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Mutation Rates in E. coli MC4100 and Hfq -. Biomath Research - Summer ‘08 Glen Hamman Jan Varada. Goals. To determine the effect of the Hfq protein in the deletion of quadruplex-forming DNA sequences.
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Mutation Rates in E. coli MC4100 and Hfq- Biomath Research - Summer ‘08 Glen Hamman Jan Varada
Goals • To determine the effect of the Hfq protein in the deletion of quadruplex-forming DNA sequences. • If the Hfq protein is involved in removing the quadruplex structures, hfq+ cells with the protein should revert slower than hfq- cells without the protein.
Approach • Insert a DNA quadruplex-forming structure in the TET gene of the pBR325 plasmid. • Do a transformation into the E. coli HB101 strain, and plate to select AMP resistant colonies which have the plasmid. • Patch in grid in AMP and TET and select those that do not grow in TET because they have the quadruplex DNA structure. • Select those colonies, purify DNA and do transformations into the MC4100 and Hfq- strains and compare reversion rates.
Results so far… AMP plate TET plate
Results so far… CAP plate AMP plate
To do… • Purify DNA from viable colonies and do transformations into the MC4100 and Hfq- strains. • Calculate the reversion frequency and complete the mutation rate experiment. • Follow up on the mathematical models describing the mutation behavior and compare predictions with experimental data.