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dc.contributor.authorLiao, LCen_US
dc.contributor.authorHo, CSen_US
dc.contributor.authorWu, WTen_US
dc.date.accessioned2014-12-08T15:46:24Z-
dc.date.available2014-12-08T15:46:24Z-
dc.date.issued1999-07-01en_US
dc.identifier.issn0032-9592en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0032-9592(98)00099-5en_US
dc.identifier.urihttp://hdl.handle.net/11536/31232-
dc.description.abstractThe deacylation of Pen G was carried out by using recombinant E. coli in an aqueous two-phase system consisting of polyethylene glycol and potassium phosphate solution, which partitions the cells to the bottom phase and the products to the top phase. Bioconversion and product separation were carried out in the same reactor. Repeated batch conversion was employed ten times and enzymic activity showed only a slight decline. When pure enzyme was used for bioconversion in an aqueous two-phase system, the decline was fast and bioconversion using whole cell penicillin acylase was better than that obtained using the pure acylase. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectpenicillin acylaseen_US
dc.subjectwhole cellen_US
dc.subjectaqueous two-phase systemen_US
dc.subjectE. colien_US
dc.subject6-APAen_US
dc.subjectrepeated batchen_US
dc.titleBioconversion with whole cell penicillin acylase in aqueous two-phase systemsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0032-9592(98)00099-5en_US
dc.identifier.journalPROCESS BIOCHEMISTRYen_US
dc.citation.volume34en_US
dc.citation.issue5en_US
dc.citation.spage417en_US
dc.citation.epage420en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000081912700001-
dc.citation.woscount11-
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