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Bacterial Genetics
Learning the Basics
1
Dr.T.V.Rao MD
Dr.T.V.Rao MD
Genetics Guide Life
2
Dr.T.V.Rao MD
Genes are Eternal
Run In Progeny
3
Dr.T.V.Rao MD
Understanding Genetics
We resemble and differ because of
Genetic configurations
Parents - Son - Daughter, how they
resemble each other.
They breed true from Generation to
Generation
But vary in small proportions in
progeny.
Bacteria too obey the laws of
Genetics 4
Dr.T.V.Rao MD
Watson - Crick
Discovery of DNA
5
Dr.T.V.Rao MD
Beginning of Bacterial
Genetics
• The principles of Genetics were applied to
bacteria and viruses
• Advances in Genetic process also of lead
to fundamental advances in Biology and
Biochemistry.
A Birth of New Branch of Science
Molecular Biology
6
Dr.T.V.Rao MD
DNA
A Complex Structure
Makes Life
7
Dr.T.V.Rao MD
DNA
( Deoxyribonucleic Acid )
• DNA is composed of Many Units of
Adenine – Thymine A – T
Guanine – Cytosine G - C
A+ T
G+C proportion differ for each species
DNA replicates first unwinding at one end to form a
fork
Each strand of fork acting as template for the
synthesis of complementary strand
8
Dr.T.V.Rao MD
9
Dr.T.V.Rao MD
Structure of DNA
10
Dr.T.V.Rao MD
DNA
• A DNA molecule is
composed of two
chains of Nucleotides
wound together in the
form of a Double
Helix
• Each chain has back
bone of Deoxyribose
and Phosphates
residues arranged
alternatively 11
Dr.T.V.Rao MD
Structure of DNA
• Attached to each
Deoxyribose and
phosphate residues
arranged alternatively
• Attached to each
Deoxyribose are of four
nitrogen bases
• Purines - Adenine,
Guanine
• Pyramidine
Thymidine and Cytosine
12
Dr.T.V.Rao MD
How RNA differs from DNA
• RNA contains - Sugar Ribose instead
of Deoxyribose
• Uracil is present instead of Thymine
• Types of RNA
Messenger RNA mRNA
Ribosomal RNA rRNA
Transfer RNA tRNA
13
Dr.T.V.Rao MD
DNA - RNA
14
Dr.T.V.Rao MD
Knowledge on DNA lead to
advances in Molecular Biology
• Central dogma of Life – Deoxyribonucleic acid
• DNA carries the Genetic information
• DNA is transcribed to RNA – Polypeptides
Cell Function depends upon specific
polypeptides – Proteins – Enzymes
DNA is a store house of Protein synthesis
DNA acts a Template for synthesis of mRNA
Virus differs from other as they contains either
DNA or RNA
15
Dr.T.V.Rao MD
What is a Code in Genetics
• Code is a unit consists of sequence of three
Bases
• Code is triplet A-T- C
• A code can make single Amino acid
• More than one code present for making similar
sequence of Amino acid
• AGA make Arginine
• AGC, CGU, CGG, also code for similar Amino
acid
• Some Codons UAA don't code for any Amino
acid called as Nonsense codon
16
Dr.T.V.Rao MD
What is a Gene
• Gene is a sequence
of DNA carrying
codons specifying for
particular polypeptide.
• DNA contains many
Genes( A
combinations of
hundreds and
thousands of
Nucleotides )
17
Dr.T.V.Rao MD
Bacterial Chromosome
• Contains a Double stranded molecules of
DNA arranged in circular form.
• Length 1,ooo microns.
• Bacterial DNA contains about
4,000kilobases
• I kb = 1000 base pairs ( A-T ) ( G-C)
• Humans have about 3,000 kb pairs.
18
Dr.T.V.Rao MD
How bacterial Genome differs
from Higher forms of Life
• Several stretches of DNA don't appear to
function as codons, occurs between the
coding sequences of Gene. called as
INTRONS.
• Coded are called as EXONS
• In transcription introns are excised when
form RNA before translated by ribosomal
proteins.
19
Dr.T.V.Rao MD
Extra chromosomal
Genetic Elements
Bacteria posses Extra chromosomal
genetic elements
Not Essential for survival of Bacteria
But makes the Bacteria Resistant to
antibiotics, and makes them survive
Able to produce toxins
20
Dr.T.V.Rao MD
Plasmids
• Plasmids are circular
DNA molecules present
in the cytoplasm of the
Bacteria
• Capable of Autonomous
replication
• Can transfer genes from
one cell to other
• Act as vectors in Genetic
engineering.
• Can also present in
Yeasts
21
Dr.T.V.Rao MD
Plasmid ( Blue )
22
Dr.T.V.Rao MD
Plasmids
• Plasmid seem to be ubiquitous in bacteria, May
encode genetic information for properties
1 Resistance to Antibiotics
2 Bacteriocins production
3 Enterotoxin production
4 Enhanced pathogen city
5 Reduced Sensitivity to
mutagens
6 Degrade complex organic molecules
23
Dr.T.V.Rao MD
R plasmid
R: drug resistance
RTF: transfer of R
plasmid
24
Dr.T.V.Rao MD
Plasmids
• Can be integrated
with Chromosomal
DNA
• Episomes -
Integrated form of
plasmid with DNA
25
Dr.T.V.Rao MD
Potentials of Plasmids
• Plasmids can be self
transmissible and
Non transmissible
• Transfers the Sex and
Drug resistance with
the help of restriction
end nucleases
26
Dr.T.V.Rao MD
Classification of Plasmids
• Incompatibility typing
• Don't accommodate
others which are
similar
• Other methods of
Classification
Centrifugation
Electrophoresis
Genetic methods
27
Dr.T.V.Rao MD
Genotypic and Phenotypic
variation
• Genome – Sum total of Gene that make
up the genetic apparatus of cell
established as Genotype.
• Hereditary constitution of cell this
transmitted to its progeny
• Phenotype – is the physical expression in
a environment. Change according to
environment.
