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拟南芥中茉莉酸生物合成需要过氧化物酶体β-氧化酶——pex6和aim1特性的进一步证据

Jasmonate biosynthesis in Arabidopsis thaliana requires peroxisomal beta-oxidation enzymes--additional proof by properties of pex6 and aim1.

作者信息

Delker Carolin, Zolman Bethany K, Miersch Otto, Wasternack Claus

机构信息

Leibniz Institute of Plant Biochemistry, Department of Natural Product Biotechnology, Weinberg 3, D-06120 Halle/S., Germany.

出版信息

Phytochemistry. 2007 Jun;68(12):1642-50. doi: 10.1016/j.phytochem.2007.04.024. Epub 2007 Jun 4.

Abstract

Jasmonic acid (JA) is an important regulator of plant development and stress responses. Several enzymes involved in the biosynthesis of JA from alpha-linolenic acid have been characterized. The final biosynthesis steps are the beta-oxidation of 12-oxo-phytoenoic acid. We analyzed JA biosynthesis in the Arabidopsis mutants pex6, affected in peroxisome biogenesis, and aim1, disrupted in fatty acid beta-oxidation. Upon wounding, these mutants exhibit reduced JA levels compared to wild type. pex6 accumulated the precursor OPDA. Feeding experiments with deuterated OPDA substantiate this accumulation pattern, suggesting the mutants are impaired in the beta-oxidation of JA biosynthesis at different steps. Decreased expression of JA-responsive genes, such as VSP1, VSP2, AtJRG21 and LOX2, following wounding in the mutants compared to the wild type reflects the reduced JA levels of the mutants. By use of these additional mutants in combination with feeding experiments, the necessity of functional peroxisomes for JA-biosynthesis is confirmed. Furthermore an essential function of one of the two multifunctional proteins of fatty acid beta-oxidation (AIM1) for wound-induced JA formation is demonstrated for the first time. These data confirm that JA biosynthesis occurs via peroxisomal fatty acid beta-oxidation machinery.

摘要

茉莉酸(JA)是植物发育和应激反应的重要调节因子。几种参与从α-亚麻酸生物合成JA的酶已被鉴定。生物合成的最后步骤是12-氧代-植物二烯酸的β-氧化。我们分析了拟南芥突变体pex6(过氧化物酶体生物发生受影响)和aim1(脂肪酸β-氧化被破坏)中的JA生物合成。受伤后,与野生型相比,这些突变体的JA水平降低。pex6积累了前体OPDA。用氘代OPDA进行的饲喂实验证实了这种积累模式,表明突变体在JA生物合成的β-氧化不同步骤中受损。与野生型相比,突变体受伤后JA响应基因(如VSP1、VSP2、AtJRG21和LOX2)的表达降低,反映了突变体JA水平的降低。通过使用这些额外的突变体并结合饲喂实验,证实了功能性过氧化物酶体对JA生物合成的必要性。此外,首次证明了脂肪酸β-氧化的两种多功能蛋白之一(AIM1)对伤口诱导的JA形成具有重要作用。这些数据证实JA生物合成是通过过氧化物酶体脂肪酸β-氧化机制进行的。

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