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Molecular Analysis of the Diversity of Sulfate-Reducing and Sulfur-Oxidizing Prokaryotes in the Environment, Using aprA as Functional Marker Gene

机译:使用aprA作为功能性标记基因的环境中硫酸盐还原和硫氧化原核生物多样性的分子分析

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The dissimilatory adenosine-5′-phosposulfate reductase is a key enzyme of the microbial sulfate reduction and sulfur oxidation processes. Because the alpha- and beta-subunit-encoding genes, aprBA, are highly conserved among sulfate-reducing and sulfur-oxidizing prokaryotes, they are most suitable for molecular profiling of the microbial community structure of the sulfur cycle in environment. In this study, a new aprA gene-targeting assay using a combination of PCR and denaturing gradient gel electrophoresis is presented. The screening of sulfate-reducing and sulfur-oxidizing reference strains as well as the analyses of environmental DNA from diverse habitats (e.g., microbial mats, invertebrate tissue, marine and estuarine sediments, and filtered hydrothermal water) by the new primer pair revealed an improved microbial diversity coverage and less-pronounced template-to-PCR product bias in direct comparison to those of the previously published primer set (B. Deplancke, K. R. Hristova, H. A. Oakley, V. J. McCracken, R. Aminov, R. I. Mackie, and H. R. Gaskins, Appl. Environ. Microbiol. 66:2166-2174, 2000). The concomitant molecular detection of sulfate-reducing and sulfur-oxidizing prokaryotes was confirmed. The new assay was applied in comparison with the 16S rRNA gene-based analysis to investigate the microbial diversity of the sulfur cycle in sediment, seawater, and manganese crust samples from four study sites in the area of the Lesser Antilles volcanic arc, Caribbean Sea (Caribflux project). The aprA gene-based approach revealed putative sulfur-oxidizing Alphaproteobacteria of chemolithoheterotrophic lifestyle to have been abundant in the nonhydrothermal sediment and water column. In contrast, the sulfur-based microbial community that inhabited the surface of the volcanic manganese crust was more complex, consisting predominantly of putative chemolithoautotrophic sulfur oxidizers of the Betaproteobacteria and Gammaproteobacteria.
机译:异化腺苷5'-磷酸磷酸还原酶是微生物硫酸盐还原和硫氧化过程的关键酶。由于编码α和β亚基的基因aprBA在硫酸盐还原和硫氧化原核生物中高度保守,因此它们最适合在环境中对硫循环的微生物群落结构进行分子分析。在这项研究中,提出了一种使用PCR和变性梯度凝胶电泳相结合的新的aprA基因靶向测定方法。通过新的引物对筛选硫酸盐还原和硫氧化的参考菌株,以及分析来自不同栖息地(例如微生物垫,无脊椎动物组织,海洋和河口沉积物以及过滤后的热水)的环境DNA,发现改进了与先前发表的引物组(B.Deplancke,KR Hristova,HAakley,VJ McCracken,R.Aminov,RI Mackie和HR Gaskins, Appl.Environ.Microbiol.66:2166-2174,2000)。证实了同时进行硫酸盐还原和硫氧化原核生物的分子检测。这项新方法与基于16S rRNA基因的分析方法进行了比较,以研究加勒比海小安地列斯火山弧地区四个研究点的沉积物,海水和锰结壳样品中硫循环的微生物多样性( Caribflux项目)。基于aprA基因的方法表明,在非水热沉积物和水柱中,化学石化异养型生活方式的推定的硫氧化阿尔法变形杆菌已经很多。相反,居住在火山锰壳表面的基于硫的微生物群落则更为复杂,主要由β变形蛋白细菌和γ变形蛋白细菌的假定的化学自养型硫氧化剂组成。

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