28
Dr.T.V.Rao MD
What is Phenotypic expression
• Exhibit – different phenotypes
• Appearance differs in different situations.
• Eg Typhoid bacilli flagellated normally
• But grown in Phenol agar don't grow flagella So
flagella are lost physical variation
• Lactose fermentation in E.coli dependent on
Beta Galactosidase
When lactose present - test is positive
When lactose is absent - test turns negative
29
Dr.T.V.Rao MD
Different Enzymes Guided by
Genomic configurations
• Inducer enzyme acts in the presence
of substrate
• Constitutive enzyme acts irrespective
of presence or absence of enzyme.
• Phenotypic variations influenced by
environment limited in range by
genes
• Genotypic variations are stable not
influenced by environment. 30
Dr.T.V.Rao MD
Principles of Genotypic
variations
• Mutations
• Genotypic by transfer of genes
Transformation
Transduction
(Lysogenic conversion)
Conjugation
31
Dr.T.V.Rao MD
Replica Plating, pt. 2
32
Dr.T.V.Rao MD
Mutations in Bacteria
• Bacteria Multiply by asexual binary fission
• Altered Nucleotide sequence in expresses new
or altered characteristics
• Selective value to the organism
• Evolutionary value
• Acquires Antibiotic resistance grows in body
without inhibition
• Become a prominent organism
• Phenotypic variation occurs when genes
changes in response to the environment but
reversible.
T.V.Rao MD
33
Dr.T.V.Rao MD
Mutations
• Mutation is a Random, Undirected,
Heritable variation
• Caused by alteration in the Nucleotide
sequence at some point of DNA which can
occur due to
Addition
Deletion
Substitution
of one or more bases
34
Dr.T.V.Rao MD
Mutation Type
Frameshift (deletion)
(leu) (ser) (arg)
Normal AAT AGT GCC
(leu) (val) (pro)
Mutant AAT AGT GCC A
35
Dr.T.V.Rao MD
Mutation Type
Frameshift (insertion)
(leu) (ser) (arg)
Normal AAT AGT GCC
(leu) (glut) (cyst)
Mutant AAT CAGT GCC
36
Dr.T.V.Rao MD
37
Dr.T.V.Rao MD
Mutations can occur in any
sequence,inveitable, useful for
Survival
38
Dr.T.V.Rao MD
Multiple Mutations
• Causes extensive chromosomal rearrangement
• Missense mutation -Triplet code is acted so as
to specify an Aminoacid different from that
normally located at particular position in the
protein
• Nonsense mutation - Deletion of nucleotide
within a gene may cause premature polypeptide
chain termination by nonsense codon
• Tran version is Substitution of purine for
pyramidine or vice versa in the base pairing
39
Dr.T.V.Rao MD
Mutations
• Suppressor Mutation is reversal of mutant
phenotype by another mutation at a point of
DNA distant from that of original mutation.
• All genes are susceptible for mutations, but all
mutations are not expressed
• Lethal mutation is harmful destroy the vital
functions
40
Dr.T.V.Rao MD
Mutations
• Conditional Lethal mutant may be Live under
certain conditions
• Common example is temperature ( its ) mutant
• Temp sensitive ( ts) mutant lives at 350c but not
at 390c
• Each gene undergoes mutation at a fixed
frequency.
Bacteria undergo mutations at 10-4 - to 10-10
• Tutomerisim T – A is replaced by G - A
41
Dr.T.V.Rao MD
Mutagenic Agents
• U V rays
• Alkyl ting
agents
• Arcidine Dyes
42
Dr.T.V.Rao MD
GENE TRANSFER
Occurs by Complex Mechanisms
43
Dr.T.V.Rao MD
The three bacterial sexual
processes
– 1. Conjugation: direct transfer of
DNA from one bacterial cell to
another.
–2. Transduction: use of a
Bacteriophages (bacterial virus) to
transfer DNA between cells.
–3. Transformation: naked DNA is
taken up from the environment by
bacterial cells.
44
Dr.T.V.Rao MD
Transformation of Genetic
material
( Gene Transfer )
• Different
Mechanisms
Transformation
Transduction
Conjugation
45
Dr.T.V.Rao MD
Gene Transfer Processes for
Bacteria and Their Viruses
1. Conjugation
2. Transformation
3. Transduction
4. Infection with
bacteriophage
46
Dr.T.V.Rao MD
What is Transformation
• Transformation is defined as transfer of Genetic
information through the activity of DNA
• Griffith experiment
Mice injected with Live non capsulated ( R )
Pneumococci
with heat killed capsulated (S) Pneumococci
Lead to death of Mice with isolation of Live
capsulated Pneumococci
It means that some factor from Dead
pneumococci transferred to live non pathogenic
Pneumococci
Avery, McCleod, Mc Cartny in 1944 identified to be DNA 47
Dr.T.V.Rao MD
Griffith Phenomenon
48
Dr.T.V.Rao MD
Demonstration of
transformation
Avery, MacLeod, and
McCarty (1944)
49
Dr.T.V.Rao MD
Transduction
• Generalized involve any segment of DNA
• Restricted when specific Bacteriophages
traduces only a particular genetic trait.
