Department of Food and Bioproduct Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5A8.
Plant Physiol. 2011 Sep;157(1):454-63. doi: 10.1104/pp.111.178822. Epub 2011 Jul 22.
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.
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。