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ENZYMATIC SYNTHESIS OF N-FORMYL-ALPHA-L-ASPARTYL-L-PHENYLALANINE METHYL ESTER

机译:酶法合成N-甲酰基-L-天冬氨酰-L-苯丙氨酸甲基酯

摘要

PROBLEM TO BE SOLVED: To efficiently obtain the subject compound useful for artificial sweetener, etc., by adding a water-immiscible solvent to an aqueous solution of a thermolysin-like metal protease and condensing a protected aspartic acid with a phenylalanine ester in an aqueous solution. ;SOLUTION: In this method for synthesizing N-formyl-α-L-aspartyl-L- phenylalanine methyl ester (F-APM) by an enzyme by a condensation reaction between N-formyl-L-aspartic acid and L-phenylalanine methyl ester or D,L- phenylalanine methyl ester, an organic phase comprising a water-immiscible solvent (e.g. tributyl phosphate) is supplied to an aqueous solution phase containing a thermolysin-like metal protease, the condensation reaction is advanced in the aqueous solution phase and the formed F-APM is transferred from the aqueous solution phase to the organic phase to efficiently give the objective compound useful as aspartame as an artificial sweetener having degree of sweetness of 200 times as much as sugar.;COPYRIGHT: (C)1998,JPO
机译:解决的问题:为了有效地获得用于人造甜味剂等的主题化合物,方法是将不与水混溶的溶剂添加到类似嗜热菌蛋白酶的金属蛋白酶的水溶液中,然后将受保护的天冬氨酸与苯丙氨酸酯在水溶液中缩合。解。 ;解决方案:该方法通过酶通过N-甲酰基-L-天冬氨酸和L-苯丙氨酸甲酯之间的缩合反应合成N-甲酰基-α-L-天冬氨酰-L-苯丙氨酸甲酯(F-APM)或D,L-苯丙氨酸甲酯,将包含与水不混溶的溶剂(例如磷酸三丁酯)的有机相供应到包含嗜热菌蛋白酶样金属蛋白酶的水溶液相中,在水溶液相中进行缩合反应,然后形成的F-APM从水溶液相转移到有机相,以有效地获得可用作甜味剂的阿斯巴甜的目标化合物,其甜度为糖的200倍。;版权所有:(C)1998,JPO

著录项

  • 公开/公告号JPH10174597A

    专利类型

  • 公开/公告日1998-06-30

    原文格式PDF

  • 申请/专利权人 TOSOH CORP;

    申请/专利号JP19970263482

  • 发明设计人 HIRATA AKIRA;

    申请日1997-09-29

  • 分类号C12P21/02;

  • 国家 JP

  • 入库时间 2022-08-22 03:04:43

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