• Transduction effects Plasmids ,and Episomes
• Plasmid transfer induces Penicillin resistance in
Staphylococcus
• Helps Genetic mapping, also in eukaryotic cell
• Helps Genetic Engineering
T.V.Rao MD
50
Dr.T.V.Rao MD
Transduction
• Transduction is
defined as
transfer of
portion of DNA
from one
bacteria to
another by
Bacteriophages,
is known as
Transduction 51
Dr.T.V.Rao MD
DNA transfer through
Bacteriophages
• When the Phage
particle infects
another bacteria
DNA transfer is
effected and the
recipient cell
acquires new
characters coded
by donor DNA
52
Dr.T.V.Rao MD
Bacteriophages
• Are viruses that
parasitize bacteria
and consists of
Nucleic acid core and
a protein coat
• A phage particle may
have at its core
besides its own
nucleic acid and a
segment of the Host
DNA 53
Dr.T.V.Rao MD
Transduction Types
• Two types of Transduction
• 1 Lytic and 2 Lysogenic
• 1 Virulent or Lytic cycle after
large number of progeny are
built up inside the host
bacterium ruptures and
phages are released 54
Dr.T.V.Rao MD
Lysogenicity creates new
characters
• Eg - Lysogenic conversion in
Diphtheria bacilli which
acquires toxigenicity by
lysogenization with phage beta
• Elimination of phage for
toxigenic strain renders
nontoxigenic 55
Dr.T.V.Rao MD
Conjugation
Lederberg - Tatum
• A process by which a Donor cell or male cell
makes contact with another cell, the recipient or
Female cell.
• DNA is directly transferable
• Plasmid Carry genetic information necessary for
conjugation to occur.
• Only cell that contain such plasmids can act as
donor. the cell lacking a corresponding plasmid
act as recipient.
• Requires direct contact between donor and
recipient
56
Dr.T.V.Rao MD
Conjugation
• The ability to conjugate is
conferred by the F plasmid. A
plasmid is a small circle of DNA
that replicates independently of
the chromosome. Bacterial cells
that contain an F plasmid are
called “F+”. Bacteria that don’t
have an F plasmid are called “ 57
Dr.T.V.Rao MD
Conjugation - Transferring
genes with plasmids
• Plasmids
mediating
conjugation carry
genes coding for
properties, of 1-2
microns long
protein appendage
termed Pilus on the
Donor cell
58
Dr.T.V.Rao MD
Mechanism of Transfer I:
Conjugation
59
Dr.T.V.Rao MD
Conjugation
60
Dr.T.V.Rao MD
Simple Conjugation
61
Dr.T.V.Rao MD
Conjugation
62
Dr.T.V.Rao MD
Pilus helps Conjugation
• Different types of Pilus
are specified by different
types of plasmids and
can help in aid of plasmid
classification.
• Only one strand of
circular DNA of the
plasmid nicked upon at a
specific site and passed
into a recipient.
• Spread to all other cells.
63
Dr.T.V.Rao MD
F factor
• Transfer factor that
contains the genetic
information necessary
for synthesis of Sex
Pilus and for self
transfer without any
other identifiable
genetic materials
such as drug
resistance
T.V.Rao MD
64
Dr.T.V.Rao MD
F factor helps transformation
• F+ called as Donor bacteria can transform
F- into F+ cell
Can be Episomes able to exist in some cells in the
integrated state in the donor cell chromosome
Can transform chromosomal genes to recruitment with
high frequency are known as Hfr cells
Conversion of F+ cells into Hfr state is reversible.
F factor incorporates some chromosomal genes and is
called as F’
Sexduction The process of transfer of host genes
through F’ factor
65
Dr.T.V.Rao MD
DNA transfer through
Bacteriophages
• When the Phage
particle infects
another bacteria
DNA transfer is
effected and the
recipient cell
acquires new
characters coded
by donor DNA
66
Dr.T.V.Rao MD
Types of DNA transfer through
Bacteriophages
67
Dr.T.V.Rao MD
Colicinogenic ( Col ) Factor
• Coli form Bacteria
produce Colicins
• Colicins are lethal to
other Enterobacteriaceae
• Pyocins produce by
Pseudomonas
• Diptherocins produced
by C.diptheria
• Plasmid transmits col factor
leads to self transfer of
chromosomal segments
T.V.Rao MD
68
Dr.T.V.Rao MD
Resistance Transfer Factor
RTF
• Plasmids – helps to spread multiple drug
resistance
• Discovered in 1959 Japan
• Infections caused due to Shigella spread
resistance to following Antibiotics
Sulphonamides
Streptomycin
Chloramphenicol,
Tetracycline
69
Dr.T.V.Rao MD
RTF
• Shigella + E.coli
excreted in the stool
resistant to several
drugs in vivo and vitro
• Plasmid mediated –
transmitted by
Conjugation
• Episomes spread the
resistance
70
Dr.T.V.Rao MD
Bacterial Conjugation:
High Frequency Transfer (Her) Cells
71
Dr.T.V.Rao MD
Hfr Conjugation
72
Dr.T.V.Rao MD
Sequence of RTF transmission
73
Dr.T.V.Rao MD
Hfr cell conjugating a Normal cell
74
Dr.T.V.Rao MD
Composition of RTF
• Plasmid consists of two
components
• A transfer factor RT, helps
conjugational transfer and
resistant determinants ( r ) to
each of the several drugs
• RTF + r determinants are known
as R factor
75
Dr.T.V.Rao MD
R factor
• R factor can contain
several determinants as
many as 8 or > 8 drugs
• Guide the cell for
production of
Enterotoxins too
• But R factors can be
inhibited by
Bile salts
R factors can be
transferred to animals
76
Dr.T.V.Rao MD
Genesis of R factors
• In discriminate use of
Antibiotics in vet nary Medicine
has increased the spread of R
factors to Human
• Addition of Antibiotics to
Animal feeds to be prohibited.
77
Dr.T.V.Rao MD
Genetic Mechanisms of Drug
Resistance
• Bacteria acquire drug resistance through several
Mechanisms
• Mutations
• Genetic transfer
Transformation,
Transduction
Conjugation
Several Biochemical Mechanisms
Decreasing permeability of drugs,
Attaining alternative pathways
Produce enzymes and inactivate drugs
78
Dr.T.V.Rao MD
Genetic Mechanisms in Bacteria helps to
Spread the Infectious diseases
79
Dr.T.V.Rao MD
Mutations
• Mutilations can be
1 Stepwise mutation as in Penicillin use
2 One step mutation
Streptomycin use
May show low resistance or High resistance
If tuberculosis is treated with sole drug as of Only
Streptomycin some resistant mutants appear
and replaces sensitive bacteria in due course
so the occurrence of MDR - TB
80
Dr.T.V.Rao MD
Other Mechanisms
• Use of Penicillin created resistant
Staphylococcus by transduction
• R factors created resistance to several drugs,
caused increased virulence
• Spread to several humans and animals
Best option- To restrict use of
Antibiotics
81
Dr.T.V.Rao MD
Transposable Genetic Elements
Structurally / Genetically – Discrete sequence of
DNA – Move around in a cut and paste manner
between Chromosomal and Extra chromosomal
DNA molecules within cells.
