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Molecular cloning, characterization and function analysis of a GDH gene from Sclerotinia sclerotiorum in rice

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Abstract

The full-length cDNA encoding a glutamate dehydrogenase (GDH) which catalyzes the reaction of reductive amination of α-oxoglutarate (α-OG) to glutamate (the anabolic activity) and the reverse reaction of oxidative deamination of glutamate (the catabolic activity) was isolated from Sclerotinia sclerotiorum, we designated it as SsGDH. Bioinformatics analysis revealed that SsGDH had a typical GDH spatial structure and extensive homology with other fungal or bacteria GDHs. To evaluate its function in rice, rice (Oryza sativa L. cv. ‘kitaake) was transformed with SsGDH in a binary vector construct by Agrobacterium-mediated transformation. Transgenic rice plants showed that transcripts and proteins of SsGDH accumulated at higher levels and GDH enzymatic activity was obviously higher in transgenic rice plants compared with the non-transformant rice plants (CK), though phenotype including plant height, fresh weight and dry weight became slightly weaker compared with CK under 50, 500 and 5,000 μM nitrogen gradient nutrient solution treatment (NH4NO3 as a nitrogen source) after introducing SsGDH into rice. For enzymatic activity assay in vitro, recombinant His6-SsGDH protein was expressed in Escherichia coli BL21 (DE3) and purified by Ni-NTA agarose. Results suggested that recombinant His6-SsGDH protein had GDH activity using ammonium, α-OG, and l-glutamate separately as a substrate at two different concentrations, especially the affinity for ammonium was very high, and its Km value was only 0.28 ± 0.03 mM, indicating that SsGDH can assimilate more ammonium into rice. According to previous reports, transgenic plants expressing fungal or bacteria GDHs might show improved herbicide resistance. Basta resistance test showed that SsGDH expression in rice can significantly enhanced their tolerance to Basta than CK. In conclusion, our results may provide some clues for further investigation on nitrogen utilization via introducing exogenous GDHs from lower organisms into rice.

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Abbreviations

Ss :

Sclerotinia sclerotiorum

GDH:

Glutamate dehydrogenase

GOGAT:

Glutamate synthase

GS:

Glutamine synthetase

PCR:

Polymerase chain reaction

α-OG:

α-Oxoglutarate

References

  1. Hirel B, Le Gouis J, Ney B, Gallais A (2007) The challenge of improving nitrogen use efficiency in crop plants: towards a more central role for genetic variability and quantitative genetics within integrated approaches. J Exp Bot 58:2369–2387

    Article  CAS  PubMed  Google Scholar 

  2. Raun WR, Johnson GV (1999) Improving nitrogen use efficiency for cereal production. Agron J 91:357–363

    Article  Google Scholar 

  3. Lea PJ, MiXin BJ (1974) Alternative route for nitrogen assimilation in higher plants. Nature 18:614–616

    Article  Google Scholar 

  4. Wootton JC (1983) Re-assessment of ammonium-ion affinities of NADP-specific glutamate dehydrogenases. Activation of the Neurospora crassa enzyme by ammonium and rubidium ions. Biochem J 209(2):527–531

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Melo-Oliveira R, Oliveira IC, Coruzzi GM (1996) Arabidopsis mutant analysis and gene regulation define a non-redundant role for glutamate dehydrogenase in nitrogen assimilation. Proc Natl Acad Sci USA 93:4718–4723

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  6. Purnell MP, Skopelitis DS, Roubelakis-Angelakis KA, Botella JR (2005) Modulation of higher-plant NAD(H)-dependent glutamate dehydrogenase activity in transgenic tobacco via alteration of beta subunit levels. Planta 222:167–180

    Article  CAS  PubMed  Google Scholar 

  7. Yamaya T, Oaks A, Matsumoto H (1984) Characteristics of glutamate dehydrogenase in mitochondria prepared from corn shoots. Plant Physiol 76:1009–1013

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  8. Lea PJ, Thurman DA (1972) Intracellular location and properties of plant L-glutamate dehydrogenases. J Exp Bot 23:440–449

    Article  CAS  Google Scholar 

  9. Ameziane R, Bernhard K, Lightfoot D (2000) Expression of the bacterial gdhA gene encoding a NADPH glutamate dehydrogenase in tobacco affects plant growth and development. Plant Soil 221:47–57

