...
首页> 外文期刊>FEMS Microbiology Letters >Construction of fusion vectors of corynebacteria: expression of glutathione-S-transferase fusion protein in Corynebacterium acetoacidophilum ATCC 21476
【24h】

Construction of fusion vectors of corynebacteria: expression of glutathione-S-transferase fusion protein in Corynebacterium acetoacidophilum ATCC 21476

机译:棒状杆菌融合载体的构建:谷胱甘肽-S-转移酶融合蛋白在丙酮酸嗜酸杆菌ATCC 21476中的表达

获取原文
获取原文并翻译 | 示例

摘要

A series of fusion vectors containing glutathione-S-transferase (GST) were constructed by inserting GST fusion cassette of Escherichia coli vectors pGEX4T-1, -2 and -3 in corynebacterial vector pBK2. Efficient expression of GST driven by inducible tac promoter of E. coli was observed in Corynebacterium acetoacidophilum. Fusion of enhanced green fluorescent protein (EGFP) and streptokinase genes in this vector resulted in the synthesis of both the fusion proteins. The ability of this recombinant organism to produce several-fold more of the product in the extracellular medium than in the intracellular space would make this system quite attractive as far as the downstream processing of the product is concerned. (C) 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 26]
机译:通过将大肠杆菌载体pGEX4T-1,-2和-3的GST融合盒插入棒状杆菌载体pBK2中,构建了一系列包含谷胱甘肽-S-转移酶(GST)的融合载体。在棒状杆菌嗜酸杆菌中观察到由大肠杆菌的可诱导tac启动子驱动的GST的有效表达。增强的绿色荧光蛋白(EGFP)和链激酶基因在该载体中的融合导致两种融合蛋白的合成。该重组生物在细胞外培养基中产生的产物比在细胞内空间中产生产物的能力高出几倍,这使得该系统在涉及产物的下游加工方面具有相当大的吸引力。 (C)2002年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:26]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号