Skip to main content
Log in

Isolation and sequence analysis of cDNAs encoding phosphoenolpyruvate carboxykinase from the PCK-type C4 grass Urochloa panicoides

  • Research Article
  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

A rabbit antiserum was raised against phosphoenolpyruvate carboxykinase (PCK) purified from Urochloa panicoides, a PCK-type C4 monocot. The antiserum was used to screen a cDNA expression library constructed from U. panicoides leaf poly(A)+RNA. Inserts from immunoreactive clones were used to rescreen the library and obtain three overlapping cDNAs comprising a 2220 bp composite sequence. The single complete open reading frame of 1872 bp encodes PCK1, a 624 amino acid polypeptide with a predicted molecular mass of 68474 Da. Comparison of PCK1 with other ATP-dependent PCKs indicates that PCK1 is significantly larger, mainly due to an N-terminal extension of greater than 65 residues, and reveals high sequence identity across the central portion of the protein, especially over seven sub-sequences. One of these sub-sequences spans motifs common to several ATP-utilising enzymes for phosphate and divalent cation binding. The anti-PCK antiserum recognises a 69 kDa polypeptide on immunoblots of either purified PCK or U. panicoides leaf extracts. However, polypeptides of 63, 62, 61 and 60 kDa are also immunoreactive. Amino terminal sequencing of polypeptides from preparations of purified PCK demonstrates that these smaller polypeptides are related to PCK1, and time course experiments show that these polypeptides arise from the breakdown of PCK during isolation. Northern blot analysis indicates that the 2.7 kb PCK mRNA is abundant in green leaves but not in roots or etiolated shoots. Moreover, PCK mRNA levels increase gradually during greening, reaching maximum levels after about 84 h.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Arnelle DR, O'Leary MH: Binding of carbon dioxide to phosphoenolpyruvate carboxykinase deduced from carbon kinetic isotope effects. Biochemistry 31: 4363–4368 (1992).

    Google Scholar 

  2. Bennetzen JL, Hall BD: Codon selection in yeast. J Biol Chem 257: 3026–3031 (1982).

    Google Scholar 

  3. Burnell JN: Purification and properties of phosphoenolpyruvate carboxykinase from C4 plants. Aust J Plant Physiol 13: 577–587 (1986).

    Google Scholar 

  4. Campbell WH, Gowri G: Codon usage in higher plants, green algae, and cyanobacteria. Plant Physiol 92: 1–11 (1990).

    Google Scholar 

  5. Chapman KSR, Hatch MD: Intracellular location of phosphoenolpyruvate carboxykinase and other C4 photosynthetic enzymes in mesophyll and bundle sheath protoplasts of Panicum maximum. Plant Sci Lett 29: 145–154 (1983).

    Google Scholar 

  6. Chomczynski P, Sacchi N: Single-step method of RNA isolation by acid guanidinium thiocyanate phenol chloroform extraction. Anal Biochem 162: 156–159 (1987).

    Google Scholar 

  7. Cook JS, Weldon SL, Garcia-Ruiz JP, Hod Y, Hanson RW: Nucleotide sequence of the mRNA encoding the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) from the chicken. Proc Natl Acad Sci USA 83: 7583–7587 (1986).

    Google Scholar 

  8. Gancedo C, Schwerzman K: Inactivation by glucose of phosphoenolpyruvate carboxykinase from Saccharomyces cerevisiae. Arch Microbiol 109: 221–225 (1976).

    Google Scholar 

  9. Goldie AH, Sanwal BD: Genetic and physiological characterisation of Escherichia coli mutants defective in phosphoenolpyruvate carboxykinase activity. J Bact 141: 1115–1121 (1980).

    Google Scholar 

  10. Gutierrez M, Gracen VE, Edwards GE: Biochemical and cytological relationships in C4 plants. Planta 119: 279–300 (1974).

    Google Scholar 

  11. Hatch MD: C4 photosynthesis: an unlikely process full of surprises. Plant Cell Physiol 33: 333–342 (1992).

    Google Scholar 

  12. Hatch MD: C4 photosynthesis: a unique blend of modified biochemistry, anatomy and ultrastructure. Biochim Biophys Acta 895: 81–106 (1987).

    Google Scholar 

  13. Hatch MD, Kagawa T, Craig S: Subdivision of C4 pathway species based on differing C4 acid decarboxylating systems and ultrastructural features. Aust J Plant Physiol 2: 111–128 (1975).

    Google Scholar 

  14. Henikoff S: Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene 28: 351–359 (1984).

    Google Scholar 

  15. Higgins CF, Gallagher MP, Mimmack ML, Pearce SR: A family of closely related ATP-binding sub-units from prokaryotic and eukaryotic cells. BioEssays 8: 111–116 (1988).

    Google Scholar 

  16. Joshi CP: An inspection of the domain between putative TATA box and translation start site in 79 plant genes. Nucl Acids Res 15: 6643–6652 (1987).

    Google Scholar 

  17. Klein RD, Winterrowd CA, Hatzenbuhler NT, Shea MH, Favreau MA, Nulf SC, Geary TG: Cloning of a cDNA encoding phosphoenolpyruvate carboxykinase from Haemonchus contortus. Mol Biochem Parasitol 50: 285–294 (1992).

    Google Scholar 

  18. Ku MSB, Spalding MH, Edwards GE: Intracellular localisation of phosphoenolpyruvate carboxykinase in leaves of C4 and CAM plants. Plant Sci Lett 19: 1–9 (1980).

