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  • Molecular cloning, expression, and immunolocalization of the NAD(+)-dependent glycerol 3-phosphate dehydrogenase (GPD) from Clonorchis sinensis.

Molecular cloning, expression, and immunolocalization of the NAD(+)-dependent glycerol 3-phosphate dehydrogenase (GPD) from Clonorchis sinensis.

Parasitology research (2011-03-17)
Yongxiu Fan, Xiaoyun Wang, Chuanhuan Deng, Yan Huang, Lexun Wang, Wenjun Chen, Chi Liang, Xuerong Li, Zhongdao Wu, Xinbing Yu
ABSTRACT

Glycerol 3-phosphate dehydrogenase (GPD) plays an important role in the energy metabolism and nutrition metabolism. In order to know about the biological functions of GPD of Clonorchis sinensis (C. sinensis), we identified a complete gene coding GPD from C. sinensis metacercaria cDNA library. This novel cDNA sequence contains 1,056 bp with a putative open reading frame of 351 amino acids and shares 74% identity with GPD from Schistosoma mansoni. Recombinant CsGPD was expressed and purified from Escherichia coli BL21 (DE3). Western blot analysis displayed that recombinant CsGPD can be recognized by anti-CsGPD serum and C. sinensis-infected serum. RT-PCR and immunolocalization analysis confirmed that GPD expressed both at the stage of adult worm and metacercaria of C. sinensis and immunolocated at the tegument of adult worm, tegument and tegumentary cells of metacercaria. Our current study has paved the way for the further researches about the biological functions involved in the growth of C. sinensis.

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Sigma-Aldrich
α-Glycerophosphate Dehydrogenase-Triosephosphate Isomerase from rabbit muscle, Type III, ammonium sulfate suspension
Sigma-Aldrich
α-Glycerophosphate Dehydrogenase from rabbit muscle, Type I, ammonium sulfate suspension, 100-300 units/mg protein
Sigma-Aldrich
α-Glycerophosphate Dehydrogenase from rabbit muscle, Type X, lyophilized powder, ≥100 units/mg protein