From the Department of Plant Biochemistry, Albrecht-von-Haller-Institute for Plant Sciences, University of Goettingen, Goettingen D-37077 and.
the Service Unit for Metabolomics and Lipidomics and.
J Biol Chem. 2019 Jun 21;294(25):9858-9872. doi: 10.1074/jbc.RA119.007600. Epub 2019 May 9.
Jasmonoyl-isoleucine (JA-Ile) is a phytohormone that orchestrates plant defenses in response to wounding, feeding insects, or necrotrophic pathogens. JA-Ile metabolism has been studied intensively, but its catabolism as a potentially important mechanism for the regulation of JA-Ile-mediated signaling is not well-understood. Especially the enzyme(s) responsible for specifically glycosylating 12-hydroxy-jasmonic acid (12-OH-JA) and thereby producing 12--glucopyranosyl-jasmonic acid (12--Glc-JA) is still elusive. Here, we used co-expression analyses of available transcriptomic data, identifying four UDP-dependent glycosyltransferase (UGT) genes as wound-induced and 12-OH-JA-related, namely, , , , and We heterologously expressed and purified the corresponding proteins to determine their individual substrate specificities and kinetic parameters. We then used an metabolite-fingerprinting approach to investigate these proteins in conditions as close as possible to their natural environment, with an emphasis on greatly extending the range of potential substrates. As expected, we found that UGT76E1 and UGT76E2 are 12-OH-JA-UGTs, with UGT76E1 contributing a major UGT activity, as deduced from mutants with abolished or increased gene expression. In contrast, recombinant UGT76E11 acted on an unidentified compound and also glycosylated two other oxylipins, 11-hydroxy-7,9,13-hexadecatrienoic acid (11-HHT) and 13-hydroxy-9,11,15-octadecatrienoic acid (13-HOT), which were also accepted by recombinant UGT76E1, UGT76E2, and UGT76E12 enzymes. UGT76E12 glycosylated 12-OH-JA only to a low extent, but also accepted an artificial hydroxylated fatty acid and low amounts of kaempferol. In conclusion, our findings have elucidated the missing step in the wound-induced synthesis of 12--glucopyranosyl-jasmonic acid in .
茉莉酰异亮氨酸(JA-Ile)是一种植物激素,它协调植物防御反应,以应对创伤、取食昆虫或坏死性病原体。JA-Ile 代谢已被深入研究,但作为 JA-Ile 介导的信号转导调控的潜在重要机制,其分解代谢尚未得到很好的理解。特别是负责特异性糖基化 12-羟基茉莉酸(12-OH-JA)并产生 12--葡糖苷基茉莉酸(12--Glc-JA)的酶(s)仍然难以捉摸。在这里,我们使用可用转录组数据的共表达分析,鉴定出四个 UDP 依赖性糖基转移酶(UGT)基因作为创伤诱导和 12-OH-JA 相关基因,即 、 、 、和 我们异源表达和纯化相应的蛋白质,以确定它们各自的底物特异性和动力学参数。然后,我们使用代谢物指纹图谱方法在尽可能接近其自然环境的条件下研究这些蛋白质,重点是极大地扩展潜在底物的范围。正如预期的那样,我们发现 UGT76E1 和 UGT76E2 是 12-OH-JA-UGTs,UGT76E1 贡献了主要的 UGT 活性,这是从表达或增加 基因的突变体推断出来的。相比之下,重组 UGT76E11 作用于一种未鉴定的化合物,还糖基化了另外两种氧脂素,11-羟基-7,9,13-十六碳三烯酸(11-HHT)和 13-羟基-9,11,15-十八碳三烯酸(13-HOT),这两种氧脂素也被重组 UGT76E1、UGT76E2 和 UGT76E12 酶接受。UGT76E12 仅低程度地糖基化 12-OH-JA,但也接受人工羟基化脂肪酸和少量山柰酚。总之,我们的研究结果阐明了 在创伤诱导的 12--葡糖苷基茉莉酸合成中缺失的步骤。