Abstract
AbstractThe medicinal properties of Ashwagandha (Withania somniferaL. Dunal) are attributed to withanolides, which belong to the triterpenoid steroidal lactones class of compounds. Though it is proposed that intermediates of the universal phytosterol pathway are utilized by cytochrome P450 (CYP450) enzymes to form withanolides, studies on functional characterization of these enzymes has been sparse. This study reports the functional characterization of a CYP450 candidate fromW. somnifera(WsCYP71B35) that exhibited induced expression in response to methyl jasmonate treatment and showed higher expression in tissues that accumulate withanolides. Biochemical assay with yeast microsomal fraction expressing recombinant WsCYP71B35 indicated no activity when phytosterols and their intermediate 24-methylene cholesterol were used as substrates. However, WsCYP71B35 catalyzed product formation with withaferin A, withanolide A, withanolide B, and withanoside IV among the tested substrates. Moreover, virus-induced gene silencing (VIGS) and transient overexpression ofWsCYP71B35inW. somniferaleaves modulated the levels of withaferin A, withanolide A, and withanolide B, indicating the role ofWsCYP71B35in withanolides pathway. Furthermore, VIGS ofWsCYP71B35inW. somniferareduced its tolerance toPseudomonas syringae(DC3000) infection, whereas overexpression enhanced the tolerance to the bacterium inW. somniferaand transgenic tobacco. Overall, these results provide insights into the role ofW. somniferaWsCYP71B35 in withanolides biosynthesis and bacterial defense.
Publisher
Cold Spring Harbor Laboratory