Archives of Microbiology

, Volume 157, Issue 4, pp 375–380 | Cite as

Formation and metabolism of glycolate in the cyanobacterium Coccochloris peniocystis

  • Eric G. Norman
  • Brian Colman
Original Papers

Abstract

The formation and metabolism of glycolate in the cyanobacterium Coccochloris peniocystis was investigated and the activities of enzymes of glycolate metabolism assayed. Photosynthetic 14CO2 incorporation was O2 insensitive and no labelled glycolate could be detected in cells incubated at 2 and 21% O2. Under conditions of 100% O2 glycolate comprised less than 1% of the acid-stable products indicating ribulose 1,5 bisphosphate (RuBP) oxidation only occurs under conditions of extreme O2 stress. Metabolism of [1-14C] glycolate indicated that as much as 62% of 14C metabolized was released as 14CO2 in the dark. Metabolism of labelled glycolate, particularly incorporation of 14C into glycine, was inhibited by the amino-transferase inhibitor amino-oxyacetate. Metabolism of [2-14C] glycine was not inhibited by the serine hydroxymethyltransferase inhibitor isonicotinic acid hydrazide and little or no labelled serine was detected as a result of 14C-glycolate metabolism. These findings indicate that a significant amount of metabolized glycolate is totally oxidized to CO2 via formate. The remainder is converted to glycine or metabolized via a glyoxylate cycle. The conversion of glycine to serine contributes little to glycolate metabolism and the absence of hydroxypyruvate reductase confirms that the glycolate pathway is incomplete in this cyanobacterium.

Key words

Cyanobacteria Coccochloris peniocystis Glycolate metabolism Photosynthesis Glyoxylate cycle Photorespiration 

