Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-22T05:35:50.271Z Has data issue: false hasContentIssue false

Cloning, expression and characterization of NAD+-dependent glyceraldehyde-3-phosphate dehydrogenase of adult Haemonchus contortus

Published online by Cambridge University Press:  21 December 2010

K. Han
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, P.R. China
L. Xu
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, P.R. China
R. Yan
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, P.R. China
X. Song
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, P.R. China
X. Li*
Affiliation:
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, P.R. China
*
*Fax: +86 25 8439 8669 E-mail: lixiangrui@njau.edu.cn

Abstract

Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) regulates a wide range of biological processes, including pathogen evasion. In the present research, the GAPDH gene of Haemonchus contortus (HcGAPDH) was cloned and characterized. Specific primers for the rapid amplification of cDNA ends (RACE) were designed based on the expressed sequence tag (EST, AW670737) to amplify the 3′ and 5′ ends of HcGAPDH. The full length of cDNA from this gene was obtained by overlapping the sequences of 3′ and 5′ extremities and amplification by reverse transcription polymerase chain reaction (RT-PCR). The biochemical activities of the recombinant protein HcGAPDH, which was expressed in prokaryotic cells and purified by affinity chromatography, were analysed by assays of enzymatic activity, thermal stability and pH. The results showed that the cloned full-length cDNA comprised 1303 bp and encoded a peptide with 341 amino acid residues which showed sequence similarity to several known GAPDHs. The biochemical assay showed that the protein encoded by the HcGAPDH exhibited enzymatic activity with NAD+ as a cofactor. HcGAPDH was stable between pH 5 and 9 and maintained activity at high temperatures of up to 75°C. The natural GAPDH of Haemonchus contortus detected by immunoblot assay was approximately 38 kDa in size, and the recombinant HcGAPDH was recognized strongly by serum from naturally infected goats.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Arumugam Pillai, M., Lihuang, Z. & Akiyama, T. (2002) Molecular cloning, characterization, expression and chromosomal location of OsGAPDH, a submergence responsive gene in rice (Oryza sativa L.). Theoretical and Applied Genetics 105, 3442.CrossRefGoogle ScholarPubMed
Batthyany, C., Schopfer, F.J., Baker, P.R., Duran, R., Baker, L.M., Huang, Y., Cervenansky, C., Branchaud, B.P. & Freeman, B.A. (2006) Reversible post-translational modification of proteins by nitrated fatty acids in vivo. Journal of Biological Chemistry 281, 2045020463.CrossRefGoogle ScholarPubMed
Baxi, M.D. & Vishwanatha, J.K. (1995) Uracil DNA-glycosylase/glyceraldehyde-3-phosphate dehydrogenase is an Ap4A binding protein. Biochemistry 34, 97009707.CrossRefGoogle ScholarPubMed
Bradford, M.M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248254.CrossRefGoogle ScholarPubMed
Chomczynski, P. & Sacchi, N. (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate–phenol–chloroform extraction. Analytical Biochemistry 162, 156159.CrossRefGoogle ScholarPubMed
El Ridi, R., Farouk, F., Sherif, M., Al-Sherbiny, M., Osman, A., El Gengehi, N. & Shoemaker, C.B. (1998) T and B cell reactivity to a 42-kDa protein is associated with human resistance to both schistosomiasis mansoni and haematobium. Journal of Infectious Diseases 177, 13641372.CrossRefGoogle Scholar
Erttmann, K.D., Kleensang, A., Schneider, E., Hammerschmidt, S., Buttner, D.W. & Gallin, M. (2005) Cloning, characterization and DNA immunization of an Onchocerca volvulus glyceraldehyde-3-phosphate dehydrogenase (Ov-GAPDH). Biochimica et Biophysica Acta 1741, 8594.CrossRefGoogle ScholarPubMed
Ferdinand, W. (1964) The isolation and specific activity of rabbit-muscle glyceraldehyde phosphate dehydrogenase. Biochemical Journal 92, 578585.CrossRefGoogle ScholarPubMed
Fothergill-Gilmore, L.A. & Michels, P.A. (1993) Evolution of glycolysis. Progress in Biophysics, Molecular Biology 59, 105235.CrossRefGoogle ScholarPubMed
