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Persistent URL
http://purl.org/net/epubs/work/41454
Record Status
Checked
Record Id
41454
Title
Model for Acetylene Reduction by Nitrogenase Derived from Density Functional Theory
Contributors
J Kaestner (Clausthal U. of Technology)
,
PE Bloechl (Clausthal U. of Technology)
Abstract
The catalytic cycle of acetylene reduction at the FeMo cofactor of nitrogenase has been investigated on the basis of density functional theory. C2H2 binds to the same site as N2, but it binds to a less reduced state of the cofactor. In a manner similar to that of N2 binding, one of the sulfur bridges opens during acetylene binding. The model explains the strong noncompetitive inhibition of N2 reduction by C2H2 and the weak competitive inhibition of C2H2 reduction by N2. Our proposed mechanism is consistent with experimentally observed stereoselectivity and the ability of C2H2 to suppress H2 production by nitrogenase.
Organisation
CCLRC
Keywords
Physics
,
Chemistry
,
Biology
Funding Information
Related Research Object(s):
Licence Information:
Language
English (EN)
Type
Details
URI(s)
Local file(s)
Year
Journal Article
Inorg Chem
44, no. 13 (2005): 4568-4575.
doi:10.1021/ic0500311
2005
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