http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111394382-B

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filingDate 2020-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111394382-B
titleOfInvention Recombinant expression vector and recombinant bacterium of feruloyl esterase BpFae gene, and recombinant expression method
abstract The invention discloses a recombinant expression vector and a recombinant bacterium of feruloyl esterase BpFae gene, and provides a method for recombinant expression of the enzyme under optimized expression conditions. The starting vector is pGEX-4T-1 to construct the gene expression vector containing the ferulic acid esterase BpFae, and when IPTG is used as an inducer, the optimal conditions are as follows: adopting an SOB culture medium; initial pH: 5.0; inoculation amount: 0.8% (v/v); the induction time is as follows: 4 h; IPTG concentration: 0.05 mM; induction temperature: 26 ℃; rotating speed of a shaking table: 240 rpm; induction time: 24h, the activity of the BpFae obtained in the way can reach 2.54U/mL at most; when lactose is used as an inducer, an LB culture medium is adopted; lactose concentration: 6 g/L; initial pH: 5.5; the induction time is as follows: 5 h; induction temperature: 23 ℃; rotating speed of a shaking table: 240 rpm; liquid loading amount: 50mL/250 mL; inoculation amount: 0.2% (v/v); induction time: the activity of the BpFae obtained in the way can reach 7.43U/mL at most after 32 h. The optimal induction expression condition of the invention can prepare the ferulic acid esterase BpFae more efficiently.
priorityDate 2020-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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