The Institute for Cancer Research, Fox Chase Center for Cancer and Medical Sciences, Philadelphia, Pennsylvania 19111.
Plant Physiol. 1974 Jan;53(1):83-7. doi: 10.1104/pp.53.1.83.
When a stationary phase cell culture of Arachis hypogaea L. is diluted into fresh media, there occurs a 10-fold increase in the rate of protein synthesis. The kinetics of the activation of amino acid-incorporating capacity show a lag of 10 to 15 minutes with maximal activity reached at 2 hours after dilution. The activation of protein synthesis is oxygen-dependent and is accompanied by a 2- to 4-fold increase in polyribosome content, as well as by a 3- to 4-fold increase in the rate of mRNA synthesis. Ribosomal function, as ascertained by determination of ribosomal transit time, is about 2.5 times more efficient in 2-hour diluted cultures as in cells immediately after dilution. These observations indicate that a very early response in the transition of plant cell cultures from the stationary state is an increased capacity for protein synthesis. At a molecular level, this increase in protein synthetic capacity is due in part to an increased mobilization of mRNA into polyribosomes and in part to a more efficient ribosomal translational capacity.
当落花生(Arachis hypogaea L.)的固定相细胞培养物被稀释到新鲜培养基中时,蛋白质合成的速度会增加 10 倍。氨基酸掺入能力的激活动力学显示出 10 到 15 分钟的延迟,最大活性在稀释后 2 小时达到。蛋白质合成的激活是氧依赖性的,并伴随着多核糖体含量增加 2-4 倍,以及 mRNA 合成速率增加 3-4 倍。核糖体功能的测定表明,在 2 小时稀释培养物中的核糖体转移时间比细胞刚稀释后的核糖体转移时间效率高约 2.5 倍。这些观察结果表明,植物细胞培养物从静止状态过渡的早期反应是蛋白质合成能力的增加。在分子水平上,这种蛋白质合成能力的增加部分归因于 mRNA 向多核糖体的更多动员,部分归因于核糖体翻译能力的提高。