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PMID: 7624773 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Importance of historical contingency in the stereochemistry of hydratase-dehydratase enzymes.

Science (New York, N.Y.) ·Vol. 269 ·No. 5223 ·1995-07-28 ·Pages 527-9

Mohrig JR, Moerke KA, Cloutier DL, Lane BD, Person EC, Onasch TB

Abstract

There are two stereochemical classes of hydratase-dehydratase enzymes. Those that catalyze the addition of water to alpha, beta-unsaturated thioesters give syn addition-elimination stereochemistry, whereas those that catalyze the addition of water to conjugated carboxylate substrates give anti stereochemistry. This dichotomy could reflect different adaptive advantages or contingencies of separate evolutionary histories. Determination of the nonenzymatic stereochemistry of deuterium oxide addition to fumarate and to S-crotonyl N-acetylcysteamine has provided direct evidence for the importance of the contingencies of evolutionary history, rather than chemical efficiency, in the pathways of these hydratase-dehydratase enzymes.

MeSH Terms
Biological Evolution Catalysis Cysteamine/analogs & derivatives,chemistry Deuterium Oxide/chemistry Enoyl-CoA Hydratase/metabolism Fumarate Hydratase/metabolism Fumarates/chemistry Hydro-Lyases/metabolism Hydrolysis Molecular Conformation Temperature
Chemicals
Fumarates S-crotonyl-N-acetylcysteamine Cysteamine fumaric acid Hydro-Lyases Enoyl-CoA Hydratase Fumarate Hydratase Deuterium Oxide
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mohrig J R
Department of Chemistry, Carleton College, Northfield, MN 55057, USA.
Moerke K A
Cloutier D L
Lane B D
Person E C
Onasch T B
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1995-07-28
Pages
527-9
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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