首页> 外文期刊>Journal of bacteriology >Characterization of the Streptomyces clavuligerus argC gene encoding N-acetylglutamyl-phosphate reductase: expression in Streptomyces lividans and effect on clavulanic acid production.
【24h】

Characterization of the Streptomyces clavuligerus argC gene encoding N-acetylglutamyl-phosphate reductase: expression in Streptomyces lividans and effect on clavulanic acid production.

机译:链霉菌棒状链霉菌argC基因编码N-乙酰谷氨酰磷酸还原酶的表征:在青霉链霉菌中的表达和对克拉维酸产生的影响。

获取原文
           

摘要

The argC gene of Streptomyces clavuligerus encoding N-acetylglutamyl-phosphate reductase (AGPR) has been cloned by complementation of argC mutants Streptomyces lividans 1674 and Escherichia coli XC33. The gene is contained in an open reading frame of 1,023 nucleotides which encodes a protein of 340 amino acids with a deduced molecular mass of 35,224 Da. The argC gene is linked to argE, as shown by complementation of argE mutants of E. coli. Expression of argC from cloned DNA fragments carrying the gene leads to high levels of AGPR in wild-type S. lividans and in the argC mutant S. lividans 1674. Formation of AGPR is repressed by addition of arginine to the culture medium. The protein encoded by the argC gene is very similar to the AGPRs of Streptomyces coelicolor, Bacillus subtilis, and E. coli and, to a lesser degree, to the homologous enzymes of Saccharomyces cerevisiae and Anabaena spp. A conserved PGCYPT domain present in all the AGPR sequences suggests that this may be the active center of the protein. Transformation of S. clavuligerus 328, an argC auxotroph deficient in clavulanic acid biosynthesis, with plasmid pULML30, carrying the cloned argC gene, restored both prototrophy and antibiotic production.
机译:已通过互补argC突变体淡紫色链霉菌1674和大肠杆菌XC33克隆了克拉维链霉菌编码N-乙酰谷氨酰磷酸还原酶(AGPR)的argC基因。该基因包含在一个1023个核苷酸的开放阅读框中,该框架编码340个氨基酸的蛋白质,推导的分子量为35224 Da。 argC基因与argE连接,如大肠杆菌argE突变体的互补所示。从携带该基因的克隆DNA片段表达argC会在野生型葡萄球菌和argC突变葡萄球菌1674中导致高水平的AGPR。通过向培养基中添加精氨酸来抑制AGPR的形成。由argC基因编码的蛋白质与链霉菌,枯草芽孢杆菌和大肠杆菌的AGPR非常相似,并且在较小程度上与酿酒酵母和鱼腥藻的同源酶相似。所有AGPR序列中均存在一个保守的PGCYPT结构域,表明这可能是蛋白质的活性中心。用携带克隆的argC基因的质粒pULML30转化缺乏棒酸生物合成能力的argC营养缺陷型s。clavuligerus 328,可以恢复原营养和抗生素生产。

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