Reagents for the determination of enzymes

Claim 2

A reagent for the temperature-independent determination of an enzyme in a sample containing same, comprising: a substrate capable of releasing p-nitrophenol at a rate proportional to the amount of enzyme in the sample, said substrate selected from the group consisting of p-nitrophenyl derivatives of mono and oligosaccharides and mixtures thereof; and a buffer which affects the release of p-nitrophenol from said substrate at a temperature-independent rate, said buffer selected from the group consisting of 2-(N-morpholino)ethanesulfonic acid, N-(2-acetamido)aminodiacetic acid, 1,3-bis(tris(hydroxymethyl)methylamino)propane, N-(2-acetamido)-2-aminoethanesulfonic acid, 3-(N-morpholino)propanesulfonic acid, N-tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid, N-2-hydroxyethylpiperazine-N'-3-propanesulfonic acid, N-tris(hydroxymethyl)methylglycine,N,N-bis(2-hydroxyethyl)glycine, cyclohexylaminoethanesulfonic acid, and mixtures thereof.

Claim 3

A reagent according to claim 1 wherein said enzyme is α-amylase and said substrate is selected from the group represented by the formula ##STR3## where n is 0 to 5, and mixtures of such substrates.

Claim 4

A reagent according to claim 2 further comprising a maltase.

Claim 5

A reagent according to claim 3 wherein the maltase is α-glucosidase.

Claim 6

A reagent according to claim 1 wherein the enzyme is α-glucosidase and the substrate is selected from the group represented by the formulas ##STR4## and mixtures thereof.

Claim 7

A reagent according to claim 1 wherein the enzyme is β-glucosidase and the substrate is selected from the group represented by the formulas ##STR5## and mixtures thereof.

Claim 8

A process for determining an enzyme in a sample containing same, comprising: (1) adding to said sample, a reagent comprising: a substrate capable of releasing p-nitrophenol at a rate proportional to the amount of enzyme in the sample, said substrate selected from the group consisting of p-nitrophenyl derivatives of mono and oligosaccharides and mixtures thereof; and a buffer which affects the release of p-nitrophenol from said substrate at a temperature-independent rate, said buffer selected from the group consisting of 2-(N-morpholino)ethane-sulfonic acid, N-(2-acetamido)aminodiacetic acid, 1,3-bis(tris(hydroxymethyl)methylamino)propane,N-(2-acetamido)-2-aminoethanesulfonic acid, 3-(N-morpholino)propanesulfonic acid, N-tris(hydroxy-methyl)methyl-2-aminoethanesulfonic acid, N-2-hydroxyethylpiperazine-N'-3-propanesulfonic acid, N-tris(hydroxymethyl)methylglycine,N,N-bis(2-hydroxyethyl) glycine, cyclohexylaminoethane-sulfonic acid, and mixtures thereof and (2) determining the enzyme activity by the release of p-nitrophenol.

Claim 9

A process for determining an enzyme in a sample containing same, comprising: (1) adding to said sample, a reagent comprising: a substrate capable of releasing p-nitrophenol at a rate proportional to the amount of enzyme in the sample, said substrate selected from the group consisting of p-nitrophenyl derivatives of mono and oligosaccharides and mixtures thereof; and a buffer which affects the release of p-nitrophenol from said substrate at a temperature-independent rate, said buffer selected from the group consisting of 2-(N-morpholino)ethane-sulfonic acid, N-(2-acetamido)aminodiacetic acid, 1,3-bis(tris(hydroxymethyl)methylamino)propane,N-(2-acetamido)-2-aminoethanesulfonic acid, 3-(N-morpholino)propanesulfonic acid, N-tris(hydroxy-methyl)methyl-2-aminoethanesulfonic acid, N-2-hydroxyethylpiperazine-N'-3-propanesulfonic acid, N-tris(hydroxymethyl)methylglycine,N,N-bis(2-hydroxyethyl) glycine, cyclohexylaminoethane-sulfonic acid, and mixtures thereof and (2) determining the enzyme activity by the release of p-nitrophenol.