首页> 外文OA文献 >Cytochrome cd1 -containing nitrite reductase encoding gene nirS as a new functional biomarker for detection of anaerobic ammonium oxidizing (anammox) bacteria
【2h】

Cytochrome cd1 -containing nitrite reductase encoding gene nirS as a new functional biomarker for detection of anaerobic ammonium oxidizing (anammox) bacteria

机译:含有细胞色素cd1的亚硝酸还原酶编码基因nirs作为检测厌氧氨氧化(厌氧氨氧化)细菌的新功能生物标志物

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A newly designed primer set (AnnirS), together with a previously published primer set (ScnirS), was used to detect anammox bacterial nirS genes from sediments collected from three marine environments. Phylogenetic analysis demonstrated that all retrieved sequences were clearly different from typical denitrifiers' nirS, but do group together with the known anammox bacterial nirS. Sequences targeted by ScnirS are closely related to Scalindua nirS genes recovered from the Peruvian oxygen minimum zone (OMZ), whereas sequences targeted by AnnirS are more closely affiliated with the nirS of Candidatus 'Kuenenia stuttgartiensis' and even form a new phylogenetic nirS clade, which might be related to other genera of the anammox bacteria. Analysis demonstrated that retrieved sequences had higher sequence identities (>60%) with known anammox bacterial nirS genes than with denitrifiers' nirS, on both nucleotide and amino acid levels. Compared to the 16S rRNA and hydrazine oxidoreductase (hzo) genes, the anammox bacterial nirS not only showed consistent phylogenetic relationships but also demonstrated more reliable quantification of anammox bacteria because of the single copy of the nirS gene in the anammox bacterial genome and the specificity of PCR primers for different genera of anammox bacteria, thus providing a suitable functional biomarker for investigation of anammox bacteria. © 2011 American Chemical Society.
机译:新设计的引物组(AnnirS)与先前发布的引物组(ScnirS)一起用于检测从三个海洋环境中收集的沉积物中的厌氧细菌nirS基因。系统发育分析表明,所有检索到的序列都与典型的反硝化菌的nirS明显不同,但与已知的厌氧菌nirS一起进行了分组。 ScnirS靶向的序列与从秘鲁最低氧区(OMZ)回收的Scalindua nirS基因密切相关,而AnnirS靶向的序列与假丝酵母(Kuenenia stuttgartiensis)的nirS紧密相关,甚至形成了新的系统发育nirS进化枝。可能与厌氧细菌的其他属有关。分析表明,与已知的厌氧细菌nirS基因相比,从反硝化菌的nirS检索到的序列在核苷酸和氨基酸水平上具有更高的序列同一性(> 60%)。与16S rRNA和肼氧化还原酶(hzo)基因相比,厌氧细菌nirS不仅显示出一致的系统发生关系,而且由于厌氧细菌基因组中nirS基因的单一拷贝以及其特异性,显示出更可靠的厌氧细菌定量分析。用于不同种类厌氧细菌的PCR引物,从而为研究厌氧细菌提供了合适的功能性生物标记。 ©2011美国化学学会。

著录项

  • 作者

    Gu, JD; Li, X; Ford, T; Li, M;

  • 作者单位
  • 年度 2011
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号