http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010036408-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cea139ad438b9ce7d33159d45b154c6b
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Y301-01017
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filingDate 2009-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d212a26046526dce07fbf13c99f8ca3e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9452dee1cb924a03d572a41d3ea718ab
publicationDate 2010-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2010036408-A2
titleOfInvention Lysk endolysin is synergistic with lysostaphin against mrsa
abstract Multi-drug resistant superbugs are a persistent problem in modern health care. LysK is a staphylococcal bacteriophage endolysin from the phage K. It is a peptidoglycan hydrolase enzyme that can lyse many staphylococcal strains and thus is a potent antimicrobial against S. aureus , including MRSA. Lysostaphin is a bacteriocin secreted by S. simulans to kill S. aureus , and has been shown to also be a potent antimicrobial for many antibiotic resistant strains of S. aureus . This study describes optimal reaction conditions for the recombinant His-tagged LysK protein, compares its MIC and antimicrobial activity to lysostaphin and demonstrates synergy when the two are used in combination against the MRSA USA300.
priorityDate 2008-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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