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dc.contributor.authorKollmus, Heike
dc.contributor.authorFuchs, Helmut
dc.contributor.authorLengger, Christoph
dc.contributor.authorHaselimashhadi, Hamed
dc.contributor.authorBogue, Molly A
dc.contributor.authorÖstereicher, Manuela A
dc.contributor.authorHorsch, Marion
dc.contributor.authorAdler, Thure
dc.contributor.authorAguilar-Pimentel, Juan Antonio
dc.contributor.authorAmarie, Oana Veronica
dc.contributor.authorBecker, Lore
dc.contributor.authorBeckers, Johannes
dc.contributor.authorCalzada-Wack, Julia
dc.contributor.authorGarrett, Lillian
dc.contributor.authorHans, Wolfgang
dc.contributor.authorHölter, Sabine M
dc.contributor.authorKlein-Rodewald, Tanja
dc.contributor.authorMaier, Holger
dc.contributor.authorMayer-Kuckuk, Philipp
dc.contributor.authorMiller, Gregor
dc.contributor.authorMoreth, Kristin
dc.contributor.authorNeff, Frauke
dc.contributor.authorRathkolb, Birgit
dc.contributor.authorRácz, Ildikó
dc.contributor.authorRozman, Jan
dc.contributor.authorSpielmann, Nadine
dc.contributor.authorTreise, Irina
dc.contributor.authorBusch, Dirk
dc.contributor.authorGraw, Jochen
dc.contributor.authorKlopstock, Thomas
dc.contributor.authorWolf, Eckhard
dc.contributor.authorWurst, Wolfgang
dc.contributor.authorYildirim, Ali Önder
dc.contributor.authorMason, Jeremy
dc.contributor.authorTorres, Arturo
dc.contributor.authorBalling, Rudi
dc.contributor.authorMehaan, Terry
dc.contributor.authorGailus-Durner, Valerie
dc.contributor.authorSchughart, Klaus
dc.contributor.authorHrabě de Angelis, Martin
dc.date.accessioned2020-02-27T15:03:03Z
dc.date.available2020-02-27T15:03:03Z
dc.date.issued2020-02-14
dc.identifier.citationMammalian genome : official journal of the International Mammalian Genome Society JID - 9100916.en_US
dc.identifier.issn1432-1777
dc.identifier.pmid32060626
dc.identifier.doi10.1007/s00335-020-09827-3
dc.identifier.urihttp://hdl.handle.net/10033/622182
dc.description.abstractMyxococcus xanthus DK1622 is known as a proficient producer of different kinds of secondary metabolites (SM) with various biological activities, including myxovirescin A, myxalamide A, myxochromide A and DKxanthene. Low production of SM in the wild type bacteria makes searching for production optimization methods highly desirable. Identification and induction of endogenous key molecular feature(s) regulating the production level of the metabolites remain promising, while heterologous expression of the biosynthetic genes is not always efficient because of various complicating factors including codon usage bias. This study established proteomic and molecular approaches to elucidate the regulatory roles of the ROK regulatory protein in the modification of secondary metabolite biosynthesis. Interestingly, the results revealed that rok inactivation significantly reduced the production of the SM and also changed the motility in the bacteria. Electrophoretic mobility shift assay using purified ROK protein indicated a direct enhancement of the promoters encoding transcription of the DKxanthene, myxochelin A, and myxalamide A biosynthesis machinery. Comparative proteomic analysis by two-dimensional fluorescence difference in-gel electrophoresis (2D-DIGE) was employed to identify the protein profiles of the wild type and rok mutant strains during early and late logarithmic growth phases of the bacterial culture. Resulting data demonstrated overall 130 differently altered proteins by the effect of the rok gene mutation, including putative proteins suspected to be involved in transcriptional regulation, carbohydrate metabolism, development, spore formation, and motility. Except for a slight induction seen in the production of myxovirescin A in a rok over-expression background, no changes were found in the formation of the other SM. From the outcome of our investigation, it is possible to conclude that ROK acts as a pleiotropic regulator of secondary metabolite formation and development in M. xanthus, while its direct effects still remain speculative. More experiments are required to elucidate in detail the variable regulation effects of the protein and to explore applicable approaches for generating valuable SM in this bacterium.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.titleA comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes.en_US
dc.typeArticleen_US
dc.contributor.departmentHZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.en_US
dc.identifier.journalMammalian Genomeen_US
refterms.dateFOA2020-02-27T15:03:04Z
dc.source.journaltitleMammalian genome : official journal of the International Mammalian Genome Society


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