Reference : Purification and characterization of a microbial dehydrogenase - A vanillin : NAD(P)(...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
Life sciences : Biotechnology
Life sciences : Microbiology
http://hdl.handle.net/2268/9393
Purification and characterization of a microbial dehydrogenase - A vanillin : NAD(P)(+) oxidoreductase
English
Bare, G. [> > > >]
Swiatkowski, T. [> > > >]
Moukil, A. [> > > >]
Gerday, Charles mailto [Université de Liège - ULg > Services généraux (Faculté des sciences) > Relations académiques et scientifiques (Sciences) >]
Thonart, Philippe mailto [Université de Liège - ULg > Département des sciences de la vie > Biochimie et microbiologie industrielles >]
2002
Applied Biochemistry and Biotechnology
Humana Press Inc
98-100
Spring
415-428
Yes (verified by ORBi)
International
0273-2289
Totowa
[en] vanillin ; enzyme purification ; vanillin dehydrogenase ; Pseudomonas fluorescens ; benzaldehyde dehydrogenase
[en] Pseudomonas fluorescens (strain BTP9) was found to have at least two NAD(P)-dependent vanillin dehydrogenases: one is induced by vanillin, and the other is constitutive. The constitutive enzyme was purified by ammonium sulfate fractionation, gel-filtration, and Q-Sepharose chromatography. The subunit Mr value was 55,000, determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis. The native M, value estimated by gel-filtration chromatography gave a value of 210,000. The enzyme made use of NAD(+) less effectively than NADP(+). Benzaldehyde, 4-hydroxybenzaldehyde, hexanal, and acetaldehyde were not oxidized at detectable rates in the presence of NAD(+) or NADP(+). The ultraviolet absorption spectrum indicated that there is no cofactor or prosthetic group bound. The vanillin oxidation reaction was essentially irreversible. The pH optimum was 9.5 and the pI of the enzyme was 4.9. Enzyme activity was not affected when assayed in the presence of salts, except FeCl2. The enzyme was inhibited by the thiol-blocking reagents 4-chloromercuribenzoate and N-ethylmaleimide. NAD(+) and NADP(+) protected the enzyme against such a type of inhibition along with vanillin to a lesser extent. The enzyme exhibited esterase activity with 4-nitrophenyl acetate as substrate and was activated by low concentrations of NAD(+) or NADP(+). We compared the properties of the enzyme with those of some well-characterized microbial benzaldehyde dehydrogenases.
http://hdl.handle.net/2268/9393

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