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Cited 213 time in webofscience Cited 225 time in scopus
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dc.contributor.authorSeo, SW-
dc.contributor.authorYang, JS-
dc.contributor.authorKim, I-
dc.contributor.authorYang, J-
dc.contributor.authorMin, BE-
dc.contributor.authorKIM, SANGUK-
dc.contributor.authorJung, GY-
dc.date.accessioned2016-03-31T08:51:51Z-
dc.date.available2016-03-31T08:51:51Z-
dc.date.created2012-10-15-
dc.date.issued2013-01-
dc.identifier.issn1096-7176-
dc.identifier.other2013-OAK-0000026208-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/16199-
dc.description.abstractPrecise prediction of prokaryotic translation efficiency can provide valuable information for optimizing bacterial host for the production of biochemical compounds or recombinant proteins. However, dynamic changes in mRNA folding throughout translation make it difficult to assess translation efficiency. Here, we systematically determined the universal folding regions that significantly affect the efficiency of translation in Escherichia coli. By assessing the specific regions for mRNA folding, we could construct a predictive design method, UTR Designer, and demonstrate that proper codon optimization around the 5'-proximal coding sequence is necessary to achieve a broad range of expression levels. Finally, we applied our method to control the threshold value of input signals switching on a genetic circuit. This should increase our understanding of the processes underlying gene expression and provide an efficient design principle for optimizing various biological systems, thereby facilitating future efforts in metabolic engineering and synthetic biology. (C) 2012 Elsevier Inc. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherCADEMIC PRESS INC ELSEVIER SCIENCE-
dc.relation.isPartOfMetabolic Engineering-
dc.titlePredictive design of mRNA translation initiation region to control prokaryotic translation efficiency-
dc.typeArticle-
dc.contributor.college정보전자융합공학부-
dc.identifier.doi10.1016/J.YMBEN.2012.10.006-
dc.author.googleSeo S.W., Yang J.-S., Kim I., Yang J., Min B.E., Kim S., Jung G.Y-
dc.relation.volume15-
dc.relation.issue1-
dc.relation.startpage67-
dc.relation.lastpage74-
dc.contributor.id10136479-
dc.relation.journalMETABOLIC ENGINEERING-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationMetabolic Engineering, v.15, pp.67 - 74-
dc.identifier.wosid000313882500007-
dc.date.tcdate2019-01-01-
dc.citation.endPage74-
dc.citation.startPage67-
dc.citation.titleMetabolic Engineering-
dc.citation.volume15-
dc.contributor.affiliatedAuthorKim, I-
dc.contributor.affiliatedAuthorKIM, SANGUK-
dc.contributor.affiliatedAuthorJung, GY-
dc.identifier.scopusid2-s2.0-84870851210-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc86-
dc.description.scptc81*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusSECONDARY STRUCTURE-
dc.subject.keywordPlusSYNTHETIC BIOLOGY-
dc.subject.keywordPlusCODON-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROMOTERS-
dc.subject.keywordPlusSEQUENCE-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusSITES-
dc.subject.keywordPlusTOOLS-
dc.subject.keywordAuthor5 &apos-
dc.subject.keywordAuthor-untranslated region-
dc.subject.keywordAuthormRNA secondary structure-
dc.subject.keywordAuthorSynthetic biology-
dc.subject.keywordAuthorTranslation efficiency-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-

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김상욱KIM, SANGUK
Dept of Life Sciences
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