The complementation is dependent on having a suitable phenotype to screen, and we have made use of the complex phenotype of S. meliloti phaC mutants that includes lack of mucoidy on high carbon ratio media such as YM, absence of fluorescence on Nile red-containing media, and reduced growth on polyhydroxyalkanaote cycle intermediates (Aneja et al., 2004). We should also be able to use this strategy

to isolate other polyhydroxyalkanaote synthesis genes such as phaA and phaB from metagenomic libraries. We anticipate the use of this method for the construction of diverse collections of genes encoding polyhydroxyalkanaote synthesis enzymes that might be useful for the optimization and improvement of industrial polyhydroxyalkanaote production through pathway engineering. As more polyhydroxyalkanaote synthase genes SP600125 concentration are isolated from metagenomic libraries using these methods, it will be Linsitinib chemical structure interesting to see the full range of genes that can be captured. This work was supported by a Natural Sciences and Engineering Research Council of Canada Strategic Projects grant (T.C.C). Fig. S1. Maximum-likelihood tree inferred from coding DNA sequences of polyhydroxyalkanaote synthases listed in Table S1. Fig. S2. Maximum-likelihood

tree inferred from protein sequences of polyhydroxyalkanaote synthases listed in Table S1. Table S1. Organism names and GenBank accession numbers of related polyhydroxyalkanaote synthases. Please note: Wiley-Blackwell is not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. “
“Clostridial cellulosomes are

cellulolytic complexes that are formed by highly specific interactions between one of the repeated cohesin modules present in the scaffolding protein and a dockerin module of the catalytic components. Although Clostridium thermocellum Xyn11A dockerin Adenosine has a typical C. thermocellum dockerin sequence, in which two amino acid residues are species specifically conserved within the two segments of the dockerin modules, it can recognize Clostridium josui cohesin modules in a non-species-specific manner. The importance of these two conserved amino acids, which are part of the recognition site of the cohesin and dockerin interaction, was investigated by introducing mutations into the first and/or the second segments of the Xyn11A dockerin. Mutations in the first segment did not affect the interactions between dockerin and C. thermocellum and C. josui cohesins. However, mutations in the second segment prevented binding to cohesin proteins. A second round of mutations within the first segment re-established the affinity for both the C. thermocellum and the C. josui cohesins. However, this was not observed for a ‘conventional’ dockerin, Xyn10C.