Related Experiment Video
Updated: May 16, 2025

Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
Published on: March 20, 2018
Functional characterization of two distinct classes of NADPH-cytochrome P450 reductases in Senna alexandrina Mill
1Genetic Engineering and Translational Biology Laboratory, Integral Centre of Excellence for Interdisciplinary Research (ICEIR), Department of Biosciences, Faculty of Science, Integral University, Kursi Road, Lucknow, Uttar Pradesh, 226026, India.
Background:
Senna alexandrina Mill., an important medicinal plant of Fabaceae family, is famous for its laxative properties which are mainly due to the presence of sennosides (anthraquinone glycosides). However, the complete biosynthetic pathway of sennosides in Senna is not yet fully understood. Cytochrome P450 monooxygenases (CYPs), which are heme-containing enzymes are supposed to play key roles in sennoside biosynthesis. Cytochrome P450 reductases (CPRs) are essential for the activity of CYPs, as they function as their redox partners. However, CPRs in Senna have not yet been characterized in detail.
Methods And Results:
In this study, two different sequences of SaCPRs were retrieved from the publicly available Transcriptome Shotgun Assembly (TSA) database of S. alexandrina at National Center for Biotechnology Information (NCBI). The open reading frames of SaCPR1 and SaCPR2 were found to be 2079 and 2121 bp, encoding 693 and 707 amino acid long polypeptides, respectively. Phylogenetic and 3-D structure analysis predicted that these two SaCPRs (i.e. SaCPR1 and SaCPR2) were grouped with the members of Class I and Class II CPRs, respectively. Analysis of SaCPR1 and SaCPR2 sequences showed that the conserved domains commonly found in CPRs such as FMN- (Flavin adenine mononucleotide), FAD-(Flavin adenine dinucleotide), NADPH-(Nicotinamide adenine dinucleotide phosphate hydrogen) and cytochrome P450 binding region, were also present in SaCPRs. SaCPR1 and SaCPR2 were cloned and expressed in yeast for functional characterization. In cytochrome P450 reductase assay, both SaCPR1 and SaCPR2 reduced cytochrome c in the presence of NADPH as an electron donor, however, SaCPR1 showed higher specific activity than SaCPR2. The real time expression analysis of SaCPRs performed in the leaf, stem and root tissues of Senna showed that SaCPR1 was expressed more in leaf tissue while SaCPR2 expressed more in stem tissue. Furthermore, both the SaCPRs were found to be induced by salicylic acid as well as wound treatment (up to two hr).
Conclusion:
Two different classes of cytochrome P450 reductases were identified and functionally characterized. SaCPR1 showed higher in vitro activity than SaCPR2 in cytochrome c reduction assay.
More Related Videos
08:03Unveiling Xenobiotic Transport and Effects in Isolated Mitochondria: Insights from Respirometric and Enzymatic Assays
Published on: March 7, 2025
08:04A New Approach for the Comparative Analysis of Multiprotein Complexes Based on 15N Metabolic Labeling and Quantitative Mass Spectrometry
Published on: March 13, 2014
Related Concept Videos
Role of Reduced Coenzymes NADH and FADH₂
Phase I Reactions: Reductive Reactions
Electron Transport Chain: Complex I and II
ROS generation is regulated and maintained at moderate levels necessary...
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
Electron Transport Chain: Complex III and IV
The Z-Scheme of Electron Transport in Photosynthesis