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Quantification of mcrA by fluorescent PCR in methanogenic and methanotrophic microbial communities
Authors:Nunoura Takuro  Oida Hanako  Miyazaki Junichi  Miyashita Ai  Imachi Hiroyuki  Takai Ken
Institution:Subground Animalcule Retrieval (SUGAR) Program, Extremobiosphere Research Center, Japan Agency for Marine-Earth Science and Technology (JAMSTEC), Yokosuka, Japan. takuron@jamstec.go.jp
Abstract:A quantitative fluorogenic PCR method for detecting methanogenic and methanotrophic orders was established using a refined primer set for the methyl coenzyme M reductase subunit A gene (mcrA). The method developed was applied to several microbial communities in which diversity and abundance of methanogens or anaerobic methanotrophs (ANMEs) was identified by 16S rRNA gene clone analysis, and strong correlations between the copy numbers of mcrA with those of archaeal 16S rRNA genes in the communities were observed. The assay can be applied to detecting and assessing the abundance of methanogens and/or ANMEs in anoxic environments that could not be detected by 16S rRNA gene sequence analyses.
Keywords:methanogen  anaerobic methanotroph  methanogenesis  anaerobic oxidation of methane              mcrA            quantitative fluorescent PCR
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