dc.contributor.authorPenesyan, Anahit
dc.contributor.authorBallestriero, Francesco
dc.contributor.authorDaim, Malak
dc.contributor.authorKjelleberg, Staffan
dc.contributor.authorThomas, Torsten
dc.contributor.authorEgan, Suhelen
dc.date.accessioned2014-01-10T02:49:25Z
dc.date.available2014-01-10T02:49:25Z
dc.date.copyright2013en_US
dc.date.issued2013
dc.identifier.citationPenesyan, A., Ballestriero, F., Daim, M., Kjelleberg, S., Thomas, T., & Egan, S. (2013). Assessing the effectiveness of functional genetic screens for the identification of bioactive metabolites. Marine drugs, 11(1), 40-49.en_US
dc.identifier.issn1660-3397en_US
dc.identifier.urihttp://hdl.handle.net/10220/18428
dc.description.abstractA common limitation for the identification of novel activities from functional (meta) genomic screens is the low number of active clones detected relative to the number of clones screened. Here we demonstrate that constructing libraries with strains known to produce bioactives can greatly enhance the screening efficiency, by increasing the “hit-rate” and unmasking multiple activities from the same bacterial source.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesMarine drugsen_US
dc.rights© 2013 The Authors (published by MDPI). This paper was published in Marine Drugs and is made available as an electronic reprint (preprint) with permission of the authors. The paper can be found at the following official DOI: [http://dx.doi.org/10.3390/md11010040]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.en_US
dc.subjectDRNTU::Science::Biological sciences
dc.titleAssessing the effectiveness of functional genetic screens for the identification of bioactive metabolitesen_US
dc.typeJournal Article
dc.identifier.doihttp://dx.doi.org/10.3390/md11010040
dc.description.versionPublished versionen_US


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