Ochiai Akihito, Hashimoto Wataru, Murata Kousaku
Laboratory of Basic and Applied Molecular Biotechnology, Graduate School of Agriculture, Kyoto University, Uji, Kyoto 611-0011, Japan.
Res Microbiol. 2006 Sep;157(7):642-9. doi: 10.1016/j.resmic.2006.02.006. Epub 2006 Mar 2.
The Gram-negative bacterium Sphingomonas sp. strain A1 (strain A1) has a peculiar biosystem to directly import and depolymerize a macromolecule, alginate, which is encoded by a cluster of genes on the genome. We identified five clustered ORFs homologous to some genes of the strain A1 cluster in the genome of Agrobacterium tumefaciens strain C58 (strain C58). These ORFs are Atu3021, Atu3022, Atu3023, and Atu3024, encoding a putative sugar ABC transporter system and Atu3025, which encodes a putative alginate lyase. We analyzed the involvement of this gene cluster in alginate metabolism. Strain C58 cells grew significantly on low-molecular-weight (LMW) alginate (average molecular weight, 1000), and we detected specific alginate-induced expression of Atu3024 and Atu3025. This strain does not grow on alginate (average molecular weight, 25,600), suggesting that the strain C58 gene cluster is involved in importing and degrading LMW alginate. One protein, Atu3025, purified from strain C58, was identified as an alginate lyase, and the enzyme overexpressed in Escherichia coli was further characterized. Atu3025 released monosaccharides specifically from alginate most efficiently at pH 7.3 and 30 degrees C through a beta-elimination reaction, indicating that Atu3025 is an exotype alginate lyase potentially involved in the assimilation of LMW alginate in strain C58.
革兰氏阴性细菌鞘氨醇单胞菌属菌株A1(菌株A1)具有一种独特的生物系统,可直接导入并解聚大分子海藻酸盐,该系统由基因组上的一组基因编码。我们在根癌土壤杆菌菌株C58(菌株C58)的基因组中鉴定出五个与菌株A1基因簇的某些基因同源的成簇开放阅读框(ORF)。这些ORF分别是Atu3021、Atu3022、Atu3023和Atu3024,它们编码一个假定的糖类ABC转运系统,以及Atu3025,其编码一个假定的海藻酸裂解酶。我们分析了该基因簇在海藻酸盐代谢中的作用。菌株C58细胞在低分子量(LMW)海藻酸盐(平均分子量为1000)上生长显著,并且我们检测到Atu3024和Atu3025有特异性的海藻酸盐诱导表达。该菌株不能在平均分子量为25,600的海藻酸盐上生长,这表明菌株C58基因簇参与低分子量海藻酸盐的导入和降解。从菌株C58中纯化出的一种蛋白质Atu3025被鉴定为海藻酸裂解酶,并且对在大肠杆菌中过表达的该酶进行了进一步表征。Atu3025在pH 7.3和30℃时通过β-消除反应从海藻酸盐中最有效地特异性释放单糖,这表明Atu3025是一种可能参与菌株C58中低分子量海藻酸盐同化作用的胞外型海藻酸裂解酶。