首页> 美国卫生研究院文献>Journal of Bacteriology >Structure and comparative analysis of the genes encoding component C of methyl coenzyme M reductase in the extremely thermophilic archaebacterium Methanothermus fervidus.
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Structure and comparative analysis of the genes encoding component C of methyl coenzyme M reductase in the extremely thermophilic archaebacterium Methanothermus fervidus.

机译:嗜热古细菌Methanothermus fervidus中甲基辅酶M还原酶C组分编码基因的结构和比较分析。

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摘要

A 6-kilobase-pair (kbp) region of the genome of the extremely thermophilic arachaebacterium Methanothermus fervidus which encodes the alpha, beta, and gamma subunit polypeptides of component C of methyl coenzyme M reductase was cloned and sequenced. Genes encoding the beta (mcrB) and gamma (mcrG) subunits were separated by two open reading frames (designated mcrC and mcrD) which encode unknown gene products. The M. fervidus genes were preceded by ribosome-binding sites, separated by short A + T-rich intergenic regions, contained unexpectedly few NNC codons, and exhibited inflexible codon usage at some locations. Sites of transcription initiation and termination flanking the mcrBDCGA cluster of genes in M. fervidus were identified. The sequences of the genes, the encoded polypeptides, and transcription regulatory signals in M. fervidus were compared with the functionally equivalent sequences from two mesophilic methanogens (Methanococcus vannielii and Methanosarcina barkeri) and from a moderate thermophile (Methanobacterium thermoautotrophicum Marburg). The amino acid sequences of the polypeptides encoded by the mcrBCGA genes in the two thermophiles were approximately 80% identical, whereas all other pairs of these gene products contained between 50 and 60% identical amino acid residues. The mcrD gene products have diverged more than the products of the other mcr genes. Identification of highly conserved regions within mcrA and mcrB suggested oligonucleotide sequences which might be developed as hybridization probes which could be used for identifying and quantifying all methanogens.
机译:克隆和测序了极端嗜热的阿拉伯拟杆菌Methanothermus fervidus基因组的6-千碱基对(kbp)区,该区编码甲基辅酶M还原酶的组分C的α,β和γ亚基多肽。编码β(mcrB)和γ(mcrG)亚基的基因被两个开放阅读框(命名为mcrC和mcrD)分开,它们编码未知的基因产物。狂犬分枝杆菌基因之前有核糖体结合位点,被短的富含A + T的基因间区域隔开,意外地含有少量NNC密码子,并且在某些位置表现出不灵活的密码子用法。鉴定了M. fervidus基因mcrBDCGA簇侧翼的转录起始和终止位点。将狂犬分枝杆菌中的基因序列,编码的多肽和转录调控信号与来自两种嗜温产甲烷菌(Methanococcus vannielii和Methanosarcina barkeri)和中等嗜热菌(Methanobacterium thermoautotrophicum Marburg)的功能等效序列进行了比较。在两个嗜热菌中,由mcrBCGA基因编码的多肽的氨基酸序列具有大约80%的同一性,而这些基因产物的所有其他对均含有50%至60%的相同氨基酸残基。 mcrD基因产物的差异大于其他mcr基因的产物。在mcrA和mcrB中高度保守的区域的鉴定提示了寡核苷酸序列,可以将其开发为可用于鉴定和定量所有产甲烷菌的杂交探针。

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