plymuthica IC1270 which showed very weak production of the predicted 3-hydroxy-C6-HSL by TLC analysis [30]. It is worth noting that there might be differences between AHL ratios from SplI and SpsI expressed in the wild type G3 and E. coli. Table 2 AHL production by E. col i expressing either splI or spsI from G3 AHL produced by G3 WT[23] AHL expressed in E. coli/splI# AHL expressed in E. coli/spsI# C4-HSL + ++++ C5-HSL STI571 + +++ C6-HSL ++ ++ C7-HSL ++ + C8-HSL + + 3-oxo-C6-HSL +++ – 3-oxo-C7-HSL ++ – 3-oxo-C8-HSL + – 3-hydroxy-C6-HSL ++ – 3-hydroxy-C8-HSL + – AHL profiles identification was performed by LC-MS/MS

from two independent experiments. # AHL mass abundance (relative quantity of íons from a particular AHL relative to that of a known standard) on LC-MS/MS: ++++ indicates 107; +++ indicates 106; ++ indicates 105; + indicates ≤104. Heterologous FGFR inhibitor expression of aiiA in G3 abolishes AHL accumulation and has an impact on biocontrol traits A number of bacteria are known to regulate various cell processes, including biocontrol activities

through AHL-mediated quorum sensing systems. To determine the ability of the Bacillus A24 lactonase AiiA in degrading AHL signal molecules in G3, the plasmid pME6863-aiiA, and the control vector pME6000 (lacking the aiiA gene) were introduced into the wild type G3 by mating with the E. coli donor strain S17-1. Overnight culture supernatants Ro 61-8048 supplier from these transconjugants were extracted in duplicate with solvent and subjected to LC-MS/MS semiquantitative analysis based on MRM mode showing that G3 harbouring the pME6000 vector control exhibited similar AHL patterns and concentration to the wild type (data not shown). Phosphoribosylglycinamide formyltransferase In contrast, AHL production was practically abolished in G3 expressing aiiA from pME6863-aiiA (more than 99% reduction), with only trace amounts of C4-HSL remaining which could not be detected by the biosensor CV026 and hence were unlikely to influence

gene expression. This result suggested that AiiA can efficiently degrade all series of AHLs, including unsubstituted, 3-oxo, and 3-hydroxy at the third carbon position as it has been previously shown [39]. Impairment in AHL accumulation resulted in down-regulation of the chitinolytic and proteolytic activities in G3/pME6863-aiiA. In contrast, biosynthesis of IAA increased five-fold and there was no effect on production of siderophores, compared to the wild type G3 and the control G3/pME6000 (see Additional file 2). This is in agreement with previous observations in S. plymuthica HRO-C48 heterologously expressing aiiA [14]. Swimming motility was also assayed to determine the role of quorum quenching by AiiA in motility. The swimming zones of the wild type G3, the AHL quenched strain G3/pME6863-aiiA and the vector control G3/pME6000 after incubation for 16 h at 28°C were 33.75 ± 0.75 mm, 33.08 ± 0.80 mm, and 32.83 ± 0.14 mm, respectively. The results suggest that, in contrast to S.