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嗜热自养甲烷杆菌δH和坎氏甲烷球菌中依赖辅酶F420的N5,N10-亚甲基四氢甲蝶呤还原酶编码基因的克隆、测序及生长阶段依赖性转录

Cloning, sequencing, and growth phase-dependent transcription of the coenzyme F420-dependent N5,N10-methylenetetrahydromethanopterin reductase-encoding genes from Methanobacterium thermoautotrophicum delta H and Methanopyrus kandleri.

作者信息

Nölling J, Pihl T D, Reeve J N

机构信息

Department of Microbiology, Ohio State University, Columbus 43210, USA.

出版信息

J Bacteriol. 1995 Dec;177(24):7238-44. doi: 10.1128/jb.177.24.7238-7244.1995.

Abstract

The mer genes, which encode the coenzyme F420-dependent N5,N10-methylenetetrahydromethanopterin reductases (CH2 = H4MPT reductases), and their flanking regions have been cloned from Methanobacterium thermoautotrophicum delta H and Methanopyrus kandleri and sequenced. The mer genes have DNA sequences that are 57% identical and encode polypeptides with amino acid sequences that are 57% identical and 71% similar, with calculated molecular masses of 33.6 and 37.5 kDa, respectively. In M. thermoautotrophicum, mer transcription has been shown to initiate 10 bp upstream from the ATG translation initiating codon and to generate a monocistronic transcript approximately 1 kb in length. This transcript was synthesized at all stages of M. thermoautotrophicum delta H growth in batch cultures but was found to increase in abundance from the earliest stages of exponential growth, reaching a maximum level at the mid-exponential growth phase. For comparison, transcription of the ftr gene from M. thermoautotrophicum delta H that encodes the formylmethanofuran:tetrahydromethanopterin formyltransferase (A. A. DiMarco, K. A. Sment, J. Konisky, and R. S. Wolfe, J. Biol. Chem. 265:472-476, 1990) was included in this study. The ftr transcript was found similarly to be monocistronic and to be approximately 1 kb in length, but, in contrast to the mer transcript, the ftr transcript was present at maximum levels at both the early and the mid-exponential growth stages.

摘要

编码依赖辅酶F420的N5,N10-亚甲基四氢甲蝶呤还原酶(CH2 = H4MPT还原酶)的mer基因及其侧翼区域已从嗜热自养甲烷杆菌δH和坎氏甲烷球菌中克隆并测序。mer基因的DNA序列有57%的同一性,编码的多肽氨基酸序列有57%的同一性和71%的相似性,计算得到的分子量分别为33.6 kDa和37.5 kDa。在嗜热自养甲烷杆菌中,已表明mer转录起始于ATG翻译起始密码子上游10 bp处,并产生一个长度约为1 kb的单顺反子转录本。该转录本在嗜热自养甲烷杆菌δH分批培养的所有生长阶段均有合成,但发现其丰度从指数生长的最早阶段开始增加,在指数生长中期达到最高水平。作为比较,本研究纳入了嗜热自养甲烷杆菌δH中编码甲酰甲烷呋喃:四氢甲蝶呤甲酰转移酶的ftr基因的转录(A. A. 迪马尔科、K. A. 斯门特、J. 科尼斯基和R. S. 沃尔夫,《生物化学杂志》265:472 - 476, 1990)。发现ftr转录本同样是单顺反子,长度约为1 kb,但与mer转录本不同的是,ftr转录本在指数生长早期和中期均处于最高水平。

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Methanogenesis: genes, genomes, and who's on first?甲烷生成:基因、基因组以及谁先发?
J Bacteriol. 1997 Oct;179(19):5975-86. doi: 10.1128/jb.179.19.5975-5986.1997.

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