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PMID: 3390431 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Studies of electron-transfer properties of salicylate hydroxylase from Pseudomonas cepacia and effects of salicylate and benzoate binding.

Biochemistry ·Vol. 27 ·No. 9 ·1988-05-03 ·Pages 3277-85

Einarsdottir GH, Stankovich MT, Tu SC

Abstract

The pH dependence of the redox behavior of salicylate hydroxylase from Pseudomonas cepacia as well as the effects of salicylate, benzoate, and chloride binding is described. At pH 7.6 in 0.02 M potassium phosphate buffer E1(0')(EFl ox/EFl.-) is -0.150 V and E2(0')(EFl.-/EFl red H-) is -0.040 V versus the standard hydrogen electrode (SHE). A maximum of 5% of FAD anion semiquinone is thermodynamically stabilized under these conditions. However, in coulometric and dithionite titrations more semiquinone is kinetically formed, indicating slow transfer of the second electron. The potential/pH dependence is consistent with a two-electron, one-proton transfer. Upon salicylate binding the midpoint potential is shifted 0.020 V negative from -0.094 to -0.114 V vs SHE at pH 7.6. A maximum of 7% of the neutral semiquinone is stabilized both in potentiometric and coulometric titrations. This small potential shift indicates that the substrate is bound nearly to the same extent to all three oxidation states of the enzyme. It is clear that the substrate binding does not make the reduction of the flavin thermodynamically more favorable. In contrast to salicylate, the potential shift caused by the effector, benzoate, is much more significant. (A maximum potential shift of -0.07 V is calculated.) Benzoate binds most tightly to the oxidized form and is least tightly bound to the two-electron-reduced form of the enzyme. For the reduction of the free enzyme the transfer of the second electron or the transfer of the proton is rate limiting, as is shown by the kinetic formation of the anionic semiquinone.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Benzoates/pharmacology Benzoic Acid Chlorides/pharmacology Dithionite/pharmacology Electron Transport Kinetics Mixed Function Oxygenases/metabolism Oxidation-Reduction Potentiometry Protein Binding Pseudomonas/enzymology Salicylates/pharmacology
Chemicals
Benzoates Chlorides Salicylates Dithionite Benzoic Acid Mixed Function Oxygenases salicylate 1-monooxygenase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Einarsdottir G H
Department of Chemistry, University of Minnesota, Minneapolis 55455.
Stankovich M T
Tu S C
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1988-05-03
Pages
3277-85
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM 25953 · United States
NIGMS NIH HHS · GM 29344 · United States
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