Shimazu Y, Morimyo M, Suzuki K
J Bacteriol. 1971 Sep;107(3):623-32. doi: 10.1128/jb.107.3.623-632.1971.
URT-43 is a mutant of Escherichia coli K-12 which gives a much larger number of survivors when ultraviolet (UV)-irradiated bacteria are incubated on agar medium at 30 C than when they are incubated on the medium at 41 C, although in both cases the number of survivors is fewer than that given by its wild-type ancestor. The UV sensitivity of this mutant was found to be markedly influenced by the presence of a high concentration of NaCl or sucrose in the plating medium. Thus, when irradiated bacteria were plated on agar medium containing 2% NaCl or 0.5 m sucrose at 30 C, they exhibited a resistance similar to that of their wild-type ancestor. At 30 C, there was also an extensive recovery in liquid M9 medium supplemented with all of the nutrients required for growth and NaCl or sucrose. At 41 C, however, the recovery was greatly inhibited. Direct chemical analysis of thymine dimers has revealed that no significant amount of the dimer was released from deoxyribonucleic acid during the period of extensive recovery. It was concluded, therefore, that the temperature-sensitive recovery of URT-43 does not accompany excision of the bulk of pyrimidine dimers. To learn the gene function involved in the recovery, double mutants carrying an additional mutation either in a uvr or a rec gene have been investigated for their UV sensitivities and recovery in liquid medium. It was found that recA(-) and recB(-) derivatives retain the ability of undergoing an efficient recovery at a low temperature, whereas uvrB(-) and uvrC(-) derivatives have completely lost this ability. For these reasons, it was concluded that the mechanism responsible for the recovery of URT-43 involves the function controlled by the uvr genes. The results of photoreactivation suggested that most of the entities dealt with during recovery were pyrimidine dimers.
URT - 43是大肠杆菌K - 12的一个突变体,当紫外线(UV)照射后的细菌在30℃的琼脂培养基上培养时,其存活菌数比在41℃的培养基上培养时多得多,尽管在这两种情况下存活菌数都比其野生型祖先少。发现该突变体的UV敏感性受到平板培养基中高浓度NaCl或蔗糖的显著影响。因此,当将照射后的细菌接种在含有2% NaCl或0.5 M蔗糖的30℃琼脂培养基上时,它们表现出与野生型祖先相似的抗性。在30℃时,在补充了生长所需的所有营养物质以及NaCl或蔗糖的液体M9培养基中也有广泛的恢复。然而,在41℃时,恢复受到极大抑制。对胸腺嘧啶二聚体的直接化学分析表明,在广泛恢复期间,没有大量的二聚体从脱氧核糖核酸中释放出来。因此得出结论,URT - 43的温度敏感恢复并不伴随着大部分嘧啶二聚体的切除。为了了解恢复过程中涉及的基因功能,研究了在uvr或rec基因中携带额外突变的双突变体的UV敏感性以及在液体培养基中的恢复情况。发现recA(-)和recB(-)衍生物在低温下仍保留有效恢复的能力,而uvrB(-)和uvrC(-)衍生物则完全丧失了这种能力。基于这些原因,得出结论,负责URT - 43恢复的机制涉及uvr基因控制的功能。光复活的结果表明,恢复过程中处理的大多数实体是嘧啶二聚体。