Bio-indigo production in two different fermentation systems using recombinant Escherichia coli cells harboring a flavin-containing monooxygenase gene (fmo) SCIE SCOPUS

DC Field Value Language
dc.contributor.author Han, Gui Hwan -
dc.contributor.author Bang, Seong Eun -
dc.contributor.author Babu, Bandamaravuri Kishore -
dc.contributor.author Chang, Man -
dc.contributor.author Shin, Hyun-Jae -
dc.contributor.author Kim, Si Wouk -
dc.date.accessioned 2020-04-20T07:55:03Z -
dc.date.available 2020-04-20T07:55:03Z -
dc.date.created 2020-01-28 -
dc.date.issued 2011-03 -
dc.identifier.issn 1359-5113 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/3909 -
dc.description.abstract Bio-indigo was produced in 3000-L batch and 5-L continuous fermentation of a recombinant Escherichia coli DH5 alpha harboring a novel gene encoding flavin-containing monooxygenase (FMO). Batch fermentation in a 3000-L fermenter produced 911 +/- 22 mg L-1 of indigo from 2 g L-1 tryptophan as a substrate (yield 46.9%) under the following culture conditions as follows: culture temperature 30 degrees C, pH 7.0, agitation speed 200 rpm, and aeration 3 vvm. Sufficient oxygen (aeration rate and agitation speed) was critical for bio-indigo production. For continuous fermentation in a 5-L fermenter, the volumetric productivity was found to be 11.3 mg L-1 h(-1) up to 110 h (final accumulated bio-indigo was 23 g) with a constant dilution rate (D) of 0.084 h(-1) (constant feeding rate of 0.167 L h(-1) with medium containing 3 g L-I tryptophan). Recombinant E. coli cells have the ability to withstand the toxicity of high concentration of accumulated indigo in batch fermentation. In continuous fermentation, the recombinant cells exhibited high plasmid stability up to 110 h, after which they lost the plasmid. (C) 2010 Elsevier Ltd. All rights reserved. -
dc.description.uri 1 -
dc.language English -
dc.publisher ELSEVIER SCI LTD -
dc.subject INDOLE -
dc.subject BIOSYNTHESIS -
dc.subject OXIDATION -
dc.subject ACID -
dc.title Bio-indigo production in two different fermentation systems using recombinant Escherichia coli cells harboring a flavin-containing monooxygenase gene (fmo) -
dc.type Article -
dc.citation.endPage 791 -
dc.citation.startPage 788 -
dc.citation.title PROCESS BIOCHEMISTRY -
dc.citation.volume 46 -
dc.citation.number 3 -
dc.contributor.alternativeName 장만 -
dc.identifier.bibliographicCitation PROCESS BIOCHEMISTRY, v.46, no.3, pp.788 - 791 -
dc.identifier.doi 10.1016/j.procbio.2010.10.015 -
dc.identifier.scopusid 2-s2.0-79951518313 -
dc.identifier.wosid 000288419900027 -
dc.type.docType Article -
dc.description.journalClass 1 -
dc.subject.keywordPlus INDOLE -
dc.subject.keywordPlus BIOSYNTHESIS -
dc.subject.keywordPlus OXIDATION -
dc.subject.keywordPlus ACID -
dc.subject.keywordAuthor Bio-indigo -
dc.subject.keywordAuthor Plasmid stability -
dc.subject.keywordAuthor Flavin-containing monooxygenase -
dc.subject.keywordAuthor Batch fermentation -
dc.subject.keywordAuthor Continuous fermentation -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology -
dc.relation.journalWebOfScienceCategory Biotechnology & Applied Microbiology -
dc.relation.journalWebOfScienceCategory Engineering, Chemical -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Biochemistry & Molecular Biology -
dc.relation.journalResearchArea Biotechnology & Applied Microbiology -
dc.relation.journalResearchArea Engineering -
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