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filingDate 2011-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1af97384c9abcf9544586e3e4841a052
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publicationDate 2014-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102618604-B
titleOfInvention Preparation method of cyclic lipopeptide compound
abstract The invention discloses a fermentation medium which comprises 0.5-5.0 wt% of amino acid or its derivative, 0.5-3.0 wt% of hard-soluble organic nitrogen source, and 1.0-10.0 wt% of carbon source. By using the medium of the invention to carry out biologic fermentation of the compound of formula I, the fermentation level can stably reach more than 0.5g/L, with the highest fermentation level being 1.0g/L. By using the strain mutagenized with Coleophoma empetri F-11899 (FERM BP2635), the fermentation level can even reach 1.5 g/L. Because the fermentation level is high and the amount of organic solvent used in the post-treatment is relatively reduced, the production cost is reduced, and the invention has high economic value and meets the need of industrial production.
priorityDate 2011-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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