Kubitschek H E
Biological and Medical Research Division, Argonne National Laboratory, Illinois 60439.
J Bacteriol. 1990 Jan;172(1):94-101. doi: 10.1128/jb.172.1.94-101.1990.
Synchronous cultures of Escherichia coli 15-THU and WP2s, which were selected by velocity sedimentation from exponential-phase cultures growing in an acetate-minimal salts medium, were shifted to richer media at various times during the cell cycle by the addition of glucose or nutrient broth. Cell numbers and mean cell volumes were measured electronically. The duration of the division cycle of the shifted generation was not altered significantly by the addition of either nutrient. Growth rates, measured as rates of cell volume increase, were constant throughout the cycle in unshifted acetate control cultures. When glucose was added, growth rates also remained unchanged during the remainder of the cell cycle and then increased abruptly at or after cell division. When nutrient broth was added, growth rates remained unchanged from periods of 0.2 to 0.4 generations and then increased abruptly to their final values. In all cases, the cell volume increase was linear both before and after the growth rate transition. The strongest support for a linear cell volume increase during the cell cycle of E. coli in slowly growing acetate cultures, however, was obtained in unshifted cultures, in complete agreement with earlier observations of cell volumes at much more rapid growth rates. Although cell growth and division are under the control of the synthesizing machinery in the cell responsible for RNA and protein synthesis, the results indicate that growth is also regulated by membrane-associated transport systems.
通过速度沉降从在乙酸盐 - 基本盐培养基中生长的指数生长期培养物中选出的大肠杆菌15 - THU和WP2s同步培养物,在细胞周期的不同时间通过添加葡萄糖或营养肉汤转移到更丰富的培养基中。用电学方法测量细胞数量和平均细胞体积。添加任何一种营养物质均未显著改变转移代的分裂周期持续时间。在未转移的乙酸盐对照培养物中,以细胞体积增加率衡量的生长速率在整个周期内保持恒定。添加葡萄糖后,在细胞周期的剩余时间内生长速率也保持不变,然后在细胞分裂时或分裂后突然增加。添加营养肉汤后,生长速率在0.2至0.4代期间保持不变,然后突然增加到最终值。在所有情况下,生长速率转变前后细胞体积的增加都是线性的。然而,在未转移的培养物中获得了对在缓慢生长的乙酸盐培养物中大肠杆菌细胞周期期间细胞体积线性增加的最强支持,这与早期在更快生长速率下对细胞体积的观察结果完全一致。虽然细胞生长和分裂受细胞内负责RNA和蛋白质合成的合成机制控制,但结果表明生长也受膜相关转运系统调节。