dc.creatorMarem, Alyne
dc.creatorOkamoto, Debora N.
dc.creatorOliveira, Lilian C.G.
dc.creatorRuiz, Diego M.
dc.creatorPaggi, Roberto Alejandro
dc.creatorKondo, Marcia Y.
dc.creatorGouvea, Iuri E.
dc.creatorJuliano, Maria A.
dc.creatorde Castro, Rosana Esther
dc.creatorJuliano, Luiz
dc.creatorIcimoto, Marcelo Y.
dc.date.accessioned2019-10-29T18:53:11Z
dc.date.accessioned2022-10-15T16:02:03Z
dc.date.available2019-10-29T18:53:11Z
dc.date.available2022-10-15T16:02:03Z
dc.date.created2019-10-29T18:53:11Z
dc.date.issued2018-07-07
dc.identifierMarem, Alyne; Okamoto, Debora N.; Oliveira, Lilian C.G.; Ruiz, Diego M.; Paggi, Roberto Alejandro; et al.; Functional roles of C-terminal extension (CTE) of salt-dependent peptidase activity of the Natrialba magadii extracellular protease (NEP); Elsevier Science; International Journal of Biological Macromolecules; 113; 7-7-2018; 1134-1141
dc.identifier0141-8130
dc.identifierhttp://hdl.handle.net/11336/87573
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4406407
dc.description.abstractNep (Natrialba magadii extracellular protease) is a halolysin-like peptidase secreted by the haloalkaliphilic archaeon Natrialba magadii. Many extracellular proteases have been characterized from archaea to bacteria as adapted to hypersaline environments retaining function and stability until 4.0 M NaCl. As observed in other secreted halolysins, this stability can be related to the presence of a C-terminal extension (CTE) sequence. In the present work, we compared the biochemical properties of recombinant Nep protease with the truncated form at the 134 amino acids CTE (Nep∆CTE), that was more active in 4 M NaCl than the non-truncated wild type enzyme. Comparable to the wild type, Nep∆CTE protease is irreversibly inactivated at low salt solutions. The substrate specificity of the truncated Nep∆CTE was similar to that of wild type form as demonstrated by a combinatorial library of FRET substrates. The enzyme stability, the effect of different salts and the thermodynamics assays using different lengths of substrates demonstrated similarities between the two forms. Altogether, these data provide further information on the stability and structural determinants of halolysins under different salinities, especially concerning the enzymatic behavior.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://linkinghub.elsevier.com/retrieve/pii/S0141813018305579
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ijbiomac.2018.03.026
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectHalophilic protease
dc.subjectNatrialba magadii
dc.subjectSerine protease
dc.titleFunctional roles of C-terminal extension (CTE) of salt-dependent peptidase activity of the Natrialba magadii extracellular protease (NEP)
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


Este ítem pertenece a la siguiente institución