نمایش مختصر رکورد

dc.contributor.authorKorbekandi, Hen_US
dc.contributor.authorDarkhal, Pen_US
dc.contributor.authorHojati, Zen_US
dc.contributor.authorAbedi, Den_US
dc.contributor.authorMeraj Pourhosein, Men_US
dc.date.accessioned1399-07-09T06:56:26Zfa_IR
dc.date.accessioned2020-09-30T06:56:26Z
dc.date.available1399-07-09T06:56:26Zfa_IR
dc.date.available2020-09-30T06:56:26Z
dc.date.issued2010-04-01en_US
dc.date.issued1389-01-12fa_IR
dc.date.submitted2010-11-20en_US
dc.date.submitted1389-08-29fa_IR
dc.identifier.citationKorbekandi, H, Darkhal, P, Hojati, Z, Abedi, D, Meraj Pourhosein, M. (2010). Overproduction of Clavulanic Acid by UV Mutagenesis of Streptomyces clavuligerus. Iranian Journal of Pharmaceutical Research, 9(2), 177-181. doi: 10.22037/ijpr.2010.854en_US
dc.identifier.issn1735-0328
dc.identifier.issn1726-6890
dc.identifier.urihttps://dx.doi.org/10.22037/ijpr.2010.854
dc.identifier.urihttp://ijpr.sbmu.ac.ir/article_854.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/312410
dc.description.abstractClavulanic acid is produced industrially by fermentation of Streptomyces clavuligerus and researches have increased its production by strain improvement, recombinant DNA technology, and media composition and growth condition optimization. The main objective of this study was to increase the level of clavulanic acid production from Streptomyces clavuligerus (DSM 738), using UV irradiation. After incubation, the spores and aerial mycelia were scraped off the agar plate by a sterile loop. After passing through a cotton wool, the serially diluted spore suspension was spread on GYM- agar containing caffeine. The plates were irradiated with UV light, wrapped in aluminum foil and incubated. The colonies were sub-cultured again to express the mutations. An aliquot of the spore suspension prepared from the resulted culture was poured in GYM agar plates and incubated. The plates were overlaid with nutrient-agar containing penicillin G and Klebsiela pneumoniae, and incubated. The inhibition zone diameter was measured and compared with the wild type colony. Repeating this procedure, the overproducer mutants were selected. Concentration of clavulanic acid was determined by HPLC analysis. It was concluded that secondary metabolites, mainly antibiotics containing clavulanic acid, were produced about 6–7 days after the growth, and concentration of clavulanic acid was increased up to two-folds after UV mutagenesis.en_US
dc.format.extent449
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSchool of Pharmacy, Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Pharmaceutical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22037/ijpr.2010.854
dc.subjectStreptomyces clavuligerusen_US
dc.subjectClavulanic aciden_US
dc.subjectUV mutagenesisen_US
dc.subjectOverproductionen_US
dc.subjectFermentationen_US
dc.subjectUV irradiationen_US
dc.titleOverproduction of Clavulanic Acid by UV Mutagenesis of Streptomyces clavuligerusen_US
dc.typeTexten_US
dc.citation.volume9
dc.citation.issue2
dc.citation.spage177
dc.citation.epage181


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