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. 1988 Dec;88(4):1235–1239. doi: 10.1104/pp.88.4.1235

Sugar Uptake by Maize Endosperm Suspension Cultures

Frederick C Felker 1, James C Goodwin 1
PMCID: PMC1055747  PMID: 16666450

Abstract

Maize (Zea mays L.) endosperm suspension cultures are a useful model system for studying biochemical and physiological events in developing maize endosperm. In this report, sugar uptake by the cultures is characterized. Uptake of 14C-labeled fructose and l-glucose was linear with time, while the rate of uptake of radioactivity from sucrose increased over a 120 min period. Both saturable and linear components of uptake were observed for fructose, glucose, sucrose, 1′-deoxy-1′-fluorosucrose, and maltose. Uptake of mannitol, sorbitol, and l-glucose took place at lower rates and was linear with concentration. Rates of incorporation of radioactivity from fructose and glucose exceeded that of sucrose at all concentrations tested. Kinetics of 1′-deoxy-1′-fluorosucrose uptake indicated that 14C from sucrose can be taken up by a saturable carrier of intact sucrose as well as by invertase hydrolysis and subsequent uptake of hexoses. Cell wall invertase was demonstrated histochemically. Further study of fructose uptake at a concentration at which the saturable component predominated revealed sensitivity to metabolic inhibitors, respiratory uncouplers, the nonpermeant sulfhydryl reagent p-chloromercuribenzenesulfonic acid, and nigericin. Uptake was not affected by valinomycin plus K+ and was stimulated by fusicoccin. Fructose and glucose uptake was not pH-sensitive below pH 7.0, whereas uptake of radioactivity from sucrose and 1′-deoxy-1′-fluorosucrose declined as the pH was increased above 5.0. Fructose uptake was not completely inhibited by glucose and vice versa, suggesting the presence of specific carriers. These results indicate that maize endosperm suspension cultures (a) absorb fructose via a typical, energy-requiring, carrier-mediated proton cotransport system; (b) possess saturable carriers for glucose and sucrose; and (c) also absorb sucrose via hexose uptake after sucrose hydrolysis by extracellular invertase.

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Selected References

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  1. Doehlert D. C. Ketose reductase activity in developing maize endosperm. Plant Physiol. 1987 Jul;84(3):830–834. doi: 10.1104/pp.84.3.830. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Felker F. C., Shannon J. C. Movement of C-labeled Assimilates into Kernels of Zea mays L: III. AN ANATOMICAL EXAMINATION AND MICROAUTORADIOGRAPHIC STUDY OF ASSIMILATE TRANSFER. Plant Physiol. 1980 May;65(5):864–870. doi: 10.1104/pp.65.5.864. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Garland W. J., Dennis D. T. Steady-state kinetics of glutamate dehydrogenase from Pisum sativum L. mitochondria. Arch Biochem Biophys. 1977 Aug;182(2):614–625. doi: 10.1016/0003-9861(77)90542-2. [DOI] [PubMed] [Google Scholar]
  4. Griffith S. M., Jones R. J., Brenner M. L. In Vitro Sugar Transport in Zea mays L. Kernels : I. Characteristics of Sugar Absorption and Metabolism by Developing Maize Endosperm. Plant Physiol. 1987 Jun;84(2):467–471. doi: 10.1104/pp.84.2.467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hanft J. M., Jones R. J. Kernel abortion in maize : I. Carbohydrate concentration patterns and Acid invertase activity of maize kernels induced to abort in vitro. Plant Physiol. 1986 Jun;81(2):503–510. doi: 10.1104/pp.81.2.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hitz W. D., Schmitt M. R., Card P. J., Giaquinta R. T. Transport and metabolism of 1'-fluorosucrose, a sucrose analog not subject to invertase hydrolysis. Plant Physiol. 1985 Feb;77(2):291–295. doi: 10.1104/pp.77.2.291. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kanabus J., Bressan R. A., Carpita N. C. Carbon assimilation in carrot cells in liquid culture. Plant Physiol. 1986 Oct;82(2):363–368. doi: 10.1104/pp.82.2.363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Lichtner F. T., Spanswick R. M. Sucrose uptake by developing soybean cotyledons. Plant Physiol. 1981 Sep;68(3):693–698. doi: 10.1104/pp.68.3.693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Maynard J. W., Lucas W. J. A Reanalysis of the Two-Component Phloem Loading System in Beta vulgaris. Plant Physiol. 1982 Mar;69(3):734–739. doi: 10.1104/pp.69.3.734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Pressman B. C. Biological applications of ionophores. Annu Rev Biochem. 1976;45:501–530. doi: 10.1146/annurev.bi.45.070176.002441. [DOI] [PubMed] [Google Scholar]
  11. Schmalstig J. G., Hitz W. D. Transport and Metabolism of a Sucrose Analog (1'-Fluorosucrose) into Zea mays L. Endosperm without Invertase Hydrolysis. Plant Physiol. 1987 Dec;85(4):902–905. doi: 10.1104/pp.85.4.902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Schmitt M. R., Hitz W. D., Lin W., Giaquinta R. T. Sugar Transport into Protoplasts Isolated from Developing Soybean Cotyledons : II. Sucrose Transport Kinetics, Selectivity, and Modeling Studies. Plant Physiol. 1984 Aug;75(4):941–946. doi: 10.1104/pp.75.4.941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Shannon J. C. Carbon-14 Distribution in Carbohydrates of Immature Zea mays. Kernels Following CO(2) Treatment of Intact Plants. Plant Physiol. 1968 Aug;43(8):1215–1220. doi: 10.1104/pp.43.8.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Shannon J. C. Movement of C-Labeled Assimilates into Kernels of Zea mays L: I. Pattern and Rate of Sugar Movement. Plant Physiol. 1972 Feb;49(2):198–202. doi: 10.1104/pp.49.2.198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Shannon J. C. Movement of C-Labeled Assimilates into Kernels of Zea mays L: II. Invertase Activity of the Pedicel and Placento-Chalazal Tissues. Plant Physiol. 1972 Feb;49(2):203–206. doi: 10.1104/pp.49.2.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Shimamoto K., Ackermann M., Dierks-Ventling C. Expression of zein in long term endosperm cultures of maize. Plant Physiol. 1983 Dec;73(4):915–920. doi: 10.1104/pp.73.4.915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Thorne J. H. Characterization of the active sucrose transport system of immature soybean embryos. Plant Physiol. 1982 Oct;70(4):953–958. doi: 10.1104/pp.70.4.953. [DOI] [PMC free article] [PubMed] [Google Scholar]

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