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Nucleotide sequence and mutational analysis of an immunity repressor gene from Bacillus subtilis temperate phage phi 105.

机译:枯草芽孢杆菌温带噬菌体phi 105免疫抑制基因的核苷酸序列和突变分析。

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摘要

We have identified and sequenced a bacteriophage phi 105 gene encoding an immunity repressor, the first to be characterized from a temperate phage infecting a Gram-positive host. Using superinfection immunity as an assay for repressor function, the phi 105 repressor gene was located within a 740-bp PvuII-HindIII subfragment near the left end of the phi 105 EcoRI-F fragment. We show that the repressor is specified by the 5'-proximal coding sequence of a translationally overlapping gene pair, transcribed from right to left on the conventional phi 105 map. Comparison of its amino acid sequence (146 residues) with that of a large number of Gram-negative bacterial and phage repressors revealed a putative DNA-binding region between positions 20 and 39. The coding region is preceded by a strong Shine-Dalgarno sequence 5' AAAGGAG 3'. Deletion analysis of the 5'-flanking DNA allowed to identify transcriptional control elements. Their structure, 5' TTGTAT 3' at -35 and 5' TATAAT 3' at -10, strongly suggests that the phi 105 repressor gene is transcribed by the major vegetative form of B. subtilis RNA polymerase, as would be expected for an early phage gene.
机译:我们已经鉴定并测序了编码免疫抑制因子的噬菌体phi 105基因,第一个以感染革兰氏阳性宿主的温和噬菌体为特征。使用超级感染免疫作为阻遏物功能的检测方法,phi 105阻遏物基因位于phi 105 EcoRI-F片段左端附近的740 bp PvuII-HindIII亚片段内。我们表明,阻遏物是由翻译重叠基因对的5'-近端编码序列指定的,在常规phi 105图谱上从右向左转录。将其氨基酸序列(146个残基)与大量革兰氏阴性细菌和噬菌体阻遏物的氨基酸序列进行比较,发现在20位和39位之间存在一个假定的DNA结合区。编码区之前是一个很强的Shine-Dalgarno序列5 'AAAGGAG 3'。 5'侧翼DNA的缺失分析允许鉴定转录控制元件。它们的结构,-35处的5'TTGTAT 3'和-10处的5'TATAAT 3',强烈暗示phi 105阻遏物基因是由枯草芽孢杆菌RNA聚合酶的主要营养形式转录的,正如早期所预期的那样噬菌体基因。

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