Iddar, A., Valverde, F., Serrano, A. & Soukri, A. (2002) Expression, purification, and characterization of recombinant nonphosphorylating NADP-dependent glyceraldehyde-3-phosphate dehydrogenase from Clostridium acetobutylicum. Protein Expression and Purification 25, 519526.CrossRefGoogle ScholarPubMed
Iddar, A., Valverde, F., Serrano, A. & Soukri, A. (2003) Purification of recombinant non-phosphorylating NADP-dependent glyceraldehyde-3-phosphate dehydrogenase from Streptococcus pyogenes expressed in E. coli. Molecular and Cellular Biochemistry 247, 195203.CrossRefGoogle ScholarPubMed
Kasuga-Aoki, H., Tsuji, N., Suzuki, K., Matsumoto, Y., Arakawa, T. & Isobe, T. (2002) Molecular characterization of a glyceraldehyde-3-phosphate dehydrogenase from the swine roundworm Ascaris suum. Molecular and Biochemical Parasitology 119, 135139.CrossRefGoogle ScholarPubMed
Kohler, P. (1985) The strategies of energy conservation in helminths. Molecular and Biochemical Parasitology 17, 118.CrossRefGoogle ScholarPubMed
Maltagliati, F., Belcari, P., Casu, D., Casu, M., Sartor, P., Vargiu, G. & Castelli, A. (2002) Allozyme genetic variability and gene flow in Octopus vulgaris (Cephalopoda, Octopodidae) from the Mediterranean Sea. Bulletin of Marine Science 71, 473486.Google Scholar
McDonald, B., Reep, B., Lapetina, E.G. & Molina y Vedia, L. (1993) Glyceraldehyde-3-phosphate dehydrogenase is required for the transport of nitric oxide in platelets. Proceedings of the National Academy of Sciences, USA 90, 1112211126.CrossRefGoogle ScholarPubMed
Muleke, C.I., Ruofeng, Y., Lixin, X., Yanming, S. & Xiangrui, L. (2006) Characterization of HC58cDNA, a putative cysteine protease from the parasite Haemonchus contortus. Journal of Veterinary Science 7, 249255.CrossRefGoogle ScholarPubMed
Newton, S.E. & Munn, E.A. (1999) The development of vaccines against gastrointestinal nematode parasites, particularly Haemonchus contortus. Parasitology Today 15, 116122.CrossRefGoogle ScholarPubMed
Nikolaou, S. & Gasser, R.B. (2006) Prospects for exploring molecular developmental processes in Haemonchus contortus. International Journal for Parasitology 36, 859868.CrossRefGoogle ScholarPubMed
Oukhattar, L., Baibai, T., Moutaouakkil, A., Assobhei, O. & Soukri, A. (2008) Isolation and characterization of glyceraldehyde-3-phosphate dehydrogenase from the common octopus (Octopus vulgaris Cuvier, 1797). Reviews in Fish Biology and Fisheries 18, 263271.CrossRefGoogle Scholar
Quinones, W., Pena, P., Domingo-Sananes, M., Caceres, A., Michels, P.A., Avilan, L. & Concepcion, J.L. (2007) Leishmania mexicana: molecular cloning and characterization of enolase. Experimental Parasitology 116, 241251.CrossRefGoogle ScholarPubMed
Singh, R. & Green, M.R. (1993) Sequence-specific binding of transfer RNA by glyceraldehyde-3-phosphate dehydrogenase. Science 259, 365368.CrossRefGoogle ScholarPubMed
Sirover, M.A. (1999) New insights into an old protein: the functional diversity of mammalian glyceraldehyde-3-phosphate dehydrogenase. Biochimica et Biophysica Acta 1432, 159184.CrossRefGoogle ScholarPubMed
Stover, N.A. & Steele, R.E. (2001) Trans-spliced leader addition to mRNAs in a cnidarian. Proceedings of the National Academy of Sciences, USA 98, 56935698.CrossRefGoogle Scholar
Villamon, E., Villalba, V., Nogueras, M.M., Tomas, J.M., Gozalbo, D. & Gil, M.L. (2003) Glyceraldehyde-3-phosphate dehydrogenase, a glycolytic enzyme present in the periplasm of Aeromonas hydrophila. Antonie Van Leeuwenhoek 84, 3138.CrossRefGoogle ScholarPubMed
Williams, C., Xu, L. & Blumenthal, T. (1999) SL1 trans splicing and 3′-end formation in a novel class of Caenorhabditis elegans operon. Molecular and Cellular Biology 19, 376383.CrossRefGoogle Scholar
Yanming, S., Ruofeng, Y., Muleke, C.I., Guangwei, Z., Lixin, X. & Xiangrui, L. (2007) Vaccination of goats with recombinant galectin antigen induces partial protection against Haemonchus contortus infection. Parasite Immunology 29, 319326.CrossRefGoogle ScholarPubMed
Yi, D., Xu, L., Yan, R. & Li, X. (2010) Haemonchus contortus: cloning and characterization of serpin. Experimental Parasitology 125, 363370.CrossRefGoogle ScholarPubMed
Zorio, D.A., Cheng, N.N., Blumenthal, T. & Spieth, J. (1994) Operons as a common form of chromosomal organization in C. elegans. Nature 372, 270272.CrossRefGoogle ScholarPubMed