Patent classifications
C07H1/08
METHOD FOR MANUFACTURING REVAUDIOSIDE-D-CONTAINING CRYSTALLIZED PRODUCT, AND REVAUDIOSIDE-D-CONTAINING CRYSTALLIZED PRODUCT
There is demand for a novel method for manufacturing a RebD crystallized product. The present invention provides a method for manufacturing a RebD-containing crystallized product, including: a step for mixing a stevia plant-derived crude product having a total steviol glycoside content of 50-95 mass %, and containing at least RebA and RebD, into a solvent containing methanol or ethanol so that the supersaturation of RebD at 10° C. is at least 10 and the supersaturation of RebA at 10° C. does not exceed 18, and adjusting a crystallization solution; and a step for cooling the crystallization solution under stirring and causing RebD to precipitate.
IMPROVED DEMINERALIZATION OF FERMENTATION BROTHS AND PURIFICATION OF FINE CHEMICALS SUCH AS OLIGOSACCHARIDES
The present invention relates to a method for improved demineralization of fermentation broths, including the steps of providing a solution comprising one or more oligosaccharides, carrying out a first membrane filtration and preferably being a microfiltration or ultrafiltration, a second membrane filtration of the permeate of the first membrane filtration and a first nanofiltration step; with a sub-step of concentration and/or a sub-step of diafiltration. Moreover, the present invention is directed to an improved purification of fine chemicals from a fermentation broth.
IMPROVED DEMINERALIZATION OF FERMENTATION BROTHS AND PURIFICATION OF FINE CHEMICALS SUCH AS OLIGOSACCHARIDES
The present invention relates to a method for improved demineralization of fermentation broths, including the steps of providing a solution comprising one or more oligosaccharides, carrying out a first membrane filtration and preferably being a microfiltration or ultrafiltration, a second membrane filtration of the permeate of the first membrane filtration and a first nanofiltration step; with a sub-step of concentration and/or a sub-step of diafiltration. Moreover, the present invention is directed to an improved purification of fine chemicals from a fermentation broth.
GLYCOLIPOPEPTIDE BIOSURFACTANTS
Surfactants based on a newly discovered class of compounds include a hydrophobic lipid oligomer covalently linked to a peptide or peptide-like chain and a carbohydrate moiety, and a serine-leucinol dipeptide linked to the lipid oligomer. Such surfactants can be used to create an oil-in-water or water-in-oil emulsion by mixing together a polar component; a non-polar component; and the surfactant. Biosurfactants of the newly discovered class can be made by isolating and culturing a microorganism which produces the biosurfactant, and then isolating the biosurfactant from the culture. A microorganism can be engineered to produce biosurfactant of this newly discovered class by expressing a set of heterologous genes involved in the biosynthesis of the biosurfactant in the microorganism.
GLYCOLIPOPEPTIDE BIOSURFACTANTS
Surfactants based on a newly discovered class of compounds include a hydrophobic lipid oligomer covalently linked to a peptide or peptide-like chain and a carbohydrate moiety, and a serine-leucinol dipeptide linked to the lipid oligomer. Such surfactants can be used to create an oil-in-water or water-in-oil emulsion by mixing together a polar component; a non-polar component; and the surfactant. Biosurfactants of the newly discovered class can be made by isolating and culturing a microorganism which produces the biosurfactant, and then isolating the biosurfactant from the culture. A microorganism can be engineered to produce biosurfactant of this newly discovered class by expressing a set of heterologous genes involved in the biosynthesis of the biosurfactant in the microorganism.
A Method for Drying Human Milk Oligosaccharides
The present invention relates to a method for drying human milk oligosaccharides (HMOs). More specifically, the present invention is related to a method of roller drying or drum drying of human milk oligosaccharides in a simple and economical way.
SYNTHESIS OF OLIGOSACCHARIDES AS PREBIOTICS FROM SIMPLE SUGARS AND POLYSACCHARIDES IN CONCENTRATED ACIDS
Provided herein are methods for preparing a product including predominantly prebiotic oligosaccharides by non-enzymatic methods of glycosylation of monosaccharides, disaccharides, and/or polysaccharides. The methods may include mixing one or more types of monosaccharides, disaccharides, and/or polysaccharides with an effective amount of a dehydrating acid at a temperature sufficient to form a product including predominantly prebiotic oligosaccharides.
SYNTHESIS OF OLIGOSACCHARIDES AS PREBIOTICS FROM SIMPLE SUGARS AND POLYSACCHARIDES IN CONCENTRATED ACIDS
Provided herein are methods for preparing a product including predominantly prebiotic oligosaccharides by non-enzymatic methods of glycosylation of monosaccharides, disaccharides, and/or polysaccharides. The methods may include mixing one or more types of monosaccharides, disaccharides, and/or polysaccharides with an effective amount of a dehydrating acid at a temperature sufficient to form a product including predominantly prebiotic oligosaccharides.
MANGIFERIN AND PREPARATION METHOD THEREOF
The present disclosure belongs to the technical field of plant extraction, and particularly relates to mangiferin and a preparation method thereof. The present disclosure includes activated carbon treatment and extraction of raw materials successively to obtain the mangiferin; the raw materials are mango leaves and/or almond leaves; the extraction is absolute methanol extraction, and the extraction is conducted at 60-65° C. Results of examples indicate that mangiferin obtained by the preparation method of mangiferin provided by the present disclosure has a purity of 98% to 99.5%, and mangiferin yield is as high as 66.7% of total mangiferin content in the mango leaves or almond leaves. The preparation method of mangiferin provided by the present disclosure is simple to operate, which obtains high-yield and highly pure mangiferin while reducing production costs of the mangiferin, and realizes the industrial production of the mangiferin.
MANGIFERIN AND PREPARATION METHOD THEREOF
The present disclosure belongs to the technical field of plant extraction, and particularly relates to mangiferin and a preparation method thereof. The present disclosure includes activated carbon treatment and extraction of raw materials successively to obtain the mangiferin; the raw materials are mango leaves and/or almond leaves; the extraction is absolute methanol extraction, and the extraction is conducted at 60-65° C. Results of examples indicate that mangiferin obtained by the preparation method of mangiferin provided by the present disclosure has a purity of 98% to 99.5%, and mangiferin yield is as high as 66.7% of total mangiferin content in the mango leaves or almond leaves. The preparation method of mangiferin provided by the present disclosure is simple to operate, which obtains high-yield and highly pure mangiferin while reducing production costs of the mangiferin, and realizes the industrial production of the mangiferin.