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. 1966 Dec;101(3):636–641. doi: 10.1042/bj1010636

Some effects of sugars and sugar phosphates on carbon dioxide fixation by isolated chloroplasts

C Bucke 1, D A Walker 1, C W Baldry 1
PMCID: PMC1270165  PMID: 16742437

Abstract

1. Carbon dioxide fixation by isolated pea chloroplasts was stimulated by the addition of intermediates of the Calvin photosynthesis cycle and by some related compounds. 2. Ribose 5-phosphate and fructose 1,6-diphosphate consistently produced the largest effects; free sugars such as erythrose and sedoheptulose and acids such as glycollate and glyoxylate were largely ineffective or even inhibitory. 3. Small effects were produced by fructose and ribose but not by their isomers, glucose and xylose. 4. Maximal rates in the presence of ribose 5-phosphate varied between 10 and 50μmoles of carbon dioxide fixed/mg. of chlorophyll/hr.

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Selected References

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

  1. ARNON D. I., ALLEN M. B., WHATLEY F. R. Photosynthesis by isolated chloroplasts. Nature. 1954 Aug 28;174(4426):394–396. doi: 10.1038/174394a0. [DOI] [PubMed] [Google Scholar]
  2. Baldry C. W., Walker D. A., Bucke C. Calvin-cycle intermediates in relation to induction phenomena in photosynthetic carbon dioxide fixation by isolated chloroplasts. Biochem J. 1966 Dec;101(3):642–646. doi: 10.1042/bj1010642. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bamberger E. S., Gibbs M. Effect of Phosphorylated Compounds and Inhibitors on CO(2) Fixation by Intact Spinach Chloroplasts. Plant Physiol. 1965 Sep;40(5):919–926. doi: 10.1104/pp.40.5.919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. GOOD N. E. Uncoupling of the Hill reaction from photophosphorylation by anions. Arch Biochem Biophys. 1962 Mar;96:653–661. doi: 10.1016/0003-9861(62)90352-1. [DOI] [PubMed] [Google Scholar]
  5. Gibbs M., Calo N. Factors Affecting Light Induced Fixation of Carbon Dioxide by Isolated Spinach Chloroplasts. Plant Physiol. 1959 May;34(3):318–323. doi: 10.1104/pp.34.3.318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. HAVIR E. A., GIBBS M. STUDIES ON THE REDUCTIVE PENTOSE PHOSPHATE CYCLE IN INTACT AND RECONSTITUTED CHLOROPLAST SYSTEMS. J Biol Chem. 1963 Oct;238:3183–3187. [PubMed] [Google Scholar]
  7. MEDINA A., SOLS A. A specific fructokinase in peas. Biochim Biophys Acta. 1956 Feb;19(2):378–379. doi: 10.1016/0006-3002(56)90445-0. [DOI] [PubMed] [Google Scholar]
  8. WHATLEY F. R., ALLEN M. B., ROSENBERG L. L., CAPINDALE J. B., ARNON D. I. Photosynthesis by isolated chloroplasts. V. Phosphorylation and carbon dioxide fixation by broken chloroplasts. Biochim Biophys Acta. 1956 Jun;20(3):462–468. doi: 10.1016/0006-3002(56)90340-7. [DOI] [PubMed] [Google Scholar]
  9. Walker D. A. Correlation between Photosynthetic Activity and Membrane Integrity in Isolated Pea Chloroplasts. Plant Physiol. 1965 Nov;40(6):1157–1161. doi: 10.1104/pp.40.6.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Wang C. H., Doyle W. P., Ramsey J. C. Role of Hexose Monophosphate Pathway in Tomato Catabolism. Plant Physiol. 1962 Jan;37(1):1–7. doi: 10.1104/pp.37.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]

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