Restricted Evolution of Gph to Rescue ΔserB E. coli through Motility Selection Public

Li, Aaron (2017)

Permanent URL: https://etd.library.emory.edu/concern/etds/tb09j656m?locale=fr
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Abstract

Under selective conditions, the promiscuous catalytic functions by enzymes can often be targets for evolution. Enzymes with beneficial mutations that affect its catalytic ability with these side-reactions can evolve to become more efficient at its new function. This phenomenon has been demonstrated in auxotrophic ΔserB Escherichia coli where the phosphoglycolate phosphatase, or Gph, protein was found to be one of three proteins that rescued the phosphoserine phosphatase ability of the E. coli. However, mutation suppression is often achieved through multiple, different mechanisms and so the evolutionary extent of any particular mechanism cannot be easily elucidated. Using plates with semisolid media and chemoattractants, the auxotrophic cells with the fittest mutations were selected for through their extent of motility. Alternating between using this motility selection to evolve the Gph protein in E.coli with mutations in serine catalysis, ΔserB, and DNA repair mechanisms, ΔmutS, and then chemically transforming its gph plasmid, we demonstrate a method to specifically evolve the gph gene without accumulating mutations in the genome, thereby restricting evolution to only Gph. A custom plasmid containing the gph gene and other inducer and antibiotic genes was first constructed and transformed into ΔserB ΔmutS E. coli before evolution on the semisolid media. We also use a similar method to show the possibility of semi-continuous evolution of Gph. Instead of selecting for and transforming the plasmids of the fittest cells into new ones, we aimed to show that conjugation can be an alternative mechanism of gene transfer to evolve the gph plasmid.

Table of Contents

Table of Contents

Introduction 1

Material and Methods 3

Figure 1 9

Figure 2 9

Figure 3 10

Figure 4 10

Figure 5 11

Results 15

Figure 6 15

Figure 7 16

Figure 8 16

Figure 9 17

Figure 10 17

Discussion 19

References 24

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