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Sequence and Expression Analyses of Cytophaga-Like Hydrolases in a Western Arctic Metagenomic Library and the Sargasso Sea

机译:北极北极超基因组文库和Sargasso海中类似细胞噬菌体的水解酶的序列和表达分析

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Sequence analysis of environmental DNA promises to provide new insights into the ecology and biogeochemistry of uncultured marine microbes. In this study we used the Sargasso Sea Whole Genome Sequence (WGS) data set to search for hydrolases used by Cytophaga-like bacteria to degrade biopolymers such as polysaccharides and proteins. Analysis of the Sargasso WGS data for contigs bearing both the 16S rRNA genes of Cytophaga-like bacteria and hydrolase genes revealed a cellulase gene (celM) most similar to the gene found in Cytophaga hutchinsonii. A BLAST search of the entire Sargasso Sea WGS data set indicated that celM was the most abundant cellulase-like gene in the Sargasso Sea. However, the similarity between CelM-like cellulases and peptidases belonging to metalloprotease family M42 led us to question whether CelM is involved in the degradation of polysaccharides or proteins. PCR primers were designed for the celM genes in the Sargasso Sea WGS data set and used to identify celM in a fosmid library constructed with prokaryotic DNA from the western Arctic Ocean. Expression analysis of the Cytophaga-like Arctic CelM, which is 63% identical and 77% similar to CelM in C. hutchinsonii, indicated that there was peptidase activity, whereas cellulase activity was not detected. Our analysis suggests that the celM gene plays a role in the degradation of protein by Cytophaga-like bacteria. The abundance of peptidase genes in the Cytophaga-like fosmid clone provides further evidence for the importance of Cytophaga-like bacteria in the degradation of protein in high-molecular-weight dissolved organic matter.
机译:环境DNA的序列分析有望为未培养的海洋微生物的生态学和生物地球化学提供新的见解。在这项研究中,我们使用了Sargasso海洋全基因组序列(WGS)数据集来搜索类吞噬细胞所使用的水解酶,以降解生物聚合物,例如多糖和蛋白质。对Sargasso WGS数据进行分析,发现同时含有胞吞噬菌样细菌的16S rRNA基因和水解酶基因的重叠群,发现纤维素酶基因(celM)与哈氏胞吞噬菌体中发现的最相似。 BLAST搜索整个Sargasso Sea WGS数据集表明celM是Sargasso Sea中最丰富的纤维素酶样基因。但是,CelM样纤维素酶和属于金属蛋白酶家族M42的肽酶之间的相似性使我们质疑CelM是否参与多糖或蛋白质的降解。 PCR引物是为Sargasso Sea WGS数据集中的celM基因设计的,用于鉴定由北冰洋西部原核DNA构建的fosmid文库中的celM。对细胞噬菌样北极CelM的表达分析表明,它与C. hutchinsonii中的CelM具有63%的相同性和77%的相似性,表明存在肽酶活性,而未检测到纤维素酶活性。我们的分析表明,celM基因在类吞噬细胞细菌降解蛋白质中起作用。 Cytophaga-like fosmid克隆中丰富的肽酶基因为Cytophaga-like细菌在高分子量溶解有机物中蛋白质降解中的重要性提供了进一步的证据。

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