Method for producing lacto-N-biose I and galacto-N-biose
View Patent ↗A method for producing lacto-N-biose I and galacto-N-biose inexpensively and conveniently is provided. The method for producing lacto-N-biose I or galacto-N-biose, characterized in that the method comprises causing: (i) a combination of a carbohydrate raw material with an enzyme that catalyzes phosphorolysis of the carbohydrate raw material to give α-glucose-1-phosphate; and (ii) a combination of an enzyme that converts α-glucose-1-phosphate to UDP-glucose and an enzyme that converts UDP-galactose to galactose-1-phosphate with their cofactors, and/or a combination of an enzyme (UDP-Gly synthase) that converts α-glucose-1-phosphate and UDP-galactose to UDP-glucose and α-galactose-1-phosphate, respectively, with its cofactor(s) to act in the presence of N-acetylglucosamine or N-acetylgalactosamine, phosphoric acid, lacto-N-biose phosphorylase (EC 2.4.1.211), and UDP-glucose-4-epimerase (EC 5.1.3.2).
1. A method for producing lacto-N-biose I,
wherein the method comprises causing:
(i) a combination of a carbohydrate raw material with an enzyme that catalyzes phosphorolysis of the carbohydrate raw material to give α-glucose-1-phosphate; and
(ii) (a) an enzyme that converts α-glucose-1-phosphate and UDP-galactose to UDP-glucose and α-galactose-1-phosphate, respectively, with cofactor(s) and substrate(s) of said enzyme of (a); and/or (b) a combination of an enzyme that converts α-glucose-1-phosphate to UDP-glucose and an enzyme that converts UDP-galactose to α-galactose-1-phosphate with cofactor(s) and substrate(s) of said enzymes of (b); and/or (c) a combination of an enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase and cofactor(s) and substrate(s) of said enzyme of (c);
to act in the presence of N-acetylglucosamine, phosphoric acid, lacto-N-biose phosphorylase (EC 2.4.1.211), 1,3-β-galactosyl-N-acetylhexosamine phosphorylase, and UDP-glucose-4-epimerase (EC 5.1.3.2), wherein lacto-N-biose I is obtained.
2. The method according to claim 1 , wherein the combination of (i) is one combination or more selected from the group consisting of sucrose with sucrose phosphorylase (EC 2.4.1.7); starch or dextrin with phosphorylase (EC 2.4.1.1); cellobiose with cellobiose phosphorylase (EC 2.4.1.20); cellodextrin(s) with cellodextrin phosphorylase (EC 2.4.1.49) and cellobiose phosphorylase (EC 2.4.1.20); laminarioligosaccharide(s) with laminaribiose phosphorylase (EC 2.4.1.31) and/or β-1,3 oligoglucan phosphorylase (EC 2.4.1.30); and trehalose with trehalose phosphorylase (EC 2.4.1.231).
3. The method according to claim 1 , wherein
the enzyme of (a) is UDP-glucose-hexose-1-phosphate uridylyltransferase (EC 2.7.7.12), and cofactor(s) thereof, with UDP-glucose, UDP-galactose, or a mixture thereof; wherein
the combination of (b) is selected from the group consisting of:
a combination of glucose-1-phosphate uridylyltransferase (EC 2.7.7.9), and cofactor(s) thereof, and galactose-1-phosphate uridylyltransferase (EC 2.7.7.10)), and cofactor(s) thereof, with UTP;
a combination of glucose-1-phosphate uridylyltransferase (EC 2.7.7.9), and cofactor(s) thereof, and galactose-1-phosphate uridylyltransferase (EC 2.7.7.10), and cofactor(s) thereof, with UDP-glucose and/or UDP-galactose and pyrophosphate; and
a combination of glucose-1-phosphate uridylyltransferase (EC 2.7.7.9), and cofactor(s) thereof, and galactose-1-phosphate uridylyltransferase (EC 2.7.7.10), and cofactor(s) thereof, with UTP and UDP-glucose and/or UDP-galactose and pyrophosphate; wherein
the combination of (c) is selected from the group consisting of the enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase, and cofactor(s) thereof, with UTP;
the enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase, and cofactor(s) thereof, with UDP-glucose and/or UDP-galactose and pyrophosphate; and
the enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase, and cofactor(s) thereof, with UTP and UDP-glucose and/or UDP-galactose and pyrophosphate.