    Article  CAS  Google Scholar 

  10. Kisaka H, Kida T (2003) Transgenic tomato plant carrying a gene for NADP-dependent glutamate dehydrogenase (gdhA) from Aspergillus nidulans. Plant Sci 164:35–42

    Article  CAS  Google Scholar 

  11. Abawi GS, Grogan RG (1979) Epidemiology of diseases caused by Sclerotinia species. Phytopathology 69:899–904

    Article  Google Scholar 

  12. Adams PB, Ayers WA (1979) Ecology of Sclerotinia species. Phytopathology 69:896–899

    Article  Google Scholar 

  13. Huang HC (1985) Factors affecting myceliogenic germination of sclerotia of Sclerotinia sclerotiorum. Phytopathology 75:433–437

    Article  Google Scholar 

  14. Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays of tobacco tissue cultures. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  15. Mae T, Ohira K (1981) the remobilization of nitrogen related to leaf growth and senescence in rice plants (Oryza sativa L.). Plant Cell Physiol 22:1067–1074

    CAS  Google Scholar 

  16. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1994) the ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25:4876–4882

    Article  Google Scholar 

  17. Schwede T, Kopp J, Guex N, Peitsch MC (2003) SWISSMODEL: an automated protein homology-modeling server. Nucleic Acids Res 31:3381–3385

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  18. Cao X, Zong Z, Xiuyun J, Sun Y, Dai C, Liu Q, Jiang J (2010) Molecular cloning, characterization and function analysis of the gene encoding HMG-CoA reductase from Euphorbia Pekinensis Rupr. Mol Biol Rep 37:1559–1567

    Article  CAS  PubMed  Google Scholar 

  19. Haruhiko Washida Okita Lab. IBC, WSU Agrobacterium-Mediated Transformation for Rice May 2007

  20. Rogers SO, Bendich AJ (1988) Extraction of DNA from plant tissues. In: Gelvin SB, Schilperoort RA (eds) Plant molecular biology manual, pp A6: l-10. Kluwer Academic Publishers, Boston, MA

    Google Scholar 

  21. Loulakakis KA, Roubelakis-Angelakis KA (1991) Plant NAD (H)-glutamate dehydrogenase consists of two subunit polypeptides and their participation in the seven isoenzymes occurs in an ordered ratio. Plant Physiol 97:104–111

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  22. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  23. Noor S, Punekar NS (2005) Allosteric NADP-glutamate dehydrogenase from aspergilli: purification, characterization and implications for metabolic regulation at the carbon–nitrogen interface. Microbiology 151:1409–1419

    Article  CAS  PubMed  Google Scholar 

  24. Ouyang S-Q, Liu Y-F, Liu P, Lei G, He S-J, Ma B, Zhang W-K, Zhang J-S, Chen S-Y (2010) Receptor-like kinase OsSIK1 improves drought and salt stress tolerance in rice (Oryza sativa) plants. The Plant Journal 62:316–329

    Article  CAS  PubMed  Google Scholar 

  25. Ishiyama K, Inoue E, Watanabe-Takahashi A, Obara M, Yamaya T, Takahashi H (2004) Kinetic properties and ammonium-dependent regulation of cytosolic isoenzymes of glutamine synthetase in Arabidopsis. J Biol Chem 16(279):16598–16605

    Article  Google Scholar 

  26. Lin C, Ahmad M, Cashmore AR (1996) Plant J 10:893–902

    Article  CAS  PubMed  Google Scholar 

  27. Huang GC, Meng SD, Wang R, Yang HY, Tian B (2002) Cloning of glutamate dehydrogenase cDNA from Chlorella sorokiniana and analysis of transgenic tobacco plants. Acta Bot Sin 44:318–324

    CAS  Google Scholar 

Download references

Acknowledgments

This research is financially supported by Important National Science and Technology Specific Projects (No. 2009ZX08001-030B), National Science Foundation of China (No. 31170172), Hunan Provincial Natural Science Foundation of China (No.12JJ3024), Fundamental Research Funds for the Central Universities, National Key Laboratory of Plant Molecular Genetics (NKLPMG).

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Correspondence to Xuanming Liu.

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Changqing Du and Jianzhong Lin have contributed equally to this work.

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Du, C., Lin, J., Yang, Y. et al. Molecular cloning, characterization and function analysis of a GDH gene from Sclerotinia sclerotiorum in rice. Mol Biol Rep 41, 3683–3693 (2014). https://doi.org/10.1007/s11033-014-3233-3

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