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Conservation of cell wall peptidoglycan by strains of Streptococcus mutans and Streptococcus sanguis.

机译:变形链球菌和血链球菌菌株对细胞壁肽聚糖的保守性。

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摘要

Turnover of the cell wall peptidoglycan fraction of six different strains of Streptococcus mutans and eight different strains of Streptococcus sanguis was examined. Cells were grown in the presence of [3H]lysine and [14C]leucine for at least eight generations and then chased in growth medium lacking the two labels. At intervals during the chase, samples of cultures were removed, and the amounts of the two labeled precursors remaining in the peptidoglycan and protein fractions were quantitated. Similar experiments were done in which the pulse-labeling technique was used. In addition, cells were labeled in the presence of tetracycline or penicillin, chased with growth medium containing no inhibitor, and assayed at intervals during the chase for the amount of [3H]lysine present in peptidoglycan fractions. Studies of cultures of S. mutans strains FA-1, OMZ-61, OMZ-176, 6715, GS-5, and Ingbritt and of S. sanguis strains 10558, M-5, Wicky, DL-101, DL-1, 71X26, and 71X48 maintained in the exponential phase of growth in a chemically defined medium failed to show evidence of loss of insoluble peptidoglycan via turnover. Similarly, for the strains of S. mutans, insoluble peptidoglycan assembled during 2 h of benzylpenicillin or tetracycline treatment was also conserved during recovery from growth inhibition.
机译:检查了六种不同变形链球菌菌株和八种不同血色链球菌菌株的细胞壁肽聚糖馏分的周转率。细胞在[3H]赖氨酸和[14C]亮氨酸存在下生长至少八代,然后在缺少这两种标记的生长培养基中追踪。在追逐过程中的间隔时间,移出培养样品,并对肽聚糖和蛋白质级分中残留的两种标记前体的量进行定量。进行了类似的实验,其中使用了脉冲标记技术。另外,在四环素或青霉素的存在下标记细胞,用不含抑制剂的生长培养基进行追踪,并在追踪过程中的间隔中分析肽聚糖级分中存在的[3H]赖氨酸的量。变形链球菌FA-1,OMZ-61,OMZ-176、6715,GS-5和Ingbritt菌株以及血统链球菌10558,M-5,Wicky,DL-101,DL-1, 71X26和71X48维持在化学定义的培养基中的指数增长期,未能显示出通过营业额损失不溶性肽聚糖的证据。类似地,对于变形链球菌菌株,在从苄基青霉素或四环素处理的2小时过程中组装的不溶性肽聚糖在从生长抑制恢复的过程中也被保存。

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