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Different Rates of Synthesis and Degradation of Two Chloroplastic Ammonium-Inducible NADP-Specific Glutamate Dehydrogenase Isoenzymes during Induction and Deinduction in Chlorella sorokiniana Cells

机译:Sorokiniana细胞诱导和还原过程中两种叶绿素铵诱导的NADP特异性谷氨酸脱氢酶同工酶的合成和降解速率不同。

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摘要

The kinetics of accumulation (per milliliter of culture) of the α- and β- subunits, associated with chloroplast-localized ammonium inducible nicotinamide adenine dinucleotide phosphate-specific glutamate dehydrogenase (NADP-GDH) isoenzymes, were measured during a 3 hour induction of synchronized daughter cells of Chlorella sorokiniana in 29 millimolar ammonium medium under photoautotrophic conditions. The β-subunit holoenzyme(s) accumulated in a linear manner for 3 hours without an apparent induction lag. A 40 minute induction lag preceded the accumulation of the α-subunit holoenzyme(s). After 120 minutes, the α-subunit ceased accumulating and thereafter remained at a constant level (i.e. steady state between synthesis and degradation). From pulsechase experiments, using 35SO4 and immunochemical procedures, the rate of synthesis of the α-subunit was shown to be greater than the β-subunit during the first 80 minutes of induction. The α- and β-subunits had different rates of degradation during the induction period (t½ = 50 versus 150 minutes, respectively) and during the deinduction period (t½ = 5 versus 13.5 minutes) after removal of ammonium from the culture. During deinduction, total NADP-GDH activity decreased with a half-time of 9 minutes. Cycloheximide completely inhibited the synthesis and degradation of both subunits. A model for regulation of expression of the NADP-GDH gene was proposed.
机译:在同步诱导3小时的诱导过程中,测量了与叶绿体定位的铵诱导型烟酰胺腺嘌呤二核苷酸磷酸特异性谷氨酸脱氢酶(NADP-GDH)同工酶相关的α-和β-亚基累积(每毫升培养物)的动力学。在光养养条件下,在29毫摩尔铵盐培养基中的Sorokiniana小球藻的子细胞。 β亚基全酶以线性方式累积3小时,没有明显的诱导滞后。 α-亚基全酶积累之前有40分钟的诱导滞后。 120分钟后,α-亚基停止积累,此后保持恒定水平(即合成和降解之间的稳态)。通过脉冲追踪实验,使用 35 SO4和免疫化学方法,在诱导的前80分钟内,α-亚基的合成速率显示大于β-亚基。从培养物中去除铵后,在诱导期(分别为t½= 50对150分钟)和在诱导期(t½= 5对13.5分钟)期间,α-和β亚基的降解速率不同。在还原过程中,总的NADP-GDH活性下降了9分钟的一半时间。环己酰亚胺完全抑制了两个亚基的合成和降解。提出了调控NADP-GDH基因表达的模型。

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