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Chloroplast pigments, proteins, lipid peroxidation and activities of antioxidative enzymes during maturation and senescence of leaves and reproductive organs of Cajanus cajan L.

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Abstract

A comparative investigation was undertaken with pigeon pea leaves and attached flower buds/flowers/pods during their developmental stages including senescence in a natural system in experimental plots. Alterations in chloroplast pigments, total soluble proteins, lipid peroxidation, malondialdehyde (MDA) content and activities of guaiacol peroxidase (POD, EC 1.11.1.7) and superoxide dismutase (SOD, EC 1.15.1.1) were studied at 5-day interval from initial to 40-day stage. Chloroplast pigments and proteins of leaves increased upto 15 and 20-day stages respectively followed by a steady decline. Reproductive parts, however, exhibited rise in chloroplast pigments upto 25-day and protein till last stage as developing pods gain the amount from the senescing leaves which are nearest to them. Senescing leaves show very high POD activity than the developing and senescing pods and POD appears to be associated with chlorophyll degradation. Considerably higher activity and amount of LOX and MDA respectively have been noticed in senescing leaves than in flowers and pods. Increase in SOD activity during early stage of leaf growth and maturation indicates protective role that declined at senescent stages. Pods are unique in having very high SOD activity, only last stage of senescence does show a decline.

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References

  • Abeles FB, Dunn LJ (1989) Role of peroxidase during ethylene-induced chlorophyll breakdown in Cucumis sativus cotyledons. J Plant Growth Regul 8:319–325

    Article  CAS  Google Scholar 

  • Arnon DI (1949) Copper enzymes in isolated chloroplasts: polyphenoloxidase in Beta vulgaris. Plant Physiol 24:1–15

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

  • Dhindsa RS, Plumb-Dhindsa PL, Thorpe TA (1981) Leaf senescence correlated with increased levels of membrane permeability and lipid peroxidation and decreased levels of superoxide dismutase and catalase. J Exp Bot 32:93–101

    Article  CAS  Google Scholar 

  • Doderer A, Kokkelink I, Vander Veen S, Valk BE, Schram AW, Douma AC (1992) Purification and characterization of two lipoxygenase isoenzymes from germinating barley. Biochem Biophys Acta 1120:97–104

    CAS  PubMed  Google Scholar 

  • Eriksson CE, Svensson SG (1970) Lipoxygenase from peas, purification and properties of the enzyme. Biochem Biophys Acta 198:449–459

    CAS  PubMed  Google Scholar 

  • Galliard T, Phillips DR (1971) Lipoxygenases from potato tubers. Partial purification and properties of enzyme that specifically oxygenates the 9-positon of linoleic acid. Biochem J 124:431–438

    CAS  PubMed Central  PubMed  Google Scholar 

  • Gan S, Amasino RM (1997) Making sense of senescence: molecular genetic regulation and manipulation of leaf senescence. Plant Physiol 113:313–319

    CAS  PubMed Central  PubMed  Google Scholar 

  • Giannopolitis CN, Ries SK (1977) Superoxide dismutase. I. Occurrence in higher plants. Plant Physiol 59:309–314

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Grossman S, Leshem Y (1983) Lowering of endogenous lipoxygenase activity in Pisum sativum foliage by cytokinin as related to senescence. Physiol Plant 43:359–362

    Article  Google Scholar 

  • Grover A, Koundal KR, Sinha SK (1985) Senescence of attached leaves: regulation by developing pods. Physiol Plant 63:87–92

    Article  CAS  Google Scholar 

  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplast I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198

    Article  CAS  PubMed  Google Scholar 

  • Holden M (1965) In: Goodwin TW (ed) Chemistry and biochemistry of plant pigments. Academic, New York, pp 462–468

    Google Scholar 

  • Hossain Z, Mandal AKA, Datta SK, Biswas AK (2006) Decline in ascorbate peroxidase activity—a prerequisite factor for tepal senescence in gladiolus. J Plant Physiol 163:186–194

    Article  CAS  PubMed  Google Scholar 

  • Huff A (1981) Peroxidase catalysed oxidation of chlorophyll by hydrogen peroxide. J Phytochem 21:261–265

    Article  Google Scholar 

  • Hurng WP, Kao CH (1994) Lipid peroxidation and antioxidative enzymes in senescing tobacco leaves during post flooding. Plant Sci 96:41–44

