Modern Research Center for Traditional Chinese Medicine, the Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Shanxi University, Taiyuan, 030006, Shanxi, China.
BMC Plant Biol. 2022 Aug 23;22(1):410. doi: 10.1186/s12870-022-03769-5.
At present, Astragalus mongholicus products on the market represent two growth patterns: imitative wild A. mongholicus (WAM) and cultivated A. mongholicus (CAM). The 6-year-old WAM (A6) and 2-year-old CAM (B2) products are often sold as commodities. This study aimed to explore the effects of the abovementioned growth patterns on the biosynthetic mechanisms of isoflavone accumulation in A. mongholicus products.
In this paper, the content of calycosin-7-O-β-D-glucoside in 6-year-old WAM (A6) was significantly higher than that in 2-year-old CAM (B2) based on high-performance liquid chromatography. Tissue anatomy indicated that A6 has developed phloem fibers, thickened secondary walls, and a more well-developed vascular system than B2. Thirteen differentially accumulated metabolites were found in A6 and B2 by UHPLC-ESI-Q-TOF-MS/MS, of which isoflavones were highly and significantly enriched in A6. By combining transcriptomics and metabolomics analysis, we found that the metabolomics profile was the same as the transcriptomics profile in both A6 and B2. In total, 11 novel isoflavone-related genes were isolated using BLAST and functional annotation through RNA-Seq and Iso-Seq. The results of integrated analysis, Short Time-series Expression Miner analysis, and Pearson correlation analysis showed that the regulation of four key enzymes, cinnamate 4-hydroxylase, 6-deoxychalcone synthase, chalcone reductase, and chalcone isomerase, led to the high accumulation of isoflavones in A6. In addition, AmUFGT (c778119) and AmUCGT (c303354) were predicted to be 7-O-glycosyltransferases by phylogenetic analysis; these genes catalyze formononetin and calycosin, respectively.
The findings of this work will clarify the differences in the biosynthetic mechanism of isoflavone accumulation between A6 and B2, which will guide the cultivation of A. mongholicus.
目前市场上的蒙古黄芪产品代表了两种生长模式:模拟野生蒙古黄芪(WAM)和栽培蒙古黄芪(CAM)。6 年生的 WAM(A6)和 2 年生的 CAM(B2)产品常作为商品出售。本研究旨在探讨上述生长模式对蒙古黄芪产品中异黄酮积累的生物合成机制的影响。
本文采用高效液相色谱法,发现 6 年生 WAM(A6)中的毛蕊异黄酮-7-O-β-D-葡萄糖苷含量明显高于 2 年生 CAM(B2)。组织解剖表明,A6 比 B2 发育出韧皮纤维、加厚的次生壁和更发达的脉管系统。通过 UHPLC-ESI-Q-TOF-MS/MS 在 A6 和 B2 中发现了 13 种差异积累代谢物,其中异黄酮在 A6 中高度富集。通过转录组学和代谢组学分析相结合,我们发现 A6 和 B2 的代谢组学图谱与转录组学图谱相同。总共通过 BLAST 分离了 11 个新的异黄酮相关基因,并通过 RNA-Seq 和 Iso-Seq 进行功能注释。综合分析、短时间序列表达 Miner 分析和 Pearson 相关分析的结果表明,四个关键酶肉桂酸 4-羟化酶、6-去氧查尔酮合酶、查尔酮还原酶和查尔酮异构酶的调控导致 A6 中异黄酮的高积累。此外,AmUFGT(c778119)和 AmUCGT(c303354)通过系统发育分析预测为 7-O-糖基转移酶;这些基因分别催化芒柄花素和毛蕊异黄酮。
本工作的结果将阐明 A6 和 B2 中异黄酮积累的生物合成机制差异,这将指导蒙古黄芪的栽培。