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dc.creatorAndersen, Mikael R.es
dc.creatorSalazar, Margarita P.es
dc.creatorSchaap, Peter J.es
dc.creatorVondervoort, Peter J.I. van dees
dc.creatorCulley, Davides
dc.creatorThykaer, Jettees
dc.creatorFrisvad, Jens C.es
dc.creatorNielsen, Kristian F.es
dc.creatorAlbang, Richardes
dc.creatorAlbermann, Kajes
dc.creatorBerka, Randy M.es
dc.creatorBraus, Gerhard H.es
dc.creatorBraus-Stromeyer, Susanna A.es
dc.creatorCorrochano Peláez, Luis Maríaes
dc.creatorDai, Ziyues
dc.creatorDijck, Piet W.M. vanes
dc.creatorHofmann, Geraldes
dc.creatorLasure, Linda L.es
dc.creatorMagnuson, Jon K.es
dc.creatorMenke, Hildegardes
dc.creatorMeijer, Martines
dc.creatorMeijer, Susan L.es
dc.creatorNielsen, Jakob B.es
dc.creatorNielsen, Michael L.es
dc.creatorOoyen, Albert J.J. vanes
dc.creatorPel, Herman J.es
dc.creatorPoulsen, Larses
dc.creatorSamson, Rob A.es
dc.creatorStam, Heines
dc.creatorTsang, Adrianes
dc.creatorBrink, Johannes M. van denes
dc.creatorAtkins, Alexes
dc.creatorAerts, Andreaes
dc.creatorShapiro, Harrises
dc.creatorPangilinan, Jasmynes
dc.creatorSalamov, Asafes
dc.creatorYigong Loues
dc.creatorLindquist, Erikaes
dc.creatorLucas, Susan M.es
dc.creatorGrimwood, Janees
dc.creatorGrigoriev, Igor V.es
dc.creatorKubicek, Christian P.es
dc.creatorMartinez, Diegoes
dc.creatorPeij, Noe¨l N.M.E. vanes
dc.creatorRoubos, Johannes A.es
dc.creatorNielsen, Jenses
dc.creatorBaker, Scott E.es
dc.date.accessioned2016-05-03T07:36:16Z
dc.date.available2016-05-03T07:36:16Z
dc.date.issued2011
dc.identifier.issn1088-9051es
dc.identifier.urihttp://hdl.handle.net/11441/40640
dc.description.abstractThe filamentous fungus Aspergillus niger exhibits great diversity in its phenotype. It is found globally, both as marine and terrestrial strains, produces both organic acids and hydrolytic enzymes in high amounts, and some isolates exhibit pathogenicity. Although the genome of an industrial enzyme-producing A. niger strain (CBS 513.88) has already been sequenced, the versatility and diversity of this species compel additional exploration. We therefore undertook whole- genome sequencing of the acidogenic A. niger wild-type strain (ATCC 1015) and produced a genome sequence of very high quality. Only 15 gaps are present in the sequence, and half the telomeric regions have been elucidated. Moreover, sequence information from ATCC 1015 was used to improve the genome sequence of CBS 513.88. Chromosome-level comparisons uncovered several genome rearrangements, deletions, a clear case of strain-specific horizontal gene transfer, and identi- fication of 0.8 Mb of novel sequence. Single nucleotide polymorphisms per kilobase (SNPs/kb) between the two strains were found to be exceptionally high (average: 7.8, maximum: 160 SNPs/kb). High variation within the species was con- firmed with exo-metabolite profiling and phylogenetics. Detailed lists of alleles were generated, and genotypic differences were observed to accumulate in metabolic pathways essential to acid production and protein synthesis. A transcriptome analysis supported up-regulation of genes associated with biosynthesis of amino acids that are abundant in glucoamylase A, tRNA-synthases, and protein transporters in the protein producing CBS 513.88 strain. Our results and data sets from this integrative systems biology analysis resulted in a snapshot of fungal evolution and will support further optimization of cell factories based on filamentous fungi.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherCold Spring Harbor Laboratory Presses
dc.relation.ispartofGenome Research, 21, 885-897es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCitric acides
dc.subjectGlucan 1es
dc.subject4 alpha glucosidasees
dc.subjectTransfer RNAes
dc.titleComparative genomics of citric-acid-producing Aspergillus niger ATCC 1015 versus enzyme-producing CBS 513.88es
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Genéticaes
dc.relation.publisherversion10.1101/gr.112169.110es
dc.identifier.doihttp://dx.doi.org/10.1101/gr.112169.110es
idus.format.extent14 p.es
dc.identifier.idushttps://idus.us.es/xmlui/handle/11441/40640

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