Abstract

The limited bioavailability of plant-derived natural products with anticancer activity poses major challenges to the pharmaceutical industry. An example of this is camptothecin, a monoterpene indole alkaloid with potent anticancer activity that is extracted at very low concentrations from woody plants. Recently, camptothecin biosynthesis has been shown to become biotechnologically amenable in hairy-root systems of the natural producer Ophiorrhiza pumila. Here, time-course expression and metabolite analyses were performed to identify novel transcriptional regulators of camptothecin biosynthesis in O. pumila. It is shown here that camptothecin production increased over cultivation time and that the expression pattern of the WRKY transcription factor encoding gene OpWRKY2 is closely correlated with camptothecin accumulation. Overexpression of OpWRKY2 led to a more than three-fold increase in camptothecin levels. Accordingly, silencing of OpWRKY2 correlated with decreased camptothecin levels in the plant. Further detailed molecular characterization by electrophoretic mobility shift, yeast one-hybrid and dual-luciferase assays showed that OpWRKY2 directly binds and activates the central camptothecin pathway gene OpTDC. Taken together, the results of this study demonstrate that OpWRKY2 acts as a direct positive regulator of camptothecin biosynthesis. As such, a feasible strategy for the over-accumulation of camptothecin in a biotechnologically amenable system is presented.

Highlights

  • Camptothecin (CPT) is a monoterpenoid indole alkaloid (MIA) originally isolated from Chinese happy tree (Camptotheca acuminata)[1]

  • Since camptothecin in O. pumila hairy roots could be excreted into the culture medium, we analyzed hairy roots and liquid medium separately by High-performance liquid chromatography (HPLC) analysis to monitor the accumulation of camptothecin in O. pumila (Fig. 2c)

  • This study found that camptothecin accumulation in O. pumila hairy roots is positively correlated with increasing culture time

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Summary

Introduction

Camptothecin (CPT) is a monoterpenoid indole alkaloid (MIA) originally isolated from Chinese happy tree (Camptotheca acuminata)[1]. This natural product exhibits potent antitumor activity by inhibiting DNA topoisomerase I1–3. Commercial exploitation of camptothecin largely depends on extraction from natural woody plant resources such as C. acuminata and Nothapodytes foetida[4]. These plants typically show low camptothecin concentrations and are not suitable for modern biotechnological applications due to their long growth cycles. The O. pumila hairy-root system has been shown to produce up to 0.1–0.2% dry weight of camptothecin[6,7,8]. To further enhance camptothecin production in O. pumila by biotechnological engineering, it is crucial to

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