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Appl Environ Microbiol. 1980 Aug;40(2):274-81. doi: 10.1128/aem.40.2.274-281.1980.
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Separate branches of the uvr gene-dependent excision repair process in ultraviolet-irradiated Escherichia coli K-12 cells; their dependence upon growth medium and the polA, recA, recB, and exrA genes.紫外线照射的大肠杆菌K-12细胞中uvr基因依赖性切除修复过程的不同分支;它们对生长培养基以及polA、recA、recB和exrA基因的依赖性。
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BOUND WATER, METABOLITES AND GENETIC CONTINUITY.结合水、代谢物与遗传连续性
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PHOTOREVERSAL AND "DARK REPAIR" OF MUTATIONS TO PROTOTROPHY INDUCED BY ULTRAVIOLET LIGHT IN PHOTOREACTIVABLE AND NON-PHOTOREACTIVABLE STRAINS OF ESCHERICHIA COLI.紫外线诱导的大肠杆菌光可活化和非光可活化菌株中向原养型突变的光逆转和“暗修复”
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Ultraviolet-induced mutation and DNA repair.紫外线诱导的突变与DNA修复。
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X-ray sensitivity and repair capacity of a polA1 exrA strain of Escherichia coli K-12.大肠杆菌K-12的polA1 exrA菌株的X射线敏感性和修复能力
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大肠杆菌在疏水滤膜上干燥诱导的突变。

Mutation induced by drying of Escherichia coli on a hydrophobic filter membrane.

作者信息

Asada S, Takano M, Shibasaki I

出版信息

Appl Environ Microbiol. 1980 Aug;40(2):274-81. doi: 10.1128/aem.40.2.274-281.1980.

DOI:10.1128/aem.40.2.274-281.1980
PMID:7008692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC291565/
Abstract

Drying of Escherichia coli to a required cellular water level was conducted on a hydrophobic membrane at the corresponding relative humidity. Mutation from an arginine auxotroph to the prototroph was induced by drying to a water activity (aw) of 0.53 and below, but not to an aw of 0.75 and above. The critical aw below which mutation occurred in the course of drying was similar to that for induction of deoxyribonucleic acid (DNA) strand breakage in the bacteria. Some ultraviolet or gamma-irradiation-sensitive strains, e.g., strains of carrying recA, recB, and uvrA recA were more sensitive to drying than the wild-type strains or strains carrying uvrA and polA. The DNA strand breakage of every strain was observed to be to a similar extent after drying to an aw of less than 0.53. The drying-resistant strains repaired the damaged DNA partially during postdrying incubation in a growth medium but not in phosphate buffer solution, while the drying-sensitive strains could not at all. Significant mutation on drying occurred in the wild-type strains, strains carrying uvrA and polA, but not in strains carrying recA. It is, therefore, concluded that the mutation is caused by errors in rec-dependent repair of the drying-induced breakage in DNA.

摘要

在相应的相对湿度下,于疏水膜上对大肠杆菌进行干燥处理,使其达到所需的细胞含水量。将精氨酸营养缺陷型菌株干燥至水分活度(aw)为0.53及以下时,可诱导其突变为原养型,但干燥至aw为0.75及以上时则不会发生突变。干燥过程中发生突变的临界aw与细菌中脱氧核糖核酸(DNA)链断裂诱导的临界aw相似。一些对紫外线或γ射线敏感的菌株,如携带recA、recB和uvrA recA的菌株,比野生型菌株或携带uvrA和polA的菌株对干燥更敏感。将每种菌株干燥至aw小于0.53后,观察到DNA链断裂程度相似。抗干燥菌株在干燥后于生长培养基中培养期间可部分修复受损的DNA,但在磷酸盐缓冲溶液中则不能,而对干燥敏感的菌株则完全无法修复。野生型菌株、携带uvrA和polA的菌株在干燥时会发生显著突变,但携带recA的菌株则不会。因此,得出结论,突变是由DNA干燥诱导断裂的rec依赖性修复错误引起的。