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大豆植保素黄豆抗毒素生物合成中催化关键异戊烯基化步骤的紫檀素4-二甲基烯丙基转移酶cDNA的分子克隆与特性分析

Molecular cloning and characterization of a cDNA for pterocarpan 4-dimethylallyltransferase catalyzing the key prenylation step in the biosynthesis of glyceollin, a soybean phytoalexin.

作者信息

Akashi Tomoyoshi, Sasaki Kanako, Aoki Toshio, Ayabe Shin-ichi, Yazaki Kazufumi

机构信息

Department of Applied Biological Sciences, Nihon University, Fujisawa, Kanagawa 252-8501, Japan.

出版信息

Plant Physiol. 2009 Feb;149(2):683-93. doi: 10.1104/pp.108.123679. Epub 2008 Dec 17.

Abstract

Glyceollins are soybean (Glycine max) phytoalexins possessing pterocarpanoid skeletons with cyclic ether decoration originating from a C5 prenyl moiety. Enzymes involved in glyceollin biosynthesis have been thoroughly characterized during the early era of modern plant biochemistry, and many genes encoding enzymes of isoflavonoid biosynthesis have been cloned, but some genes for later biosynthetic steps are still unidentified. In particular, the prenyltransferase responsible for the addition of the dimethylallyl chain to pterocarpan has drawn a large amount of attention from many researchers due to the crucial coupling process of the polyphenol core and isoprenoid moiety. This study narrowed down the candidate genes to three soybean expressed sequence tag sequences homologous to genes encoding homogentisate phytyltransferase of the tocopherol biosynthetic pathway and identified among them a cDNA encoding dimethylallyl diphosphate: (6aS, 11aS)-3,9,6a-trihydroxypterocarpan [(-)-glycinol] 4-dimethylallyltransferase (G4DT) yielding the direct precursor of glyceollin I. The full-length cDNA encoding a protein led by a plastid targeting signal sequence was isolated from young soybean seedlings, and the catalytic function of the gene product was verified using recombinant yeast microsomes. Expression of the G4DT gene was strongly up-regulated in 5 to 24 h after elicitation of phytoalexin biosynthesis in cultured soybean cells similarly to genes associated with isoflavonoid pathway. The prenyl part of glyceollin I was demonstrated to originate from the methylerythritol pathway by a tracer experiment using [1-(13)C]Glc and nuclear magnetic resonance measurement, which coincided with the presumed plastid localization of G4DT. The first identification of a pterocarpan-specific prenyltransferase provides new insights into plant secondary metabolism and in particular those reactions involved in the disease resistance mechanism of soybean as the penultimate gene of glyceollin biosynthesis.

摘要

大豆抗毒素是大豆(Glycine max)的植保素,具有紫檀烷类骨架,并带有源自C5异戊烯基部分的环状醚修饰。在现代植物生物化学的早期,参与大豆抗毒素生物合成的酶已得到充分表征,许多编码异黄酮生物合成酶的基因已被克隆,但一些后期生物合成步骤的基因仍未确定。特别是,负责将二甲基烯丙基链添加到紫檀烷上的异戊烯基转移酶,由于多酚核心和类异戊二烯部分的关键偶联过程,引起了许多研究人员的大量关注。本研究将候选基因范围缩小至三个与生育酚生物合成途径中编码尿黑酸植基转移酶的基因同源的大豆表达序列标签序列,并在其中鉴定出一个编码二甲基烯丙基二磷酸:(6aS, 11aS)-3,9,6a-三羟基紫檀烷[(-)-大豆醇] 4-二甲基烯丙基转移酶(G4DT)的cDNA,该酶产生大豆抗毒素I的直接前体。从年轻大豆幼苗中分离出编码由质体靶向信号序列引导的蛋白质的全长cDNA,并使用重组酵母微粒体验证了该基因产物的催化功能。与异黄酮途径相关的基因类似,在培养的大豆细胞中诱导植保素生物合成后的5至24小时内,G4DT基因的表达强烈上调。通过使用[1-(13)C]葡萄糖的示踪实验和核磁共振测量,证明大豆抗毒素I的异戊烯基部分源自甲基赤藓糖醇途径,这与G4DT假定的质体定位一致。首次鉴定出紫檀烷特异性异戊烯基转移酶,为植物次生代谢,特别是大豆抗病机制中涉及的那些反应,提供了新的见解,因为它是大豆抗毒素生物合成的倒数第二个基因。

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