Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Synergistic Coordination of Polyethylene Glycol with ClpB/DnaKJE Bichaperone for Refolding of Heat-Denatured Malate Dehydrogenase

Full metadata record
DC Field Value Language
dc.contributor.authorRui Nian-
dc.contributor.authorKim, Duck Sang-
dc.contributor.authorTan, Lihan-
dc.contributor.authorKim, Chan-Wha-
dc.contributor.authorChoe, Woo-Seok-
dc.date.accessioned2021-09-08T15:39:11Z-
dc.date.available2021-09-08T15:39:11Z-
dc.date.created2021-06-10-
dc.date.issued2009-07-
dc.identifier.issn8756-7938-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/119698-
dc.description.abstractThe use of polyethylene glycol (PEG) as a refolding additive to a refolding cocktail comprising the molecular bichaperone ClpB and DnaKJE significantly enhances chaperone-mediated refolding of heat-denatured malate dehydrogenase (MDH). The critical factor to affect the refolding yield is the time point of introducing PEG to the refolding cocktail. The refolding efficiency reached approximately 90% only when PEG was added at the beginning of refolding reaction. The synergistic coordination of an inexpensive refolding additive PEG with the ClpB/DnaKJE bichaperone system may provide an economical route to further enhance the efficacy of ClpB/DnaKJE refolding cocktail approach, facilitating its implementation in large-scale refolding processes. (C) 2009 American Institute of Chemical Engineers Biotechnol. Prog., 25: 1078-1085, 2009-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectAGGREGATED PROTEINS-
dc.subjectCHAPERONE SYSTEM-
dc.subjectGROEL-GROES-
dc.subjectCLPB-
dc.subjectDNAK-
dc.subjectSOLUBILIZATION-
dc.subjectMECHANISM-
dc.subjectGRPE-
dc.subjectRENATURATION-
dc.subjectINTERMEDIATE-
dc.titleSynergistic Coordination of Polyethylene Glycol with ClpB/DnaKJE Bichaperone for Refolding of Heat-Denatured Malate Dehydrogenase-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chan-Wha-
dc.identifier.doi10.1002/btpr.175-
dc.identifier.wosid000269403000021-
dc.identifier.bibliographicCitationBIOTECHNOLOGY PROGRESS, v.25, no.4, pp.1078 - 1085-
dc.relation.isPartOfBIOTECHNOLOGY PROGRESS-
dc.citation.titleBIOTECHNOLOGY PROGRESS-
dc.citation.volume25-
dc.citation.number4-
dc.citation.startPage1078-
dc.citation.endPage1085-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusAGGREGATED PROTEINS-
dc.subject.keywordPlusCHAPERONE SYSTEM-
dc.subject.keywordPlusGROEL-GROES-
dc.subject.keywordPlusCLPB-
dc.subject.keywordPlusDNAK-
dc.subject.keywordPlusSOLUBILIZATION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusGRPE-
dc.subject.keywordPlusRENATURATION-
dc.subject.keywordPlusINTERMEDIATE-
dc.subject.keywordAuthorMalate dehydrogenase (MDH)-
dc.subject.keywordAuthorpolyethylene glycol (PEG)-
dc.subject.keywordAuthormolecular bichaperone-
dc.subject.keywordAuthorprotein refolding-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Life Sciences and Biotechnology > Division of Life Sciences > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE