Milborrow B V
School of Biochemistry and Molecular Genetics, The University of New South Wales, Sydney, NSW 2052, Australia.
J Exp Bot. 2001 Jun;52(359):1145-64.
The pathway of biosynthesis of abscisic acid (ABA) can be considered to comprise three stages: (i) early reactions in which small phosphorylated intermediates are assembled as precursors of (ii) intermediate reactions which begin with the formation of the uncyclized C40 carotenoid phytoene and end with the cleavage of 9'-cis-neoxanthin (iii) to form xanthoxal, the C15 skeleton of ABA. The final phase comprising C15 intermediates is not yet completely defined, but the evidence suggests that xanthoxal is first oxidized to xanthoxic acid by a molybdenum-containing aldehyde oxidase and this is defective in the aba3 mutant of Arabidopsis and present in a 1-fold acetone precipitate of bean leaf proteins. This oxidation precludes the involvement of AB-aldehyde as an intermediate. The oxidation of the 4'-hydroxyl group to the ketone and the isomerization of the 1',2'-epoxy group to the 1'-hydroxy-2'-ene may be brought about by one enzyme which is defective in the aba2 mutant and is present in the 3-fold acetone fraction of bean leaves. Isopentenyl diphosphate (IPP) is now known to be derived by the pyruvate-triose (Methyl Erythritol Phosphate, MEP) pathway in chloroplasts. (14C)IPP is incorporated into ABA by washed, intact chloroplasts of spinach leaves, but (14C)mevalonate is not, consequently, all three phases of biosynthesis of ABA occur within chloroplasts. The incorporation of labelled mevalonate into ABA by avocado fruit and orange peel is interpreted as uptake of IPP made in the cytoplasm, where it is the normal precursor of sterols, and incorporated into carotenoids after uptake by a carrier in the chloroplast envelope. An alternative bypass pathway becomes more important in aldehyde oxidase mutants, which may explain why so many wilty mutants have been found with this defect. The C-1 alcohol group is oxidized, possibly by a mono-oxygenase, to give the C-1 carboxyl of ABA. The 2-cis double bond of ABA is essential for its biological activity but it is not known how the relevant trans bond in neoxanthin is isomerized.
脱落酸(ABA)的生物合成途径可分为三个阶段:(i)早期反应,在此阶段,小分子磷酸化中间体被组装成(ii)中间反应的前体,该中间反应始于未环化的C40类胡萝卜素八氢番茄红素的形成,并以9'-顺式新黄质的裂解(iii)结束,形成黄氧醛,即ABA的C15骨架。包含C15中间体的最后阶段尚未完全明确,但有证据表明,黄氧醛首先被含钼的醛氧化酶氧化为黄氧酸,这在拟南芥的aba3突变体中存在缺陷,并且存在于豆叶蛋白的1倍丙酮沉淀物中。这种氧化排除了AB-醛作为中间体的参与。4'-羟基被氧化为酮以及1',2'-环氧基异构化为1'-羟基-2'-烯可能由一种酶完成,该酶在aba2突变体中存在缺陷,并且存在于豆叶的3倍丙酮级分中。现在已知异戊烯基二磷酸(IPP)是通过叶绿体中的丙酮酸-磷酸甘油醛(甲基赤藓糖醇磷酸,MEP)途径产生的。菠菜叶经洗涤的完整叶绿体将(14C)IPP掺入ABA中,但(14C)甲羟戊酸则不然,因此,ABA生物合成的所有三个阶段都发生在叶绿体内。鳄梨果实和橙皮将标记的甲羟戊酸掺入ABA中,这被解释为细胞质中产生的IPP的摄取,在细胞质中IPP是甾醇的正常前体,并在被叶绿体包膜中的载体摄取后掺入类胡萝卜素中。在醛氧化酶突变体中,一条替代的旁路途径变得更加重要,这可能解释了为什么发现了如此多具有这种缺陷的萎蔫突变体。C-1醇基可能被单加氧酶氧化,生成ABA 的C-1羧基。ABA的2-顺式双键对其生物活性至关重要,但尚不清楚新黄质中相关的反式键是如何异构化的。