Biology
1. Biosphere Land – water – atmosphere (inhabited by life).
2. Ecosystem Living thing and non-living thing with which life
interacts in particular area (forests or oceans or
deserts).
3. Community living different species in particular
ecosystem.
4. Population one species.
5. Organism one individual (Body).
6. Organs
7. Tissues
8. Cells
9. Organelles
10. Molecules
Molecules
1. Organic compounds
(macromolecules)
Carbohydrates, lipid, proteins, vitamins and nucleic acid
1. Inorganic compounds
(micromolecules)
Water and minerals
THE STRUCTURE AND FUNCTION
OF MACROMOLECULES
Polymer principles
And
Macromolecules
Introduction (Polymers principles)
• Cells link smaller organic molecules together to form larger
molecules.
• These larger molecules called macromolecules.
• The four major classes of macromolecules are: carbohydrates,
lipids, proteins, and nucleic acids.
• Most macromolecules are polymers
– Polymers consist of many similar or identical building blocks,
called monomers. Linked by covalent bonds.
• Covalent bonds are formed by a
dehydration reaction .تفاعل نزع الماء
– One monomer provides a hydroxyl group and
the other provides a hydrogen to form water.
– This process requires energy and is aided by
enzymes.
وبالعكسVise versa
• The covalent bonds connecting monomers in a polymer are disassembled
تـُكســرby hydrolysis (hydration) . بإضافة الماء
َ
– In hydrolysis as the covalent bond is broken a
hydrogen atom and hydroxyl group from a split
water molecule attaches where the covalent
bond used to be.
– Hydrolysis reactions dominate the digestive
process, guided by specific enzymes.
(Carbohydrates, Lipids, Proteins and nucleic acids)
Mono-mer Di-mer Poly-mer
أحادى ثنائى عديد
Polymer is a long molecule consists of a chain of similar
building molecules (monomers) covalently bounded together.
Polymer can be built up يـُبـ َنىby linking its monomers by
ْ
dehydration (removing H2O).
َ
Polymer can be broken down يـُكســًر إلىto its monomers by
hydrolysis (adding H2O).
THE STRUCTURE AND FUNCTION
OF MACROMOLECULES
1- Carbohydrates
Fuel and Building Material () مادة الطاقة و البناء
1. Sugars, the smallest carbohydrates, serve as fuel and carbon
sources
2. Polysaccharides, the polymers of sugars, have storage and
structural roles
Carbohydrates include sugars.
• Monosaccharides, are the simplest carbohydrates (simple sugars).
• Disaccharides, double sugars, consist of two monosaccharides joined
by dehydration.
• Polysaccharides, are polymers of many monosaccharides.
___________________
• Monosaccharides have a carbonyl group (C=O) and multiple hydroxyl
groups (O-H) .
– If the carbonly group is at the end of C chain, the sugar is called aldose
(aldehyde sugar), if not, the sugars is called ketose (Ketone sugar).
– Glucose called “aldose”, and fructose called “ketose”. They are structural
isomers.
1- Monosaccharides
Aldose Ketose
H O H
H OH
C C
Glucose Fructose
C6H12O6 H C OH O C6H12O6
C
OH C H OH H
C
H C OH H C OH
H C OH H C OH
H C OH H C OH
H H
Triose Sugar Tetrose Sugar Pentose Sugar Hexose Sugar
H
H OH
H O H O C
H O
C C C C O
H C OH H C OH H C OH OH C H
H C OH H C OH H C OH H C OH
H H C OH H C OH H C OH
H H C OH H OH
C
Types of monosaccharides, based
on the number of C atoms H H
• Monosaccharides are also classified by the number of carbons in the backbone.
– Glucose and other six carbon sugars are hexoses .سداسى
– Five carbon backbones are pentoses خماسىand three carbon sugars are trioses .ثالثى
Aldehyde
sugars
Ketone
sugars
Summary
Monosaccharides are classified into :-
A- Based on the location of C=O
Aldoses: are the monosaccharides of carbonyle group (C=O)
at the end of C chain (e.g. Glucose).
Ketoses: are the monosaccharides of C=O carbonyle
group within داخلthe C chain (e.g. Fructose).
B- Based on the number of C in the skeleton
Triose (3C): e.g. Glyceraldehyde.
Pentose (5C): e.g. Ribose.
Hexose (6C): e.g. Glucose, Fructose and Galactose.
2- Disaccharides السكر الثنائى
Consist of 2 monosaccharide molecules during a dehydration
reaction .تفاعل نزع الماء
1- Maltose (malt sugar)
2(C6H12O6) C12H22O11 + H2O
2 Glucose Maltose
2- Lactose (milk sugar): consists of Glucose + Galactose.
3- Sucrose (table sugar): consists of Glucose + Fructose.
3- Polysaccharides السكر العديد
Consist of few hundreds to few thousands of monosaccharides.
They are two types:
1- Storage .تخزينية Provide sugar for cell, when needs, by hydrolysis
2- Structural .تركيبية Serve as building materials for the organism
A)- Storage Polysaccharides
I- Starch النشا
A storage polysaccharide of plants (within plastids).
It is consisted of thousands of α glucose molecules.
Thus, it gives glucose when hydrolysed بإضافة الماءby special enzymes
in human.
Potatos and grains are the major source of starch.
II- Glycogen
Stored in animal cells (e.g. liver and muscle cells in Human).
It is consisted of thousands of glucose molecules.
Thus, it gives glucose when hydrolysed.
B)- Structural Polysaccharides
I- Cellulose
It is the building material of plants (cell wall).
Forms the micro-fibrils and cell wall in plants.
It is consisted of thousands of β glucose molecules.
Human cannot digest it, but some bacteria and protozoa can (e.g.
in Termites and Cows stomach).
Arrangement
of cellulose
in plants
• The enzymes that digest starch cannot hydrolyze
the beta linkages in cellulose.
– Cellulose in our food passes through the digestive tract
and is eliminated in feces as “insoluble fiber”.
– As it travels through the digestive tract, it abrades يثيرthe
intestinal walls and stimulates the secretion of mucus.
• Some microbes can digest cellulose to its glucose
monomers through the use of cellulase enzymes.
• Many eukaryotic herbivores ,آكالت العشبlike cows and
termites, have symbiotic relationships with
cellulolytic microbes, allowing them access to this
rich source of energy.
II- Chitin الكيتين
It is the building material of the cuticle الجـلَيدin insects.
ُ
It is consisted of thousands of glucose molecules with a N atom
in one end.
It is used to manufacture the surgical threads.
Carbohydrates
No. of C atoms No. of sugar molecules
Triose (3C) Pentose (5C) Hexose (6C)
Glyceraldehyde Ribose Glucose
Monosaccharides Disaccharides Polysaccharides
Glucose, galactose & Fructose Maltose, Lactose & Sucrose
Location of Carbonyl Group
Storage Structural
Starch (in plants) Cellulose (in plants)
Aldose Ketose & &
Glycogen (in animals) Chitin (in insects)
C=O group C=O group
is Terminal in middle
THE STRUCTURE AND FUNCTION
OF MACROMOLECULES
3) Proteins :- Many Structures, Many Functions
1. A polypeptide is a polymer of amino acids connected in a specific sequence
2. A protein’s function depends on its specific conformation
3) Proteins
Their functions include structural support, storage, transport of
other substances, intercellular signaling ,اإلشارات بين الخلويةmovement,
defense against microbes and work as enzymes in the cell that
regulate metabolism .األيض
Humans have tens of thousands of different proteins, each with
their own structure and function.
All protein polymers are constructed from تتركب منthe same set of 20
monomers, called amino acids.
Polymers of proteins are called polypeptides .ببتيدات عديدة
A protein consists of one or more polypeptides folded and coiled
into a specific conformation
- Monomer of amino acid includes a hydrogen atom, a carboxyl
group, an amino group, and a variable متغيرةR group (or side chain),
all covalently bonded to C atom.
General Formula H H O
of the Amino
Acid: N C C
H OH Carboxyl
Amino
group
R group
Side chain
- The side chain R links with ترتبط بـdifferent compounds
- Differences in R groups produce the 20 different amino acids.
- The physical and chemical characteristics صفاتof the R group
determine تحددthe unique characteristics of a particular amino acid.
Amino acids األحماض األمينية
1. Hydrophobic: the amino acids that have hydrophobic R groups
(non-polar).
2- Hydrophilic: the amino acids that have polar R groups, making
them hydrophilic.
3- Ionized: the amino acids with functional groups that are charged
(ionized) at cellular pH (7). So, some R groups are bases, others are
acids.
The Peptide Bond الرابطة البيبتيدية
Peptide bond formed between the carboxyl group of one amino acid
and the amino group of the other by dehydration.
H H O H H O
N C C N C C
H OH H OH
R R
Dehydration
Peptide bond
نزع الماء
Amino acids Peptide Polypeptide (Protein)
• Amino acids are joined together when a dehydration reaction removes a
hydroxyl group from the carboxyl end of one amino acid and a hydrogen
from the amino group of another. The resulting covalent bond is called a
peptide bond.
• Repeating the process over and over عدة مراتcreates a long polypeptide chain.
– At one end is an amino acid with a free amino group the (the N-terminus)
and at the other is an amino acid with a free carboxyl group the (the C-
terminus).
• The repeated sequence (N-C-C) is the polypeptide backbone.
• Attached to the backbone are the various R groups.
• Polypeptides range in size from a few monomers to thousands.
Levels of Protein Structure
• The folding إلتفافof a protein from a chain of amino acids
occurs spontaneously .ذاتيا
• There are three levels of structure:
primary ,أولىsecondary ,ثانوىand tertiary ثالثىstructure,
are used to organize the folding within a single peptide
chain.
• Quaternary رُباعىstructure arises when two or more
polypeptides (proteins) join to form another kind of
protein.
1. Primary structure:
It is a single peptide
chain of amino acids.
– Lysozyme, an enzyme that
attacks bacteria, consists of a
polypeptide chain of 129
amino acids.
– A slight change تغيير طفيفin the
primary structure can affect a
protein’s conformation and
ability to function.
• Sickle cell disease :خاليا الدم المنجلية
an abnormal hemoglobin because of a single amino acid
substitution .تغيير
– These abnormal hemoglobin crystallize, deforming يكسرthe red blood
ُ
cells and leading to clogs إنسدادin tiny blood vessels .أوعية
2. The secondary structure:
Results from hydrogen bonds at regular intervals على أبعاد متساويةalong
the polypeptide backbone.
A. Coils ( الحلزونىα-helix)
are typical shapes
that develop from
secondary structure
B. Folds (β-pleated sheets)
.الشيت المجعـدComposed
ُ
of several parallel α-helix
coils attached by H bonds
An example for folds (β-pleated sheets) :الشيت المُجعد
Is the structural properties of silk الحريرbecause of the presence of
so many hydrogen bonds makes each silk fiber stronger than steel.
3. Tertiary structure:
is determined by a variety of interactions among خاللR groups and
between R groups and the polypeptide backbone.
– These interactions include weak bonds like hydrogen bonds
among polar areas, ionic bonds between charged R groups,
and hydrophobic interactions and Van der Waals interactions
among hydrophobic R groups.
- Also include disulfide bridges,
strong covalent bonds that
form between the sulfhydryl
groups (SH) of cysteine
monomers, stabilize the
structure.
4- The quaternary structure:
Results from the aggregation تجمعof two or more
polypeptide chains.
Collagen is a fibrous protein of three polypeptides that are
supercoiled, and function in connective tissues.
Hemoglobin
is a globular protein with
two copies of two kinds
of polypeptides (2α and
2β).
Collagen Hemoglobin
The 4 forms of protein
Denaturation of protein فرد البروتين
ْ
• It is the change of protein’s conformation in response to
إستجابة لـthe physical and chemical conditions.
