摘要:
The invention provides novel and improved methods that allow effective capture of valuable active ingredients in biomass (e.g., DDGS) at cost-effective commercial scale. The invention also provides novel compositions of active ingredients with unique properties (e.g., nutritional values and enhanced bioavailability).
摘要:
A novel use of uridine diphosphate glucose 4-epimerase (also called uridine diphosphate galactose 4-epimerase). A method of converting uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) into uridine diphosphate N-acetylgalactoasmine (UDP-GalNAc) by using the above-described enzyme. Because of being practically usable and efficient, the method of synthesizing UDP-GalNAc by using the uridine diphosphate glucose 4-epimerase as described above and an UDP-GalNAc supplying system are highly useful industrially.
摘要:
A novel use of uridine diphosphate glucose 4-epimerase (also called uridine diphosphate galactose 4-epimerase). A method of converting uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) into uridine diphosphate N-acetylgalactoasmine (UDP-GalNAc) by using the above-described enzyme. Because of being practically usable and efficient, the method of synthesizing UDP-GalNAc by using the uridine diphosphate glucose 4-epimerase as described above and an UDP-GalNAc supplying system are highly useful industrially.
摘要:
The present invention relates to a new use of uridine diphosphate glucose 4-epimerase (also called uridine diphosphate galactose 4-epimerase), and a method of converting uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) to uridine diphosphate N-acetylgalactosamine (UDP-GalNAc) by using the said enzyme. The process for producing UDP-GalNAc by using the uridine diphosphate glucose 4-epimerase and the UDP-GalNAc supply system according to the present invention are practical and efficient, and greatly beneficial to the industries.
摘要:
A process for producing uridine diphosphate-N-acetylglucosamine (UDPAG) from uridylic acid (UMP) and N-acetylglucosamine by use of microorganism cells, characterized by adding N-acetylglucosamine kinase thereto. According to the present invention, UDPAG can be efficiently produced even when N-acetylglucosamine is used as a substrate.
摘要:
There is disclosed a method for measuring the activity of a-N-acetylgalactosaminyl transferase by means of the conversion of Type O red blood cells to Type A ones, characterized by the direct use, as the substrate for the conversion reaction, of a reaction solution obtained by enzymatically converting uridine diphosphate-N-acetylglucosamine to uridine diphosphate-N-acetylgalactosamine.
摘要:
The invention relates to a new synthethic process for obtaining compounds of formula (I) from compounds of formula (II) by means of deaminase enzymes.
摘要:
The present invention relates to a process for attaching an N-acetylgalactosamine- (hetero)arylmoiety to an N-acetylglucosaminemoiety, the process comprising the step of contacting the N-acetylgalactosamine-(hetero)arylmoiety with the N- acetylglucosaminemoiety in the presence of a mutant galactosyltransferase, wherein the N-acetylglucosaminemoiety is according to Formula (1)the N- acetylgalactosamine-(hetero)arylmoiety is according to Formula (2): In a particularly preferred embodiment of the process according to the invention, the N-acetylgalactosamine-(hetero)arylmoiety comprises a 1,3-dipole functional group, and the N-acetylglucosaminemoiety is a terminal GlcNAc moiety of a glycoprotein glycan. The invention further relates to a productobtainable by the process according to the invention, in particular to glycoproteins. Also, the invention relates to several compounds comprising an N-acetylgalactosamine-(hetero)arylmoiety.