Kinetic assay for inorganic phosphates and composition therefore

Claim 2

A reagent system for an inorganic phosphate assay comprising: (a) maltose; (b) maltose phosphorylase; (c) a co-enzyme selected from a group consisting of beta-nicotinamide-adenine dinucleotide, beta-nicotinamide-adenine dinucleotide phosphate, and mixtures thereof; (d) glucose-6-phosphate dehydrogenase; (e) beta-D-phosphoglucomutase; wherein the above are present in amounts such that the inorganic phosphate to be assayed is the limiting component, and (f) a non-phosphate buffer having a pH of from about 6 to about 8.

Claim 3

The reagent system of claim 1 wherein said buffer is selected from a group consisting of piperzin-N ,N'-bis(2-ethanesulfonic acid), N,N-bis(2-hydroxyethyl)-2-aminoethane-sulphanic acid, triethanolamine.HCl, and tris(hydroxymethyl) aminomethane.

Claim 4

The reagent system of claim 1 further comprising glucose-1,6-diphosphate.

Claim 5

The reagent system of claim 3 further comprising 6-phosphogluconate dehydrogenase.

Claim 6

The reagent system of claim 3 further comprising a cation selected from a group consisting of Mn +2 , Mg +2 , Co +2 , Zn +2 , Ni +2 , and mixtures thereof.

Claim 7

The reagent system of claim 3 further comprising 6-phosphogluconate dehydrogenase and a cation selected from a group consisting of Mn +2 , Mg +2 , Co +2 , Zn +2 , Ni +2 , and mixtures thereof.

Claim 8

The reagent system of claim 6 wherein said cation is selected from the group consisting of Mg +2 , Mn +2 , Co +2 , and mixtures thereof.

Claim 9

The reagent system of claim 7 wherein aid glucose-1,6-diphosphate consists essentially of the beta form thereof.

Claim 10

The reagent system of claim 1 wherein said reagents are present in amounts such that the inorganic phosphate to be assayed is rate-limiting so that the reagent system is a kinetic reagent system.

Claim 11

The kinetic reagent system of claim 9 for an inorganic phosphate assay comprising per liter of reagent: (a) about 50 millimoles of N,N-bis-(2-hydroxyethyl)-2-aminoethane-sulphanic acid; (b) about 13.9 millimoles of maltose (c) about 2 millimoles of magnesium chloride; (d) about 2 millimoles of said co-enzyme; (e) about 1600 International Units of maltose phosphorylase; (f) about 400 International Units of β-phosphoglucomutase; (g) about 700 International Units of 6-phosphogluconate dehydrogenase; (h) about 5000 International Units of glucose-6-phosphate dehydrogenase; and (i) about 0.05 millimole of sodium glucose-1,6-diphosphate.

Claim 12

The reagent system of claim 1 wherein maltose and said co-enzyme are present in molar excess of the inorganic phosphate to be assayed so that said reagent system is an end-point reagent system.

Claim 13

The end-point reagent system of claim 11 for an inorganic phosphate assay comprising per liter of reagent: (a) about 50 millimole of piperazin-N,N' -bis)2-ethanesulfonic acid); (b) about 13.9 millimoles of maltose; (c) about 1.6 millimoles of said co-enzyme; (d) about 2 millimoles of magnesium chloride; (e) about 0.05 millimole of sodium glucose-1,6-diphosphate; (f) about 3000 International Units of maltose phosphorylase; (g) about 600 International Units of β-phosphoglucomutase; and (h) about 5000 International Units of glucose-6-phosphate dehydrogenase.

Claim 14

An inorganic phosphate assay comprising: (a) performing coupled reactions, at a pH of from about 6 to about 8, which comprise: (i) reacting maltose with an inorganic phosphate specimen in the presence of maltose phosphorylase to form glucose and β-D-glucose-1-phosphate; (ii) reacting β-D-glucose-1-phosphate in the presence of β-D-phosphoglucomutase to form glucose-6-phosphate; and (iii) reacting glucose-6-phosphate in the presence of glucose-6-phosphate dehydrogenase and a co-enzyme selected from a group consisting of β-nicotinamide-adenine dinucleotide, β-nicotinamide-adenine dinucleotide phosphate and mixtures thereof to form the reduced form of said co-enzyme and 6-phosphogluconate; and (b) measuring the production of said reduced co-enzyme, wherein the inorganic phosphate being measured is the limiting component and wherein a non-phosphate buffer is used to control said pH.

Claim 15

An inorganic phosphate assay comprising: (a) performing coupled reactions, at a pH of from about 6 to about 8, which comprise: (i) reacting maltose with an inorganic phosphate specimen in the presence of maltose phosphorylase to form glucose and β-D-glucose-1-phosphate; (ii) reacting β-D-glucose-1-phosphate in the presence of β-D-phosphoglucomutase to form glucose-6-phosphate; and (iii) reacting glucose-6-phosphate in the presence of glucose-6-phosphate dehydrogenase and a co-enzyme selected from a group consisting of β-nicotinamide-adenine dinucleotide, β-nicotinamide-adenine dinucleotide phosphate and mixtures thereof to form the reduced form of said co-enzyme and 6-phosphogluconate; and (b) measuring the production of said reduced co-enzyme, wherein the inorganic phosphate being measured is the limiting component and wherein a non-phosphate buffer is used to control said pH.

Claim 16

The inorganic phoshate assay of claim 13 wherein said β-D-glucose-1-phosphate is reacted in the presence of β-D-phosphoglucomutase and glucose-1,6-diphosphate to form glucose-6-phosphate.

Claim 17

The inorganic phosphate assay of claim 14 wherein said β-D-glucose-1-phosphate is reacted in the presence of β-D-phosphoglucomutase, glucose-1,6-diphosphate and a cation selected from a group consisting of Mn +2 , Mg +2 , Co +2 , Zn.sup.°2, Ni +2 , and mixtures thereof to form glucose-6-phosphate.

Claim 18

The inorganic phosphate assay of claim 15 wherein the total production of said reduced co-enzyme is measured and wherein maltose and said co-enzyme are present in molar excess of the inorganic phosphate to be assayed.

Claim 19

The inorgaic phosphate assay of claim 15 wherein the rate of production of said reduced co-enzyme is measured and wherein the inorganic phosphate being measured is rate-limiting.

Claim 20

The inorganic phosphate assay of claim 17 further comprising: reacting 6-phosphogluconate in the presence of said co-enzyme and 6-phosphogluconate dehydrogenase to form the reduced form of said co-enzyme, ribulose-5-phosphate and CO 2 .