| Peer-Reviewed

Regulation of Physiological and Biochemical Processes in an Intact Plant Is Determined by Interaction of Flows of Substance Bulk Transfer

Received: 12 June 2017    Accepted: 19 June 2017    Published: 17 August 2017
Views:       Downloads:
Abstract

The analysis of characteristic features of photosynthesis alterations, assimilate transport, growth function, and plant leaf ultrastructure under the changes in sink-source relations (SSR) between photosynthetic and sink organs is carried out, as well as the level of nitrogen (nitrate) nutrition. Under modeling conditions, there is shown NO-triggering mechanism of inhibition of assimilate export from leaves which becomes involved with the increase in the plant apoplast nitrate level. The concept that the plant metabolism regulation under the changes of environmental conditions is realized through the interaction of counter flows of nitrates and photoassimilates. This interaction involves changing in the degree of reduction of absorbed nitrates resulting in NO formation. By activating the callose synthesis, NO plugs pores in sieve tubes and inhibits sugar transport along the phloem. Numerous genes are activated under the effect of NO signal system. Out of all enzymes synthesized due to the expression of these genes, there function and change the metabolism only the ones for which cofactors and substrates resulting from SSR disturbance exist. Such reorganization of metabolism occurs every new photoperiod in accordance with new levels of assimilates and nitrates in plants.

Published in Journal of Plant Sciences (Volume 5, Issue 4)
DOI 10.11648/j.jps.20170504.13
Page(s) 110-119
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Photosynthesis, Nitric Oxide, Apoplast, Regulation

