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. 1983 Oct;73(2):370–376. doi: 10.1104/pp.73.2.370

Transport of Purine and Pyrimidine Bases and Nucleosides from Endosperm to Cotyledons in Germinating Castor Bean Seedlings 1

Erich Kombrink 1, Harry Beevers 1
PMCID: PMC1066467  PMID: 16663222

Abstract

During germination and early growth of castor bean (Ricinus communis), all cellular constituents of the endosperm are eventually transferred to the growing embryo. The present results bear on the transport of breakdown products of nucleic acids. The total content of nucleic acids and nucleotides declines rapidly between day 4 and day 8 of seedling development. Concomitant with this decline, a secretion of adenosine, guanosine, and adenine from excised endosperms into the incubation medium takes place, accompanying a much more extensive release of sucrose and amino acids. Release of nucleotides could not be detected. The rates of release were linear for at least 5 hours for all compounds measured, indicating that they were liberated due to a coordinated metabolism. Uptake studies with cotyledons removed from the seedling showed that these have the ability to absorb all the substances released from the endosperm. Besides sucrose and amino acids, both nucleosides and free purine and pyrimidine bases were taken up by the cotyledons with high efficiency. AMP was also transported whereas ATP was not. Kinetic analyses were carried out to estimate the maximal uptake capacities of the cotyledons. Rates of uptake were linear for at least 1 to 2 hours and saturation kinetics were observed for all substances investigated. It is concluded that nucleosides can serve best as transport metabolites of nucleic acids, inasmuch as they are taken up by the cotyledons with the highest efficiency, the Vmax/Km ratios being considerably higher than those found for free purine and pyrimidine bases. For both adenosine and adenine transport, the Vmax was about 2 micromoles per hour per gram fresh weight, and the Km values were 0.12 and 0.37 millimolar, respectively. The rates of metabolite release from the endosperm and the capacity of the absorption system in the cotyledons are shown to account for the observed rates of disappearance of nucleic acids from the endosperm and efficient transport to the growing embryo.

