Acyl-homoserine lactone production is more common among plant-associated Pseudomonas spp. than among soilborne Pseudomonas spp.

Citation
M. Elasri et al., Acyl-homoserine lactone production is more common among plant-associated Pseudomonas spp. than among soilborne Pseudomonas spp., APPL ENVIR, 67(3), 2001, pp. 1198-1209
Citations number
52
Categorie Soggetti
Biology,Microbiology
Journal title
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
ISSN journal
00992240 → ACNP
Volume
67
Issue
3
Year of publication
2001
Pages
1198 - 1209
Database
ISI
SICI code
0099-2240(200103)67:3<1198:ALPIMC>2.0.ZU;2-G
Abstract
A total of 137 soilborne and plant-associated bacterial strains belonging t o different Pseudomonas species were tested for their ability to synthesize N-acyl-homoserine lactones (NAHL). Fifty-four strains synthesized NAHL. In terestingly, NAHL production appears to be more common among plant-associat ed than among soilborne Pseudomonas spp. Indeed, 40% of the analyzed Pseudo monas syringae strains produced NAHL which were identified most often as th e short-chain NAHL, N-hexanoyl-L-homoserine lactone, N-(3-oxo-hexanoyl)-ham oserine lactone, and N-(3-oxo-octanoyl)-L-homoserine lactone (no absolute c orrelation between genomospecies of P. syringae and their ability to produc e NAHL could be found). Six strains of fluorescent pseudomonads, belonging to the species P. chlororaphis, P. fluorescens, and P. putida, isolated fro m the plant rhizosphere produced different types of NAHL. In contrast, none of the strains isolated from soil samples were shown to produce NAHL. The gene encoding the NAHL synthase in P. syringae pv. maculicola was isolated by complementation of an NAHL-deficient Chromobacterium mutant. Sequence an alysis revealed the existence of a luxI homologue that we named psmI. This gene is sufficient to confer NAHL synthesis upon its bacterial host and has strong homology to psyI and ahlI, two genes involved in NAHL production in P. syringae pv. tabaci and P. syringae pu. syringae, respectively. We iden tified another open reading frame that we termed psmR, transcribed converge ntly in relation to psmI and partly overlapping psmI; this gene encodes a p utative LuxR regultory protein. This gene organization, with luxI and luxR homologues facing each other and overlapping, has been found so far only in the enteric bacteria Erwinia and Pantoea and in the related species P. syr ingae pv. tabaci.