Börmann E R, Eikmanns B J, Sahm H
Institut für Biotechnologie 1 des Forschungszentrums Jülich GmbH, Germany.
Mol Microbiol. 1992 Feb;6(3):317-26. doi: 10.1111/j.1365-2958.1992.tb01474.x.
The Corynebacterium glutamicum gdh gene encoding NADP-dependent glutamate dehydrogenase (GDH) has been isolated by complementation of the Escherichia coli gdh mutant PA340. The gdh gene was subcloned into the E. coli/C. glutamicum shuttle vector pEK0 and introduced into C. glutamicum. Recombinant strains showed approximately eightfold higher specific GDH activity (15U mg protein-1) relative to the wild type (1.8U mg protein-1). Physiological studies with wild-type and recombinant C. glutamicum strains revealed no indication of significant regulation of gdh expression. The DNA sequence of 2082 bp, including the gdh gene, 5'-, and 3'-flanking regions, was determined. The structural gene consists of 1344 bp and codes for a polypeptide of 448 amino acid residues (Mr 49,152) showing up to 53.6% identity with reported amino acid sequences of glutamate dehydrogenases from other organisms. Northern blot hybridization revealed a 1.65kb mRNA transcript, indicating that the gdh gene of C. glutamicum is monocistronic. Transcription occurred from a G residue located 284 bp upstream of the AUG considered to be the translational initiation codon.
通过对大肠杆菌gdh突变体PA340进行互补,分离出了编码依赖NADP的谷氨酸脱氢酶(GDH)的谷氨酸棒杆菌gdh基因。将gdh基因亚克隆到大肠杆菌/谷氨酸棒杆菌穿梭载体pEK0中,并导入谷氨酸棒杆菌。重组菌株的比GDH活性(15U mg蛋白-1)相对于野生型(1.8U mg蛋白-1)高出约8倍。对野生型和重组谷氨酸棒杆菌菌株的生理学研究表明,没有迹象表明gdh表达受到显著调控。测定了包括gdh基因、5'-和3'-侧翼区域在内的2082 bp的DNA序列。结构基因由1344 bp组成,编码一个448个氨基酸残基的多肽(Mr 49,152),与其他生物体中报道的谷氨酸脱氢酶氨基酸序列的同一性高达53.6%。Northern印迹杂交显示有一个1.65kb的mRNA转录本,表明谷氨酸棒杆菌的gdh基因是单顺反子的。转录从位于被认为是翻译起始密码子AUG上游284 bp处的一个G残基开始。