A new acidophilic thermostable endo-1,4-β-mannanase from Penicillium oxalicum GZ-2: cloning, characterization and functional expression in Pichia pastorisReportar como inadecuado

A new acidophilic thermostable endo-1,4-β-mannanase from Penicillium oxalicum GZ-2: cloning, characterization and functional expression in Pichia pastoris - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

BMC Biotechnology

, 14:90

Protein and enzyme technology


BackgroundEndo-1,4-β-mannanase is an enzyme that can catalyze the random hydrolysis of β-1, 4-mannosidic linkages in the main chain of mannans, glucomannans and galactomannans and has a number of applications in different biotechnology industries. Penicillium oxalicum is a powerful hemicellulase-producing fungus Bioresour Technol 123:117-124, 2012; however, few previous studies have focused on the cloning and expression of the endo-1,4-β-mannanase gene from Penicillium oxalicum.

ResultsA gene encoding an acidophilic thermostable endo-1,4-β-mannanase E.C. from Penicillium oxalicum GZ-2, which belongs to glycoside hydrolase family 5, was cloned and successfully expressed in Pichia pastoris GS115. A high enzyme activity 84.4 U mL was detected in the culture supernatant. The recombinant endo-1,4-β-mannanase rPoMan5A was tagged with 6 × His at its C-terminus and purified using a Ni-NTA Sepharose column to apparent homogeneity. The purified rPoMan5A showed a single band on SDS-PAGE with a molecular mass of approximately 61.6 kDa. The specific activity of the purified rPoMan5A was 420.9 U mg using locust bean gum as substrate. The optimal catalytic temperature 10 min assay and pH value for rPoMan5A are 80°C and pH 4.0, respectively. The rPoMan5A is highly thermostable with a half-life of approximately 58 h at 60°C at pH 4.0. The Km and Vmax values for locust bean gum, konjac mannan, and guar gum are 7.6 mg mL and 1425.5 μmol min mg, 2.1 mg mL and 154.8 μmol min mg, and 2.3 mg mL and 18.9 μmol min mg, respectively. The enzymatic activity of rPoMan5A was not significantly affected by an array of metal ions, but was inhibited by Fe and Hg. Analytical results of hydrolytic products showed that rPoMan5A could hydrolyze various types of mannan polymers and released various mannose and manno-oligosaccharides, with the main products being mannobiose, mannotriose, and mannopentaose.

ConclusionOur study demonstrated that the high-efficient expression and secretion of acid stable and thermostable recombinant endo-1, 4-β-mannanase in Pichia pastoris is suitable for various biotechnology applications.

KeywordsEndo-1,4-β-mannanase Gene cloning Expression system Pichia pastoris Penicillium oxalicum Electronic supplementary materialThe online version of this article doi:10.1186-s12896-014-0090-z contains supplementary material, which is available to authorized users.

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Autor: Hanpeng Liao - Shuixian Li - Haiping Zheng - Zhong Wei - Dongyang Liu - Waseem Raza - Qirong Shen - Yangchun Xu

Fuente: https://link.springer.com/

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