2. Lederberg and Tatum (1946) discovered conjugation in e.coli
Detailed structure studies were made by Woodman and Jacob
(1956)
It was defined as process by which genetic material is transferred
from one bacterial cell (“donor cell or male cell”) to another
(“recipient cell or female cell”) through a specialized intercellular
connection called Sex pilus or Conjugation tube.
Conjugation
3. The maleness and femaleness of bacterial cells are determined by
presence or absence of F- plasmid also called f- factor or sex- factor.
F-plasmid , an extra chromosomal genetic material is always present
in cytoplasm of donor or male cell.
And the later develop specialised cell surface appendages called “F-
pili” or “sex pili” under the control of f- plasmid where , in recipient or
female cells always lack f-plasmid .
4.
5. F-plasmid can exist in two different states:-
The autonomous state in which it lies free in cytoplasm and replicate
independent of bacterial chromosome (DNA): a donor or male cell
containing f-factor in autonomous state is called F+ cell.
The integrated state in which it is integrated into the bacterial
chromosome (DNA) and replicates along with it ; a donor or male cell
containing f-factor in integrated state is called Hfr cell or male cell,
however the recipient or female cell lacks f-factor and this is called F-
cell.
6. Conjugation between f+ cell & f- cell
Step 1: F+ cell produce hair like appendages called sex pili which
facilitates cell to cell contact with f-strain by forming conjugation tube.
Step 2: Replication of F factor making copy.
Step 3: Transfer of copy of F plasmid to recipient cell via conjugation
tube.
Step 4: Conjugation tube dissolves
Now the f- stain is also f+ but, here bacterial genome is not involved.
f+ cell + f-cell= f+cell + f+cell
7.
8. Conjugation
between Hfr
cell and f-cell :-
Step 1:-Hfr donor cell produce hair like
appendages called sex pili which facilitates cell to
cell contact with f- strain by forming conjugation
tube.
Step 2:- Hfr undergoes replication by rolling
circle mechanism.
Step 3:- Circular Hfr DNA breaks open and
become linear. A portion of F plasmid occupies the
leading end.
Step 4:- The leading end moves to recipient cell
via conjugation tube.
Step 5:- During this transfer, conjugation tube
abruptly breaks up , so that only part of Hfr DNA
is transferred to the recipient.
9. Step 6:- The transferred donor
DNA gets integrated to the
recipient chromosome. This
bring about genetic variability
10. Conjugation
between f’cell
& f-cell:-
It is also called sex duction.
Transfer of f’ factor to receipt
occur in mating between f’ and f-
.
The transfer of f’ to recipient
produce partial diploids .
Recombination occur between
recipient chromosome and f’,
producing recombinant.
Recombination of this type
mediated as sex duction
12. Transduction was first discovered in 1952 by Joshua Lederberg and
Norton Zinder.
Studied in Salmonella typhimurium
It is special method of genetic recombination where genetic material is
transferred from the donor to recipient cell through a non- replicating
bacteriophage- temperate bacteriophage.
In this process, a small fragment of bacterial DNA is incorporated into an
attacking bacteriophage and when this bacteriophage infects a new
bacterial cell, it transfers the genetic material into it, and thus genetic
recombination takes place.
13. Transduction are of two types:-
Specialised transduction
Generalised transduction
14. Specialised
transduction
In this process , DNA fragment is transferred from
one bacterium to another bacterium by temperate
bacteriophage that is now carrying donor bacterial
DNA due to an error in spontaneous induction
during lysogenic cycle.
15. STEPS INVOLVED IN SPECIALISED
TRANSDUCTION
1. A temperate bacteriophage infect susceptible bacterium into bacterium.
2. The DNA of bacteriophage, incorporated into genome of bacterium called
PROPHASE.
3. Occasionally, during spontaneous induction, a small piece of donor bacterial
DNA is picked up as part of the phage genome.
4. As bacteriophage replicate, the replicates the segment of bacterial genome also
replicate along with phage genome.
5. When this phage infect another bacterium, the donor DNA along with phage
genome inserted into a recipient bacterial genome form recombinant DNA.
16.
17.
18. Generalised
transduction
A DNA fragment is transferred from one bacterium to another
by a lytic bacteriophage that is now carrying donor bacterial
DNA due to an error in maturation during the lytic life cycle.
19. Steps involved in generalised transduction
1) A lytic bacteriophages infect a susceptible bacterium.
2) The phage genome enters into the bacterium. The genome directs a
bacterium’s metabolic machinery to manufacture bacteriophage
components and enzyme.
3) Occasionally, a bacterial genome get into a phage coat by mistake
and the bacteriophage released.
4) When this phage having bacterial DNA infect another bacterium, the
previous bacterial DNA incorporated into new bacterial genome
forming recombinant DNA.
20.
21.
22. Significance of transduction
It transfer genetic material from one cell to another cell and alter
genetic characteristics.
For example , In specialized transduction a cell lacking ability to
metabolize galactose could acquired ability.
It shows evolutionary relationship between the prophage and host
bacterial cell
Prophage can exist in a cell for long period suggest a possible
mechanism for viral origin of cancer.
It provide a way to study the gene linkage.