• For example, alterations تغييرin pH, salt concentration,
temperature, or other factors can denature يفردa protein.
– These forces break the hydrogen bonds, ionic bonds, and
disulfide bridges that maintain the protein’s complicated shape.
• Some proteins can return to their original shape again
after denaturation, but others cannot.
فرد البروتين Denaturation of protein
فرد
مفرود
إعادة إلى طبيعته
Hydrophobic (non-polar R group)
Amino
Hydrophilic (polar R group)
acids
Ionized (charged functional groups)
Peptides Polypeptides Proteins
Primary Secondary Tertiary Quaternary
structure structure structure structure
Single chain H bonds 1- Hydrophobic two or more
of amino acids Interaction polypeptide
Coils & (Van der Waals chains
e.g. Lysozyme Folds interaction);
2- H bonds; e.g. Collagen
e.g. silk 3- Ionic bonds; & Hemoglobin
4- Di-sulfide
bridges;
Lipids;
The Hydrophobic Molecules
1. Fats store large amounts of energy
2. Phospholipids are major components of cell membranes
3. Steroids include cholesterol and certain hormones
1) Fats:
• Lipids are an exception among macromolecules
because they do not have polymers.
• The unifying feature الصفة المميـٍزةof lipids is that they all
َُ
have little or no affinity for water .ال تـَمتزج بالماء
– This is because their structures are dominated by non-polar
covalent bonds.
• Lipids are the components مكوناتof fats, and are highly
ُ
diverse in form and function.
• Although fats are not polymers, they are large
molecules assembled from تتكون منsmaller molecules by
dehydration reactions.
• A fat is constructed from two kinds of smaller
molecules, glycerol and fatty acids .أحماض دُهنية
Glycerol H
O H H
Fatty Acid
H H
H C C C H
OH C C C
H C OH H H
Ester link H H H
H C OH
H C OH Dehydration
H
A fat is composed of three fatty acids linked with one glycerol molecule.
Fats are classified into Saturated مشبعand Un-saturated غير مشبعfats
Glycerol consists of a three C skeleton with an OH group attached to each C.
A fatty acid consists of a carboxyl group (COOH) attached to a long
carbon skeleton, often 16 to 18 carbons long.
• The many non-polar C-H bonds in the long hydrocarbon skeleton
make fats hydrophobic.
• In a fat, three fatty acids are joined to glycerol by an ester linkage,
رابطة إستيريةcreating a triacylglycerol.
• Fatty acids may vary تختلفin length (number of carbons) and in the
number and locations of double bonds.
– If there are no carbon-carbon double bonds, then the molecule is a
saturated fatty acid ( مشبعhas H at every possible position).
•If there are one or more carbon-carbon double bonds, then the
molecule is an unsaturated fatty acid - حامض دهنى غير مشبعformed by the
removal of H atoms from the carbon skeleton.
A)- Saturated Fats الدهون المشبعة
The Fatty acid components are saturated (there is no double bonds
between the carbons. All C are linked with H.
Thus, it is saturated with H.
Most animal fats are saturated.
They are solid at room temperature.
Saturated fats-rich diet results in Atherosclerosis .التصلب الشريانى
B)- Un-saturated Fats الغير مشبعة الدهون
These double bonds are formed by the removal of H atoms.
Most vegetable fats (oils) and fish fats are unsaturated.
They are liquid at room temperature.
They can be synthetically converted to saturated (solid) by adding H
(Hydrogenation .)الهدْ رﭽـَة
َ َ
• The major function of fats is energy storage.
– A gram of fat stores more than twice as much energy as a
gram of a polysaccharide.
– Humans and other mammals store fats as long-term
energy reserves كمخزون طاقة طويل المدىin adipose cells .خاليا دهنية
2) Phospholipids;
Are major components of cell membranes
• Phospholipids have two fatty acids attached to glycerol and a
phosphate group at the third position.
– The phosphate group carries a negative charge.
• The interaction of
phospholipids with
water is complex.
• The fatty acid tails are
hydrophobic, but the
phosphate group and
its attachments form
a hydrophilic head.
• When phospholipids are added to
water, they self-assemble تتشكل ذاتيا
into aggregates تجمعاتwith the
hydrophobic tails pointing toward
the center and the hydrophilic
heads on the outside.
– This type of structure is called a
micelle .الزهرة
• At the surface of a cell
phospholipids are arranged as a
bilayer .طبقة مزدوجة
– Again, the hydrophilic heads are on
the outside in contact with the
aqueous solution المحلول المائىand the
hydrophobic tails in the core .المركز
– The phospholipid bilayer طبقة مزدوجة
forms a barrier حاجزbetween the cell
and the external environment البيئة
.الخارجية
• They are the major component of cell
membranes.
3) Steroids:
Include cholesterol and certain hormones
• Steroids are lipids with a carbon skeleton consisting of four fused
ملتحمةcarbon rings.
– Different steroids are created by varying functional groups attached to
the rings.
• Cholesterol, an important
steroid, is a component in
animal cell membranes.
• Cholesterol is also the precursor المادة الخامfrom which all other
steroids are synthesized.
• Many of these other steroids are hormones, including the sex
hormones.
• While cholesterol is clearly an essential molecule, high levels of
cholesterol in the blood may contribute to Atherosclerosis تصلب الشرايين
Fats
(Composed of Lipids)
Saturated Unsaturated Phospholipids Steroids
Animal Fats Vegetable Fats Bi-layer of cell Sex Hormones
membrane & Cholesterol
Hydrogenation
هَـدْ رﭽـَــــــــة
َ
CHAPTER FUNCTION
THE STRUCTURE AND 5
THE STRUCTURE AND FUNCTION
OF MACROMOLECULES
OF MACROMOLECULES
4- Nucleic Acids:
The Informational Polymers
1. Nucleic acids store and transmit
hereditary information المعلومات الوراثية
2. A nucleic acid strand is a polymer
of nucleotides
3. Inheritance is based on
replication of the DNA
double helix
DNA Structure
• DNA is located in the nucleus
• There are two types of nucleic acids
ribonucleic acid (RNA)
And
deoxyribonucleic acid (DNA).
Structures of nucleic acids (DNA & RNA)
3 5 o Phosphate Bases
group
o P o
o DNA Adenine
Base nucleotide
(A)
5 CH2 o Purine
4 H H 1
H
H
Guanine
3 2H (G)
o
Deoxyribose sugar
o P o
o
Base Cytosine
CH2 o (C) Pyrimidine
H H
H
H Thymine
3
5 3 H
(T)
Sugar-phosphate backbone
• The PO4 group of one
nucleotide is attached
to the sugar of the
next nucleotide in line
.فى صف مستقيم
• The result is a
“backbone” of
alternating تبادل
phosphates and
sugars, from which
the bases starts.
Nitrogenous bases القواعد النيتروجينية
3 5
Hydrogen bonds
Nitrogenous bases
Cytosine Guanine
(C) (G)
Thymine Adenine
(T) (A)
Uracil (U)
Pyrimidines Purine
5 3
Sugar-phosphate
backbones
DNA
• Adenine (A) would
form 2 hydrogen
bonds only with
thymine (T)
• Guanine (G) would
form 3 hydrogen
bonds only with
cytosine (C).
DNA & RNA
CH2 o CH2 o
H H
H H H
H H
H H
OH
Deoxyribose sugar Ribose sugar
(O on C2 is missed) (no missed O)
Deoxiribo-Nucleic-Acid Ribo-Nucleic-Acid
Double stranded nucleic acid Single stranded nucleic acid
Bases: A, G, C, T Bases: A, G, C, U
The nucleic acid strand is
a polymer of nucleotides
• Nucleic acids are polymers of monomers called nucleotides.
• Each nucleotide consists of three parts: a nitrogen base, a pentose
sugar, and a phosphate group.
• The nitrogen bases (rings of carbon and nitrogen) come in two types:
Purines and Pyrimidines.
• The pentose sugar joined to the nitrogen base is ribose in
nucleotides of RNA and deoxyribose in DNA.
• The only difference between the sugars is the lack نقصof an oxygen
atom on carbon 2 in deoxyribose.
• Polynucleotides are synthesized by connecting the
sugars of one nucleotide to the phosphate of the next
with a phosphodiester link.
• This creates a repeating backbone of sugar-phosphate
units with the nitrogen bases as appendages.
• The sequence of nitrogen bases along a DNA or mRNA
polymer is unique for each gene.
• Genes are normally hundreds to thousands of
nucleotides long.
• The linear order الترتيب التتابعىof bases in a gene specifies
يحددthe order of amino acids ( ترتيب األحماض األمينيةthe monomers of a
ُ
protein).
Inheritance is based on replication of the DNA double helix
• An RNA molecule is single polynucleotide chain (single strand).
• DNA molecules have two polynucleotide strands (double strand)
that spiral around تدور حلزونياto form a double helix .حلزون مزدوج
• The sugar-phosphate
backbones of the two
polynucleotides are on
the outside of the helix.
• Pairs of nitrogenous
bases (one from each
strand) connect the
polynucleotide chains
with hydrogen bonds.
• Most DNA molecules
have thousands to
millions of base pairs
( زوج من القواعدbP).
• Because of their shapes, only some bases are compatible متوافقة
with each other.
– Adenine (A) always pairs with thymine (T) and guanine (G) with
cytosine (C).
• With these base-pairing rules, if we know the sequence of bases on
one strand, we know the sequence on the opposite المقابلstrand.
• The two strands are complementary .مكملين لبعضهما
• During preparations for cell division each of the strands serves as
a template قالب نسخto order nucleotides into a new complementary
strand.
• This results in two identical copies نسختين طبق األصلof the original
double-stranded DNA molecule.
– The copies are then distributed توزعto the daughter cells.
• This mechanism ensures that the genetic information is
transmitted to the new cells.
Repeated Sugar - Phosphate DNA backbone
Sugar–Phosphate-Base One nucleotide
Polynucleotide
DNA Molecule
DNA Double stranded
RNA single stranded
DNA A G C T A T C
mRNA U
T C G A T
U A G
A TOUR OF THE CELL
Panoramic View of the Cell
Cell Theory
1- All organisms are composed of one or
more of cells.
2- Cell is the basic unit of life.
3- The new cell arises only from pre-existing
الموجودة cell.
The Cell Cellulae (Small room)
The Organism’s Basic Unit of Structure and Function
Types of cells
متقدمة
بدائية
Prokaryotic Eukaryotic
Micro-organisms All other forms
الكائنات الدقيقة of life
Prokaryotic and eukaryotic cells
differ in size and complexity
Similarities أوجه ألتشابه
• All cells are surrounded by a plasma membrane .غشاء بالزمى
• The semi-fluid substance المادة النصف سائلةwithin the cell is the cytosol,
السيتوبالزمcontaining the cell organelles .عِ ضيات الخلية
• All cells contain chromosomes which have genes in the form of DNA.
• All cells also have Ribosomes, tiny organelles عضيات صغيرةthat make
proteins using the instructions التعليماتcontained in genes.
Prokaryotic and eukaryotic cells
differ in size and complexity
Differences أوجه ألختالف
إ
• A major difference الفرق األساسىbetween prokaryotic and
eukaryotic cells is the location of chromosomes .موضع الصبغيات
– In an eukaryotic cell, chromosomes are contained in a true nucleus (.) النواة
– In a prokaryotic cell, the DNA is concentrated in the nucleoid ()شـبه نواة
without a membrane ( ) بدون غـشاءseparating it from the rest of the cell.
– In prokaryotic cell, DNA is a single strand ( )أحادى الشريطor double strand
( )ثنائى الشريطDNA. But in eukaryotic cell, DNA is double strand.
Eukaryotic Cell
Eu: True
Karyon: Nucleus
Animal Cell Plant Cell
What are the functions of cell organelles ?