References
[1] Ainsworth EA, Bush DR. 2011. Carbohydrate export from the Leaf: A highly regulated process and target to enhance photosynthesis and productivity. Plant Physiology. 155, 64-69.
[2] Ayre BG, Keller F, and Turgeon, R. 2003. Symplastic continuity between companion cell and the translocation stream: long-distance transport is controlled by retention and retrieval mechanisms in the phloem. Plant Physiology 131, 1518-1528.
[3] Batasheva S, Abdrakhimov F, Bakirova G, Isaeva E, Chikov V. 2007. Effect of nitrates supplied with the transpiration flow on assimilate translocation. Rus. J. Plant Physiology 54, 373-380. [in rus].
[4] Batasheva S, Abdrakhimov F, Bakirova G, Isaeva E, Chikov V. 2010. Effects of sodium nitroprusside, the nicric oxyde donor, on photosynthesis and ultrastructure of common flax leave blades. Rus. J. Plant Physiology 57, 376-381. [in rus].
[5] Batasheva S, Isaeva E, Chikov V, and Ratushnyk A. 2011. The Influence of Suddenly Changing Quantity of Produced Photosynthetic Products on its Export from Donor-Leave. Middle-East Journal of Scientific Research. 10, 188-190.
[6] Bethke PC, Badger MR, Jones RL. 2004. Apoplastic synthesis of nitric oxide by plant tissue. The Plant Cell 16. 332-341.
[7] Chikov VI. 1987. Photo¬synthesis and Assimilate Transport. Moscow: Nauka. [in rus].
[8] Chikov VI. 1996. Photorespiration. Soros Educate Journal. (11) 2-8. [in rus].
[9] Chikov VI, Abdrakhimov FA, Bakirova GG, Batasheva SN. 2007. The role of sink-source relationship between different organs in regulation of photosynthesis and productivity. Acta Horticulturae, Proceedings of the International Symposium on Source-Sinc relationsheps in Plants. (835) 87-98.
[10] Chikov, V. I., Abdrakhimov, F. A., Batasheva, S. N., and Khamidullina L. A.: Characteristics of Photosynthesis in Maize Leaves (С4 Plants) upon Changes in the Level of Illuminance and Nitrate Nutrition. − Russ. J. Plant Physiol. 63: 620-625, 2016b. (In Rus).
[11] Chikov V. I., Akhtyamova G. A., Batasheva S. N., D. S. Dyurbin, М. Ш. Tagirov M. Sh., Blokhin V. I. Root formation in the pre-heading period in different morphobiotypes of barley // Niva Tatarstana. 2017. N. 2. P. 27-29. (In Rus).
[12] Chikov VI, Avvakumova NY, Bakirova GG, Belova LA, Zaripova L. 2001. Apoplastic transport of 14C-photosynthates measured under drought and nitrogen supply. Biollogia Plantarum 44 (4), 517-521.
[13] Chikov VI, Bakirova GG. 1999. Relationship between carbon and nitrogen metabolisms in photosynthesis. The role of photooxidation processes. Photosynthetica 37 (4), 519-527.
[14] Chikov VI, Bakirova GG, Batasheva SN, Sergeeva AA. 2005. Effect of Defoliation or Excision of Growing Axillary Shoots on the Composition of Labeled Products od Photosynthesis in the leaves and Xylem Sap of Kidney Bean. Rus. J. Plant Physiology 52, 459-462. [in rus].
[15] Chikov VI, Batasheva SN. 2012. The role of C to N balance in the regulation of photosynthesis function. Function Advances in Photosynthesis - Fundamental Aspects ISBN 978-953-307-928-8 Edited by: Mohammad Mahdi Najafpour Publisher: InTech, 273-298.
[16] Chikov VI, Bulka ME, Lozovaya VV. 1972. Effect of insecticides on 14C distribution in the products of photosynthesis. Sov. J. Plant Physiology 19, 190-193. [in rus].
[17] Chikov VI, Bulka ME, Yargunov, VG. 1985. Effects of fruit removal on photosynthctic metabolism of 14C in cotton leaves. Sov. J. Plant Physiol. 32, 1055-1063. [in russ].
[18] Chikov VI, Chemikosova SB, Bakirova GG, Gazizova NI. 1984. Influence of removal of a portion of spike or leaves on assimilate transport and photosynthetic productivity in spring wheat. Sov. J. Plant Physiol 31 475-481. [in russ].
[19] Chikov V, Chemikosova S, Nesterova T, Zernova O. 1988. Peculiarity of photosynthesis and export function of leaf under Enhanced Nitrogen Nutrition. Photosynthesis and productive process. Ed. Mokronosov, A. T. Sverdlovsk. Russia. 145-154. [in rus].
[20] Chikov VI, Isfandiyarov NI. 1978. Effects of the rate of assimilate efflux on the ratio between some components of plant gas exchange. Abst. All-Union Conf. “Biochemical and Biophysical Mechanisms of Substance Transport in Plants and its Regulation”. Gorky. 182. [in russ].
