Zhang Shouan, Sundin George W
National Center for Agricultural Utilization Research, USDA Agricultural Research Service, Peoria, Illinois, USA.
J Bacteriol. 2004 Nov;186(22):7807-10. doi: 10.1128/JB.186.22.7807-7810.2004.
Forty replicate lineages of Pseudomonas syringae B86-17 cells expressing the rulAB mutagenic DNA repair (MDR) determinant or the rulB::Km MDR-deficient mutant GWS242 were passaged through single-cell bottlenecks (60 cycles), with a UV radiation (UVR) exposure given to half of the lineages at the beginning of each cycle. After every 10th bottleneck cycle, single-colony isolates from all 80 lineages were subjected to 39 phenotypic screens, with newly arising mutations detected in 60 and 0% of UVR-exposed or non-UVR-exposed B86-17 lineages, respectively, by the 60th cycle. Cellular fitness, measured as growth rate in a minimal medium, of UVR-exposed lineages of both B86-17 and GWS242 after 60 cycles was not significantly different from that of the ancestral strains. Although UVR exposure and MDR activity increased the occurrence of mutations in cells, a significant reduction in overall fitness was not observed.
表达rulAB诱变DNA修复(MDR)决定簇的丁香假单胞菌B86 - 17细胞的40个重复谱系或rulB::Km MDR缺陷型突变体GWS242通过单细胞瓶颈传代(60代),每个传代周期开始时,对一半的谱系进行紫外线辐射(UVR)照射。在每第10代瓶颈传代后,对所有80个谱系的单菌落分离株进行39种表型筛选,到第60代时,在UVR照射的B86 - 17谱系中有60%检测到新出现的突变,而未照射UVR的B86 - 17谱系中该比例为0%。以基本培养基中的生长速率衡量的细胞适应性,在60代后,UVR照射的B86 - 17和GWS242谱系与原始菌株相比无显著差异。虽然UVR照射和MDR活性增加了细胞中的突变发生率,但未观察到总体适应性的显著降低。