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Mechanistic Investigation of Methylphosphonate Synthase, a Non-Heme Iron-Dependent Oxygenase
[Image: see text] Methylphosphonate synthase is a non-heme iron-dependent oxygenase that converts 2-hydroxyethylphosphonate (2-HEP) to methylphosphonate. On the basis of experiments with two enantiomers of a substrate analog, 2-hydroxypropylphosphonate, catalysis is proposed to commence with stereos...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458437/ https://www.ncbi.nlm.nih.gov/pubmed/22957470 http://dx.doi.org/10.1021/ja306777w |
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author | Cooke, Heather A. Peck, Spencer C. Evans, Bradley S. van der Donk, Wilfred A. |
author_facet | Cooke, Heather A. Peck, Spencer C. Evans, Bradley S. van der Donk, Wilfred A. |
author_sort | Cooke, Heather A. |
collection | PubMed |
description | [Image: see text] Methylphosphonate synthase is a non-heme iron-dependent oxygenase that converts 2-hydroxyethylphosphonate (2-HEP) to methylphosphonate. On the basis of experiments with two enantiomers of a substrate analog, 2-hydroxypropylphosphonate, catalysis is proposed to commence with stereospecific abstraction of the pro-S hydrogen on C2 of the substrate. Experiments with isotopologues of 2-HEP indicate stereospecific hydrogen transfer of the pro-R hydrogen at C2 of the substrate to the methyl group of methylphosphonate. Kinetic studies with these substrate isotopologues reveal that neither hydrogen transfer is rate limiting under saturating substrate conditions. A mechanism is proposed that is consistent with the available data. |
format | Online Article Text |
id | pubmed-3458437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-34584372012-09-27 Mechanistic Investigation of Methylphosphonate Synthase, a Non-Heme Iron-Dependent Oxygenase Cooke, Heather A. Peck, Spencer C. Evans, Bradley S. van der Donk, Wilfred A. J Am Chem Soc [Image: see text] Methylphosphonate synthase is a non-heme iron-dependent oxygenase that converts 2-hydroxyethylphosphonate (2-HEP) to methylphosphonate. On the basis of experiments with two enantiomers of a substrate analog, 2-hydroxypropylphosphonate, catalysis is proposed to commence with stereospecific abstraction of the pro-S hydrogen on C2 of the substrate. Experiments with isotopologues of 2-HEP indicate stereospecific hydrogen transfer of the pro-R hydrogen at C2 of the substrate to the methyl group of methylphosphonate. Kinetic studies with these substrate isotopologues reveal that neither hydrogen transfer is rate limiting under saturating substrate conditions. A mechanism is proposed that is consistent with the available data. American Chemical Society 2012-09-08 2012-09-26 /pmc/articles/PMC3458437/ /pubmed/22957470 http://dx.doi.org/10.1021/ja306777w Text en Copyright © 2012 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Cooke, Heather A. Peck, Spencer C. Evans, Bradley S. van der Donk, Wilfred A. Mechanistic Investigation of Methylphosphonate Synthase, a Non-Heme Iron-Dependent Oxygenase |
title | Mechanistic Investigation
of Methylphosphonate Synthase,
a Non-Heme Iron-Dependent Oxygenase |
title_full | Mechanistic Investigation
of Methylphosphonate Synthase,
a Non-Heme Iron-Dependent Oxygenase |
title_fullStr | Mechanistic Investigation
of Methylphosphonate Synthase,
a Non-Heme Iron-Dependent Oxygenase |
title_full_unstemmed | Mechanistic Investigation
of Methylphosphonate Synthase,
a Non-Heme Iron-Dependent Oxygenase |
title_short | Mechanistic Investigation
of Methylphosphonate Synthase,
a Non-Heme Iron-Dependent Oxygenase |
title_sort | mechanistic investigation
of methylphosphonate synthase,
a non-heme iron-dependent oxygenase |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458437/ https://www.ncbi.nlm.nih.gov/pubmed/22957470 http://dx.doi.org/10.1021/ja306777w |
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