1932

Abstract

This review examines deoxyadenosylcobalamin (Ado-B) 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 ) and an anaerobic pathway (in and )–that differ in the point of cobalt insertion. Analysis of B transport in 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 B in living forms, we suggest that the B 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 (O production), and heme (aerobic respiration). As oxygen became a larger part of the atmosphere, many organisms lost fermentative functions and retained dependence on newer, B functions that did not involve fermentation. Paradoxically, spp. synthesize B only anaerobically but can use B (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 B 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 spp. and evolved appears to have lost the ability to synthesize B and the ability to use it in propanediol and glycerol degradation. spp., but not , have acquired by horizontal transfer the ability to synthesize B and degrade propanediol. The acquired ability to degrade propanediol provides the selective force that maintains B synthesis in this group.

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/content/journals/10.1146/annurev.micro.50.1.137
1996-10-01
2024-04-14
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  • Article Type: Review Article
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