Morihara K
Department of Enzymology, University of East Asia, Yamaguchi, Japan.
J Mol Recognit. 1990 Oct-Dec;3(5-6):181-6. doi: 10.1002/jmr.300030502.
Peptide bond formation can be enzymatically catalysed by the reverse reaction of proteases. Application is seen in the industrial production of human insulin. Human insulin derivative can be enzymatically prepared using either porcine insulin or the single chain B(1-29)-A(1-21) insulin precursor as the starting material. This is accomplished by either (1) digesting the starting material at Lys29 with Achromobacter lyticus protease I (Ach) and then coupling with Thr-X (X = blocking residue) (two-step reaction) or (2) subjecting Ala-B30 of porcine insulin or Gly-A1 of the single chain insulin precursor to transpeptidation with Thr-X (one-step reaction). Trypsin and Ach can be used for either type of reaction and, in the immobilized form, for the two-step reaction. Since the single chain insulin precursor can be produced by gene technology (yeast), use of immobilized trypsin or Ach and the two-step reaction using the single chain insulin precursor as the starting material ensures the continuous production of human insulin making it a feasible method for industrial manufacture.
肽键形成可通过蛋白酶的逆反应进行酶催化。其应用见于人胰岛素的工业生产。人胰岛素衍生物可使用猪胰岛素或单链B(1 - 29)-A(1 - 21)胰岛素前体作为起始原料通过酶法制备。这可通过以下两种方式实现:(1) 用溶杆菌属无色杆菌蛋白酶I(Achromobacter lyticus protease I,Ach)在Lys29处消化起始原料,然后与Thr-X(X = 封闭残基)偶联(两步反应);或(2) 使猪胰岛素的Ala-B30或单链胰岛素前体的Gly-A1与Thr-X进行转肽反应(一步反应)。胰蛋白酶和Ach可用于任何一种反应类型,并且以固定化形式用于两步反应。由于单链胰岛素前体可通过基因技术(酵母)生产,使用固定化胰蛋白酶或Ach以及以单链胰岛素前体作为起始原料的两步反应可确保人胰岛素的连续生产,使其成为工业制造的可行方法。