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史氏甲烷球形菌的基因组序列揭示了为何这种人类肠道古菌仅利用甲醇和氢气来生成甲烷及合成ATP。

The genome sequence of Methanosphaera stadtmanae reveals why this human intestinal archaeon is restricted to methanol and H2 for methane formation and ATP synthesis.

作者信息

Fricke Wolfgang F, Seedorf Henning, Henne Anke, Krüer Markus, Liesegang Heiko, Hedderich Reiner, Gottschalk Gerhard, Thauer Rudolf K

机构信息

Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg August University, Grisebachstr. 8, D-37077 Göttingen, Germany.

出版信息

J Bacteriol. 2006 Jan;188(2):642-58. doi: 10.1128/JB.188.2.642-658.2006.

Abstract

Methanosphaera stadtmanae has the most restricted energy metabolism of all methanogenic archaea. This human intestinal inhabitant can generate methane only by reduction of methanol with H2 and is dependent on acetate as a carbon source. We report here the genome sequence of M. stadtmanae, which was found to be composed of 1,767,403 bp with an average G+C content of 28% and to harbor only 1,534 protein-encoding sequences (CDS). The genome lacks 37 CDS present in the genomes of all other methanogens. Among these are the CDS for synthesis of molybdopterin and for synthesis of the carbon monoxide dehydrogenase/acetyl-coenzyme A synthase complex, which explains why M. stadtmanae cannot reduce CO2 to methane or oxidize methanol to CO2 and why this archaeon is dependent on acetate for biosynthesis of cell components. Four sets of mtaABC genes coding for methanol:coenzyme M methyltransferases were found in the genome of M. stadtmanae. These genes exhibit homology to mta genes previously identified in Methanosarcina species. The M. stadtmanae genome also contains at least 323 CDS not present in the genomes of all other archaea. Seventy-three of these CDS exhibit high levels of homology to CDS in genomes of bacteria and eukaryotes. These 73 CDS include 12 CDS which are unusually long (>2,400 bp) with conspicuous repetitive sequence elements, 13 CDS which exhibit sequence similarity on the protein level to CDS encoding enzymes involved in the biosynthesis of cell surface antigens in bacteria, and 5 CDS which exhibit sequence similarity to the subunits of bacterial type I and III restriction-modification systems.

摘要

史氏甲烷短杆菌具有所有产甲烷古菌中最为有限的能量代谢方式。这种人类肠道寄居菌仅能通过氢气还原甲醇来产生甲烷,并且依赖乙酸盐作为碳源。我们在此报告史氏甲烷短杆菌的基因组序列,发现其由1,767,403碱基对组成,平均G+C含量为28%,仅含有1,534个蛋白质编码序列(CDS)。该基因组缺少所有其他产甲烷菌基因组中存在的37个CDS。其中包括钼蝶呤合成以及一氧化碳脱氢酶/乙酰辅酶A合成酶复合物合成的CDS,这解释了为什么史氏甲烷短杆菌不能将二氧化碳还原为甲烷或将甲醇氧化为二氧化碳,以及为什么这种古菌在细胞成分生物合成中依赖乙酸盐。在史氏甲烷短杆菌的基因组中发现了四组编码甲醇:辅酶M甲基转移酶的mtaABC基因。这些基因与先前在甲烷八叠球菌属物种中鉴定出的mta基因具有同源性。史氏甲烷短杆菌的基因组还包含至少323个在所有其他古菌基因组中不存在的CDS。其中73个CDS与细菌和真核生物基因组中的CDS具有高度同源性。这73个CDS包括12个异常长(>2,400碱基对)且具有明显重复序列元件的CDS,13个在蛋白质水平上与编码细菌细胞表面抗原生物合成相关酶的CDS具有序列相似性的CDS,以及5个与细菌I型和III型限制修饰系统亚基具有序列相似性的CDS。

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