Bacterial conjugation is a fascinating process where one bacterium transfers genetic material to another. This exchange, facilitated by structures like the F pilus, plays a key role in genetic diversity and the spread of traits such as antibiotic resistance among bacteria.
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Formation of F pilus
- The F pilus is a hair-like appendage produced by F+ (donor) bacteria.
- It is composed of pilin protein and is essential for establishing contact with recipient cells.
- The pilus extends from the donor cell and can retract, bringing the two cells closer together.
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Contact between donor and recipient cells
- The F pilus attaches to specific receptors on the surface of the recipient (F-) cell.
- This initial contact is crucial for the subsequent steps of conjugation.
- The interaction is often mediated by surface proteins and can vary between different bacterial species.
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Stabilization of mating pair
- Once contact is established, the cells stabilize their connection to prevent disconnection.
- This stabilization may involve additional surface interactions and adhesion factors.
- A stable mating pair is necessary for the efficient transfer of genetic material.
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Formation of conjugation bridge
- The conjugation bridge is formed as the cells draw closer together, allowing for direct transfer of DNA.
- This bridge is a channel through which the DNA will pass from the donor to the recipient.
- It is essential for the physical connection required for DNA transfer.
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Nicking of F plasmid DNA
- The F plasmid DNA is nicked at a specific site by an enzyme called relaxase.
- This nicking creates a single-stranded DNA molecule that can be transferred.
- The process is crucial for initiating the transfer of genetic material.
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Transfer of single-stranded DNA
- The single-stranded DNA is transferred from the donor to the recipient through the conjugation bridge.
- This transfer is typically unidirectional, meaning only one strand is sent at a time.
- The process is facilitated by the relaxase enzyme, which helps guide the DNA through the bridge.
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Synthesis of complementary strand
- Once the single-stranded DNA enters the recipient cell, a complementary strand is synthesized.
- This synthesis is carried out by the recipient's DNA polymerase.
- The result is a double-stranded DNA molecule that is now part of the recipient's genetic material.
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Circularization of transferred DNA
- The transferred DNA, if it is a plasmid, will circularize within the recipient cell.
- This circularization is important for the stability and functionality of the plasmid.
- It allows the plasmid to replicate independently within the recipient cell.
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Integration into recipient chromosome (if F+ donor)
- If the donor is F+, the transferred DNA may integrate into the recipient's chromosome.
- This integration can lead to the recipient acquiring new traits, such as antibiotic resistance.
- The integration process is facilitated by homologous recombination.
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Separation of donor and recipient cells
- After the transfer is complete, the donor and recipient cells separate.
- This separation can occur naturally as the cells grow apart or through the retraction of the pilus.
- Both cells can now replicate and pass on the new genetic material to their progeny.