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DNA超螺旋对在海水中培养的大肠杆菌细胞可培养性丧失的影响。

Influence of DNA supercoiling on the loss of culturability of Escherichia coli cells incubated in seawater.

作者信息

Gauthier M J, Labedan B, Breittmayer V A

机构信息

INSERM Unité 303, Nice, France.

出版信息

Mol Ecol. 1992 Oct;1(3):183-90. doi: 10.1111/j.1365-294x.1992.tb00174.x.

Abstract

The relationship between the loss of culturability of Escherichia coli cells in seawater and the DNA supercoiling level of a reporter plasmid (pUC8) have been studied under different experimental conditions. Transfer to seawater of cells grown at low osmolarity decreased their ability to grow without apparent modification of the plasmid supercoiling. We found that E. coli cells could be protected against seawater-induced loss of culturability by increasing their DNA-negative supercoiling in response to environmental factors: either a growth at high osmolarity before the transfer to seawater, or addition of organic matter (50-mg/l peptone) in seawater. We further found conditions where a DNA-induced relaxation was accompanied by an increase in seawater sensitivity. Indeed, inactivation of either one of the subunits A and B of DNA gyrase, which leads to important DNA relaxation, was accompanied in both cases by an increased loss of culturability of conditional mutants after transfer to seawater which could not be explained uniquely by the increase in the temperature required to inactivate the gyrase. Similarly, a strain harbouring a mutation in topoisomerase I, compensated by another mutation in subunit B of the gyrase, was more sensitive to seawater than the isogenic wild-type cell and this greater sensitivity was correlated to a relaxation of plasmid DNA. Again, in these different cases, a previous growth at high osmolarity protected against this seawater sensitivity. We thus propose that the ability of E. coli cells to survive in seawater and maintain their ability to grow on culture media could be linked, at least in part, to the topological state of their DNA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在不同实验条件下,研究了海水中大肠杆菌细胞可培养性丧失与报告质粒(pUC8)DNA超螺旋水平之间的关系。将在低渗透压下生长的细胞转移至海水中,其生长能力下降,但质粒超螺旋无明显改变。我们发现,通过响应环境因素增加其DNA负超螺旋,大肠杆菌细胞可免受海水诱导的可培养性丧失:要么在转移至海水之前在高渗透压下生长,要么在海水中添加有机物(50mg/L蛋白胨)。我们进一步发现,DNA诱导的松弛伴随着海水敏感性增加的情况。实际上,DNA促旋酶亚基A和B之一失活导致重要的DNA松弛,在这两种情况下,条件突变体转移至海水后可培养性丧失均增加,这不能仅由促旋酶失活所需温度的升高来解释。同样,拓扑异构酶I发生突变且由促旋酶亚基B中的另一个突变补偿的菌株,比同基因野生型细胞对海水更敏感,且这种更高的敏感性与质粒DNA的松弛相关。同样,在这些不同情况下,之前在高渗透压下生长可防止这种海水敏感性。因此,我们提出,大肠杆菌细胞在海水中存活并维持其在培养基上生长能力的能力,至少部分可能与其DNA的拓扑状态有关。(摘要截短于250字)

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