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PROTEINS HAVING IMIDAZOLE DIPEPTIDE SYNTHESIS ACTIVITY AND IMIDAZOLE DIPEPTIDE PRODUCTION METHOD

机译:具有咪唑二肽合成活性的蛋白质和咪唑二肽的生产方法

摘要

PROBLEM TO BE SOLVED: To address the problem of simply providing a low cost imidazole dipeptide, to thereby provide proteins that produce imidazole dipeptides with high efficiency such as carnosine, anserine and balenine, and a production method using same.;SOLUTION: A modified protein comprises an L-amino acid α-ligase illustrated by sequence number 1 in which at least 1-3 amino acid residues of an amino acid sequence of YwfE are substituted wherein the asparagine (N) residue at position 108 from the N terminal is substituted for an alanine (A) residue, glutamic acid (E) residue or glutamine (Q) residue, or additionally, the isoleucine (I) residue at position 112 is substituted for a valine (V) residue, and/or the histidine (H) residue at position 378 is substituted for a lysine (K) residue or an arginine (R) residue.;SELECTED DRAWING: Figure 1;COPYRIGHT: (C)2018,JPO&INPIT
机译:解决的问题:为了解决简单地提供低成本的咪唑二肽的问题,从而提供能高效产生咪唑二肽的蛋白质,例如肌肽,反肌氨酸和苯丙氨酸,以及使用该蛋白质的生产方法。包含由序列号1所示的L-氨基酸α-连接酶,其中YwfE的氨基酸序列的至少1-3个氨基酸残基被取代,其中从N末端起的位置108的天冬酰胺(N)残基被取代为丙氨酸(A)残基,谷氨酸(E)残基或谷氨酰胺(Q)残基,或另外,位置112处的异亮氨酸(I)残基取代缬氨酸(V)残基和/或组氨酸(H) 378位残基被赖氨酸(K)残基或精氨酸(R)残基取代;选图:图1;版权:(C)2018,JPO&INPIT

著录项

  • 公开/公告号JP2018102287A

    专利类型

  • 公开/公告日2018-07-05

    原文格式PDF

  • 申请/专利权人 TOKAI BUSSAN KK;

    申请/专利号JP20170165715

  • 发明设计人 KINO KUNIKI;

    申请日2017-08-30

  • 分类号C12N15/09;C12N1/15;C12N1/19;C12N1/21;C12N5/10;C12N9/00;C12P21/02;C07K5/06;

  • 国家 JP

  • 入库时间 2022-08-21 13:11:58

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