Called as Transposons _ Jumping Genes
Genetic transfer due to Transposition
Small Transposons 1 – 2 Kb
Not self replicating and depend on Plasmid or
Chromosome for replication.
A chunk of DNA is added by Transposons.
82
Dr.T.V.Rao MD
Transposons and R factor
• R forms may have evolved as a collection of
Transposons
• Each carrying Genes that confers resistance to
one or several Antibiotics
• Seen in Plasmids,
Microorganisms
Animals
Laboratory Manipulations are called as Genetic
Engineering
83
Dr.T.V.Rao MD
Molecular Genetics
• Analysis and
manipulation of
DNA using
Biochemical
and
Microbiological
techniques 84
Dr.T.V.Rao MD
Genetic Engineering
• Under standing Molecular
genetics in Biochemistry
fuels genetic Engineering
• Recombinant DNA
(renal) techniques
changed the ideals of
Medicine
• Genetic Engineering
await many
surprises?
85
Dr.T.V.Rao MD
Genetic Engineering Was Born from
Genetic Recombination
•Genetic engineering involves changing
the genetic material in an organism to
alter its traits or products
•A recombinant DNA molecule contains
DNA fragments spliced together from 2 or
more organisms
Genetic Engineering
86
Dr.T.V.Rao MD
Modern applications
• Pharmaceutical production
–Insulin, interferon, hormones, vaccines
etc.
• Genetically engineered plants
• Animal gene alterations
• Gene probes
• DNA fingerprinting
• The human genome initiative
Dr.T.V.Rao MD 87
Genetic Engineering
• Isolation of Genes coding for any
desired protein from Microorganism
or from cell of higher life forms
including human beings and their
introduction into a suitable
microorganism in which genes would
function directing the production of
specific proteins
88
Dr.T.V.Rao MD
Genetic Engineering changing
the Diagnostic and Therapeutic
Protocols in
MEDICINE
89
Dr.T.V.Rao MD
Research on Gene transfer
shapes the future of Science
90
Dr.T.V.Rao MD
Genetically Engineered Products
• Can prepare desired
protein in pure form in
economic way
Somatostatin
• Commercial
preparations pdf
Cloned Human
Insulin
Interferons
Hepatitis B
vaccine 91
Dr.T.V.Rao MD
Restriction Endonucleases
• A restriction enzyme (or restriction
endonuclease) is an enzyme that cuts
double-stranded DNA. The enzyme
makes two incisions, one through each of
the sugar-phosphate backbones (i.e., each
strand) of the double helix without
damaging the nitrogenous bases They
work with cutting up foreign DNA, a
process called
92
Dr.T.V.Rao MD
Restriction Endonucleases
Made the advances in Genetic
Engineering
93
Dr.T.V.Rao MD
DNA Probes
• There are Radioactive
Biotinylated otherwise
labeled copies united
single stranded DNA
Contains 20 -25 nucleotides
Helps detection of
Homology DNA by
Hybridization.
Helps Diagnosis of
Infectious Diseases
Minute quantities of DNA
can be detected.
94
Dr.T.V.Rao MD
Blotting Techniques
• Drug fragments obtained by restriction
enzyme digestion on separation Gel can
be transferred to Nitrocellulose or nylon
membranes
• Several methods
1 Southern blotting
2 Northern Blotting
3 Western blotting
95
Dr.T.V.Rao MD
western blot
• The western blot (alternatively, protein
immunoblot) is an analytical technique
used to detect specific proteins in a given
sample of tissue homogenate or extract. It
uses gel electrophoresis to separate
native or denatured proteins by the length
of the polypeptide (denaturing conditions)
or by the 3-D structure of the protein
(native/ non-denaturing conditions)
96
Dr.T.V.Rao MD
Western Blotting
• In Western Blot Protein (
Antigen ) mixture is
separated by SDS (
Sodium dodecyl sulfate –
polyacrylamide gel
electrophoresis ) Blotted
on to Nitro cellulose strips
and identified by radio
labeled or enzyme
labeled antibodies as
probes
97
Dr.T.V.Rao MD
Western Blot
98
Dr.T.V.Rao MD
Western Blot to confirm
HIV Infections made land mark
Diagnostic tool
• Western Blot testing
is confirmatory test for
diagnosis of
HIV/AIDS
• Identifies antibodies
directed against
different antigens in
pathogen
Surface,
Core
RT antigen 99
Dr.T.V.Rao MD
Polymerase chain reaction
Kary B Mullis 1983
• Rapid
• Automatic
amplification of
specific DNA
sequences
• Nobel prize winning
Technology 1993
100
Dr.T.V.Rao MD
PCR -Sequences
• PCR consists of several
cycles of sequential DNA
replication where the
products of first cycle
becomes the template for
the Next
• It makes available
abundant quantities of
specific DNA sequences
starting
101
Dr.T.V.Rao MD
Genetic Mapping
• Genetic sequences
for Bacteriophages
and virus
• Genetic mapping is
done most of the
Human Genes
102
Dr.T.V.Rao MD
Newer Understanding on
GENES
103
Dr.T.V.Rao MD
Human Genome Project
104
Dr.T.V.Rao MD
Human Genome Project
• Completed in 2003, the Human Genome
Project (HGP) was a 13-year project
coordinated by the U.S. Department of
Energy and the National Institutes of
Health. During the early years of the HGP,
the Welcome Trust (U.K.) became a major
partner; additional contributions came from
Japan, France, Germany, China, and
others
105
Dr.T.V.Rao MD
Genetics are Complex - Leading
the birth of BIOINFORMATICS
106
Dr.T.V.Rao MD
Genes Evolved and made us
Men
What NEXT ?
