Enhancement of operational stability of immobilized whole cell D-hydantoinase

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dc.contributor.authorKim, D.M.ko
dc.contributor.authorKim, G.J.ko
dc.contributor.authorKim, Hak-Sungko
dc.date.accessioned2013-02-27T07:29:02Z-
dc.date.available2013-02-27T07:29:02Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1994-09-
dc.identifier.citationBIOTECHNOLOGY LETTERS, v.16, no.1, pp.11 - 16-
dc.identifier.issn0141-5492-
dc.identifier.urihttp://hdl.handle.net/10203/67257-
dc.description.abstractA bacterium Pseudomonas sp. KBEL 101 isolated from soil was immobilized within polyacrylamide gel and used for the synthesis of D-p-hydroxyphenylglycine from DL-5-substituted hydantoin. The half-life of immobilized whole cell D-hydantoinase was found to be about 50 hrs. In order to increase the operational stability of immobilized whole cell D-hydantoinase, a carbon or nitrogen source was supplied with the reaction mixture in the continuous stirred tank reactor. As a sole source of carbon, glycerol was found to be most effective, and the activity of immobilized whole cell enzyme was maintained stably during 7 days when O.1%(W/V) glycerol solution was provided. In the case of nitrogen source, supplying of O.1%(W/V) yeast extract prolonged the half-life of immobilized whole cell D-hydantoinase to about 25 days.-
dc.languageEnglish-
dc.publisherSPRINGER-
dc.subjectAMINO-ACIDS-
dc.titleEnhancement of operational stability of immobilized whole cell D-hydantoinase-
dc.typeArticle-
dc.identifier.wosidA1994MU96100003-
dc.identifier.scopusid2-s2.0-0028014309-
dc.type.rimsART-
dc.citation.volume16-
dc.citation.issue1-
dc.citation.beginningpage11-
dc.citation.endingpage16-
dc.citation.publicationnameBIOTECHNOLOGY LETTERS-
dc.contributor.localauthorKim, Hak-Sung-
dc.contributor.nonIdAuthorKim, D.M.-
dc.contributor.nonIdAuthorKim, G.J.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusAMINO-ACIDS-
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