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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K2319-02
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-6467
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-06
filingDate 2000-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b95da10ac61c80cf30ea310d1d827fe3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e366bbbbd4a56ec0fd0599b5bc887d3c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51b6eb574d7d171e61ea3a249e012f73
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a19a02004c5d1a70d53f38da3b81e199
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10ccaed1f78f4cf3d65bb0b89facd31e
publicationDate 2001-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2403330-A1
titleOfInvention Method for producing active serine proteases and inactive variants
abstract The invention relates to a method for producing biologically active serine proteases, isolated serine protease domains and their amino-acid variants in a prokaryotic host. The method is characterised by an N-terminal addition of a helper sequence consisting of a dipeptide which is suitable for degradation by a dipeptidyl amino peptidase, by the expression of the serine protease(s) and/or their fragments containing the N-terminal dipeptide helper sequence, optionally as inclusion bodies, and by the renaturation of the expressed proteins and the activation of the serine protease(s) and/or serine protease domains by splitting-off the helper sequence using an exopeptidase.
priorityDate 1999-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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