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이성국

Lee, Sung Kuk
Synthetic Biology & Metabolic Engineering Lab.
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dc.citation.endPage 203 -
dc.citation.number 2 -
dc.citation.startPage 197 -
dc.citation.title PROTEIN EXPRESSION AND PURIFICATION -
dc.citation.volume 61 -
dc.contributor.author Lee, Sung Kuk -
dc.contributor.author Keasling, Jay D. -
dc.date.accessioned 2023-12-22T08:36:37Z -
dc.date.available 2023-12-22T08:36:37Z -
dc.date.created 2014-09-29 -
dc.date.issued 2008-10 -
dc.description.abstract We examined expression of two plant genes encoding coclaurine N-methyltransferase (CMT) and norcoclaurine synthase (NCS) in Escherichia coli from the Salmonella enterica prpBCDE promoter (Pp,B) and compared it to that from the strongest IPTG-inducible promoter, P-T7. In contrast to our previous study showing slightly higher production of green fluorescent protein (GFP) from the pPro system compared to that from the T7 system, production of two plant proteins CMT and NCS from P-prpB was 2- to 4-fold higher than that from P-T7. Unlike P-T7, expression from P-prB did not reduce cell growth even when highly induced, indicating that this propionate-inducible system is more efficient for overproduction of proteins that result in growth inhibition. In an auto-induction experiment, which does not require monitoring the culture or adding inducer during cell growth, the pPro system exhibited much higher protein production than the T7 system. These results strongly indicate that the pPro system is well-suited for overproduction of recombinant proteins. Published by Elsevier Inc. -
dc.identifier.bibliographicCitation PROTEIN EXPRESSION AND PURIFICATION, v.61, no.2, pp.197 - 203 -
dc.identifier.doi 10.1016/j.pep.2008.06.008 -
dc.identifier.issn 1046-5928 -
dc.identifier.scopusid 2-s2.0-50049109691 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/6730 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=50049109691 -
dc.identifier.wosid 000259172100015 -
dc.language 영어 -
dc.publisher ACADEMIC PRESS INC ELSEVIER SCIENCE -
dc.title Heterologous protein production in Escherichia coli using the propionate-inducible pPro system by conventional and auto-induction methods -
dc.type Article -
dc.description.journalRegisteredClass scopus -

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