[21] Chikov, V. I., Mikhailov, A. L., Timofeeva, O. A., and Khamidullina, L. A2016a.. Photosynthetic carbon metabolism in potato leaves under changes in light intensity. − Russ. J. Plant Physiol. 63: 70–76, (In Rus).
[22] Chikov VI, Salyakhova GA, Safiullina GF, Zamalieva FF. 2012. Photosynthesis, assimilates transport and productivity in potato plants of the nevskii variety grown under different insolation. Agricultural biology. No 1, 72-77. (in rus).
[23] Chikov VI, Yargunov VG, Fedoseeva, Chemikosova SB. 1982. Influence of the regulationship between production and consumption of photosynthates on the operation of photosynthetic apparatus in plants. Sov. J. Plant Physiology (Moscow) 29 (6) 1141-1146. [in russ].
[24] Crawford NM. 1995. Nitrate: nutrient and signal for plant growth. The Plant Cell. 7, 859-868.
[25] Eickenbusch JD, Beck E. 1973. Evidence for involvement of 2 types of reaction in glycolate formation during photosynthesis in isolated spinach chloroplasts. FEBS Lett. 31, 225-228.
[26] Foyer CH, Parry M, Noctor G. 2003. Markers and signals associated with nitrogen assimilation in higher plants. Journal of Experimenta Botany 54, 585-593.
[27] Fritz C, Mueller C, Matt P, Feil R, Stitt M. 2006. Impact of C-N status on the amino acids profile in tobacco sourse leaves. Plant, Cell and Environment 29, 2055-2076.
[28] Hall AJ, Brady CJ. 1977. Assimilate source-sink relationships in Capsicum annuum L II Effects fruiting and defloration on the photosynthetic capacity and senescence of the leaves. Aust J Plant Phisiol 4, 771-783.
[29] Henkes S, Sonnewald U, Flachmann R, Stitt M. 2001. A small decrease of plastid transketolase expression in antisence tobacco transformants has dramatic effects on photosynthesis and pheniltropanoid metabolism. The Plant Cell. 13, 535-551.
[30] Kaiser WM, Kandlbinder A, Stoimenova M, Glaab J. 2000. Discrepancy between nitrate reduction rates in intact leaves and nitrate reductase activity in leaf extracts: what limits nitrate reduction in satu? Planta 210, 801-807.
[31] Khamidullina LA, Abdrakhimov FA, Batasheva SN, Frolov DA, Chikov VI. 2011. Effect of nitrate infusion into the shoot apoplast on photosynthesis and assimilate transport in symplastic and apoplastic plants Rus. J. Plant Physiology 57, 484-490. [in rus].
[32] Khalilova LA. 2008. The ways of transport Cl⁻ in the whole plant sistem halophyte Suaeda antissima (L.) Thesis of Dissertation. Institute of plant physiology, Moscow. Russia. [in rus].
[33] Krapp A, Saliba-Colombani V, Daniel-Vedelr F 2005. Analisis of C and N metabolisms and of C/N integrations using quantitative genetics. Photosynthesis Research 83, 251-263.
[34] Kursanov AL. 1976. Assimilate transport in plants. Nauka, Moscow. 1976. [in rus].
[35] Kursanov AL. 1984. Endogenous regulation of assimilate transport and source-sink relation in plant. Soviet J. Plant Physiology. 31, 579-595. [in rus].
[36] Lamattina L. & Polaco J. C. 2006. Nitric Oxide in Plant Growth. Springer-Verlag Berlin Heidelberg.
[37] Leggewie G, Kolbe A, Lemoine R, Roessner U, Lytovchenko A, Zuther E, Kehr J, Frommer WB, Riesmeier JW, Willmitzer, et al 2003. Overexpression of the sucrose transporter So SUT1 in potato results in alterations in leaf carbon partitioning and in tuber metabolism byt has little impact on tuber morphology. Planta 217, 158-167.
[38] Lenz F. 1977. Einflüβ der Frucht auf Photosynthese und atmung. Ztschr. Pflanzenenernahr. Und Bodenk. 140, 51-61.
[39] Lips SN. 1997. The role of InorganicNitrogen Ions in Plant Adaptation Process. Rus. J. Plant Physiology 44, 487-498. [in rus].
[40] Lawlor D. W. Genetic engineering to improve plant performance under drought: physiological evaluation of achievements, limitations, and possibilities // Journal of Experimental Botany. 2013. Volume 64, Issue 1. Pp. 83-108.
[41] Majumder SK, Leopold AC. 1967. Callose formation in response to low temperature. Plant and Cell Physiol. 8, 775-778.
[42] Matt P, Geiger M, Walch-Liu P, Engels C, Krapp A, Stitt M. 2001. Elevated carbon dioxide increases nitrate uptake and nitrate reductase activity when tobacco is growing on nitrate, but increases ammonium uptake and inhibits nitrate reductase activity when tobacco is growing on ammonium nitrate. Plant Cell and Environment 24, 1119-1137.
