Murphy G, Lynen F
Eur J Biochem. 1975 Oct 15;58(2):467-75. doi: 10.1111/j.1432-1033.1975.tb02394.x.
The ring hydroxylation of m-hydroxybenzyl alcohol to gentisyl alcohol by a particulate preparation from Penicillium patulum has been characterised. The activity was shown to be closely associated with, but not necessarily identical to, m-cresol 2-hydroxylase activity of the 105 000 X g microsomal fraction. As with both the m-cresol hydroxylases of this system, m-hydroxybenzyl alcohol hydroxylase required oxygen and NADPH for activity. A Km value for m-hydroxybenzyl alcohol of 15 muM was measured. Inhibition of the hydroxylase activity and its reversal by light, as well as the action of cytochrome c, KCN and other effectors suggested a mixed-function oxidase reaction of the cytochrome P-450, NADPH-cytochrome reductase type. m-Hydroxybenzaldehyde was not ring hydroxylated by any preparation from P. patulum. Apart from the previously described conversion to m-hydroxybenzyl alcohol by a predominantly soluble dehydrogenase, m-hydroxybenzaldehyde was metabolized to m-hydroxybenzoic acid by a particulate fraction. This activity required NADPH. It was concluded that the main biosynthetic pathway to patulin must be through m-hydroxybenzyl alcohol, gentisyl alcohol and gentisaldehyde.
来自展青霉的微粒体制剂将间羟基苯甲醇环羟基化生成龙胆醇的过程已得到表征。该活性显示与105000×g微粒体部分的间甲酚2-羟化酶活性密切相关,但不一定相同。与该系统的两种间甲酚羟化酶一样,间羟基苯甲醇羟化酶的活性需要氧气和NADPH。测得间羟基苯甲醇的Km值为15μM。羟化酶活性的抑制及其光逆转作用,以及细胞色素c、KCN和其他效应物的作用表明这是一种细胞色素P-450、NADPH-细胞色素还原酶类型的混合功能氧化酶反应。展青霉的任何制剂都不能将间羟基苯甲醛环羟基化。除了先前描述的通过主要是可溶性脱氢酶转化为间羟基苯甲醇外,间羟基苯甲醛还通过微粒体部分代谢为间羟基苯甲酸。该活性需要NADPH。得出的结论是,棒曲霉素的主要生物合成途径必定是通过间羟基苯甲醇、龙胆醇和龙胆醛。