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诺卡氏菌内酰胺杜兰α-氨基己二酰-半胱氨酰-缬氨酸合成酶在淡紫链霉菌中的过表达。纯化的多酶以胱硫醚和6-氧代哌啶-2-羧酸为底物合成三肽。

Overexpression of the Nocardia lactamdurans alpha-aminoadipyl-cysteinyl-valine synthetase in Streptomyces lividans. The purified multienzyme uses cystathionine and 6-oxopiperidine 2-carboxylate as substrates for synthesis of the tripeptide.

作者信息

Coque J J, de la Fuente J L, Liras P, Martín J F

机构信息

Faculty of Biology, Department of Ecology, Genetics and Microbiology, University of León, Spain.

出版信息

Eur J Biochem. 1996 Dec 1;242(2):264-70. doi: 10.1111/j.1432-1033.1996.0264r.x.

Abstract

Formation of the tripeptide delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine (Aad-Cys-Val) is catalyzed by a multienzyme peptide synthetase encoded by the pcbAB gene in producers of beta-lactam antibiotics. The pcbAB gene of Nocardia lactamdurans was overexpressed in Streptomyces lividans giving a high Aad-Cys-Val synthetase activity. The synthetase was purified 2785-fold to near homogeneity showing a molecular mass of 430 kDa by SDS/PAGE. The protein was identified in the gels with antibodies to Aad-Cys-Val synthetase and by the formation of aminoacyl-synthetase thioester complex with [14C]valine. The purified synthetase used alpha-aminoadipic acid or its lactam 6-oxopiperidine 2-carboxylic acid but was unable to use piperideine 6-carboxylic acid or pipecolic acid as substrates to form Aad-Cys-Val. L-Cystathionine, (2-amino-2-carboxyethyl)-L-homocysteine, was used as substrate and formed Aad-Cys-Val with the same efficiency as L-cysteine. The product of the reaction eluted with authentic Aad-Cys-Val. The synthetase preparation was able to hydrolyze L-cystathionine by a pyridoxal-phosphate-independent mechanism which is not inhibited by propargylglycine, to form Aad-Cys-Val.

摘要

β-内酰胺抗生素产生菌中,由pcbAB基因编码的多酶肽合成酶催化三肽δ-(L-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸(Aad-Cys-Val)的形成。诺卡氏菌的pcbAB基因在变铅青链霉菌中过表达,产生了高活性的Aad-Cys-Val合成酶。该合成酶经纯化后比活性提高了2785倍,达到近乎均一的状态,SDS/PAGE显示其分子量为430 kDa。通过用Aad-Cys-Val合成酶抗体以及与[14C]缬氨酸形成氨酰合成酶硫酯复合物,在凝胶中鉴定出了该蛋白。纯化后的合成酶使用α-氨基己二酸或其内酯6-氧代哌啶-2-羧酸,但不能使用哌啶-6-羧酸或哌可酸作为底物来形成Aad-Cys-Val。L-胱硫醚、(2-氨基-2-羧乙基)-L-高半胱氨酸用作底物时,形成Aad-Cys-Val的效率与L-半胱氨酸相同。反应产物与纯品Aad-Cys-Val一起洗脱。该合成酶制剂能够通过一种不依赖磷酸吡哆醛且不受炔丙基甘氨酸抑制的机制水解L-胱硫醚,从而形成Aad-Cys-Val。

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