Hort. Sci. (Prague), 2021, 48(4):149-157 | DOI: 10.17221/123/2020-HORTSCI

Response of sweet cherry buds and twigs to temperature changes - evaluated by the determination of the degradation and synthesis of sucroseOriginal Paper

Klaus-Peter Götz ORCID...*, Frank-Michael Chmielewski
Faculty of Life Science, Humboldt-University of Berlin, Berlin, Germany

This study was undertaken to determine the degradation and synthesis of sucrose (Suc) in sweet cherry buds and the twig tissue response to a sequence of environmental temperature changes (cold (orchard) - warm (controlled temperature of ∼22 °C) - cold (orchard)). The results of two years' (2016, 2017) findings were compared with the buds of trees and the buds of twigs in November/December in northeast Germany. The Suc content in the buds of trees and the buds of twigs under natural conditions was stable. Temperatures of ∼22 °C resulted in a significant (Suc) degradation (62%, from 39 to 15 mg/g DW) in the buds of twigs after 21 days (day of the year (DOY) 340). The significant re-synthesis (66%, to 25 mg/g DW after 21 days, DOY 361) in the orchard is noteworthy, and highlights the Suc value as a cryoprotective saccharide. The marked changes in the Suc, glucose, and fructose contents of the twigs exposed to a cold-warm-cold sequence (< DOY 319, DOY 319-340, DOY 340-361), lead to the conclusion that this adaptation is the result of tissue- and cold-specific sucrose invertases/synthases. The effect of low-temperature-active enzymes explains the role of Suc in the buds of trees during the winter rest. When using twigs for plant physiological examinations during the winter rest, results on a metabolite level should be considered when drawing conclusions concerning the overall tree physiology.

Keywords: Prunus avium L.; buds; trees; twigs; saccharides; air temperature

Published: April 15, 2021  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Götz K, Chmielewski F. Response of sweet cherry buds and twigs to temperature changes - evaluated by the determination of the degradation and synthesis of sucrose. Hort. Sci. (Prague). 2021;48(4):149-157. doi: 10.17221/123/2020-HORTSCI.
Download citation

