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A cell contains host chromosome (large loop of DNA), F plasmid (small loop of DNA) and a pilus (projection out of the cell). The F plasmid is inserted into the host chromosome to become Hfr male (donor). When the plasmid is removed from the host chromosome, genes from the chromosome (such as lac) may move from the chromosome to the plasmid. In this case the cell becomes an F’ cell.
(a) The F plasmid can occasionally integrate into the bacterial chromosome, producing an Hfr cell. (b) Imprecise excision of the F plasmid from the chromosome of an Hfr cell may lead to the production of an F’ plasmid that carries chromosomal DNA adjacent to the integration site. This F’ plasmid can be transferred to an F cell by conjugation.
a) Diagram showing one cell with multiple genes on its chromosome as well as an integrated F plasmid. This cell begins copying and transferring its entire genome but conjugation ends before the entire chromosome is transferred. B) A sample plasmid showing the variety of genes on the plasmid. Some sample genes include: argG, pabB, metA, argR, polA, and oriC. Numbers in the center of the plasmid indicate the location of genes; these numbers show a plasmid of 1000bp total.
(a) An Hfr cell may attempt to transfer the entire bacterial chromosome to an F cell, treating the chromosome like an extremely large F plasmid. However, contact between cells during conjugation is temporary. Chromosomal genes closest to the integration site (gene 1) that are first displaced during rolling circle replication will be transferred more quickly than genes far away from the integration site (gene 4). Hence, they are more likely to be recombined into the recipient F cell’s chromosome. (b) The time it takes for a gene to be transferred, as detected by recombination into the F cell’s chromosome, can be used to generate a map of the bacterial genome, such as this genomic map of E. coli . Note that it takes approximately 100 minutes for the entire genome (4.6 Mbp) of an Hfr strain of E. coli to be transferred by conjugation.

Consequences and applications of conjugation

Plasmids are an important type of extrachromosomal DNA element in bacteria and, in those cells that harbor them, are considered to be part of the bacterial genome. From a clinical perspective, plasmid s often code for genes involved in virulence. For example, genes encoding proteins that make a bacterial cell resistant to a particular antibiotic are encoded on R plasmids . R plasmids, in addition to their genes for antimicrobial resistance, contain genes that control conjugation and transfer of the plasmid. R plasmids are able to transfer between cells of the same species and between cells of different species. Single R plasmids commonly contain multiple genes conferring resistance to multiple antibiotics.

Genes required for the production of various toxins and molecules important for colonization during infection may also be found encoded on plasmids. For example, verotoxin-producing strains of E. coli ( VTEC ) appear to have acquired the genes encoding the Shiga toxin from its gram-negative relative Shigella dysenteriae through the acquisition of a large plasmid encoding this toxin. VTEC causes severe diarrheal disease that may result in hemolytic uremic syndrome (HUS), which may be lead to kidney failure and death.

In nonclinical settings, bacterial genes that encode metabolic enzymes needed to degrade specialized atypical compounds like polycyclic aromatic hydrocarbons (PAHs) are also frequently encoded on plasmids. Additionally, certain plasmids have the ability to move from bacterial cells to other cell types, like those of plants and animals, through mechanisms distinct from conjugation. Such mechanisms and their use in genetic engineering are covered in Modern Applications of Microbial Genetics .

Practice MCQ 4

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Source:  OpenStax, Microbiology. OpenStax CNX. Nov 01, 2016 Download for free at http://cnx.org/content/col12087/1.4
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