Modified α-glucosidase and applications of same
The object is to provide an α-glucosidase in which a transglycosylation activity predominates, and use thereof, and the like. A modified α-glucosidase consisting of an amino acid sequence in which one or two or more of the amino acid(s) is selected from a group of specific amino acids.
1. A modified α-glucosidase which (a) consists of an amino acid sequence which is identical to SEQ ID NO: 2 except for a substitution at a position corresponding to position 343 of SEQ ID NO: 2, or (b) comprises an amino acid sequence which has 95% or more identity with SEQ ID NO: 2 and comprises a substitution corresponding to position 343 of SEQ ID NO: 2,
wherein the amino acid at position 343 is substituted by a cysteine, aspartic acid, methionine, histidine, alanine, phenylalanine, glycine, threonine, glutamic acid, valine, glutamine, asparagine or isoleucine, and
wherein the modified α-glucosidase has at least one of: improved transglycosylation activity compared to the α-glucosidase of SEQ ID NO: 2, and decreased hydrolysis activity compared to the α-glucosidase of SEQ ID NO: 2.
2. The modified α-glucosidase according to claim 1 , wherein said α-glucosidase consists of the amino acid sequence of SEQ ID No: 20.
3. An enzyme agent comprising the modified α-glucosidase according to claim 2 .
4. A pharmaceutical composition, a composition, a cosmetic composition, a food composition or a feed composition, comprising the modified α-glucosidase according to claim 2 .
5. The α-glucosidase according to claim 2 , having a transglycosylation activity to form α-1,4 or α-1,6 glucosidic linkages.
6. The modified α-glucosidase according to claim 1 , wherein said α-glucosidase (a) consists of the amino acid sequence of SEQ ID No: 20, or (b) comprises an amino acid sequence which has 95% or more identity with the sequence of SEQ ID NO: 20.
7. The modified α-glucosidase according to claim 1 , wherein said α-glucosidase (a) consists of the amino acid sequence of SEQ ID NO.: 20 or (b) comprises an amino acid sequence which has 98% or more identity with the sequence of SEQ ID NO.: 20.
8. The modified α-glucosidase of claim 1 , wherein said modified α-glucosidase comprises an amino acid sequence which has 95% or more identity with SEQ ID NO: 2 and comprises a substitution corresponding to position 343 of SEQ ID NO: 2, wherein the amino acid at position 343 is substituted by a cysteine, aspartic acid, methionine, histidine, alanine, phenylalanine, glycine, threonine, glutamic acid, valine, glutamine, asparagine or isoleucine, wherein the modified α-glucosidase has at least one of: improved transglycosylation activity compared to the α-glucosidase of SEQ ID NO: 2, and decreased hydrolysis activity compared to the α-glucosidase of SEQ ID NO: 2, and wherein said modified α-glucosidase further comprises one or more amino acid substitutions at an amino acid selected from the group consisting of:
(i) an amino acid corresponding to the amino acid at position 452 of SEQ ID NO: 2;
(ii) an amino acid corresponding to the amino acid at position 496 of SEQ ID NO: 2;
(iii) an amino acid corresponding to the amino acid at position 410 of SEQ ID NO: 2;
(iv) an amino acid corresponding to the amino acid at position 495 of SEQ ID NO: 2;
(v) an amino acid corresponding to the amino acid at position 498 of SEQ ID NO: 2;
(vi) an amino acid corresponding to the amino acid at position 499 of SEQ ID NO: 2;
(vii) an amino acid corresponding to the amino acid at position 531 of SEQ ID NO: 2;
(viii) an amino acid corresponding to the amino acid at position 533 of SEQ ID NO: 2;
(ix) an amino acid corresponding to the amino acid at position 579 of SEQ ID NO: 2;
(x) an amino acid corresponding to the amino acid at position 585 of SEQ ID NO: 2;
(xi) an amino acid corresponding to the amino acid at position 662 of SEQ ID NO: 2;
(xii) an amino acid corresponding to the amino acid at position 715 of SEQ ID NO: 2; and
(xiii) an amino acid corresponding to the amino acid at position 721 of SEQ ID NO: 2.
9. The modified α-glucosidase of claim 8 , wherein the modified α-glucosidase comprises a substitution at an amino acid corresponding to the amino acid at position 452 of SEQ ID NO: 2, and the amino acid after the substitution is glycine, aspartic acid or glutamic acid.
10. The modified α-glucosidase of claim 8 , wherein the modified α-glucosidase comprises a substitution at an amino acid corresponding to the amino acid at position 496 of SEQ ID NO: 2, and the amino acid after the substitution is valine, asparagine or glutamine.
11. The modified α-glucosidase of claim 8 , wherein the amino acid corresponding to position 343 of SEQ ID NO: 2 is substituted with aspartic acid, and wherein the amino acid corresponding to position 452 of SEQ ID NO: 2 is substituted with alanine or glycine.
12. The modified α-glucosidase of claim 8 , wherein the amino acid corresponding to position 343 of SEQ ID NO: 2 is substituted with aspartic acid or methionine, and wherein the amino acid corresponding to position 496 of SEQ ID NO: 2 is substituted with isoleucine, arginine, cysteine or threonine.
13. The modified α-glucosidase of claim 8 , wherein the modified α-glucosidase comprises a substitution at an amino acid corresponding to the amino acid at position 495 of SEQ ID NO: 2, and the amino acid after the substitution is glycine, proline or valine.
14. The modified α-glucosidase of claim 8 , wherein the modified α-glucosidase comprises a substitution at an amino acid corresponding to the amino acid at position 498 of SEQ ID NO: 2, and the amino acid after the substitution is leucine or serine.
15. A method for producing an oligosaccharide comprising reacting the modified α-glucosidase of claim 1 with an oligosaccharide or polysaccharide having an α-1,4 glucosidic linkage.
16. A method for producing an oligosaccharide comprising reacting the modified α-glucosidase of claim 13 with an oligosaccharide or polysaccharide having an α-1,6 glucosidic linkage.