Uhlenhopp E L, Zimm B H
Biophys J. 1975 Mar;15(3):223-32. doi: 10.1016/S0006-3495(75)85813-9.
Single-stranded DNA released from E. coli wild type and mutant cells by alkaline-EDTA-detergent was analyzed using the recently developed biophysical technique of viscoelastometry. Under the lysis conditions used, it was possible to detect single strands of molecular weight approximately 2 times 10-9 daltons. Little difference was detected in the size of single-stranded DNA from log phase vs. stationary phase cultures, or from cells treated with chloramphenicol to allow completion of replicating chromosomes. The largest single strands from ligase overproducing, endonuclease minus, and pol A1 mutants were likewise of approximately the same size as wild type, but were present in smaller yields. The reduction in single-strand molecular weight as a result of heating intact cells was investigated as a function of time and temperature. Heating at 37 degrees C for up to 20 min produced no additional single-strand breaks, but temperatures from 45 to 65 degrees introduced breaks. Solutions maintained at pH 12.5 were not stable indefinitely, and the relative viscosity of such solutions was found to decrease over a period of several hours.
使用最近开发的粘弹性测定生物物理技术,对通过碱性 - EDTA - 去污剂从大肠杆菌野生型和突变细胞中释放的单链DNA进行了分析。在所使用的裂解条件下,能够检测到分子量约为2×10⁻⁹道尔顿的单链。对数期与稳定期培养物中的单链DNA大小,或用氯霉素处理以允许复制染色体完成的细胞中的单链DNA大小,几乎没有差异。来自连接酶高产、核酸内切酶缺陷和pol A1突变体的最大单链同样与野生型大小大致相同,但产量较低。研究了完整细胞加热导致的单链分子量降低与时间和温度的关系。在37℃加热长达20分钟不会产生额外的单链断裂,但45至65℃的温度会引入断裂。保持在pH 12.5的溶液不会无限期稳定,并且发现此类溶液的相对粘度在数小时内会降低。