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钴胺素(辅酶B12):合成与生物学意义

Cobalamin (coenzyme B12): synthesis and biological significance.

作者信息

Roth J R, Lawrence J G, Bobik T A

机构信息

Department of Biology, University of Utah, Salt Lake City 84112, USA.

出版信息

Annu Rev Microbiol. 1996;50:137-81. doi: 10.1146/annurev.micro.50.1.137.

Abstract

This review examines deoxyadenosylcobalamin (Ado-B12) biosynthesis, transport, use, and uneven distribution among living forms. We describe how genetic analysis of enteric bacteria has contributed to these issues. Two pathways for corrin ring formation have been found-an aerobic pathway (in P. denitrificans) and an anaerobic pathway (in P. shermanii and S. typhimurium)-that differ in the point of cobalt insertion. Analysis of B12 transport in E. coli reveals two systems: one (with two proteins) for the outer membrane, and one (with three proteins) for the inner membrane. To account for the uneven distribution of B12 in living forms, we suggest that the B12 synthetic pathway may have evolved to allow anaerobic fermentation of small molecules in the absence of an external electron acceptor. Later, evolution of the pathway produced siroheme, (allowing use of inorganic electron acceptors), chlorophyll (O2 production), and heme (aerobic respiration). As oxygen became a larger part of the atmosphere, many organisms lost fermentative functions and retained dependence on newer, B12 functions that did not involve fermentation. Paradoxically, Salmonella spp. synthesize B12 only anaerobically but can use B12 (for degradation of ethanolamine and propanediol) only with oxygen. Genetic analysis of the operons for these degradative functions indicate that anaerobic degradation is important. Recent results suggest that B12 can be synthesized and used during anaerobic respiration using tetrathionate (but not nitrate or fumarate) as an electron acceptor. The branch of enteric taxa from which Salmonella spp. and E. coli evolved appears to have lost the ability to synthesize B12 and the ability to use it in propanediol and glycerol degradation. Salmonella spp., but not E. coli, have acquired by horizontal transfer the ability to synthesize B12 and degrade propanediol. The acquired ability to degrade propanediol provides the selective force that maintains B12 synthesis in this group.

摘要

本综述探讨了脱氧腺苷钴胺素(Ado - B12)的生物合成、运输、利用及其在生物界中的不均匀分布。我们描述了对肠道细菌的遗传分析如何为这些问题提供了线索。已发现两种形成咕啉环的途径——需氧途径(在反硝化假单胞菌中)和厌氧途径(在谢氏丙酸杆菌和鼠伤寒沙门氏菌中),这两种途径在钴插入点上有所不同。对大肠杆菌中B12运输的分析揭示了两个系统:一个(由两种蛋白质组成)用于外膜,另一个(由三种蛋白质组成)用于内膜。为了解释B12在生物界中的不均匀分布,我们认为B12合成途径可能是为了在没有外部电子受体的情况下允许小分子进行厌氧发酵而进化的。后来,该途径的进化产生了尿卟啉原Ⅲ(允许使用无机电子受体)、叶绿素(产生氧气)和血红素(有氧呼吸)。随着氧气在大气中所占比例增加,许多生物失去了发酵功能,转而依赖不涉及发酵的更新的B12功能。矛盾的是,沙门氏菌属仅在厌氧条件下合成B12,但仅在有氧条件下才能利用B12(用于乙醇胺和丙二醇的降解)。对这些降解功能操纵子的遗传分析表明厌氧降解很重要。最近的研究结果表明,在以连四硫酸盐(而非硝酸盐或富马酸盐)作为电子受体的厌氧呼吸过程中,可以合成并利用B12。沙门氏菌属和大肠杆菌所进化而来的肠道分类群分支似乎已失去了合成B12以及在丙二醇和甘油降解中利用它的能力。沙门氏菌属通过水平转移获得了合成B12和降解丙二醇的能力,而大肠杆菌则没有。获得的降解丙二醇的能力提供了在该群体中维持B12合成的选择压力。

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