Alleviation of aluminum toxicity by hydrogen sulfide is related to elevated ATPase, and suppressed aluminum uptake and oxidative stress in barley

Journal of Hazardous Materials

Volumn 209-210, Issue , 2012, Pages 121-128

  Dawood, Muhammad ^a   Cao, Fangbin ^a   Jahangir, Muhammad Muzammil ^a   Zhang, Guoping ^a   Wu, Feibo ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

Adenosine triphosphatase (ATPase); Aluminum (Al); Barley (Hordeum vulgare L.); Hydrogen sulfide (H 2S); Mineral elements; Oxidative stress

Indexed keywords

ADENOSINE TRIPHOSPHATASE; AL TOXICITY; ALUMINUM TOXICITY; BARLEY SEEDLINGS; CHLOROPHYLL CONTENTS; DOSE-DEPENDENT; ELECTROLYTE LEAKAGE; ELEVATED CONCENTRATIONS; HORDEUM VULGARE; HYDROPONIC EXPERIMENTS; LIPID PEROXIDATION; MINERAL ELEMENTS; NET PHOTOSYNTHETIC RATE; PHOTOCHEMICAL EFFICIENCY; ROOT ELONGATION;

CHLOROPHYLL; MINERALS; OXIDATIVE STRESS; PRINCIPAL COMPONENT ANALYSIS; SODIUM; SULFUR DETERMINATION; TOXICITY;

ALUMINUM;

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ALUMINUM; CALCIUM; CATALASE; CHLOROPHYLL; ELECTROLYTE; HYDROGEN POTASSIUM ADENOSINE TRIPHOSPHATASE; HYDROGEN SULFIDE; IRON; MAGNESIUM; MALONALDEHYDE; PHOSPHORUS; SODIUM HYDROGEN SULFIDE; SULFUR; UNCLASSIFIED DRUG;

ALUMINUM; BARLEY; BIOACCUMULATION; BIOLOGICAL UPTAKE; CHLOROPHYLL; ECOTOXICOLOGY; ENZYME ACTIVITY; EXPERIMENTAL STUDY; GREENHOUSE ECOSYSTEM; HYDROGEN SULFIDE; HYDROPONICS; LIPID; PHOTOSYNTHESIS; ROOT SYSTEM; SEEDLING;

ALUMINUM OVERLOAD; ARTICLE; BARLEY; CHLOROPHYLL CONTENT; CONTROLLED STUDY; DOSE RESPONSE; ENZYME ACTIVITY; LIPID PEROXIDATION; NONHUMAN; OXIDATIVE STRESS; PHOTOCHEMICAL EFFICIENCY; PHOTOSYNTHETIC RATE; PLANT ROOT; ROOT GROWTH; SEEDLING;

ADENOSINE TRIPHOSPHATASES; ALUMINUM; BIOMASS; CHLOROPHYLL; DOSE-RESPONSE RELATIONSHIP, DRUG; HORDEUM; HYDROGEN SULFIDE; MALONDIALDEHYDE; OXIDATIVE STRESS; PHOTOSYNTHESIS;

HORDEUM; HORDEUM VULGARE SUBSP. VULGARE;

EID: 84862809336     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2011.12.076     Document Type: Article

References (40)