107
Dr.T.V.Rao MD
Are We Playing with Genes in the
Right Direction ?
108
Dr.T.V.Rao MD
Understanding of human Genome is
Changing the Future of Medicine
109
Dr.T.V.Rao MD
• Programmed Created by Dr.T.V.Rao MD
for Undergraduate Medical Students in
the Developing World
• Email
• doctortvrao@gmail.com
110
Dr.T.V.Rao MD

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  • 1. Bacterial Genetics Learning the Basics 1 Dr.T.V.Rao MD Dr.T.V.Rao MD
  • 3. Genes are Eternal Run In Progeny 3 Dr.T.V.Rao MD
  • 4. Understanding Genetics We resemble and differ because of Genetic configurations Parents - Son - Daughter, how they resemble each other. They breed true from Generation to Generation But vary in small proportions in progeny. Bacteria too obey the laws of Genetics 4 Dr.T.V.Rao MD
  • 5. Watson - Crick Discovery of DNA 5 Dr.T.V.Rao MD
  • 6. Beginning of Bacterial Genetics • The principles of Genetics were applied to bacteria and viruses • Advances in Genetic process also of lead to fundamental advances in Biology and Biochemistry. A Birth of New Branch of Science Molecular Biology 6 Dr.T.V.Rao MD
  • 7. DNA A Complex Structure Makes Life 7 Dr.T.V.Rao MD
  • 8. DNA ( Deoxyribonucleic Acid ) • DNA is composed of Many Units of Adenine – Thymine A – T Guanine – Cytosine G - C A+ T G+C proportion differ for each species DNA replicates first unwinding at one end to form a fork Each strand of fork acting as template for the synthesis of complementary strand 8 Dr.T.V.Rao MD
  • 11. DNA • A DNA molecule is composed of two chains of Nucleotides wound together in the form of a Double Helix • Each chain has back bone of Deoxyribose and Phosphates residues arranged alternatively 11 Dr.T.V.Rao MD
  • 12. Structure of DNA • Attached to each Deoxyribose and phosphate residues arranged alternatively • Attached to each Deoxyribose are of four nitrogen bases • Purines - Adenine, Guanine • Pyramidine Thymidine and Cytosine 12 Dr.T.V.Rao MD
  • 13. How RNA differs from DNA • RNA contains - Sugar Ribose instead of Deoxyribose • Uracil is present instead of Thymine • Types of RNA Messenger RNA mRNA Ribosomal RNA rRNA Transfer RNA tRNA 13 Dr.T.V.Rao MD
  • 15. Knowledge on DNA lead to advances in Molecular Biology • Central dogma of Life – Deoxyribonucleic acid • DNA carries the Genetic information • DNA is transcribed to RNA – Polypeptides Cell Function depends upon specific polypeptides – Proteins – Enzymes DNA is a store house of Protein synthesis DNA acts a Template for synthesis of mRNA Virus differs from other as they contains either DNA or RNA 15 Dr.T.V.Rao MD
  • 16. What is a Code in Genetics • Code is a unit consists of sequence of three Bases • Code is triplet A-T- C • A code can make single Amino acid • More than one code present for making similar sequence of Amino acid • AGA make Arginine • AGC, CGU, CGG, also code for similar Amino acid • Some Codons UAA don't code for any Amino acid called as Nonsense codon 16 Dr.T.V.Rao MD
  • 17. What is a Gene • Gene is a sequence of DNA carrying codons specifying for particular polypeptide. • DNA contains many Genes( A combinations of hundreds and thousands of Nucleotides ) 17 Dr.T.V.Rao MD
  • 18. Bacterial Chromosome • Contains a Double stranded molecules of DNA arranged in circular form. • Length 1,ooo microns. • Bacterial DNA contains about 4,000kilobases • I kb = 1000 base pairs ( A-T ) ( G-C) • Humans have about 3,000 kb pairs. 18 Dr.T.V.Rao MD
  • 19. How bacterial Genome differs from Higher forms of Life • Several stretches of DNA don't appear to function as codons, occurs between the coding sequences of Gene. called as INTRONS. • Coded are called as EXONS • In transcription introns are excised when form RNA before translated by ribosomal proteins. 19 Dr.T.V.Rao MD
  • 20. Extra chromosomal Genetic Elements Bacteria posses Extra chromosomal genetic elements Not Essential for survival of Bacteria But makes the Bacteria Resistant to antibiotics, and makes them survive Able to produce toxins 20 Dr.T.V.Rao MD
  • 21. Plasmids • Plasmids are circular DNA molecules present in the cytoplasm of the Bacteria • Capable of Autonomous replication • Can transfer genes from one cell to other • Act as vectors in Genetic engineering. • Can also present in Yeasts 21 Dr.T.V.Rao MD
  • 22. Plasmid ( Blue ) 22 Dr.T.V.Rao MD
  • 23. Plasmids • Plasmid seem to be ubiquitous in bacteria, May encode genetic information for properties 1 Resistance to Antibiotics 2 Bacteriocins production 3 Enterotoxin production 4 Enhanced pathogen city 5 Reduced Sensitivity to mutagens 6 Degrade complex organic molecules 23 Dr.T.V.Rao MD
  • 24. R plasmid R: drug resistance RTF: transfer of R plasmid 24 Dr.T.V.Rao MD
  • 25. Plasmids • Can be integrated with Chromosomal DNA • Episomes - Integrated form of plasmid with DNA 25 Dr.T.V.Rao MD
  • 26. Potentials of Plasmids • Plasmids can be self transmissible and Non transmissible • Transfers the Sex and Drug resistance with the help of restriction end nucleases 26 Dr.T.V.Rao MD
  • 27. Classification of Plasmids • Incompatibility typing • Don't accommodate others which are similar • Other methods of Classification Centrifugation Electrophoresis Genetic methods 27 Dr.T.V.Rao MD
  • 28. Genotypic and Phenotypic variation • Genome – Sum total of Gene that make up the genetic apparatus of cell established as Genotype. • Hereditary constitution of cell this transmitted to its progeny • Phenotype – is the physical expression in a environment. Change according to environment. 28 Dr.T.V.Rao MD
