Cargando…
Characterization of diverse homoserine lactone synthases in Escherichia coli
Quorum sensing networks have been identified in over one hundred bacterial species to date. A subset of these networks regulate group behaviors, such as bioluminescence, virulence, and biofilm formation, by sending and receiving small molecules called homoserine lactones (HSLs). Bioengineers have in...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107141/ https://www.ncbi.nlm.nih.gov/pubmed/30138364 http://dx.doi.org/10.1371/journal.pone.0202294 |
_version_ | 1783349918454251520 |
---|---|
author | Daer, René Barrett, Cassandra M. Melendez, Ernesto Luna Wu, Jiaqi Tekel, Stefan J. Xu, Jimmy Dennison, Brady Muller, Ryan Haynes, Karmella A. |
author_facet | Daer, René Barrett, Cassandra M. Melendez, Ernesto Luna Wu, Jiaqi Tekel, Stefan J. Xu, Jimmy Dennison, Brady Muller, Ryan Haynes, Karmella A. |
author_sort | Daer, René |
collection | PubMed |
description | Quorum sensing networks have been identified in over one hundred bacterial species to date. A subset of these networks regulate group behaviors, such as bioluminescence, virulence, and biofilm formation, by sending and receiving small molecules called homoserine lactones (HSLs). Bioengineers have incorporated quorum sensing pathways into genetic circuits to connect logical operations. However, the development of higher-order genetic circuitry is inhibited by crosstalk, in which one quorum sensing network responds to HSLs produced by a different network. Here, we report the construction and characterization of a library of ten synthases including some that are expected to produce HSLs that are incompatible with the Lux pathway, and therefore show no crosstalk. We demonstrated their function in a common lab chassis, Escherichia coli BL21, and in two contexts, liquid and solid agar cultures, using decoupled Sender and Receiver pathways. We observed weak or strong stimulation of a Lux receiver by longer-chain or shorter-chain HSL-generating Senders, respectively. We also considered the under-investigated risk of unintentional release of incompletely deactivated HSLs in biological waste. We found that HSL-enriched media treated with bleach were still bioactive, while autoclaving deactivates LuxR induction. This work represents the most extensive comparison of quorum signaling synthases to date and greatly expands the bacterial signaling toolkit while recommending practices for disposal based on empirical, quantitative evidence. |
format | Online Article Text |
id | pubmed-6107141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61071412018-08-30 Characterization of diverse homoserine lactone synthases in Escherichia coli Daer, René Barrett, Cassandra M. Melendez, Ernesto Luna Wu, Jiaqi Tekel, Stefan J. Xu, Jimmy Dennison, Brady Muller, Ryan Haynes, Karmella A. PLoS One Research Article Quorum sensing networks have been identified in over one hundred bacterial species to date. A subset of these networks regulate group behaviors, such as bioluminescence, virulence, and biofilm formation, by sending and receiving small molecules called homoserine lactones (HSLs). Bioengineers have incorporated quorum sensing pathways into genetic circuits to connect logical operations. However, the development of higher-order genetic circuitry is inhibited by crosstalk, in which one quorum sensing network responds to HSLs produced by a different network. Here, we report the construction and characterization of a library of ten synthases including some that are expected to produce HSLs that are incompatible with the Lux pathway, and therefore show no crosstalk. We demonstrated their function in a common lab chassis, Escherichia coli BL21, and in two contexts, liquid and solid agar cultures, using decoupled Sender and Receiver pathways. We observed weak or strong stimulation of a Lux receiver by longer-chain or shorter-chain HSL-generating Senders, respectively. We also considered the under-investigated risk of unintentional release of incompletely deactivated HSLs in biological waste. We found that HSL-enriched media treated with bleach were still bioactive, while autoclaving deactivates LuxR induction. This work represents the most extensive comparison of quorum signaling synthases to date and greatly expands the bacterial signaling toolkit while recommending practices for disposal based on empirical, quantitative evidence. Public Library of Science 2018-08-23 /pmc/articles/PMC6107141/ /pubmed/30138364 http://dx.doi.org/10.1371/journal.pone.0202294 Text en © 2018 Daer et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Daer, René Barrett, Cassandra M. Melendez, Ernesto Luna Wu, Jiaqi Tekel, Stefan J. Xu, Jimmy Dennison, Brady Muller, Ryan Haynes, Karmella A. Characterization of diverse homoserine lactone synthases in Escherichia coli |
title | Characterization of diverse homoserine lactone synthases in Escherichia coli |
title_full | Characterization of diverse homoserine lactone synthases in Escherichia coli |
title_fullStr | Characterization of diverse homoserine lactone synthases in Escherichia coli |
title_full_unstemmed | Characterization of diverse homoserine lactone synthases in Escherichia coli |
title_short | Characterization of diverse homoserine lactone synthases in Escherichia coli |
title_sort | characterization of diverse homoserine lactone synthases in escherichia coli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107141/ https://www.ncbi.nlm.nih.gov/pubmed/30138364 http://dx.doi.org/10.1371/journal.pone.0202294 |
work_keys_str_mv | AT daerrene characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT barrettcassandram characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT melendezernestoluna characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT wujiaqi characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT tekelstefanj characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT xujimmy characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT dennisonbrady characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT mullerryan characterizationofdiversehomoserinelactonesynthasesinescherichiacoli AT hayneskarmellaa characterizationofdiversehomoserinelactonesynthasesinescherichiacoli |