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首页> 外文期刊>FEMS Microbiology Letters >CHARACTERIZATION OF PEPR1, A GENE CODING FOR A POTENTIAL TRANSCRIPTIONAL REGULATOR OF LACTOBACILLUS DELBRUECKII SUBSP LACTIS DSM7290
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CHARACTERIZATION OF PEPR1, A GENE CODING FOR A POTENTIAL TRANSCRIPTIONAL REGULATOR OF LACTOBACILLUS DELBRUECKII SUBSP LACTIS DSM7290

机译:PEPR1的特性,一种编码乳杆菌的潜在转录调节子的基因编码DSM7290

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摘要

The gene designated pepRI, 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 pepRI 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 pepRI gene has the potential to encode a protein of 333 amino acids with a calculated molecular mass of 36 955 Da and a calculated pI 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 pepRI-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 pepRI. [References: 25]
机译:命名为pepRI的基因,编码潜在的德氏乳杆菌亚种的转录调节子。乳酸DSM7290,通过以相反方向定位的蛋白水解酶pepQ上游的开放阅读框的序列相似性鉴定。 pepQ和pepRI编码区相隔152个核苷酸。在pepQ -35区域的上游,可以鉴定出与分解代谢物响应元件同源的14 bp回文序列。 pepRI基因具有编码333个氨基酸的蛋白质的潜力,计算的分子量为36 955 Da,计算的pI为5.5。推导的蛋白质序列与芽孢杆菌的分解代谢物控制蛋白具有明显的同一性。研究了在pepRI-pepQ基因间区域融合了无启动子的β-半乳糖苷酶报道基因的大肠杆菌中的共表达。 pepQ-β-半乳糖苷酶杂化物在克隆的pepRI存在下显示出增强的表达。 [参考:25]

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