Koch A L
J Gen Microbiol. 1980 Jan;116(1):165-71. doi: 10.1099/00221287-116-1-165.
It is generally agreed that ribosomes function with reduced efficiency (i.e. a smaller proportion is actually engaged in protein synthesis) in bacteria growing at low growth rates (doubling times greater than 2 h). This paper examines whether the efficiency is constant in bacteria growing at various rates corresponding to doubling times of less than 2 h. Because isotopic methods cannot be used in very rich media, turbidimetric methods have been extended to follow the kinetics of growth immediately following the shift-up of cultures of Escherichia coli ML308 growing in glucose minimal medium or succinate minimal medium into a very rich medium supporting a balanced doubling time of 17.4 min. It is concluded that the efficiency of ribosome participation in protein synthesis is higher in the very rich medium than in the two minimal media, which support doubling times of 43 and 65 min, respectively, at 37 degrees C.
普遍认为,在生长速率较低(倍增时间大于2小时)的细菌中,核糖体的功能效率会降低(即实际参与蛋白质合成的比例较小)。本文研究了在对应于倍增时间小于2小时的各种生长速率下生长的细菌中,这种效率是否恒定。由于同位素方法不能用于非常丰富的培养基中,因此已扩展了比浊法,以跟踪在葡萄糖基本培养基或琥珀酸基本培养基中生长的大肠杆菌ML308培养物转移到支持平衡倍增时间为17.4分钟的非常丰富的培养基后立即生长的动力学。得出的结论是,在非常丰富的培养基中,核糖体参与蛋白质合成的效率高于在两种基本培养基中,这两种基本培养基在37℃时分别支持43分钟和65分钟的倍增时间。