McDonald I R, Murrell J C
Department of Biological Sciences, University of Warwick, United Kingdom.
Appl Environ Microbiol. 1997 Aug;63(8):3218-24. doi: 10.1128/aem.63.8.3218-3224.1997.
The methanol dehydrogenase gene mxaF, encoding the large subunit of the enzyme, was amplified from the DNA of a number of representative methanotrophs, methyletrophs, and environmental samples by PCR using primers designed from regions of conserved amino acid sequence identified by comparison of three known sequences of the large subunit of methanol dehydrogenase. The resulting 550-bp PCR products were cloned and sequenced. Analysis of the predicted amino acid sequences corresponding to these mxaF genes revealed strong sequence conservation. Of the 172 amino acid residues, 47% were conserved among all 22 sequences obtained in this study. Phylogenetic analysis of these MxaF sequences showed that those from type I and type II methanotrophs form two distinct clusters and are separate from MxaF sequences of other gram-negative methylotrophs. MxaF sequences retrieved by PCR from DNA isolated from a blanket bog peat core sample formed a distinct phylogenetic cluster within the MxaF sequences of type II methanotrophs and may originate from a novel group of acidophilic methanotrophs which have yet to be cultured from this environment.
甲醇脱氢酶基因mxaF编码该酶的大亚基,利用根据甲醇脱氢酶大亚基三个已知序列比对确定的保守氨基酸序列区域设计的引物,通过聚合酶链式反应(PCR)从多个代表性甲烷营养菌、甲基营养菌的DNA以及环境样品中扩增出该基因。将得到的550个碱基对的PCR产物进行克隆和测序。对与这些mxaF基因相对应的预测氨基酸序列分析显示出很强的序列保守性。在本研究获得的所有22个序列中,172个氨基酸残基中有47%是保守的。对这些MxaF序列的系统发育分析表明,来自I型和II型甲烷营养菌的序列形成两个不同的簇,并且与其他革兰氏阴性甲基营养菌的MxaF序列分开。通过PCR从毯状沼泽泥炭芯样品分离的DNA中检索到的MxaF序列在II型甲烷营养菌的MxaF序列中形成一个独特的系统发育簇,可能源自一组尚未从该环境中培养出来的新型嗜酸甲烷营养菌。