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1.
Biotechnol Lett ; 33(1): 131-7, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-20872163

RESUMEN

A hyperthermostable glycoside hydrolase family 51 (GH51) α-L-arabinofuranosidase from Thermotoga petrophila RKU-1 (TpAraF) was cloned, overexpressed, purified and characterized. The recombinant enzyme had optimum activity at pH 6.0 and 70°C with linear α-1,5-linked arabinoheptaose as substrate. The substrate cleavage pattern monitored by capillary zone electrophoresis showed that TpAraF is a classical exo-acting enzyme producing arabinose as its end-product. Far-UV circular dichroism analysis displayed a typical spectrum of α/ß barrel proteins analogously observed for other GH51 α-L-arabinofuranosidases. Moreover, TpAraF was crystallized in two crystalline forms, which can be used to determine its crystallographic structure.


Asunto(s)
Bacterias/enzimología , Glicósido Hidrolasas/genética , Glicósido Hidrolasas/metabolismo , Arabinosa/metabolismo , Dicroismo Circular , Clonación Molecular , Cristalización , ADN Bacteriano/química , ADN Bacteriano/genética , Estabilidad de Enzimas , Expresión Génica , Glicósido Hidrolasas/química , Glicósido Hidrolasas/aislamiento & purificación , Calor , Concentración de Iones de Hidrógeno , Datos de Secuencia Molecular , Conformación Proteica , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/aislamiento & purificación , Proteínas Recombinantes/metabolismo , Análisis de Secuencia de ADN , Especificidad por Sustrato
2.
Acta Crystallogr Sect F Struct Biol Cryst Commun ; 66(Pt 9): 1078-81, 2010 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-20823531

RESUMEN

Endo-1,4-beta-D-mannanases play key roles in seed germination and fruit ripening and have recently received much attention owing to their potential applications in the food, detergent and kraft pulp industries. In order to delineate their structural determinants for specificity and stability, X-ray crystallographic investigations combined with detailed functional studies are being performed. In this work, crystals of the catalytic domain of a hyperthermostable endo-1,4-beta-D-mannanase from Thermotoga petrophila RKU-1 were obtained from three different conditions, resulting in two crystalline forms. Crystals from conditions with phosphate or citrate salts as precipitant (CryP) belonged to space group P2(1)2(1)2(1), with unit-cell parameters a=58.76, b=87.99, c=97.34 A, while a crystal from a condition with ethanol as precipitant (CryE) belonged to space group I2(1)2(1)2(1), with unit-cell parameters a=91.03, b=89.97, c=97.89 A. CryP and CryE diffracted to resolutions of 1.40 and 1.45 A, respectively.


Asunto(s)
Dominio Catalítico , Bacilos Gramnegativos Anaerobios Rectos, Curvos y Espirales/enzimología , Manosidasas/química , Clonación Molecular , Cristalización , Cristalografía por Rayos X , Estabilidad de Enzimas , Expresión Génica , Manosidasas/genética , Manosidasas/aislamiento & purificación
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