Affiliation:
1. Institut für Biologie, Humboldt-Universität zu Berlin, 10115 Berlin, Germany,1 and
2. Swammerdam Institute for Life Sciences, Biochemistry, University of Amsterdam, NL-1018 TV Amsterdam, The Netherlands2
Abstract
ABSTRACT
The biosynthesis of [NiFe] hydrogenases is a complex process that requires the function of the Hyp proteins HypA, HypB, HypC, HypD, HypE, HypF, and HypX for assembly of the H
2
-activating [NiFe] site. In this study we examined the maturation of the regulatory hydrogenase (RH) of
Ralstonia eutropha
. The RH is a H
2
-sensing [NiFe] hydrogenase and is required as a constituent of a signal transduction chain for the expression of two energy-linked [NiFe] hydrogenases. Here we demonstrate that the RH regulatory activity was barely affected by mutations in
hypA
,
hypB
,
hypC
, and
hypX
and was not substantially diminished in
hypD
- and
hypE
-deficient strains. The lack of HypF, however, resulted in a 90% decrease of the RH regulatory activity. Fourier transform infrared spectroscopy and the incorporation of
63
Ni into the RH from overproducing cells revealed that the assembly of the [NiFe] active site is dependent on all Hyp functions, with the exception of HypX. We conclude that the entire Hyp apparatus (HypA, HypB, HypC, HypD, HypE, and HypF) is involved in an efficient incorporation of the [NiFe] center into the RH.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
43 articles.
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