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燕麦中环氧化脂肪酸生物合成中涉及的过氧物酶途径。

A peroxygenase pathway involved in the biosynthesis of epoxy fatty acids in oat.

机构信息

Department of Food and Bioproduct Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5A8.

出版信息

Plant Physiol. 2011 Sep;157(1):454-63. doi: 10.1104/pp.111.178822. Epub 2011 Jul 22.

Abstract

While oat (Avena sativa) has long been known to produce epoxy fatty acids in seeds, synthesized by a peroxygenase pathway, the gene encoding the peroxygenase remains to be determined. Here we report identification of a peroxygenase cDNA AsPXG1 from developing seeds of oat. AsPXG1 is a small protein with 249 amino acids in length and contains conserved heme-binding residues and a calcium-binding motif. When expressed in Pichia pastoris and Escherichia coli, AsPXG1 catalyzes the strictly hydroperoxide-dependent epoxidation of unsaturated fatty acids. It prefers hydroperoxy-trienoic acids over hydroperoxy-dienoic acids as oxygen donors to oxidize a wide range of unsaturated fatty acids with cis double bonds. Oleic acid is the most preferred substrate. The acyl carrier substrate specificity assay showed phospholipid and acyl-CoA were not effective substrate forms for AsPXG1 and it could only use free fatty acid or fatty acid methyl esters as substrates. A second gene, AsLOX2, cloned from oat codes for a 9-lipoxygenase catalyzing the synthesis of 9-hydroperoxy-dienoic and 9-hydroperoxy-trienoic acids, respectively, when linoleic (18:2-9c,12c) and linolenic (18:3-9c,12c,15c) acids were used as substrates. The peroxygenase pathway was reconstituted in vitro using a mixture of AsPXG1 and AsLOX2 extracts from E. coli. Incubation of methyl oleate and linoleic acid or linolenic acid with the enzyme mixture produced methyl 9,10-epoxy stearate. Incubation of linoleic acid alone with a mixture of AsPXG1 and AsLOX2 produced two major epoxy fatty acids, 9,10-epoxy-12-cis-octadecenoic acid and 12,13-epoxy-9-cis-octadecenoic acid, and a minor epoxy fatty acid, probably 12,13-epoxy-9-hydroxy-10-transoctadecenoic acid. AsPXG1 predominately catalyzes intermolecular peroxygenation.

摘要

虽然燕麦(Avena sativa)长期以来一直被认为能在种子中产生环氧脂肪酸,这些脂肪酸由过氧化物酶途径合成,但编码过氧化物酶的基因尚未确定。在这里,我们报告了从小麦种子中鉴定出一种过氧化物酶 cDNA AsPXG1。AsPXG1 是一种长度为 249 个氨基酸的小蛋白,含有保守的血红素结合残基和钙结合基序。当在巴斯德毕赤酵母和大肠杆菌中表达时,AsPXG1 催化不饱和脂肪酸的严格依赖于氢过氧化物的环氧化作用。它更喜欢氢过氧三烯酸而不是氢过氧二烯酸作为氧供体,以氧化具有顺式双键的广泛的不饱和脂肪酸。油酸是最优选的底物。酰基载体底物特异性测定表明,磷脂和酰基辅酶 A 不是 AsPXG1 的有效底物形式,它只能使用游离脂肪酸或脂肪酸甲酯作为底物。从小麦克隆的第二个基因 AsLOX2 编码一种 9-脂氧合酶,当使用亚油酸(18:2-9c,12c)和亚麻酸(18:3-9c,12c,15c)作为底物时,分别催化 9-氢过氧二烯酸和 9-氢过氧三烯酸的合成。在体外使用大肠杆菌的 AsPXG1 和 AsLOX2 提取物的混合物重建了过氧化物酶途径。用酶混合物孵育甲基油酸和亚油酸或亚麻酸生成甲基 9,10-环氧硬脂酸。单独用亚油酸与 AsPXG1 和 AsLOX2 的混合物孵育产生两种主要的环氧脂肪酸,9,10-环氧-12-顺-十八烯酸和 12,13-环氧-9-顺-十八烯酸,以及一种次要的环氧脂肪酸,可能是 12,13-环氧-9-羟基-10-反-十八烯酸。AsPXG1 主要催化分子间过氧反应。

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