الشبكة اإلندوبالزمية المادة الوراثية
نوية
النواة
الجدار النووى
سوط حركى
جسم مركزى
ريبوسوم
حلمات دقيقة حهاز جولـﭽـى
غشاء بالزمى
ميتوكوندريا
الهيكل الخلوى جسم محلل
ُ
The Cell Organelles
عضيــات ألخلي ـ ـ ـ ــة
1. The nucleus
- The nucleus contains most of the genes in an eukaryotic cell.
- The nucleus averages about 5 µm in diameter.
• a. Nuclear envelope
Structure:
• The nucleus is separated from the cytoplasm by a
double membrane .غشاء مزدوج
• Where the double membranes are fused, a pore ثقوبis
formed
Functions:
• 1. Pores allows macromolecules to pass through.
• 2. The nuclear membrane الغالف النووىis maintaining the
• shape of the nucleus
• b. Chromatin
Structure:
• Within the nucleus, the DNA and associated proteins are
organized into fibrous material, chromatin.
• At the time of division, the chromatin fibers coil up تلتفto be
seen as separate structures, chromosomes.
• Each eukaryotic species has a characteristic number of
َُ
chromosomes .رقم مميـ ٍز من الكروموسومات
- A typical human cell has 46 chromosomes (23 pairs), but sex
cells (ovum and sperm) have only 23 chromosomes.
Functions:
1. Chromatin have genes that determine تحددthe general
characters الصفات العامةof organism.
2. The nucleus directs protein synthesis by synthesizing
messenger RNA (mRNA).
– The mRNA travels to the cytoplasm and combines with ribosomes
where the primary structure of a specific protein is formed.
c. Nucleolus
• Nucleolus is a dark region involved in
the production of ribosomes.
2. Ribosomes
• Ribosomes contain ribosomal RNA (rRNA) and protein.
• A ribosome is composed of two subunits وحدتينthat combine تتحدto
direct protein synthesis .تخليق البروتين
حرة
مرتبطة
• In the nucleolus, ribosomal RNA (rRNA) is synthesized
into ribosomal subunits (rRNA + proteins).
• The subunits pass from the nuclear pores to the
cytoplasm where they combine to form ribosomes.
• - Cell types that synthesize large quantities of proteins (e.g.,
pancreas) have large numbers of ribosomes.
• Ribosomes are 2 types:-
1. Free ribosomes are suspended معلقin the cytosol and
synthesize proteins that function within the cytosol.
2. Bound ribosomes are attached to ملتصق بـthe outside of the
endoplasmic reticulum.
– This type of ribosomes synthesize proteins that are either
included into membranes or for secretion outside the cell.
3- The Endomembrane System
a) The endoplasmic reticulum manufacturers membranes
and performs many other biosynthetic functions
b) The Golgi apparatus finishes, sorts, and ships cell
products
c) The Lysosomes are digestive compartments
d) The Vacuoles have diverse functions in cell
maintenance
a)- Endoplasmic reticulum
manufacturers membranes and performs many other
biosynthetic functions
• The ER includes
membranous tubules
• There are two types of ER
that differ in structure and
function.
1. Smooth ER looks smooth
because it lacks ribosomes.
2. Rough ER looks rough خشنة
because ribosomes (bound
ribosomes) are attached to
its membranes, including the
outside of the nuclear
envelope.
• The smooth ER:
- It is rich in enzymes and plays a role in metabolic
processes.
- Its enzymes synthesize lipids ( دهونoils, phospholipids,
and steroids) including the sex hormones .الهرمونات الحنسية
- Extensive توجد بكثرةin the liver, it helps detoxify إبطال األثر السام
drugs المخدراتand poisons السموم
• The rough ER: it contains ribosomes
- is the main site of protein synthesis.
- It is especially abundant متوفرةin those cells that secrete
proteins.
- These secretory proteins are packaged in transport
vesicles that carry them to their next stage.
b)- Golgi apparatus:
finishes, sorts ,تـُجهزpackaging and ships تنقلcell products
َ
• Many transport vesicles أوعية ناقلةfrom the ER travel to the
Golgi apparatus for modification تطويرof their contents.
• The Golgi function is manufacturing ,تصنيعwarehousing
,تغليفsorting ( تـَجْ هيزPackaging), and shipping نقلmaterials to
outside the cell.
• The Golgi apparatus is extensive specially in secretory
cells .خاليا إفرازية
• The Golgi also manufactures polysaccharides.
وعاء ناقل
c)- Lysosomes األجسام المُحللة are digestive components
• The lysosome is a membrane-bounded sac of enzymes that digests
macromolecules.
• Lysosomal enzymes can hydrolyse proteins, fats,
polysaccharides, and nucleic acids.
• These enzymes work best at pH = 5 (acidic).
• While rupturing إنفجارlysosomes can destroy the cell by
autodigestion (autophagy) .الهضم الذاتى
• The lysosomal enzymes and membrane are
synthesized by rough ER and then transferred to تنقل إلى
the Golgi then to lysosomes.
• Lysosomes can fuse with food vacuoles الفحجوة الغذائيةto
digest food, (when a food item is brought into the cell
by phagocytosis).
• Lysosomes can also fuse with another organelle or
part of the cytosol. This process of autophagy called
recycling which renews the cell
d)- Vacuoles الفجواتhave diverse functions وظائف متنوعة
in cell maintenance للحفاظ على الخلية
• Vesicles أوعـيةand vacuoles فجواتare
membrane-bound sacs أكياس ذات أغشيةwith varied
functions.
1. Food vacuoles ,فجوة غذائيةfrom phagocytosis, fuse with lysosomes.
2. Contractile vacuoles ,فجوة منقبضةfound in freshwater protists, pump
excess water out of the cell.
3. Central vacuoles فجوة مركزيةare found in many mature plant cells.
Animal cell
Other Membranous Organelles
1)- Peroxisomes (exists in the liver cells):
generate and degrade H2O2 in performing various metabolic functions
• Peroxisomes contain enzymes that transfer hydrogen from various
substrates to oxygen
– An intermediate product of this process
is hydrogen peroxide (H2O2), a poison,
but the peroxisome has another enzyme
that converts H2O2 to water.
– Some peroxisomes break fatty acids down
to smaller molecules that are transported to
mitochondria for fuel .إلنتاج الطاقة
– They detoxify alcohol and other harmful
compounds. Thus, it exists extensively in
the liver cells
2- Mitochondrium: is the main energy transformer of cells
• Mitochondria organelles converts energy to forms that cells can
use for work.
• Mitochondria are the sites of cellular respiration, generating تـُنتِج
ATP (Adenosine TriPhosphate) from the catabolism هدمof sugars,
fats, and other fuel sources مصادر طاقةin the presence of oxygen.
• Mitochondria are mobile and move around the cell along tracks in
the cytoskeleton.
• Mitochondria have a smooth outer membrane and a highly folded
inner membrane forming cristae .نتوءات
• The inner membrane encloses the mitochondrial matrix, a fluid-filled
space with DNA, ribosomes, and enzymes.
The Cytoskeleton الهيكل الخلوى
The cytoskeleton is a network of fibers extending throughout تمتد عبرthe cytoplasm
Functions:
• The cytoskeleton organizes يرتب
the structures and activities of the cell.
• functions in cell motility.
Cytoskeleton
Intermediate
Microtubules Microfilaments filaments
أنيبيبات دقيقة ألياف دقيقة ألياف متوسطة
Thick Thin Middle
سميكة رفيعة متوسطة
Responsible for cell Transport Reinforcing the cell
motility, and materials within shape and fixing
separation of the cell. position of
chromosome during organelles.
(Actin protein)
cell division.
(Fibrous protein)
(Tubulin protein)
• The cytoskeleton provides mechanical support and maintains
shape of the cell.
• The cytoskeleton is dynamic, حركيdismantling يتفككin one part and
reassembling يتركبin another to change cell shape.
• The cytoskeleton also plays a major role in cell motility حركة الخليةby
interacting with motor proteins .البروتين الحركى
– In cilia, flagella and muscle cells
motor proteins pull components
of the cytoskeleton past each
other.
• Microtubules functions as tracks قضيبthat guide motor proteins
to circulates materials within the cell.
• Motor molecules carry vesicles or organelles to various
destinations إلى أماكن مختلفةinside cell.
• They move chromosomes during cell division
• In many cells, microtubules grow out from a centrosome
الجسم المركزىnear the nucleus.
• In animal cells, the centrosome has a pair of centrioles,
each with 9 triplets of microtubules تسعة مجموعات كل منها مكون من ثالثة أنيبيبات
arranged in a ring .مرتبة دائريا
ُ
Cilia and Flagella
• Microtubules are the central structural supports both
cilia األهدابand flagella .األسواط
– Both can move unicellular and small multicellular organisms by
propelling water outside the organism.
• Cilia usually occur in large numbers on the cell surface.
• Flagella usually occur in just one or a few per cell.
• Cilia move more like oars مجاديفwith alternating power
and recovery strokes.
• Flagella have an undulatory movement .حركة تموجية
• So, They differ in their beating pattern .أسلوب الحركة
cilia
flagellum
Both cilia and flagella have the same ultrastructure .التركيب الدقيق
Both have a core مركزof microtubules sheathed by the plasma
membrane.
Nine doublets (9 + 2 pattern) تسعة مجموعات كل منها مكون من أنيبيبتانof
microtubules arranged around a pair at the center.
Flexible “wheels” of proteins connect outer doublets to each other
and to the core.
The outer doublets
are also connected
by motor proteins.
The structure of cilium
and flagellum is
identical to that of
centriole.
• Cilia and flagella are formed of arms of a motor
protein (dynein .)بروتين الداينين
– Addition phosphate group from ATP to dynein and its
removal causes conformation changes in the protein.
– Dynein arms alternately
grab, move, and release
the outer microtubules.
– Protein cross-links limit
sliding and the force is
expressed as bending.
7- Cell membrane
• The plasma
membrane
functions as a
selective barrier
حاجز إختيارىthat
allows passage
of oxygen,
nutrients, and
wastes for the
whole volume of
the cell.
Cell membrane
Composed of lipids (phospholipids) and proteins
Lipid layer contains hydrophilic and hydrophobic regions
Carbohydrate chains
Hydrophilic مُحب للماء
Phospholipid
Hydrophobic كاره للماء
Proteins
CHAPTER 5
MEMBRANE STRUCTURE AND
THE STRUCTURE AND FUNCTION OF
MACROMOLECULES
FUNCTION
How things get into and out of the cell
Section A: Membrane Structure
The plasma membrane separates the living cell from its nonliving
surroundings.
This thin barrier, 8 nm thick, controls traffic into and out of the cell.
Like other membranes, the plasma membrane is selectively
permeable, allowing some substances to cross more easily than
others.
The main macromolecules in membranes are lipids and proteins,
but include some carbohydrates.
The most abundant lipids are phospholipids.
Phospholipids and most other membrane constituents are
amphipathic molecules.
Amphipathic molecules have both hydrophobic regions and
hydrophilic regions.
The phospholipids and proteins in membranes create a fluid
mosaic model.
proteins embedded or attached to a double layer of phospholipids.
The molecules in the bilayer طبقة مزدوجةare arranged as hydrophobic
fatty acid tails are sheltered محميةfrom water while the hydrophilic
phosphate groups interact with water.
Membrane proteins are amphipathic, with
hydrophobic and hydrophilic regions.
If at the surface, the hydrophilic regions
Fig. 8.1b
would be in contact with water.
In this fluid mosaic
model, the hydrophilic
regions of proteins and
phospholipids are in
contact with water and
the hydrophobic regions
are in a nonaqueous environment.
Fig. 8.2b
Cell membrane is fluid
• Most of the lipids and some proteins can drift
laterally in the plane of the membrane, but
rarely flip-flop from one layer to the other.
• The lateral movements of phospholipids are
rapid, about 2 µm/second.
