A radiochemical assay for argininosuccinate synthetase with [U-14C]aspartate
β Scribed by Sarah Ratner
- Book ID
- 102984873
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 901 KB
- Volume
- 135
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
A simple and sensitive radiochemical procedure to assay argininosuccinate synthetase activity in crude tissue homogenates and lysates of cultured cells is described. The new method depends on the location of 14C, uniformly, in the four carbons of aspartate. On incubation in the presence of excess of L-[U-14C]aspartate, L-citrulline, ATP, and an ATP-generating system, argininosuccinase and arginase, the [14C]fumarate formed is measured as the sum of malate and fumarate. After acidification the latter two acids are separated from [14C]aspartate on a small Dowex-50 column by elution with a few milliliters of water; the unutilized amino acid substrates remain on the column. With a specific radioactivity of 9 X 10(4) cpm, 1 to 2 nmol of product can be accurately measured under kinetically optimum conditions.
π SIMILAR VOLUMES
A radiochemical assay was developed to measure the activity of β€-ureidopropionase in human liver homogenates which is based on the detection of the reaction product 14 CO 2 by liquid scintillation counting. Radiolabeled N-carbamyl-β€-alanine was prepared within 15 min by a simple hydrolysis of [2-14
&Aminolevulinic acid (ALA) synthetase activities in the range of 0.1 to 100 U/ml of enzyme are routinely assayed using a modified Beckman Model 121 amino acid analyzer. This method reproducibly and specifically quantitates [Wlaminolevulinate from a mixture of [Wlsuccinate metabolites known to interf