PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2009 | 31 | 1 |

Tytuł artykułu

Inhibition of monoterpene biosynthesis accelerates oxidative stress and leads to enhancement of antioxidant defenses in leaves of rubber tree (Hevea brasiliensis)

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
This paper mainly studies the possible antioxidant of monoterpene and effects of its absence on other antioxidant defense. The leaves of rubber tree (Hevea brasiliensis) were fed with fosmidomycin through transpiration stream, in the dark, at room temperature for 2 h, and were then exposed to bright illumination (1,500 lmol m⁻² s⁻¹) and moderately high temperature (30°C) for 1 h. The results showed that monoterpene biosynthesis in leaves was considerably inhibited by fosmidomycin, and the elevated levels of both hydrogen peroxide and malondialdehyde were observed in the leaves fed with fosmidomycin (LFF). Compared to the control leaves (CK), ΔF/Fm' in the LFF was markedly lower during the first 20 min; however, there were no significant differences in non-photochemical quenching and photosynthetic pigments (chlorophylls and carotenoids). In contrast, the activities of antioxidant enzymes (superoxide dismutase, catalase, guaiacol peroxidase, ascorbate peroxidase, and glutathione reductase) were enhanced in the LFF. Meanwhile, the contents of antioxidant metabolites (ascorbate and glutathione) were also elevated in the LFF, when compared with the CK. The results obtained here suggest that monoterpene may be very effective molecule in protecting plants against oxidative stress, the absence of monoterpene leads to the increased responses of the enzymatic and non-enzymatic antioxidant defenses to oxidative stress, and the enhancement of the enzymatic and nonenzymatic antioxidant defenses may, in part, compensate for the loss of antioxidant conferred by monoterpene.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

31

Numer

1

Opis fizyczny

p.95-101,fig.,ref.

Twórcy

autor
  • Kunming Division, Xishuangbanna Tropical Botanical Garden, The Chinese Academy of Sciences, 88 Xuefu Road, 650223 Kunming, Yunnan, People's Republic of China
  • Graduate School of the Chinese Academy of Sciences, 100049 Beijing, People's Republic of China
autor
  • Kunming Division, Xishuangbanna Tropical Botanical Garden, The Chinese Academy of Sciences, 88 Xuefu Road, 650223 Kunming, Yunnan, People's Republic of China
  • Graduate School of the Chinese Academy of Sciences, 100049 Beijing, People's Republic of China
autor
  • Kunming Division, Xishuangbanna Tropical Botanical Garden, The Chinese Academy of Sciences, 88 Xuefu Road, 650223 Kunming, Yunnan, People's Republic of China

