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2019 | 41 | 07 |

Tytuł artykułu

Mitigation of As toxicity in wheat by exogenous application of hydroxamate siderophore of Aspergillus origin

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Siderophores are secondary metabolites having molecular weight less than 10 KD. They are specifically meant for chelation of ferric ions. They also tend to chelate metals under heavy metal stress, thus reducing their toxic effects. In the current study, experiments have been conducted on wheat plants to analyse siderophore’s ability to counteract the adverse impact of arsenic (As) toxicity on physiology of plant seedlings along with biochemical response. As toxicity has been observed to adversely affect the lengths of root and shoot, chlorophyll and carotenoid contents, and activities of various antioxidative enzymes. The present study revealed that the application of hydroxamate-type siderophore isolated from Aspergillus nidulans under toxic condition significantly recovered the growth and helped in amending the enzymatic activities of superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD) of wheat genotype (NW1014). At the same time, injury caused by lipid peroxidation was significantly reduced. In silico studies revealed better binding affinity of ferricrocin–arsenate complex leading to thermodynamically stable complex. Encouraging results of As containment by organic biomolecule-siderophore can lead to an emerging bioremediation mechanism brimming with opportunities for agricultural field and environmental clean-up.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

41

Numer

07

Opis fizyczny

Article 107 [11p.], fig.,ref.

Twórcy

autor
  • Department of Life Science, School of Earth, Biological and Environmental Sciences, Central University of South Bihar, Panchanpur, Gaya 824 236, India
autor
  • Department of Life Science, School of Earth, Biological and Environmental Sciences, Central University of South Bihar, Panchanpur, Gaya 824 236, India
autor
  • Department of Life Science, School of Earth, Biological and Environmental Sciences, Central University of South Bihar, Panchanpur, Gaya 824 236, India
autor
  • ICAR-Research Complex for Eastern Region, Patna 800 014, India
autor
  • Department of Bioinformatics, Central University of South Bihar, Panchanpur, Gaya 824 236, India
  • Department of Life Science, School of Earth, Biological and Environmental Sciences, Central University of South Bihar, Panchanpur, Gaya 824 236, India

