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dc.contributor.authorOlivera, Elías R.-
dc.contributor.authorCarnicero, David-
dc.contributor.authorJodra, Ruth-
dc.contributor.authorMiñambres Rodríguez, Baltasar-
dc.contributor.authorGarcía, Belén-
dc.contributor.authorAbraham, Gustavo A.-
dc.contributor.authorGallardo Ruiz, Alberto-
dc.contributor.authorSan Román, Julio-
dc.contributor.authorGarcía, José Luis-
dc.contributor.authorNaharro, Germán-
dc.contributor.authorLuengo, José M.-
dc.date.accessioned2009-04-01T12:30:05Z-
dc.date.available2009-04-01T12:30:05Z-
dc.date.issued2001-10-
dc.identifier.citationEnvironmental Microbiology 3(10): 612-618 (2001)en_US
dc.identifier.issn1462-2912-
dc.identifier.urihttp://hdl.handle.net/10261/12031-
dc.description7 páginas, 4 figuras, 1 tabla.-- PMID: 11722541 [PubMed].en_US
dc.description.abstractNew bioplastics containing aromatic or mixtures of aliphatic and aromatic monomers have been obtained using genetically engineered strains of Pseudomonas putida. The mutation (-) or deletion (Delta) of some of the genes involved in the beta-oxidation pathway (fadA(-), fadB(-) Delta fadA or Delta fad BA mutants) elicits a strong intracellular accumulation of unusual homo- or co-polymers that dramatically alter the morphology of these bacteria, as more than 90% of the cytoplasm is occupied by these macromolecules. The introduction of a blockade in the beta-oxidation pathway, or in other related catabolic routes, has allowed the synthesis of polymers other than those accumulated in the wild type (with regard to both monomer size and relative percentage), the accumulation of certain intermediates that are rapidly catabolized in the wild type and the accumulation in the culture broths of end catabolites that, as in the case of phenylacetic acid, phenylbutyric acid, trans-cinnamic acid or their derivatives, have important medical or pharmaceutical applications (antitumoral, analgesic, radiopotentiators, chemopreventive or antihelmintic). Furthermore, using one of these polyesters (poly 3-hydroxy-6-phenylhexanoate), we obtained polymeric microspheres that could be used as drug vehicles.en_US
dc.description.sponsorshipThis work was supported by grants 1FD97-0245 from the Fondo Europeo de Desarrollo Regional and BMC2000-0125-C04 from the Ministerio de Ciencia y Tecnología.en_US
dc.format.extent94510 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherBlackwell Publishingen_US
dc.rightsclosedAccessen_US
dc.titleGenetically engineered Pseudomonas: a factory of new bioplastics with broad applicationsen_US
dc.typeartículoen_US
dc.identifier.doi10.1046/J.1462-2920.2001.00224.x-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1046/J.1462-2920.2001.00224.xen_US
dc.contributor.funderEuropean Commission-
dc.contributor.funderMinisterio de Ciencia y Tecnología (España)-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100006280es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeartículo-
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