Nölling J, Pihl T D, Vriesema A, Reeve J N
Department of Microbiology, Ohio State University, Columbus 43210, USA.
J Bacteriol. 1995 May;177(9):2460-8. doi: 10.1128/jb.177.9.2460-2468.1995.
Two regions of the Methanobacterium thermoautotrophicum genome containing genes that encode enzymes involved in methanogenesis (methane genes) have been cloned and sequenced to determine the extent of methane gene clustering and conservation. One region from the M. thermoautotrophicum strains delta H and Winter, extending approximately 13.5 kb upstream from the adjacent mvhDGAB and mrtBDGA operons that encode the methyl-viologen-reducing hydrogenase (MVH) and the methyl coenzyme M reductase II (MRII), respectively, was sequenced, and 76% sequence identity and very similar gene organizations were demonstrated. Five closely linked open reading frames were located immediately upstream of the mvh operon and were designated flpECBDA. The flpCBD genes encode amino acid sequences that are 31, 47, and 65% identical to the primary sequences of the alpha and beta subunits of formate dehydrogenase and the delta subunit of MVH, respectively. Located immediately upstream of the flp genes was the mth gene, which encodes the H2-dependent methylene-tetrahydromethanopterin dehydrogenase (MTH). In contrast to this mth-flp-mvh-mrt cluster of methane genes, a separate approximately 5.4-kb genomic fragment cloned from M. thermoautotrophicum delta H contained only one methane gene, the mtd gene, which encodes the 8-hydroxy-5-deazaflavin (H2F420)-dependent methylene-tetrahydromethanopterin dehydrogenase (MTD). Northern (RNA) blot experiments demonstrated that mth was transcribed only at early growth stages in fermentor-grown cultures of M. thermoautotrophicum delta H, whereas mtd was transcribed at later growth stages and in the stationary phase. Very similar transcription patterns have been observed by T.D. Pihl, S. Sharma, and J. N. Reeve (J. Bacteriol. 176:6384-6391, 1994) for the MRI- and MRII-encoding operons, mrtBDGA and mcrBDCGA, im M. thermoautotrophicum deltaH, suggesting coordinated regulation of methane gene expression. In contrast to the growth phase-dependent transcription of the mth/mrt and mtd/mcr genes, transcription of the mvhDGAB and frhADGB operons, which encode the two (NiFe) hydrogenases in M. thermoautotrophicum deltaH, was found to occur at all growth stages.
嗜热自养甲烷杆菌基因组中包含编码参与甲烷生成相关酶的基因(甲烷基因)的两个区域已被克隆和测序,以确定甲烷基因的聚类程度和保守性。对嗜热自养甲烷杆菌菌株δH和Winter的一个区域进行了测序,该区域从分别编码甲基紫精还原氢化酶(MVH)和甲基辅酶M还原酶II(MRII)的相邻mvhDGAB和mrtBDGA操纵子上游约13.5 kb处开始,结果显示序列同一性为76%,且基因组织非常相似。五个紧密相连的开放阅读框位于mvh操纵子的紧邻上游,被命名为flpECBDA。flpCBD基因编码的氨基酸序列分别与甲酸脱氢酶的α和β亚基以及MVH的δ亚基的一级序列有31%、47%和65%的同一性。flp基因的紧邻上游是mth基因,它编码依赖H2的亚甲基四氢甲蝶呤脱氢酶(MTH)。与这个mth-flp-mvh-mrt甲烷基因簇不同,从嗜热自养甲烷杆菌δH克隆的一个单独的约5.4 kb基因组片段仅包含一个甲烷基因mtd基因,它编码依赖8-羟基-5-脱氮黄素(H2F420)的亚甲基四氢甲蝶呤脱氢酶(MTD)。Northern(RNA)印迹实验表明,在嗜热自养甲烷杆菌δH的发酵罐培养物中,mth仅在生长早期转录,而mtd在生长后期和稳定期转录。T.D. Pihl、S. Sharma和J.N. Reeve(《细菌学杂志》176:6384 - 6391,1994年)在嗜热自养甲烷杆菌δH中对编码MRI和MRII的操纵子mrtBDGA和mcrBDCGA观察到了非常相似的转录模式,这表明甲烷基因表达存在协同调控。与mth/mrt和mtd/mcr基因的生长阶段依赖性转录不同,嗜热自养甲烷杆菌δH中编码两种(NiFe)氢化酶的mvhDGAB和frhADGB操纵子的转录在所有生长阶段都发生。