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dc.contributor.authorTelke, Amar
dc.contributor.authorOvchinnikov, Kirill
dc.contributor.authorVuoristo, Kiira
dc.contributor.authorMathiesen, Geir
dc.contributor.authorThorstensen, Tage
dc.contributor.authorDiep, Dzung B.
dc.date.accessioned2020-01-03T11:14:50Z
dc.date.available2020-01-03T11:14:50Z
dc.date.created2019-04-08T14:28:53Z
dc.date.issued2019
dc.identifier.citationFrontiers Microbiology, 05 March 2019nb_NO
dc.identifier.issn1664-302X
dc.identifier.urihttp://hdl.handle.net/11250/2634763
dc.description.abstractThe leaderless bacteriocin Garvicin KS (GarKS) is a potent antimicrobial, being active against a wide range of important pathogens. GarKS production by the native producer Lactococcus garvieae KS1546 is, however, relatively low (80 BU/ml) under standard laboratory growth conditions (batch culture in GM17 at 30°C). To improve the production, we systematically evaluated the impact of different media and media components on bacteriocin production. Based on the outcomes, a new medium formulation was made that increased GarKS production about 60-fold compared to that achieved in GM17. The new medium was composed of pasteurized milk and tryptone (PM-T). GarKS production was increased further 4-fold (i.e., to 20,000 BU/ml) by increasing the gene dose of the bacteriocin gene cluster (gak) in the native producer. Finally, a combination of the newly composed medium (PM-T), an increased gene dose and cultivation at a constant pH 6 and a 50–60% dissolved oxygen level in growth medium, gave rise to a GarKS production of 164,000 BU/ml. This high production, which is about 2000-fold higher compared to that initially achieved in GM17, corresponds to a GarKS production of 1.2 g/L. To our knowledge, this is one of the highest bacteriocin production reported hitherto.nb_NO
dc.language.isoengnb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleOver 2000-Fold Increased Production of the Leaderless Bacteriocin Garvicin KS by Increasing Gene Dose and Optimization of Culture Conditionsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume10nb_NO
dc.source.journalFrontiers in Microbiologynb_NO
dc.identifier.doi10.3389/fmicb.2019.00389
dc.identifier.cristin1690882
dc.relation.projectNorges forskningsråd: 254784nb_NO
cristin.unitcode192,12,0,0
cristin.unitcode192,0,0,0
cristin.unitnameKjemi, bioteknologi og matvitenskap
cristin.unitnameNorges miljø- og biovitenskapelige universitet
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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