    Article  CAS  Google Scholar 

  • Jakhar S, Mukherjee D (2006) Chloroplast pigments, free and bound amino acids, activities of protease and peroxidase during development and senescence of attached nodal leaves of Cajanus cajan L. J Plant Biol 33:125–132

    CAS  Google Scholar 

  • Kanazawa S, Savo S, Koshiba T, Ushimaru T (2000) Changes in antioxidative enzymes in cucumber cotyledons during natural senescence: comparison with those during dark induced senescence. Plant Physiol 109:211–216

    Article  CAS  Google Scholar 

  • Kato M, Shimizu S (1985) Chlorophyll metabolism in higher plants. VI, involvement of peroxidase in chlorophyll degradation. Plant Cell Physiol 26:1291–1301

    CAS  Google Scholar 

  • Kaup MT, Froese CD, Thompson JE (2002) A role of diacylglycerolacyltransferase during leaf senescence. Plant Physiol 129:1616–1626

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Klein BP, Grossman S, King D, Cohen BS, Pinsky A (1984) Pigment bleaching carbonyl production and antioxidant effect during the anaerobic lipoxygenase reaction. Biochem Biophys Acta 793:72–79

    Article  CAS  Google Scholar 

  • Lee D, Polisensky DH, Braam J (2005) Genome-wide identification of touch- and darkness-regulated Arabidopsis genes: a focus on calmodulin-like and XTH genes. New Phytol 165:429–444

    Article  CAS  PubMed  Google Scholar 

  • Lesham YY (1988) Plant senescence processes and free radicals. Free Radic Biol Med 5:39–49

    Article  Google Scholar 

  • Lindoo SJ, Nooden LD (1976) The inter-relation of fruit development and leaf senescence in ‘Anoka’ soybeans. Bot Gaz 137:218–223

    Article  Google Scholar 

  • Maehly AC (1954) Determination of peroxidase activity. In: Glick D (ed) Methods of biochemical analysis, vol 2. Interscience, New York, pp 385–386

    Google Scholar 

  • Marie O (1995) Alteration in lipid composition and antioxidative protection during senescence in drought-stressed plants and non drought-stressed plants of Pisum sativum. Plant Physiol Biochem 33:547–553

    Google Scholar 

  • Martinoia E, Dalling MJ, Matile P (1982) Catabolism of chlorophyll: demonstration of chloroplast-localized peroxidative and oxidative activities. Z Pflanzenphysiol 107:269–279

    Article  CAS  Google Scholar 

  • Matile P (1980) Catabolism of chlorophyll: involvement of peroxidase? Z Pflanzenphysiol 99:475–478

    Article  CAS  Google Scholar 

  • Mukherjee D, Kumar R (2007) Kinetin regulates plants growth and senescence of leaves, flowers and pods of Cajanus cajan L. J Biol Plant 51(1):80–85

    Article  CAS  Google Scholar 

  • Mukherjee D, Ponmeni G (2004) Effect of kinetin on the regulation of abscission and senescence in pigeon pea. Physiol Mol Biol Plants 10:223–231

    CAS  Google Scholar 

  • Nene YL, Sheila VK (1990) Pigeonpea: geography and importance. In: Nene YL, Hall SH, Sheila VK (eds) The pigeonpea. CAB International, Wellingford, pp 1–14

    Google Scholar 

  • Nooden LD, Guiamet JJ, John I (1997) Senescence mechanisms. Physiol Plant 101:746–753

    Article  CAS  Google Scholar 

  • Palma JM, Jimenez R, Sandalio LM, Corbas FJ, Lundquist M, Gomez M, Sevilla F, Del-Rio LA (2006) Antioxidant enzymes from chloroplasts, mitochondria and peroxisomes during leaf senescence of nodulated pea plants. J Exp Bot 57:1747–1758

    Article  CAS  PubMed  Google Scholar 

  • Pastori GM, del Rio LA (1997a) An activated-oxygen-mediated role for peroxisomes in the mechanism of senescence of Pisum sativum L. leaves. Planta 193:385–391

    Google Scholar 

  • Pastori GM, del Rio LA (1997b) Natural senescence of pea leaves. Activated oxygen mediated function for peroxisome. J Plant Physiol 113:411–418

