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Involvement of abscisic acid in photosynthetic process in Hordeum vulgare L. during salinity stress

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Abstract

In Hordeum vulgare L. plants, NaCl stress imposed through the root medium for a period of 8 days decreased the rate of CO2 assimilation, the chlorophyll and protein leaf content, and the activity of ribulose-1,5-bisphosphate carboxylase. The activity of phosphoenolpyruvate carboxylase was twofold over the control. Pretreatment with abscisic acid (ABA) for 3 days before salinization diminished the inhibitory effect of NaCl on the rate of CO2 fixation. The leaf Na+ and Cl content decreased in ABA-pretreated plants. Both ABA and NaCl treatments led to an increase in the endogenous level of ABA in the plant leaves. Patterns of total proteins extracted from the leaves of control or ABA- and salt-treated plants were compared. Both ABA and NaCl induced marked quantitative and qualitative changes in the polypeptide profiles concerning mainly the proteins with approximately equal mobility. The results are discussed in terms of a possible role of ABA in increasing the salt tolerance when ABA is applied to the plants for a short period before exposure to salinity stress, thus improving the invulnerability to unfavorable conditions.

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Abbreviations

RuBPC:

ribulose-1,5-bisphosphate carboxylase

PSII:

photosystem II

ABA:

abscisic acid

PEPC:

phosphoenolpyruvate carboxylase

DTTr:

dithiothreitol

BSA:

bovine serum albumin

ELISA:

enzyme-linked immunosorbent assay

SDS:

sodium dodecyl sulfate

PAGEr:

polyacrylamide gel electrophoresis

References

  • Amzallag GN, Lerner HR, Poljakoff-Mayber A (1990) Exogenous ABA as a modulator of the response of sorghum to high salinity. J Exp Bot 41:1529–1534

    Article  CAS  Google Scholar 

  • Arnon DI (1949) Cooper enzymes in isolated chloroplasts: Polyphenol-oxidase in Beta vulgaris. Plant Physiol 24:1–15

    PubMed  CAS  Google Scholar 

  • Behl R, Raschke K (1986) Effect of abscisic acid on sequestration and exchange of Na+ by barley roots. Planta 167:563–568

    Article  CAS  Google Scholar 

  • Bethke PC, Drew MC (1992) Stomatal and nonstomatal components to inhibition of photosynthesis in leaves of Capsicum annuum during progressive exposure to NaCl salinity. Plant Physiol 99:219–226

    PubMed  CAS  Google Scholar 

  • Claes B, Dekeyser R, Villarroel P, van denBulcke M, Bauw G, Montagu VM, Caplan A (1990) Characterization of a rice gene showing organ-specific expression in response to salt stress and drought. Plant Cell 2:19–27

    Article  PubMed  CAS  Google Scholar 

  • Cotlove E (1963) Determination of the true chloride content of biological fluids and tissues: Analysis by simple nonisotopic methods. Anal Chem 35:101–105

    Article  Google Scholar 

  • Downton WJ, Loveys BR (1981) Abscisic acid content and osmotic relations of salt stressed grapevine leaves. J Plant Physiol 8:443–453

    CAS  Google Scholar 

  • Eberhardt HJ, Wegmann K (1989) Effect of abscisic acid and proline on adaptation of tobacco callus cultures to salinity and osmotic shock. Physiol Plant 76:283–288

    CAS  Google Scholar 

  • Harris MJ, Outlaw WH, Mertens R, Weiler EW (1988) Water stress-induced changes in the abscisic acid content of guard cells and other cells of Vicia faba L. leaves as determined by enzyme-amplified immunoassay. Proc Natl Acad Sci USA 85:2584–2588

    Article  PubMed  CAS  Google Scholar 

  • Henson IE, Quarrie SA (1981) Abscisic acid accumulation in detached cereal leaves in response to water stress. I. Effect of incubation time and sevirety of stress. Z Pflanzenphysiol 101:431–438

    CAS  Google Scholar 

  • Hurkman WJ, Fornari CS, Tanaka CK (1989) A comparison of the effect of salt on polypeptides and translatable mRNAs in roots of a salt-tolerant and salt-sensitive cultivar of barley. Plant Physiol 60:1444–1456

    Google Scholar 

  • Greenway H, Munns R (1980) Mechanism of salt tolerance in nonhalophytes. Annu Rev Plant Physiol 31:149–190

    Article  CAS  Google Scholar 

  • Kurth E, Gramer GR, Lauchli A, Epstein E (1986) Effects of NaCl and CaCl2 on cell enlargement and cell production in cotton roots. Plant Physiol 82:1102–1106

    PubMed  CAS  Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    Article  PubMed  CAS  Google Scholar 

  • LaRosa PC, Handa AK, Hasegawa PM, Bressan RA (1985) Abscisic acid accelerates adaptation of cultured tobacco cells to salt. Plant Physiol 79:138–142

    Google Scholar 

  • Lauchli A, Wieneke J (1979) Studies on growth and distribution of Na+, K+, and Cl in soybean varieties differing in salt tolerance. Z Pflanzenernaehr Bobenkd 142:3–13

    Article  Google Scholar 

  • Leopold AC, Willing RP (1984) Evidence for toxicity effect of salt on membranes. In: Staples RC, Toenniessen GH (eds): Salinity tolerance in plants: Strategies for crop improvement. John Wiley & Sons, New York, pp 67–75

