, 2004). In the current report,

we describe the use of this method for the isolation and characterization of novel polyhydroxyalkanaote synthesis genes from a soil metagenomic library. Many bacteria found in heterogeneous and diverse soil habitats are known to accumulate polyhydroxyalkanaote. this website In several cases it has been demonstrated that the ability to store carbon as polyhydroxyalkanaote contributes to survival under fluctuating environmental conditions of the soil and rhizosphere (recently reviewed in Castro-Sowinski et al., 2010). Our methods should be useful for the isolation of additional novel polyhydroxyalkanaote synthesis genes from uncultivated bacteria inhabiting environments such as soil. This work continues our development of the Alphaproteobacteria as surrogate hosts for functional metagenomic studies (Wang et al., 2006) (Hao et al., 2010). Strains and plasmids are listed in Table 1. Luria–Bertani and yeast extract–mannitol (YM) medium supplemented

with appropriate antibiotics were used as described previously (Aneja et al., 2004). The metagenomic library was maintained as pooled Escherichia coli HB101 culture, stored long-term at −70 °C in the presence of 7% dimethyl sulphoxide. Nile red (Sigma-Aldrich, N3013, technical grade) added to agar media at a concentration of 0.5 μg mL−1 facilitated the visual identification of stained colonies containing polyhydroxyalkanaote accumulating cells (Spiekermann

et al., 1999). Sinorhizobium meliloti genetics (Glazebrook & Walker, 1991) and standard techniques for molecular biology Dasatinib were used. The metagenomic library was transferred to recipient S. meliloti cells by triparental conjugation, and screens for complementation of polyhydroxyalkanaote synthesis were performed by examination of transconjugant colonies for restoration of mucoid phenotype or Nile Red staining on YM agar (Aneja et al., 2004). Along with end sequencing of subcloned cosmid insert fragments, the EZ∷TN 〈KAN-2〉 insertion kit (Epicentre) was used to generate transposon mutations that facilitated sequencing using the recommended transposon-sequencing primers. Primer walking was used to close gaps when necessary, and trimming and assembly were performed manually. The Clomifene sequence was obtained at MOBIX (McMaster University) using an ABI 3100 Gene Analyzer instrument, and at the Institut für Mikrobiologie und Genetik, Universität Göttingen. Potential protein-coding sequences were identified using genemark.hmm (Lukashin & Borodovsky, 1998), and supported by blastx analysis (Altschul et al., 1997). The predicted ORFs were further analysed by blastp and blastn. For polyhydroxyalkanaote analysis 1-mL precultures were used to inoculate 200 mL YM broth in 500-mL Erlenmeyer flasks. Incubation was carried out at 30 °C on a shaker at 200 r.p.m. for 48 h. Cells were recovered by centrifugation at 5855 g for 15 min in a GSA rotor.