  • 29. What is Phenotypic expression • Exhibit – different phenotypes • Appearance differs in different situations. • Eg Typhoid bacilli flagellated normally • But grown in Phenol agar don't grow flagella So flagella are lost physical variation • Lactose fermentation in E.coli dependent on Beta Galactosidase When lactose present - test is positive When lactose is absent - test turns negative 29 Dr.T.V.Rao MD
  • 30. Different Enzymes Guided by Genomic configurations • Inducer enzyme acts in the presence of substrate • Constitutive enzyme acts irrespective of presence or absence of enzyme. • Phenotypic variations influenced by environment limited in range by genes • Genotypic variations are stable not influenced by environment. 30 Dr.T.V.Rao MD
  • 31. Principles of Genotypic variations • Mutations • Genotypic by transfer of genes Transformation Transduction (Lysogenic conversion) Conjugation 31 Dr.T.V.Rao MD
  • 32. Replica Plating, pt. 2 32 Dr.T.V.Rao MD
  • 33. Mutations in Bacteria • Bacteria Multiply by asexual binary fission • Altered Nucleotide sequence in expresses new or altered characteristics • Selective value to the organism • Evolutionary value • Acquires Antibiotic resistance grows in body without inhibition • Become a prominent organism • Phenotypic variation occurs when genes changes in response to the environment but reversible. T.V.Rao MD 33 Dr.T.V.Rao MD
  • 34. Mutations • Mutation is a Random, Undirected, Heritable variation • Caused by alteration in the Nucleotide sequence at some point of DNA which can occur due to Addition Deletion Substitution of one or more bases 34 Dr.T.V.Rao MD
  • 35. Mutation Type Frameshift (deletion) (leu) (ser) (arg) Normal AAT AGT GCC (leu) (val) (pro) Mutant AAT AGT GCC A 35 Dr.T.V.Rao MD
  • 36. Mutation Type Frameshift (insertion) (leu) (ser) (arg) Normal AAT AGT GCC (leu) (glut) (cyst) Mutant AAT CAGT GCC 36 Dr.T.V.Rao MD
  • 38. Mutations can occur in any sequence,inveitable, useful for Survival 38 Dr.T.V.Rao MD
  • 39. Multiple Mutations • Causes extensive chromosomal rearrangement • Missense mutation -Triplet code is acted so as to specify an Aminoacid different from that normally located at particular position in the protein • Nonsense mutation - Deletion of nucleotide within a gene may cause premature polypeptide chain termination by nonsense codon • Tran version is Substitution of purine for pyramidine or vice versa in the base pairing 39 Dr.T.V.Rao MD
  • 40. Mutations • Suppressor Mutation is reversal of mutant phenotype by another mutation at a point of DNA distant from that of original mutation. • All genes are susceptible for mutations, but all mutations are not expressed • Lethal mutation is harmful destroy the vital functions 40 Dr.T.V.Rao MD
  • 41. Mutations • Conditional Lethal mutant may be Live under certain conditions • Common example is temperature ( its ) mutant • Temp sensitive ( ts) mutant lives at 350c but not at 390c • Each gene undergoes mutation at a fixed frequency. Bacteria undergo mutations at 10-4 - to 10-10 • Tutomerisim T – A is replaced by G - A 41 Dr.T.V.Rao MD
  • 42. Mutagenic Agents • U V rays • Alkyl ting agents • Arcidine Dyes 42 Dr.T.V.Rao MD
  • 43. GENE TRANSFER Occurs by Complex Mechanisms 43 Dr.T.V.Rao MD
  • 44. The three bacterial sexual processes – 1. Conjugation: direct transfer of DNA from one bacterial cell to another. –2. Transduction: use of a Bacteriophages (bacterial virus) to transfer DNA between cells. –3. Transformation: naked DNA is taken up from the environment by bacterial cells. 44 Dr.T.V.Rao MD
  • 45. Transformation of Genetic material ( Gene Transfer ) • Different Mechanisms Transformation Transduction Conjugation 45 Dr.T.V.Rao MD
  • 46. Gene Transfer Processes for Bacteria and Their Viruses 1. Conjugation 2. Transformation 3. Transduction 4. Infection with bacteriophage 46 Dr.T.V.Rao MD
  • 47. What is Transformation • Transformation is defined as transfer of Genetic information through the activity of DNA • Griffith experiment Mice injected with Live non capsulated ( R ) Pneumococci with heat killed capsulated (S) Pneumococci Lead to death of Mice with isolation of Live capsulated Pneumococci It means that some factor from Dead pneumococci transferred to live non pathogenic Pneumococci Avery, McCleod, Mc Cartny in 1944 identified to be DNA 47 Dr.T.V.Rao MD
  • 49. Demonstration of transformation Avery, MacLeod, and McCarty (1944) 49 Dr.T.V.Rao MD
  • 50. Transduction • Generalized involve any segment of DNA • Restricted when specific Bacteriophages traduces only a particular genetic trait. • Transduction effects Plasmids ,and Episomes • Plasmid transfer induces Penicillin resistance in Staphylococcus • Helps Genetic mapping, also in eukaryotic cell • Helps Genetic Engineering T.V.Rao MD 50 Dr.T.V.Rao MD
  • 51. Transduction • Transduction is defined as transfer of portion of DNA from one bacteria to another by Bacteriophages, is known as Transduction 51 Dr.T.V.Rao MD
  • 52. DNA transfer through Bacteriophages • When the Phage particle infects another bacteria DNA transfer is effected and the recipient cell acquires new characters coded by donor DNA 52 Dr.T.V.Rao MD
  • 53. Bacteriophages • Are viruses that parasitize bacteria and consists of Nucleic acid core and a protein coat • A phage particle may have at its core besides its own nucleic acid and a segment of the Host DNA 53 Dr.T.V.Rao MD