Abbreviations

AAN

aminoacetonitrile

AOA

aminooxyacetate

DIC

dissolved inorganic carbon

INH

isonicotinic acid hydrazide

PEP

phosphoenolpyruvate

PEPcase

phosphoenolpyruvate carboxylase

PG

phosphoglycolate

PGA

phosphoglyceric acid

PGPase

phosphoglycolate phosphatase

PR

photorespiration

Rubisco

ribulose-1,5-bisphosphate carboxylase oxygenase

TCA

trichloroacetic acid

RuBP

ribulose-1,5-bisphosphate

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References

  1. Bergman B, Renstrom E, Hallbom L, Codd GA (1985) Effects of aminooxyacetate and aminoacetonitrile on glycolate and ammonia release by the cyanobacterium Anabaena cylindrica. Plant Physiol 77: 536–539Google Scholar
  2. Bergman BE, Codd GA, Hallbom L (1984) Glycollate excretion by N2-fixing cyanobacteria treated with photorespiratory inhibitors. Z Pflanzenphysiol 113: 451–460Google Scholar
  3. Birmingham BC, Coleman JR, Colman B (1982) Measurement of photorespiration in algae. Plant Physiol 69: 259–262Google Scholar
  4. Cheng KH, Miller AG, Colman B (1972) An investigation of glycolate excretion in two species of blue-green algae. Planta 103: 109–116Google Scholar
  5. Clagget CO, Tolbert NE, Burris RN (1949) Oxidation of α-hydroxy acids by enzyme from plants. J Biol Chem 178: 977–987Google Scholar
  6. Codd GA, Stewart WDP (1973) Pathways of glycolate metabolism in the blue-green alga Anabaena cylindrica. Arch Mikrobiol 94: 11–28Google Scholar
  7. Colman B (1989) Photosynthetic carbon assimilation and the suppression of photorespiration in the cyanobacteria. Aquatic Bot 34: 211–231Google Scholar
  8. Coleman JR, Colman B (1980) Demonstration of C3-photosynthesis in a blue-green alga. Planta 149: 318–320Google Scholar
  9. Coleman JR, Colman B (1981) Photosynthetic carbon assimilation in the blue-green alga Coccochloris peniocystis. Plant Cell Environ 4: 285–290Google Scholar
  10. Daron HH, Gunsalus IC (1965) Citratase and isocitrase. In: Colowick SP, Kaplan NO (eds) Methods in enzymology V. Academic Press, New York, pp 628–633Google Scholar
  11. Dixon GH, Kornberg HL (1965) Malate synthetase from Baker's yeast. In: Colowick SP, Kaplan NO (eds) Methods in Enzymology V: Academic Press, New York, pp. 633–637Google Scholar
  12. Eley JH (1988) Glyoxylate cycle enzyme activities in the cyanobacterium Anacystis nidulans. J Phycol 24: 586–588Google Scholar
  13. Grodzinski B, Colman B (1970) Glycolic acid oxidase activity in cell-free preparations of blue-green algae. Plant Physiol 45: 735–737Google Scholar
  14. Grodzinski B, Colman B (1975) The effect of osmotic stress on the oxidation of glycolate by the blue-green alga Anacystis nidulans. Planta 124: 125–133Google Scholar
  15. Grodzinski B (1971) Studies with a glycolate oxidizing enyme from blue-green algae. MSc York UniversityGoogle Scholar
  16. Holden M (1965) Chlorophylls: Goodwin TW, ed Chemistry and biochemistry of plant pigments. Academic Press, New York, pp 461–488Google Scholar
  17. Husic HD, Tolbert NE (1985) Properties of phosphoglycolate phosphatase from Chlamydomonas reinhardtii and Anacystis nidulans. Plant Physiol 79: 394–399Google Scholar
  18. Ingle RK, Colman B (1976) The relationship between carbonic anhydrase activity and glycolate excretion in the blue-green alga Cocchochloris peniocystis. Planta 128: 217–223Google Scholar
  19. Jansz ER, Maclean EI (1973) CO2 fixation by the blue-green alga Anacystis nidulans. Can J Microbiol 19: 497–503Google Scholar
  20. Markwell MAK, Maas SM, Bieber LL, Tolbert NE (1978) A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples. Analyt Biochem 87: 206–210Google Scholar
  21. Miller AG, Colman B (1980) Evidence for HCO3 transport by the blue-green alga (cyanobacterium) Coccochloris peniocystis. Plant Physiol 65: 397–402Google Scholar
  22. Miller AG, Cheng KH, Colman B (1971) The uptake and oxidation of glycolic acid by blue-green algae. J Phycol 7: 97–100Google Scholar
  23. Murray EW, Adams RE (1980) Embryonic control of isocitrate lyase activity in the megagametophyte of ponderosa pine seeds. Plant Physiol 49: 21–26Google Scholar
  24. Norman EG; Colman B (1991a) Purification and characterization of phosphoglycolate phosphatase from the cyanobacterium Coccochloris peniocystis. Plant Physiol 95: 693–698Google Scholar
  25. Norman EG, Colman B (1991b) Characterization of a malate dehydrogenase in the cyanobacterium Coccochloris peniocystis. Arch Microbiol 156: 28–33Google Scholar
  26. Norman EG, Colman B (1988) Evidence for an incomplete glycolate pathway in cyanobacteria. J Plant Physiol 132: 766–768Google Scholar
  27. Norris L, Norris RE, Calvin M (1955) A survey of the rates and products of short term photosynthesis in plants of nine phyla. J Exp Bot 6: 64–74Google Scholar
  28. Owttrim GW, Colman B (1988) Phosphoenolpyruvate carboxylase mediated carbon flow in a cyanobacterium. Biochem Cell Biol 66: 93–99Google Scholar
  29. Pearce J, Carr NG (1967) The metabolism of acetate by the blue-green algae Anabaena variabilis and Anacystis nidulans. J Gen Microbiol 49: 301–313Google Scholar
  30. Renstrom E, Bergman B (1989) Glycolate metabolism in cyanobacteria. I. Glycolate excretion and phosphoglycolate phosphatase activity. Physiologia Plantarum 43: 137–143Google Scholar
  31. Richardson KE, Tolbert NE (1961) Phosphoglycolic acid phosphatase. J Biol Chem 236: 1285–1290Google Scholar
  32. Tarant AA, Colman B (1972) Dark assimilation of acetate 14C by Anabaena flos-aquae. Can J Bot 50: 2067–2071Google Scholar
  33. Wolfendon R (1970) Binding of substrate and transition state analogs to triosephosphate isomerase. Biochemistry 9: 3404–3407Google Scholar
  34. Yokota A, Kitaoka S (1987) The mechanism of induction of glycolate excretion by aminooxyacetate in low CO2-grown Euglena gracilis Z. J Biol Chem 51: 665–670Google Scholar
  35. Zelitch I (1955) Glycolic acid oxidase and glyoxylic acid reductase. In: Colowick SP, Kaplan NO (eds) Methods in enzymology I: Academic Press, New York, pp 528–535Google Scholar

Copyright information

© Springer-Verlag 1992

Authors and Affiliations

  • Eric G. Norman
    • 1
  • Brian Colman
    • 1
  1. 1.Department of BiologyYork UniversityNorth YorkCanada

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