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2014 | 36 | 01 |

Tytuł artykułu

Jatropha is vulnerable to cold injury due to impaired activity and expression of plasma membrane H+-ATPase

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Cold stress is one of the major environmental factors limiting the amount of plant mass for bioenergy production. A chilling-sensitive Jatropha (Jatropha curcas L.) as a bioenergy crop was used to investigate the cold injury process at the physiological and biochemical levels. Various physiological parameters such as leaf length, width, stomatal conductance, chlorophyll fluorescence, and electrolyte leakage were measured to determine the growth rate of leaves cold-treated (7 and 2°C) for 5 days. These parameters of cold-treated Jatropha were significantly reduced from day 1 compared with control (23°C). Using the pH indicator bromocresol purple, it was shown that surface pH of Jatropha root in control was strongly acidified by time only from the starting pH 6, while H⁺-efflux of the surface of cold-treated roots did not change. H⁺- ATPase activity of plasma membrane (PM) isolated from leaves and roots of cold-treated Jatropha was decreased in a time-dependent manner. The expression of PM H⁺-ATPase and 14-3-3 protein, which participates in phosphorylation of PM H⁺-ATPase was reduced in the presence of cold stress. Interestingly, fusicoccin, an activator of the PM H⁺- ATPase, alleviated cold-injury by stimulating the enzyme in leaves. These results may suggest that the activity and expression of PM H⁺-ATPase in Jatropha is closely related to the overcoming of cold stress.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

01

Opis fizyczny

p.231-241,fig.,ref.

Twórcy

autor
  • Bioenergy Research Center, Department of Bioenergy Science and Technology, Chonnam National University, Gwangiu 500-757, South Korea
autor
  • Bioenergy Research Center, Department of Bioenergy Science and Technology, Chonnam National University, Gwangiu 500-757, South Korea
autor
  • Bioenergy Research Center, Department of Bioenergy Science and Technology, Chonnam National University, Gwangiu 500-757, South Korea
autor
  • Bioenergy Research Center, Department of Bioenergy Science and Technology, Chonnam National University, Gwangiu 500-757, South Korea

