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Kinetics of Accumulation of Ribulose-1,5-bisphosphate Carboxylase during Greening in Euglena gracilis1: Nutritional Regulation

机译:裸眼藻绿化过程中1,5-双磷酸核糖1,5-二磷酸羧化酶积累的动力学:营养调控

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摘要

The accumulation of ribulose-1,5-bisphosphate carboxylase (RuBPCase) in resting Euglena gracilis strain Z during greening is photo-regulated (Freyssinet, Eichholz, Buetow 1984 Plant Physiol 75: 850-857. Greening resting cells are not photosynthetically competent for about the first 24 hours in the light. Therefore, substrates for a net synthesis of the enzyme must come from endogenous constituents. During this time, degradation of endogenous paramylum (carbohydrate) reserves provides the main source of substrates. By about 24 hours of greening, resting cells are photosynthetically competent and RuBPCase accumulation becomes highly sensitive to 3-(3,4 dichlorophenyl)-1,1-dimethylurea. Therefore, from about 24 hours of greening onward, substrates (and/or energy) for RuBPCase synthesis are provided by photosynthesis. Ethanol, a nutritional substrate ordinarily used constitutively by Euglena for growth, inhibits RuBPCase accumulation when added to the resting medium in the light. The alcohol exerts this negative regulatory effect by limiting the availability of substrates needed for a net synthesis of the enzyme.
机译:绿化过程中静止的Euglena gracilis菌株Z中核糖1,5-双磷酸羧化酶(RuBPCase)的积累受到光调节(Freyssinet,Eichholz,Buetow 1984 Plant Physiol 75:850-857。绿化的静止细胞不能光合作用约在光照下的最初24小时内,因此,用于酶的净合成的底物必须来自内源性成分。在这段时间内,内源性副淀粉(碳水化合物)储备的降解提供了底物的主要来源。静止细胞具有光合作用能力,RuBPCase的积累对3-(3,4二氯苯基)-1,1-二甲基脲高度敏感,因此,从大约24小时的绿化开始,RuBPCase的合成所需的底物(和/或能量)由光合作用:乙醇是Euglena通常用于生长的营养底物,当添加到光照下的静止培养基中时,它会抑制RuBPCase的积累。通过限制酶的净合成所需的底物的可用性,Ol1发挥了这种负调节作用。

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