Sequence characteristics, expression and subcellular localization of gene from cytochrome P450 family in willd.

The Cytochrome P450 (CYP450) family is the largest enzyme protein family in plants, distributed across various organs and involved in significant catalytic activities in primary and secondary metabolic processes. In this study, we cloned the gene, characterized its open reading frame (ORF), and conducted comprehensive analyses including physicochemical properties, evolutionary relationships, subcellular localization, prokaryotic expression, and correlation between the relative expression of different parts and the content of tenuifolin, hormones, and abiotic stress response associated with the encoded protein. The ORF of was 1,521 bp, with a secondary structure predominantly composed of α-helices and random coils. Subcellular localization experiments confirmed the presence of in the endoplasmic reticulum. For prokaryotic expression, we constructed the recombinant plasmid pET28a- using pET28a as the vector, which was then transformed into BL21(DE3). Induction with Isopropyl β-D-1-thiogalactopyranoside (IPTG) at temperatures of 16 and 25 °C and varying concentrations (0.1, 0.2, 0.5, 1, 2 mM) resulted in the formation of inclusion bodies, with higher expression observed at 25 °C. Our qPCR analyses revealed that exhibited the highest expression in the cortex of , followed by roots and xylem, correlating with the observed tenuifolin content distribution. Induction with abscisic acid (ABA) and chitosan (CHT) initially decreased expression followed by a subsequent increase, peaking at 48 h. Similarly, drought stress induced a gradual increase in expression, also peaking at 48 h. NaCl treatment for 6 h significantly upregulated expression. In conclusion, our study provides foundational insights into the gene in , laying the groundwork for further exploration of its role in the biosynthesis pathway of triterpenoid saponins.