首页> 外文期刊>Journal of Rapid Methods and Automation in Microbiology >New primers for amplification of the planctomycetes 16S rRNA gene from environmental samples.
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New primers for amplification of the planctomycetes 16S rRNA gene from environmental samples.

机译:用于从环境样品中扩增轮生菌16S rRNA基因的新引物。

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Although the 16S rDNA primer set Pla-46-F/1392-R is often used to explore the planctomycetes community, the universal reverse primer 1392-R limits the capability of the forward primer Pla-46-F. Here we report two new reverse primers (Pla-1097-R and Pla-1368-R), which greatly promote the potential ability of the forward primer Pla-46-F, both theoretically and experimentally. The tests with field samples showed that PCR induced by the new primer sets both reduced mismatches to non-planctomycetes and supplemented the diversity of planctomycetes, particularly increasing the numbers of planctomycetes genera in both seawater and sediment samples. Our results strongly suggest that the diversity of planctomycetes revealed by the previously used primer set Pla-46F/1392-R has been underestimated.
机译:尽管通常使用16S rDNA引物对Pla-46-F / 1392-R探索扁平菌群落,但通用反向引物1392-R限制了正向引物Pla-46-F的功能。在这里,我们报告了两个新的反向引物(Pla-1097-R和Pla-1368-R),它们在理论上和实验上都大大提高了正向引物Pla-46-F的潜在能力。对现场样品的测试表明,新引物组诱导的PCR既减少了与非浮生菌的错配,又增加了浮生菌的多样性,特别是增加了海水和沉积物样品中浮生菌属的数量。我们的结果有力地表明,先前使用的引物对Pla-46F / 1392-R揭示的轮菌的多样性被低估了。

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