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传代培养对变形链球菌细胞表面蛋白抗原表达的影响。

Effect of subculturing on expression of a cell-surface protein antigen by Streptococcus mutans.

作者信息

Koga T, Asakawa H, Okahashi N, Takahashi I

机构信息

Department of Dental Research, National Institute of Health, Tokyo, Japan.

出版信息

J Gen Microbiol. 1989 Dec;135(12):3199-207. doi: 10.1099/00221287-135-12-3199.

Abstract

Two freshly isolated strains, Xc and Yc, of Streptococcus mutans serotype c from human dental plaque were subcultured 100 times in Brain Heart Infusion broth. The cell-surface hydrophobicity of strain Xc markedly decreased after subculturing 60 times, but that of strain Yc remained unaltered. Radioimmunoassay showed a close correlation between surface hydrophobicity and the amount of a cell-surface protein antigen (PAc) of Mr 190,000. One hydrophilic variant (strain Xc100L), one relatively hydrophobic variant (strain Xc100H), and two hydrophobic variants (strains Yc100H1 and Yc100H2) were isolated from the 100-fold subcultures of hydrophobic strains Xc and Yc, respectively. SDS-PAGE showed that the amount of cell-associated and cell-free PAc of strain Xc100L was smaller than that of strains Xc and Xc100H. Strain Yc100H2 produced larger amounts of cell-associated PAc than strains Yc and Yc100H1. Resting cells of hydrophilic strain Xc100L attached in smaller numbers to saliva-coated hydroxyapatite than did other hydrophobic strains. RNA dot-blot analysis demonstrated a significant decrease in PAc-specific mRNA in strain Xc100L, as compared with strains Xc and Xc100H. Neither rearrangement nor deletion in the structural gene (pac) for PAc of these strains was observed by Southern blot analysis. These findings suggest that a mechanism which regulates the transcription of the pac gene participates in the quantitative variation of PAc after repeated subculturing.

摘要

从人类牙菌斑中分离出的两种变形链球菌血清型c的新鲜菌株Xc和Yc,在脑心浸液肉汤中传代培养100次。菌株Xc在传代培养60次后细胞表面疏水性显著降低,但菌株Yc的细胞表面疏水性保持不变。放射免疫分析表明表面疏水性与分子量为190,000的细胞表面蛋白抗原(PAc)的量密切相关。分别从疏水性菌株Xc和Yc的100代传代培养物中分离出一个亲水性变体(菌株Xc100L)、一个相对疏水性变体(菌株Xc100H)和两个疏水性变体(菌株Yc100H1和Yc100H2)。SDS-PAGE显示菌株Xc100L的细胞相关和无细胞PAc的量低于菌株Xc和Xc100H。菌株Yc100H2产生的细胞相关PAc比菌株Yc和Yc100H1多。与其他疏水性菌株相比,亲水性菌株Xc100L的静息细胞附着在唾液包被的羟基磷灰石上的数量较少。RNA斑点印迹分析表明,与菌株Xc和Xc100H相比,菌株Xc100L中PAc特异性mRNA显著减少。通过Southern印迹分析未观察到这些菌株PAc结构基因(pac)的重排或缺失。这些发现表明,一种调节pac基因转录的机制参与了重复传代培养后PAc的定量变化。

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