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Biphasic kinetic behavior of E. coli WrbA, an FMN-dependent NAD(P)H:quinone oxidoreductase

Authors :
Kishko, Iryna
Harish, Balasubramanian
Zayats, Vasilina
Reha, David
Tenner, Brian
Beri, Dhananjay
Gustavsson, Tobias
Ettrich, Rüdiger
Carey, Jannette
Kishko, Iryna
Harish, Balasubramanian
Zayats, Vasilina
Reha, David
Tenner, Brian
Beri, Dhananjay
Gustavsson, Tobias
Ettrich, Rüdiger
Carey, Jannette
Source :
Kishko , I , Harish , B , Zayats , V , Reha , D , Tenner , B , Beri , D , Gustavsson , T , Ettrich , R & Carey , J 2012 , ' Biphasic kinetic behavior of E. coli WrbA, an FMN-dependent NAD(P)H:quinone oxidoreductase ' , PLOS ONE , vol. 7 , no. 8 , pp. e43902 .
Publication Year :
2012

Abstract

The E. coli protein WrbA is an FMN-dependent NAD(P)H:quinone oxidoreductase that has been implicated in oxidative defense. Three subunits of the tetrameric enzyme contribute to each of four identical, cavernous active sites that appear to accommodate NAD(P)H or various quinones, but not simultaneously, suggesting an obligate tetramer with a ping-pong mechanism in which NAD departs before oxidized quinone binds. The present work was undertaken to evaluate these suggestions and to characterize the kinetic behavior of WrbA. Steady-state kinetics results reveal that WrbA conforms to a ping-pong mechanism with respect to the constancy of the apparent Vmax to Km ratio with substrate concentration. However, the competitive/non-competitive patterns of product inhibition, though consistent with the general class of bi-substrate reactions, do not exclude a minor contribution from additional forms of the enzyme. NMR results support the presence of additional enzyme forms. Docking and energy calculations find that electron-transfer-competent binding sites for NADH and benzoquinone present severe steric overlap, consistent with the ping-pong mechanism. Unexpectedly, plots of initial velocity as a function of either NADH or benzoquinone concentration present one or two Michaelis-Menten phases depending on the temperature at which the enzyme is held prior to assay. The effect of temperature is reversible, suggesting an intramolecular conformational process. WrbA shares these and other details of its kinetic behavior with mammalian DT-diaphorase, an FAD-dependent NAD(P)H:quinone oxidoreductase. An extensive literature review reveals several other enzymes with two-plateau kinetic plots, but in no case has a molecular explanation been elucidated. Preliminary sedimentation velocity analysis of WrbA indicates a large shift in size of the multimer with temperature, suggesting that subunit assembly coupled to substrate binding may underlie the two-plateau behavior. An additional aim o

Details

Database :
OAIster
Journal :
Kishko , I , Harish , B , Zayats , V , Reha , D , Tenner , B , Beri , D , Gustavsson , T , Ettrich , R & Carey , J 2012 , ' Biphasic kinetic behavior of E. coli WrbA, an FMN-dependent NAD(P)H:quinone oxidoreductase ' , PLOS ONE , vol. 7 , no. 8 , pp. e43902 .
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1322714379
Document Type :
Electronic Resource