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利用玉米脂氧合酶制备亚油酸和亚麻酸9(S)-氢过氧化物的方法。

Method to produce 9(S)-hydroperoxides of linoleic and linolenic acids by maize lipoxygenase.

作者信息

Gardner H W, Grove M J

机构信息

Mycotoxin Research, NCAUR, ARS, USDA, Peoria, Illinois 61604, USA.

出版信息

Lipids. 2001 May;36(5):529-33. doi: 10.1007/s11745-001-0753-1.

DOI:10.1007/s11745-001-0753-1
PMID:11432467
Abstract

Seed from maize (corn) Zea mays provides a ready source of 9-lipoxygenase that oxidizes linoleic acid and linolenic acid into 9(S)-hydroperoxy-10(E),12(Z)-octadecadienoic acid and 9(S)-hydroperoxy-10(E),12(Z),15(Z)-octadecatrienoic acid, respectively. Corn seed has a very active hydroperoxide-decomposing enzyme, allene oxide synthase (AOS), which must be removed prior to oxidizing the fatty acid. A simple pH 4.5 treatment followed by centrifugation removes most of the AOS activity. Subsequent purification by ammonium sulfate fractional precipitation results in negligible improvement in 9-hydroperoxide formation. This facile alternative method of preparing 9-hydroperoxides has advantages over other commonly used plant lipoxygenases.

摘要

玉米(Zea mays)种子是9-脂氧合酶的现成来源,该酶可将亚油酸和亚麻酸分别氧化为9(S)-氢过氧-10(E),12(Z)-十八碳二烯酸和9(S)-氢过氧-10(E),12(Z),15(Z)-十八碳三烯酸。玉米种子具有一种非常活跃的氢过氧化物分解酶——丙二烯氧化物合酶(AOS),在氧化脂肪酸之前必须将其去除。简单的pH 4.5处理后再进行离心,可去除大部分AOS活性。随后通过硫酸铵分级沉淀进行纯化,9-氢过氧化物的生成量几乎没有改善。这种制备9-氢过氧化物的简便替代方法比其他常用的植物脂氧合酶具有优势。

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本文引用的文献

1
Product specificity of rice germ lipoxygenase.水稻胚芽脂氧合酶的产物特异性
Lipids. 1980 Jan;15(1):1-5. doi: 10.1007/BF02534108.
2
Sequential enzymes of linoleic acid oxidation in corn germ: lipoxygenase and linoleate hydroperoxide isomerase.玉米胚芽中亚油酸氧化的顺序酶:脂氧合酶和亚油酸氢过氧化物异构酶。
J Lipid Res. 1970 Jul;11(4):311-21.
3
Steric analysis of hydroperoxides formed by lipoxygenase oxygenation of linoleic acid.对由脂氧合酶催化亚油酸氧化形成的氢过氧化物的空间分析。
Anal Biochem. 1971 Oct;43(2):515-26. doi: 10.1016/0003-2697(71)90282-x.
4
Positional specificity of corn germ lipoxygenase as a function of pH.玉米胚芽脂氧合酶的位置特异性与pH的关系
Biochem Biophys Res Commun. 1972 Apr 14;47(1):22-6. doi: 10.1016/s0006-291x(72)80004-4.
5
Lipoxygenase from potato tubers. Partial purification and properties of an enzyme that specifically oxygenates the 9-position of linoleic acid.来自马铃薯块茎的脂氧合酶。一种特异性氧化亚油酸9位的酶的部分纯化及性质
Biochem J. 1971 Sep;124(2):431-8. doi: 10.1042/bj1240431.
6
The enzymic conversion of linoleic acid into 9-(nona-1',3'-dienoxy)non-8-enoic acid, a novel unsaturated ether derivative isolated from homogenates of Solanum tuberosum tubers.亚油酸向9-(壬-1',3'-二烯氧基)壬-8-烯酸的酶促转化,9-(壬-1',3'-二烯氧基)壬-8-烯酸是一种从马铃薯块茎匀浆中分离出的新型不饱和醚衍生物。
Biochem J. 1972 Sep;129(3):743-53. doi: 10.1042/bj1290743.
7
Specificity of lipoxygenases. Separation of isomeric hydroperoxides by high performance liquid chromatography.
Biochim Biophys Acta. 1975 Jan 24;380(1):141-4.
8
A simple method for the preparation of pure 9-D-hydroperoxide of linoleic acid and methyl linoleate based on the positional specificity of lipoxygenase in tomato fruit.基于番茄果实中脂氧合酶的位置特异性,一种制备纯亚油酸9-D-氢过氧化物和亚油酸甲酯的简单方法。
Lipids. 1977 Mar;12(3):324-6. doi: 10.1007/BF02533358.
9
Enzymic reactions of fatty acid hydroperoxides in extracts of potato tuber. II. Conversion of 9- and 13-hydroperoxy-octadecadienoic acids to monohydroxydienoic acid, epoxyhydroxy- and trihydroxymonoenoic acid derivatives.
Biochim Biophys Acta. 1975 Nov 21;409(2):157-71. doi: 10.1016/0005-2760(75)90151-4.