College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, 08826, Republic of Korea.
Department of Plant Science, Plant Genomics and Breeding Institute, Research Institute of Agriculture and Life Sciences, College of Agriculture and Life Sciences, Seoul National University, Seoul, 08826, Republic of Korea.
Sci Rep. 2018 Aug 6;8(1):11744. doi: 10.1038/s41598-018-30262-7.
Ginsenosides are dammarane-type or triterpenoidal saponins that contribute to the various pharmacological activities of the medicinal herb Panax ginseng. The putative biosynthetic pathway for ginsenoside biosynthesis is known in P. ginseng, as are some of the transcripts and enzyme-encoding genes. However, few genes related to the UDP-glycosyltransferases (UGTs), enzymes that mediate glycosylation processes in final saponin biosynthesis, have been identified. Here, we generated three replicated Illumina RNA-Seq datasets from the adventitious roots of P. ginseng cultivar Cheongsun (CS) after 0, 12, 24, and 48 h of treatment with methyl jasmonate (MeJA). Using the same CS cultivar, metabolomic data were also generated at 0 h and every 12-24 h thereafter until 120 h of MeJA treatment. Differential gene expression, phylogenetic analysis, and metabolic profiling were used to identify candidate UGTs. Eleven candidate UGTs likely to be involved in ginsenoside glycosylation were identified. Eight of these were considered novel UGTs, newly identified in this study, and three were matched to previously characterized UGTs in P. ginseng. Phylogenetic analysis further asserted their association with ginsenoside biosynthesis. Additionally, metabolomic analysis revealed that the newly identified UGTs might be involved in the elongation of glycosyl chains of ginsenosides, especially of protopanaxadiol (PPD)-type ginsenosides.
人参中的三萜皂苷类化合物(ginsenosides)主要为达玛烷型或齐墩果烷型,这是其发挥各种药理活性的物质基础。人参中已鉴定出一些与糖基化过程相关的 UGT 基因,但关于人参皂苷生物合成的假定生物合成途径及其相关的转录本和酶编码基因,目前还知之甚少。本研究以 12 年生的人参加工厂 Cheongsun(CS)的不定根为材料,在添加茉莉酸甲酯(MeJA)处理 0、12、24 和 48 h 后,生成了 3 个 Illumina RNA-Seq 数据集。采用相同的 CS 品种,在添加 MeJA 0 h 和之后每隔 12-24 h 生成代谢组学数据,直到添加 MeJA 120 h。通过差异基因表达分析、系统发育分析和代谢谱分析,鉴定候选 UGT 基因。鉴定到 11 个可能参与人参皂苷糖基化的候选 UGT。其中 8 个被认为是新的 UGT,本研究中首次发现,3 个与之前鉴定到的人参 UGT 同源。系统发育分析进一步证实了它们与人参皂苷生物合成的关系。此外,代谢组学分析表明,新鉴定的 UGT 可能参与了人参皂苷糖基链的延伸,特别是原人参二醇(PPD)型人参皂苷。