Lehmacher A, Klenk H P
Max-Planck-Institut für Biochemie, Martinsried, Germany.
Mol Gen Genet. 1994 Apr;243(2):198-206. doi: 10.1007/BF00280317.
A 5.7 kb region of chromosomal DNA from Methanothermus fervidus, harbouring a second mcr gene cluster, was cloned and sequenced. This gene cluster, termed mcrII, encodes an isoenzyme of methyl coenzyme M reductase (MCR). In contrast to the known mcr gene clusters from other methanogens, mcrII lacks mcrC, a gene of unknown function. But the remaining mcrII genes B, D, G and A are arranged in the same order as in previously sequenced mcr gene clusters. The mcrII genes from M. fervidus are located 3' to the open reading frame (ORF) B of the methylviologen-reducing hydrogenase (mvh) gene cluster. The genes of mcrII are cotranscribed, resulting in an mRNA of 4500 nucleotides. The transcriptional initiation and termination sites were identified. Phylogenetic reconstructions reveal that the mcr gene clusters fall into two different types, I and II, and that the ancestral mcr gene cluster was duplicated before the segregation of methanogens into three major orders occurred.
来自嗜热甲烷热菌(Methanothermus fervidus)的一段5.7 kb染色体DNA区域被克隆并测序,该区域含有第二个mcr基因簇。这个基因簇被命名为mcrII,编码甲基辅酶M还原酶(MCR)的一种同工酶。与其他产甲烷菌已知的mcr基因簇不同,mcrII缺少功能未知的基因mcrC。但是其余的mcrII基因B、D、G和A的排列顺序与先前测序的mcr基因簇相同。嗜热甲烷热菌的mcrII基因位于甲基紫精还原氢化酶(mvh)基因簇的开放阅读框(ORF)B的3'端。mcrII的基因共转录,产生一个4500个核苷酸的mRNA。确定了转录起始和终止位点。系统发育重建表明,mcr基因簇分为I和II两种不同类型,并且在产甲烷菌分化为三个主要目之前,祖先mcr基因簇发生了复制。