UDC 633.11:58.056:[581.1+575.1/.2

doi: 10.15389/agrobiology.2016.1.68eng

Acknowledgements:
Study of root exudates isolation was supported by Russian Foundation for Basic Research (15-04-09023-а). Experiments on root exudates chromatography were supported by Russian Science Foundation grant (14-26-00094). Experiments in CIMMYT-Turkey were supported by CRP WHEAT and Republic of Turkey Ministry of Food, Agriculture and Livestock.

COMPARATIVE CHARACTERISTICS OF ROOT SYSTEMS AND ROOT EXUDATION OF SYNTHETIC, LANDRACE AND MODERN WHEAT VARIETIES

A.I. Shaposhnikov1, A.I. Morgounov2, B. Akin2, N.M. Makarova1,
A.A. Belimov1, I.A. Tikhonovich1, 3

1All-Russian Research Institute for Agricultural Microbiology, Federal Agency of Scientific Organizations,
3, sh. Podbel’skogo, St. Petersburg, 196608 Russia,
e-mail belimov@rambler.ru; ai-shaposhnikov@mail.ru;
2International Maize and Wheat Improvement Center (CIMMYT),
P.K. 39 Emek, 06511, Ankara, Turkey,
e-mail a.morgounov@CGIAR.ORG;
3Saint Petersburg State University,
7-9, Universitetskaya nab., St. Petersburg, 199034 Russia

Received April 24, 2015

Finding ways to increase the wheat adaptation to drought is now considered as a major problem in breeding new varieties of this crop. This study was conducted to evaluate genotypic differences in fundamental root traits which may have effect on wheat adaptation to unfavorable environments, including drought. Three wheat genotypes representing various evolution levels of hexaploid bread wheat (Triticum aestivum L.) were used: synthetic wheat developed by crossing variety LEUCURUM 84693 of durum wheat (Triticum durum Desf., genome АВ, Ukraine) with wild Tausch's goat grass (Aegilops tauschii Coss., genome D, Turkey), landrace of bread wheat Albostan (genome ABD, Turkey, province Nevsehir), and a modern cultivar Karahan (genome ABD, Turkey). The varieties differed in root diameter, shoot biomass and shoot/root ratio. The removal of above ground biomass caused increase in the root length, number of tips, number of forks, number of crosses and shoot/root biomass ratio of synthetic wheat and Albostan, but decreased these parameters in Karahan. Averaged values of ten measured growth parameters of the plants with removed above ground biomass relatively to the control plants were +28 % for synthetic wheat, 0 % for landrace Albostan and -37 % for cultivar Karahan. These results showed a higher ability of synthetic wheat but lower ability of Karahan to recover from cutting stress and to revegetate. For the first time a comparative analysis of root exudation (amino acids, sugars and organic acids) by wheat genotypes having different levels of evolution was performed. It was shown that Karahan was characterized by high exudation of tryptophan (0.05 mg/g dry roots per day), histidine (0.12 mg/g dry roots per day) and phenylalanine (0.45 mg/g dry roots per day). Total amount of sugars (mostly fructose, glucose and maltose) exuded by Karahan was 55 mg/g dry roots per day, that was 5 and 3 times higher as compared to synthetic genotype and Albastan. The quantum of organic acids in exudates of all studied genotypes was approximately similar and amounted to about 1.8 mg/g of dry roots per day. The results suggested low ability of Karahan to control the flow rate of carbohydrates from roots to the environment. We propose that high root exudation of tryptophane (precursor in biosynthesis of auxins) and sugars may result in deficit of these compounds and involved in impaired shoot regeneration of Karahan. The results demonstrated differences in the functioning of the root system of primitive hexaploid wheat (synthetic) compared to landrace and modern cultivated variety. The nature of these differences requires more investigation.

Keywords: wheat, root exudation, revegetation, drought stress adaptation.

 

Full article (Rus)

Full text (Eng)

 

