Control of oxygenation in lipoxygenase and cyclooxygenase catalysis

被引:244
作者
Schneider, Claus
Pratt, Derek A.
Porter, Ned A.
Brash, Alan R.
机构
[1] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA
[4] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
来源
CHEMISTRY & BIOLOGY | 2007年 / 14卷 / 05期
关键词
D O I
10.1016/j.chembiol.2007.04.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipoxygenases (LOX) and cyclooxygenases (COX) react an achiral polyunsaturated fatty acid with oxygen to form a chiral peroxide product of high regio- and stereochemical purity. Both enzymes employ free radical chemistry reminiscent of hydrocarbon autoxidation but execute efficient control during catalysis to form a specific product over the multitude of isomers found in the nonenzymatic reaction. Exactly how both dioxygenases achieve this positional and stereos control is far from clear. We present four mechanistic models, not mutually exclusive, that could account for the specific reactions of molecular oxygen with a fatty acid in the LOX or COX active site.
引用
收藏
页码:473 / 488
页数:16
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