Bibliografia

  • Abedin MJ, Meharg AA (2002) Relative toxicity of arsenite and arsenate on germination and early seedling growth of rice (Oryza sativa L). Plant Soil 243:57–66. https://doi.org/10.1023/A:1019918100451
  • Aebi H (1984) Catalase in vitro. Methods in enzymology, vol 105. Academic Press, Florida, pp 114–121
  • Ahmad FD, Ahmad N, Masood KR, Hussain M, Malik MF, Qayyum A (2018) Phytoremediation of arsenic-contaminated soils by Eucalyptus camaldulensis, Terminalia arjuna and Salix tetrasperma. J App Bot Food Qual 91:8–13. https://doi.org/10.5073/JABFQ.2018.091.002
  • Arnon DI (1949) Copper enzymes in isolated chloroplast, polyphenol-oxidase in Beta vulgaris. Plant Physiol 24:1–15. https://doi.org/10.1104/pp.24.1.1
  • Atkin CL, Neilands JB, Phaff H (1970) Rhodotorulic acid from species of Rhodospirillum, Rhodotorula, Sporidiobolus and Sporobolomyces. J Bacteriol 103:722–733
  • Baran A, Antonkiewicz J (2017) Phytotoxicity and extractability of heavy metals from industrial wastes. Environ Prot Eng 43:143–155. https://doi.org/10.5277/epe170212
  • Dhindsa RS, Dhindsa P, Thorpe T (1981) Leaf senescence correlated with increased levels of membrane permeability and lipid peroxidation and decrease levels of superoxide dismutase and catalase. J Exp Bot 32:93–101. https://doi.org/10.1093/jxb/32.1.93
  • Duckworth O, Bargar J, Sposito G (2009) Quantitative structure–activity relationships for aqueous metal–siderophore complexes. Environ Sci Technol 43:343–349. https://doi.org/10.1021/es802044y
  • Grobelak A, Hiller J (2017) Bacterial siderophores promote plant growth: screening of catechol and hydroxamate siderophores. Int J Phytorem 19(9):825–833
  • Gusain P, Singh V (2016) Hydroxamate and catecholate siderophore synthesizing As resistant pgpr. J Environ Appl Biores 4:01–04
  • Gwóźdź EA, Przymusiński R, Rucińska R et al (1997) Plant cell responses to heavy metals: molecular and physiological aspects. Acta Physiol Plant 19:459–465. https://doi.org/10.1007/s11738-997-0042-5
  • Hartley-Whitaker J, Ainsworth G, Meharg AA (2001) Copper- and arsenate-induced oxidative stress in Holcus lanatus L. clones with differential sensitivity. Plant Cell Environ 24:713–722. https://doi.org/10.1046/j.0016-8025.2001.00721.x
  • Hasanuzzaman M, Fujita M (2013) Exogenous sodium nitroprusside alleviates As-induced oxidative stress in wheat (Triticum aestivum L.) seedlings by enhancing antioxidant defense and glyoxalase system. Ecotoxicology 22:584–596. https://doi.org/10.1007/s10646-013-1050-4
  • Heath R, Packer L (1968) Photoperoxidation in isolated chloroplasts. Arch Biochem Biophys 125(1):189–198
  • Hindmarsh JT, Mccurdy RF (1986) Clinical and environmental aspects of As toxicity. Crit Rev Clin Lab Sci 23:315–347. https://doi.org/10.3109/10408368609167122
  • Hoagland DR, Arnon DI (1938) The water-culture method for growing plants without soil. Circ Calif Agric Exp Sta 347:1–35
  • Jeong S, Hee Sun Moon HS, Nam K (2014) Enhanced uptake and translocation of arsenic in cretain brake fern (Pteris cretica L.) through siderophore arsenic complex formation with an aid of rhizospheric bacterial activity. J Haz Mater 280:536–543
  • Khan A, Singh P, Srivastava A (2018) Synthesis, nature and utility of universal iron chelator-siderophore: a review. Microbiol Res 212–213:103–111
  • Kraemer SM, Crowley DE, Kretzschmar R (2006) Geochemical aspects of phytosiderophore promoted iron acquisition by plants. Adv Agron 91:1–46. https://doi.org/10.1021/es5031728
  • Lichtenthaler HK, Wellburn AR (1983) Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochem Soc Trans 11:591–592. https://doi.org/10.1042/bst0110591
  • McLaren RG, Naidu R, Smith J, Tiller KG (1998) Fractionation and distribution of arsenic in soils contaminated by cattle dip. J Environ Qual 27:348–354
  • Morton WE, Dunnette DA (1994) Health effects of environmental As. In: Nriagu JO (ed) As in the environment. Part II. Human health and ecosystem effects. Wiley, New York, pp 17–34
  • Mylona PV, Polidoros AN, Scandalios JG (1998) Modulation of antioxidant responses by As in maize. Free Radic Biol Med 25:576–585
  • Neilands JB (1981) Iron absorption and transport in microorganisms. Annu Rev Nutr 1:27–46. https://doi.org/10.1007/s11270-006-9263-2