  • 54. Transduction Types • Two types of Transduction • 1 Lytic and 2 Lysogenic • 1 Virulent or Lytic cycle after large number of progeny are built up inside the host bacterium ruptures and phages are released 54 Dr.T.V.Rao MD
  • 55. Lysogenicity creates new characters • Eg - Lysogenic conversion in Diphtheria bacilli which acquires toxigenicity by lysogenization with phage beta • Elimination of phage for toxigenic strain renders nontoxigenic 55 Dr.T.V.Rao MD
  • 56. Conjugation Lederberg - Tatum • A process by which a Donor cell or male cell makes contact with another cell, the recipient or Female cell. • DNA is directly transferable • Plasmid Carry genetic information necessary for conjugation to occur. • Only cell that contain such plasmids can act as donor. the cell lacking a corresponding plasmid act as recipient. • Requires direct contact between donor and recipient 56 Dr.T.V.Rao MD
  • 57. Conjugation • The ability to conjugate is conferred by the F plasmid. A plasmid is a small circle of DNA that replicates independently of the chromosome. Bacterial cells that contain an F plasmid are called “F+”. Bacteria that don’t have an F plasmid are called “ 57 Dr.T.V.Rao MD
  • 58. Conjugation - Transferring genes with plasmids • Plasmids mediating conjugation carry genes coding for properties, of 1-2 microns long protein appendage termed Pilus on the Donor cell 58 Dr.T.V.Rao MD
  • 59. Mechanism of Transfer I: Conjugation 59 Dr.T.V.Rao MD
  • 63. Pilus helps Conjugation • Different types of Pilus are specified by different types of plasmids and can help in aid of plasmid classification. • Only one strand of circular DNA of the plasmid nicked upon at a specific site and passed into a recipient. • Spread to all other cells. 63 Dr.T.V.Rao MD
  • 64. F factor • Transfer factor that contains the genetic information necessary for synthesis of Sex Pilus and for self transfer without any other identifiable genetic materials such as drug resistance T.V.Rao MD 64 Dr.T.V.Rao MD
  • 65. F factor helps transformation • F+ called as Donor bacteria can transform F- into F+ cell Can be Episomes able to exist in some cells in the integrated state in the donor cell chromosome Can transform chromosomal genes to recruitment with high frequency are known as Hfr cells Conversion of F+ cells into Hfr state is reversible. F factor incorporates some chromosomal genes and is called as F’ Sexduction The process of transfer of host genes through F’ factor 65 Dr.T.V.Rao MD
  • 66. DNA transfer through Bacteriophages • When the Phage particle infects another bacteria DNA transfer is effected and the recipient cell acquires new characters coded by donor DNA 66 Dr.T.V.Rao MD
  • 67. Types of DNA transfer through Bacteriophages 67 Dr.T.V.Rao MD
  • 68. Colicinogenic ( Col ) Factor • Coli form Bacteria produce Colicins • Colicins are lethal to other Enterobacteriaceae • Pyocins produce by Pseudomonas • Diptherocins produced by C.diptheria • Plasmid transmits col factor leads to self transfer of chromosomal segments T.V.Rao MD 68 Dr.T.V.Rao MD
  • 69. Resistance Transfer Factor RTF • Plasmids – helps to spread multiple drug resistance • Discovered in 1959 Japan • Infections caused due to Shigella spread resistance to following Antibiotics Sulphonamides Streptomycin Chloramphenicol, Tetracycline 69 Dr.T.V.Rao MD
  • 70. RTF • Shigella + E.coli excreted in the stool resistant to several drugs in vivo and vitro • Plasmid mediated – transmitted by Conjugation • Episomes spread the resistance 70 Dr.T.V.Rao MD
  • 71. Bacterial Conjugation: High Frequency Transfer (Her) Cells 71 Dr.T.V.Rao MD
  • 73. Sequence of RTF transmission 73 Dr.T.V.Rao MD
  • 74. Hfr cell conjugating a Normal cell 74 Dr.T.V.Rao MD
  • 75. Composition of RTF • Plasmid consists of two components • A transfer factor RT, helps conjugational transfer and resistant determinants ( r ) to each of the several drugs • RTF + r determinants are known as R factor 75 Dr.T.V.Rao MD
  • 76. R factor • R factor can contain several determinants as many as 8 or > 8 drugs • Guide the cell for production of Enterotoxins too • But R factors can be inhibited by Bile salts R factors can be transferred to animals 76 Dr.T.V.Rao MD
  • 77. Genesis of R factors • In discriminate use of Antibiotics in vet nary Medicine has increased the spread of R factors to Human • Addition of Antibiotics to Animal feeds to be prohibited. 77 Dr.T.V.Rao MD
  • 78. Genetic Mechanisms of Drug Resistance • Bacteria acquire drug resistance through several Mechanisms • Mutations • Genetic transfer Transformation, Transduction Conjugation Several Biochemical Mechanisms Decreasing permeability of drugs, Attaining alternative pathways Produce enzymes and inactivate drugs 78 Dr.T.V.Rao MD
  • 79. Genetic Mechanisms in Bacteria helps to Spread the Infectious diseases 79 Dr.T.V.Rao MD
  • 80. Mutations • Mutilations can be 1 Stepwise mutation as in Penicillin use 2 One step mutation Streptomycin use May show low resistance or High resistance If tuberculosis is treated with sole drug as of Only Streptomycin some resistant mutants appear and replaces sensitive bacteria in due course so the occurrence of MDR - TB 80 Dr.T.V.Rao MD
  • 81. Other Mechanisms • Use of Penicillin created resistant Staphylococcus by transduction • R factors created resistance to several drugs, caused increased virulence • Spread to several humans and animals Best option- To restrict use of Antibiotics 81 Dr.T.V.Rao MD
