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<titleInfo><title>Adaptive mutation in E. coli modulated by luxS</title></titleInfo>

  
  
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  <title>ISTA Thesis</title>
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<name type="personal">
  <namePart type="given">Mike</namePart>
  <namePart type="family">Hennessey-Wesen</namePart>
  <role><roleTerm type="text">author</roleTerm> </role><identifier type="local">3F338C72-F248-11E8-B48F-1D18A9856A87</identifier></name>





<name type="personal">
  
  <namePart type="given">Björn</namePart>
  
  
  <namePart type="family">Hof</namePart>
  
  <role> <roleTerm type="text">supervisor</roleTerm> </role>
</name>



<name type="corporate">
  <namePart></namePart>
  <identifier type="local">GradSch</identifier>
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  </role>
</name>

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  <identifier type="local">BjHo</identifier>
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    <roleTerm type="text">department</roleTerm>
  </role>
</name>





<name type="corporate">
  <namePart>International IST Doctoral Program</namePart>
  <role><roleTerm type="text">project</roleTerm></role>
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<abstract lang="eng">Mutation rates represent the net result of complex interactions among various
cellular processes and can dramatically influence the evolutionary fate of
microbial populations. However, many popular techniques used to study
mutations are subject to the confounding effects of heredity and the subtleties
of adaptation to selection, all of which make it difficult to observe any dynamic
responses of mutation rates to fitness challenges. Furthermore, in spite of the
ubiquity of quorum sensing systems across the bacterial domain and relevance
for many physiological behaviors, the effects of such mechanisms on mutation
rate and adaptation remain poorly understood. In the following work, I
present the development of a microfluidic droplet-based method to measure
single base-pair mutation rates in growing populations of the bacterium
Escherichia coli. I use this method to observe a stress-induced increase in
mutation rate that is mediated by luxS, a highly conserved bacterial quorum
sensing component. I also show that the aforementioned increase in mutation
rate, and its associated control by luxS, corresponds to a higher degree of
adaptability under competitive environments.</abstract>

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<originInfo><publisher>Institute of Science and Technology Austria</publisher><dateIssued encoding="w3cdtf">2023</dateIssued>
</originInfo>
<language><languageTerm authority="iso639-2b" type="code">eng</languageTerm>
</language>

<subject><topic>microfluidics</topic><topic>miceobiology</topic><topic>mutations</topic><topic>quorum sensing</topic>
</subject>


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  <identifier type="issn">2663-337X</identifier><identifier type="doi">10.15479/at:ista:14641</identifier>
<part><extent unit="pages">104</extent>
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<extension>
<bibliographicCitation>
<apa>Hennessey-Wesen, M. (2023). &lt;i&gt;Adaptive mutation in E. coli modulated by luxS&lt;/i&gt;. Institute of Science and Technology Austria. &lt;a href=&quot;https://doi.org/10.15479/at:ista:14641&quot;&gt;https://doi.org/10.15479/at:ista:14641&lt;/a&gt;</apa>
<ieee>M. Hennessey-Wesen, “Adaptive mutation in E. coli modulated by luxS,” Institute of Science and Technology Austria, 2023.</ieee>
<ista>Hennessey-Wesen M. 2023. Adaptive mutation in E. coli modulated by luxS. Institute of Science and Technology Austria.</ista>
<mla>Hennessey-Wesen, Mike. &lt;i&gt;Adaptive Mutation in E. Coli Modulated by LuxS&lt;/i&gt;. Institute of Science and Technology Austria, 2023, doi:&lt;a href=&quot;https://doi.org/10.15479/at:ista:14641&quot;&gt;10.15479/at:ista:14641&lt;/a&gt;.</mla>
<chicago>Hennessey-Wesen, Mike. “Adaptive Mutation in E. Coli Modulated by LuxS.” Institute of Science and Technology Austria, 2023. &lt;a href=&quot;https://doi.org/10.15479/at:ista:14641&quot;&gt;https://doi.org/10.15479/at:ista:14641&lt;/a&gt;.</chicago>
<ama>Hennessey-Wesen M. Adaptive mutation in E. coli modulated by luxS. 2023. doi:&lt;a href=&quot;https://doi.org/10.15479/at:ista:14641&quot;&gt;10.15479/at:ista:14641&lt;/a&gt;</ama>
<short>M. Hennessey-Wesen, Adaptive Mutation in E. Coli Modulated by LuxS, Institute of Science and Technology Austria, 2023.</short>
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