A new method for the determination of adenine phosphoribosyltransferase (APRT) activity in human erythrocytes is described. APRT activity was assayed by a non-radiochemical method in which adenosine mnnophosphate (AMP) and AMY metabolites produced from a substrate adenine were converted to inosine b
Determination of nicotinamide phosphoribosyltransferase activity in human erythrocytes: High-performance liquid chromatography-linked method
β Scribed by Marina Rocchigiani; Vanna Micheli; John A. Duley; H. Anne Simmonds
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 326 KB
- Volume
- 205
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
A radiochemical reverse-phase-high-performance liquid chromatography-linked method to measure the activity of nicotinamide phosphoribosyltransferase (EC 2.4.2.12) in crude lysates of human red blood cells is described. The apparent Km for nicotinamide was in the micromolar range, much lower than that described in human erythrocytes in the past. The enzyme activity in crude hemolysates was found to be extremely low (21 +/- 3.5 nmol x h-1 x g-1 Hb); nevertheless, the low Km for nicotinamide might account for the production of pyridine nucleotides reported by us for intact erythrocytes incubated at low, physiological concentrations of this substrate.
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A method for the measurement of erythrocyte 5-phosphoribosyl 1-pyrophosphate (PP-ribose-P) using HPLC is described. lnosinic acid formed from the enzyme-catalyzed reaction of hypoxanthine and PP-ribose-P using partially purified hypoxanthine-guanine phosphoribosyltransferase is measured after chroma
## Abstract A reversedβphase HPLC method for the analysis of cephalexin (7β[(aminophenylacetyl)amino]β3βmethylβ8βoxoβ5βthiaβ1βazabicyclo[4.2.0]octβ2βeneβ2βcarboxylic acid) by isocratic separation is described. A comparison is made between the ultrafiltration land the extraction procedure developed