Affiliation:
1. Department of Microbiology and Center for Biocatalysis and Bioprocessing, University of Iowa, Iowa City, Iowa 52242
Abstract
ABSTRACT
Naphthalene dioxygenase (NDO) is a multicomponent enzyme system that oxidizes naphthalene to (+)-
cis
-(1
R
,2
S
)-1,2-dihydroxy-1,2-dihydronaphthalene with consumption of O
2
and two electrons from NAD(P)H. In the presence of benzene, NADH oxidation and O
2
utilization were partially uncoupled from substrate oxidation. Approximately 40 to 50% of the consumed O
2
was detected as hydrogen peroxide. The rate of benzene-dependent O
2
consumption decreased with time, but it was partially increased by the addition of catalase in the course of the O
2
consumption by NDO. Detailed experiments showed that the total amount of O
2
consumed and the rate of benzene-induced O
2
consumption increased in the presence of hydrogen peroxide-scavenging agents, and further addition of the terminal oxygenase component (ISP
NAP
) of NDO. Kinetic studies showed that ISP
NAP
was irreversibly inactivated in the reaction that contained benzene, but the inactivation was relieved to a high degree in the presence of catalase and partially relieved in the presence of 0.1 mM ferrous ion. Benzene- and naphthalene-reacted ISP
NAP
gave almost identical visible absorption spectra. In addition, hydrogen peroxide added at a range of 0.1 to 0.6 mM to the reaction mixtures inactivated the reduced ISP
NAP
containing mononuclear iron. These results show that hydrogen peroxide released during the uncoupling reaction acts both as an inhibitor of benzene-dependent O
2
consumption and as an inactivator of ISP
NAP
. It is proposed that the irreversible inactivation of ISP
NAP
occurs by a Fenton-type reaction which forms a strong oxidizing agent, hydroxyl radicals (
·
OH), from the reaction of hydrogen peroxide with ferrous mononuclear iron at the active site. Furthermore, when [
14
C]benzene was used as the substrate,
cis
-benzene 1,2-dihydrodiol formed by NDO was detected. This result shows that NDO also couples a trace amount of benzene to both O
2
consumption and NADH oxidation.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference56 articles.
1. Metabolic switching in cytochrome P-450cam: deuterium isotope effects on regiospecificity and monooxygenase/oxidase ratio;Atkins W. M.;J. Am. Chem. Soc.,1987
2. Batie
C. J.
Ballou
D. P.
Corell
C. C.
Phthalate dioxygenase reductase and related flavin-iron-sulfur containing electron transferases
Chemistry and biochemistry of flavoenzymes.
Müller
F.
1991
543
556
CRC Press
Boca Raton Fla
3. A SPECTROPHOTOMETRIC METHOD FOR MEASURING THE BREAKDOWN OF HYDROGEN PEROXIDE BY CATALASE
4. Spin trapping: ESR parameters of spin adducts;Buettner G. R.;Free Radic. Biol. Med.,1987
5. Oxidative metabolism of naphthalene by soil pseudomonads: the ring-fission mechanism;Davies J. I.;Biochem. J.,1964
Cited by
92 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献