Skip to main content

Research Repository

Advanced Search

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.

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 Thumbnail


Authors

Han Ming Gan

Lucas Dailey

Peter Wengert

Nigel Halliday

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/#

Files

peerj-18657 (14.3 Mb)
PDF

Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/

Copyright Statement
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.





You might also like



Downloadable Citations