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噬菌体P22不太可能作为鼠伤寒沙门氏菌内膜与外膜之间黏附区域的探针。

Bacteriophage P22 is not a likely probe for zones of adhesion between the inner and outer membranes of Salmonella typhimurium.

作者信息

Crowlesmith I, Schindler M, Osborn M J

出版信息

J Bacteriol. 1978 Jul;135(1):259-69. doi: 10.1128/jb.135.1.259-269.1978.

DOI:10.1128/jb.135.1.259-269.1978
PMID:353032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC224814/
Abstract

Thin-section electron micrographs of plasmolyzed Salmonella typhimurium infected with bacteriophage P22 demonstrated that phage adsorbed to cells over sites of inner- and outer-membrane contact. Efforts were made to isolate such adsorption sites by infection of cells with 35S- and 32P-labeled phage and by separation of the membranes on sucrose gradients. At 37 degrees C, about 75% of the 35S radioactivity could be recovered in a region of intermediate density between the inner and outer membranes. This region (phi band) did not contain 32P. The gradient profile was independent of the multiplicity of infection (between 0.2 and 50) and of the presence or absence of chloramphenicol, dinitrophenol, or cyanide. However, ethylenediaminetetraacetate, when present during the infection step, prevented the formation of phi band. The density of phi band was at least 1.30 g/cm3, as demonstrated by prolonged centrifugation on a D2O-sucrose gradient. phi Band was shown by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and electron microscopy to contain empty phage heads and contaminating cellular debris. In purified preparations, phage heads were the only structures, visible by negative staining, and very little cellular phospholipid or protein was associated with the phage proteins (less than 2% and 30% by weight, respectively, as determined by using [3H]glycerol or [3H]leucine). The residual cellular protein included all of the major outer-membrane proteins rather than any one specific protein. These results are interpreted as indicating that phi band probably does not contain adhesion site material stably associated with phage heads.

摘要

用噬菌体P22感染后发生质壁分离的鼠伤寒沙门氏菌的超薄切片电子显微镜照片显示,噬菌体吸附在细胞内膜与外膜接触的部位。通过用35S和32P标记的噬菌体感染细胞,并在蔗糖梯度上分离膜,努力分离出这样的吸附位点。在37℃时,约75%的35S放射性可在内膜和外膜之间的中等密度区域中回收。该区域(φ带)不含32P。梯度分布与感染复数(在0.2至50之间)以及氯霉素、二硝基苯酚或氰化物的存在与否无关。然而,在感染步骤中存在乙二胺四乙酸时,会阻止φ带的形成。如在D2O-蔗糖梯度上长时间离心所示,φ带的密度至少为1.30 g/cm3。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和电子显微镜显示,φ带含有空噬菌体头部和污染的细胞碎片。在纯化的制剂中,噬菌体头部是通过负染色可见的唯一结构,并且与噬菌体蛋白质相关的细胞磷脂或蛋白质很少(分别使用[3H]甘油或[3H]亮氨酸测定,重量分别小于2%和30%)。残留的细胞蛋白质包括所有主要的外膜蛋白质,而不是任何一种特定的蛋白质。这些结果被解释为表明φ带可能不包含与噬菌体头部稳定相关的粘附位点物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/84c42536b0e0/jbacter00290-0274-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/42d6a2636001/jbacter00290-0267-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/5ab7470dbf08/jbacter00290-0269-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/1e35537aee93/jbacter00290-0270-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/16934bb5cc4b/jbacter00290-0272-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/84c42536b0e0/jbacter00290-0274-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/42d6a2636001/jbacter00290-0267-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/5ab7470dbf08/jbacter00290-0269-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/1e35537aee93/jbacter00290-0270-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/16934bb5cc4b/jbacter00290-0272-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/757b/224814/84c42536b0e0/jbacter00290-0274-a.jpg

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