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. 1970 Mar;45(3):249–254. doi: 10.1104/pp.45.3.249

The Development of Glyoxysomes in Peanut Cotyledons and Maize Scutella 1

Claudio P Longo a,2, Giovanna P Longo a,2
PMCID: PMC396392  PMID: 4316376

Abstract

The development of glyoxysomes during germination has been studied in isolated peanut (Arachis hypogaea L.) cotyledons and in maize (Zea mays L.) scutella. In peanut cotyledons isocitratase, malate synthetase, and protein associated with the glyoxysomal fraction increase simultaneously from the 3rd to the 8th day of incubation. In scutella of germinating maize seeds the specific activities of isocitratase, malate synthetase, and catalase associated with the glyoxysomes rise until the 4th day of germination and then decline while the total amount of protein present in the fraction stays constant during the first 5 days. If the peanut cotyledons are cultured in 2% glucose, the development of isocitratase and malate synthetase is severely inhibited, but the level of the glyoxysomal protein is not measurably affected.

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Selected References

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  1. Baudhuin P., Beaufay H., De Duve C. Combined biochemical and morphological study of particulate fractions from rat liver. Analysis of preparations enriched in lysosomes or in particles containing urate oxidase, D-amino acid oxidase, and catalase. J Cell Biol. 1965 Jul;26(1):219–243. doi: 10.1083/jcb.26.1.219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Breidenbach R. W., Beevers H. Association of the glyoxylate cycle enzymes in a novel subcellular particle from castor bean endosperm. Biochem Biophys Res Commun. 1967 May 25;27(4):462–469. doi: 10.1016/s0006-291x(67)80007-x. [DOI] [PubMed] [Google Scholar]
  3. Breidenbach R. W., Castelfranco P., Criddle R. S. Biogenesis of Mitochondria in Germinating Peanut Cotyledons II. Changes in Cytochromes and Mitochondrial DNA. Plant Physiol. 1967 Aug;42(8):1035–1041. doi: 10.1104/pp.42.8.1035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Breidenbach R. W., Kahn A., Beevers H. Characterization of glyoxysomes from castor bean endosperm. Plant Physiol. 1968 May;43(5):705–713. doi: 10.1104/pp.43.5.705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Carpenter W. D., Beevers H. Distribution and Properties of Isocitritase in Plants. Plant Physiol. 1959 Jul;34(4):403–409. doi: 10.1104/pp.34.4.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gientka-Rychter A., Cherry J. H. De Novo Synthesis of Isocitritase in Peanut (Arachis hypogaea L.) Cotyledons. Plant Physiol. 1968 Apr;43(4):653–659. doi: 10.1104/pp.43.4.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lado P., Schwendimann M., Marrè E. Repression of isocitrate lyase synthesis in seeds germinated in the presence of glucose. Biochim Biophys Acta. 1968 Mar 18;157(1):140–148. doi: 10.1016/0005-2787(68)90272-4. [DOI] [PubMed] [Google Scholar]
  8. Longo C. P. Evidence for de novo synthesis of isocitratase and malate synthesis in germinating peanut cotyledons. Plant Physiol. 1968 Apr;43(4):660–664. doi: 10.1104/pp.43.4.660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Yamamoto Y., Beevers H. Malate Synthetase in Higher Plants. Plant Physiol. 1960 Jan;35(1):102–108. doi: 10.1104/pp.35.1.102. [DOI] [PMC free article] [PubMed] [Google Scholar]

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