4. The method according to claim 1 , wherein one of said enzymes or more is/are immobilized on a carrier.
5. A method for producing galacto-N-biose, wherein the method comprises causing:
(i) a combination of a carbohydrate raw material with an enzyme that catalyzes phosphorolysis of the carbohydrate raw material to give α-glucose-1-phosphate; and
(ii) (a) an enzyme that converts α-glucose-1-phosphate and UDP-galactose to UDP-glucose and α-galactose-1-phosphate, respectively, with cofactor(s) and substrate(s) of said enzyme of (a); and/or (b) a combination of an enzyme that converts α-glucose-1-phosphate to UDP-glucose and an enzyme that converts UDP-galactose to α-galactose-1-phosphate with cofactor(s) and substrate(s) of said enzymes of (b); and/or (c) a combination of an enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase and cofactor(s) and substrate(s) of said enzyme of (c);
to act in the presence of N-acetylgalactosamine, phosphoric acid, lacto-N-biose phosphorylase (EC 2.4.1.211), and UDP-glucose-4-epimerase (EC 5.1.3.2), wherein galacto-N-biose is obtained.
6. The method according to claim 5 , wherein the combination of
(i) is one combination or more selected from the group consisting of sucrose with sucrose phosphorylase (EC 2.4.1.7); starch or dextrin with phosphorylase (EC 2.4.1.1); cellobiose with cellobiose phosphorylase (EC 2.4.1.20); cellodextrin(s) with cellodextrin phosphorylase (EC 2.4.1.49) and cellobiose phosphorylase (EC 2.4.1.20); laminarioligosaccharide(s) with laminaribiose phosphorylase (EC 2.4.1.31) and/or β-1,3 oligoglucan phosphorylase (EC 2.4.1.30); and trehalose with trehalose phosphorylase (EC 2.4.1.231).
7. The method according to claim 5 , wherein
the enzyme of (a) is UDP-glucose-hexose-1-phosphate uridylyltransferase (EC 2.7.7.12), and cofactors thereof, with UDP-glucose, UDP-galactose, or a mixture thereof; wherein
the combination of (b) is selected from the group consisting of:
a combination of glucose-1-phosphate uridylyltransferase (EC 2.7.7.9), and cofactor(s) thereof, and galactose-1-phosphate uridylyltransferase (EC 2.7.7.10), and cofactor(s) thereof, with UTP;
a combination of glucose-1-phosphate uridylyltransferase (EC 2.7.7.9), and cofactor(s) thereof, and galactose-1-phosphate uridylyltransferase (EC 2.7.7.10), and cofactor(s) thereof, with UDP-glucose and/or UDP-galactose and pyrophosphate; and
a combination of glucose-1-phosphate uridylyltransferase (EC 2.7.7.9), and cofactor(s) thereof, and galactose-1-phosphate uridylyltransferase (EC 2.7.7.10), and cofactor(s) thereof, with UTP and UDP-glucose and/or UDP-galactose and pyrophosphate; wherein
the combination of (c) is selected from the group consisting of the enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase, and cofactor(s) thereof, with UTP;
the enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase, and cofactor(s) thereof, with UDP-glucose and/or UDP-galactose and pyrophosphate; and
the enzyme having both activity of glucose-1-phosphate uridylyltransferase and activity of galactose-1-phosphate uridylyltransferase, and cofactor(s) thereof, with UTP and UDP-glucose and/or UDP-galactose and pyrophosphate.
8. The method according to claim 5 , wherein one of said enzymes or more is/are immobilized on a carrier.