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N-acetyl-(L-Ala) 3 -p-nitroanilide as a new chromogenic substrate for elastase
Authors:G Feinstein  A Kupfer  M Sokolovsky
Affiliation:Department of Biochemistry, Tel Aviv University, Tel Aviv, Israel.
Abstract:The introduction of a useful new chromogenic substrate for the determination of elastase (EC 3.4.4.7) activity is described. N-acetyl-L-Ala-L-Ala-L-Ala-p-nitroanilide (AcAla3NA) is a new specific elastase substrate whose hydrolysis can be followed spectrophotometrically at 410 nm in a wide pH range. Its rate of hydrolysis by α-chymotrypsin (EC 3.4.4.5) and trypsin (EC 3.4.4.4.) is 0.02% and 0.001% respectively compared to its rate of hydrolysis by elastase. As little as 0.1 μg elastase/ml can be satisfactorily determined. At pH 8, Km = 0.88 mM and kcat = 11.9 sec?1.
Keywords:AcAlaOMe  N-acetyl-L-ala methyl ester  BzAlaOMe  N-benzoyl-L-Ala methyl ester  N-acetyl-L-Ala-L-Ala-L-Ala methyl ester  N-acetyl-L-Ala-L-Ala-L-Alaninamide  BocAlaNP  ZAlaNP
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