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渗透休克对携带R因子的大肠杆菌四环素抗性的影响。

Effect of osmotic shock on tetracycline resistance in Escherichia coli bearing an R-factor.

作者信息

Franklin T J, Foster S J

出版信息

Biochem J. 1971 Jan;121(2):287-92. doi: 10.1042/bj1210287.

Abstract
  1. Escherichia coli with an R-factor conferring resistance to tetracycline was induced to high-degree resistance by pre-exposure to the antibiotic. The degree of resistance was drastically lowered by subjecting the cells to osmotic shock. 2. Resistance to tetracycline was rapidly restored by incubating the shocked cells in a glucose-salts medium containing shock proteins prepared from tetracycline-sensitive and -resistant cells. Resistance was also restored by incubating the cells in a complex medium without shock protein. 3. The initial recovery of resistance was followed by a secondary fall in resistance when the cells were cultured in complex medium; this secondary fall was largely prevented by the addition of a low concentration (10mug/ml) of tetracycline to cells. The secondary fall was significantly less in shocked E. coli cells harbouring a mutant R-factor in which tetracycline resistance is largely constitutive. 4. Tetracycline resistance was also transiently depressed by treating R-factor-bearing cells with EDTA in tris buffer. 5. The significance of these results in relation to the mechanism of tetracycline resistance in R-factor-bearing cells is discussed.
摘要
  1. 携带赋予四环素抗性的R因子的大肠杆菌通过预先暴露于抗生素而被诱导产生高度抗性。通过对细胞进行渗透压休克处理,抗性程度急剧降低。2. 通过将受到休克处理的细胞在含有从对四环素敏感和抗性细胞制备的休克蛋白的葡萄糖盐培养基中培养,对四环素的抗性迅速恢复。通过将细胞在不含休克蛋白的复合培养基中培养,抗性也得以恢复。3. 当细胞在复合培养基中培养时,抗性的初始恢复之后是抗性的二次下降;向细胞中添加低浓度(10微克/毫升)的四环素可在很大程度上防止这种二次下降。在携带突变R因子的休克大肠杆菌细胞中,二次下降明显较少,在该突变R因子中,四环素抗性很大程度上是组成型的。4. 通过在三羟甲基氨基甲烷缓冲液中用乙二胺四乙酸处理携带R因子的细胞,四环素抗性也会短暂降低。5. 讨论了这些结果与携带R因子的细胞中四环素抗性机制的相关性。

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75.
2
RESISTANCE OF ESCHERICHIA COLI TO TETRACYCLINES.
Biochem J. 1965 Jan;94(1):54-60. doi: 10.1042/bj0940054.
3
A NONSPECIFIC INCREASE IN PERMEABILITY IN ESCHERICHIA COLI PRODUCED BY EDTA.
Proc Natl Acad Sci U S A. 1965 Apr;53(4):745-50. doi: 10.1073/pnas.53.4.745.
7
Active accumulation of tetracycline by Escherichia coli.
Biochem J. 1970 Jan;116(2):287-97. doi: 10.1042/bj1160287.
8
Lack of synergy of EDTA with antimicrobials in resistant enterobacteriaceae.
Nature. 1970 Feb 21;225(5234):763. doi: 10.1038/225763a0.
10
Aminoglycoside antibiotics: inactivation by phosphorylation in Escherichia coli carrying R factors.
J Bacteriol. 1969 Nov;100(2):1144-6. doi: 10.1128/jb.100.2.1144-1146.1969.

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