    CAS  Google Scholar 

  • Ponmeni G, Mukherjee D (1997) Kinetin-induced alteration in senescence of redgram leaves. Indian J Plant Physiol New Ser 2:250–251

    CAS  Google Scholar 

  • Prochazkova D, Wilhelmova N (2004) Changes in antioxidative protection in bean cotyledons during natural and continous irradiation-accelerated senescence. Biol Plant 48:33–39

    Article  CAS  Google Scholar 

  • Prochazkova D, Sairam RK, Srivastava GC, Singh DV (2001) Oxidative stress and antioxidant activity as the basis of senescence in maize leaves. Plant Sci 161:765–771

    Article  CAS  Google Scholar 

  • Rao KUM, Mikherjee D (1990) Some metabolic changes during development and senescence in the leaves of Cajanus cajan. J Indian Bot Soc 69:311–314

    Google Scholar 

  • Sairam RK, Prochazkova D, Srivastava GC, Singh DV (2001) Oxidative stress and antioxidant activity as the basis of senescence in maize leaves. Plant Sci 161:765–771

    Article  Google Scholar 

  • Sheldrake AR, Narayanan A (1979) Comparison of earlier and later formed pods of pigeon pea [Cajanus cajan (L.) Millsp.]. Ann Bot 43:459–466

    Google Scholar 

  • Shioi Y, Tatsumi Y, Shimokawa K (1991) Enzymatic degradation of chlorophyll in Chenopodium album. Plant Cell Physiol 32:87–93

    CAS  Google Scholar 

  • Simpson RJ, Lamber H, Dalling MJ (1983) Nitrogen redistribution during grain growth in wheat (Triticum aestivum L.) IV. Development of a quantitative model of the translocation of nitrogen to the grains. Plant Physiol 71:7–14

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Sinha SK (1974) Yield of grain legumes: problems and prospects. Indian J Genet 34A:988–994

    Google Scholar 

  • Srivalli B, Khanna-Chopra R (2001) Induction of new isoforms of superoxide dismutase and catalase enzymes in the flag leaf of wheat during monocarpic senescence. Biochem Biophys Res Commun 288:1037–1042

    Article  CAS  PubMed  Google Scholar 

  • Thompson JE, Todd JF, Paliyath G (1990) Characterization of a membrane-associated lipoxygenase in tomato fruit. Plant Physiol 94:1225–1232

    Article  PubMed Central  PubMed  Google Scholar 

  • Thompson JE, Froese CD, Madey E, Smith MD, Hong Y (1998) Lipid metabolism during plant senescence. Prog Lipid Res 37:119–141

    Article  CAS  PubMed  Google Scholar 

  • Yamauchi N, Minamide T (1986) Chlorophyll degradation by peroxidase in parsley leaves. J Jpn Soc Hortic Sci 54:265–271

    Article  Google Scholar 

  • Ye Z, Rodriguez R, Tran A, Hoang H, de los Santos D, Brown S, Ellanoweth RLV (2000) The developmental transition to flowering repress ascorbate peroxidase activity and induces enzymatic lipid peroxidation in leaf tissue in Arabidopsis thaliana. Plant Sci 158:115–127

    Article  CAS  PubMed  Google Scholar 

  • Yoshida S (2003) Molecular regulation of leaf senescence. Curr Opin Plant Biol 6:1–16

    Article  Google Scholar 

Download references

Acknowledgments

Financial assistance from University Grants Commission, New Delhi, India as a Research Project, No. F.3-6/2004 (SR) to DM and Project Fellow to SJ are gratefully acknowledged.

Author contribution

Somveer Jakhar has carried out experiments, obtained results, analyzed data and took photographs. D. Mukherjee was responsible for designing experiments, standardizing methods and verifying data. Both the authors contributed in preparing the manuscript.

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Correspondence to Somveer Jakhar.

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Jakhar, S., Mukherjee, D. Chloroplast pigments, proteins, lipid peroxidation and activities of antioxidative enzymes during maturation and senescence of leaves and reproductive organs of Cajanus cajan L.. Physiol Mol Biol Plants 20, 171–180 (2014). https://doi.org/10.1007/s12298-013-0219-x

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  • DOI: https://doi.org/10.1007/s12298-013-0219-x

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