Sada E, Katoh S, Kheirolomoom A
Department of Chemical Engineering, Kyoto University, Japan.
Appl Biochem Biotechnol. 1989 Dec;22(3):247-61. doi: 10.1007/BF02921760.
The reaction characteristics of prostaglandin E2 biosynthesis by PGH-synthase and PGE2 isomerase and the substrate dependency of this biosynthesis were studied. The activity of PG-synthases was blocked by the inhibitory action of one or more byproducts, probably resulting from the action of PGH-synthase. This inhibitory action then appeared to be partly reversible, indicating that the substrate and the inhibitor compete for the catalytic sites. According to these findings, the feasibility of a successful semibatch biosynthesis was investigated. A combination of the substrate concentration reducing procedure and the semibatch process resulted in an about 3.5-fold higher increase in the total amount of PGE2 formed in comparison with the batch results obtained at the substrate concentration of 1.0 mg/cm3. Since the cost of enzyme is a governing factor in this biosynthesis, development of semibatch biosynthesis of PGE2 becomes a matter of economic importance.
研究了PGH合酶和PGE2异构酶合成前列腺素E2的反应特性以及该生物合成的底物依赖性。PG合酶的活性被一种或多种副产物的抑制作用所阻断,这些副产物可能是PGH合酶作用产生的。然后这种抑制作用似乎部分是可逆的,这表明底物和抑制剂竞争催化位点。根据这些发现,研究了成功进行半间歇生物合成的可行性。底物浓度降低程序和半间歇过程相结合,与在底物浓度为1.0 mg/cm3时获得的批次结果相比,形成的PGE2总量增加了约3.5倍。由于酶的成本是这种生物合成中的一个关键因素,PGE2半间歇生物合成的开发具有重要的经济意义。