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Bacterial Genetics (Ch18). Genetic diversity caused by Rapid reproduction Mutation Recombination. Bacteria One of the simplest genetic model systems to study the mechanisms of molecular genetics Escherichia coli (E. coli) Intestinal flora “lab rat” of molecular biology.
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Bacterial Genetics (Ch18) Genetic diversity caused by Rapid reproduction Mutation Recombination Bacteria • One of the simplest genetic model systems to study the mechanisms of molecular genetics Escherichia coli(E. coli) • Intestinal flora • “lab rat” of molecular biology
Replication of bacterial genome • One circular DNA genome • Single origin of replication (Ori) • Bidirectional DNA replication • May have plasmids • smaller circular DNA molecules • Autonomously replicated (contain ori) • Bacteria divide by binary fission • asexual reproduction • Progeny are genetically identical to parent (clones)
Bacterial DNA replication Replication fork LE 18-14 Origin of replication Both genome & plasmid replicate in this manner Termination of replication
Bacterial DNA Mutation Caused spontaneously (mistakes in DNA synthesis) • Physicochemical forces (UV, X rays, chemical mutagens, etc.) • Since reproduction is quick e.g.doubling time=20 min • New mutations spread quickly
Calculation of incidence of mutations If doubling time= 20 min, then 23cells/hr Over 12 hr, 236 cells (~1010)produced from a single cell If spontaneous mutation rate = 1 x 10-7 / gene, then in 12 hr (day) (1010) (10-7)= 103 mutations/gene/day If bacteria have ~4000 genes then (4x103genes)(103)= 4 x 109 mutations/day
Take home message: bacterial mutations rare per gene But due to rapid cell division, become frequent Major contribution to genetic diversity and ability to adapt
Another source of bacterial genetic diversity:Genetic Recombination • Three processes bring bacterial DNA from different individuals together: • Transduction • Transformation • Conjugation
Transduction • Bacteriophages (bacterial viruses) transfer bacterial genes from one host cell to another
Phage DNA A+ B+ LE 18-16 A+ B+ Donor cell A+ Crossing over A+ A- B– Recipient cell A+ B– Recombinant cell
Transformation • Alteration of a bacterial cell’s genotype and phenotype • by the uptake of naked, foreign DNA from the surrounding environment • For example, harmless Streptococcus pneumoniae bacteria can be transformed to pneumonia-causing cells • Uptake of ampicillin resistant/ GFP-carrying plasmid (done in lab) (pGLO)
Conjugation • Direct transfer of DNA between live bacterial cells that are temporarily joined • Transfer one-way: • “Male” donates DNA • “Female” receives DNA
“Maleness,” • Contains F (fertility) genes on plasmid or in genome • Encode sex pilus • Forms passage way for DNA from donor to recipient
LE 18-17 Sex pilus 5 µm
Donor cells containing the F plasmid: F+ • Recipient cells: F- • Cells with F factor integrated into genome: Hfr cell (high frequency of recombination) • Hfr cells • Transfer some genomic DNA to recipient cell
F plasmid Bacterial chromosome F+cell F+ cell Mating bridge LE 18-18_4 F– cell F+ cell Bacterial chromosome Conjugation and transfer of F plasmid from and F+ donor to an F– recipient Formation of Hfr (high frequency of recombination) cell Hfr cell F+ cell F factor Hfr cell F– cell Temporary partial diploid Recombinant F– bacterium Conjugation and transfer of part of the bacterial chromosome from an Hfr donor to an F– recipient, resulting in recombiination