References

  1. Barrero-Gil J., Salinas J. (2013): Post-translational regulation of cold acclimation response. Plant Science, 205-206: 48-54. Go to original source... Go to PubMed...
  2. Castède S., Campoy J.A., Le Dantec L., Quero-García J., Barreneche T., Wenden B., Dirlewanger E. (2015): Mapping of candidate genes involved in bud dormancy and flowering time in sweet cherry (Prunus avium). PLoS ONE 10: e0143250. Go to original source... Go to PubMed...
  3. Chmielewski F.M., Götz K.P. (2016): Performance of models for the beginning of sweet cherry blossom under current and changed climate conditions. Agricultural and Forest Meteorology, 218-219: 85-91. Go to original source...
  4. Chmielewski F.M., Götz K.P., Homann T., Huschek G., Rawel H.M. (2017): Identification of endodormancy release for cherries (Prunus avium L.) by abscisic acid and sugars. Journal of Horticulture, 4: 210.
  5. da Silveira Falavigna V., Port D.D., Miotto Y.E., Pessoa dos Santos H., de Oliveira P.R.D., Margis-Pinheiro M., Pasquali G., Revers L.F. (2018): Evolutionary diversification of galactinol synthases in Rosaceae: adaptive roles of glactionol and raffinose during apple bud dormancy. Journal of Experimental Botany, 69: 1247-1259. Go to original source... Go to PubMed...
  6. Fu Y.H., Campioli M., Deckmyn G., Janssens I.A. (2013): Sensitivity of leaf unfolding to experimental warming in three temperate tree species. Agricultural and Forest Meteorology, 181: 125-132. Go to original source...
  7. Gariglio N., González-Rossia D.E., Mendow M., Reig C., Agusti M. (2006): Effect of artificial chilling on the depth of endodormancy and vegetative and flower bud break of peach and nectarine cultivars using excised shoots. Scientia Horticulturae, 108: 371-377. Go to original source...
  8. Gholizadeh J., Sadeghipour H.R., Abdolzahde A., Hemmati K., Hassani D., Vahdati K. (2017): Redox rather than carbohydrate metabolism differentiates endodormant lateral buds in walnut cultivars with contrasting chilling requirements. Scientia Horticulturae, 225: 29-37. Go to original source...
  9. González-Rossia D.E., Reig C., Dovis V., Gariglio N., Agustí M. (2008): Changes on carbohydrates and nitrogen content in the bark tissues induced by artificial chilling and its relationship with dormancy bud break in Prunus sp. Scientia Horticulturae, 118: 275-281. Go to original source...
  10. Hoermiller I.I., Naegele T., Augustin H., Stutz S., Weckwerth W., Heyer A.G. (2017): Subcellular reprogramming of metabolism during cold acclimation in Arabidopsis thaliana. Plant, Cell and Environment, 40: 602-610. Go to original source... Go to PubMed...
  11. Lattanzi F.A., Ostler U., Wild M., Morvan-Bertrand A., Decau M.L., Lehmeier C.A. Meuriot F., Prud'homme M.P., Schäufele R., Schnyder H. (2012): Fluxes in central carbohydrate metabolism of source leaves in a fructan-storing C3 grass: rapid turnover and futile cycling of sucrose in continuous light under contrasted nitrogen nutrition status. Journal of Experimental Botany, 63: 2363-2375. Go to original source... Go to PubMed...
  12. Levizou E., Manetas Y. (2007): Photosynthetic pigment contents in twigs of 24 woody species assessed by in vivo reflectance spectroscopy indicate low chlorophyll levels but high carotenoid/chlorophyll ratios. Environmental and Experimental Biology, 59: 293-298. Go to original source...
  13. Miki Y., Takahashi D., Kawamura Y., Uemura M. (2019): Temporal proteomics of Arabidopsis plasma membrane during cold- and de-acclimation. Journal of Proteomics, 197: 71-81. Go to original source... Go to PubMed...
  14. Parada F., Noriega X., Dantas D., Bressan-Smith R., Perérez F.J. (2016): Differences in respiration between dormant and non-dormant buds suggest the involvement of ABA in the development of endodormancy in grapevines. Journal of Plant Physiology, 201: 71-78. Go to original source... Go to PubMed...
  15. Peresa-Resa C., Rodrígues-Milla M.A., Iniesto E., Rubio V., Salinas J. (2017): Prefoldins negatively regulate cold acclimation in Arabidopsis thaliana by promoting nuclear proteasomemediated HY5 degradation. Molecular Plant, 10: 791-804. Go to original source... Go to PubMed...
  16. Sin'kevich M.S., Sabel'nikova E.P., Deryabin A.N., Astakhova N.V., Dubinina I.M., Burakhanova E.A., Trunova T.I. (2008): The changes in invertase activity and the content of sugars in the course of adaptation of potato plants to hypothermia. Russian Journal of Plant Physiology, 55: 449-454. Go to original source...
  17. Stitt M., Hurry V. (2002): A plant for all seasons: alterations in photosynthetic carbon metabolism during cold acclimation in Arabidopsis. Current Opinion in Plant Biology, 5: 199-206. Go to original source... Go to PubMed...
  18. Sturm A. (1999): Invertases. Primary structures, functions, and roles in plant development and sucrose partitioning. Plant Physiology, 121: 1-7. Go to original source... Go to PubMed...
  19. Tiessen A., Padilla-Chacon D. (2013): Subcellular compartmentation of sugar signalling: links among carbon cellular status, route of sucrolysis, sink-source allocation, and metabolic partitioning. Frontiers in Plant Science: 3. Go to original source... Go to PubMed...
  20. Turhan E., Ergin S. (2012): Soluble sugars and sucrose-metabolizing enzymes related to cold acclimation of sweet cherry cultivars grafted on different rootstocks. The Scientific World Journal, Article ID 979682. Go to original source... Go to PubMed...
  21. Weiß K., Alt M. (2017): Determination of single sugars, including inulin, in plants and feed materials by HighPerformance Liquid Chromatography and Refraction Index Detection. Fermentation, 3: 36. Go to original source...
  22. Xin Z., Browse J. (2000): Cold comfort farm: the acclimation of plants to freezing temperatures. Plant, Cell and Environment, 23: 893-902. Go to original source...
  23. Yu D.J., Hwang J.Y., Chung S.W., Oh H.D., Yun S.K., Lee H.J. (2017): Changes in cold hardiness and carbohydrate content in peach (Prunus persica) trunk bark and wood tissues during cold acclimation and deacclimation. Scientia Horticulturae, 219: 45-52. Go to original source...
  24. Zhou J., He L., Gao Y., Han N., Zhang R., Wu Q., Li J., Tang X., Xu B., Ding J., Huang Z. (2016): Characterization of a novel low-temperature-active, alkaline and sucrose-tolerant invertase. Scientific Reports, 6: 32081. Go to original source... Go to PubMed...
  25. Zuther E., Büchel K., Hundertmark M., Stitt M., Hincha D.K., Heyer A.G. (2004): The role of raffinose in the cold acclimation response of Arabidopsis thaliana. FEBS Letters, 576: 169-173. Go to original source... Go to PubMed...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.