Pihl T D, Sharma S, Reeve J N
Department of Microbiology, Ohio State University, Columbus 43210.
J Bacteriol. 1994 Oct;176(20):6384-91. doi: 10.1128/jb.176.20.6384-6391.1994.
The genes encoding the two isoenzymes of methyl coenzyme M reductase (MRI and MRII) in Methanobacterium thermoautotrophicum delta H have been cloned and sequenced. The MRI-encoding mcr operon (mcrBDCGA) has been located immediately upstream from the mtr operon (mtrEDCBA) that encodes N5-methyltetrahydromethanopterin:coenzyme M methyltransferase, the enzyme that catalyzes the step preceding the MR-catalyzed reaction in methanogenesis. The MRII-encoding mrt operon (mrtBDGA) has been located between the operon that encodes the methyl viologen-reducing hydrogenase and an open reading frame (designated pyrC) predicted to encode dihydroorotase. Surprisingly, the mrt operon has been found to contain only four genes (mrtBDGA), lacking the equivalent of the mcrC gene that is present in all mcr operons. A protocol that isolates transcripts intact from M. thermoautotrophicum delta H cells has been developed and used, with primer extension and Northern (RNA) blot procedures, to identify the sites of transcription initiation upstream of the mcr, mrt, and mtr operons and to determine the relative numbers of these transcripts in cells at different growth stages. Transcription of the mrt operon was found to occur only at early times in batch cultures and was then replaced by transcription of the mcr operon. Transcripts of the mtr operon were detectable at all times; however, at early times, all mtr transcripts were initiated at the mtr promoter, whereas at later times, during mcr transcription, approximately 3% of mcr transcripts were extended to generate mcr plus mtr transcripts that constituted approximately 20% of all mtr transcripts present.
嗜热自养甲烷杆菌δH中编码甲基辅酶M还原酶两种同工酶(MR I和MR II)的基因已被克隆和测序。编码MR I的mcr操纵子(mcrBDCGA)位于mtr操纵子(mtrEDCBA)的紧上游,mtr操纵子编码N5-甲基四氢甲蝶呤:辅酶M甲基转移酶,该酶催化产甲烷过程中MR催化反应之前的步骤。编码MR II的mrt操纵子(mrtBDGA)位于编码甲基紫精还原氢化酶的操纵子和一个预测编码二氢乳清酸酶的开放阅读框(命名为pyrC)之间。令人惊讶的是,已发现mrt操纵子仅包含四个基因(mrtBDGA),缺少所有mcr操纵子中都存在的相当于mcrC基因的基因。已开发并使用了一种从嗜热自养甲烷杆菌δH细胞中完整分离转录本的方案,通过引物延伸和Northern(RNA)印迹程序,来鉴定mcr、mrt和mtr操纵子上游的转录起始位点,并确定不同生长阶段细胞中这些转录本的相对数量。发现mrt操纵子的转录仅在分批培养的早期发生,然后被mcr操纵子的转录所取代。mtr操纵子的转录本在所有时间都可检测到;然而,在早期,所有mtr转录本都在mtr启动子处起始,而在后期,在mcr转录期间,约3%的mcr转录本会延伸产生mcr加mtr转录本,这些转录本约占所有存在的mtr转录本的20%。