Bibliografia

  • Ahn SJ, Im YJ, Chung GC, Cho BH, Suh SR (1999) Physiological responses of grafted-cucumber leaves and rootstock roots affected by low root temperature. Sci Hortic-Amsterdam 81(4):397–408. doi:10.1016/S0304-4238(99)00042-4
  • Ahn SJ, Im YJ, Chung GC, Seong KY, Cho BH (2000) Sensitivity of plasma membrane H⁺-ATPase of cucumber root system in response to low root temperature. Plant Cell Rep 19(8):831–835.
  • Ahn SJ, Sivaguru M, Osawa H, Chung GC, Matsumoto H (2001) Aluminum inhibits the H⁺-ATPase activity by permanently altering the plasma membrane surface potentials in squash roots. Plant Physiol 126(4):1381–1390. doi:10.1104/pp.126.4.1381
  • Ahn SJ, Sivaguru M, Chung GC, Rengel Z, Matsumoto H (2002) Aluminium-induced growth inhibition is associated with impaired efflux and influx of H⁺ across the plasma membrane in root apices of squash (Cucurbita pepo). J Exp Bot 53(376):1959–1966. doi:10.1093/Jxb/Erf049
  • Ao PX, Li ZG, Fan DM, Gong M (2013) Involvement of antioxidant defense system in chill hardening-induced chilling tolerance in Jatropha curcas seedlings. Acta Physiol Plant 35(1):153–160.
  • Arango M, Gevaudant F, Oufattole M, Boutry M (2003) The plasma membrane proton pump ATPase: the significance of gene subfamilies. Planta 216(3):355–365. doi:10.1007/s00425-002-0856-8
  • Babakov AV, Chelysheva VV, Klychnikov OI, Zorinyanz SE, Trofimova MS, De Boer AH (2000) Involvement of 14-3-3 proteins in the osmotic regulation of H⁺-ATPase in plant plasma membranes. Planta 211(3):446–448. doi:10.1007/s004250000347
  • Baunsgaard L, Venema K, Axelsen KB, Villalba JM, Welling A, Wollenweber B, Palmgren MG (1996) Modified plant plasma membrane H⁺-ATPase with improved transport coupling efficiency identified by mutant selection in yeast. Plant J 10(3):451–458. doi:10.1046/j.1365-313X.1996.10030451.x
  • Berchmans HJ, Hirata S (2008) Biodiesel production from crude Jatropha curcas L. seed oil with a high content of free fatty acids. Bioresour Technol 99(6):1716–1721. doi:10.1016/j.biortech.2007.03.051
  • Bobik K, Duby G, Nizet Y, Vandermeeren C, Stiernet P, Kanczewska J, Boutry M (2010) Two widely expressed plasma membrane H⁺-ATPase isoforms of Nicotiana tabacum are differentially regulated by phosphorylation of their penultimate threonine. Plant J 62(2):291–301. doi:10.1111/j.1365-313X.2010.04147.x
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254.
  • Calba H, Jaillard B, Fallavier P, Arvieu JC (1996) Agarose as a suitable substrate for use in the study of Al dynamics in the rhizosphere. Plant Soil 178(1):67–74. doi:10.1007/Bf00011164
  • Chelysheva VV, Smolenskaya IN, Trofimova MC, Babakov AV, Muromtsev GS (1999) Role of the 14-3-3 proteins in the regulation of H⁺-ATPase activity in the plasma membrane of suspension-cultured sugar beet cells under cold stress. FEBS Lett 456(1):22–26. doi:10.1016/S0014-5793(99)00923-0
  • Díaz-López L, Gimeno V, Simón I, Martínez V, Rodríguez-Ortega WM, García-Sánchez F (2012) Jatropha curcas seedlings show a water conservation strategy under drought conditions based on decreasing leaf growth and stomatal conductance. Agric Manag Water Qual 105:48–56. doi:10.1016/j.agwat.2012.01.001
  • Fuglsang AT, Visconti S, Drumm K, Jahn T, Stensballe A, Mattei B, Jensen ON, Aducci P, Palmgren MG (1999) Binding of 14-3-3 protein to the plasma membrane H⁺-ATPase AHA2 involves the three C-terminal residues Tyr(946)-Thr-Val and requires phosphorylation of Thr(947). J Biol Chem 274(51):36774–36780.
