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1.
Electron. j. biotechnol ; 29: 7-12, sept. 2017. ilus, graf, tab
Artículo en Inglés | LILACS | ID: biblio-1016095

RESUMEN

Background: DegP is a serine protease that specifically cleaves and refolds unfolding proteins in the periplasmic space of the cells. To date, there is no information regarding DegP from halophilic bacteria. Chromohalobacter salexigens BKL5 is a moderately halophilic bacterium that has the ability to grow in a media containing more than 15% salt. Therefore, the objectives of this work were to clone and overexpress DegP-encoding gene from C. salexigens BKL5 and characterize its biochemical properties. Results: DegP-encoding gene was overexpressed in Escherichia coli BL21(DE3) CodonPlus in an active form. SDS-PAGE analysis showed that the molecular weight of the recombinant DegP was 45 kDa. Size-exclusion chromatography analysis suggested that recombinant DegP was present in two multimeric states, hexameric and dodecameric, with molecular weights of 297.9 and 579.12 kDa, respectively. Both conformations were enzymatically active when casein was used as substrate for enzymatic assay. Circular dichroism analysis showed that recombinant DegP was composed of 0.21­0.29 helical content, which was comparable to the helical content in the crystal structure of E. coli DegP. The basic/acidic residue ratio of recombinant DegP was 0.56, which was slightly higher than that of DegP from extreme halophiles (average, 0.45) but significantly lower than that of DegP from nonhalophiles (average, 0.94). Conclusions: Recombinant DegP from C. salexigens BKL5 showed proteolytic activity when ß-casein was used as a substrate. In silico analysis indicated that recombinant DegP had characteristics similar to those of halophilic proteins depending on its amino acid composition.


Asunto(s)
Serina Endopeptidasas/genética , Proteínas Periplasmáticas/genética , Chromohalobacter/enzimología , Proteolisis , Proteínas de Choque Térmico/genética , Proteínas Recombinantes , Serina Endopeptidasas/metabolismo , Caseínas , Cromatografía en Gel , Dicroismo Circular , Clonación Molecular , Proteínas Periplasmáticas/metabolismo , Electroforesis en Gel de Poliacrilamida , Escherichia coli , Salinidad , Chromohalobacter/genética , Proteínas de Choque Térmico/metabolismo , Peso Molecular
2.
Braz. j. microbiol ; 46(3): 879-883, July-Sept. 2015. tab
Artículo en Inglés | LILACS | ID: lil-755800

RESUMEN

Studies investigating rickettsial infections in ticks parasitizing wild animals in the Northeast region of Brazil have been confined to the detection of Rickettsia amblyommii in immature stages of Amblyomma longirostre collected from birds in the state of Bahia, and in immatures and females of Amblyomma auriculariumcollected from the striped hog-nosed skunk (Conepatus semistriatus) and armadillos (Euphractus sexcinctus) in the state of Pernambuco. The current study extends the distribution of R. amblyommii (strain Aranha), which was detected in A. longirostre collected from the thin-spined porcupine Chaetomys subspinosus and the hairy dwarf porcupine Coendou insidiosus. In addition, we report the first detection of Rickettsia bellii in adults of A. longirostre collected from C. insidiosus in the state of Bahia.

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Asunto(s)
Animales , Ixodidae/microbiología , Infecciones por Rickettsia/microbiología , Rickettsia/genética , Rickettsia/aislamiento & purificación , Infestaciones por Garrapatas/microbiología , Animales Salvajes , Armadillos , Secuencia de Bases , Aves , Brasil , Proteínas de la Membrana Bacteriana Externa/genética , Proteínas Bacterianas/genética , Citrato (si)-Sintasa/genética , ADN Bacteriano , Proteínas de Choque Térmico/genética , Mephitidae , Datos de Secuencia Molecular , Tipificación Molecular , Puercoespines , Proteínas Periplasmáticas/genética , Análisis de Secuencia de ADN , Serina Endopeptidasas/genética
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