Biochemical characterization of NADH:FMN oxidoreductase HcbA3 from <i>Nocardioides</i> sp. PD653 in catalyzing aerobic HCB dechlorination

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  • Ito Koji
    Hazardous Chemical Division, Institute for Agro-Environmental Sciences, National Agriculture and Food Research Organisation
  • Takagi Kazuhiro
    Hazardous Chemical Division, Institute for Agro-Environmental Sciences, National Agriculture and Food Research Organisation
  • Kataoka Ryota
    Department of Environmental Sciences, University of Yamanashi
  • Kiyota Hiromasa
    Graduate School of Environmental and Life Science, Okayama University

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  • Biochemical characterization of NADH:FMN oxidoreductase HcbA3 from Nocardioides sp. PD653 in catalyzing aerobic HCB dechlorination

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Abstract

<p>Nocardioides sp. PD653 genes hcbA1, hcbA2, and hcbA3 encode enzymes that catalyze the oxidative dehalogenation of hexachlorobenzene (HCB), which is one of the most recalcitrant persistent organic pollutants (POPs). In this study, HcbA1, HcbA2, and HcbA3 were heterologously expressed and characterized. Among the flavin species tested, HcbA3 showed the highest affinity for FMN with a Kd value of 0.75±0.17 µM. Kinetic assays revealed that HcbA3 followed a ping-pong bi–bi mechanism for the reduction of flavins. The Km for NADH and FMN was 51.66±11.58 µM and 4.43±0.69 µM, respectively. For both NADH and FMN, the Vmax and kcat were 2.21±0.86 µM and 66.74±5.91 sec−1, respectively. We also successfully reconstituted the oxidative dehalogenase reaction in vitro, which consisted of HcbA1, HcbA3, FMN, and NADH, suggesting that HcbA3 may be the partner reductase component for HcbA1 in Nocardioides sp. PD653.</p>

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