Daneo-Moore L, Terleckyj B, Shockman G D
Infect Immun. 1975 Nov;12(5):1195-205. doi: 10.1128/iai.12.5.1195-1205.1975.
In the presence of sucrose, Streptococcus mutans grows in large glucan-containing aggregates. Because of reports of linear rather than exponential growth of sucrose-grown cultures, the kinetics of growth of sucrose-grown cultures of S. mutans strain OMZ-176 were compared with those of glucose-grown cultures. Culture turbidity measurements indicated that growth of sucrose cultures was slower, did not follow exponential kinetics, and slowed and stopped at lower absorbance values than did glucose-grown cultures. However, measurements of the rates of accumulation of deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and protein using fully equilibrated radioactively labeled precursors of each of these macromolecular species in sucrose and glucose-grown cultures showed that: (i) for glucose cultures the synthesis of each of the three informational molecules occurred at the same exponential rate, which was identical to the rate of turbidity increase; (ii) for sucrose cultures each macromolecular species was synthesized at the same exponential rate and these rates were identical to the rate of increase of turbidity of the glucose-grown culture for periods of up to 7 h. Furthermore, the ratios of DNA to RNA, RNA to protein, and protein to DNA for the sucrose cultures were identical to those for the glucose cultures for up to 10 doublings. From these data it was concluded that in the presence of sucrose S. mutans grows in a balanced fashion at the same exponential rate as it does in glucose. The deviation from an exponential growth model of the absorbance in sucrose cultures was attributed to an optical artifact due to the formation of large glucan-containing aggregates of cells. The addition of dextranase to sucrose cultures resulted in cultures which increased in turbidity at the same exponential rate as glucose-grown cultures, without affecting the rate or extent of macromolecular synthesis.
在有蔗糖存在的情况下,变形链球菌会形成大量含葡聚糖的聚集体生长。由于有报道称蔗糖培养的菌呈现线性而非指数生长,因此将变形链球菌菌株OMZ - 176在蔗糖培养基中的生长动力学与在葡萄糖培养基中的生长动力学进行了比较。培养物浊度测量表明,蔗糖培养基中的生长较慢,不符合指数动力学,且在吸光度值低于葡萄糖培养物时生长减缓并停止。然而,使用每种大分子物质的完全平衡的放射性标记前体,对蔗糖和葡萄糖培养物中脱氧核糖核酸(DNA)、核糖核酸(RNA)和蛋白质的积累速率进行测量后发现:(i)对于葡萄糖培养物,三种信息分子的合成以相同的指数速率进行,这与浊度增加速率相同;(ii)对于蔗糖培养物,每种大分子物质以相同的指数速率合成,并且在长达7小时的时间段内,这些速率与葡萄糖培养物的浊度增加速率相同。此外,在多达10次倍增的情况下,蔗糖培养物中DNA与RNA、RNA与蛋白质以及蛋白质与DNA的比率与葡萄糖培养物中的比率相同。从这些数据可以得出结论,在有蔗糖存在的情况下,变形链球菌以与在葡萄糖中相同的指数速率平衡生长。蔗糖培养物中吸光度偏离指数生长模型归因于细胞形成大量含葡聚糖的聚集体导致的光学假象。向蔗糖培养物中添加葡聚糖酶后,培养物的浊度以与葡萄糖培养物相同的指数速率增加,而不影响大分子合成的速率或程度。