Luo Pan, Huang Jia-Hua, Lv Jian-Ming, Wang Gao-Qian, Hu Dan, Gao Hao
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 Chinese Ministry of Education of China, Jinan University, Guangzhou 510632, China.
Nat Prod Rep. 2024 May 22;41(5):748-783. doi: 10.1039/d3np00052d.
Covering: up to August 2023Terpenoids, which are widely distributed in animals, plants, and microorganisms, are a large group of natural products with diverse structures and various biological activities. They have made great contributions to human health as therapeutic agents, such as the anti-cancer drug paclitaxel and anti-malarial agent artemisinin. Accordingly, the biosynthesis of this important class of natural products has been extensively studied, which generally involves two major steps: hydrocarbon skeleton construction by terpenoid cyclases and skeleton modification by tailoring enzymes. Additionally, fungi (Ascomycota and Basidiomycota) serve as an important source for the discovery of terpenoids. With the rapid development of sequencing technology and bioinformatics approaches, genome mining has emerged as one of the most effective strategies to discover novel terpenoids from fungi. To date, numerous terpenoid cyclases, including typical class I and class II terpenoid cyclases as well as emerging UbiA-type terpenoid cyclases, have been identified, together with a variety of tailoring enzymes, including cytochrome P450 enzymes, flavin-dependent monooxygenases, and acyltransferases. In this review, our aim is to comprehensively present all fungal terpenoid cyclases identified up to August 2023, with a focus on newly discovered terpenoid cyclases, especially the emerging UbiA-type terpenoid cyclases, and their related tailoring enzymes from 2015 to August 2023.
截至2023年8月
萜类化合物广泛分布于动物、植物和微生物中,是一大类结构多样、具有多种生物活性的天然产物。它们作为治疗药物,如抗癌药物紫杉醇和抗疟药物青蒿素,对人类健康做出了巨大贡献。因此,这类重要天然产物的生物合成已得到广泛研究,其一般涉及两个主要步骤:由萜类环化酶构建碳氢化合物骨架以及由修饰酶进行骨架修饰。此外,真菌(子囊菌门和担子菌门)是发现萜类化合物的重要来源。随着测序技术和生物信息学方法的迅速发展,基因组挖掘已成为从真菌中发现新型萜类化合物的最有效策略之一。迄今为止,已鉴定出众多萜类环化酶,包括典型的I类和II类萜类环化酶以及新出现的UbiA类萜类环化酶,还有多种修饰酶,包括细胞色素P450酶、黄素依赖性单加氧酶和酰基转移酶。在本综述中,我们的目的是全面介绍截至2023年8月已鉴定出的所有真菌萜类环化酶,重点关注新发现的萜类环化酶,尤其是2015年至2023年8月新出现的UbiA类萜类环化酶及其相关修饰酶。