Skip to main content
Log in

The role of nitrate reduction in the anoxic metabolism of roots I. Characterization of root morphology and normoxic metabolism of wild type tobacco and a transformant lacking root nitrate reductase

  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

Two tobacco lines with (Nicotiana tabacum cv. Gatersleben, WT) or without (transformant LNR-H) nitrate reductase in roots were chosen as model systems to re-evaluate the role of root nitrate reduction for survival of anoxia. In this first paper, the two hydroponically grown lines were compared with respect to their root morphology, root respiration and the root content of inorganic cations, anions, and metabolites. Leaf transpiration in relation to root morphology was also determined. In comparison to WT roots containing NR, the NR-free LNR-H transformants had slightly shorter and thicker roots with a lower root surface area per g leaf FW. Consistent with that, LNR-H leaves had lower transpiration rates than WT. LNR-H-roots also showed consistently higher respiration and higher contents of ATP, starch and hexose monophosphates than WT roots. Concentrations of free sugars were only slightly higher in LNR-H roots. Total soluble protein content was identical in both lines, whereas amino acids were higher in LNR-H. Contents of major inorganic cations and anions were also almost identical in both lines. We conclude that WT versus LNR-H plants are a suitable tool to re-evaluate the role of nitrate reduction in flooding tolerance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Apostolova E and Georgieva M 1990 Effect of nitrate and ammonium on the accumulation of biomass nitrogen and ash elements in the overground parts and roots of Virginia cultivar tobacco. Pochvoznanie I Agrochimia25, 47-54.

    Google Scholar 

  • Arnon D I 1937 Ammonium and nitrate nitrogen nutrition of barley at different seasons in relation to hydrogen ion concentration, manganese, copper and oxygen supply. Soil Sci. 44, 91-121.

    Google Scholar 

  • Back E 1996 Regulation of root:shoot ratio by cytokinins from roots in Urtica dioica. Opinion. Plant Soil 185, 3-12.

    Google Scholar 

  • Botrel A and Kaiser W M 1997 Nitrate reductase activation state in barley roots in relation to the energy and carbohydrate status. Planta 201, 496-501.

    Google Scholar 

  • Botrel A, Magne C and Kaiser W M 1996 Nitrate reduction, nitrite reduction and ammonium assimilation in barley roots in response to anoxia. Plant Physiol. Biochem. 34, 645-652.

    Google Scholar 

  • Cheeseman J M 1993 Plant growth modeling without integrating mechanisms. Plant Cell Environ. 16, 137-147.

    Google Scholar 

  • Cooper H D and Clarkson D T 1989 Cycling of amino nitrogen and other nutrients between shoots and roots in cereals: a possible mechanism integrating shoot and root in the regulation of nutrient uptake. J. Exp. Bot. 40, 753-762.

    Google Scholar 

  • Crawford N M 1995 Nitrate: nutrient and signal for plant growth. Plant Cell 7, 859-868.

    Google Scholar 

  • Cruz C, Lips S H and Martins-Loucao M A 1997 Changes in the morphology of roots and leaves of carob seedlings induced by nitrogen source and atmospheric carbon dioxide. Ann. Bot. 80, 817-823.

    Google Scholar 

  • Drew M C, Saker L R and Ashley T W 1973 Nutrient supply and the growth of the seminal root system in barley. I. The effect of nitrate concentration on the growth of axes and laterals. J. Exp. Bot. 24, 1189-1202.

    Google Scholar 

  • Fitter A H 1985 Functional significance of root morphology and root system architecture. In Ecological Interactions in Soil, Special publication of the British ecological survey No 4, 87-106, Blackwell Scientific, Oxford.

    Google Scholar 

  • Forde B and Lorenzo H 2001 The nutritional control of plant development. Plant Soil 232, 51-68.

    Google Scholar 

  • Fox G G, McCallan N R and Ratcliffe R G 1995 Manipulating cytoplasmic pH under anoxia: a critical test of the role of pH in the switch from aerobic to anaerobic metabolism. Planta 195, 324-30.

