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变形链球菌的遗传异质性。

Genetic heterogeneity in Streptococcus mutans.

作者信息

Coykendall A L

出版信息

J Bacteriol. 1971 Apr;106(1):192-6. doi: 10.1128/jb.106.1.192-196.1971.

DOI:10.1128/jb.106.1.192-196.1971
PMID:5551636
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC248661/
Abstract

The genetic homogeneity among eight cariogenic strains of Streptococcus mutans was assessed by deoxyribonucleic acid (DNA)-DNA reassociation experiments. DNA species were extracted from strains GS5, Ingbritt, 10449, FAl, BHT, E49, SLl, and KlR. Labeled DNA ((14)C-DNA) was extracted from strains 10449, FAl, and SLl. Denatured (14)C-DNA fragments were allowed to reassociate, i.e., form hybrid duplexes, with denatured DNA immobilized on membrane filters incubated in 0.45 m NaCl-0.045 m sodium citrate at 67 or 75 C. At 67 C, 10449 (14)C-DNA reassociated extensively only with GS5 and Ingbritt DNA. FAl (14)C-DNA hybridized extensively only with BHT DNA, and SLl (14)C-DNA reassociated with KlR and E49 DNA. DNA which hybridized extensively at 67 C also reassociated to a high degree at 75 C. Thermal elution of (14)C-FAl-BHT duplexes showed that the hybrid duplexes were thermostable. The results indicate that S. mutans is a genetically heterogeneous species. The strains studied can be divided into three (possibly four) genetic groups, and these groups closely parallel antigenic groups.

摘要

通过脱氧核糖核酸(DNA)-DNA重缔合实验评估了8株变形链球菌致龋菌株间的基因同质性。从GS5、Ingbritt、10449、FAl、BHT、E49、SLl和KlR菌株中提取DNA样本。从10449、FAl和SLl菌株中提取标记DNA((14)C-DNA)。使变性的(14)C-DNA片段与固定在膜滤器上的变性DNA重缔合,即在0.45 m NaCl-0.045 m柠檬酸钠中于67或75℃孵育。在67℃时,10449(14)C-DNA仅与GS5和Ingbritt DNA广泛重缔合。FAl(14)C-DNA仅与BHT DNA广泛杂交,而SLl(14)C-DNA与KlR和E49 DNA重缔合。在67℃广泛杂交的DNA在75℃时也高度重缔合。(14)C-FAl-BHT双链体的热洗脱表明杂交双链体具有热稳定性。结果表明变形链球菌是一个基因异质的物种。所研究的菌株可分为三个(可能四个)基因群,且这些基因群与抗原群密切平行。

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本文引用的文献

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The Hydrolysis of Arginine by Streptococci.链球菌对精氨酸的水解作用
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