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The Methanol Dehydrogenase Gene, mxaF, as a Functional and Phylogenetic Marker for Proteobacterial Methanotrophs in Natural Environments

机译:甲醇脱氢酶基因mxaF,作为自然环境中变形细菌甲烷营养菌的功能和系统发生标记

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摘要

The mxaF gene, coding for the large (α) subunit of methanol dehydrogenase, is highly conserved among distantly related methylotrophic species in the Alpha-, Beta- and Gammaproteobacteria. It is ubiquitous in methanotrophs, in contrast to other methanotroph-specific genes such as the pmoA and mmoX genes, which are absent in some methanotrophic proteobacterial genera. This study examined the potential for using the mxaF gene as a functional and phylogenetic marker for methanotrophs. mxaF and 16S rRNA gene phylogenies were constructed based on over 100 database sequences of known proteobacterial methanotrophs and other methylotrophs to assess their evolutionary histories. Topology tests revealed that mxaF and 16S rDNA genes of methanotrophs do not show congruent evolutionary histories, with incongruencies in methanotrophic taxa in the Methylococcaceae, Methylocystaceae, and Beijerinckiacea. However, known methanotrophs generally formed coherent clades based on mxaF gene sequences, allowing for phylogenetic discrimination of major taxa. This feature highlights the mxaF gene’s usefulness as a biomarker in studying the molecular diversity of proteobacterial methanotrophs in nature. To verify this, PCR-directed assays targeting this gene were used to detect novel methanotrophs from diverse environments including soil, peatland, hydrothermal vent mussel tissues, and methanotroph isolates. The placement of the majority of environmental mxaF gene sequences in distinct methanotroph-specific clades (Methylocystaceae and Methylococcaceae) detected in this study supports the use of mxaF as a biomarker for methanotrophic proteobacteria.
机译:编码甲醇脱氢酶大(α)亚基的mxaF基因在Alpha,Beta和Gammaproteobacteria的远缘甲基营养物种中高度保守。与其他甲烷营养特异的基因(例如pmoA和mmoX基因)相比,它在甲烷营养中普遍存在,而基因在某些甲基营养蛋白中没有。这项研究检查了使用mxaF基因作为甲烷营养生物的功能和系统发生标记的潜力。 mxaF和16S rRNA基因系统发育是基于已知蛋白菌甲烷营养生物和其他甲基营养生物的100多个数据库序列构建的,以评估其进化历史。拓扑测试显示,甲烷氧化菌的mxaF和16S rDNA基因没有显示出一致的进化历史,甲基球菌科,甲基囊藻科和贝氏菊科的甲烷氧化菌群没有一致性。但是,已知的甲烷营养生物通常基于mxaF基因序列形成连贯进化枝,从而可以对主要类群进行系统发育区分。此功能凸显了mxaF基因作为研究自然界中细菌性甲烷氧化菌的分子多样性的生物标记物的有用性。为了验证这一点,针对该基因的PCR导向检测被用于检测来自土壤,泥炭地,热液喷口贻贝组织和甲烷营养菌分离物等多种环境的新型甲烷营养菌。在这项研究中检测到的大多数环境mxaF基因序列在不同的甲烷营养生物特有的进化枝(甲基囊藻科和甲基球菌科)中的位置都支持将mxaF用作甲烷营养生物蛋白菌的生物标记。

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