Functional identification of the terpene synthase family involved in diterpenoid alkaloids biosynthesis in Aconitum carmichaelii

被引:1
|
作者
Liuying Mao [1 ,2 ]
Baolong Jin [2 ]
Lingli Chen [2 ]
Mei Tian [2 ]
Rui Ma [2 ]
Biwei Yin [2 ]
Haiyan Zhang [2 ]
Juan Guob [1 ]
Jinfu Tang [2 ]
Tong Chen [2 ]
Changjiangsheng Lai [2 ]
Guanghong Cui [2 ]
Luqi Huang [1 ,2 ]
机构
[1] College of Pharmacy, Shandong University of Chinese Medicine
[2] State Key Laboratory of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences
基金
国家自然科学基金重大项目; 国家重点研发计划; 中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
R284 [中药化学];
学科分类号
摘要
Aconitum carmichaelii is a high-value medicinal herb widely used across China, Japan,and other Asian countries. Aconitine-type diterpene alkaloids(DAs) are the characteristic compounds in Aconitum. Although six transcriptomes, based on short-read next generation sequencing technology, have been reported from the Aconitum species, the terpene synthase(TPS) corresponding to DAs biosynthesis remains unidentified. We apply a combination of Pacbio isoform sequencing and RNA sequencing to provide a comprehensive view of the A. carmichaelii transcriptome. Nineteen TPSs and five alternative splicing isoforms belonging to TPS-b, TPS-c, and TPS-e/f subfamilies were identified. In vitro enzyme reaction analysis functional identified two sesqui-TPSs and twelve di TPSs.Seven of the TPS-c subfamily genes reacted with GGPP to produce the intermediate ent-copalyl diphosphate. Five Ac KSLs separately reacted with ent-CPP to produce ent-kaurene, ent-atiserene,and ent-13-epi-sandaracopimaradie: a new diterpene found in Aconitum. Ac TPSs gene expression in conjunction DAs content analysis in different tissues validated that ent-CPP is the sole precursor to all DAs biosynthesis, with Ac KSL1, Ac KSL2 s and Ac KSL3-1 responsible for C20atisine and napelline type DAs biosynthesis, respectively. These data clarified the molecular basis for the C20-DAs biosynthetic pathway in A. carmichaelii and pave the way for further exploration of C19-DAs biosynthesis in the Aconitum species.
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收藏
页码:3310 / 3321
页数:12
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