  • Geilfus CM, Muhling KH (2013) Ratiometric monitoring of transient apoplastic alkalinization in the leaf apoplast of living Vicia fava plants: chloride primes and PM H⁺-ATPase shapes NaClinduced systemic alkalinizations. New Phytol 197:1117–1129.
  • Hayashi Y, Nakamura S, Takemiya A, Takahashi Y, Shimazaki K, Kinoshita T (2010) Biochemical characterization of in vitro phosphorylation and dephosphorylation of the plasma membrane H⁺-ATPase. Plant Cell Physiol 51(7):1186–1196. doi:10.1093/pcp/pcq078
  • Iglesias-Acosta M, Martínez-Ballesta MC, Teruel JA, Carvajal M (2010) The response of broccoli plants to high temperature and possible role of root aquaporins. Environ Exp Bot 68(1):83–90.doi:10.1016/j.envexpbot.2009.10.007
  • Jan N, ul-Hussain M, Andrabi KI (2009) Cold resistance in plants: a mystery unresolved. Electron J Biotechnol 12:14–15. doi:10.2225/vol12-issue3-fulltext-3
  • Janicka-Russak M, Kabala K, Wdowikowska A, Klobus G (2012) Response of plasma membrane H⁺-ATPase to low temperature in cucumber roots. J Plant Res 125(2):291–300. doi:10.1007/s10265-011-0438-6
  • Johansson F, Sommarin M, Larsson C (1993) Fusicoccin activates the plasma membrane H⁺-ATPase by a mechanism involving the C-terminal inhibitory domain. Plant Cell 5(3):321–327. doi:10.1105/tpc.5.3.321
  • Kalberer SR, Wisniewski M, Arora R (2006) Deacclimation and reacclimation of cold-hardy plants: current understanding and emerging concepts. Plant Sci 171(1):3–16. doi:10.1016/j.plantsci.2006.02.013
  • Kim JS, Jung HJ, Lee HJ, Kim KA, Goh CH, Woo YM, Oh SH, Han YS, Kang H (2008) Glycine-rich RNA-binding protein7 affects abiotic stress responses by regulating stomata opening and closing in Arabidopsis thaliana. Plant J 55(3):455–466. doi:10.1111/j.1365-313X.2008.03518.x
  • Kim HS, Oh JM, Luan S, Carlson JE, Ahn S-J (2013) Cold stress causes rapid but differential changes in properties of plasma membrane H⁺-ATPase of camelina and rapeseed. J Plant Physiol 170(9):828–837. doi:10.1016/j.jplph.2013.01.007
  • Kinoshita T, Shimazaki K (1999) Blue light activates the plasma membrane H⁺-ATPase by phosphorylation of the C-terminus in stomatal guard cells. EMBO J 18(20):5548–5558. doi:10.1093/emboj/18.20.5548
  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227(5259): 680–685.
  • Li W, Li M, Zhang W, Welti R, Wang X (2004) The plasma membrane-bound phospholipase Ddelta enhances freezing tolerance in Arabidopsis thaliana. Nat Biotechnol 22(4):427–433.doi:10.1038/nbt949
  • Liang Y, Chen H, Tang M-J, Yang P-F, Shen S-H (2007) Responses of Jatropha curcas seedlings to cold stress: photosynthesisrelated proteins and chlorophyll fluorescence characteristics. Physiol Plant 131(3):508–517. doi:10.1111/j.1399-3054.2007.00974.x
  • Liu Y, Liu H, Pan Q, Yang H, Zhan J, Huang W (2009) The plasma membrane H⁺-ATPase is related to the development of salicylic acid-induced thermotolerance in pea leaves. Planta 229(5):1087–1098. doi:10.1007/s00425-009-0897-3
  • Martz F, Sutinen ML, Kiviniemi S, Palta JP (2006) Changes in freezing tolerance, plasma membrane H⁺-ATPase activity and fatty acid composition in Pinus resinosa needles during cold acclimation and de-acclimation. Tree Physiol 26(6):783–790.
  • Matos FS, de Oliveria LR, Galvão de Freitas R, Evaristo AB, Missio RF, Oliva Cano MA, Antônio dos Santos Dias L (2012) Physiological characterization of leaf senescence of Jatropha curcas L. populations. Biomass Bioenergy 45(0):57–64. doi:10.1016/j.biombioe.2012.05.012
  • Matteucci M, D’Angeli S, Errico S, Lamanna R, Perrotta G, Altamura MM (2011) Cold affects the transcription of fatty acid desaturases and oil quality in the fruit of Olea europaea L. genotypes with different cold hardiness. J Exp Bot 62(10):3403–3420. doi:10.1093/Jxb/Err013
