, 2012a, b). RNA Synthesis inhibitor Although in some Mesorhizobium strains, no ACC deaminase activity was detected under free-living conditions (Ma et al., 2003b; Nascimento et al., 2012a), it has been shown that Mesorhizobium. sp. MAFF303099 expresses ACC deaminase under symbiotic conditions, in a NifA2-dependent manner (Uchiumi et al., 2004; Nukui et al., 2006). One explanation for these somewhat

disparate results includes the possibility that those acdS genes under the transcriptional control of a NifA-regulated promoter are either exclusively or primarily expressed within nodules resulting in a decreased rate of nodule senescence. On the other hand, those acdS genes under the transcriptional control of an Lrp-regulated promoter (Ma et al., 2003a)

are primarily involved in facilitating the nodulation process and are not expressed within the nodule itself. The aim of the present study was to assess the prevalence and phylogeny of acdS genes in selleck chemicals Mesorhizobium strains including isolates from a collection of chickpea mesorhizobia from Portuguese soils. In the present study, 12 Mesorhizobium type strains as well as 18 chickpea Mesorhizobium isolates from Portugal were tested for the presence of acdS genes and ACC deaminase activity under free-living conditions. The chickpea Mesorhizobium isolates from Portugal were collected from different sites throughout the country, as previously described (Alexandre et al., 2009). Mesorhizobium strains were grown at 28 °C in TY medium (Beringer, 1974), in YMA medium (Vincent, 1970), and in modified M9 minimal medium (Robertsen et al., 1981) when necessary. The bacterial strains used in this work are presented in Table 1. Mesorhizobium strains and isolates were grown in 5 mL of

TY medium at 28 °C for 2–4 days. The bacterial cultures were centrifuged at 16 000 g for 1 min and used for genomic DNA isolation using the E.Z.N.A bacterial DNA kit (Omega Bio-tek) following the manufacturer’s suggested protocol. To amplify the acdS gene HSP90 in Mesorhizobium type strains and chickpea Mesorhizobium isolates, PCR primers were designed based on the Mesorhizobium sp. MAFF303099 and M. ciceri bv. biserrulae WSM1271 acdS gene sequences, resulting in primers F2 (5′-CAAGCTGCGCAAGCTCGAATA-3′) and R6 (5′-CATCCCTTGC ATCGATTTGC-3′). The acdS gene was amplified in a ‘T Personal Cycler’ (Biometra) thermocycler using the following program: 3 min of initial denaturation at 95 °C, 35 cycles of 1 min denaturation at 94 °C, followed by 1 min and 30 s of primer annealing at 49 °C and 1 min of elongation at 72 °C, and a final elongation step of 5 min at 72 °C. The amplification product is a 760-bp fragment. After amplification, the PCR product was purified using the GFX DNA purification Kit (GE Healthcare, UK) and sequenced by Macrogen Inc. (Seoul, Korea). The obtained acdS gene sequences are presented in Table 1.