DC Field | Value | Language |
---|---|---|
dc.contributor.author | Moon Sun Hahm | - |
dc.contributor.author | Jung Hoon Bae | - |
dc.contributor.author | Eui Sung Choi | - |
dc.contributor.author | Bong Hyun Chung | - |
dc.date.accessioned | 2017-04-19T08:56:42Z | - |
dc.date.available | 2017-04-19T08:56:42Z | - |
dc.date.issued | 1999 | - |
dc.identifier.issn | 0141-5492 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/4956 | - |
dc.description.abstract | The genes encoding pro-carboxypeptidase Ys (pro-CPYs) from Saccharomyces cerevisiae and Hansenula polymorpha were cloned and expressed in Escherichia coli. Most of the expressed pro-CPY was present in the form of inclusion bodies, accounting for about 35% of the total cellular protein. The inclusion bodies solubilized in 6 M guanidinum chloride were renatured by dilution 1:60 into renaturation buffer. Further refolding and activation were followed by the addition of 60 μg ml-1 proteinase K into the diluted solution. The specific activities of in vitro activated S. cerevisiae and H. polymorpha CPYs were found to be similar, representing about 25% of that of native S. cerevisiae CPY. | - |
dc.publisher | Springer | - |
dc.title | In vitro activation of yeast pro-carboxypeptidase Y expressed as inclusion bodies in Escherichia coli | - |
dc.title.alternative | In vitro activation of yeast pro-carboxypeptidase Y expressed as inclusion bodies in Escherichia coli | - |
dc.type | Article | - |
dc.citation.title | Biotechnology Letters | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 885 | - |
dc.citation.startPage | 881 | - |
dc.citation.volume | 21 | - |
dc.contributor.affiliatedAuthor | Jung Hoon Bae | - |
dc.contributor.affiliatedAuthor | Eui Sung Choi | - |
dc.contributor.affiliatedAuthor | Bong Hyun Chung | - |
dc.contributor.alternativeName | 함문선 | - |
dc.contributor.alternativeName | 배정훈 | - |
dc.contributor.alternativeName | 최의성 | - |
dc.contributor.alternativeName | 정봉현 | - |
dc.identifier.bibliographicCitation | Biotechnology Letters, vol. 21, pp. 881-885 | - |
dc.identifier.doi | 10.1023/A:1005506119165 | - |
dc.subject.keyword | E. coli | - |
dc.subject.keyword | H. polymorpha | - |
dc.subject.keyword | in vitro activation | - |
dc.subject.keyword | pro-carboxypeptidase Y | - |
dc.subject.keyword | proteinase K | - |
dc.subject.local | E. Coli | - |
dc.subject.local | E. coli | - |
dc.subject.local | E.coli | - |
dc.subject.local | Escherichia Coli | - |
dc.subject.local | Escherichia coli | - |
dc.subject.local | Escherichia coli. | - |
dc.subject.local | escherichia coil | - |
dc.subject.local | escherichia coli | - |
dc.subject.local | H. polymorpha | - |
dc.subject.local | in vitro activation | - |
dc.subject.local | pro-carboxypeptidase Y | - |
dc.subject.local | pro-carboxypeptidase Y (pro-CPY) | - |
dc.subject.local | proteinase K | - |
dc.description.journalClass | Y | - |
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