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一种新型镰刀菌烷型二萜合酶及相关细胞色素P450酶的表征

Characterization of a new fusicoccane-type diterpene synthase and an associated P450 enzyme.

作者信息

Huang Jia-Hua, Lv Jian-Ming, Xiao Liang-Yan, Xu Qian, Lin Fu-Long, Wang Gao-Qian, Chen Guo-Dong, Qin Sheng-Ying, Hu Dan, Gao Hao

机构信息

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.

Clinical Experimental Center, First Affiliated Hospital of Jinan University, Guangzhou 510630, China.

出版信息

Beilstein J Org Chem. 2022 Oct 5;18:1396-1402. doi: 10.3762/bjoc.18.144. eCollection 2022.

Abstract

Fusicoccane-type terpenoids are a subgroup of diterpenoids featured with a unique 5-8-5 ring system. They are widely distributed in nature and possess a variety of biological activities. Up to date, only five fusicoccane-type diterpene synthases have been identified. Here, we identify a two-gene biosynthetic gene cluster containing a new fusicoccane-type diterpene synthase gene and an associated cytochrome P450 gene from ATCC 26942. Heterologous expression reveals that TadA catalyzes the formation of a new fusicoccane-type diterpene talaro-7,13-diene. DO isotope labeling combined with site-directed mutagenesis indicates that TadA might employ a different C2,6 cyclization strategy from the known fusicoccane-type diterpene synthases, in which a neutral intermediate is firstly formed and then protonated by an environmental proton. In addition, we demonstrate that the associated cytochrome P450 enzyme TadB is able to catalyze multiple oxidation of talaro-7,13-diene to yield talaro-6,13-dien-5,8-dione.

摘要

壳梭孢烷型萜类化合物是二萜类化合物的一个亚群,具有独特的5-8-5环系。它们在自然界中广泛分布,并具有多种生物活性。截至目前,仅鉴定出5种壳梭孢烷型二萜合酶。在此,我们从ATCC 26942中鉴定出一个包含新的壳梭孢烷型二萜合酶基因和一个相关细胞色素P450基因的双基因生物合成基因簇。异源表达表明,TadA催化形成一种新的壳梭孢烷型二萜塔拉罗-7,13-二烯。氘代同位素标记结合定点诱变表明,TadA可能采用与已知壳梭孢烷型二萜合酶不同的C2,6环化策略,即首先形成一个中性中间体,然后由环境质子进行质子化。此外,我们证明相关的细胞色素P450酶TadB能够催化塔拉罗-7,13-二烯的多次氧化,生成塔拉罗-6,13-二烯-5,8-二酮。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2721/9551204/8e25fa302c89/Beilstein_J_Org_Chem-18-1396-g002.jpg

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