Pellon J R, Gomez R F
J Bacteriol. 1981 Mar;145(3):1456-8. doi: 10.1128/jb.145.3.1456-1458.1981.
The folded chromosome or nucleoid of Escherichia coli was analyzed by low-speed sedimentation in neutral sucrose gradients after heat treatment (30 min at 50 degrees C) and subsequent incubation of cells at 37 degrees C for various times. Heat treatment resulted in in vivo association of the nucleoids with cellular protein and in an increase in sedimentation coefficient. During incubation at 37 degrees C, a fraction of the nucleoids, from heated cells, because dissociated from cellular protein and regained their characteristic sedimentation coefficients. The percentage of nucleoids which returned to their control sedimentation position in the sucrose gradients corresponded to the percentage of cells able to repair thermal damage as assayed by enumeration on agar plates.
对大肠杆菌折叠的染色体或类核进行分析,方法是在热处理(50℃ 30分钟)后,在中性蔗糖梯度中进行低速沉降,随后将细胞在37℃孵育不同时间。热处理导致类核在体内与细胞蛋白结合,并使沉降系数增加。在37℃孵育期间,来自受热细胞的一部分类核从细胞蛋白中解离出来,恢复其特征性沉降系数。在蔗糖梯度中回到其对照沉降位置的类核百分比,与通过在琼脂平板上计数测定的能够修复热损伤的细胞百分比相对应。