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用于新型类似物组合生物合成的抗真菌蕨烷型三萜类化合物多聚多酚的生物合成表征

Biosynthetic characterization of the antifungal fernane-type triterpenoid polytolypin for generation of new analogues combinatorial biosynthesis.

作者信息

Li Xin-Yu, Lv Jian-Ming, Cao Zhi-Qin, Wang Gao-Qian, Lin Fu-Long, Chen Guo-Dong, Qin Sheng-Ying, Hu Dan, Gao Hao, Yao Xin-Sheng

机构信息

School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, Liaoning, China.

Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy/Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research/International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Ministry of Education (MOE) of China, Jinan University, Guangzhou 510632, China.

出版信息

Org Biomol Chem. 2023 Jan 25;21(4):851-857. doi: 10.1039/d2ob02158g.

Abstract

Fernane-type triterpenoids are a small group of natural products mainly found in plants and fungi with a wide range of biological activities. Polytolypin is a representative fernane-type triterpenoid from fungi and possesses potent antifungal activity. So far, biosynthesis of fungal-derived fernane-type triterpenoids has not been characterized, which hinders the expansion of their structural diversity using biosynthetic approaches. Herein, we identified the biosynthetic gene cluster of polytolypin and elucidated its biosynthetic pathway through heterologous expression in NSAR1, which involves a new triterpene cyclase for the biosynthesis of the hydrocarbon skeleton motiol, followed by multiple oxidations three P450 enzymes. Moreover, two new triterpene cyclases for the biosynthesis of two other fernane-type skeletons isomotiol and fernenol were identified from fungi, and were individually co-expressed with the three P450 enzymes involved in polytolypin biosynthesis. These studies led to the generation of 13 fernane-type triterpenoids including eight new compounds, and two of them showed stronger antifungal activity towards FIM709 than polytolypin.

摘要

蕨烷型三萜类化合物是一小类主要存在于植物和真菌中的天然产物,具有广泛的生物活性。多聚多酚是一种来自真菌的代表性蕨烷型三萜类化合物,具有强大的抗真菌活性。到目前为止,真菌来源的蕨烷型三萜类化合物的生物合成尚未得到表征,这阻碍了利用生物合成方法扩展其结构多样性。在此,我们鉴定了多聚多酚的生物合成基因簇,并通过在NSAR1中的异源表达阐明了其生物合成途径,该途径涉及一种用于烃骨架莫替醇生物合成的新三萜环化酶,随后由三种P450酶进行多次氧化。此外,还从真菌中鉴定出另外两种用于合成其他两种蕨烷型骨架异莫替醇和蕨烯醇的新三萜环化酶,并分别与参与多聚多酚生物合成的三种P450酶共表达。这些研究产生了13种蕨烷型三萜类化合物,包括8种新化合物,其中两种对FIM709的抗真菌活性比多聚多酚更强。

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