Hagmann M L, Heller W, Grisebach H
Eur J Biochem. 1984 Jul 2;142(1):127-31. doi: 10.1111/j.1432-1033.1984.tb08259.x.
A microsomal preparation from elicitor-challenged soybean cell suspension cultures catalyzes an NADPH-dependent and dioxygen-dependent 6a-hydroxylation of 3,9-dihydroxypterocarpan to 3,6a,9-trihydroxypterocarpan. The latter is a precursor for the soybean phytoalexin glyceollin. No reaction is observed with NADH. The 6a-hydroxylase is inhibited by cytochrome c. Optical rotatory dispersion spectra of the enzymatic product formed from racemic dihydroxypterocarpan and of the remaining unreacted substrate proved that the product has the natural (6aS, 11aS)-configuration and that hydroxylation proceeds with retention of configuration. The 6a-hydroxylase was also found in elicitor-challenged soybean seedlings. The results indicate that the 6a-hydroxylase is specifically involved in the biosynthesis of glyceollin.
来自激发子刺激的大豆细胞悬浮培养物的微粒体制剂催化3,9 - 二羟基紫檀素依赖NADPH和双加氧的6a - 羟基化反应生成3,6a,9 - 三羟基紫檀素。后者是大豆植保素黄豆苷元的前体。用NADH未观察到反应。6a - 羟化酶被细胞色素c抑制。由外消旋二羟基紫檀素形成的酶促产物和剩余未反应底物的旋光色散光谱证明产物具有天然的(6aS, 11aS) - 构型,并且羟基化反应构型保持不变。在激发子刺激的大豆幼苗中也发现了6a - 羟化酶。结果表明6a - 羟化酶特别参与了黄豆苷元的生物合成。