• Many larger membrane proteins move more
slowly but do drift.
• As temperatures cool, membranes switch
from a fluid state to a solid state as the
phospholipids are more closely packed.
• Membranes rich in unsaturated fatty acids
are more fluid than those dominated by
saturated fatty acids because the kinks
in the unsaturated fatty acid tails prevent
tight packing.
• To work properly with permeability, membrane must be fluid, about
as fluid as oil.
Membranes are mosaics of structure and function
• A membrane is a collage تـَجمُّعof different proteins embedded
َ
مُـ ْنغمسin the fluid matrix of the lipid bilayer.
ِ َ
A)- The plasma membrane has a unique collection تجمع مميـزof proteins.
َ
• There are two populations of membrane proteins.
1. Integral proteins مُندَمجpenetrate the hydrophobic core of the lipid
bilayer (transmembrane protein).
2. Peripheral proteins طرفىare not embedded in the lipid bilayer at all.
Instead, they are loosely bounded to the surface of the integral
proteins.
• The integral proteins has a middle
area, hydrophobic regions with
Periphera
nonpolar amino acids. Integral
l proteins
proteins
• And surface area, in contact with the
aqueous environment, they have
hydrophilic regions of amino acids.
Periphera
l proteins
• The proteins in the plasma membrane may provide a variety of major
cell functions.
B)- Membrane carbohydrates are important for cell-cell
recognition
• The membrane plays the key role in cell-cell recognition.
– Cell-cell recognition is the ability of a cell to distinguish one type
of neighboring المجاورةcell from another.
– It is the basis for rejection of foreign cells by the immune system.
– Cells recognize other cells by recognizing the surface molecules,
often carbohydrates, on the plasma membrane.
– Membrane carbohydrates may be covalently bonded either to
lipids, forming glycolipids, or, to proteins, forming glycoproteins.
– The four human blood groups (A, B, AB, and O) differ in the
external carbohydrates on red blood cells.
1- Selective permeability النفاذية اإلختيارية
one of the most important functions of cell membrane (Plasma membrane)
A steady traffic العبور المنتطمof small molecules and ions move across
the plasma membrane in both directions.
For example, sugars, amino acids, and other nutrients enter a muscle
cell and metabolic waste products leave it.
The cell absorbs O2 and expels CO2.
It also regulates concentrations of inorganic ions, like Na+, K+, Ca2+,
and Cl-, by passing them across the membrane.
However, substances do not move across the membrane barrier
indiscriminately .عشوائيا
Hydrophobic molecules, like hydrocarbons, CO2, and O2, can
dissolve in the lipid bilayer and cross easily.
Ions and polar molecules, like water, glucose and sugars pass
through with difficulty.
Proteins can assist and regulate يساعد و ينظمthe transport of ions and
polar molecules.
Selective Permeability
CO2
CO2
Nucleus
O2
O2
The cell is able to take up تـنـتـقىparticular
molecules and exclude تـتجنبothers
2- Passive transport اإلنتقال السلبىis diffusion across a membrane
• Diffusion: اإلنتشار
Is the tendency إستعدادof molecules of any substance to spread out لإلنتشارin the
available space randomly .عشوائيا
• For example, a permeable membrane غشاء منفذseparating a solution with dye
molecules from pure water, dye molecules will cross the barrier randomly.
• The dye will cross the membrane until both solutions have equal
concentrations of the dye (dynamic equilibrium .)التعادل الديناميكى
• A substance will diffuse from where it is more concentrated to where
it is less concentrated, down its concentration gradient .مـُنحدر التركيز
• Passive transport: اإلنتقال السلبى
is the diffusion of a substance across a biological membrane which
requires no energy.
• The concentration gradient drives diffusion.
Osmosis : األسموزيةis the passive transport of water
• Differences in concentration of dissolved materials in two solutions
can lead to the movement of ions from one to the other.
• The solution with the higher concentration of solutes is hypertonic.
• The solution with the lower concentration of solutes is hypotonic.
• Solutions with equal solute concentrations are isotonic.
• Osmosis:
Is a passive transport in which water
diffuses across a selectively permeable
membrane from the hypotonic solution
to the hypertonic solution until the
solutions become isotonic.
Principal of water movement
Osmosis Osmosis
Isotonic
Selectively
permeable
membrane
Low conc. of sugar High conc. of sugar
hypotonic hypertonic
Passive transport of water (Osmosis)
• Hypertonic solution: عالى التركيز
contains high concentration of solute مُذابmolecules.
• Hypotonic solution: منخفض التركيز
contains low concentration of solute molecules.
• Isotonic solution: متعادل
contains equal concentrations of solute molecules
Biological
Membrane
H2O
Hypertonic Hypotonic
Osmoregulation التوازن األسموزى
• A cell in a hypotonic solution will
gain تسحبwater, swell, and burst.
• The cell in a hypertonic
environment will loose water,
shrivel ,تنكمشand die.
• Organisms without rigid walls
have osmotic problems in either
a hypertonic or hypotonic
environment and must have
adaptations for osmoregulation
to maintain للحفاظ علىtheir internal
environment.
• Example, Paramecium have a
specialized organelle (the
contractile vacuole), that
functions as a pump to force يطرد
water out of the cell.
Specific proteins facilitate تـُسهـِّلpassive transport
َ
• Many polar molecules and ions diffuse passively through the lipid bilayer
with the help of transport proteins (gated channels .)قنوات م َبوبة
ُ
• The passive movement of molecules down its concentration gradient via a
transport protein is called facilitated diffusion.
• Many transport proteins simply provide
channels allowing a specific molecule or
ion to cross the membrane.
• Other transport proteins translocate
ينقلthe molecules across the
membrane as the protein changes
shape (active transport)
Active Transport النقل النشط
Active transport is the pumping ضخof solutes against their
َ
concentration gradients تزايد التركيز
• Some facilitated transport
proteins can move solutes
against their concentration
gradient, from the side where
they are less concentrated to
the side where they are more
concentrated.
• This active transport requires
metabolic energy via ATP.
• Active transport is critical بالغ األهميةfor a cell to maintain its internal
concentrations.
• Active transport is performed by specific proteins embedded in
the membranes (transport protein).
1)- Small molecules (Ions )
• The sodium-potassium pump Outside the cell
actively maintains the gradient
of sodium (Na+) and potassium Na
ions (K+) across the membrane. Na Protein
– The animal cell has higher Na molecule
concentrations of K+ and lower Na
concentrations of Na+ inside
the cell.
– The sodium-potassium pump
(T. protein) uses the energy of
one ATP to pump 3 Na+ ions
out and 2 K+ ions in. ATP
Cellular
1ATP T. protein
membrane
Low conc. High conc.
+ 2 of K
+
of K
High conc. Low conc. Inside the cell
of Na
+ 3 of Na+
Adenosine Tri-Phosphate (ATP)
Adenosine
P P P
+ H2O
Triphosphate
Energy P P P
Adenosine Di-Phosphate
Two roles of
membrane protein
Both diffusion and facilitated diffusion are forms of passive transport of molecules
down their concentration gradient, while active transport requires an investment of
energy to move molecules against their concentration gradient.
2)- Large molecules (macromolecules)
Large molecules are transported by Exocytosis and endocytosis
Small molecules and water enter or leave the cell through the lipid
bilayer or by transport proteins.
Large molecules, such as polysaccharides and proteins, cross the
membrane by vesicles .أوعية
1. Exocytosis :اإلخراج الخلوى
a transport vesicle budded from ينشأ منthe Golgi apparatus is moved
by the cytoskeleton to the plasma membrane.
When the two membranes come in contact ,تالمسthe bilayers fuse
يندمجand spill يُفرعthe contents to the outside.
2- Endocytosis ,اإلدخال الخلوى
a cell brings in macromolecules and particulate matter by forming
new vesicles from the plasma membrane and include the
following:
A)- Phagocytosis :اإلبتالع الخلوى
Called “cellular eating”. The
cell engulfs تـَ ْبلَعa particle by
extending pseudopodia أقدام
كاذبةaround it and packaging
it تـُغلفهاin a large vacuole.
• The contents of the vacuole
are digested when the
vacuole fuses with a
lysosome.
B)- Pinocytosis, الشرب الخلوى
“cellular drinking”,
a cell creates a vesicle
around droplets نقاطof
extracellular fluid السائل
.الموجود خارج الخلية
– This is a non-specific
process .عملية غير متخصصة
C)- Receptor-mediated endocytosis: اإلدخال الخلوى عن طريق المستقبالت المتخصصة
It Is called (Selective eating) which very specific in what substances are
being transported.
• It is triggered تـُستـَحثwhen extracellular substances bind to special
receptors ,مُستقبـِالت خاصةon the membrane surface. This triggers the
formation of a vesicle وعاء
• It enables a cell to take large quantities of specific materials that may
be in low concentrations in the environment.
Transport
Active Passive
Large Small Facilitated Diffusion
molecules Molecules/ions diffusion
(Membrane) (T. protein) (T. protein) (Membrane)
Exocytosis Endocytosis
Pinocytosis Receptor-mediated
Phagocytosis endocytosis
Cellular eating Cellular drinking Selective eating
Using specific
receptors (coated
vesicles) that bind to
specific legends and
engulf it. It is specific
INTRODUCTION
CHAPTER 5
TO
THE STRUCTURE AND FUNCTION
OF MACROMOLECULES
METABOLISM
Section B: Enzymes
1. Enzymes speed up metabolic reactions by lowering energy barriers
2. Enzymes are substrate specific
3. The active site in an enzyme’s catalytic center
4. A cell’s physical and chemical environment affects enzyme activity
Pages 96 - 103
Hydrolysis of sucrose (table sugar)
Dehydration
Glucose + Fructose Sucrose
Hydration (H2O)
Glucose + Fructose
Sucrase
Hydrolysis of sucrose in the presence of Sucrase results
in its two monosaccharide components.
This process include:
1- breaking the bond between Glucose and Fructose;
2- Then, forming new bonds with H+ and OH- from water
This process consumes تستهلكenergy (Activation Energy; EA)
Enzymes speed up metabolic reactions by lowering
energy barriers حواجز الطاقة
A catalyst المُحفزis a chemical agent that changes the rate of a
reaction without being consumed دون أن يستهلكby the reaction.
ُ
An enzyme is a catalytic protein.
Chemical reactions between molecules involve both bond breaking
and bond forming.
To hydrolyze (hydration) sucrose, the bond between glucose and
fructose must be broken via hydrolysis in the presence of sucrase (the
catalyst).
Sucrase
Enzymes and Activation Energy
Activation Energy: is the amount of energy needed for the
reaction (between enzyme & substrate) to complete (to break the bonds)
Raising the temperature for these reactions to complete
will either denature the compounds or kill the cell.
Thus, organisms must therefore use a catalyst .عامل محفز
Catalyst: is a chemical agent that accelerate the reaction
without being consumed by the reaction.
Enzyme is a catalytic protein بروتين مساعد/محفز
Enzyme is a specific متخصصcatalyst for specific reactants
at any time in the cell (e.g. Sucrase for only Sucrose).
Activation energy: is the amount of energy necessary to push the
reactants over an energy barrier.
At the transition state, the molecules
are at an unstable point.
The difference between free energy
of the products and the free energy
of the reactants is the delta G.
Enzyme speed reactions by
lowering EA. The transition
state can then be reached
even at moderate temperatures.
Enzymes are substrate specific
• The substrate المادة المطلوب هضمهاis a reactant which binds to an enzyme.
• When a substrate binds to an enzyme, the enzyme catalyzes يسهلthe
conversion تحويلof the substrate to the product .مكوناتها البنائية
– Sucrase (catalyst) is an enzyme that binds to sucrose (substrate) and
breaks the disaccharide into fructose and glucose (products).