    Google Scholar 

  • Foyer C H, Lescure J C, Lefebvre C, Morot G J F, Vincentz M and Vaucheret H 1994 Adaptations of photosynthetic electron transport, carbon assimilation and carbon partitioning in transgenic Nicotiana plumbaginifolia plants to changes in nitrate reductase activity. Plant Physiol. 104, 171-178.

    Google Scholar 

  • Friend A L, Eide M R and Hinckley T M 1990 Nitrogen stress alters root proliferation in Douglas fir seedlings. Can. J. For. Res. 20, 1524-1529.

    Google Scholar 

  • Gojon A, Dapoigny L, Lejay L, Tillard P and Rufty T W 1998 Effects of genetic modification of nitrate reductase expression on 15NO3 uptake and reduction in Nicotiana plants. Plant Cell Environ. 21, 43-53.

    Google Scholar 

  • Hackett C 1972 A method of applying nutrients locally to roots under controlled conditions and some morphological effects of locally applied nitrate on the branching of wheat roots. Aust. J. Biol. Sci. 25, 1169-1180.

    Google Scholar 

  • Hänsch R, Gómez Fessel D, Witt C, Hesberg C, Hoffmann G, Walch-Liu P, Engels C, Jörg Kruse, Rennenberg H, Kaiser W M and Mendel R R 2001 Tobacco plants that lack expression of functional nitrate reductase in roots show changes in growth rates and metabolite accumulation. J. Exp. Bot. 52, 1251-1258.

    Google Scholar 

  • Imsande J and Touraine B 1994 N demand and the regulation of nitrate uptake. Plant Physiol. 105, 3-7.

    Google Scholar 

  • Johnson C, Stout P, Broyer T and Carlton A 1957 Comparative chlorine requirements of different plant species. Plant Soil 8, 337-353.

    Google Scholar 

  • Kronzucker H J, Schjoerring J K, Erner Y, Kirk G J D, Siddiqi M Y and Glass A D M 1998 Dynamic interaction between root NH4 + influx and long distance N translocation in rice: Insights into feedback processes. Plant Cell Physiol. 39, 1287-1293.

    Google Scholar 

  • Lang B and Kaiser W M 1994 Solute content and energy status of roots of barley plants cultivated at different pH on nitrate-or ammonium-nitrogen. New Phytol. 128, 451-459.

    Google Scholar 

  • Roberts J K M, Callies J, Jardetzky O, Walbot V and Freeling M 1984 Cytoplasmic acidosis as a determinant of flooding intolerance in plants. Proc. Natl. Acad. Sci. USA 81, 6029-33.

    Google Scholar 

  • Scheible W R, Lauerer M, Schulze E D, Caboche M and Stitt M 1997 Accumulation of nitrate in the shoot acts as a signal to regulate shoot-root allocation in tobacco. Plant J. 11, 671-691.

    Google Scholar 

  • Stoimenova M, Libourel I G L, Ratcliffe R G and Kaiser WM 2002 The role of nitrate reduction in the anoxic metabolism of roots. II. Anoxic metabolism of tobacco roots with or without nitrate reductase activity. Plant Soil 253, 155-167.

    Google Scholar 

  • Walch-Liu P, Neumann G and Engels C 2001 Response to shoot and root growth to supply of different nitrogen forms is not related to carbohydrate and nitrogen status of tobacco plants. J. Plant Nutr. Soil Sci. 164, 97-103.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to W.M. Kaiser.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Stoimenova, M., Hänsch, R., Mendel, R. et al. The role of nitrate reduction in the anoxic metabolism of roots I. Characterization of root morphology and normoxic metabolism of wild type tobacco and a transformant lacking root nitrate reductase. Plant and Soil 253, 145–153 (2003). https://doi.org/10.1023/A:1024563507275

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1024563507275

Navigation