Since the released fatty acids would be further metabolized by β-oxidation during Histone Methyltransferase inhibitor cultivation [41], excessively long digestion times should be avoided. The digestion mixture was directly used as a sample

to perform ESI-MS Nutlin 3 analysis. The reaction buffers were observed to have a decisive effect on ESI-MS analysis. When 100 mM sodium phosphate (pH 7.0) was used as a reaction buffer, only the phosphate ([M-H] m/z = 97) was found in the ESI–MS pattern, wherein the fatty acid was still not detectable (data not shown). In contrast, when 10 mM ammonia acetate was used as a reaction buffer to avoid the phosphate effect, the fatty acid was detected by ESI–MS (Fig. 3B). Among the reported AHL-acylases, only AiiC can deacylate the short chain C6-HSL Seliciclib molecular weight [18]. In addition, PvdQand QuiP were verified to express C7-HSL-degrading activity. However, the substrate specificity of the Aac for AHLs is within the limits of more than six carbon-acyl chain (Table

4). Moreover, transferring the aac gene into C. violaceum CV026 significantly influenced violacein production and chitinase activity (Fig. 4). These results indicated that Aac has the potential to be a quorum- quenching agent. Although the quorum-sensing signal for controlling the virulence factors of R. solanacearum is 3-OH-PAME, solI and solR are members of the 3-OH-PAME communication system regulon [25]. In our study, no 3-OH-PAME-degrading enzyme has been found using the BLASTP search when interrogated with the beta-hydroxypalmitate methyl ester hydrolase (BAF64544) [42]. There are SolI (NP 521405) and SolR (NP 521406) proteins of R. solanacearumGMI1000 sharing 86% and 87% identity, respectively, with that of not SolI (O30920) and SolR (AAC45947) from R. solanacearumAW1. Because the SolI (O30920) synthesizes C6- and C8-HSLs, the GMI1000 strain might be expected to produce both of them. Although the physiological role of AHL-acylase

in R. solanacearum is unclear yet, we consider that R. solanacearum might adopt a unique signal turnover system to control existing signals from a quorum-sensing mode [43]. The AHL-acylase would be a mechanism of interference to degrade exogenous signals produced by competitors. It may also be possible that these acylase prevent the accumulation of self generated signals, allowing the quorum response to switch off as is seen in Agrobacterium tumefaciens [43]. Recently, several reports indicated that quorum-quenching enzymes, such as lactonase, AHL-acylase, and oxidoreductase, have potential to be used as peptide drugs. Among them, AHL-lactonase has been applied in genetically engineered procedures to control plant diseases [35, 44]. Eventually such enzymes would lead to the attenuation of the expression of quorum-sensing regulated functions in microorganisms.