Enzyme (a catalyst)
Substrate Product (s)
Sucrase
Sucrose + H2O Glucose + Fructose
Specificity of enzyme تخصصية اإلنزيمrefers to its Active Site المركز
النشطwhich fit to يـُناسبthe surface of substrate.
The active site is an enzyme’s catalytic center
The active site of an enzymes is typically a pocket or groove شكل الجيب
on the surface of the enzyme into which the substrate fits.
The specificity of an enzyme is due to the fit between the active site
and that of the substrate.
As the substrate binds, the enzyme changes shape to fit the
substrate, bringing chemical groups in position to catalyze the
reaction.
Fig. 6.14
Catalytic Cycle of Enzyme
Active site of enzyme and Catalytic Cycle
Sucrose Sucrase
Glucose
Fructose
H 2O
Catalytic Cycle of Enzyme
1- The substrate binds to the active cite of enzyme.
2- This forms an Enzyme-Substrate complex (via weak
hydrogen bonds).
3- The active cite catalyses the conversion of the
substrate to final products (original components) by
breaking bonds.
4- The resulting products release from the enzyme.
5- The enzyme starts another reaction over and over again.
6- Thus, the enzyme can have a huge metabolic effects in
the catalytic cycle.
A single enzyme molecule can catalyze thousands or more reactions
a second.
Enzymes are unaffected by the reaction and are reusable .يـُعاد استخدامها
Most metabolic enzymes اإلنزيمات األيضيةcan catalyze a reaction in both
the forward and reverse direction.
The actual direction depends on the relative concentrations of products
and reactants.
Enzymes catalyze reactions in the direction of equilibrium .التعادل
Enzymes lower activation energy and speed a reaction.
The rate that a specific number of enzymes converts substrates to
products depends in part on substrate concentrations.
At some substrate concentrations, the active sites on all enzymes are
engaged ,مشغولةcalled enzyme saturation .التشبع اإلنزيمى
Cellular factors affecting enzyme activity
• Some conditions lead to the most active conformation and lead to
optimal rate of reaction. These factors are:-
1. Temperature: has a major
impact on reaction rate.
As temperature increases,
reaction between substrate
and active sites occur faster.
However, at some point
thermal increase begins to
denature the substrate.
Each enzyme has an optimal
temperature . درجة حرارة مُثلى
Cellular factors affecting enzyme activity
2. pH also influences the reaction rate, each enzyme has
an optimal pH falls between pH 6 - 8 for most
enzymes.
• However, digestive enzymes in the
stomach are designed to work best
at pH 2 while those in the intestine
are optimal at pH 8, both matching
their working environments.
Fig. 6.16b, page 100
3. Cofactors (coenzymes): العوامل المساعدة
A non-protein helpers for catalytic activity of enzymes. They bind
permanently دائماto the enzyme and include two types:-
a) Inorganic cofactors, include zinc, iron, and copper.
b) Organic cofactors, include vitamins or molecules derived
from vitamins.
Enzyme inhibitors: مُـثـبِّطات اإلنزيمات
They are molecules that prevent enzymes from catalyzing reactions.
– If thy covalently bind with enzyme, inhibition is irreversible .غير منعكس
– If binding is weak, inhibition may be reversible .مُنعكس
• If the inhibitor binds to the same site as the substrate, then it
called competitive inhibition .تثبيط تنافسى
• If the inhibitor binds somewhere
other than the active site, then it
called noncompetitive inhibition.
Types of Inhibitors:
A- Competitive: That resemble the substrate molecule and thus competes
the attach to the active site (blocking the active site).
B- Noncompetitive: They do not compete the substrate directly at the active
site. Rather, they bind with another part of the enzyme resulting in
changing enzyme shape. Finally, deactivate يـُخمدthe active site.
Activation and inhibition of enzymes are essential
for metabolic control
The insecticide DDT is inhibitor for key enzymes of nervous system.
Many antibiotics (e.g. Penicillin) inhibits enzymes that help bacteria
to make their cell walls.
CHAPTER 5
THE STRUCTURE AND FUNCTION
Control of Metabolism
The OF MACROMOLECULES
1. Metabolic control often depends on allosteric regulation التحكم الجانبى
2. The localization of enzymes within a cell helps order metabolism
The control of metabolism (i.e. enzyme activity)
The cell is controlling its metabolism by regulating enzyme activity:
1)- Allosteric Regulation:
Regulatory molecules that bind weakly to an Alosteric site of the enzyme
(Allosteric Enzymes) in order to inhibit or stimulate the enzyme activity.
A)- Allosteric activator.
B)- Allosteric inhibitor
C)- Feedback inhibition.
2- Cooperativity.
Stabilizes favorable conformational changes at all other
subunits to make enzyme more efficient.
Metabolic control often depends on allosteric regulation
• In many cases, the molecules that naturally
regulate enzyme activity behave like reversible
Allosteric
noncompetitive inhibitors or activators. site
• These molecules often bind weakly to an allosteric
site which is a specific receptor on the enzyme
that is not the active site.
• These molecules can either inhibit or stimulate
enzyme activity.
1)- Allosteric Regulation: التنظيم األلوستيرى
• Most allosterically regulated enzymes
are constructed of two or more
polypeptide chains.
• Each subunit has its own active site.
The allosteric sites are often located
where subunits are joined.
• The whole protein exists in two
conformational shapes, one is active,
and one is inactive.
A)- Allosteric activators :منشطات
It makes active site functional
(connection of substrate with
enzyme).
B)- Allosteric inhibitors :مثبطات
It makes active site non-
functional .
• In many cases, both inhibitors and activators are similar enough in
shape that they compete for the same allosteric sites.
– These molecules may be products and substrates of a metabolic
pathway.
– For example, some catabolic pathways have allosteric sites that are
inhibited when ATP binds, but activated when AMP (adenosine
monophosphate) binds.
– When ATP levels are low, AMP levels are high, and the pathway is turned
on until ATP levels rise, AMP levels fall and inhibition by ATP occurs.
C)- Feedback inhibition
:التثبيط باألثر الراجعى
It is one of the common
methods of metabolic control
in which a metabolic pathway
is turned off يتوقفby its end
product .الناتج النهائى
• Example:
the production of Isoleucine
from Thereonine by
Thereonine deaminase:-
• The end product acts as an
inhibitor of an enzyme in the
pathway.
• When the product is
abundant ,متوفرthe pathway is
turned off, when rare قليلthe
pathway is active.
2)- Cooperativity regulation التنظيم التضامنى
• It occurs In enzymes with
multiple catalytic subunits,
binding by a substrate to
one active site stabilizes
favorable conformational
changes at all other
subunits, a process called
cooperativity .التضامنية
• This mechanism amplifies يـُزيدthe response استجابةof
enzymes to substrates, making the enzyme to accept
additional إضافىsubstrates.
The localization of enzymes within a cell وضع اإلنزيمات بالخليةhelps
order metabolism تنظيم األيض
• Some enzymes and enzyme complexes have fixed locations موضع ثابت
within the cells as structural components of particular membranes.
• Others are confined
within membrane-
enclosed organelles
• (lysosomes and mitochondria).
• Both methods concentrate
enzymes for efficiency.
لزيادة الفاعلية
Respiration
Alveoli
External respiration
الــدم
Internal respiration
خاليا
Cellular respiration الجـسـم
CELLULAR RESPIRATION:
HARVESTING CHEMICAL ENERGY
Section A: The Principles of Energy Harvest
Section A: The Principles of Energy Harvest
1. Cells recycle the ATP they use for work
2. Redox reactions تفاعالت األكسدة-اإلختزالrelease energy when
electrons move closer to electronegative atoms
3. Electrons “fall” تنتقلfrom organic molecules to oxygen
during cellular respiration
4. The “fall” of electrons during respiration is stepwise ,مرْ حلى
َ َ
via NAD+ and an Electron Transport Chain
Respiration
Cellular Respiration
O2 H2O
Food
(Fuel of energy)
Respiration Energy
+
O2 CO2
Cellular Activities
Organic compounds + O2 Energy + CO2 + H2O
1. Cells recycle the ATP they use for work
• ATP (Adenosine Tri-Phosphate) is the important
molecule in cellular energetics .عمليات إنتاج الطاقة
– The attachment of three negatively-charged phosphate groups
(P) is an unstable ,غير مستقرenergy-storing مخزن للطاقةarrangement.
– Loss of the end phosphate group release energy
• The price of most cellular work is the conversion of
ATP to ADP and phosphate (P).
• An animal cell regenerates تعيد إنتاجATP from ADP by
adding P via the catabolism هدمof organic molecules.
Adenosine Tri-Phosphate (ATP)
Adenosine
P P P
+ H2O
Triphosphate
Energy P P P
Adenosine Di-Phosphate
The transfer of the terminal phosphate group from ATP to
another molecule is phosphorylation .فـَسْ ـفـَرة
This changes the shape
of the receiving molecule
in order to work
(transport, mechanical,
or chemical).
When the phosphate
groups leaves the
molecule, the
molecule returns to
its original shape (stop).
How dose ATP drive cellular work ?
P P P
Organelle
Motor P
Protein
Microtubule
Energy
2. Redox reactions release energy when electrons move
closer to electronegative atoms
• Catabolic pathways relocate يبدل أماكنthe electrons stored in food
molecules, releasing energy that is used to synthesize لتخليقATP.
• Oxidation-reduction reactions (Redox reactions):
Are reactions that result in the transfer of one or more electrons
from one reactant to another
• Oxidation:
Redox reactions require
Is the loss فقـدof electrons.
• Reduction: both a donor and acceptor of e.
Is the addition إكتسابof electrons.
+
X e- + Y X + Y
Oxidation Reduction
Na + Cl Na+ + Cl- Energy
3. Electrons “fall” from organic molecules to oxygen
during cellular respiration
• In cellular respiration, glucose and other fuel molecules are oxidized, releasing
energy.
e -
C6H12O6 + 6O2 6CO2 + 6H2O + (ATP + Heat)
Reducing Oxidizing Energy = 686 kcal/mol
agent agent Energy
• Glucose is oxidized, oxygen is reduced, and electrons loose potential energy.
• H is the source of electrons that transfere to O.
• Thus, molecules that have an abundance of وفرة منhydrogen are excellent fuels
because their bonds are a source of electrons that “fall” closer to oxygen.
• Enzymes lower the barrier of activation energy, allowing these fuels to be
oxidized slowly.
• The resulting energy is used by the cell to synthesis ATP .
4. The “fall” of electrons اإلنحدار اإلليكترونىduring respiration is
stepwise ,مرحلىby NAD+ and an electron transport chain
• Cellular respiration does not oxidize glucose in a single step that
transfers all the hydrogen in glucose to oxygen at one time.
• Rather, glucose and other fuels are broken down gradually تدريجياin
a series of steps, each catalyzed by a specific enzyme.
• At key steps ,فى الخطوات األساسيةhydrogen atoms move from glucose
and passed first to the coenzyme NAD+ (Nicotinamide Adenine
Dinucleotide).
• Dehydrogenase enzymes strip two hydrogen atoms from the fuel
(e.g., glucose), pass two electrons to NAD+ and release H+.
Dehydrogenase
H-C-OH + NAD+ C=O + NADH + H+
• This changes the oxidized form, NAD+, to the reduced form
NADH.
• NAD + functions as the oxidizing agent in many of the redox steps
during the catabolism of glucose.
As electrons “fall” from NADH to oxygen,
Their energy is tapped to synthesize ATP.
• Cellular respiration uses an electron transport chain سلسلة نقل اإلليكترونات
to break يـُقـَسمthe fall of electrons to O2 into several steps .عدة خطوات
• The electron transport chain, consisting
of several molecules (primarily proteins),
is built into the inner membrane of a
mitochondrion.
• NADH takes electrons from food at the
“top” of the chain.
• At the “bottom”, oxygen captures the
electrons and H+ to form water.