  • 82. Transposable Genetic Elements Structurally / Genetically – Discrete sequence of DNA – Move around in a cut and paste manner between Chromosomal and Extra chromosomal DNA molecules within cells. Called as Transposons _ Jumping Genes Genetic transfer due to Transposition Small Transposons 1 – 2 Kb Not self replicating and depend on Plasmid or Chromosome for replication. A chunk of DNA is added by Transposons. 82 Dr.T.V.Rao MD
  • 83. Transposons and R factor • R forms may have evolved as a collection of Transposons • Each carrying Genes that confers resistance to one or several Antibiotics • Seen in Plasmids, Microorganisms Animals Laboratory Manipulations are called as Genetic Engineering 83 Dr.T.V.Rao MD
  • 84. Molecular Genetics • Analysis and manipulation of DNA using Biochemical and Microbiological techniques 84 Dr.T.V.Rao MD
  • 85. Genetic Engineering • Under standing Molecular genetics in Biochemistry fuels genetic Engineering • Recombinant DNA (renal) techniques changed the ideals of Medicine • Genetic Engineering await many surprises? 85 Dr.T.V.Rao MD
  • 86. Genetic Engineering Was Born from Genetic Recombination •Genetic engineering involves changing the genetic material in an organism to alter its traits or products •A recombinant DNA molecule contains DNA fragments spliced together from 2 or more organisms Genetic Engineering 86 Dr.T.V.Rao MD
  • 87. Modern applications • Pharmaceutical production –Insulin, interferon, hormones, vaccines etc. • Genetically engineered plants • Animal gene alterations • Gene probes • DNA fingerprinting • The human genome initiative Dr.T.V.Rao MD 87
  • 88. Genetic Engineering • Isolation of Genes coding for any desired protein from Microorganism or from cell of higher life forms including human beings and their introduction into a suitable microorganism in which genes would function directing the production of specific proteins 88 Dr.T.V.Rao MD
  • 89. Genetic Engineering changing the Diagnostic and Therapeutic Protocols in MEDICINE 89 Dr.T.V.Rao MD
  • 90. Research on Gene transfer shapes the future of Science 90 Dr.T.V.Rao MD
  • 91. Genetically Engineered Products • Can prepare desired protein in pure form in economic way Somatostatin • Commercial preparations pdf Cloned Human Insulin Interferons Hepatitis B vaccine 91 Dr.T.V.Rao MD
  • 92. Restriction Endonucleases • A restriction enzyme (or restriction endonuclease) is an enzyme that cuts double-stranded DNA. The enzyme makes two incisions, one through each of the sugar-phosphate backbones (i.e., each strand) of the double helix without damaging the nitrogenous bases They work with cutting up foreign DNA, a process called 92 Dr.T.V.Rao MD
  • 93. Restriction Endonucleases Made the advances in Genetic Engineering 93 Dr.T.V.Rao MD
  • 94. DNA Probes • There are Radioactive Biotinylated otherwise labeled copies united single stranded DNA Contains 20 -25 nucleotides Helps detection of Homology DNA by Hybridization. Helps Diagnosis of Infectious Diseases Minute quantities of DNA can be detected. 94 Dr.T.V.Rao MD
  • 95. Blotting Techniques • Drug fragments obtained by restriction enzyme digestion on separation Gel can be transferred to Nitrocellulose or nylon membranes • Several methods 1 Southern blotting 2 Northern Blotting 3 Western blotting 95 Dr.T.V.Rao MD
  • 96. western blot • The western blot (alternatively, protein immunoblot) is an analytical technique used to detect specific proteins in a given sample of tissue homogenate or extract. It uses gel electrophoresis to separate native or denatured proteins by the length of the polypeptide (denaturing conditions) or by the 3-D structure of the protein (native/ non-denaturing conditions) 96 Dr.T.V.Rao MD
  • 97. Western Blotting • In Western Blot Protein ( Antigen ) mixture is separated by SDS ( Sodium dodecyl sulfate – polyacrylamide gel electrophoresis ) Blotted on to Nitro cellulose strips and identified by radio labeled or enzyme labeled antibodies as probes 97 Dr.T.V.Rao MD
  • 99. Western Blot to confirm HIV Infections made land mark Diagnostic tool • Western Blot testing is confirmatory test for diagnosis of HIV/AIDS • Identifies antibodies directed against different antigens in pathogen Surface, Core RT antigen 99 Dr.T.V.Rao MD
  • 100. Polymerase chain reaction Kary B Mullis 1983 • Rapid • Automatic amplification of specific DNA sequences • Nobel prize winning Technology 1993 100 Dr.T.V.Rao MD
  • 101. PCR -Sequences • PCR consists of several cycles of sequential DNA replication where the products of first cycle becomes the template for the Next • It makes available abundant quantities of specific DNA sequences starting 101 Dr.T.V.Rao MD
  • 102. Genetic Mapping • Genetic sequences for Bacteriophages and virus • Genetic mapping is done most of the Human Genes 102 Dr.T.V.Rao MD
  • 105. Human Genome Project • Completed in 2003, the Human Genome Project (HGP) was a 13-year project coordinated by the U.S. Department of Energy and the National Institutes of Health. During the early years of the HGP, the Welcome Trust (U.K.) became a major partner; additional contributions came from Japan, France, Germany, China, and others 105 Dr.T.V.Rao MD
  • 106. Genetics are Complex - Leading the birth of BIOINFORMATICS 106 Dr.T.V.Rao MD
  • 107. Genes Evolved and made us Men What NEXT ? 107 Dr.T.V.Rao MD
  • 108. Are We Playing with Genes in the Right Direction ? 108 Dr.T.V.Rao MD
  • 109. Understanding of human Genome is Changing the Future of Medicine 109 Dr.T.V.Rao MD
  • 110. • Programmed Created by Dr.T.V.Rao MD for Undergraduate Medical Students in the Developing World • Email • doctortvrao@gmail.com 110 Dr.T.V.Rao MD