Bibliografia

  • Bukhov HG, Wiese C, Neimanis S, Heber U (1999) Heat sensitivity of chloroplasts and leaves: leakage of protons from thylakoids and reversible activation of cyclic electron transport. Photosynth Res 59:81–83
  • Dat J, Vandenabeele S, Vranová E, Van Montagu M, Inzé D, Van Breusegem F (2000) Dual action of the reactive oxygen species during plant stress responses. Cell Mol Life Sci 57:779–795
  • Doulis A, Debian N, Kingston-Smith AH, Foyer CH (1997) Characterization of chilling sensitivity in maize. I. Differential localization of antioxidants in maize leaves. Plant Physiol 114:1031–1037
  • Etienne P, Petitot AS, Houot V, Blein JP, Suty L (2000) Induction of tcl 7, a gene encloding a β-subunit of proteasome, in tobacco plants treated with elicitin, salicylic acid or hydrogen peroxide. FEBS Lett 466:213–218
  • Foyer CH, Lopez-Delgado H, Dat JF, Scott IM (1997) Hydrogen peroxide and glutathione-associated mechanisms of acclamatory stress tolerance and signals. Physiol Plant 100:241–254
  • Giannopolitis N, Ries SK (1977) Superoxide dismutase. I. Occurrence in higher plants. Plant Physiol 59:309–314
  • Heath RL, Parker L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Hodges DM, Delong JM, Forney CF, Prange RK (1999) Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and interfering compounds. Planta 207:604–611
  • Klinger LF, Li QJ, Guenther AB, Greenberg JP, Baker B, Bai JH (2002) Assessment of volatile organic compound emissions from ecosystems of China. J Geophys Res 107:4603–4624
  • Laule O, Fuerholz A, Chang HS, Zhu T, Wang X, Heifetz PB, Gruissen W, Lange BM (2003) Crosstalk between cytosolic and plastidial pathways of isoprenoid biosynthesis in Arabidopsis thaliana. Proc Natl Acad Sci 100:6866–6871
  • Levine A, Tenhaken R, Dixon R, Lamb C (1994) H₂O₂ from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 79:583–593
  • Lichtenthaler HK, Wellburn AR (1983) Determinations of total carotenoids and chlorophyll and chlorophyll a and b of leaf extracts in different solvents. Biochem Soc Trans 603:591–592
  • Llusià J, Peňuelas J (2000) Seasonal patterns of terpene content and emission from seven Mediterranean woody species in field conditions. Am J Bot 87:133–140
  • Loreto F, Förster A, Dürr M, Csiky O, Seufert G (1998) On the monoterpene emission under heat stress and on the increased thermotolerance of leaves of Quercus ilex L. fumigated with selected monoterpenes. Plant Cell Environ 21:101–107
  • Loreto F, Pinelli P, Manes F, Kollist H (2004) Impact of zone on monoterpene emissions and evidence for an isoprene-like antioxidant action of monoterpenes emitted by Quercus iles leaves. Tree Physiol 24:361–367
  • Loreto F, Velikova V (2001) Isoprene produced by leaves protects the photosynthetic apparatus against ozone damage, quenches ozone products, and reduces lipid peroxidation of cellular membranes. Plant Physiol 127:1781–1787
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275
  • Mahmoud SS, Croteau BR (2002) Strategies for transgenic manipulation of monoterpene biosynthesis in plants. Trends Plant Sci 7:366–373
  • Nakagawara S, Sagisaka S (1984) Increase in enzyme activities related to ascorbate metabolism during cold acclimation in poplar twigs. Plant Cell Physiol 25:899–906
  • Neill SJ, Desikan R, Clarke A, Hurst RD, Hancock JT (2002) Hydrogen peroxide and nitric oxide as signaling molecules in plants. J Exp Bot 53:1237–1247
  • Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–279
  • Pastenes C, Horton P (1996) Effects of high temperature on photosynthesis in beans. 1. Oxygen evolution and chlorophyll fluorescence. Plant Physiol 112:1245–1251
  • Peňuelas J, Llusià J (2002) Linking photorespiration, monoterpenes and thermotolerance in Quercus. New Phytol 155:227–237
  • Peňuelas J, Llusià J, Asensio D, Munné-Bosch S (2005) Linking isoprene with plant monoterpene, antioxidants and monoterpene emissions. Plant Cell Environ 28:278–286
  • Peňuelas J, Munné-Bosch S (2005) Isoprenoids: an evolutionary pool for photoprotection. Trends Plant Sci 10:166–169
  • Schreiber U, Bilger W, Neubauer C (1994) Chlorophyll fluorescence as a nonintrusive indictor for rapid assessment of in vivo photosynthesis. In: Schulze DD, Caldwell MM (eds) Ecophysiology of photosynthesis. Springer, Berlin, pp 49–70
  • Sharkey TD, Singsaas EL (1995) Why plants emit isoprene? Nature 374:769
  • Sharkey TD, Yeh S (2001) Isoprene emission from plants. Annu Rev Plant Physiol Plant Mol Biol 52:407–436
  • Sharkey TD, Chen X, Yeh S (2001) Isoprene increases thermotolerance of fosmidomycin-fed leaves. Plant Physiol 125:2001–2006
  • Singsaas EL (2000) Terpenes and the thermotolerance of photosynthesis. New Phytol 146:1–4
  • Tichy M, Vermaas V (1999) In vivo role of catalase-peroxidase in Synechocystis sp. Strain PCC6803. J Bacteriol 181:1875–1882
  • Velikova V, Loreto F (2005) On the relationship between isoprene emission and thermotolerance in Phragmites australis leaves exposed to high temperatures and during the recovery from a heat stress. Plant Cell Environ 28:318–327
  • Velikova V, Yordanov I, Edreva A (2000) Oxidative stress and some antioxidant system in acid rain-treated bean plants. Protective role of exogenous polymines. Plant Sci 151:59–66
  • Willekens H, Inze D, van Montagu M, van Camp W (1995) Catalases in plants. Mol Breeding 1:207–222
  • Zeidler J, Schwender J, Müller C, Wiesner J, Weidemeyer C, Back E, Jomaa H, Lichtenthaler HK (1998) Inhibition of the nonmevalonate 1-deoxy-d-xylulose-5-phosphate pathway of plant isoprenoid biosynthesis by fosmidomycin. Z Naturforsch 53c:980–986

Uwagi

Rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-4b8477db-fa79-4c56-96d9-048bb8b97be1
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.