• The free energy change from “top” to
“bottom” is -53 kcal/mole of NADH.
• Electrons are passed by increasingly
electronegative molecules in the chain
until they are caught by oxygen (the
most electronegative).
Summary of electron “Fall” steps during respiration
- Falling of all H atoms from glucose to O is gradually not at once.
- It occurs in steps, each one is catalyzed by an enzyme.
- H atoms of glucose pass first to the co-enzyme NAD+ to form NADH
- Then from NADH to electron transport chain, and finally to O and
releases energy to form ATP.
Mitochondrion
NAD+ e e
Food H NADH Transport chain Oxygen
Energy
ATP ADP
CELLULAR RESPIRATION:
HARVESTING CHEMICAL ENERGY
Section B:
The Process of Cellular
Respiration
1. Respiration involves glycolysis, the Krebs cycle, and
electron transport
2. Glycolysis (in cytoplasm): harvests chemical energy by
oxidizing glucose (breaking glucose into 2 molecules of
pyruvate).
3. The Krebs cycle (in motochonderial matrix): completes the
energy harvest by oxidizing the organic molecules.
4. The electron transport chain (inner mitochondrial
membrane): to synthesis ATP.
Cellular respiration generates 38 ATP molecules
for each sugar molecule it oxidizes.
Summary of Glycolysis (Splitting of glucose)
It is the process of breaking a glucose into 2 Pyruvate.
It is a source for some ATP & NADH and occurs in the
CYTOSOL (cytoplasm).
It has two phases
A)- Energy investment phase
1)- Glucose is phosphorylated twice by adding 2 P
coming from 2 ATP (substrate-level-phosphorylation).
2)- Thus, Glucose (6-C) splits into two small sugar
molecules (each with 3-C).
Summary of Glycolysis (Splitting of glucose)
B)- Energy pay-off phase
3)- The two resulting 3-C-sugars are then oxidized (losing e- (H)).
4)- The resulting e- from the two 3-C-sugar are used for reducing 2
NAD+ into 2 NADH molecules via dehydrogenase.
5)- 4 ATP are formed by adding 4P to 4ADP molecules.
6)- The net yield of this process is the formation of 2 NADH,
2 ATP and 2 pyruvate molecules.
7)- Now pyruvate is ready for Krebs Cycle.
2. The Krebs cycle completes the energy harvest by
oxidizing organic molecules (in mitochondrial matrix):
• If O2 is present, pyruvate enters the mitochondrion where enzymes of
the Krebs cycle complete the oxidation of this organic fuel to CO2.
• As pyruvate enters the mitochondrion which modifies pyruvate
to acetyl-CoA which enters the Krebs cycle in the matrix.
– A carboxyl group is removed as CO2.
– A pair of electrons is
transferred from the
remaining two-carbon
fragment to NAD+ to form
NADH.
– The oxidized fragment,
acetate, combines with
coenzyme A to form
acetyl-CoA.
Summary of Respiration
- Glycolysis occurs in the cytosol and breaks glucose into 2 pyruvates
- Krebs Cycle takes place within the mitochondrial matrix, and breaks
a pyruvate into CO2 and produce some ATP and NADH.
- Some of ATP is produced at these tow steps via (substrate-level-
phosphorylation).
- Electron Transport Chain accepts e- from NADH and passes these e-
from one protein molecule to another.
- At the end of the chain, e- combine with both H+ and O2 to form H2O
and release energy.
- These energy are used by mitochondria to synthesis 90% of the cellular
ATP via ATP-synthase, a process called Oxidative Phosphorylation, in
the inner membrane of mitochondria.
Summary of cell respiration
CHEMICAL SIGNALS IN ANIMALS
Egg Larva Pupa Adult
Introduction
• Nervous and endocrine systems are the main internal
communication and regulation systems.
• The animal hormone-secreting cells constitute the endocrine
system.
• Hormone secreting organs are called endocrine glands (ductless
glands).
• Hormone is a chemical signal secreted into blood stream and
regulates communicating messages within the body.
• Target cell is the site that reached by the hormone to which it
responds.
• Complete changes in the body is regulated by hormones (e.g.
metamorphosis in insects).
• Types of hormones are [ Polypeptide H., Steroid H. or Amino acid
derivatives H ].
• Many endocrine organs contain specialized nerve cells called
neurosecretory cells that secret hormones.
• The hormone epinephrine has two functions:
– As a hormone of the endocrine system.
– As a signal in the nervous system.
• Feedback is common in regulation the activity of both endocrine
and nervous systems (homeostasis) (Fig. 45.1, page 956):
– Calcitonin and parathyroid hormones play an important role in
maintaining the concentration of the blood calcium constant.
– They are secreted from thyroid and parathyroid glands respictively.
• Hormones regulate the development of
invertebrates (e.g. insects)
A variety of local regulators affect neighboring target cells
• Growth factors:
Are proteins and polypeptides that stimulate cell proliferation
• Example: nerve growth factor (NGF) affects certain embryonic cells,
developing white blood cells, and other kinds of cells.
• Nitric oxide (NO):
– Though a gas, NO is an important local regulator.
– When secreted by neurons, it acts as a neurotransmitter.
– When secreted by white blood cells, it kills bacteria and cancer cells.
– And when secreted by endothelial cells, it dilates the walls of blood
vessels.
• Prostaglandins (PGs): modified fatty acids.
– PGs secreted by the placenta stimulate uterine contractions during
childbirth.
– Other PGs play a role in inflammation and the blood flow to the lungs.
Most chemical signals bind to plasma-membrane proteins,
initiating signal-transduction pathways.
Mechanism of chemical signaling:
The chemical signals secreted by a cell either:
a): Bind to a receptor protein on the surface of the target cell. This will
trigger signal transduction pathway. For example protein hormones.
a): Penetrate the cell and bind to a receptor protein inside the target cell.
This also will trigger signal transduction pathway (e.g. steroid hormones
for synthesizing a specific protein).
Steroid hormones, thyroid hormones, and some local regulators enter
target cells and bind to intracellular receptors
• Estrogen, progesterone, vitamin D and NO.
– Usually, the intracellular receptor activated by a hormone is a
transcription factor.
• Ecdysone (insect molting hormone).
– A steroid hormone triggers the special cells to secrete new
exoskeleton.
• Different signal-transduction pathways in different cells can lead
to different responses to the same signal.
The Vertebrate Endocrine System
الصنوبرية
Tropic hormones المنبه للغدد النخامية
target other endocrine الدرقية
glands and are
important to understanding
chemical coordination. الكظرية
• Humans have nine
endocrine glands.
Fig. 45.5, Page 960
The hypothalamus and pituitary integrate many
functions of the vertebrate endocrine system
• The hypothalamus integrates endocrine and
nervous function.
– Neurosecretory cells of the hypothalamus produce
hormones.
a) Releasing hormones stimulate the anterior pituitary
(adenohypophysis) to secrete hormones.
b) Inhibiting hormones prevent the anterior pituitary from
secreting hormones.
1)- Pituitary gland: secrets 9 hormones ( 7 hormones by the
anterior part and 2 hormones by the posterior part).
A)- Anterior pituitary hormones.
1) Growth hormone (GH): a protein.
• Stimulates growth and metabolism.
• Secretion regulated by hypothalamic hormones.
• Acts directly on tissues or acts via growth factors.
• Gigantism: العملقةexcessive GH during development.
• Acromegaly: excessive GH production during adulthood.
• Hypopituitary dwarfism :القزميةchildhood GH deficiency.
2) Prolactin (PRL): a protein.
• Stimulates milk production and secretion.
• Secretion regulated by hypothalamic hormones.
3) Gonadotropins: glyocoproteins.
• Follicle-stimulating hormone (FSH).
– Stimulates production of sperm and ova.
– Secretion regulated by hypothalamic hormones.
• Luteinizing hormone (LH) .المحفز لتكوين الجسم األصفر
ُ
– Stimulates ovaries and testes.
– Secretion regulated by hypothalamic hormones.
4) Thyroid-stimulating hormone (TSH): a glycoprotein.
• Stimulates thyroid gland.
• Secretion regulated by thyroxine in blood.
• Secretion regulated by hypothalamic hormones.
5) Adrenocorticotropic hormone (ACTH): a peptide
• Stimulates adrenal cortex secretion of glucocorticoids
• Secretion regulated by glucocorticoids and hypothalamic
hormones.
6) Melanocyte-stimulating hormone (MSH): a peptide.
• May play a role in fat metabolism.
7) Endorphins: peptides.
• Inhibit pain perception.
• Effects mimicked by heroin and other opiate drugs.
The anterior pituitary gland hormones
Melanocyte-
stimulating H.
Adrenocorticotropic
Also called gonadotropine
hormones هرمونات المناسل
B)- Posterior pituitary hormones.
– Oxytocin: a peptide.
• Stimulates contraction of the uterus and mammary glands.
• Secretion regulated by the nervous system.
– Antidiuretic hormone (ADH): مضاد إلدرار البولa peptide.
ُ
• Promotes retention of water by the kidneys.
• High level decreases urination and vice versa.
• Secretion regulated by water/salt balance.
2- Pineal gland: الغدة الصنوبرية
is a small mass of tissue near the center of the mammalian brain
and involved in biorhythms.
– The pineal gland secretes the hormone, melatonin, an amine.
• Involved in biological rhythms associated with reproduction.
• Secretion regulated by light/dark cycles.
Posterior pituitary
(neurohypophysis)
stores and secretes
hormones produced
by the hypothalamus.
Antidiuretic H
3. Thyroid gland: secrets hormones function in development,
bioenergetics, and homeostasis ثبات البيئة الفسيولوﭽـية الداخلية
• The thyroid gland of mammals consists
of two lobes located on the ventral
surface of the trachea. It contains 4
small Parathyroid glands. It plays role in
maintaining normal blood pressure, Thyroid
heart rate digestion ..etc. releasing H.
• Thyroid glands secretes 3
hormones:
I. Tri-iodothyronine [(T3), 3 I
atoms]: amino acid derivative.
Thyroid
stimulating H.
II. Thyroxine [(T4), 4 I atoms]:
amino acid derivative.
– Stimulates and maintain metabolic
processes.
– Secretion regulated by TSH
hormones.
III. Calcitonin: a peptide.
Lowers blood Ca2+ levels.
Its secretion regulated by calcium in blood.
a) Hyperthyroidism: the excessive secretion of thyroid
hormones causes:
• high body temperature
• sweating
• weight loss
• Irritability
• high blood pressure.
b) Hypothyroidism: an insufficient قليلamount of thyroid
hormones because deficiency of I in human diet (causes Goiter).
Infants: cretinism.
Adults: weight gain, lethargy, cold intolerance.
Goiter :تضخم الغدةoften associated with iodine deficiency .نقص
Parathyroid gland: Parathyroid hormone (PTH): a peptide
• PTH is secreted by The four parathyroid glands which embedded
in the surface of the thyroid gland. It functions as:
– Raises blood Ca2+ levels.
– Secretion regulated by calcium in the blood.
– Causes osteoclasts فقد الكالسيومto break down bone, releasing Ca2+ into
the blood.
– Stimulates the kidneys to reabsorb تعيد إمتصاصCa2+.
– Stimulates kidneys to convert vitamin D to its active form, which
stimulate intestine to absorb Ca2+.
– PTH and calcitonin are antagonistic متضادينhormones. Thus PTH and
calcitonin regulate blood calcium level (important role in homeostasis).
• Hypoparathyoidism (tetany): it is a lack of PTH which causes:
– Ca2+ levels in the blood drop.
– Convulsive contractions of the skeletal muscles.
Hormonal control of Ca2+ homeostasis in mammals blood
5. Pancreas: Endocrine tissues of the pancreas secrete insulin and
glucagon, antagonistic hormones that regulate blood glucose
• The pancreas has both endocrine and exocrine functions.