    Google Scholar 

  19. Kyte J, Doolittle RF: A simple method for displaying the hydropathic character of a protein. J Mol Biol 157: 105–132 (1982).

    Google Scholar 

  20. Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685 (1970).

    Google Scholar 

  21. Linss J, Goldenberg S, Urbina JA, Amzel LM: Cloning and characterisation of the gene encoding ATP-dependent phosphoenolpyruvate carboxykinase in Trypanosoma cruzi: comparison of primary and predicted secondary structure with the host GTP-dependent enzyme. Gene 136: 69–77 (1993).

    Google Scholar 

  22. Medina V, Pontarollo R, Glaeske D, Tabel H, Goldie H: Sequence of the pckA gene of Escherichia coli K-12: relevance to genetic and allosteric regulation and homology of E. coli phosphoenolpyruvate carboxykinase with the enzymes from Trypanosoma brucei and Saccharomyces cerevisiae. J Bact 172: 7151–7156 (1990).

    Google Scholar 

  23. Muirhead H, Clayden DA, Cuffe SP, Davies C: Crystallographic studies on the structure and catalytic activity of pyruvate kinase from skeletal muscle. Biochem Soc Trans 15: 996–999 (1987).

    Google Scholar 

  24. Muller M, Muller H, Holzer H: Immunochemical studies on catabolite inactivation of phosphoenolpyruvate carboxykinase in Saccharomyces cerevisiae. J Biol Chem 256: 723–727 (1981).

    Google Scholar 

  25. Osteras M, Finan TM, Stanley J: Site-directed mutagenesis and DNA sequence of pckA of Rhizobium NGR234, encoding phosphoenolpyruvate carboxykinase: gluconeogenesis and host-dependent symbiotic phenotype. Mol Gen Genet 230: 257–269 (1991).

    Google Scholar 

  26. Popot J-L, deVitry C: On the microassembly of integral membrane proteins. Annu Rev Biophys Biophys Chem 19: 369–403 (1990).

    Google Scholar 

  27. Reymond P, Geourjon C, Roux B, Durand R, Fevre M: Sequence of the phosphoenolpyruvate carboxykinase-encoding cDNA from the rumen anaerobic fungus Neocallimastix frontalis: comparison of the amino acid sequence with animals and yeast. Gene 110: 57–63 (1992).

    Google Scholar 

  28. Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989).

    Google Scholar 

  29. Sanger F, Nicklen S, Coulson AR: DNA sequencing with chain terminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467 (1977).

    Google Scholar 

  30. Sanwal BD: Allosteric controls of amphibolic pathways in bacteria. Bact Rev 34: 20–39 (1970).

    Google Scholar 

  31. Saz HJ, Lescure OL: The functions of phosphoenolpyruvate carboxykinase and malic enzyme in the anaerobic formation of succinate by Ascaris lumbricoides. Comp Biochem Physiol 30: 49–60 (1969).

    Google Scholar 

  32. Stucka R, Valdes-Hevia MD, Gancedo C, Schwarzlose C, Feldman H: Nucleotide sequence of the phosphoenolpyruvate carboxykinase gene from Saccharomyces cerevisiae. Nucl Acids Res 16: 10926 (1988).

    Google Scholar 

  33. Ting C-N, Burgess DL, Chamberlain JS, Keith TP, Falls K, Meisler MH: Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20. Genomics 16: 698–706 (1993).

    Google Scholar 

  34. Urbina JA: The phosphoenolpyruvate carboxykinase of Trypanosoma (Schizotrypanum) cruzi epimastigotes: molecular, kinetic and regulatory properties. Arch Biochem Biophys 258: 186–195 (1987).

    Google Scholar 

  35. Utter MF, Kolenbrander HM: Formation of oxaloacetate by CO2 fixation on phosphoenolpyruvate. In: Boyer PD (ed) The Enzymes, 3rd ed., vol. 6, pp. 117–168. Academic Press, New York (1972).

    Google Scholar 

  36. Weldon SL, Rando A, Matathias AS, Hod Y, Kalonick PA, Savon S, Cook JS, Hanson RW: Mitochondrial phosphoenolpyruvate carboxykinase from the chicken: comparison of the cDNA and protein sequences with the cytosolic isozyme. J Biol Chem 265: 7308–7317 (1990).

    Google Scholar 

  37. Walker JE, Saraste M, Runswick MJ, Gay NJ: Distantly related sequences in the α and β-subunits of ATP-synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold. EMBO J 1: 945–951 (1982).

    Google Scholar 

  38. Watford M, Hod Y, Chiao Y-B, Utter MF, Hanson RW: The unique role of the kidney in gluconeogenesis in chicken: the significance of a cytosolic form of phosphoenolpyruvate carboxykinase. J Biol Chem 256: 10023–10027 (1981).

    Google Scholar 

  39. Yie Y, Wei Z, Tien P: A simplified and reliable protocol for plasmid DNA sequencing: fast miniprep and denaturation. Nucl Acids Res 21: 361 (1993).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Finnegan, P.M., Burnell, J.N. Isolation and sequence analysis of cDNAs encoding phosphoenolpyruvate carboxykinase from the PCK-type C4 grass Urochloa panicoides . Plant Mol Biol 27, 365–376 (1995). https://doi.org/10.1007/BF00020190

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00020190

Key words

Navigation