柯铃钰, 陈姿伊, 丁文文, 张智新, 何平, 刘颖. 过表达LIS基因对甘草毛状根中甘草酸生物合成的调控研究J. 药学学报, 2022, 57(12): 3686-3694. DOI: 10.16438/j.0513-4870.2022-0666
引用本文: 柯铃钰, 陈姿伊, 丁文文, 张智新, 何平, 刘颖. 过表达LIS基因对甘草毛状根中甘草酸生物合成的调控研究J. 药学学报, 2022, 57(12): 3686-3694. DOI: 10.16438/j.0513-4870.2022-0666
KE Ling-yu, CHEN Zi-yi, DING Wen-wen, ZHANG Zhi-xin, HE Ping, LIU Ying. Overexpression of (3S)-linalool synthase gene (LIS) regulates the glycyrrhizic acid biosynthesis in Glycyrrhiza uralensis hairy rootsJ. Acta Pharmaceutica Sinica, 2022, 57(12): 3686-3694. DOI: 10.16438/j.0513-4870.2022-0666
Citation: KE Ling-yu, CHEN Zi-yi, DING Wen-wen, ZHANG Zhi-xin, HE Ping, LIU Ying. Overexpression of (3S)-linalool synthase gene (LIS) regulates the glycyrrhizic acid biosynthesis in Glycyrrhiza uralensis hairy rootsJ. Acta Pharmaceutica Sinica, 2022, 57(12): 3686-3694. DOI: 10.16438/j.0513-4870.2022-0666

过表达LIS基因对甘草毛状根中甘草酸生物合成的调控研究

Overexpression of (3S)-linalool synthase gene (LIS) regulates the glycyrrhizic acid biosynthesis in Glycyrrhiza uralensis hairy roots

  • 摘要: 芳樟醇合酶(3S)-linalool synthase, LIS 是单萜合成途径上的关键酶。本课题组前期在甘草转录组研究中发现LIS基因与甘草酸(glycyrrhizic acid, GA) 的生物合成密切相关, 因此本研究拟利用甘草毛状根培养体系, 进一步解析LIS对甘草酸生物合成的调控作用。本研究克隆了甘草LIS基因(GenBank注册号: MZ169552); 采用基因融合法构建过表达LIS基因的植物双元表达载体pCA-LIS; 利用发根农杆菌(Agrobacterium rhizogenes ATCC15834) 介导法诱导甘草毛状根系; 通过实时荧光定量PCR (RT-qPCR) 进行LIS基因的表达水平分析; 最终采用UPLC法测定各甘草毛状根系中的甘草酸含量。结果显示, 过表达LIS基因的甘草毛状根系中, LIS基因的表达水平显著高于野生型, 而甘草酸含量则显著低于野生型和阴性对照组, 表明LIS基因的表达水平与甘草酸含量呈负相关。本研究首次克隆得到甘草LIS基因, 通过反向遗传学策略证实了LIS基因对甘草酸生物合成的负调控作用, 为进一步完善甘草酸生物合成的分子调控网络提供了依据。

     

    Abstract: (3S)-Linalool synthase (LIS) is a key enzyme involved in the monoterpene biosynthetic pathway. Based on our previous transcriptome study, the expression level of LIS gene was exceedingly related to glycyrrhizic acid (GA) biosynthesis. Therefore, we used hairy root culturing to further investigate the effect of LIS on the GA biosynthesis. A LIS gene (GenBank accession number: MZ169552) was cloned from Glycyrrhiza uralensis. The plant binary overexpression vector pCA-LIS was constructed by gene fusion. G. uralensis hairy roots overexpressing LIS were induced by the Agrobacterium rhizogenes ATCC15834. The expression levels of LIS were analyzed by real-time quantitative PCR (RT-qPCR) and the contents of GA in hairy root lines were determined by UPLC. It was found that in the hairy root lines overexpressing LIS, the expression levels of LIS were significantly higher than that in the wild type, while the contents of GA were remarkably lower than those in the wild type and negative control. These findings indicate that the expression level of LIS is negatively correlated with the accumulation of GA. In this study, LIS was cloned from G. uralensis for the first time and the negative regulatory effect of LIS on GA biosynthesis was confirmed by reverse genetics. This work provides support for further improvement of the molecular regulatory network of GA biosynthesis in G. uralensis.

     

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