– Exocrine function: secretion of bicarbonate ions and digestive
enzymes.
– Endocrine function: insulin and glucagon secreted by beta and alpha
cells of islets of Langerhans .جيوب النجرانز
1. Insulin: a protein secreted by beta cells.
• Lowers blood glucose levels.
– Stimulates all body cells (except brain cells) to take up glucose.
– Slows glycogenolysis ( يبطىء تحلل الجليكوجينa source of glucose).
– Inhibits gluconeogenesis .يوقف تكوين الجلوكوز
• Secretion regulated by glucose in blood (negative feedback).
– Hypoinsulinism: diabetes mellitus .نقص اإلنسولين
• Hereditary factors عامل وراثىand play a role in its development.
• High blood sugar levels – sugar excreted in the urine.
• Symptoms: excessive urination كثرة التبولand excessive thirst .العطش
a) Type I diabetes mellitus (insulin-dependent diabetes).
• Autoimmune disorder.
• Usually appears in childhood .الطفولة
• Treatment: insulin injections.
b) Type II diabetes mellitus (non-insulin-dependent diabetes).
• Usually due to target cells having a decreased responsiveness to
insulin .قلة اإلستجابة لإلنسولين
• Usually occurs after age 40 – risk increases with age.
• Accounts for over 90% of diabetes cases.
2. Glucagon: a protein secreted by alpha cells.
• Raises blood glucose levels.
– Stimulates glycogenolysis تحلل الجليكوجينin the liver and skeletal
muscle to produce glucose.
– Secretion regulated by glucose in blood (negative feedback).
6. The adrenal gland: adrenal medulla and adrenal cortex help
the body manage stress
• The adrenal glands are located adjacent to the kidneys.
– The adrenal cortex القشرةis the outer portion.
– The adrenal medulla is the inner portion.
I- Adrenal medulla .المركز
– Developmentally and functionally related to the nervous system.
– It produces the following hormones (in response to stress):
a) Epinephrine (adrenaline .)هرمون القلب
b) Norepinephrine (noradrenaline).
They are amino acid derivatives (synthesized from tyrosine)
and function as:
• Raises blood glucose level and blood fatty acid level.
• Increases heart rate and stroke volume and dilates bronchioles.
• Shunts blood away from skin, digestive organs, and kidneys,
and increases blood flow to heart, brain, and skeletal muscle.
II- Adrenal cortex: reacts to stress.
• Secretion of corticosteroids (a family of steroid hormones) is
regulated by the nervous system in response to stress for example:
a) Glucocorticoids.
• Raises blood glucose level.
• Secretion regulated by ACTH (Adrenocorticotropic hormone).
• Abnormally high doses are administered as medication to
suppress the inflammation response.
b) Mineralocorticoids (example: aldosterone, which affects salt and
water balance).
• Promotes re-absorption of Na+ and excretion of K+ in kidneys.
• Their secretion regulated by K+ in blood.
– A third group of corticosteriods are Sex hormones.
• Androgens secreted by the adrenal cortex may account for the female
sex drive.
• The adrenal cortex also secretes small amounts of estrogens and
progesterone.
7. Tests and ovaries: Gonadal steroids regulate growth,
development, reproductive cycles, and sexual behavior
a) Testes hormones:
– Testosterone: steroids.
• Supports sperm formation.
• Promote development and maintenance of male sex characteristics.
• Secretion regulated by FSH and LH.
b) Ovaries hormones:
1) Estrogens: steroids.
• Stimulate uterine lining growth.
• Promote development and maintenance of female sex
characteristics.
• Secretion regulated by FSH and LH.
2) Progesterone: steroids.
• Promotes uterine lining growth.
• Secretion regulated by FSH and LH.
8- Thymus gland:
Secretes Thymosin: a peptide.
It stimulates T lymphocytes.
Protein hormones affect target cells via
receptors on the membrane protein
Steroid hormones inter the target cells
and trigger protein synthesis via
receptors in the nucleus.
MENDEL AND THE GENE IDEA
Section A: Gregor Mendel’s Discoveries
Mendel brought an experimental and quantitative approach
to genetics
• Around 1857, Mendel began breeding
garden peas to study inheritance .وراثة
Because they are available in many
varieties with distinct heritable مُتوارث
characters صفاتwith different traits
(genes).
• Each pea plant has male (stamens)
and female (carpal) sexual organs.
• In nature, pea plants typically
self-fertilize ,تلقيح ذاتىfertilizing ova
with their own pollens.
• However, Mendel could also move
pollens حبوب اللقاحfrom one plant to
another to cross-pollinate يُـلقحplants.
• In a breeding experiment, Mendel would cross-pollinate
( تلقيح خلطىhybridize )هجنtwo contrasting ,متباينينtrue-
َ
breeding pea varieties .أنواع
– The true-breeding parents are the P (Parental generation) and
their hybrid offspring النسل المُهجنare the F1 (1st Filial generation) .
• Mendel would then allow the F1 (1st Filial generation) hybrids
to self-pollinate to produce an F2 generation.
• It was mainly Mendel’s quantitative analysis تحليل كمىof F2
plants that revealed the two fundamental lows of
heredity:
A)- The law of segregation.
B)- The law of independent assortment.
A)- Law of segregation: ) )قانون اإلنعزالthe two alleles ﭽـيناتfor a
character are isolated into separate gametes
• The F1 hybrids from a cross تلقيح
between purple-flowered and white-
flowered pea plants would have pale
purple flowers .بنفسجى باهت
• Instead, ولكنthe F1 hybrids all have
purple flowers, just a purple like their
parents.
• This cross produced a 3 purple to 1
white ratio of traits in the F2 offspring,
• Mendel reasoned that the heritable
factor for white flowers was present
in the F1 plants, but it did not affect
flower color.
• Thus, purple flower is a dominant color
) (صفة سائدةand white flower is a recessive
color ).(صفة مُتنحية
• Mendel found similar 3 to 1 ratios of two traits among
F2 offspring when he conducted crosses for six other
characters, each represented by two different varieties
.صفتين مختلفتين
• For example, when Mendel crossed two true-breeding
varieties, one of which produced round seeds ,بذور مُستديرة
the other of which produced wrinkled seeds ,بذور مُجعدةall
َ
the F1 offspring had round seeds, but among the F2
plants, 75% of the seeds were round and 25% were
wrinkled (see second low in the next lecture).
• Mendel developed a hypothesis إفتراضto explain these results that
consisted of four related ideas.
1. Alternative version of genes (different alleles )الـﭽينين المتقابلينaccount
for variations in inherited characters.
– Different alleles vary somewhat in
the sequence of nucleotides at
the specific locus موضعof a gene.
2. For each character, an organism
inherits يرثtwo alleles, one from
each parent.
– These homologous loci موقعُه على الكروموسوم
ِ َ
may be differ
– In the flower-color example, the F1 plants
inherited a purple-flower allele from one
parent and a white-flower allele from the
other.
3. If two alleles differ, then, the dominant allele is fully expressed in
the organism’s appearance and the recessive allele has no effect
on the organism’s appearance.
4. The two alleles for each character segregate (separate) ينفصل
during gamete production.
– This segregation of alleles because of the distribution of homologous
chromosomes to different gametes in meiosis.
– If an organism has identical allele for a particular character, then that
allele exists as a single copy in all gametes.
– If different alleles are present, then 50% of the gametes will receive one
allele and 50% will receive the other.
• The separation of alleles into separate gametes
is summarized as Mendel’s law of segregation.
Summary
Mendelian inheritance reflects rules of probability for the
behaviour of genes.
For each character, an organism inherit two alleles (one from each
parent).
Red colour
gene (allele)
Homologous
chromosomes
White colour
gene (allele)
If the two alleles differ, one of them will be Dominant, and the other
is Recessive.
The two alleles (genes) for a character are separated (segregated)
into separate gametes and aggregated again by fertilization.
• Mendel’s law of segregation accounts
for the 3:1 ratio in the F2 generation.
• The F1 hybrids will produce two
classes of gametes, half with the
purple-flower allele and half with the
white-flower allele.
• During self-pollination, the gametes
of these two classes unite randomly.
• This can produce four equally likely
combinations of sperm and ovum.
• A Punnett square predicts the results
of a genetic cross between individuals
of known genotype.الطرز الـﭽينى
• A Punnett square analysis of the
flower-color example demonstrates
Mendel’s model.
• Mendel’s model accounts for the 3:1
ratio in the F2 generation
Pea plant
PP X pp Pp X Pp
P p P p
P p
Dominant Recessive
allele Pp allele PP Pp Pp pp
100% Purple
3 Purple : 1 White
Homozygous Heterozygous
F1 generation F2 generation
Phenotype:
Phenotype Is the organism’s appearance .المظهر
(Colour)
Genotype:
Is the organism’s genetic makeup
.الطرز الـﭽينى
PP PP Homozygous pp
An organism having a pair of
identical alleles
Genotype Pp Heterozygous
(Genetic make up)
An organism having a pair of two
different alleles
• Dominant character (allele) الصفة السائدة
Is fully expressed in the organism’s appearance.
• Recessive character (allele) الصفة المُتنحية
Has no noticeable effect تأثير غير ملحوظon the organism’s appearance.
• Homozygous متماثل الجينات
ُ
An organism with two identical alleles for a character.
• Heterozygous مختلف الجينات
ُ
An organism with two different alleles for a character.
• Karyotype الطرز الكروموسومى
The display of an organism’s chromosomal pattern
• Phenotype الطرز المظهرى
A description of an organism’s traits (feature .)مظهر
• Genotype الطرز الجينى
A description of an organism’s genetic makeup.
• For flower color in peas, both PP and Pp plants have
the same phenotype (purple) but different genotypes
(homozygous and heterozygous).
• The only way to
produce a white
phenotype is to
be homozygous
recessive (pp)
for the flower-
color gene.
• It is not possible to predict the genotype of an
organism with a dominant phenotype.
– The organism must have one dominant allele, but it could be
homozygous dominant or heterozygous.
• A test cross, breeding a
homozygous recessive
with dominant phenotype,
but unknown genotype,
can determine the identity
of the unknown allele.
Q: What is the result of
Cross hybridization of
purple X white colored
flowers ?
MENDEL AND THE GENE IDEA
Section C: Mendelian Inheritance in Humans
2- The law of Independent Assortment: التوزيع الحر للـﭽـينات
each pair of alleles segregates into gametes independently
• Mendel’s experiments that followed the inheritance of flower color or
other characters focused on only a single character via monohybrid
crosses .التزاوج أحادى الصفة
• He conduced other experiments in which he followed the inheritance
of two different characters (a dihybrid cross .)التزاوج ثنائى الصفة
• In one dihybrid cross experiment, Mendel studied the inheritance of
seed color and seed shape.
– The allele for yellow seeds (Y) is dominant to the allele for green
seeds (y).
– The allele for round seeds (R) is dominant to the allele for wrinkled seeds
(r)
• Mendel crossed true-breeding plants that had yellow & round seeds
(YYRR) with true-breeding plants that has green & wrinkled seeds
(yyrr).
• The two pairs of alleles segregate independently of each other.
– The presence of one specific allele for one trait has no impact تأثيرon
the presence of a specific allele for the second trait.
• When sperm and ova each with
four classes of alleles
combine, there would be 16
equally probable ways in which
the alleles can combine
in the F2 generation.
• These combinations produce
four distinct phenotypes in a
9:3:3:1 ratio.
• This was consistent with
Mendel’s results.
• Each character appeared to be
inherited independently.
Mendel’s low of Independent (Dihybrid cross)
It is a mating between two parent plants differing in two characters.
YY RR X yy r r
Y
R
YR y r
y
Y y Rr
r
F1 Yellow Round
Yy Rr X Yy Rr
YR Yr yR yr
YR YYRR
Yellow Round
Yr YYrr
Yellow Wrinkled
yR yyRR
Green Round
yr yyrr
Green Wrinkled
F2: % of Phenotype ?
