Rodrigues L E, Gonnard P
Rev Bras Pesqui Med Biol. 1977 Jun;10(3):181-6.
Using the cytoplasmic soluble fraction from rat brain as a source of glutamate decarboxilase, its enzymatic activity was induced by electrical stimulation and determined by gas release. Modified Warburg's flasks were used for such determination. The limits of frequency and the use of sinusoidal waves were based on normal cerebral rhythms. At low frequencies, GAD activity is markedly enhanced (1-10 Hz, 2v, 500 muA). Activation of the enzyme may be due to distortion of the tertiary structure promoting thus an increased coupling between the substrate and the enzyme complex.
以大鼠脑细胞质可溶部分作为谷氨酸脱羧酶的来源,其酶活性通过电刺激诱导,并通过气体释放来测定。采用改良的瓦氏呼吸瓶进行该测定。频率极限和正弦波的使用基于正常脑节律。在低频时,谷氨酸脱羧酶活性显著增强(1 - 10赫兹,2伏,500微安)。酶的激活可能是由于三级结构的扭曲,从而促进了底物与酶复合物之间更强的结合。