Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1982 Aug;70(2):469–475. doi: 10.1104/pp.70.2.469

The Effects of Cyanide and Azide on the Photoreduction of 3-Phosphoglycerate and Oxaloacetate by Wild Type and Two Reductive Pentose Phosphate Cycle Mutants of Chlamydomonas reinhardtii1

William R Belknap 1, Robert K Togasaki 1
PMCID: PMC1067172  PMID: 16662518

Abstract

3-Phosphoglycerate- and oxaloacetate-dependent O2 photoevolution by permeabilized cell preparations (Pressates), prepared from wild type (Wt) and two reductive pentose phosphate cycle mutants of Chlamydomonas reinhardtii showed different sensitivities to the inhibitors sodium cyanide and sodium azide. NaCN (1.5 millimolar) severely inhibits both CO2- and 3-phosphoglycerate-dependent O2 photoevolution by the Wt Pressate, but does not inhibit 3-phosphoglycerate-dependent O2 photoevolution by Pressates prepared from the mutants rcl-u-1-10-6C (which lacks ribulose, 1-5, bisphosphate carboxylase activity) and F60 (which lacks phosphoribulokinase activity). NaN3 (0.5 millimolar) inhibits 3-phosphoglycerate-dependent O2 photoevolution by the rcl-u-1-10-6C Pressate more severely than in the Pressates prepared from F60 and Wt. A higher concentration of NaN3 (2.0 millimolar) severely inhibited oxaloacetate-dependent O2 photoevolution by the rcl-u-1-10-6C, but not by the F60 Pressate. O2 exchange-dependent upon methyl viologen was not strongly inhibited by 2 millimolar NaN3 in either of the mutant Pressates. The data suggests that the mutational lesions which resulted in decreased ribulose-1,5-bisphosphate carboxylase and phosphoribulokinase activities effected changes in other photosynthetic reactions, either by direct interactions between component proteins or by causing changes in substrate or cofactor availability to the partial reactions.

Full text

PDF
469

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bandyopadhyay A. K., Deutscher M. P. Complex of aminoacyl-transfer RNA synthetases. J Mol Biol. 1971 Aug 28;60(1):113–122. doi: 10.1016/0022-2836(71)90451-7. [DOI] [PubMed] [Google Scholar]
  2. Belknap W. R., Togasaki R. K. Chlamydomonas reinhardtii cell preparation with altered permeability toward substrates of organellar reactions. Proc Natl Acad Sci U S A. 1981 Apr;78(4):2310–2314. doi: 10.1073/pnas.78.4.2310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Forti G., Gerola P. Inhibition of photosynthesis by azide and cyanide and the role of oxygen in photosynthesis. Plant Physiol. 1977 May;59(5):859–862. doi: 10.1104/pp.59.5.859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Galmiche J. M. Studies on the mechanism of glycerate 3-phosphate synthesis in tomato and maize leaves. Plant Physiol. 1973 Mar;51(3):512–519. doi: 10.1104/pp.51.3.512. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gorman D. S., Levine R. P. Cytochrome f and plastocyanin: their sequence in the photosynthetic electron transport chain of Chlamydomonas reinhardi. Proc Natl Acad Sci U S A. 1965 Dec;54(6):1665–1669. doi: 10.1073/pnas.54.6.1665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kow Y. W., Gibbs M. Characterization of a Photosynthesizing Reconstituted Spinach Chloroplast Preparation : REGULATION BY PRIMER, ADENYLATES, FERREDOXIN, AND PYRIDINE NUCLEOTIDES. Plant Physiol. 1982 Jan;69(1):179–186. doi: 10.1104/pp.69.1.179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LYNEN F. Biosynthesis of saturated fatty acids. Fed Proc. 1961 Dec;20:941–951. [PubMed] [Google Scholar]
  8. Lilley R. M., Chon C. J., Mosbach A., Heldt H. W. The distribution of metabolites between spinach chloroplasts and medium during photosynthesis in vitro. Biochim Biophys Acta. 1977 May 11;460(2):259–272. doi: 10.1016/0005-2728(77)90212-2. [DOI] [PubMed] [Google Scholar]
  9. McNeil P. H., Walker D. A. The effect of magnesium and other ions on the distribution of ribulose 1,5-bisphosphate carboxylase in chloroplast extracts. Arch Biochem Biophys. 1981 Apr 15;208(1):184–188. doi: 10.1016/0003-9861(81)90138-7. [DOI] [PubMed] [Google Scholar]
  10. Moll B., Levine R. P. Characterization of a Photosynthetic Mutant Strain of Chlamydomonas reinhardi Deficient in Phosphoribulokinase Activity. Plant Physiol. 1970 Oct;46(4):576–580. doi: 10.1104/pp.46.4.576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Shneyour A., Avron M. High biological activity in chloroplasts from Euglena gracilis prepared with a new gas pressure device. FEBS Lett. 1970 Jun 1;8(3):164–166. doi: 10.1016/0014-5793(70)80253-8. [DOI] [PubMed] [Google Scholar]
  12. Shoaf W. T., Jones M. E. Uridylic acid synthesis in Ehrlich ascites carcinoma. Properties, subcellular distribution, and nature of enzyme complexes of the six biosynthetic enzymes. Biochemistry. 1973 Oct 9;12(21):4039–4051. doi: 10.1021/bi00745a004. [DOI] [PubMed] [Google Scholar]
  13. Spreitzer R. J., Mets L. Photosynthesis-deficient Mutants of Chlamydomonas reinhardii with Associated Light-sensitive Phenotypes. Plant Physiol. 1981 Mar;67(3):565–569. doi: 10.1104/pp.67.3.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Stitt M., Wirtz W., Heldt H. W. Metabolite levels during induction in the chloroplast and extrachloroplast compartments of spinach protoplasts. Biochim Biophys Acta. 1980 Nov 5;593(1):85–102. doi: 10.1016/0005-2728(80)90010-9. [DOI] [PubMed] [Google Scholar]
  15. Stokes D. M., Walker D. A. Photosynthesis by isolated chloroplasts. Inhibition by DL-glyceraldehyde of carbon dioxide assimilation. Biochem J. 1972 Aug;128(5):1147–1157. doi: 10.1042/bj1281147. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Welch G. R., Gaertner F. H. Enzyme organization in the polyaromatic-biosynthetic pathway: the arom conjugate and other multienzyme systems. Curr Top Cell Regul. 1980;16:113–162. [PubMed] [Google Scholar]
  17. Wishnick M., Lane M. D. Inhibition of ribulose diphosphate carboxylase by cyanide. Inactive ternary complex of enzyme, ribulose diphosphate, and cyanide. J Biol Chem. 1969 Jan 10;244(1):55–59. [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES