Fast reaction kinetics of enzymes having low activity in dry chemistry layers

1. A method for determining an analyte, comprising:

(a) contacting a sample containing the analyte with a diagnostic element comprising a dry reagent layer which contains:

(i) a mutated glucose dehydrogenase obtained by mutating a wild type glucose dehydrogenase from Bacillus megaterium or Bacillus subtilis , wherein the wild type glucose dehydrogenase comprises an amino acid sequence selected from the group consisting of SEQ ID NOS:2, 3 and 4, and wherein the mutated glucose dehydrogenase includes mutations at positions 170 and 252 when compared to the amino acid sequence of SEQ ID NOS:2, 3 and 4, and wherein the mutation at position 170 is an amino acid substitution to lysine and the mutation at position 252 is an amino acid substitution to leucine; and

(ii) an artificial coenzyme, wherein the artificial coenzyme is carbaNAD

(b) determining at least one of analyte presence and an amount of the analyte.

2. The method according to claim 1 , wherein the diagnostic test element includes a turnover rate of the analyte higher than a turnover rate of the analyte in a corresponding diagnostic element which comprises a corresponding wild type coenzyme instead of the artificial coenzyme.

3. The method according to claim 2 , wherein the diagnostic test element includes a turnover rate of the analyte at least 20% higher than the turnover rate of the analyte in the corresponding diagnostic element.

4. The method according to claim 1 , wherein the mutated glucose dehydrogenase has a reduced specific enzyme activity compared to a corresponding wild type dehydrogenase.

5. The method according to claim 1 , wherein the mutated glucose dehydrogenase is a nicotinamide adenine dinucleotide (NAD/NADH)-dependent mutated glucose dehydrogenase or nicotinamide adenine dinucleotide phosphate (NADP/NADPH)-dependent mutated glucose dehydrogenase.

6. The method according to claim 1 , wherein the mutated glucose dehydrogenase is obtained by mutation of the wild type glucose dehydrogenase from Bacillus subtilis having the amino acid sequence shown in SEQ ID NO:2.

7. The method according to claim 1 , wherein the mutated glucose dehydrogenase has the amino acid sequence shown in SEQ ID NO:1.

8. The method according to claim 1 , wherein the diagnostic element is one of a test tape, a test disk, a test pad, a test strip and a test strip drum.

9. The method according to claim 1 , which further includes photometrically or fluorometrically determining at least one of the analyte presence and the amount of the analyte.

10. A diagnostic element for determining an analyte, comprising a dry reagent layer which contains:

(a) a mutated dehydrogenase obtained by mutating a wild type glucose dehydrogenase comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:2, 3 and 4, and wherein the mutated glucose dehydrogenase includes mutations at positions 170 and 252 when compared to the amino acid sequence of SEQ ID NOS:2, 3 and 4, and wherein the mutation at position 170 is an amino acid substitution to lysine and the mutation at position 252 is an amino acid substitution to leucine, and

(b) an artificial coenzyme, wherein the artificial coenzyme is carbaNAD.

11. The diagnostic element according to claim 10 , wherein the mutated dehydrogenase has the amino acid sequence shown in SEQ ID NO:1.

12. The method according to claim 1 , wherein the mutated glucose dehydrogenase is obtained by mutation of the wild type glucose dehydrogenase from Bacillus megaterium having the amino acid sequence shown in SEQ ID NO:3.

13. The method according to claim 1 , wherein the mutated glucose dehydrogenase is obtained by mutation of the wild type glucose dehydrogenase from Bacillus subtilis having the amino acid sequence shown in SEQ ID NO:4.