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首页> 外文期刊>Marine biotechnology >Actinomycetal Community Structures in Seawater and Freshwater Examined by DGGE Analysis of 16S rRNA Gene Fragments.
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Actinomycetal Community Structures in Seawater and Freshwater Examined by DGGE Analysis of 16S rRNA Gene Fragments.

机译:通过16S rRNA基因片段的DGGE分析检查海水和淡水中的放线菌群落结构。

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摘要

The actinomycetal community structures in marine and freshwater environments (the Pacific Ocean, East China Sea, Tokyo Bay, and Arakawa River) were investigated by a culture-independent molecular method to clarify spatial and seasonal distributions. Deoxyribonucleic acid (DNA) was extracted from environmental water samples, and a community analysis was carried out on polymerase chain reaction-amplified 16S ribosomal DNA. The amplified DNA fragments were analyzed by denaturing gradient gel electrophoresis (DGGE) and nonmetric multidimensional scaling analysis, followed by sequencing analysis. The actinomycetal community structures were different at each station in the Pacific Ocean, the East China Sea, Tokyo Bay, and Arakawa River, and different populations predominated in each area. There were vertical variations in actinomycetal communities in the Pacific Ocean and East China Sea between the surface and 100-m depth, but communities were similar from 200- to 1,000-m depths. There were also distinct seasonal variations in communities in Tokyo Bay. Phylogenetic analysis of DNA fragments recovered from DGGE bands revealed that most of the predominant actinomycetal strains were uncultured and were quite different from well known culturable strains, such as the Streptomyces, Micromonospora, Microbispora, Salinispora, and Actinoplanes groups. These results suggest that the marine environment is an attractive target for discovering new actinomycetal populations producing bioactive compounds and that sampling depth and season are important considerations for isolating various populations effectively.
机译:通过与文化无关的分子方法研究了海洋和淡水环境(太平洋,东海,东京湾和荒川河)中的放线菌群落结构,以阐明空间和季节分布。从环境水样中提取脱氧核糖核酸(DNA),并对聚合酶链反应扩增的16S核糖体DNA进行群落分析。通过变性梯度凝胶电泳(DGGE)和非度量多维标度分析,然后测序分析,分析了扩增的DNA片段。太平洋,东中国海,东京湾和荒川河的每个站点的放线菌群落结构都不同,并且每个地区的种群均不同。太平洋和东中国海的放线菌群落在地表深度和100-m之间存在垂直变化,但在200-1000 m的深度上相似。东京湾的社区也有明显的季节性变化。从DGGE谱带回收的DNA片段的系统发育分析表明,大多数主要的放线菌菌株未经培养,并且与众所周知的可培养菌株(如链霉菌,微单孢菌,微双孢菌,Salinispora和放线菌群)完全不同。这些结果表明,海洋环境是发现产生生物活性化合物的放线菌新种群的一个有吸引力的目标,并且采样深度和季节是有效隔离各种种群的重要考虑因素。

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