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马铃薯植株中水杨酸的生物合成

The biosynthesis of salicylic acid in potato plants.

作者信息

Coquoz JL, Buchala A, Metraux JP

机构信息

Departement de Biologie, Route Albert-Gockel 3, Universite de Fribourg, CH-1700 Fribourg, Switzerland.

出版信息

Plant Physiol. 1998 Jul;117(3):1095-101. doi: 10.1104/pp.117.3.1095.

Abstract

Spraying potato (Solanum tuberosum L.) leaves with arachidonic acid (AA) at 1500 &mgr;g mL-1 led to a rapid local synthesis of salicylic acid (SA) and accumulation of a SA conjugate, which was shown to be 2-O-beta-glucopyranosylsalicylic acid. Radiolabeling studies with untreated leaves showed that SA was synthesized from phenylalanine and that both cinnamic and benzoic acid were intermediates in the biosynthesis pathway. Using radiolabeled phenylalanine as a precursor, the specific activity of SA was found to be lower when leaves were treated with AA than in control leaves. Similar results were obtained when leaves were fed with the labeled putative intermediates cinnamic acid and benzoic acid. Application of 2-aminoindan-2-phosphonic acid at 40 &mgr;M, an inhibitor of phenylalanine ammonia-lyase, prior to treatment with AA inhibited the local accumulation of SA. When the putative intermediates were applied to leaves in the presence of 2-aminoindan-2-phosphonic acid, about 40% of the expected accumulation of free SA was recovered, but the amount of the conjugate remained constant.

摘要

用1500μg/mL的花生四烯酸(AA)喷洒马铃薯(Solanum tuberosum L.)叶片,导致水杨酸(SA)迅速在局部合成并积累一种SA共轭物,该共轭物被证明是2-O-β-吡喃葡萄糖基水杨酸。对未处理叶片的放射性标记研究表明,SA由苯丙氨酸合成,肉桂酸和苯甲酸都是生物合成途径中的中间体。以放射性标记的苯丙氨酸为前体,发现用AA处理叶片时SA的比活性低于对照叶片。当用标记的假定中间体肉桂酸和苯甲酸处理叶片时,也得到了类似的结果。在用AA处理之前,施加40μM的2-氨基茚-2-膦酸(一种苯丙氨酸解氨酶抑制剂)可抑制SA在局部的积累。当在2-氨基茚-2-膦酸存在的情况下将假定中间体施用于叶片时,回收了约40%预期积累的游离SA,但共轭物的量保持不变。

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