Construction of new variants of dextransucrase DSR-S by genetic engineering
The present invention relates to a recombinant process for the production of truncated or mutated dextransucrases while conserving the enzymatic activity or their specificity in the synthesis of the α-1,6 bonds. The present invention relates to nucleic acid sequences of truncated or mutated dextransucrases, vectors containing the nucleic acid sequences and host cells transformed by sequences encoding truncated or mutated dextransucrases. In another aspect, the invention concerns a method for producing, in a recombinant manner, truncated or mutated dextransucrases which conserve their enzymatic activity or which conserve their specificity in the synthesis of α-1,6 bonds and can produce, from saccharose, dextrans with high molar mass and modified rheological properties compared with the properties of dextran obtained with the native enzyme and isomalto-oligosaccharides with a controlled molar mass and dextrans. The dextrans and isomalto-oligosaccharides of the invention can be used namely as texturing agents or as prebiotics.
1. A prebiotic composition comprising dextrans with a controlled size of 1,300 to 5,200 Da centered around 10,000 Da, dextrans with a controlled size of 7,000 to 1.7×10 5 Da centered around 40,000 Da, dextrans with a high molar mass of 2×10 6 Da to 10 9 Da or isomalto-oligosaccharides of 342 to 5,000 Da having a degree of polymerization of 2 to 60 glycosyl units and a food quality vehicle, wherein said dextrans or isomalto-oligosaccharides are obtained by reacting sucrose with a dextransucrase consisting of SEQ ID NOs 6, 7, 8, 9 or 10.
2. The prebiotic according to claim 1 , wherein said dextrans with a high molar mass have non-Newtonian behavior.
3. A prebiotic composition comprising a dextran with a controlled molar mass obtained by reacting sucrose with a dextransucrase consisting of a fragment of said dextransucrase of SEQ ID NO:6 from amino acid at position 125 to amino acid at position 1423, SEQ ID NO:7 from amino acid at position 125 to amino acid at position 1335, SEQ ID NO:8 from amino acid at position 125 to amino acid at position 1136, SEQ ID NO:9 from amino acid at position 125 to amino acid at position 1006, or SEQ ID NO:10 from amino acid at position 125 to amino acid at position 1423.
4. The prebiotic composition according to claim 3 , further comprising reacting said dextransucrase with at least one acceptor.
5. The prebiotic composition according to claim 4 , wherein the at least one acceptor is glucose, isomalto-oligosaccharides, maltose or isomalto-oligosaccharides.
6. A prebiotic composition comprising an isomaltose-oligosaccharide with a controlled molar mass obtained by reacting sucrose with a dextransucrase consisting of SEQ ID NOs 6, 7, 8, 9 or 10.
7. The prebiotic composition according to claim 3 , further comprising reacting said dextransucrase with at least one acceptor.
8. The prebiotic composition according to claim 7 , wherein the at least one acceptor is glucose, isomalto-oligosaccharides, maltose or isomalto-oligosaccharides.
9. A prebiotic composition comprising dextrans with a controlled size of 1,300 to 5,200 Da centered around 10,000 Da, dextrans with a high molar mass of 2×10 6 Da to 10 9 Da or isomalto-oligosaccharides of 342 to 5,000 Da, wherein said dextrans or isomalto-oligosaccharides are obtained by reacting sucrose with a dextransucrase consisting of SEQ ID NOs 6, 7, 8, 9 or 10.
10. A prebiotic composition comprising dextrans with a controlled size of 1,300 to 5,200 Da centered around 10,000 Da, dextrans with a controlled size of 7,000 to 1.7×10 5 Da centered around 40,000 Da, dextrans with a high molar mass of 2×10 6 Da to 10 9 Da or isomalto-oligosaccharides of 342 to 5,000 Da having a degree of polymerization of 2 to 60 glycosyl units, said dextrans have non-Newtonian behavior, wherein said dextrans or isomalto-oligosaccharides are obtained by reacting sucrose with a dextransucrase consisting of SEQ ID NOs 6, 7, 8, 9 or 10.