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链球菌中多糖抗原合成类型及溶血素合成的转变

Transformation of type polysaccharide antigen synthesis and hemolysin synthesis in streptococci.

作者信息

Willers J M, Deddish P A, Slade H D

出版信息

J Bacteriol. 1968 Oct;96(4):1225-30. doi: 10.1128/jb.96.4.1225-1230.1968.

Abstract

Transformation of the ability to synthesize type polysaccharide antigen and beta-hemolysin has been obtained in group F streptococci. Colonies possessing cells transformed to antigen synthesis were detected on the agar surface with fluorescein-labeled anti-type serum. This selection method, in contrast to those with antibiotics, allowed both transformed and nontransformed cells to grow, resulting in sectored colonies. These colonies could be subcultured to further establish the synthesis of antigen. Group F, group A, and group-like z deoxyribonucleic acid (DNA) labeled with type II antigen and hemolysin, and streptomycin resistance transferred each marker to a group F strain lacking a type antigen. DNA from group F and z3 strains labeled with type III antigen, and streptomycin resistance transferred both markers to group F and z3 strains lacking type antigen. A second F strain without type antigen was not transformed with any of these markers. A group H strain was transformed to streptomycin resistance only by the same types of DNA. Transformation to type II antigen synthesis always resulted in the formation of beta-hemolysin. All strains isolated from natural sources contained both markers. A mutant, obtained by nitrosoguanidine treatment of an FII(sr) strain, did not synthesize either the hemolysin or the antigen. This mutant still possessed the group antigen and streptomycin resistance. A close linkage of type II antigen and beta-hemolysin is indicated. The fluorescent-antibody staining of cells containing both group and type antigens showed a more intense ultraviolet adsorption for type than group antigen. A surface location (microcapsular) for the type antigen appeared likely. These results are of interest for studies on antigen biosynthesis, genetics, and classification of the streptococci.

摘要

在F组链球菌中已实现了合成多糖抗原和β-溶血素能力的转化。用荧光素标记的抗型血清在琼脂表面检测到具有转化为抗原合成细胞的菌落。与使用抗生素的选择方法不同,这种选择方法允许转化细胞和未转化细胞都生长,从而产生扇形菌落。这些菌落可以进行传代培养以进一步确定抗原的合成。用II型抗原和溶血素标记的F组、A组和类z组脱氧核糖核酸(DNA)以及链霉素抗性将每个标记转移到缺乏型抗原的F组菌株中。用III型抗原标记的F组和z3组菌株的DNA以及链霉素抗性将两个标记都转移到缺乏型抗原的F组和z3组菌株中。第二个无型抗原的F组菌株未被这些标记中的任何一个转化。一个H组菌株仅被相同类型的DNA转化为链霉素抗性。向II型抗原合成的转化总是导致β-溶血素的形成。从自然来源分离的所有菌株都含有这两个标记。通过亚硝基胍处理FII(sr)菌株获得的一个突变体既不合成溶血素也不合成抗原。这个突变体仍然具有组抗原和链霉素抗性。这表明II型抗原和β-溶血素之间存在紧密连锁。对同时含有组抗原和型抗原的细胞进行荧光抗体染色显示,型抗原的紫外线吸附比组抗原更强。型抗原似乎位于表面(微荚膜)。这些结果对于链球菌抗原生物合成、遗传学和分类的研究具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8a6/252438/4255be955ceb/jbacter00397-0401-a.jpg

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