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谷氨酸棒杆菌leuB基因的分析

Analysis of the leuB gene from Corynebacterium glutamicum.

作者信息

Pátek M, Hochmannová J, Jelínková M, Nesvera J, Eggeling L

机构信息

Institute of Microbiology, Academy of Sciences of the Czech Republic, Praha, Czech Republic.

出版信息

Appl Microbiol Biotechnol. 1998 Jul;50(1):42-7. doi: 10.1007/s002530051254.

Abstract

The leuB gene of Corynebacterium glutamicum was found to be present on a 2.2-kb BamHI-SacI chromosomal fragment which complemented the leuB mutation of Escherichia coli. The activity of 3-isopropylmalate dehydrogenase (EC 1.1.1.85), encoded by the leuB gene, was significantly increased in C. glutamicum cells harbouring a plasmid containing the 2.2-kb fragment. The nucleotide sequence of the C. glutamicum leuB coding region (an open reading frame, ORF, of 1020 bp encoding a polypeptide of 340 amino acids with M(r) of 36 144) was determined. The deduced amino acid sequence of the product of this ORF is highly homologous to those of 3-isopropylmalate dehydrogenases from three species of mycobacteria. The transcriptional start site of the leuB gene was localized 35 bp upstream of its translational start; a functional terminator was detected in the 3' flanking region. Northern hybridization analysis showed that the C. glutamicum leuB gene is transcribed as a single monocistronic RNA (approximately 1.2 kb in size). Activity of the leuB promoter was significantly reduced when leucine was present in the growth medium. This suggests the negative regulation of the leuB expression on the transcriptional level in C. glutamicum cells.

摘要

发现谷氨酸棒杆菌的leuB基因存在于一个2.2kb的BamHI-SacI染色体片段上,该片段可互补大肠杆菌的leuB突变。在携带含有2.2kb片段质粒的谷氨酸棒杆菌细胞中,由leuB基因编码的3-异丙基苹果酸脱氢酶(EC 1.1.1.85)的活性显著增加。测定了谷氨酸棒杆菌leuB编码区的核苷酸序列(一个1020bp的开放阅读框,ORF,编码一个340个氨基酸的多肽,M(r)为36144)。该ORF产物的推导氨基酸序列与三种分枝杆菌的3-异丙基苹果酸脱氢酶的氨基酸序列高度同源。leuB基因的转录起始位点位于其翻译起始位点上游35bp处;在3'侧翼区域检测到一个功能性终止子。Northern杂交分析表明,谷氨酸棒杆菌leuB基因转录为单一的单顺反子RNA(大小约为1.2kb)。当生长培养基中存在亮氨酸时,leuB启动子的活性显著降低。这表明在谷氨酸棒杆菌细胞中,leuB表达在转录水平上受到负调控。

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