Many human disorders أمراضfollow Mendelian
patterns of inheritance
• Thousands of genetic disorders ,أمراض وراثيةincluding disabling اإلعاقةor
deadly hereditary diseases ,األمراض الوراثية المُميتةare inherited as simple
recessive traits .صفات وراثية مُتنحية
• These range from the relatively mild (albinism )األلبينو، البُهاقto life-threatening
(cystic fibrosis).
• Heterozygotes have a normal phenotype because one “normal” allele
produces enough of the required factors (for normal trait).
• A recessively inherited disorder shows up يظهرonly in the
individuals who inherit homozygous recessive allele from parents.
• Thus, individuals who lack the disorder are either homozgyous dominant
or heterozygous.
• Heterozygous member may have no clear phenotypic effects, but is a
carrier who may transmit a recessive allele to their offspring.
• Most people with recessive disorders are born from carrier parents with
normal phenotypes.
– Two carriers have a 1/4 chance of having a child with the disorder, 1/2 chance of
a carrier, and 1/4 free.
A- Recessively inherited disorders الصفات المرضية المتنحية
1. Cystic fibrosis: a lethal recessive disorder
– One in 25 person is a carrier.
– The normal allele codes for a membrane protein that transports
Cl- between cells and the environment.
– If these channels are absent, there are abnormally high
extracellular levels of chloride that causes the mucus coats of
certain cells to become thicker سميكةand stickier لزجةthan normal.
– This mucus build-up in the pancreas, lungs, digestive tract, and
elsewhere favors bacterial infections.
– Without treatment, affected children die before five, but with
treatment can live past their late 20’s.
2. Tay-Sachs disease a lethal recessive disorder.
– It is caused by a dysfunctional enzyme إنزيم غير عاملthat fails to break
down specific brain lipids.
– The symptoms begin with seizures ,حولblindness, and degeneration
of motor and mental performance a few months after birth.
– Inevitably, the child dies after a few years.
3. Sickle-cell disease .خاليا الدم الهاللية
– It is caused by the substitution of a single amino acid in
hemoglobin.
– When oxygen levels in
the blood of an affected
individual are low,
sickle-cell hemoglobin
crystallizes into long
rods.
– This deforms red blood
cells into a sickle shape.
– Doctors can use regular
blood transfusions to
prevent brain damage
and new drugs to
prevent or treat other
problems.
• The two alleles are codominant as both normal and abnormal
hemoglobins are synthesized.
• Normally it is relatively unlikely that two carriers of the same rare
harmful allele will meet and mate.
• However, consanguineous mating ,زواج األقاربthose between
close relatives, increase the risk.
– These individuals who share a recent common ancestor are more
likely to carry the same recessive alleles.
• Most societies and cultures have laws or taboos forbidding
marriages between close relatives.
B- Dominantly inherited disorders الصفات المرضية السائدة
• Although most harmful alleles are recessive, many human disorders
are due to dominant alleles.
1. Achondroplasia, a form of dwarfism ,القزميةhas an incidence of one
case in 10,000 people.
– Heterozygous individuals have the dwarf phenotype.
– Those who are not achodroplastic dwarfs are homozygous recessive for this
trait.
• Lethal dominant alleles are much less common than lethal recessives
because if a lethal dominant kills an offspring before it can mature and
reproduce, the allele will not be passed on to future generations.
2. Huntington’s disease: a degenerative ضُمورdisease of the nervous system.
The dominant lethal allele has no obvious phenotypic effect until an
individuals is about 35 to 45 years old.
– The deterioration of the nervous system is irreversible and inevitably
fatal .مُميت
• Recently, molecular geneticists have used pedigree analysis تحليل السجل العائلى
of affected families to track down لنزعthe Huntington’s allele to a locus
near the tip of chromosomes 4.
Many other disorders have a multifactorial متعدد العواملbasis.
– These have a genetic component plus a significant environmental
influence.
– Multifactorial disorders include heart disease, diabetes, cancer,
alcoholism, and certain mental illnesses, such a schizophrenia and
manic-depressive disorder.
– The genetic component is typically polygenic .متعدد الجينات
• At present, little is understood about the genetic contribution to most
multifactorial diseases
THE CHROMOSOMAL BASIS
OF INHERITANCE
Section B: Sex Chromosomes
1. The chromosomal basis of sex varies with the organism
2. Sex-linked genes have unique patterns of inheritance
1. The chromosomal basis of sex varies with the organism
• In human and other mammals, there are
two varieties of sex chromosomes, X & Y.
– An individual who inherits two X
chromosomes usually develops as a female.
– An individual who inherits an X and a Y
chromosome usually develops as a male.
• This X-Y system of mammals is not the
only chromosomal mechanism of
determining sex.
• Other options include the X-0 (in locust)
system, the Z-W system (in birds), and the
haplo-diploid system (in bees).
• In Human, the SRY gene (Sex-determining
Region of the Y chromosome) modifies
embryonic gonads into testes.
• Females lack the SRY gene, thus, the
embryonic gonads develop into ovaries.
• In the X-Y system, Y and X chromosomes behave as
homologous chromosomes during meiosis.
– In reality, they are only partially homologous and rarely
undergo crossing over
• In both testes (XY) and ovaries (XX), the two sex
chromosomes segregate during meiosis and each
gamete receives one.
– Each egg receives an X chromosome.
– Half the sperm receive an X chromosome and half receive a Y
chromosome.
• Because of this, each conception has about a fifty-fifty
chance of producing a particular sex.
2. Sex-linked genes have unique patterns of inheritance
• The sex chromosomes, especially the
X chromosome, have genes for many
characters unrelated to sex.
• These sex-linked genes جينات مرتبطة بالجنس
follow the same pattern of inheritance
as the white-eye locus in Drosophila.
• If a sex-linked trait is due to a recessive
allele, a female have this phenotype
only if homozygous.
– Heterozygous females will be carriers.
• Because males have only one X chromosome
(hemizygous), any male receiving the recessive allele
from his mother will express the trait.
• Therefore, males are far more likely to inherit sex-
linked recessive disorders مرضthan are females.
الصفات المرتبطة بالجنس تورث لألبناء الذكور من األم
الحامل لهذا النوعX فقط ألنهم يرثون منها الكروموسوم
ال يحمل شىءY من الـﭼـينات، حيث إن
Sex-linked disorders األمراض المرتبطة بالجنس in human.
1. Duchenne muscular dystrophy: وهن العضالت
affects one in 3,500 males born in the United States.
– Affected individuals rarely live past their early 20s.
– This disorder is due to the absence of an X-linked gene for a key
muscle protein, called dystrophin.
– The disease is characterized by a weakening ضعفof the muscles and
loss of coordination .فـقـد التوازن
ْ
2. Hemophilia: النزيف الدموىis a sex-linked recessive trait defined by
the absence of one or more clotting factors .عوامل تجلط
– These proteins normally slow and then stop bleeding.
– Individuals with hemophilia have prolonged bleeding نزيف مستمر
because a firm clot تجلطforms slowly.
– Individuals can be treated with intravenous injections of the missing
protein.
– This gene is transmitted to offspring via the mothers.
– Thus, Sons borne from hemophilic woman should be exempted يستثنى ُ
from circumcision .الختان
3. Color blindness: عمى األلوانis a
disorder inherited as a recessive sex-
linked character and affect both males
and females.
– A color blind female (XaXa) may be born to
a color blind father (XaY) and a carrier
mother (XAXa)
• Although female mammals الثديياتinherit
two X chromosomes, only one X chromosome is active.
• Therefore, males and females have the same effective dose (one
copy ) of genes on the X chromosome.
– During female development, one X chromosome per cell condenses into
a compact object, a Barr body ( جسم بارin somatic cells).
– This inactivates most of its genes.
• The condensed Barr body chromosome is reactivated in ovarian
cells that produce ova.
Chromosomal aberration .الشذوذ الكروموسومى
• It is common شائعin meiosis and includes:
a) Chromosomal deletions/translocations نقص أو فقد جزء
Homologous chromatids may break تـَنكسرand rejoin و تلتحم مرة أخرى
at incorrect places, thus, one chromatid will loose more genes
than it receives.
b) Chromosomal duplications ( تضاعُفPolyploidy .)تعدد الكروموسومات
result from nondisjunction عدم اإلنفصال الكامل للكروموسومات أثناء اإلنقسام الميوزى
during gamete production in one parent.
• A diploid embryo that is homozygous for a large deletion
or male with a large deletion to its single X chromosome
is usually missing يفتقدmany essential genes and this
ُِ
leads to a lethal مميتoutcome.
– Duplications and translocations تغيير أماكن األجزاء المقطوعةare very harmful.
• Translocation or inversion can alter phenotype because
a gene’s expression is influenced by its location.
• Several serious human disorders are due to these
alterations تغييراتof chromosome number and structure.
• Although the frequency َيحدث مراراof aneuploid zygotes
ُ
الالقحة الـمتعددة الكروموسوماتmay be quite high in humans, most of
these alterations result in abortion إجهاضlong time before
birth .قبل الوالدة
– These developmental problems results from an imbalance
عدم توازنamong gene products.
• Certain aneuploid conditions decrease the imbalance
effect, leading to survival to birth .المولود
– But these individuals have a set of symptoms أعراض
َُ
(syndromes) characteristic مميـِزةof the type of aneuploidy as
following:-
A)- Aneuploidy (Chromosomal duplication) ,التعدد الكروموسومى غير التام
1- Down syndrome [Polyploidy (2n + 1), trisomy in autosomes]:
Is due to three copies of chromosome 21 (Trisomies .)مجموعات كروموسومية ثالثية
Although chromosome 21 is the smallest human chromosome, it
severely alters يُغيرan individual’s phenotype in specific ways.
• Most cases of Down syndrome result from nondisjunction
عدم اإلنفصال الكامل للكروموسومات أثناء اإلنقسام الميوزىduring gamete production in
one parent.
• The frequency تِكرارof Down syndrome correlates with the age of the
mother.
– This may be linked to some age-dependent abnormality in the spindle
checkpoint during meiosis I, leading to nondisjunction.
2- Klinefelter’s syndrome [Polyploidy (2n + 1), trisomy in sex chromosomes ],
(a)- An XXY male, occurs once in every 2000 live births.
• These individuals have male sex organs, but are sterile.
• There may be feminine characteristics ,له صفات أنثويةbut their intelligence is
normal.
(b)- An XYY male, tend to somewhat taller than average.
(c)- A trisomy female (XXX), which occurs once in every 2000 live
births, produces healthy females.
3- Turner’s syndrome, a monosomy female (X0), which occurs
once in every 5000 births, produces phenotypic, but immature
females .غير ناضجة جنسيا
B)- Chromosomal structure-alterations:
It can also cause human disorders.
• Deletions ,حزفeven in a heterozygous state, cause severe physical
and mental problems.
1. Cri-du-chat ,عارض مواء القط
results from a specific deletion in chromosome 5.
– These individuals are mentally retarded, have a small head with
unusual facial features, and a cry like the mewing of a distressed cat.
– This syndrome is fatal in infancy الطفويةor early childhood.
2. Myelogenous, [leukemia (CML)].
Caused by chromosomal translocations since a fragment of
chromosome 22 switches places with a small fragment from the
tip of chromosome 9.
erozygous state, cause severe physical
and mental problems.
1. Cri-du-chat ,عارض مواء القط
results from a specific deletion in chromosome 5.
– These individuals are mentally retarded, have a small head with
unusual facial features, and a cry like the mewing of a distressed cat.
– This syndrome is fatal in infancy الطفويةor early childhood.
2. Myelogenous, [leukemia (CML)].
Caused by chromosomal translocations since a fragment of
chromosome 22 switches places with a small fragment from the
tip of chromosome 9.