Bruttin A, Brüssow H
Nestlé Research Centre, Lausanne, Switzerland.
Virology. 1996 May 1;219(1):96-104. doi: 10.1006/viro.1996.0226.
Site-specific spontaneous deletions were observed with high frequency in three regions of the genome of the temperate Streptococcus thermophilus phage phi SFi21. Deletion sizes were 750 bp (type 1), 2.7 kb (type 2), and 1 kb (type 3). Combinations of types 1 and 3 and 2 and 3 were observed. The mutants grew lytically although with reduced burst sizes. Type 2 mutants lost the capacity to lysogenize host cells. Upon serial passage, the deletion mutants overgrew the wild-type phage. No direct or inverted DNA repeats were associated with type 1 or 2 deletion sites. Several independent phage isolates showed deletions at identical nucleotide positions, suggesting a site-specific recombination system. Sequencing of an Xbal restriction fragment covering the type 1 deletion predicted a single long open reading frame (ORF) showing a high degree of amino acid similarity with two proteins from bacteriophage P1 implicated in its immunity control (KiIA, Ant). Type 1 deletion leads to a loss of the conserved C-terminal part of this ORF.
在温和嗜热链球菌噬菌体phi SFi21的基因组三个区域中高频观察到位点特异性自发缺失。缺失大小分别为750 bp(1型)、2.7 kb(2型)和1 kb(3型)。观察到1型和3型以及2型和3型的组合。突变体进行裂解生长,不过裂解量减少。2型突变体失去了使宿主细胞溶原化的能力。经过连续传代,缺失突变体的生长超过了野生型噬菌体。1型或2型缺失位点未发现直接或反向DNA重复序列。几个独立的噬菌体分离株在相同核苷酸位置出现缺失,提示存在位点特异性重组系统。对覆盖1型缺失的Xbal限制片段进行测序,预测有一个单一的长开放阅读框(ORF),其氨基酸序列与噬菌体P1中参与免疫控制的两种蛋白(KiIA、Ant)高度相似。1型缺失导致该ORF保守的C末端部分缺失。