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. 1964 Jun;51(6):1226–1231. doi: 10.1073/pnas.51.6.1226

ACTION SPECTRUM FOR FERRICYANIDE PHOTOREDUCTION AND REDOX POTENTIAL OF CHLOROPHYLL 683*

Takekazu Horio 1,†, Anthony San Pietro 1
PMCID: PMC300241  PMID: 14218065

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Selected References

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

  1. AVRON M. Photophosphorylation by swiss-chard chloroplasts. Biochim Biophys Acta. 1960 May 20;40:257–272. doi: 10.1016/0006-3002(60)91350-0. [DOI] [PubMed] [Google Scholar]
  2. Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BLACK C. C., TURNER J. F., GIBBS M., KROGMANN D. W., GORDON S. A. Studies on photosynthetic processes. II. Action spectra and quantum requirement for triphosphopyridine nucleotide reduction and the formation of adenosine triphosphate by spinach chloroplasts. J Biol Chem. 1962 Feb;237:580–583. [PubMed] [Google Scholar]
  4. Brown J. S., French C. S. Absorption Spectra and Relative Photostability of the Different Forms of Chlorophyll in Chlorella. Plant Physiol. 1959 May;34(3):305–309. doi: 10.1104/pp.34.3.305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chen S. L. The Action Spectrum for the Photochemical Evolution of Oxygen by Isolated Chloroplasts. Plant Physiol. 1952 Jan;27(1):35–48. doi: 10.1104/pp.27.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. DAVENPORT H. E., HILL R. The preparation and some properties of cytochrome f. Proc R Soc Lond B Biol Sci. 1952 Apr 24;139(896):327–345. doi: 10.1098/rspb.1952.0016. [DOI] [PubMed] [Google Scholar]
  7. Fork D. C. Action Spectra of O(2) Evolution by Chloroplasts with & without Added Substrate, for Regeneration of O(2) Evolving Ability by Far-red, & for O(2) Uptake. Plant Physiol. 1963 May;38(3):323–332. doi: 10.1104/pp.38.3.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Jagendorf A. T., Hendricks S. B., Avron M., Evans M. B. The Action Spectrum for Photosynthetic Phosphorylation by Spinach Chloroplasts. Plant Physiol. 1958 Jan;33(1):72–73. doi: 10.1104/pp.33.1.72. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. KEISTER D. L., SAN PIETRO A., STOLZENBACH F. E. Pyridine nucleotide transhydrogenase from spinach. II. Requirement of enzyme for photochemical accumulation of reduced pyridine nucleotides. Arch Biochem Biophys. 1962 Aug;98:235–244. doi: 10.1016/0003-9861(62)90178-9. [DOI] [PubMed] [Google Scholar]
  10. NIELSEN S. O., LEHNINGER A. L. Phosphorylation coupled to the oxidation of ferrocytochrome c. J Biol Chem. 1955 Aug;215(2):555–570. [PubMed] [Google Scholar]
  11. SAN PIETRO A., HENDRICKS S. B., GIOVANELLI J., STOLZENBACH F. E. Action spectrum for triphosphopyridine nucleotide reduction by illuminated chloroplasts. Science. 1958 Oct 10;128(3328):845–845. doi: 10.1126/science.128.3328.845. [DOI] [PubMed] [Google Scholar]
  12. STILLER M., VENNESLAND B. Photophosphorylation accompanying the Hill reaction with ferricyanide. Biochim Biophys Acta. 1962 Jul 16;60:562–579. doi: 10.1016/0006-3002(62)90875-2. [DOI] [PubMed] [Google Scholar]
  13. THOMAS J. B. On the role of the carotenoids in photosynthesis in Rhodospirillum rubrum. Biochim Biophys Acta. 1950 Apr;5(2):186–196. [PubMed] [Google Scholar]
  14. WHATLEY F. R., TAGAWA K., ARNON D. I. Separation of the light and dark reactions in electron transfer during photosynthesis. Proc Natl Acad Sci U S A. 1963 Feb 15;49:266–270. doi: 10.1073/pnas.49.2.266. [DOI] [PMC free article] [PubMed] [Google Scholar]

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