Bacterial Genetics
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Transcript of Bacterial Genetics
Prokaryotic Cell• Circular (and
naked) double stranded DNA
• Bacteria have very short generation spans (ex. E.coli divides every 20 minutes)
Plasmid – small circular DNA found in some bacteria
– Contain a few accessory genes (e.g. antibiotic resistance)
– NOT required for bacterial cell reproduction or survival
Bacterial Cell Reproduction• Binary fission – asexual (production of offspring
from one parent) process for prokaryotic cell division
• Each fission results in two daughter cells each with 1 copy of the original chromosome
Why bother?• Bacteria rapidly reproduce which leads to
increase in genetic diversity (due to mutations that may or may not confer advantages to offspring)– 9 million mutations per day per human host– Beneficial mutations allow bacteria to continue
to survive in host and contribute to evolution of bacterial populations
Mechanisms for gene transfer:
• Mutations cannot account for all bacterial diversity
• Bacteria have three mechanisms for exchanging genetic information between themselves:– 1. Transformation– 2. Transduction– 3. Conjugation
• These exchanges create new strains of bacteria
Transposable Elements
• In addition to the transfer of genetic material (DNA) b/n bacterial cells, DNA of a single bacterium can undergo recombination via transposable elements
• Essentially, DNA “jumps” from one part of chromosome to another
Regulation of gene expression• Individual bacterium have to deal with
fluctuations in host environment so they have developed levels to control gene expression
• 2 types of genes in bacteria:– Regulatory genes – produce proteins that
control gene expression – Structural genes – produce proteins that do
something (e.g. break down lactose)
2 Levels for Metabolic Control1. Use allosteric control (e.g. feedback inhibition)
– Ex: Negative feedback to stop production of tryptophan after thanksgiving dinner
2. Regulate expression of genes using an operon system
3 parts to an operon
1. Operator – controls access of RNA polymerase to the promoter
2. Promoter – where RNA polymerase attaches to begin transcription of genes
3. Genes – code for expression of proteins related to one particular function (e.g. breaking down galactosidase)
Regulatory gene
• Located away from operon itself• Produce repressor protein that is able to
bind to operator and prevent RNA polymerase from attaching to promoter
2 types of operons1. Repressible – normally on but can be inhibited (i.e. IS REPRESSIBLE)
– Usually anabolic (building essential molecules)– Repressible protein (coded for by the regulatory
gene) is inactive– If the essential molecule is present, it binds to the
repressible protein, activates it, and this activated protein binds to the operator and turns operon OFF (blocks RNA polymerase thus REPRESSED!)
2. Inducible – normally off but can be turned on (i.e. IS INDUCIBLE)
– Usually catabolic (breaking down food for energy)
– Repressible protein is active– Inducer (small molecule) binds to & inactivates
the repressible protein, preventing it from binding to the operator. Now RNA polymerase transcribes the genes (INDUCED!)