Han Ming Gan
Quorum sensing signals of the grapevine crown gall bacterium, Novosphingobium sp. Rr2-17: use of inducible expression and polymeric resin to sequester acyl-homoserine lactones
Gan, Han Ming; Dailey, Lucas; Wengert, Peter; Halliday, Nigel; Williams, Paul; Hudson, Andre; Savka, Michael A.
Authors
Lucas Dailey
Peter Wengert
Nigel Halliday
Professor PAUL WILLIAMS PAUL.WILLIAMS@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR MICROBIOLOGY
Andre Hudson
Michael A. Savka
Abstract
Background: A grapevine crown gall tumor strain, Novosphingobium sp. strain Rr2- 17 was previously reported to accumulate copious amounts of diverse quorum sensing signals during growth. Genome sequencing identified a single luxI homolog in strain Rr2-17, suggesting that it may encode for a AHL synthase with broad substrate range, pending functional validation. The exact identity of the complete suite of AHLs formed by novIspR1 is largely unknown. Methods: This study validates the function of novIspR1 through inducible expression in Escherichia coli and in the wild-type parental strain Rr2-17. We further enhanced the capture of acyl homoserine lactone (AHL) signals produced by novIspR1 using polymeric resin XAD-16 and separated the AHLs by one- and two-dimensional thin layer chromatography followed by detection using AHL-dependent whole cell biosensor strains. Lastly, the complete number of AHLs produced by novIspR1 in our system was identified by LC-MS/MS analyses. Results: The single LuxI homolog of N. sp. Rr2-17, NovIspR1, is able to produce up to eleven different AHL signals, including AHLs: C8-, C10-, C12-, C14-homoserine lactone (HSL) as well as AHLs with OH substitutions at the third carbon and includes 3-OH-C6-, 3-OH-C8-, 3-OH-C10-, 3-OH-C12- and 3-OH-C14-HSL. The most abundant AHL produced was identified as 3-OH-C8-HSL and isopropyl-D-1- thiogalactopyranoside (IPTG) induction of novIspR1 expression in wild type parental Rr2-17 strain increased its concentration by 6.8-fold when compared to the same strain with the vector only control plasmid. Similar increases were identified with the next two most abundant AHLs, 3-OH-C10- and unsubstituted C8-HSL. The presence of 2% w/v of XAD-16 resin in the growth culture bound 99.3 percent of the major AHL (3-OH-C8-HSL) produced by IPTG-induced overexpression of novIspR1 in Rr2-17 strain. This study significantly adds to our understanding of the AHL class of quorum sensing system in a grapevine crown gall tumor associated Novosphingobium sp. Rr2-17 strain. The identity of nine AHL signals produced by this bacterium will provide a framework to identify the specific function(s) of the AHL-mediated quorum-sensing associated genes in this bacterium.
Citation
Gan, H. M., Dailey, L., Wengert, P., Halliday, N., Williams, P., Hudson, A., & Savka, M. A. (2024). Quorum sensing signals of the grapevine crown gall bacterium, Novosphingobium sp. Rr2-17: use of inducible expression and polymeric resin to sequester acyl-homoserine lactones. PeerJ, 12, Article e18657. https://doi.org/10.7717/peerj.18657
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 17, 2024 |
Online Publication Date | Dec 20, 2024 |
Publication Date | Dec 20, 2024 |
Deposit Date | Dec 28, 2024 |
Publicly Available Date | Jan 6, 2025 |
Journal | PeerJ |
Electronic ISSN | 2167-8359 |
Publisher | PeerJ |
Peer Reviewed | Peer Reviewed |
Volume | 12 |
Article Number | e18657 |
DOI | https://doi.org/10.7717/peerj.18657 |
Keywords | Acyl-homoserine lactones, Novosphingobium. sp., Quorum sensing, Inducible expression, Resin, NovI, Grapevine crown gall tumor, Agrobacterium vitis tumor |
Public URL | https://nottingham-repository.worktribe.com/output/43213164 |
Publisher URL | https://peerj.com/articles/18657/# |
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This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
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