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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...

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Autores principales: Cooke, Heather A., Peck, Spencer C., Evans, Bradley S., van der Donk, Wilfred A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2012
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.
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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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