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Taming of a Poison: Biosynthesis of the...
Journal article

Taming of a Poison: Biosynthesis of the NiFe-Hydrogenase Cyanide Ligands

Abstract

NiFe-hydrogenases have an Ni-Fe site in which the iron has one CO and two CN groups as ligands. Synthesis of the CN ligands requires the activity of two hydrogenase maturation proteins: HypF and HypE. HypF is a carbamoyltransferase that transfers the carbamoyl moiety of carbamoyladenylate to the COOH-terminal cysteine of HypE and thus forms an enzyme-thiocarbamate. HypE dehydrates the S-carbamoyl moiety in an adenosine triphosphate-dependent process to yield the enzyme thiocyanate. Chemical model reactions corroborate the feasibility of this unprecedented biosynthetic route and show that thiocyanates can donate CN to iron. This finding underscores a striking parallel between biochemistry and organometallic chemistry in the formation of an iron-cyano complex.

Authors

Reissmann S; Hochleitner E; Wang H; Paschos A; Lottspeich F; Glass RS; Böck A

Journal

Science, Vol. 299, No. 5609, pp. 1067–1070

Publisher

American Association for the Advancement of Science (AAAS)

Publication Date

February 14, 2003

DOI

10.1126/science.1080972

ISSN

0036-8075

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