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with Folin phenol reagent. J Biol Chem 193:265–275

    PubMed  CAS  Google Scholar 

  • Maslenkova LT, Gambarova N, Miteva T, Zanev Y (1991) Changes in the oxygen evolving activity of barley plants grown under NaCl salinity. CR Acad Bulg Sci 44:103–105

    CAS  Google Scholar 

  • Maslenkova LT, Miteva T, Popova L (1992) Changes in the polypeptide patterns of barley seedlings exposed to jasmonic acid and salinity. Plant Physiol 98:700–707

    PubMed  CAS  Google Scholar 

  • Maslenkova L, Zanev Y, Popova P (1993) Adaptation to salinity as monitored by PS II oxygen evolving reactions in barley thylakoids. J Plant Physiol 142:629–643

    CAS  Google Scholar 

  • Miteva T, Popova L (1991) Photosynthetic carbon metabolism at NaCl salinity. CR Acad Bulg Sci 44:97–100

    CAS  Google Scholar 

  • Miteva T, Vaklinova S (1989) Salt stress and activity of some photosynthetic enzymes. CR Acad Bulg Sci 42:87–89

    CAS  Google Scholar 

  • Miteva T, Vaklinova S (1991) Photosynthesis, photorespiration and respiration in young barley plants upon influence of NaCl. CR Acad Bulg Sci 44:89–92

    CAS  Google Scholar 

  • Miteva T, Zhelev N, Popova L (1992) Effect of salinity on the synthesis of ribulose-1–5-bisphosphate carboxylase/oxygen in barley leaves. J Plant Physiol 140:46–51

    CAS  Google Scholar 

  • Mohanty AP, Saradhi PP (1992) Effect of sodium chloride on primary photochemical activities in cotyledonary leaves of Brassica juncea. Biochem Physiol Pflanzen 188:1–12

    Google Scholar 

  • Poljakoff-Mayber A, Gale J (1975) Plants in saline environments. Springer-Verlag, New York, pp 97–117

    Google Scholar 

  • Popova LP, Kolev K, Stoinova Z (1994) Effect of abscisic acid on the polypeptide patterns of leaf soluble proteins of barley leaves. CR Acad Bulg Sci 47:77–80

    CAS  Google Scholar 

  • Popova LP, Tsonev TD, Lazova G, Stoinova Z (1995) Drought- and ABA-induced changes in photosynthetic response of barley plants. Physiol Plant, in press

  • Popova LP, Tsonev TD, Vaklinova SG (1987) A possible role for abscisic acid in regulation of photosynthetic and photorespiratory carbon metabolism in barley leaves. Plant Physiol 83:820–824

    PubMed  CAS  Google Scholar 

  • Rani UR, Reddy AR (1994) Salt stress responsive polypeptides in germinating seeds and young seedlings of indica rice (Oriza sativa L.). J Plant Physiol 143:250–253

    CAS  Google Scholar 

  • Rathnam CKM, Chollet R (1980) Photosynthetic and photorespiratory carbon metabolism in mesophyll protoplasts and chloroplasts isolated from isogenic diploid and tetraploid cultivars of ryegrass (Lolium perenne L.) Plant Physiol 65:489–494

    PubMed  CAS  Google Scholar 

  • Robinson SP, Downton WJS, Mulhouse JA (1983) Photosynthesis and ion content of leaves and isolated chloroplasts of salt-stressed spinach. Plant Physiol 73:238–242

    Article  PubMed  CAS  Google Scholar 

  • Seemann JR, Critchley C (1985) Effects of salt stress on the growth, ion content, stomatal behavior and photosynthetic capacity of a salt-sensitive species, Phaseolus vulgaris L. Planta 164:151–162

    Article  CAS  Google Scholar 

  • Seemann JR, Sharkey TD (1986) Salinity and nitrogen effects on photosynthesis, ribulose-1,5-bisphosphate carboxylase and metabolite pool sizes in Phaseolus vulgaris L. Plant Physiol 82:555–560

    PubMed  CAS  Google Scholar 

  • Singh NK, La Rosa PC, Bressan RA, Hasegava PM, Handa AK (1984) Protein synthesis in response to NaCl adaptation and abscisic acid. UCLA Symposium

  • Skiver K, Mundy J (1990) Gene expression in response to abscisic acid and osmotic stress. Plant Cell 2:503–512

    Article  Google Scholar 

  • Stiborova M, Ksinska S, Brezinova A (1987) Effect of NaCl on the growth and biochemical characteristics of photosynthesis of barley and maize. Photosynthetica 21:320–328

    CAS  Google Scholar 

  • Walker MA, Dumbroff EB (1981) Effect of salt stress on abscisic acid and cytokine levels in tomato. Z Pflanzenphysiol 101:461–470

    CAS  Google Scholar 

  • Zhang S, Hite DRC, Outlaw WH Jr (1991) Technical note: Modification required for abscisic acid microassay (enzyme-amplified ELISA). Physiol Plant 84:304–306

    Article  Google Scholar 

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Popova, L.P., Stoinova, Z.G. & Maslenkova, L.T. Involvement of abscisic acid in photosynthetic process in Hordeum vulgare L. during salinity stress. J Plant Growth Regul 14, 211–218 (1995). https://doi.org/10.1007/BF00204914

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  • DOI: https://doi.org/10.1007/BF00204914

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