1. Horst W.J., Wang Y.X., Eticha D. The role of the root apoplast in aluminium-induced inhibition of root elongation and in aluminium resistance of plants: a review. Ann. Bot.: Lond. 2010, 106:185-197.
2. Berthon G. Chemical speciation studies in relation to aluminium metabolism and toxicity. Coord. Chem. Rev. 1996, 149:241-280.
3. Sivaguru M., Horst W.J. The distal part of the transition zone is the most aluminum-sensitive apical root zone of maize. Plant Physiol. 1998, 116:155-163.
4. Meriga B., Reddy B.K., Rao K.R., Reddy L.A., Kishor P.B.K. Aluminium-induced production of oxygen radicals, lipid peroxidation and DNA damage in seedlings of rice (Oryza sativa). J. Plant Physiol. 2004, 161:63-68.
5. Wang Y.S., Yang Z.M. Nitric oxide reduces aluminum toxicity by preventing oxidative stress in the roots of Cassia tora L. Plant Cell Physiol. 2005, 46:1915-1923.
6. Ezaki B., Suzuki M., Motoda H., Kawamura M., Nakashima S., Matsumoto H. Mechanism of gene expression of Arabidopsis glutathione S-transferase, AtGST1, and AtGST11 in response to aluminum stress. Plant Physiol. 2004, 134:1672-1682.
7. Maron L.G., Kirst M., Mao C., Milner M.J., Menossi M., Kochian L.V. Transcriptional profiling of aluminum toxicity and tolerance responses in maize roots. New Phytol. 2008, 179:116-128.
8. +-ATPase activity in near-isogenic wheat lines differing in tolerance to aluminum. New Phytol. 2004, 162:71-79.
9. Darko E., Ambrus H., Stefanovits-Banyai E., Fodor J., Bakos F., Barnaba B. Aluminium toxicity, Al tolerance and oxidative stress in an Al-sensitive wheat genotype and in Al-tolerant lines developed by in vitro microspore selection. Plant Sci. 2004, 166:583-591.
10. Abu-Romman S., Shatnawi M. Isolation and expression analysis of chloroplastic copper/zinc superoxide dismutase gene in barley. S. Afr. J. Bot. 2011, 77:328-334.
11. +-ATPase. Plant Physiol. 2005, 138:287-296.
12. Lindberg S., Griffiths G. Aluminum effects on ATPase activity and lipid-composition of plasma-membranes in sugar-beet roots. J. Exp. Bot. 1993, 44:1543-1550.
13. 2S be the third endogenous gaseous transmitter?. FASEB J. 2002, 16:1792-1798.
14. Zhang H., Hu L.Y., Hu K.D., He Y.D., Wang S.H., Luo J.P. Hydrogen sulfide promotes wheat seed germination and alleviates oxidative damage against copper stress. J. Integr. Plant Biol. 2008, 50:1518-1529.
15. Garcia-Mata C., Lamattina L. Hydrogen sulphide, a novel gasotransmitter involved in guard cell signaling. New Phytol. 2010, 188:97-984.
16. Zhang H., Ye Y.K., Wang S.H., Luo J.P., Tang J., Ma D.F. Hydrogen sulfide counteracts chlorophyll loss in sweet potato seedling leaves and alleviates oxidative damage against osmotic stress. Plant Growth Regul. 2009, 58:243-250.
17. Wang B.L., Shi L., Li Y.X., Zhang W.H. Boron toxicity is alleviated by hydrogen sulfide in cucumber (Cucumis sativus L.) seedlings. Planta 2010, 231:1301-1309.
18. Wu F.B., Zhang G.P., Dominy P., Wu H.X., Bachir D.M.L. Differences in yield components and kernel Cd accumulation in response to Cd toxicity in four barley genotypes. Chemosphere 2007, 70:83-92.
19. Hosoki R., Matsuk N., Kimura H. The possible role of hydrogen sulfide as an endogenous smooth muscle relaxant in synergy with nitric oxide. Biochem. Biophys. Res. Commun. 1997, 237:527-531.
20. Wu F.B., Zhang G.P., Dominy P. Four barley genotypes respond differently to cadmium, lipid peroxidation and activities of antioxidant capacity. Environ. Exp. Bot. 2003, 50:67-78.