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Selected References

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  1. BEEVERS H. Metabolic production of sucrose from fat. Nature. 1961 Jul 29;191:433–436. doi: 10.1038/191433a0. [DOI] [PubMed] [Google Scholar]
  2. Berlin R. D., Oliver J. M. Membrane transport of purine and pyrimidine bases and nucleosides in animal cells. Int Rev Cytol. 1975;42:287–336. doi: 10.1016/s0074-7696(08)60983-3. [DOI] [PubMed] [Google Scholar]
  3. Berlin R. D., Stadtman E. R. A possible role of purine nucleotide pyrophosphorylases in the regulation of purine uptake by Bacillus subtilis. J Biol Chem. 1966 Jun 10;241(11):2679–2686. [PubMed] [Google Scholar]
  4. Birch B., Turnock G. The uptake and metabolism of uridine by the slime mould Physarum polycephalum. Eur J Biochem. 1976 Oct 1;69(1):257–263. doi: 10.1111/j.1432-1033.1976.tb10881.x. [DOI] [PubMed] [Google Scholar]
  5. CERIOTTI G. A microchemical determination of desoxyribonucleic acid. J Biol Chem. 1952 Sep;198(1):297–303. [PubMed] [Google Scholar]
  6. Fleck A., Begg D. The estimation of ribonucleic acid using ultraviolet absorption measurements. Biochim Biophys Acta. 1965 Nov 8;108(3):333–339. doi: 10.1016/0005-2787(65)90025-0. [DOI] [PubMed] [Google Scholar]
  7. Gordon S. A., Cameron E., Shen-Miller J. Polarity and rate of transport of cyclic adenosine 3,5'-monophosphate in the coleoptile. Plant Physiol. 1973 Aug;52(2):105–110. doi: 10.1104/pp.52.2.105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Guranowski A. Purine catabolism in plants : purification and some properties of inosine nucleosidase from yellow lupin (lupinus luteus L.) seeds. Plant Physiol. 1982 Aug;70(2):344–349. doi: 10.1104/pp.70.2.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hochstadt-Ozer J., Stadtman E. R. The regulation of purine utilization in bacteria. III. The involvement of purine phosphoribosyltransferases in the uptake of adenine and other nucleic acid precursors by intact resting cells. J Biol Chem. 1971 Sep 10;246(17):5312–5320. [PubMed] [Google Scholar]
  10. Kobr M. J., Beevers H. Gluconeogenesis in the castor bean endosperm: I. Changes in glycolytic intermediates. Plant Physiol. 1971 Jan;47(1):48–52. doi: 10.1104/pp.47.1.48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kriedemann P., Beevers H. Sugar uptake and translocation in the castor bean seedling I. Characteristics of transfer in intact and excised seedlings. Plant Physiol. 1967 Feb;42(2):161–173. doi: 10.1104/pp.42.2.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. 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]
  13. Lee H. J., Wilson I. B. Enzymic parameters: measurement of V and Km. Biochim Biophys Acta. 1971 Sep 22;242(3):519–522. doi: 10.1016/0005-2744(71)90144-6. [DOI] [PubMed] [Google Scholar]
  14. Losson R., Jund R., Chevallier M. R. Properties of three distinct pyrimide transport systems in yeast. Evidence for distinct energy coupling. Biochim Biophys Acta. 1978 Nov 2;513(2):296–300. doi: 10.1016/0005-2736(78)90182-7. [DOI] [PubMed] [Google Scholar]
  15. Magill C. W., Sabina R. L., Garber T. L., Magill J. M. Guanine uptake and metabolism in Neurospora crassa. J Bacteriol. 1982 Mar;149(3):941–947. doi: 10.1128/jb.149.3.941-947.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Munro H. N. The determination of nucleic acids. Methods Biochem Anal. 1966;14:113–176. doi: 10.1002/9780470110324.ch5. [DOI] [PubMed] [Google Scholar]
  17. Muto S., Beevers H. Lipase Activities in Castor Bean Endosperm during Germination. Plant Physiol. 1974 Jul;54(1):23–28. doi: 10.1104/pp.54.1.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Nishimura M., Beevers H. Isoenzymes of sugar phosphate metabolism in endosperm of germinating castor beans. Plant Physiol. 1981 Jun;67(6):1255–1258. doi: 10.1104/pp.67.6.1255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Pettersen R., Knutsen G. Uptake of guanine by synchronized Chlorella fusca. Characterization of the transport system in autospores. Arch Microbiol. 1974 Mar 7;96(3):233–246. doi: 10.1007/BF00590179. [DOI] [PubMed] [Google Scholar]
  20. Plagemann P. G., Richey D. P. Transport of nucleosides, nucleic acid bases, choline and glucose by animal cells in culture. Biochim Biophys Acta. 1974 Dec 16;344(3-4):263–305. doi: 10.1016/0304-4157(74)90010-0. [DOI] [PubMed] [Google Scholar]
  21. Polak A., Grenson M. Evidence for a common transport system for cytosine, adenine and hypoxanthine in Saccharomyces cerevisiae and Candida albicans. Eur J Biochem. 1973 Jan 15;32(2):276–282. doi: 10.1111/j.1432-1033.1973.tb02608.x. [DOI] [PubMed] [Google Scholar]
  22. Reichert U., Winter M. Uptake and accumulation of purine bases by stationary yeast cells pretreated with glucose. Biochim Biophys Acta. 1974 Jul 12;356(1):108–116. doi: 10.1016/0005-2736(74)90298-3. [DOI] [PubMed] [Google Scholar]
  23. Robinson S. P., Beevers H. Amino Acid transport in germinating castor bean seedlings. Plant Physiol. 1981 Sep;68(3):560–566. doi: 10.1104/pp.68.3.560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Wasternack C. H. Uptake and incorporation of pyrimidines in Euglena gracilis. Arch Microbiol. 1976 Aug;109(1-2):167–174. doi: 10.1007/BF00425131. [DOI] [PubMed] [Google Scholar]

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