Stucky K, Schick J, Klein J R, Henrich B, Plapp R
Universitat Kaiserslautern, Fachbereich Biologie, Abteilung Mikrobiologie, Germany.
FEMS Microbiol Lett. 1996 Feb 1;136(1):63-9. doi: 10.1016/0378-1097(95)00494-7.
The gene designated pepR1, encoding a potential transcription regulator of Lactobacillus delbrueckii subsp. lactis DSM7290, was identified by sequence similarity of an open reading frame located upstream of the prolidase pepQ orientated in opposite direction. pepQ and pepR1 coding regions are spaced by 152 nucleotides. Upstream of the -35 region of pepQ, a 14-bp palindromic sequence, homologous to the catabolite responsive element, could be identified. The pepRl gene has the potential to encode a protein of 333 amino acids with a calculated molecular mass of 36955 Da and a calculated pl of 5.5. The deduced protein sequence shows significant identity to the catabolite control protein of Bacillus. Co-expression in Escherichia coli was studied with the pepR1-pepQ intergenic region fused to the promoterless beta-galactosidase reporter gene. The pepQ-beta-galactosidase hybrid displayed an enhanced expression in the presence of cloned pepR1.
名为pepR1的基因编码德氏乳杆菌乳酸亚种DSM7290的一种潜在转录调节因子,该基因是通过与位于肽酶pepQ上游且方向相反的一个开放阅读框的序列相似性鉴定出来的。pepQ和pepR1的编码区相隔152个核苷酸。在pepQ的-35区上游,可鉴定出一个与分解代谢物反应元件同源的14碱基对回文序列。pepR1基因有潜力编码一种由333个氨基酸组成的蛋白质,计算分子量为36955 Da,计算pI为5.5。推导的蛋白质序列与芽孢杆菌的分解代谢控制蛋白有显著同源性。利用与无启动子β-半乳糖苷酶报告基因融合的pepR1-pepQ基因间区域,在大肠杆菌中进行了共表达研究。在克隆的pepR1存在的情况下,pepQ-β-半乳糖苷酶杂种显示出增强的表达。