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小球藻细胞周期中核酮糖二磷酸羧化酶蛋白的积累模式和催化活性的比较及其抗原半衰期的测定。

Comparison of Patterns of Accumulation of Ribulose Bisphosphate Carboxylase Antigen and Catalytic Activity and Measurement of Antigen Half-Life during the Cell Cycle of Chlorella sorokiniana.

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville, Florida 32611.

出版信息

Plant Physiol. 1985 Nov;79(3):815-9. doi: 10.1104/pp.79.3.815.

Abstract

By use of specific immunochemical procedures, ribulose-1,5-bisphosphate carboxylase (RuBPCase), antigen and catalytic activity were shown to have coincident step-patterns of accumulation during the cell cycle of Chlorella sorokiniana. Pulse-chase studies, employing radioactive sulfate, were performed during the period of rapid accumulation of enzyme activity and during the period of constant enzyme activity in the cell cycle. No degradation of RuBPCase antigen could be detected during either of these cell cycle periods. Thus, the step-pattern of accumulation of RuBPCase activity resulted from periodic synthesis of an enzyme that was stable under steady-state cell cycle conditions. Although inhibition of protein synthesis by cycloheximide, at different times in the cell cycle in the light, resulted in rapid decay of RuBPCase activity, this loss in activity occurred without detectable loss in enzyme antigen. When synchronous cells were placed into the dark, to slow the rate of protein synthesis in the absence of cycloheximide, the levels of enzyme antigen and activity decreased by 30 and 50%, respectively, during the 10-hour dark period. Thus, in C. sorokiniana changes in RuBPCase activity do not necessarily reflect parallel changes in enzyme antigen, particularly when cell growth is perturbed by changes from steady-state cultural conditions.

摘要

利用特定的免疫化学程序,发现核酮糖-1,5-二磷酸羧化酶(RuBPCase)、抗原和催化活性在集胞藻的细胞周期中具有一致的积累阶跃模式。在酶活性快速积累的时期和细胞周期中酶活性恒定的时期进行了放射性硫酸盐脉冲追踪研究。在这两个细胞周期期间,都检测不到 RuBPCase 抗原的降解。因此,RuBPCase 活性的积累阶跃模式是由于周期性合成在稳定的细胞周期条件下稳定的酶的结果。尽管在光下的细胞周期的不同时间,用环己亚胺抑制蛋白质合成会导致 RuBPCase 活性迅速下降,但这种活性的丧失没有检测到酶抗原的明显损失。当同步细胞被置于黑暗中,以在没有环己亚胺的情况下减缓蛋白质合成的速度时,在 10 小时的黑暗期间,酶抗原和活性水平分别下降了 30%和 50%。因此,在集胞藻中,RuBPCase 活性的变化不一定反映酶抗原的平行变化,特别是当细胞生长受到从稳态培养条件的变化干扰时。

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