[43] Meyer C, Lea US, Provan F, Kaizer WM, Lillo C. 2005. Is nitrate reductase a major player in the plant NO (nitric oxide) game? Photosynth. Res. 83, 181-189.
[44] Minchin PEH. & McNaughton GS. 1987. Xylem transport of recemtly fixed carbon within Lupin. Aust. Plant Physiol. 14, 325-329.
[45] Mokronosov AT. 1972. Photosynthetic Function in the System of the Whole Plant. Theoretical Basics for Photosynthetic Productivity. Nichiporovich, A. A. Ed., Moscow. Nauka. 355-361. [in rus].
[46] Mokronosov AT. 1981. Developmental aspects of Photosynthesis. Moscow. Nauka. [in russ].
[47] Mokronosov AT, Ivanova NA. 1971. Specialities of Photosynthetic Function at the Partial Defoliation of Plants Sov. Journal of Plant Physiology. (Moscow). 18, 668-676. [in rus].
[48] Moorby J. 1977. Integration and regulation of translocation within the whole plant. Symp Soc Exp Biol. 31, 425-454.
[49] Moyse A. 1980. La photorespiration: differents aspects de la respiration des vegetaux a la lumiere. Physiol. Veg. 18, 543-565.
[50] Neill SJ, Desikan R. & Hancock JT. 2003. Nitric oxide signaling in plants. New Physiologist 159, 11-35.
[51] Noctor G, Foyer CH. 1998. A re-evaluation of the ATP: NADPH budget during C3 photosynthesis. A contribution from nitrate assimilation and its associated respiratory activity? Journal of Experimental Botany 49, 1895-1908.
[52] Paris R, Lamattina L, Casalongue CA 2007. Nitric oxide promotes the wound-h.
[53] Paul MJ, Foyer CH. 2001. Sink regulation of photosynthesis. Journal of Experimental Botany 52, No 360, 1383-1400.
[54] Paul MJ, Pellny TK. 2003. Carbon metabolitefreedback regulation of leaf photosynthesis and development. Journal of Experimental Botany 54, (382), Regulation of Carbon Metabolism Special Issue, 539-547.
[55] Peuke AD, Jeschke WD, Hurtung, WW. 2002. Flows of elements, Ions and abscisic acid in Ricinus communis and Site of Nitrate Reduction under Potassium Limitation. Journal of Experimental Botany 53, pp. 241-250.
[56] Rennie EA, Turgeon R 2009. A comprehensive picture of phloem loading strategies. Proc Natl Acad Sci. USA 106, 14162-14167.
[57] Rosche E, Blackmore D, Tegeder M, Richardson T, Schroeder H, Higgins TJV, Frommer WB, Offler CE, Patrick JW. 2000. Seed-specific overexpression of a popate sucrose transporter increases sucroseuptake and growth rates of developing pea cotyledons. Plant J. 30, 165-175.
[58] Slewinski TL, Braun DM. 2010. Current perspectives on the regulation of whole-plant carbohydrate partitioning. Plant Science 178, 341-349.
[59] Stitt M, Müller C, Gibon Y, Carillo P, Morcuende R, Scheible WR, Krapp A. 2002. Steps towards an integrated view of nitrogen. Journal of Experimental Botany 53, (370), Inorganic Nitrogen Assimilation Special Issue, 959–970.
[60] Tarchevsky IA. 1965. Relationship between Photosynthetic Phosphorylation, CO2 assimilation and Other Functions of Chloroplasts and Photosynthesizing Cells. In: Biochemistry and Biophysics of Photosynthesis. Krasnovskii A. A. Ed. Moscow. 305-319. [in rus].
[61] Turgenon R, Wolf S. 2009. Phloem transport: cellular pathways and molecular trafficking. Annu Rev. Plant Bioogy 60, 207-221.
[62] Voskresenskaya NP, Wiil YA, Grishina GS, Pärnik TR. 1970. Effect of oxygen concentration and light intensity on the distribution of labeled cfrbon in photosynthesis products in bean plants. Photosynthetica 4, (1) 1-8.
[63] Walch-Liy P, Filleur S, Gan Y, Forde BG. 2005. Signaling mechanisms integrating root and shoot responses to changes in the nitrogen supply. Photosynthesis Research 83, 239-250.
[64] Wardlaw JF, Moncur L. 1976. Source, Sink and Hormonal Control of Translocation in Wheat. Planta 128 (2) 93.
[65] Webb JA, Gorham PR. 1965. The Effect of Node Temperature on Assymilation and Translocation of 14C in Squash. Can. Journal of Botany 43, 1009-1017.
[66] Zottini M, Costa A, Michele RD, Ruzzene M, Carimi F. 2007. Salicylic acis activates nitric oxide synthesis in Arabidopsis. Journal of Experimental Botany 58, 1397-1405.
Cite This Article
  • APA Style

