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Elucidation of the anaerobic pathway for the corrin component of cobalamin (vitamin B12 )

Elucidation of the anaerobic pathway for the corrin component of cobalamin (vitamin B12 )
Elucidation of the anaerobic pathway for the corrin component of cobalamin (vitamin B12 )
It has been known for the past 20 years that two pathways exist in nature for the de novo biosynthesis of the coenzyme form of vitamin B12, adenosylcobalamin, representing aerobic and anaerobic routes. In contrast to the aerobic pathway, the anaerobic route has remained enigmatic because many of its intermediates have proven technically challenging to isolate, because of their inherent instability. However, by studying the anaerobic cobalamin biosynthetic pathway in Bacillus megaterium and using homologously overproduced enzymes, it has been possible to isolate all of the intermediates between uroporphyrinogen III and cobyrinic acid. Consequently, it has been possible to detail the activities of purified cobinamide biosynthesis (Cbi) proteins CbiF, CbiG, CbiD, CbiJ, CbiET, and CbiC, as well as show the direct in vitro conversion of 5-aminolevulinic acid into cobyrinic acid using a mixture of 14 purified enzymes. This approach has resulted in the isolation of the long sought intermediates, cobalt-precorrin-6A and -6B and cobalt-precorrin-8. EPR, in particular, has proven an effective technique in following these transformations with the cobalt(II) paramagnetic electron in the dyz orbital, rather than the typical dz2. This result has allowed us to speculate that the metal ion plays an unexpected role in assisting the interconversion of pathway intermediates. By determining a function for all of the pathway enzymes, we complete the tool set for cobalamin biosynthesis and pave the way for not only enhancing cobalamin production, but also design of cobalamin derivatives through their combinatorial use and modification.
0027-8424
14906-14911
Moore, Simon J.
9a9edf57-d1ae-4078-a30d-211b62181ec3
Lawrence, Andrew D.
ce503b40-0155-486f-bb1d-26830b61b5f1
Biedendieck, Rebekka
03b1d4e9-762c-495e-b5d1-9f61c4f16859
Deery, Evelyne
16c10c8d-1383-4ce6-95dd-dfcfa0168875
Frank, Stefanie
cb728fb0-fbe4-4d4a-b4f7-fd8efbae5974
Howard, Mark J.
780e29b9-d377-47aa-b39c-18f8591fa73f
Rigby, Stephen E.J.
32656ae3-5d2f-4d00-b427-39979ffe8d00
Warren, Martin J.
4c73b491-93f5-404b-acde-4f86dbbbb130
Moore, Simon J.
9a9edf57-d1ae-4078-a30d-211b62181ec3
Lawrence, Andrew D.
ce503b40-0155-486f-bb1d-26830b61b5f1
Biedendieck, Rebekka
03b1d4e9-762c-495e-b5d1-9f61c4f16859
Deery, Evelyne
16c10c8d-1383-4ce6-95dd-dfcfa0168875
Frank, Stefanie
cb728fb0-fbe4-4d4a-b4f7-fd8efbae5974
Howard, Mark J.
780e29b9-d377-47aa-b39c-18f8591fa73f
Rigby, Stephen E.J.
32656ae3-5d2f-4d00-b427-39979ffe8d00
Warren, Martin J.
4c73b491-93f5-404b-acde-4f86dbbbb130

Moore, Simon J., Lawrence, Andrew D., Biedendieck, Rebekka, Deery, Evelyne, Frank, Stefanie, Howard, Mark J., Rigby, Stephen E.J. and Warren, Martin J. (2013) Elucidation of the anaerobic pathway for the corrin component of cobalamin (vitamin B12 ). Proceedings of the National Academy of Sciences, 110 (37), 14906-14911. (doi:10.1073/pnas.1308098110).

Record type: Article

Abstract

It has been known for the past 20 years that two pathways exist in nature for the de novo biosynthesis of the coenzyme form of vitamin B12, adenosylcobalamin, representing aerobic and anaerobic routes. In contrast to the aerobic pathway, the anaerobic route has remained enigmatic because many of its intermediates have proven technically challenging to isolate, because of their inherent instability. However, by studying the anaerobic cobalamin biosynthetic pathway in Bacillus megaterium and using homologously overproduced enzymes, it has been possible to isolate all of the intermediates between uroporphyrinogen III and cobyrinic acid. Consequently, it has been possible to detail the activities of purified cobinamide biosynthesis (Cbi) proteins CbiF, CbiG, CbiD, CbiJ, CbiET, and CbiC, as well as show the direct in vitro conversion of 5-aminolevulinic acid into cobyrinic acid using a mixture of 14 purified enzymes. This approach has resulted in the isolation of the long sought intermediates, cobalt-precorrin-6A and -6B and cobalt-precorrin-8. EPR, in particular, has proven an effective technique in following these transformations with the cobalt(II) paramagnetic electron in the dyz orbital, rather than the typical dz2. This result has allowed us to speculate that the metal ion plays an unexpected role in assisting the interconversion of pathway intermediates. By determining a function for all of the pathway enzymes, we complete the tool set for cobalamin biosynthesis and pave the way for not only enhancing cobalamin production, but also design of cobalamin derivatives through their combinatorial use and modification.

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More information

Accepted/In Press date: 17 July 2013
e-pub ahead of print date: 6 August 2013
Published date: 10 September 2013

Identifiers

Local EPrints ID: 488499
URI: http://eprints.soton.ac.uk/id/eprint/488499
ISSN: 0027-8424
PURE UUID: 646c9c80-f69c-496f-8903-25d326c88a0d
ORCID for Andrew D. Lawrence: ORCID iD orcid.org/0000-0002-5853-5409

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Date deposited: 25 Mar 2024 17:33
Last modified: 26 Mar 2024 03:05

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Contributors

Author: Simon J. Moore
Author: Andrew D. Lawrence ORCID iD
Author: Rebekka Biedendieck
Author: Evelyne Deery
Author: Stefanie Frank
Author: Mark J. Howard
Author: Stephen E.J. Rigby
Author: Martin J. Warren

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