Method for obtaining soluble fibres enzymatically
OwnerPierre LANOS, Matthieu RAMETTE +4inventors
InventorsPierre LANOS, Matthieu RAMETTE, Magali REMAUD-SIMEON, Claire MOULIS, Sandra PIZZUT-SERIN, Etienne SEVERAC
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Abstract
A method for preparing a mixture of poorly-digestible alpha-glucans from a substrate rich in oligosaccharides having a degree of polymerization (DP) of 4.
Claims15
A method for preparing a mixture of a-glucans comprising the following steps:
- providing a substrate, said substrate being a mixture of oligosaccharides and polysaccharides having a polydispersity index of between 5 and 10, preferably between 6 and 9.5, even more preferably between 7 and 9, between 8 and 8.5, most preferably about 8.4,
- a first incubation in the presence of a first enzyme,
- a second incubation with a second enzyme,
- said first and second enzymes being an α-glucanotransferase capable of cleaving alpha (1,4) glycosidic bonds and creating α(1,3) glycosidic bonds and/or an α-glucanotransferase capable of cleaving α(1,4) glycosidic bonds and creating α(1,6) glycosidic bonds.
The method according to any one of the preceding claims, wherein the substrate is introduced at a concentration of between 50 g/L and 500 g/L, preferably between 100 g/L and 200 g/L of reaction medium.
The method according to any one of the preceding claims, wherein the substrate is added between the first and second incubations.
The method according to any one of the preceding claims, wherein the first enzyme is an α-glucanotransferase capable of cleaving the α(1,4) glycosidic bonds and creating α(1,3) glycosidic bonds and the second enzyme is an α-glucanotransferase capable of cleaving the α(1,4) glycosidic bonds and creating α(1,6) glycosidic bonds.
The method according to any one of the preceding claims, wherein the α-glucanotransferase capable of cleaving the α(1,4) glycosidic bonds and creating α(1,6) glycosidic bonds is the protein having the sequence SEQ ID No:
- 1 or a protein having at least 90% identity with the protein having SEQ ID No:
- 1.
The method according to any one of the preceding claims, wherein the α-glucanotransferase capable of cleaving the α(1,4) glycosidic bonds and of creating α(1,3) glycosidic bonds is the protein having the sequence SEQ ID No:
- 2 or a protein having at least 90% identity with the protein having the sequence SEQ ID No:
- 2.
The method according to any one of the preceding claims, wherein each enzyme is at a concentration of between 0.01 and 1 mg/ml of reaction medium, preferably between 0.05 and 0.5 mg/mL, even more preferably approximately 0.1 mg/ml of reaction medium.
The method according to any one of the preceding claims, characterized in that each incubation is carried out for a period of between 12 and 48 hours, preferably approximately 24 hours and/or at a temperature comprised between 2° and 40° C., preferably approximately 37° C. and/or at a pH of between 5 and 6.5, preferably approximately 5.75.
A mixture of α-glucans capable of being obtained by the method according to any one of the preceding claims.
A mixture of α-glucans characterized in that it has:
- a content of hydrolyzable fibers less than 45%, by weight relative to the total weight of dry matter,
- and/or at least 20% of a (1,6) bonds,
- and/or at least 3% of a (1,3) bonds,
- wherein the fiber content corresponds to the hydrolyzable (i.e. non-resistant) fraction according to the AOAC 2002.02 method and the percentage of α(1,6) and α(1,3) bonds represents the molar percentage of α(1,6) and α(1,3) bonds respectively relative to the total number of glycosidic bonds, measured by the Hakomori method.
Sequential use of a glucanotransferase capable of cleaving the α(1,4) glycosidic bonds and of creating α(1,6) glycosidic bonds and of a glucanotransferase capable of cleaving the α(1,4) glycosidic bonds and of creating α(1,3) glycosidic bonds to reduce the digestibility of a mixture of α-glucans, said glucanotransferases respectively having the sequence SEQ ID No:
- 1 or a protein having at least 90% identity with the protein having SEQ ID No:
- 1 and SEQ ID No:
- 2 or a protein having at least 90% identity with the protein having SEQ ID No:
- 2.
Dependencies are inferred from the claim text.