Molecular Cloning and Identification of NADPH Cytochrome P450 Reductase from Panax ginseng

• Published in: Molecules (Basel, Switzerland) Vol. 26; no. 21; p. 6654
• Main Authors: Zou, Xian, Zhang, Yue, Zeng, Xu, Liu, Tuo, Li, Gui, Dai, Yuxin, Xie, Yuanzhu, Luo, Zhiyong
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 03.11.2021; MDPI
• Subjects: Alzheimer's disease; Amino acids; Bioinformatics; Biology; Biosynthesis; Cloning; Cytochrome; Cytochrome c; Cytochrome P450; Cytochromes P450; Enzymatic activity; Enzymes; Family studies; Ferricyanide; Gene expression; Genes; Ginseng; ginsenoside; Ginsenosides; Methyl jasmonate; NADPH-cytochrome P450 reductase; NADPH-ferrihemoprotein reductase; Panax ginseng; PgCPR1 and PgCPR2; Phylogeny; prokaryotic expression; Proteins; Reductases
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules26216654

Ginseng (Panax ginseng C.A. Mey.) is a precious Chinese traditional medicine, for which ginsenosides are the most important medicinal ingredients. Cytochrome P450 enzymes (CYP450) and their primary redox molecular companion NADPH cytochrome P450 reductase (CPR) play a key role in ginsenoside biosynthesis pathway. However, systematic studies of CPR genes in ginseng have not been reported. Numerous studies on ginsenoside synthesis biology still use Arabidopsis CPR (AtCPR1) as a reductase. In this study, we isolated two CPR genes (PgCPR1, PgCPR2) from ginseng adventitious roots. Phylogenetic tree analysis showed that both PgCPR1 and PgCPR2 are grouped in classⅡ of dicotyledonous CPR. Enzyme experiments showed that recombinant proteins PgCPR1, PgCPR2 and AtCPR1 can reduce cytochrome c and ferricyanide with NADPH as the electron donor, and PgCPR1 had the highest enzymatic activities. Quantitative real-time PCR analysis showed that PgCPR1 and PgCPR2 transcripts were detected in all examined tissues of Panax ginseng and both showed higher expression in stem and main root. Expression levels of the PgCPR1 and PgCPR2s were both induced after a methyl jasmonate (MeJA) treatment and its pattern matched with ginsenoside accumulation. The present investigation suggested PgCPR1 and PgCPR2 are associated with the biosynthesis of ginsenoside. This report will assist in future CPR family studies and ultimately improving ginsenoside production through transgenic engineering and synthetic biology.