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CbiZ, an amidohydrolase enzyme required for salvaging the coenzyme B12 precursor cobinamide in archaea.CbiZ,一种古细菌中挽救辅酶B12前体钴胺酰胺所需的酰胺水解酶。
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The cobY gene of the archaeon Halobacterium sp. strain NRC-1 is required for de novo cobamide synthesis.嗜盐古菌盐生盐杆菌属菌株NRC-1的cobY基因是从头合成钴胺素所必需的。
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Cysteinyl-tRNA synthetase is not essential for viability of the archaeon Methanococcus maripaludis.半胱氨酰 - tRNA合成酶对于嗜温甲烷球菌的生存并非必不可少。
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Resolution of component proteins in an enzyme complex from Methanosarcina thermophila catalyzing the synthesis or cleavage of acetyl-CoA.嗜热甲烷八叠球菌中催化乙酰辅酶A合成或裂解的酶复合物中各组成蛋白的解析。
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Identification of an alternative nucleoside triphosphate: 5'-deoxyadenosylcobinamide phosphate nucleotidyltransferase in Methanobacterium thermoautotrophicum delta H.嗜热自养甲烷杆菌δH中一种替代核苷三磷酸的鉴定:5'-脱氧腺苷钴胺酰胺磷酸核苷酸转移酶
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前咕啉6-X还原酶基因在嗜盐碱甲烷球菌钴胺素生物合成中的作用

Role of the precorrin 6-X reductase gene in cobamide biosynthesis in Methanococcus maripaludis.

作者信息

Kim Wonduck, Major Tiffany A, Whitman William B

机构信息

Department of Microbiology, The Ohio State University, Columbus, OH, USA.

出版信息

Archaea. 2005 Dec;1(6):375-84. doi: 10.1155/2005/903614.

DOI:10.1155/2005/903614
PMID:16243778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2685584/
Abstract

In Methanococcus maripaludis strain JJ, deletion of the homolog to cbiJ, which encodes the corrin biosynthetic enzyme precorrin 6-X reductase, yielded an auxotroph that required either cobamide or acetate for good growth. This phenotype closely resembled that of JJ117, a mutant in which tandem repeats were introduced into the region immediately downstream of the homolog of cbiJ. Mutant JJ117 also produced low quantities of cobamides, about 15 nmol g(-1) protein or 1-2% of the amount found in wild-type cells. These results confirm the role of the cbiJ homolog in cobamide biosynthesis in the Archaea and suggest the presence of low amounts of a bypass activity in these organisms.

摘要

在马氏甲烷球菌菌株JJ中,编码钴胺素生物合成酶前咕啉6-X还原酶的cbiJ同源物缺失,产生了一种营养缺陷型菌株,该菌株需要钴胺酰胺或乙酸盐才能良好生长。这种表型与JJ117非常相似,JJ117是一种突变体,其中在cbiJ同源物下游紧邻区域引入了串联重复序列。突变体JJ117也产生少量的钴胺酰胺,约15 nmol g(-1)蛋白质,或野生型细胞中发现量的1-2%。这些结果证实了cbiJ同源物在古菌钴胺酰胺生物合成中的作用,并表明这些生物体中存在少量的旁路活性。