REFERENCES

  1. Morgounov A., Haun S., Lang L., Martynov S., Sonder K. Climate change at winter wheat breeding sites in central Asia, eastern Europe, and USA, and implications for breeding. Euphytica, 2013, 194: 277-292 CrossRef
  2. Blum A. Plant breeding for water-limited environments. Springer, 2011.
  3. White R.G., Kirkegaard J.A. The distribution and abundance of wheat roots in a dense, structured subsoil — implications for water uptake. Plant Cell and Environment, 2010, 33: 133-148 CrossRef
  4. Porcel R., Ruiz-Lozano J.M. Arbuscular mycorrhizal influence on leaf water potential, solute accumulation, and oxidative stress in soybean plants subjected to drought stress. Journal of Experimental Botany, 2004, 55: 1743-1750 CrossRef
  5. Aroca R., Porcel R., Ruiz-Lozano J.M. How does arbuscular mycorrhizal symbiosis regulate root hydraulic properties and plasma membrane aquaporins in Phaseolus vulgaris under drought, cold or salinity stresses? New Phytologist, 2007, 173: 808-816 CrossRef
  6. Belimov A.A., Dodd I.C., Hontzeas N., Theobald J.C., Safronova V.I., Davies W.J. Rhizosphere bacteria containing 1-aminocyclopropane-1-carboxylate deaminase increase yield of plants grown in drying soil via both local and systemic hormone signalling. New Phytologist, 2009, 181: 413-423 CrossRef
  7. Groppa M.D., Benavides M.P., Zawoznik M.S. Root hydraulic conductance, aquaporins and plant growth promoting microorganisms: a revision. Applied Soil Ecology, 2012, 61: 247-254 CrossRef
  8. Bais H.P., Weir T.L., Perry L.G., Gilroy S., Vivanco J.M. The role of root exudates in rhizosphere interactions with plants and other organisms. Annual Review of Plant Biology, 2006, 57: 233-266 CrossRef
  9. Farrar J.F., Jones D.L. The control of carbon acquisition by roots. New Phytologist, 2000, 147: 43-53 CrossRef
  10. Plant roots. The hidden half /Y. Waisel, A. Eshel, U. Kafkafi (eds.). NY, Marcel Dekkers Inc., 1996.
  11. Blum A., Ritchie J.T. Effect of soil surface water content on sorghum root distribution in the soil. Field Crops Research, 1984, 8: 169-176 CrossRef
  12. Asseng S., Ritchie J.T., Smucker A.J.M., Robertson M.J. Root growth and water uptake during water deficit and recovering in wheat. Plant and Soil, 1998, 201: 265-273 CrossRef
  13. Reynolds M., Mujeeb-Kazi A., Sawkins M. Prospects for utilising plant-adaptive mechanisms to improve wheat and other crops in drought- and salinity-prone environments. Annals of Applied Biology, 2005, 146: 239-259 CrossRef
  14. Bell L.W., Harrison A.M., Kirkegaard B. Dual-purpose cropping — capitalising on potential grain crop grazing to enhance mixed-farming profitability. Crop and Pasture Science, 2015, 66: i-iv.
  15. Ogbonnaya F.C. Development, management and utilization of synthetic hexaploids in wheat improvement. In: The world wheat book: a history of wheat breeding. A.P. Bonjean, W.J. Angus, M. van Ginkel (eds.). Lavoisier, France, 2011, V. 2: 823-849.
  16. Vorob'ev N.I., Provorov N.A., Sviridova O.V. Programma dlya odnofaktornogo dispersionnogo analiza rendomizirovannykh biologicheskikh dannykh. Svidetel'stvo o gosudarstvennoi registratsii programmy dlya EVM № 2013615092 [The program for the one-way ANOVA for randomized biological data. State Registration Certificate № 2013615092]. Moscow, 2013.
  17. Siddique K.H.M., Belford R.K., Tennant D. Root:shoot ratios of old and modern, tall and semi-dwarf wheats in a mediterranean environment. Plant and Soil, 1990, 121: 89-98 CrossRef
  18. Kierkegaard J.A., Lilley J.M., Hunt J.R., Sprague S.J., Ytting N.K., Rasmussen I.S., Graham J.M. Effect of defoliation by grazing or shoot removal on the root growth of field-grown wheat (Triticum aestivum L.). Crop and Pasture Science, 2015, 66: 249-259.
  19. Shaposhnikov A.I., Azarova T.S., Kravchenko L.V., Bazhanova A.A., Bazhanov D.P., Babak O.G., Nekrashevich N.A., Kil'chevskii A.V. Mole-kulyarnaya i prikladnaya genetika, 2012, 14: 63-68.
  20. Kuzmicheva Yu.V., Shaposhnikov A.I., Azarova T.S., Petrova S.N., Naumkina T.S., Borisov A.Yu., Belimov A.A., Kravchenko L.V., Parakhin N.V., Tikhonovich I.A. Fiziologiya rastenii, 2014, 61(1): 121-128 CrossRef
  21. Belimov A.A., Dodd I.C., Safronova V.I., Shaposhnikov A.I., Azarova T.S., Makarova N.M., Davies W.J., Tikhonovich I.A. Rhizobacteria that produce auxins and contain ACC deaminase decrease amino acid concentrations in the rhizosphere and improve growth and yield of well-watered and water-limited potato (Solanum tuberosum). Annals of Applied Biology, 2015, 1: 11-25 CrossRef
  22. Kravchenko L.V., Shaposhnikov A.I., Makarova N.M., Azarova T.S., L'vova K.A., Kostyuk I.I., Tikhonovich I.A. Sel’skokhozyaistvennaya Biologiya [Agricultural Biology], 2011, 3: 71-75.
  23. Belimov A.A., Dodd I.C., Safronova V.I., Malkov N.V., Davies W.J., Tikhonovich I.A. The cadmium tolerant pea (Pisum sativum L.) mutant SGECdt is more sensitive to mercury: assessing plant water relations. Journal of Experimental Botany, 2015, 66(8): 2359-2369 CrossRef
  24. Tsyganov V.E., Belimov A.A., Borisov A.Y., Safronova V.I., Georgi M., Dietz K.-J., Tikhonovich I.A. A chemically induced new pea (Pisum sativum L.) mutant SGECdt with increased tolerance to and accumulation of cadmium. Annals of Botany, 2007, 99: 227-237 CrossRef
  25. Ljung K. Auxin metabolism and homeostasis during plant development. Development, 2013, 140, 5: 943-950 CrossRef
  26. Sassi M., Vernoux T. Auxin and self-organization at the shoot apical meristem. Journal of Experimental Botany, 2013, 64: 2579-2592 CrossRef
  27. Motte H., Vereecke D., Geelen D., Werbrouck S. The molecular path to in vitro shoot regeneration. Biotechnology Advantages, 2014, 32: 107-121 CrossRef

back