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. 1977 Sep;60(3):452–456. doi: 10.1104/pp.60.3.452

Light-mediated Oxygen Uptake Measured in Wheat Etioplasts 1

Thomas E Redlinger a, Robert G McDaniel a
PMCID: PMC542636  PMID: 16660113

Abstract

An in vitro O2 assay was used to measure early response of wheat (Triticum aestivum L.) etioplasts to light. A transient photoinducible O2 uptake occurred when dark-grown etioplasts were initially exposed to light. The rate of inducible O2 consumption was dependent on both the intensity of light and the quantity of organelle protein present. Higher light intensities resulted in greater O2 utilization per minute, and a greater quantity of organelle protein in the sample resulted in an increased rate of O2 uptake under the same light intensity conditions. Experiments with various plant tissues as well as with mitochondrial respiratory inhibitors indicated that etioplasts are the organelles responsible for the photoinduced O2 uptake phenomenon. A preliminary action spectrum study revealed that wavelengths 640 to 680 nm resulted in maximum O2 uptake. This indicated the presence of an etioplast red light receptor pigment which induces O2 uptake in etioplasts.

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Selected References

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  1. BOARDMAN N. K., WILDMAN S. G. Identification of proplastids by fluorescence microscopy and their isolation and purification. Biochim Biophys Acta. 1962 May 7;59:222–224. doi: 10.1016/0006-3002(62)90717-5. [DOI] [PubMed] [Google Scholar]
  2. Egan J. M., Dorsky D., Schiff J. A. Events Surrounding the Early Development of Euglena Chloroplasts: VI. Action Spectra for the Formation of Chlorophyll, Lag Elimination in Chlorophyll Synthesis, and Appearance of TPN-dependent Triose Phosphate Dehydrogenase and Alkaline DNase Activities. Plant Physiol. 1975 Aug;56(2):318–323. doi: 10.1104/pp.56.2.318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Evans A., Smith H. Localization of phytochrome in etioplasts and its regulation in vitro of gibberellin levels. Proc Natl Acad Sci U S A. 1976 Jan;73(1):138–142. doi: 10.1073/pnas.73.1.138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Gassman M., Granick S., Mauzerall D. A rapid spectral change in etiolated red kidney bean leaves following phototransformation of protochlorophyllide. Biochem Biophys Res Commun. 1968 Jul 26;32(2):295–300. doi: 10.1016/0006-291x(68)90384-7. [DOI] [PubMed] [Google Scholar]
  5. Granick S., Gassman M. Rapid regeneration of protochlorophyllide(650). Plant Physiol. 1970 Feb;45(2):201–205. doi: 10.1104/pp.45.2.201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Jacobson A. B. A procedure for isolation of proplastids from etiolated maize leaves. J Cell Biol. 1968 Jul;38(1):238–244. doi: 10.1083/jcb.38.1.238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  8. Smith J. H., Benitez A. The Effect of Temperature on the Conversion of Protochlorophyll to Chlorophyll a in Etiolated Barley Leaves. Plant Physiol. 1954 Mar;29(2):135–143. doi: 10.1104/pp.29.2.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Zelitch I. The photooxidation of glyoxylate by envelope-free spinach chloroplasts and its relation to photorespiration. Arch Biochem Biophys. 1972 Jun;150(2):698–707. doi: 10.1016/0003-9861(72)90088-4. [DOI] [PubMed] [Google Scholar]

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