dc.creatorSilva, ME
dc.creatorFranco, TT
dc.date1999
dc.dateOCT-DEC
dc.date2014-12-02T16:28:56Z
dc.date2015-11-26T16:38:02Z
dc.date2014-12-02T16:28:56Z
dc.date2015-11-26T16:38:02Z
dc.date.accessioned2018-03-28T23:21:16Z
dc.date.available2018-03-28T23:21:16Z
dc.identifierRevista De Microbiologia. Soc Brasileira Microbiologia, v. 30, n. 4, n. 324, n. 331, 1999.
dc.identifier0001-3714
dc.identifierWOS:000167874600006
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/58481
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/58481
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/58481
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1272189
dc.descriptionThis work investigated the partitioning of beta -galactosidase from Kluyveromyces fragilis in aqueous two-phase systems (ATPS) by bioaffinity. PEG 4000 was chemically activated with thresyl chloride, and the biospecific ligand p-aminophenyl 1-thio-beta -D-galactopyranoside (APGP) was attached to the activated PEG 4000. A new two-step method for extraction and purification of the enzyme beta -galactosidase from Kluyveromyces fragilis was developed. In the first step, a system composed of 6% PEG 4000-APGP and 8% dextran 505 was used, where beta -galactosidase was strongly partitioned to the top phase (K = 2,330). In the second step, a system formed of 13% PEG-APGP and 9% phosphate salt was used to revert the value of the partition coefficient of beta -galactosidase (K = 2 x 10(-5)) in order to provide the purification and recovery of 39% of the enzyme in the bottom salt-rich phase.
dc.description30
dc.description4
dc.description324
dc.description331
dc.languageen
dc.publisherSoc Brasileira Microbiologia
dc.publisherSao Paulo
dc.publisherBrasil
dc.relationRevista De Microbiologia
dc.relationRev. Microbiol.
dc.rightsaberto
dc.sourceWeb of Science
dc.subjectbeta-galactosidase
dc.subjectaqueous two-phase systems
dc.subjectprotein purification
dc.subjectdownstream-processing
dc.subjectaffinity
dc.subjectAqueous 2-phase Systems
dc.subjectImmobilization
dc.subjectExtraction
dc.subjectProteins
dc.subjectLigands
dc.subjectWhey
dc.titlePurification of microbial beta-galactosidase from Kluyveromyces fragilis by bioaffinity partitioning
dc.typeArtículos de revistas


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