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饥饿诱导纤毛虫斯坦尼科尔波虫中包囊壁蛋白的合成。

Induction of cyst coat protein synthesis by starvation in the ciliate Colpoda steinii.

作者信息

Tibbs J

出版信息

Biochem J. 1971 Sep;124(2):419-26. doi: 10.1042/bj1240419.

Abstract
  1. At 28 degrees C, synthesis of protein cyst coat in ciliates of Colpoda steinii is induced by washing with water and, as judged by glutamic acid assays and incorporation studies with l-[U-(14)C]leucine, starts about 30min after the cells have stopped swimming and is largely complete 90min later. During this time up to 70% of the protein synthesized by the cell is coat protein. 2. When cells were placed in l-[U-(14)C]leucine at low concentrations (0.25-0.76mm) during the period of coat synthesis there was no lag in uptake. Only a small proportion of the leucine incorporated into the coat was from the external substrate, implying that the rate of radioactive isotope incorporation measured the rate of transport of amino acid into the cell. Transport of l-[U-(14)C]leucine into the cell was markedly stimulated by l-glutamic acid and l-lysine. 3. When cells were placed in l-[U-(14)C]leucine at high concentrations (38mm) the rate of incorporation was considered to measure the rate of protein synthesis, but because the latter may have been affected by substrate it is concluded that such measurements are of doubtful value.
摘要
  1. 在28摄氏度时,用水冲洗可诱导斯坦尼肾形虫纤毛虫合成蛋白质囊膜,通过谷氨酸测定和用l-[U-(14)C]亮氨酸进行掺入研究判断,合成在细胞停止游动后约30分钟开始,并在90分钟后基本完成。在此期间,细胞合成的蛋白质中高达70%是囊膜蛋白。2. 在囊膜合成期间,当细胞置于低浓度(0.25 - 0.76毫米)的l-[U-(14)C]亮氨酸中时,摄取没有滞后现象。掺入囊膜的亮氨酸中只有一小部分来自外部底物,这意味着测量的放射性同位素掺入速率反映了氨基酸进入细胞的运输速率。l-[U-(14)C]亮氨酸进入细胞的运输受到l-谷氨酸和l-赖氨酸的显著刺激。3. 当细胞置于高浓度(38毫米)的l-[U-(14)C]亮氨酸中时,掺入速率被认为反映了蛋白质合成速率,但由于后者可能受到底物的影响,因此得出结论,此类测量的价值存疑。

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