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    • 9. 发明公开
    • METHOD FOR PRODUCING ALPHA-L-ASPARTYL-L-PHENYLALANINE-BETA-ESTER AND METHOD FOR PRODUCING ALPHA-L-ASPARTYL-L-PHENYLALANINE-ALPHA-METHYL ESTER
    • 用于生产ALPHA-L-天冬氨酰-L-苯丙氨酸-β-酯及其制造方法ALPHA-L-天冬氨酰-L-苯丙氨酸-α-甲基酯
    • EP1587941A4
    • 2006-06-21
    • EP04704772
    • 2004-01-23
    • AJINOMOTO KK
    • YOKOZEKI KENZOOHNO AYAKOHARA SEIICHIABE ISAO
    • C12P21/02A23L27/30C07K5/072C07K5/075C12N9/48C12N15/57C12P21/06
    • C07K5/0613A23L27/32C07K5/06113C12P21/02C12P21/06
    • A method for producing an α-L-aspartyl-L-phenylalanine-β-ester (also named α-L-(β-o-substituted aspartyl)-L-phenylalanine), which is an intermediate of an α-L-aspartyl-L-phenylalanine-α-methyl ester (also named α-L-aspartyl-L-phenylalanine methyl ester; product name: aspartame), easily, at high yield and inexpensively without going through a complex synthesis method is provided. Further, an easy, inexpensive and high-yield production method for an α-L-aspartyl-L-phenylalanine-α-methyl ester is provided. α-L-aspartyl-L-phenylalanine-α-methyl ester is produced from a L-aspartic acid-α,β-diester and L-phenylalanine using an enzyme or enzyme-containing substance that has an ability to catalyze a reaction in which L-phenylalanine performs no nucleophilic attack on a β-ester site of L-aspartic acid-α,β-diester but performs a nucleophilic attack on an α-ester site thereof.
    • 一种用于在±L-天冬氨酰-L-苯丙氨酸-SQ-酯制备(即命名为±-L(²邻substituiertem天冬氨酰)-L-苯丙氨酸)的方法,所有这是在中间的在±L-天冬氨 -L-苯丙氨酸²甲酯(因而命名±-L天冬氨酰-L-苯丙氨酸甲基酯,商品名:阿司帕坦),容易地以高收率且廉价地,而无需通过复杂的合成方法要被提供。 此外,对于在±提供L-天冬氨-L-苯丙氨酸±甲酯一种简单,廉价且高收率的制造方法。 ±-L天冬氨酰基-L-苯丙氨酸甲基酯±从L-天冬氨酸 - ±²二酯和L-苯丙氨酸在使用酶或含酶物质已做了以催化在哪一个反应能力产生 L-苯丙氨酸执行对L-天冬氨酸 - ±,²二酯的²酯站点没有亲核攻击,但执行对在其±酯位点的亲核攻击。