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大肠杆菌荚膜噬菌体。VIII. 噬菌体28-1的片段

Escherichia coli capsule bacteriophages. VIII. Fragments of bacteriophage 28-1.

作者信息

Rieger D, Freund-Mölbert E, Stirm S

出版信息

J Virol. 1976 Mar;17(3):859-64. doi: 10.1128/JVI.17.3.859-864.1976.

Abstract

As described previously, a host capsule depolymerase activity is associated with the particles of Escherichia coli capsule bacteriophage 28-1. This is a large virus with a long, contractile tail terminating in a base plate with spikes. In the present work, isolated virions were exposed to a variety of dissociative reagents and conditions. They were then tested for residual infectivity and depolymerase activity, as well as inspected under an electron microscope. Very mild acid treatment (10 to 15 min at pH 4.0 and 37 C) was found to cause a specific detachment of some phage spikes, together with a moderate drop in both infectivity and depolymerase activity. Large batches of viruses were fragmented in this manner, and the detached spikes were isolated. The host capsule depolymerase activity was found to be associated with these organelles. In negatively stained preparations, the spikes exhibited a length of approximately 18 nm and a thickness of about 5 nm. By sodium dodecyl sulfate-polyacrylamide gel electrophoresis, they were found to contain polypeptides with molecular weights of 80,000 and 145, 000.

摘要

如前所述,宿主荚膜解聚酶活性与大肠杆菌荚膜噬菌体28-1的颗粒有关。这是一种大型病毒,具有一条长的、可收缩的尾巴,末端是带有刺突的基板。在本研究中,将分离的病毒粒子暴露于各种解离试剂和条件下。然后检测它们的残余感染性和解聚酶活性,并在电子显微镜下进行观察。发现非常温和的酸处理(在pH 4.0和37℃下处理10至15分钟)会导致一些噬菌体刺突的特异性脱落,同时感染性和解聚酶活性适度下降。大量病毒以这种方式破碎,并分离出脱落的刺突。发现宿主荚膜解聚酶活性与这些细胞器有关。在负染制剂中,刺突的长度约为18nm,厚度约为5nm。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,发现它们含有分子量为80,000和145,000的多肽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d40/515486/f7f64f5a26f3/jvirol00219-0199-a.jpg

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