Li Yuanjun, Chen Fangfang, Li Zhenqiu, Li Changfu, Zhang Yansheng
CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, The Chinese Academy of Science, Wuhan 430074, China University of Chinese Academy of Sciences, Beijing 100049, China.
CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, The Chinese Academy of Science, Wuhan 430074, China.
Plant Cell Physiol. 2016 Mar;57(3):630-41. doi: 10.1093/pcp/pcw019. Epub 2016 Feb 8.
Xanthium strumarium synthesizes various pharmacologically active sesquiterpenes. The molecular characterization of sesquiterpene biosynthesis in X. strumarium has not been reported so far. In this study, the cDNAs coding for three sesquiterpene synthases (designated as XsTPS1, XsTPS2 and XsTPS3) were isolated using the X. strumarium transcriptome that we recently constructed. XsTPS1, XsTPS2 and XsTPS3 were revealed to have primary activities forming germacrene D, guaia-4,6-diene and germacrene A, respectively, by either ectopic expression in yeast cells or purified recombinant protein-based in vitro assays. Quantitative real-time PCRs and metabolite analysis for the different plant parts showed that the transcript abundance of XsTPS1-XsTPS3 is consistent with the accumulation pattern of their enzymatic products, supporting their biochemical functions in vivo. In particular, we discovered that none of the XsTPS2 product, guaia-4,6-diene, can be detected in one of the X. strumarium cultivars used in this study (it was named the Hubei-cultivar), in which a natural deletion of two A bases in the XsTPS2 cDNA disrupts its activity, which further confirmed the proposed biochemical role of XsTPS2 in X. strumarium in vivo.
苍耳合成多种具有药理活性的倍半萜。迄今为止,尚未见关于苍耳中倍半萜生物合成的分子特征的报道。在本研究中,利用我们最近构建的苍耳转录组,分离出编码三种倍半萜合酶(命名为XsTPS1、XsTPS2和XsTPS3)的cDNA。通过在酵母细胞中的异位表达或基于纯化重组蛋白的体外测定,发现XsTPS1、XsTPS2和XsTPS3分别具有形成杜松烯D、愈创木-4,6-二烯和杜松烯A的主要活性。对不同植物部位进行的定量实时PCR和代谢物分析表明,XsTPS1-XsTPS3的转录丰度与其酶产物的积累模式一致,支持它们在体内的生化功能。特别是,我们发现在本研究中使用的一个苍耳栽培品种(命名为湖北品种)中检测不到XsTPS2的产物愈创木-4,6-二烯,该品种中XsTPS2 cDNA天然缺失两个A碱基,破坏了其活性,这进一步证实了XsTPS2在苍耳体内的拟生化作用。