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Tail morphology controls DNA release in two Salmonella phages with one lipopolysaccharide receptor recognition system

机译:尾巴形态通过一个脂多糖受体识别系统控制两个沙门氏菌噬菌体中的DNA释放

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Bacteriophages use specific tail proteins to recognize host cells. It is still not understood to molecular detail how the signal is transmitted over the tail to initiate infection. We have analysed in vitro DNA ejection in long-tailed siphovirus 9NA and short-tailed podovirus P22 upon incubation with Salmonella typhimurium lipopolysaccharide (LPS). We showed for the first time that LPS alone was sufficient to elicit DNA release from a siphovirus in vitro. Crystal structure analysis revealed that both phages use similar tailspike proteins for LPS recognition. Tailspike proteins hydrolyse LPS O antigen to position the phage on the cell surface. Thus we were able to compare in vitro DNA ejection processes from two phages with different morphologies with the same receptor under identical experimental conditions. Siphovirus 9NA ejected its DNA about 30 times faster than podovirus P22. DNA ejection is under control of the conformational opening of the particle and has a similar activation barrier in 9NA and P22. Our data suggest that tail morphology influences the efficiencies of particle opening given an identical initial receptor interaction event.
机译:噬菌体使用特定的尾巴蛋白识别宿主细胞。分子细节仍不清楚,信号如何通过尾巴传播以引发感染。我们与鼠伤寒沙门氏菌脂多糖(LPS)孵育后,分析了长尾siphovirus 9NA和短尾足病毒P22的体外DNA弹出。我们首次证明,单独的LPS足以在体外诱导siphovirus释放DNA。晶体结构分析表明,两种噬菌体都使用类似的尾钉蛋白来识别LPS。尾钉蛋白水解LPS O抗原,将噬菌体定位在细胞表面。因此,我们能够在相同的实验条件下比较来自具有相同受体的两种不同形态的噬菌体的体外DNA喷射过程。 Siphovirus 9NA的DNA喷射速度比Podvirus P22快30倍。 DNA喷射受粒子构象开放的控制,并且在9NA和P22中具有类似的激活屏障。我们的数据表明,给定相同的初始受体相互作用事件,尾部形态会影响颗粒打开的效率。

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