Global Lrp regulator protein from Haloferax mediterranei: Transcriptional analysis and structural characterization

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dc.contributorBiotecnología de Extremófilos (BIOTECEXTREM)es_ES
dc.contributor.authorMatarredona, Laura-
dc.contributor.authorGarcía-Bonete, María José-
dc.contributor.authorGuío, Jorge-
dc.contributor.authorCamacho, Mónica-
dc.contributor.authorFillat, María F.-
dc.contributor.authorEsclapez, Julia-
dc.contributor.authorBonete, María-José-
dc.contributor.otherUniversidad de Alicante. Departamento de Bioquímica y Biología Molecular y Edafología y Química Agrícolaes_ES
dc.date.accessioned2024-01-26T12:36:49Z-
dc.date.available2024-01-26T12:36:49Z-
dc.date.issued2024-01-18-
dc.identifier.citationInternational Journal of Biological Macromolecules. 2024, 260(Part 2): 129541. https://doi.org/10.1016/j.ijbiomac.2024.129541es_ES
dc.identifier.issn0141-8130 (Print)-
dc.identifier.issn1879-0003 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/140040-
dc.description.abstractHaloferax mediterranei, an extreme halophilic archaeon thriving in hypersaline environments, has acquired significant attention in biotechnological and biochemical research due to its remarkable ability to flourish in extreme salinity conditions. Transcription factors, essential in regulating diverse cellular processes, have become focal points in understanding its adaptability. This study delves into the role of the Lrp transcription factor, exploring its modulation of glnA, nasABC, and lrp gene promoters in vivo through β-galactosidase assays. Remarkably, our findings propose Lrp as the pioneering transcriptional regulator of nitrogen metabolism identified in a haloarchaeon. This study suggests its potential role in activating or repressing assimilatory pathway enzymes (GlnA and NasA). The interaction between Lrp and these promoters is analyzed using Electrophoretic Mobility Shift Assay and Differential Scanning Fluorimetry, highlighting l-glutamine's indispensable role in stabilizing the Lrp-DNA complex. Our research uncovers that halophilic Lrp forms octameric structures in the presence of l-glutamine. The study reveals the three-dimensional structure of the Lrp as a homodimer using X-ray crystallography, confirming this state in solution by Small-Angle X-ray Scattering. These findings illuminate the complex molecular mechanisms driving Hfx. mediterranei's nitrogen metabolism, offering valuable insights about its gene expression regulation and enriching our comprehension of extremophile biology.es_ES
dc.description.sponsorshipFunding for this research was provided by the Ministry of Economy and Competitiveness and FEDER (BIO2013-42921-P); “Programa Propio para el Fomento de la I + D + i del Vicerrectorado de Investigación y Transferencia de Conocimiento” of the University of Alicante (Spain) (GRE20-02-C; VIGROB-016).es_ES
dc.languageenges_ES
dc.publisherElsevieres_ES
dc.rights© 2024 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).es_ES
dc.subjectLrp transcription factores_ES
dc.subjectEMSAes_ES
dc.subjectHaloarchaeaes_ES
dc.subjectX-ray crystallographyes_ES
dc.subjectSAXSes_ES
dc.subjectDSFes_ES
dc.titleGlobal Lrp regulator protein from Haloferax mediterranei: Transcriptional analysis and structural characterizationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1016/j.ijbiomac.2024.129541-
dc.relation.publisherversionhttps://doi.org/10.1016/j.ijbiomac.2024.129541es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//BIO2013-42921-Pes_ES
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