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从培养基成分中分离并纯化出无培养基成分的活解脲脲原体细胞。

Isolation and purification of viable Ureaplasma urealyticum cells free from medium components.

作者信息

Horowitz S, Gal H

机构信息

Department of Microbiology and Immunology, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.

出版信息

J Gen Microbiol. 1991 May;137(5):1087-92. doi: 10.1099/00221287-137-5-1087.

Abstract

A procedure was devised to produce Ureaplasma urealyticum preparations free of adsorbed components of the growth medium, which contains high concentrations of serum. The ureaplasmas were cultivated in a medium containing PPLO-serum fraction as a replacement for horse serum. High titres of ureaplasmas (greater than 10(7) c.f.u. ml-1) were obtained. Harvested cells were then purified by Urografin density gradient centrifugation. By use of 3H-labelled ureaplasma cells and 125I-labelled medium components, a distinct band of viable cells devoid of serum constituents was demonstrated. The absence of medium components was verified by immunoblotting cells from this band with antiserum to medium components. Medium components that had been present before the purification procedure were undetectable in the purified cell fraction obtained. The viability of the purified ureaplasma cells represented an 85% recovery rate and their antigenicity, examined with anti-serotype specific antiserum, remained intact. This easy and reproducible procedure can be used to prepare purified ureaplasmas for investigation of ureaplasmal antigens and their expression and/or role in disease.

摘要

设计了一种程序来制备不含生长培养基吸附成分的解脲脲原体制剂,该生长培养基含有高浓度血清。将脲原体在含有PPLO - 血清组分以替代马血清的培养基中培养。获得了高滴度的脲原体(大于10⁷ c.f.u. ml⁻¹)。然后通过泛影葡胺密度梯度离心法对收获的细胞进行纯化。使用³H标记的脲原体细胞和¹²⁵I标记的培养基成分,证明了一条不含血清成分的活细胞带。通过用针对培养基成分的抗血清对该条带的细胞进行免疫印迹来验证培养基成分的缺失。在获得的纯化细胞组分中未检测到纯化程序之前存在的培养基成分。纯化的脲原体细胞的活力代表85%的回收率,并且用抗血清型特异性抗血清检测其抗原性保持完整。这种简单且可重复的程序可用于制备纯化的脲原体,以研究脲原体抗原及其在疾病中的表达和/或作用。

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