BIOTRANSFORMATION OF RIFAMYCIN-B TO RIFAMYCIN-S USING IMMOBILIZED WHOLE CELLS OF HUMICOLA SPP IN A FLUIDIZED-BED REACTOR

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dc.contributor.authorLee, Gyun Minko
dc.contributor.authorChoi, CYko
dc.contributor.authorPark, JMko
dc.contributor.authorHan, MHko
dc.date.accessioned2013-02-25T14:33:48Z-
dc.date.available2013-02-25T14:33:48Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1985-03-
dc.identifier.citationJOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY. BIOTECHNOLOGY, v.35 B, no.1, pp.3 - 10-
dc.identifier.issn0264-3421-
dc.identifier.urihttp://hdl.handle.net/10203/62884-
dc.description.abstractThe biotransformation of rifamycin B to rifamycin S using immobilised whole cells of a Humicola sp. in a fluidised bed reactor exhibited a linear relationship between loading of the immobilised whole cells and conversion, in both batch and continuous operations; the conversion of rifamycin B was higher in batch than continuous operation for a given residence time. The immobilised whole cells were obtained by copolymerisation of the acetone-dried cells with acrylamide. They showed maximum activity of pH 7.8 and 50°C. It was found that aeration effects on the reaction in continuous operation were different from those in batch operation for the same residence time. In batch operation, the conversion of rifamycin B to rifamycin S increased with increased rate of aeration and reached a constant maximum value at aeration rates above 20.8 vvm. In continuous operation, the steady state conversion reached a maximum value in the range of aeration rate between 5.8 and 12.5 vvm; beyond this range the steady state conversion decreased steadily owing to cell leakage. The half life for the operational stability at 40°C was about 13 h.-
dc.languageEnglish-
dc.publisherBlackwell Publishing-
dc.titleBIOTRANSFORMATION OF RIFAMYCIN-B TO RIFAMYCIN-S USING IMMOBILIZED WHOLE CELLS OF HUMICOLA SPP IN A FLUIDIZED-BED REACTOR-
dc.typeArticle-
dc.identifier.wosidA1985AFE6200002-
dc.identifier.scopusid2-s2.0-0022039653-
dc.type.rimsART-
dc.citation.volume35 B-
dc.citation.issue1-
dc.citation.beginningpage3-
dc.citation.endingpage10-
dc.citation.publicationnameJOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY. BIOTECHNOLOGY-
dc.contributor.localauthorLee, Gyun Min-
dc.contributor.nonIdAuthorChoi, CY-
dc.contributor.nonIdAuthorPark, JM-
dc.contributor.nonIdAuthorHan, MH-
dc.type.journalArticleArticle-
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