
Biosynthesis of the [FeFe] hydrogenase H-cluster via a synthetic [Fe(ii )(CN)(CO)2(cysteinate)]− complex
Author(s) -
R. David Britt,
Thomas B. Rauchfuss
Publication year - 2021
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/d1dt02258j
Subject(s) - hydrogenase , cluster (spacecraft) , chemistry , catalysis , stereochemistry , computer science , biochemistry , operating system
The H-cluster of [Fe-Fe] hydrogenase consists of a [4Fe] H subcluster linked by the sulfur of a cysteine residue to an organometallic [2Fe] H subcluster that utilizes terminal CO and CN ligands to each Fe along with a bridging CO and a bridging SCH 2 NHCH 2 S azadithiolate (adt) to catalyze proton reduction or hydrogen oxidation. Three Fe-S "maturase" proteins, HydE, HydF, and HydG, are responsible for the biosynthesis of the [2Fe] H subcluster and its incorporation into the hydrogenase enzyme to form this catalytically active H-cluster. We have proposed that HydG is a bifunctional enzyme that uses S -adenosylmethione (SAM) bound to a [4Fe-4S] cluster to lyse tyrosine via a transient 5'-deoxyadenosyl radical to produce CO and CN ligands to a unique cysteine-chelated Fe(II) that is linked to a second [4Fe-4S] cluster via the cysteine sulfur. In this "synthon model", after two cycles of tyrosine lysis, the product of HydG is completed: a [Fe(CN)(CO) 2 (cysteinate)] - organometallic unit that is vectored directly into the synthesis of the [2Fe] H sub-cluster. However our HydG-centric synthon model is not universally accepted, so further validation is important. In this Frontiers article, we discuss recent results using a synthetic "Syn-B" complex that donates [Fe(CN)(CO) 2 (cysteinate)] - units that match our proposed HydG product. Can Syn-B activate hydrogenase in the absence of HydG and its tyrosine substrate? If so, since Syn-B can be synthesized with specific magnetic nuclear isotopes and with chemical substitutions, its use could allow its enzymatic conversions on the route to the H-cluster to be monitored and modeled in fresh detail.