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. 1972 Aug 1;54(2):279–294. doi: 10.1083/jcb.54.2.279

BIOSYNTHESIS IN ISOLATED ACETABULARIA CHLOROPLASTS

I. Protein Amino Acids

David C Shephard 1, Wendy B Levin 1
PMCID: PMC2108880  PMID: 4557310

Abstract

The ability of chloroplasts isolated from Acetabulana mediterranea to synthesize the protein amino acids has been investigated. When this chloroplast isolate was presented with 14CO2 for periods of 6–8 hr, tracer was found in essentially all amino acid species of their hydrolyzed protein Phenylalanine labeling was not detected, probably due to technical problems, and hydroxyproline labeling was not tested for The incorporation of 14CO2 into the amino acids is driven by light and, as indicated by the amount of radioactivity lost during ninhydrin decarboxylation on the chromatograms, the amino acids appear to be uniformly labeled. The amino acid labeling pattern of the isolate is similar to that found in plastids labeled with 14CO2 in vivo. The chloroplast isolate did not utilize detectable amounts of externally supplied amino acids in light or, with added adenosine triphosphate (ATP), in darkness. It is concluded that these chloroplasts are a tight cytoplasmic compartment that is independent in supplying the amino acids used for its own protein synthesis. These results are discussed in terms of the role of contaminants in the observed synthesis, the "normalcy" of Acetabularia chloroplasts, the synthetic pathways for amino acids in plastids, and the implications of these observations for cell compartmentation and chloroplast autonomy.

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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. 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]
  2. Burns L. C., O'Neal R. M., Koeppe R. E. Labeling patterns in glutamic acid in Nicotiana rustica L. from carbon-14 dioxide. J Am Chem Soc. 1967 Jul 19;89(15):3938–3939. doi: 10.1021/ja00991a069. [DOI] [PubMed] [Google Scholar]
  3. Chaudhuri T. K., Spencer R. P. Amino acid uptake in Acetabularia. Protoplasma. 1968;66(1):255–259. doi: 10.1007/BF01252536. [DOI] [PubMed] [Google Scholar]
  4. Goffeau A. Incorporation of amino acids into the soluble and membrane-bound proteins of chloroplasts isolated from enucleated Acetabularia. Biochim Biophys Acta. 1969 Jan 21;174(1):340–350. doi: 10.1016/0005-2787(69)90259-7. [DOI] [PubMed] [Google Scholar]
  5. Green B. R., Burton H. Acetabularia chloroplast DNA: electron microscopic visualization. Science. 1970 May 22;168(3934):981–982. doi: 10.1126/science.168.3934.981. [DOI] [PubMed] [Google Scholar]
  6. HAEMMERLING J., CLAUSS H., KECK K., RICHTER G., WERZ G. Growth and protein synthesis in nucleated and enucleated cells. Exp Cell Res. 1959;Suppl 6:210–226. [PubMed] [Google Scholar]
  7. Hatch M. D., Slack C. R. Photosynthesis by sugar-cane leaves. A new carboxylation reaction and the pathway of sugar formation. Biochem J. 1966 Oct;101(1):103–111. doi: 10.1042/bj1010103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hess J. L., Tolbert N. E. Glycolate pathway in algae. Plant Physiol. 1967 Mar;42(3):371–379. doi: 10.1104/pp.42.3.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hess J. L., Tolbert N. E. Glycolate, glycine, serine, and glycerate formation during photosynthesis by tobacco leaves. J Biol Chem. 1966 Dec 10;241(23):5705–5711. [PubMed] [Google Scholar]
  10. Reuter W., Schweiger H. G. Kernkontrollierte Lactatdehydrogenase in Acetabularia. Protoplasma. 1969;68(3):357–368. doi: 10.1007/BF01251620. [DOI] [PubMed] [Google Scholar]
  11. Shephard D. C. An autoradiographic comparison of the effects of enucleation and actinomycin D on the incorporation of nucleic acid and protein precursors by Acetabularia chloroplasts. Biochim Biophys Acta. 1965 Dec 9;108(4):635–643. doi: 10.1016/0005-2787(65)90059-6. [DOI] [PubMed] [Google Scholar]
  12. Spencer D. Protein synthesis by isolated spinach chloroplasts. Arch Biochem Biophys. 1965 Aug;111(2):381–390. doi: 10.1016/0003-9861(65)90200-6. [DOI] [PubMed] [Google Scholar]
  13. Trench R. K., Smith D. C. Synthesis of pigment in symbiotic chloroplasts. Nature. 1970 Jul 11;227(5254):196–197. doi: 10.1038/227196a0. [DOI] [PubMed] [Google Scholar]
  14. Walker D. A., Baldry C. W., Cockburn W. Photosynthesis by isolated chloroplasts, simultaneous measurement of carbon assimilation and oxygen evolution. Plant Physiol. 1968 Sep;43(9):1419–1422. doi: 10.1104/pp.43.9.1419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Werz G., Kellner G. Molecular characteristics of chloroplast DNA of acetabularia cells. J Ultrastruct Res. 1968 Jul;24(1):109–115. doi: 10.1016/s0022-5320(68)80020-6. [DOI] [PubMed] [Google Scholar]
  16. Woodcock C. L., Bogorad L. Evidence for variation in the quantity of DNA among plastids of Acetabularia. J Cell Biol. 1970 Feb;44(2):361–375. doi: 10.1083/jcb.44.2.361. [DOI] [PMC free article] [PubMed] [Google Scholar]

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