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filingDate 1990-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cc9ea188785140fa438469c60f24ae2
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publicationDate 1999-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-280028-B6
titleOfInvention PLASMIDES, METHODS OF PRODUCTION AND USE THEM
abstract An operon of hereby disclosed plasmides consists of a controllable Trp promotor or a cotrollable Tac promotor; a Shine-Dalgarno sequence effective as a ribosomal binding site; a translational start codon, wilst said Shine-Dalgarno sequence is separated from said start codon by from 6 to 12 nucleotides; a structural gene for single chain urinary plasminogen activator "scuPA" having 411 amino acids, wherein the triplet CGT is utilized as the codon for arginine; the triplet CTG is utilized as the codon for leucine; the triplet GTT is utilized as the codon for valine; the triplet CCG is utilized as the codon for proline; and the triplet GGT is utilized as the codon for glycine; and downstream of the structural gene at least one transcription terminator selected from the group containing trp A terminator and/or tet A/orf L-terminator from Tn 10. These plasmids are suitable for expressing a precursor protein of rscu-PA in Enterobacteriaceae, especially Escherichia coli. There is further described a process for producing novel plasmides comprising the step of: (i) removing the nic/bom-region and mutationally inactivating the tetracycline resistance gene of the plasmid pBR 322; (ii) inserting a multi-cloning site having the nucleotide sequence of FIG. 2 between the pBR 322 restriction sites Eco RI and Hind III; and (iii) inserting by means of the multi-cloning site a transcription terminator, a synthetic gene encoding scu-PA, and a Trp-promotor such that the gene is operatively linked to the promoter and the terminator.
priorityDate 1989-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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