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

• Published in: Journal of Pesticide Science Vol. 45; no. 3; pp. 125 - 131
• Main Authors: Ito, Koji, Takagi, Kazuhiro, Kataoka, Ryota, Kiyota, Hiromasa
• Format: Journal Article
• Language: English
• Published: Tokyo Pesticide Science Society of Japan 20.08.2020; Japan Science and Technology Agency
• Subjects: Dechlorination; Dehalogenation; Flavin mononucleotide; flavin reductase; HcbA3; Hexachlorobenzene; NADH; Nicotinamide adenine dinucleotide; Nocardioides sp. PD653; Original; Oxidoreductase; Persistent organic pollutants; Pollutants; Reductases; TC-FDM
• ISSN: 1348-589X; 1349-0923
• DOI: 10.1584/jpestics.D20-23

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.