Roles of pIII in filamentous phage assembly

被引:57
作者
Rakonjac, J [1 ]
Model, P [1 ]
机构
[1] Rockefeller Univ, New York, NY 10021 USA
基金
美国国家科学基金会;
关键词
filamentous phage; gene III encoded protein; gene VI encoded protein; phage assembly;
D O I
10.1006/jmbi.1998.2006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Filamentous phage protein LII (pIII), located at one end of the phage, is required for infectivity and stability of the particle. Cells infected with phage from which gene LIT has been completely deleted produce particles that are not released into the medium but stay associated at the surface. These particles are much longer than normal phage. They can be released by subsequent expression of pIII. Viewed with the electron microscope, cells infected with gene III deletion phage are decorated with structures that resemble extremely long pill. Surprisingly, such cells are viable and can form colonies. The pill deficiency can be complemented in trans, but there is a threshold concentration below which assembly does not occur. Above this threshold, pIII is used very efficiently and is incorporated into infectious but longer than unit length phage. As the concentration of pIII is increased, the number of infectious particles increases, and their average length decreases. pIII stabilizes pVI, a second phage protein found at the pIII end of the particle. Ln the absence of pIII, degradation of pVI is very rapid. pIII is thus not only required for infectivity and particle stability, but to terminate assembly and release the phage from its assembly site. (C) 1998 Academic Press.
引用
收藏
页码:25 / 41
页数:17
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