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通过超速离心和等电聚焦纯化多杀性巴氏杆菌抗原。

Purification of Pasteurella multocida antigens by ultracentrifugation and isoelectrofocusing.

作者信息

McKinney K L, Rebers P A

出版信息

Can J Microbiol. 1982 May;28(5):511-21. doi: 10.1139/m82-077.

Abstract

A procedure was developed to purify Pasteurella multocida X-731 antigens extracted by potassium thiocyanate. The crude extract was centrifuged at 105 000 x g; the antigens were then separated into a particulate (40p) fraction and a soluble (40s) fraction consisting of proteins and polysaccharides. These fractions were antigenically different. The ultracentrifuged antigens were resolved further by preparative isoelectrofocusing. The 40p antigens focused in a pH range of 3.0 to 6.0; distinctive proteins focused at pH's of 3.5, 3.6, and 3.8. The electrofocused 40p antigens were antigenically similar. The 40s antigens were initially electrofocused in a broad pH range and were found within a pH range of 4.6 to 9.0. The process was repeated with a narrower pH range and antigens that were focused in a narrower pH range could be separated and unique antigenic activities identified. Specific antigens from defined pH ranges were pooled and examined further by immunoelectrophoresis, analytical electrofocusing, and sodium dodecyl sulphate--polyacrylamide gel electrophoresis.

摘要

开发了一种纯化用硫氰酸钾提取的多杀巴斯德菌X-731抗原的方法。粗提物在105 000×g下离心;然后将抗原分离成颗粒(40p)组分和由蛋白质和多糖组成的可溶性(40s)组分。这些组分在抗原性上有所不同。超速离心的抗原通过制备性等电聚焦进一步分离。40p抗原聚焦在pH 3.0至6.0范围内;独特的蛋白质聚焦在pH 3.5、3.6和3.8处。电聚焦的40p抗原在抗原性上相似。40s抗原最初在较宽的pH范围内进行电聚焦,发现在pH 4.6至9.0范围内。用较窄的pH范围重复该过程,聚焦在较窄pH范围内的抗原可以被分离并鉴定出独特的抗原活性。将来自特定pH范围的特异性抗原合并,并通过免疫电泳、分析性电聚焦和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进一步检查。

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