Coenzyme-linked glucose dehydrogenase and polynucleotide encoding the same
The present invention provides members that produce on a large scale a coenzyme-linked glucose dehydrogenase which has excellent substrate-recognizing ability toward glucose while providing low action on maltose. The present invention relates to a polynucleotide encoding a soluble coenzyme-linked glucose dehydrogenase that catalyzes the oxidation of glucose in the presence of an electron acceptor and has an activity toward maltose of 5% or lower; a polypeptide encoded by the nucleotide sequence of the polynucleotide; a recombinant vector carrying the polynucleotide; a transformed cell produced using the recombinant vector; a method for producing a polypeptide comprising culturing the transformed cell and collecting from the cultivated products a polypeptide that links to FAD to exert the glucose dehydration activity; a method for determination of glucose using the polypeptide; a reagent composition for determination of glucose; and a biosensor.
1. A method for producing a recombinant glucose dehydrogenase (GLD) comprising:
(i) providing a transformed fungal or yeast host cell comprising a recombinant expression vector comprising a nucleic acid encoding a GLD comprising the sequences set forth in SEQ ID NOs. 8 to 12, wherein SEQ ID NO:8 is GGGTSGLVVANRLSE, SEQ ID NO:10 is SPLILELSGVGNP, and SEQ ID NO:12 is LLPFARGNIHI; culturing the transformed host cell;
(ii) recombinantly expressing the GLD: and
(iii) collecting recombinant GLD secreted from the transformed host cell.
2. The method of claim 1 , wherein the recombinant GLD has an activity toward maltose of 5% or less with respect to its activity toward glucose.
3. The method of claim 1 , wherein the recombinant GLD has a total content of galactose, glucose, mannose, and arabinose of 10 μg or less per μg of protein.
4. The method of claim 1 , wherein the recombinant GLD has a total content of galactose, glucose, mannose, and arabinose of 2 μg or less per μg of protein.
5. The method of claim 1 , wherein the transformed host cell is a fungal cell.
6. The method of claim 1 , wherein the transformed host cell is a yeast cell.
7. The method of claim 5 , wherein the collecting of the recombinant GLD comprises isolating the recombinant GLD from culture medium containing the recombinant GLD secreted outward of a fungus body.
8. The method of claim 1 , wherein the recombinant GLD is an Aspergillus species GLD.
9. The method of claim 8 , wherein the recombinant GLD is an Aspergillus oryzae species GLD.
10. The method of claim 9 , wherein SEQ ID NO:9 is RAGKALGGTSTINGMAYTRAEDVQID.
11. The method of claim 1 , wherein the recombinant GLD has at least 90% homology to the sequence set forth in residues 20 to 592 of SEQ ID NO:2.