    Chikov Vladimir. (2017). Regulation of Physiological and Biochemical Processes in an Intact Plant Is Determined by Interaction of Flows of Substance Bulk Transfer. Journal of Plant Sciences, 5(4), 110-119. https://doi.org/10.11648/j.jps.20170504.13

    Copy | Download

    ACS Style

    Chikov Vladimir. Regulation of Physiological and Biochemical Processes in an Intact Plant Is Determined by Interaction of Flows of Substance Bulk Transfer. J. Plant Sci. 2017, 5(4), 110-119. doi: 10.11648/j.jps.20170504.13

    Copy | Download

    AMA Style

    Chikov Vladimir. Regulation of Physiological and Biochemical Processes in an Intact Plant Is Determined by Interaction of Flows of Substance Bulk Transfer. J Plant Sci. 2017;5(4):110-119. doi: 10.11648/j.jps.20170504.13

    Copy | Download

  • @article{10.11648/j.jps.20170504.13,
      author = {Chikov Vladimir},
      title = {Regulation of Physiological and Biochemical Processes in an Intact Plant Is Determined by Interaction of Flows of Substance Bulk Transfer},
      journal = {Journal of Plant Sciences},
      volume = {5},
      number = {4},
      pages = {110-119},
      doi = {10.11648/j.jps.20170504.13},
      url = {https://doi.org/10.11648/j.jps.20170504.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jps.20170504.13},
      abstract = {The analysis of characteristic features of photosynthesis alterations, assimilate transport, growth function, and plant leaf ultrastructure under the changes in sink-source relations (SSR) between photosynthetic and sink organs is carried out, as well as the level of nitrogen (nitrate) nutrition. Under modeling conditions, there is shown NO-triggering mechanism of inhibition of assimilate export from leaves which becomes involved with the increase in the plant apoplast nitrate level. The concept that the plant metabolism regulation under the changes of environmental conditions is realized through the interaction of counter flows of nitrates and photoassimilates. This interaction involves changing in the degree of reduction of absorbed nitrates resulting in NO formation. By activating the callose synthesis, NO plugs pores in sieve tubes and inhibits sugar transport along the phloem. Numerous genes are activated under the effect of NO signal system. Out of all enzymes synthesized due to the expression of these genes, there function and change the metabolism only the ones for which cofactors and substrates resulting from SSR disturbance exist. Such reorganization of metabolism occurs every new photoperiod in accordance with new levels of assimilates and nitrates in plants.},
     year = {2017}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - Regulation of Physiological and Biochemical Processes in an Intact Plant Is Determined by Interaction of Flows of Substance Bulk Transfer
    AU  - Chikov Vladimir
    Y1  - 2017/08/17
    PY  - 2017
    N1  - https://doi.org/10.11648/j.jps.20170504.13
    DO  - 10.11648/j.jps.20170504.13
    T2  - Journal of Plant Sciences
    JF  - Journal of Plant Sciences
    JO  - Journal of Plant Sciences
    SP  - 110
    EP  - 119
    PB  - Science Publishing Group
    SN  - 2331-0731
    UR  - https://doi.org/10.11648/j.jps.20170504.13
    AB  - The analysis of characteristic features of photosynthesis alterations, assimilate transport, growth function, and plant leaf ultrastructure under the changes in sink-source relations (SSR) between photosynthetic and sink organs is carried out, as well as the level of nitrogen (nitrate) nutrition. Under modeling conditions, there is shown NO-triggering mechanism of inhibition of assimilate export from leaves which becomes involved with the increase in the plant apoplast nitrate level. The concept that the plant metabolism regulation under the changes of environmental conditions is realized through the interaction of counter flows of nitrates and photoassimilates. This interaction involves changing in the degree of reduction of absorbed nitrates resulting in NO formation. By activating the callose synthesis, NO plugs pores in sieve tubes and inhibits sugar transport along the phloem. Numerous genes are activated under the effect of NO signal system. Out of all enzymes synthesized due to the expression of these genes, there function and change the metabolism only the ones for which cofactors and substrates resulting from SSR disturbance exist. Such reorganization of metabolism occurs every new photoperiod in accordance with new levels of assimilates and nitrates in plants.
    VL  - 5
    IS  - 4
    ER  - 

    Copy | Download

Author Information
  • Kazan Institute of Biochemistry and Biophysics, Kazan, Russia

  • Sections