21. Zheng S.J., Yang J.L., He Y.F., Yu X.H., Zhang L., You J.F., Shen R.F., Matsumoto H. Immobilization of aluminum with phosphorus in roots is associated with high aluminum resistance in buckwheat. Plant Physiol. 2005, 138:297-303.
22. Wang F., Chen F., Cai Y., Zhang G.P., Wu F.B. Modulation of exogenous glutathione in ultrastructure and photosynthetic performance against Cd stress in the two barley genotypes differing in Cd tolerance. Biol. Trace Elem. Res 2011, 144:1275-1288.
23. Chen F., Wang F., Wu F.B., Mao W., Zhang G., Zhou M. Modulation of exogenous glutathione in antioxidant defense system against Cd stress in the two barley genotypes differing in Cd tolerance. Plant Physiol. Biochem. 2010, 48:663-672.
24. Tang Q.Y., Feng M.G. DPS Data Processing System for Practical Statistics 2002, Science, Beijing.
25. Gill S.S., Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 2010, 48:909-930.
26. Inostroza-Blancheteau C., Reyes-Díaz M., Aquea F., Nunes-Nesi A., Alberdi M., Arce-Johnson P. Biochemical and molecular changes in response to aluminium-stress in highbush blueberry (Vaccinium corymbosum L.). Plant Physiol. Biochem. 2011, 49:1005-1012.
27. Sharma P., Dubey R.S. Involvement of oxidative stress and role of antioxidative defense system in growing rice seedlings exposed to toxic concentrations of aluminum. Plant Cell 2007, 26:2027-2038.
28. Wang H.H., Huang J.J., Bi Y.R. Nitrate reductase-dependent nitric oxide production is involved in aluminum tolerance in red kidney bean roots. Plant Sci. 2010, 179:281-288.
29. Shan C.J., Zhang S.L., Li D.F., Zhao Y.Z., Tian X.L., Zhao X.L., Wu Y.X., Wei X.Y., Liu R.Q. Effects of exogenous hydrogen sulfide on the ascorbate and glutathione metabolism in wheat seedlings leaves under water stress. Acta Physiol. Plant. 2011, 33:2533-2540.
30. 2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine γ-lyase. Science 2008, 322:587-590.
31. 2S on metabolite levels, activity of enzymes and expression of genes involved in cysteine metabolism. Plant Physiol. Biochem. 2005, 43:473-483.
32. 2S as sulphur source for Brassica oleracea: consequences for the activity of the enzymes of the assimilatory sulphate reduction pathway. Plant Physiol. Biochem. 2001, 39:425-432.
33. Lisjak M., Srivastava N., Teklic T., Civale L., Lewandowski K., Wilson I., Wood M.E., Whiteman M., Hancock J.T. A novel hydrogen sulfide donor causes stomatal opening and reduces nitric oxide accumulation. Plant Physiol. Biochem. 2010, 48:931-935.
34. Poschenrieder C., Gunse B., Corrales I., Barcelo J. A glance into aluminum toxicity and resistance in plants. Sci. Total Environ. 2008, 400:356-368.
35. +-ATPase activity by permanently altering the plasma membrane surface potentials in squash roots. Plant Physiol. 2001, 126:1381-1390.
36. Dattagupta S., Redding M., Luley K., Fisher C. Comparison of proton-specific ATPase activities in plume and root tissues of two co-occurring hydrocarbon seep tubeworm species Lamellibrachia luymesi and Seepiophila jonesi. Mar. Biol. 2009, 156:779-786.
37. +-ATPase activity in organelles of wheat seedlings. Chinese Bull. Bot. 2009, 44:451-456.
38. Ali S., Zeng F., Qiu L., Zhang G.P. The effect of chromium and aluminum on growth, root morphology, photosynthetic parameters and transpiration of the two barley cultivars. Biol. Plant. 2011, 55:291-296.
39. Farquhar G.D., Sharkey T.D. Stomatal conductance and photosynthesis. J. Ann. Rev. Plant Physiol. 1982, 33:317-345.
40. Chen J., Wu F.H., Wang W.H., Zheng C.J., Lin G.H., Dong X.J., He J.X., Pei Z.M., Zheng H.L. Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in Spinacia oleracea seedlings. J. Exp. Bot. 2011, 62:4481-4493.