Affiliation:
1. Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut 06269-2131
Abstract
ABSTRACT
This study demonstrates the ability of
Desulfitobacterium
spp. to utilize aliphatic sulfonates as terminal electron acceptors (TEA) for growth. Isethionate (2-hydroxyethanesulfonate) reduction by
Desulfitobacterium hafniense
resulted in acetate as well as sulfide accumulation in accordance with the expectation that the carbon portion of isethionate was oxidized to acetate and the sulfur was reduced to sulfide. The presence of a polypeptide, approximately 97 kDa, was evident in isethionate-grown cells of
Desulfitobacterium hafniense
,
Desulfitobacterium
sp. strain PCE 1, and the two sulfate-reducing bacteria (SRB)—
Desulfovibrio desulfuricans
IC1 (T. J. Lie, J. R. Leadbetter, and E. R. Leadbetter, Geomicrobiol. J. 15:135–149, 1998) and
Desulfomicrobium norvegicum
; this polypeptide was not detected when these bacteria were grown on TEA other than isethionate, suggesting involvement in its metabolism. The sulfate analogs molybdate and tungstate, effective in inhibiting sulfate reduction by SRB, were examined for their effects on sulfonate reduction. Molybdate effectively inhibited sulfonate reduction by strain IC1 and selectively inhibited isethionate (but not cysteate) reduction by
Desulfitobacterium dehalogenans
and
Desulfitobacterium
sp. strain PCE 1.
Desulfitobacterium hafniense
, however, grew with both isethionate and cysteate in the presence of molybdate. In contrast, tungstate only partially inhibited sulfonate reduction by both SRB and
Desulfitobacterium
spp. Similarly, another inhibitor of sulfate reduction, 1,8-dihydroxyanthraquinone, effectively inhibited sulfate reduction by SRB but only partially inhibited sulfonate reduction by both SRB and
Desulfitobacterium hafniense
.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
48 articles.
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