4.7 Article

Synthesis of (-)-deoxypodophyllotoxin and (-)-epipodophyllotoxin via a multi-enzyme cascade in E. coli

期刊

MICROBIAL CELL FACTORIES
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12934-021-01673-5

关键词

E; coli; Podophyllotoxin; Deoxypodophyllotoxin; Epipodophyllotoxin; P450; Plant biosynthetic pathway; Multi-enzyme cascade; Sinopodophyllum hexandrum

资金

  1. Federal Ministry of Education and Research [031B0362A]

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Researchers have developed a multi-enzyme cascade approach to produce the anti-neoplastic compound (-)-deoxypodophyllotoxin from plant compounds. They successfully extended this method to prepare other related compounds, representing a significant advancement towards developing more sustainable supply routes for pharmaceutical production.
Background The aryltetralin lignan (-)-podophyllotoxin is a potent antiviral and anti-neoplastic compound that is mainly found in Podophyllum plant species. Over the years, the commercial demand for this compound rose notably because of the high clinical importance of its semi-synthetic chemotherapeutic derivatives etoposide and teniposide. To satisfy this demand, (-)-podophyllotoxin is conventionally isolated from the roots and rhizomes of Sinopodophyllum hexandrum, which can only grow in few regions and is now endangered by overexploitation and environmental damage. For these reasons, targeting the biosynthesis of (-)-podophyllotoxin precursors or analogues is fundamental for the development of novel, more sustainable supply routes. Results We recently established a four-step multi-enzyme cascade to convert (+)-pinoresinol into (-)-matairesinol in E. coli. Herein, a five-step multi-enzyme biotransformation of (-)-matairesinol to (-)-deoxypodophyllotoxin was proven effective with 98 % yield at a concentration of 78 mg/L. Furthermore, the extension of this cascade to a sixth step leading to (-)-epipodophyllotoxin was evaluated. To this end, seven enzymes were combined in the reconstituted pathway involving inter alia three plant cytochrome P450 monooxygenases, with two of them being functionally expressed in E. coli for the first time. Conclusions Both, (-)-deoxypodophyllotoxin and (-)-epipodophyllotoxin, are direct precursors to etoposide and teniposide. Thus, the reconstitution of biosynthetic reactions of Sinopodophyllum hexandrum as an effective multi-enzyme cascade in E. coli represents a solid step forward towards a more sustainable production of these essential pharmaceuticals.

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