http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111944865-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P19-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-2402
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y302-0104
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-70
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-60
filingDate 2020-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111944865-B
titleOfInvention Application of a bacterial-derived α-L-rhamnosidase in the efficient production of hesperetin-7-O-glucoside
abstract The invention relates to the application of a bacterial-derived α-L-rhamnosidase in the efficient production of hesperetin-7-O-glucoside. The nucleotide sequence of the α-L-rhamnosidase FjRha in the present invention is shown in SEQ ID NO. 1, and the gene is cloned from the genome of Flavobacterium johnsonii. The α-L-rhamnosidase FjRha can specifically hydrolyze artificial substrates and natural substrates containing α-1,6 rhamnoside bonds, and can efficiently and specifically catalyze hesperidin to prepare hesperetin-7-O glucoside, the conversion rate of catalyzing 3g/L of hesperidin to generate hesperetin-7-O-glucoside is up to more than 95% under the conditions of enzyme dosage 8U/mL, pH 7.0, and 37°C, and the method has simple steps. , low cost, mild conditions, environmental friendliness and other advantages, has broad application prospects.
priorityDate 2020-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 437.