Mondigler Martin, Ayoub Ahmed T, Heller Knut J
Universität Konstanz, Fachbereich Biologie, D-78457 Konstanz.
J Basic Microbiol. 2006;46(2):116-25. doi: 10.1002/jobm.200510047.
Analysis of the DNA region upstream of the BF23 hrs gene revealed a genetic organisation similar to that of closely related phage T5. A gene encoding a lipoprotein (llp(BF23)) is located directly upstream of the gene encoding the receptor binding protein (hrs) but is transcribed in opposite direction. The gene is followed by four open reading frames transcribed in the same direction. The llp (BF23) gene product does not show similarity to the corresponding T5 Llp(T5) protein, however, like Llp(T5) does for FhuA it blocks the BtuB receptor for BF23 infection. While no similarity between BF23 and T5 was observed for the DNA region encoding Llp and the receptor binding protein, the flanking regions were highly similar. Based on our results we conclude that a genetic module, the receptor-binding/receptor-blocking module, exists in phages BF23 and T5. Due to exclusion of homologous recombination within this module, it is hereditary only as an intact module: separation of the receptor-binding gene from the receptor-blocking gene, which apparently results in reduced fitness of the phage due to inactivation of progeny phage by active receptor proteins in the outer membranes of lysed cells, is thus effectively prevented.
对BF23 hrs基因上游的DNA区域分析发现,其遗传组织与密切相关的噬菌体T5相似。一个编码脂蛋白的基因(llp(BF23))直接位于编码受体结合蛋白(hrs)的基因上游,但转录方向相反。该基因后面跟着四个同向转录的开放阅读框。llp(BF23)基因产物与相应的T5 Llp(T5)蛋白没有相似性,然而,就像Llp(T5)对FhuA所起的作用一样,它能阻断BF23感染的BtuB受体。虽然在编码Llp和受体结合蛋白的DNA区域未观察到BF23与T5之间的相似性,但侧翼区域高度相似。基于我们的结果,我们得出结论,噬菌体BF23和T5中存在一个遗传模块,即受体结合/受体阻断模块。由于该模块内同源重组的排除,它仅作为一个完整模块遗传:受体结合基因与受体阻断基因的分离显然会导致噬菌体适应性降低,因为裂解细胞外膜中的活性受体蛋白会使子代噬菌体失活,因此有效地防止了这种情况的发生。