  • Morsomme P, dExaerde AD, De Meester S, Thines D, Goffeau A, Boutry M (1996) Single point mutations in various domains of a plant plasma membrane H⁺-ATPase expressed in Saccharomyces cerevisiae increase H⁺-pumping and permit yeast growth at low pH. EMBO J 15(20):5513–5526.
  • Olsson A, Svennelid F, Ek B, Sommarin M, Larsson C (1998) A phosphothreonine residue at the C-terminal end of the plasma membrane H⁺-ATPase is protected by fusicoccin-induced 14-3-3 binding. Plant Physiol 118(2):551–555. doi:10.1104/Pp.118.2.551
  • Openshaw K (2000) A review of Jatropha curcas: an oil plant of unfulfilled promise. Biomass Bioenergy 19(1):1–15. doi:10.1016/S0961-9534(00)00019-2
  • Öquist G, Wass R (1988) A portable, microprocessor operated instrument for measuring chlorophyll fluorescence kinetics in stress physiology. Physiol Plant 73(2):211–217. doi:10.1111/j.1399-3054.1988.tb00588.x
  • Palmgren MG (1998) Proton gradients and plant growth: role of the plasma membrane H⁺-ATPase. Adv Bot Res 28:1–70.
  • Palmgren MG, Askerlund P, Fredrikson K, Widell S, Sommarin M, Larsson C (1990) Sealed inside-out and right-side-out plasma membrane vesicles: optimal conditions for formation and separation. Plant Physiol 92(4):871–880.
  • Palmgren MG, Sommarin M, Serrano R, Larsson C (1991) Identification of an autoinhibitory domain in the C-terminal region of the plant plasma membrane H⁺-ATPase. J Biol Chem 266(30):20470–20475.
  • Palta JP, Whitaker BD, Weiss LS (1993) Plasma membrane lipids associated with genetic variability in freezing tolerance and cold acclimation of solanum species. Plant Physiol 103(3):793–803.
  • Portillo F (2000) Regulation of plasma membrane H⁺-ATPase in fungi and plants. Bba-Rev Biomembranes 1469(1):31–42.doi:10.1016/S0304-4157(99)00011-8
  • Rapacz M, Janowiak F (1998) Physiological effects of winter rape (Brassica napus var. oleifera) prehardening to frost. I. Frost resistance and photosynthesis during cold acclimation. J Agron Crop Sci 181(1):13–20. doi:10.1111/j.1439-037X.1998.tb00392.x
  • Santori G, Di Nicola G, Moglie M, Polonara F (2012) A review analyzing the industrial biodiesel production practice starting from vegetable oil refining. Appl Energy 92:109–132. doi:10.1016/j.apenergy.2011.10.031
  • Shen H, He LF, Sasaki T, Yamamoto Y, Zheng SJ, Ligaba A, Yan XL, Ahn SJ, Yamaguchi M, Sasakawa H, Matsumoto H (2005) Citrate secretion coupled with the modulation of soybean root tip under aluminum stress Up-regulation of transcription, translation, and threonine-oriented phosphorylation of plasma membrane H⁺-ATPase. Plant Physiol 138(1):287–296. doi:10.1104/pp.104.058065
  • Shen H, Chen J, Wang Z, Yang C, Sasaki T, Yamamoto Y, Matsumoto H, Yan X (2006) Root plasma membrane H⁺-ATPase is involved in the adaptation of soybean to phosphorus starvation. J Exp Bot 57(6):1353–1362. doi:10.1093/jxb/erj111
  • Silva EN, Ferreira-Silva SL, Fontenele Ade V, Ribeiro RV, Viegas RA, Silveira JA (2010) Photosynthetic changes and protective mechanisms against oxidative damage subjected to isolated and combined drought and heat stresses in Jatropha curcas plants. J Plant Physiol 167(14):1157–1164. doi:10.1016/j.jplph.2010.03.005
  • Suhayda CG, Giannini JL, Briskin DP, Shannon MC (1990) Electrostatic changes in Lycopersicon esculentum root plasma membrane resulting from salt stress. Plant Physiol 93(2): 471–478.
