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茚三酮法测定大鼠脑线粒体中鸟氨酸氨基转移酶的灵敏分析方法。

A sensitive assay for ornithine amino transferase in rat brain mitochondria by ninhydrin method.

作者信息

Ravi Kumar H, Ananda S, Devaraju K S, Prakash B M, Sampath Kumar S, Suresh Babu S V, Ramachandraswamy N, Puttaraju H P

机构信息

Department of Neurochemistry, National Institute of Mental Health and Neuro Sciences, Bangalore, 560029 India ; Department of Biochemistry, Central College Campus, Bangalore University, Bangalore, 560001 India ; School of Natural Sciences, Biological Sciences, Jnanabharathi Campus, Bangalore University, Bangalore, 560056 India ; School of Natural Sciences, Biological Sciences, Jnanabharathi Campus, Bangalore University, Bangalore, 560056 Karnataka India.

出版信息

Indian J Clin Biochem. 2009 Jul;24(3):275-9. doi: 10.1007/s12291-009-0052-8. Epub 2009 Sep 16.

Abstract

To establish/develop an assay method for measuring Ornithine Aminotransferase (EC.2.6.1.13) activity using rat brain mitochondria as a source of enzyme in presence and absence of Pyridoxal Phosphate (PLP). The modified method, with the improved sensitivity, is adopted for the assay of ornithine amino transferase activity in rat brain mitochondria. The enzyme activity was measured at 620 nm, the study showed that reaction was optimum at 37°C for 30 minutes. The assay is sensitive enough to detect activity at the order of nanomoles pyrroline-5-carboxylate/mg protein/minute and can be compared as an alternative to the radio isotopic method which is more cumbersome and aminobenzaldehyde method which is less sensitive. The K(m) & V(max) shows maximum activity in the presence of Pyridoxal Phosphate (Coenzyme) concentration at 0.05mM when compared with absence of Pyridoxal Phosphate as higher the concentration of Pyridoxal Phosphate affects the affinity of the enzyme to substrate. The OAT activity in different tissues of the rat was also studied and highest activity was found in liver and kidney.

摘要

建立/开发一种测定鸟氨酸转氨酶(EC.2.6.1.13)活性的方法,该方法以大鼠脑线粒体作为酶源,分别在有和没有磷酸吡哆醛(PLP)的情况下进行。采用改进后的方法测定大鼠脑线粒体中的鸟氨酸氨基转移酶活性,该方法具有更高的灵敏度。酶活性在620nm处测定,研究表明反应在37°C下进行30分钟时最为适宜。该测定方法灵敏度足够高,能够检测到以纳摩尔吡咯啉-5-羧酸/毫克蛋白质/分钟为单位的活性,并且可以作为更繁琐的放射性同位素方法和灵敏度较低的氨基苯甲醛方法的替代方法进行比较。与没有磷酸吡哆醛时相比,当磷酸吡哆醛(辅酶)浓度为0.05mM时,K(m)和V(max)显示出最大活性,因为磷酸吡哆醛浓度越高,对酶与底物亲和力的影响越大。还研究了大鼠不同组织中的鸟氨酸转氨酶活性,发现肝脏和肾脏中的活性最高。

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