Rådén B, Rutberg L
J Virol. 1984 Oct;52(1):9-15. doi: 10.1128/JVI.52.1.9-15.1984.
Temperate Bacillus subtilis phage SPO2 codes for a phage-specific DNA polymerase. The polymerase gene has been cloned, and its nucleotide sequence has been determined. Within the sequence there is an open reading frame starting with a TTG and ending with three consecutive translational stop codons. Ten base pairs upstream from the proposed TTG initiation codon there is a probable ribosome-binding site with a calculated free energy of interaction with the 3' end of B. subtilis 16S rRNA of -15 kcal (-63 kJ)/mol. Based on the sequence and the expression of the polymerase gene in three different hybrid plasmids, we conclude that this open reading frame is the structural gene for SPO2 DNA polymerase. The predicted molecular weight of the polymerase is 72,486. In hybrid plasmid pJB74, the terminal triplet of an open reading frame with coding capacity for a protein of ca. 10 kilodaltons overlaps with the translational initiation triplet TTG of the polymerase gene. We speculate that transcription and translation of this open reading frame can influence the amount of phage DNA polymerase made in SPO2-infected bacteria.
温和型枯草芽孢杆菌噬菌体SPO2编码一种噬菌体特异性DNA聚合酶。该聚合酶基因已被克隆,其核苷酸序列也已确定。在该序列中有一个开放阅读框,起始于TTG,终止于三个连续的翻译终止密码子。在所推测的TTG起始密码子上游10个碱基对处,有一个可能的核糖体结合位点,其与枯草芽孢杆菌16S rRNA 3'端相互作用的计算自由能为-15千卡(-63千焦)/摩尔。基于该序列以及聚合酶基因在三种不同杂交质粒中的表达情况,我们得出结论,这个开放阅读框是SPO2 DNA聚合酶的结构基因。该聚合酶的预测分子量为72,486。在杂交质粒pJB74中,一个对约10千道尔顿蛋白质具有编码能力的开放阅读框的末端三联体与聚合酶基因的翻译起始三联体TTG重叠。我们推测这个开放阅读框的转录和翻译会影响SPO2感染细菌中噬菌体DNA聚合酶的产生量。