http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113481249-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-6454
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-6472
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-6472
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-6458
filingDate 2021-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113481249-B
titleOfInvention Method for preparing lecithin type n-3PUFA by enzyme method
abstract The invention discloses a method for preparing lecithin type n-3PUFA by an enzyme method, belonging to the technical field of separation and application of enzyme. In a eutectic system consisting of choline chloride and glycerophosphatidylcholine, the glycerophosphatidylcholine is used as a solvent and a substrate, and lipase catalyzes the glycerophosphatidylcholine to perform an esterification reaction with n-3PUFA, so that the mass transfer of the substrate can be obviously improved, byproducts can be absorbed, the product inhibition is removed, and the lecithin content and the n-3PUFA binding rate in the product are greatly improved. Compared with the traditional lecithin type n-3PUFA prepared in a solvent-free system, a solvent-free vacuumizing system and an organic solvent system, the lecithin type n-3PUFA prepared in the system is safe, green and environment-friendly, the lecithin content in the product is greatly improved, and the n-3PUFA binding rate is high; more importantly, the immobilized lipase can be repeatedly used. The method has good social, ecological and economic benefits.
priorityDate 2021-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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