Publication: Reduction kinetics of a flavin oxidoreductase LuxG from photobacterium leiognathi (TH1): Half-sites reactivity
Issued Date
2010-11-02
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15204995
00062960
00062960
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2-s2.0-78049255927
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Mahidol University
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SCOPUS
Bibliographic Citation
Biochemistry. Vol.49, No.43 (2010), 9241-9248
Suggested Citation
Sarayut Nijvipakul, David P. Ballou, Pimchai Chaiyen Reduction kinetics of a flavin oxidoreductase LuxG from photobacterium leiognathi (TH1): Half-sites reactivity. Biochemistry. Vol.49, No.43 (2010), 9241-9248. doi:10.1021/bi1009985 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/28599
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Title
Reduction kinetics of a flavin oxidoreductase LuxG from photobacterium leiognathi (TH1): Half-sites reactivity
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Abstract
Bacterial bioluminescence is a phenomenon resulting from the reaction of a two-component FMN-dependent aldehyde monooxygenase system, which comprises a bacterial luciferase and a flavin reductase. Bacterial luciferase (LuxAB) is one of the most extensively investigated two-component monooxygenases, while its reductase partner, the flavin reductase (LuxG) from the same operon, has only been recently expressed in a functional form. This work reports transient kinetics identification of intermediates in the LuxG reaction using stopped-flow spectrophotometry. The results indicate that the overall reaction follows a sequential-ordered mechanism in which NADH binds first to the enzyme, followed by FMN, resulting in the formation of charge-transfer intermediate 1 (CT-1) typical of those between reduced pyridine nucleotides and oxidized flavins. The next step is the reduction of FMN as indicated by a large decrease in absorbance at 450 nm. The reduction of FMN is biphasic. The first phase of FMN reduction occurs concurrently with formation of charge-transfer intermediate 2 (CT-2), while the second phase is synchronous with the decay of CT-2. When the isotope-labeled substrate, 4(R)-[2H]NADH, was used, the first reduction phase showed a primary kinetic isotope effect (Dk red) of ≥3.9 and resulted in greater accumulation of CT-1. These results are consistent with CT-1 being the FMNox:NADH complex, while CT-2 is the FMNred:NAD+ complex. Because CT-2 decays with a rate constant of 2.8 ± 0.2 s-1, while the turnover number obtained from the steady-steady-state kinetics is 1.7 s-1, it is likely that the CT-2 decay step largely controls the overall reaction rate. All kinetic data are consistent with a half-sites reactivity model in which flavin reduction occurs at only one subunit at a time. The first reduction phase is due to the reduction of FMN in the first subunit, while the second phase is due to the reduction of FMN in the second subunit. The latter phase is limited by the rate of decay of CT-2 in the first subunit. The half-sites reactivity model is also supported by detection of burst kinetics during the pre-steady-state period that is correlated with 0.5 mol of the FMN being reduced/mol of the LuxG:NADH complex. The functional importance of this half-site reactivity phenomenon is still unclear. © 2010 American Chemical Society.