  • Svennelid F, Olsson A, Piotrowski M, Rosenquist M, Ottman C, Larsson C, Oecking C, Sommarin M (1999) Phosphorylation of Thr-948 at the C terminus of the plasma membrane H⁺-ATPase creates a binding site for the regulatory 14-3-3 protein. Plant Cell 11(12):2379–2391.
  • Sze H, Li X, Palmgren MG (1999) Energization of plant cell membranes by H⁺-pumping ATPases. Regulation and biosynthesis. Plant Cell 11(4):677–690.
  • Tang M, Sun J, Liu Y, Chen F, Shen S (2007) Isolation and functional characterization of the JcERF gene, a putative AP2/EREBP domain-containing transcription factor, in the woody oil plant Jatropha curcas. Plant Mol Biol 63(3):419–428. doi:10.1007/s11103-006-9098-7
  • Taylor AR, Assmann SM (2001) Apparent absence of a redox requirement for blue light activation of pump current in broad bean guard cells. Plant Physiol 125(1):329–338. doi:10.1104/Pp.125.1.329
  • Tomasi N, Kretzschmar T, Espen L, Weisskopf L, Fuglsang AT, Palmgren MG, Neumann G, Varanini Z, Pinton R, Martinoia E, Cesco S (2009) Plasma membrane H⁺-ATPase-dependent citrate exudation from cluster roots of phosphate-deficient white lupin. Plant Cell Environ 32(5):465–475. doi:10.1111/j.1365-3040.2009.01938.x
  • Tong L, Shu-Ming P, Wu-Yuan D, Dan-Wei M, Ying X, Meng X, Fang C (2006) Characterization of a new stearoyl-acyl carrier protein desaturase gene from Jatropha curcas. Biotechnol Lett 28(9):657–662. doi:10.1007/s10529-006-0034-3
  • Venema K, Palmgren MG (1995) Metabolic modulation of transport coupling ratio in yeast plasma membrane H⁺-ATPase. J Biol Chem 270(33):19659–19667.
  • Vitart V, Baxter I, Doerner P, Harper JF (2001) Evidence for a role in growth and salt resistance of a plasma membrane H⁺-ATPase in the root endodermis. Plant J 27(3):191–201. doi:10.1046/j.1365-313x.2001.01081.x
  • Williams JP, Khan MU, Mitchell K, Johnson G (1988) The effect of temperature on the level and biosynthesis of unsaturated fatty acids in diacylglycerols of Brassica napus leaves. Plant Physiol 87(4):904–910.
  • Yang Y, Zhang F, Zhao M, An L, Zhang L, Chen N (2007) Properties of plasma membrane H⁺ -ATPase in salt-treated Populus euphratica callus. Plant Cell Rep 26(2):229–235. doi:10.1007/s00299-006-0220-8
  • Yu X, Peng YH, Zhang MH, Shao YJ, Su WA, Tang ZC (2006) Water relations and an expression analysis of plasma membrane intrinsic proteins in sensitive and tolerant rice during chilling and recovery. Cell Res 16(6):599–608. doi:10.1038/sj.cr.7310077
  • Zhao SY, Colombo SJ, Blumwald E (1995) The induction of freezing tolerance in jack pine-seedlings—the role of root plasmamembrane H⁺-Atpase and redox activities. Physiol Plant 93(1):55–60. doi:10.1034/j.1399-3054.1995.930109.x
  • Zheng YL, Feng YL, Lei YB, Yang CY (2009) Different photosynthetic responses to night chilling among twelve populations of Jatropha curcas. Photosynthetica 47(4):559–566.
  • Zhou BL, Arakawa K, Fujikawa S, Yoshida S (1994) Cold-induced alterations in plasma membrane proteins that are specifically related to the development of freezing tolerance in cold-hardy winter wheat. Plant Cell Physiol 35(2):175–182.
  • Zhu J, Dong CH, Zhu JK (2007) Interplay between cold-responsive gene regulation, metabolism and RNA processing during plant cold acclimation. Curr Opin Plant Biol 10(3):290–295. doi:10.1016/j.pbi.2007.04.010
  • Zhu Y, Di T, Xu G, Chen X, Zeng H, Yan F, Shen Q (2009) Adaptation of plasma membrane H⁺-ATPase of rice roots to low pH as related to ammonium nutrition. Plant Cell Environ 32(10):1428–1440. doi:10.1111/j.1365-3040.2009.02009.x

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Bibliografia

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