State Key Laboratory of Conservation and Utilization of Bio-resources in Yunnan, The Key Laboratory of Medicinal Plant Biology of Yunnan Province, National and Local Joint Engineering Research Center on Germplasms Innovation and Utilization of Chinese Medicinal Materials in Southwest China, Yunnan Agricultural University, Kunming, 650201, China.
College of Food Science and Technology, Yunnan Agricultural University, Kunming, 650201, China.
Planta. 2019 Feb;249(2):393-406. doi: 10.1007/s00425-018-2995-6. Epub 2018 Sep 15.
Oleanolic acid glucuronosyltransferase (OAGT) genes synthesizing the direct precursor of oleanane-type ginsenosides were discovered. The four recombinant proteins of OAGT were able to transfer glucuronic acid at C-3 of oleanolic acid that yields oleanolic acid 3-O-β-glucuronide. Ginsenosides are the primary active components in the genus Panax, and great efforts have been made to elucidate the mechanisms underlying dammarane-type ginsenoside biosynthesis. However, there is limited information on oleanane-type ginsenosides. Here, high-performance liquid chromatography analysis demonstrated that oleanane-type ginsenosides (particularly ginsenoside Ro and chikusetsusaponin IV and IVa) are the abundant ginsenosides in Panax zingiberensis, an extremely endangered Panax species in southwest China. These ginsenosides are derived from oleanolic acid 3-O-β-glucuronide, which may be formed from oleanolic acid catalyzed by an unknown oleanolic acid glucuronosyltransferase (OAGT). Transcriptomic analysis of leaves, stems, main roots, and fibrous roots of P. zingiberensis was performed, and a total of 46,098 unigenes were obtained, including all the identified homologous genes involved in ginsenoside biosynthesis. The most upstream genes were highly expressed in the leaves, and the UDP-glucosyltransferase genes were highly expressed in the roots. This finding indicated that the precursors of ginsenosides are mainly synthesized in the leaves and transported to different parts for the formation of particular ginsenosides. For the first time, enzyme activity assay characterized four genes (three from P. zingiberensis and one from P. japonicus var. major, another Panax species with oleanane-type ginsenosides) encoding OAGT, which particularly transfer glucuronic acid at C-3 of oleanolic acid to form oleanolic acid 3-O-β-glucuronide. Taken together, our study provides valuable genetic information for P. zingiberensis and the genes responsible for synthesizing the direct precursor of oleanane-type ginsenosides.
发现了合成齐墩果酸型人参皂苷直接前体的齐墩果酸葡萄糖醛酸基转移酶 (OAGT) 基因。四种重组 OAGT 蛋白能够将葡萄糖醛酸转移到齐墩果酸的 C-3 位,生成齐墩果酸 3-O-β-葡萄糖醛酸。人参皂苷是人参属的主要活性成分,人们已经做出了巨大的努力来阐明达玛烷型人参皂苷生物合成的机制。然而,关于齐墩果酸型人参皂苷的信息有限。在这里,高效液相色谱分析表明,齐墩果酸型人参皂苷(特别是人参皂苷 Ro 和柴胡皂苷 IV 和 IVa)是中国西南地区极度濒危的人参属植物姜状三七中的丰富人参皂苷。这些人参皂苷来源于齐墩果酸 3-O-β-葡萄糖醛酸,可能是由未知的齐墩果酸葡萄糖醛酸基转移酶 (OAGT) 催化齐墩果酸形成的。对姜状三七的叶、茎、主根和须根进行了转录组分析,共获得 46098 个基因,其中包括所有鉴定的与人参皂苷生物合成相关的同源基因。最上游基因在叶片中高表达,UDP-葡萄糖基转移酶基因在根部高表达。这一发现表明,人参皂苷的前体主要在叶片中合成,并运输到不同部位形成特定的人参皂苷。首次通过酶活性测定鉴定了四个基因(三个来自姜状三七,一个来自另一种具有齐墩果酸型人参皂苷的人参属植物——日本三叶参)编码 OAGT,这些基因特别将葡萄糖醛酸转移到齐墩果酸的 C-3 位,形成齐墩果酸 3-O-β-葡萄糖醛酸。总之,我们的研究为姜状三七提供了有价值的遗传信息,以及负责合成齐墩果酸型人参皂苷直接前体的基因。