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Diversity of anaerobic arsenite-oxidizing bacteria in low-salt environments analyzed with a newly developed PCR-based method

机译:用新开发的基于PCR的方法分析低盐环境中厌氧砷酸盐氧化细菌的多样性

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摘要

Anaerobic arsenite oxidation is potentially important but the least understood process in the arsenic cycle. The catalytic subunit of the key enzyme for anaerobic arsenite oxidation is encoded by the arxA gene. In this study, a novel primer pair for the arxA gene was designed to detect diverse sequences of this notable gene. Further modification of the designed primer was made by adding extra bases to its 5'- end. This modification made it possible to analyze the PCR products with TA cloning, which provides higher throughput of investigations. With the combination of modified primer pair and TA cloning, diverse arxA gene sequences were effectively obtained from samples of lake water, spring water, and hot spring microbial mat. The sequences detected in the samples characterized by low salinity and nearly neutral pH were phylogenetically distinct from the majority of previously known arxA genes, found in the genome of alkaliphiles and halophiles.
机译:Anaerobic砷酸氧化可能是重要的,但最不理解的砷循环中的过程。 厌氧亚砷酸盐氧化的关键酶的催化亚基由ARXA基因编码。 在该研究中,设计用于ARXA基因的新型引物对以检测该值得注意基因的不同序列。 通过将额外的碱添加到其5'末端来进行设计的引物的进一步改变。 这种改进使得可以使用Ta克隆分析PCR产品,这提供了更高的研究吞吐量。 随着改性引物对和Ta克隆的组合,各种ARXA基因序列有效地从湖水,泉水和热弹簧微生物垫的样品中获得。 在盐度低盐度和几乎中性pH的样品中检测到的序列是从碱和卤素基因组中发现的大多数先前已知的ARXA基因。

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