  • Neilands J (1995) Siderophores: structure and function of microbial iron transport compounds. J Biol Chem 270:26723–26726. https://doi.org/10.1074/jbc.270.45.26723
  • Niazi NK, Bashir S, Bibi I, Murtaza G (2016) Phytoremediation of arsenic-contaminated soils using arsenic hyperaccumulating ferns. Phytoremediation. https://doi.org/10.1007/978-3-319-40148-5_19
  • Olsen SR, Cole CV, Watanabe FS, Dean LA (1954) Estimation of available phosphorus in soils by extraction with sodium bicarbonate. US Department of Agric. Circ p. 939
  • Payne SM (1994) Detection, isolation, and characterization of siderophores. Methods Enzymol 235:329–344. https://doi.org/10.1016/0076-6879(94)35151-1
  • Pinto L, Moore M (2009) Screening method to identify inhibitors of siderophore biosynthesis in the opportunistic fungal pathogen, Aspergillus fumigatus. Lett Appl Microbiol 49:8–13. https://doi.org/10.1111/j.1472-765X.2009.02582.x
  • Polle A, Junkermann W (1994) Inhibition of apoplastic and symplastic Arse activity from Norway spruce by the photooxidant hydroxymethyl hydroperoxide. Plant Physiol 104:617–621. https://doi.org/10.1104/pp.104.2.617
  • Poschenrieder C, Gunse B, Barcelo J (1989) Influence of cadmium on water relations, stomatal resistance, and abscisic acid content in expanding Bean leaves. Plant Physiol 90:1365–1371. https://doi.org/10.1104/pp.90.4.1365
  • Puschenreiter M, Gruber B, Wenzel WW, Schindlegger Y, Hann S, Spangl B, Schenkeveld WDC, Kraemer SM, Oburger E (2017) Phytosiderophore-induced mobilization and uptake of Cd, Cu, Fe, Ni, Pb and Zn by wheat plants grown on metal enriched soils. Environ Exp Bot 138:67–76. https://doi.org/10.1016/j.envexpbot.2017.03.011
  • Raj A, Singh N (2015) Phytoremediation of arsenic contaminated soil by arsenic accumulators: a three year study. Bull Environ Contam Toxicol 94:308–313. https://doi.org/10.1007/s00128-015-1486-8
  • Raj A, Pandey A, Sharma Y, Khare P, Srivastava P, Singh N (2011) Metabolic adaptation of Pteris vittata L. gametophyte to As induced oxidative stress. Biores Technol 102:9827–9832. https://doi.org/10.1016/j.biortech.2011.08.017
  • Saha P, Shinde O, Sarkar S (2017) Phytoremediation of industrial mines wastewater using water hyacinth. Int J Phytorem 19:87–96. https://doi.org/10.1080/15226514.2016.1216078
  • Sarkar A, Agrawal SB (2010) Identification of Ozone stress in Indian rice through foliar injury and differential protein profile. Environ Monit Assess 161:205–215. https://doi.org/10.1007/s10661-008-0738-z
  • Schwyn B, Neilands J (1987) Universal chemical assay for the detection and determination of siderophores. Anal Biochem 160:47–56
  • Shaibur M, Kitajima N, Sugawara R, Kondo T, Huq S, Kawai S (2006) Physiological and mineralogical properties of As-induced chlorosis in rice seedlings grown hydroponically. J Soil Sci Plant Nutr 52:691–700. https://doi.org/10.1111/j.1747-0765.2006.00085.x
  • Sharma S, Anand G, Singh N, Kapoor R (2017) Arbuscular mycorrhiza augments As tolerance in wheat (Triticum aestivum L.) by strengthening antioxidant defense system and thiol metabolism. Front Plant Sci 8:906. https://doi.org/10.3389/fpls.2017.00906
  • Shi P, Zing Z, Zhang U, Chai T (2017) Effect of heavy-metal on synthesis of siderophores by Pseudomonas aeruginosa ZGKD3. Earth Environ Sci 52:012103. https://doi.org/10.1088/17426596/52/1/012103 (IOP Conference Series)
  • Simola LK (1977) Effect of lead, cadmium, arsenate, and fluoride ions on growth and fine-structure of Sphagnum–Nemoreum in aseptic culture. Can J Bot-Revue Canadienne De Botanique 55:426–435. https://doi.org/10.1139/b77-052
  • Stoeva N, Bineva T (2003) Oxidative changes and photosynthesis in oat plants grown in As-contaminated soil. Bulg J Plant Physiol 29:87–95
  • Stoeva N, Berova M, Zlatev Z (2005) Effect of As on some physiological parameters in bean plants. Biol Plantarum 49:293–296. https://doi.org/10.1007/s10535-005-3296-z
  • Tripathi A, Mishra AK (2017) The wheat sector in India: production, policies and food security. In: Gomez y Paloma S, Mary S, Langrell S, Ciaian P (eds) The Eurasian wheat belt and food security. Springer, Switzerland, pp 275–296. https://doi.org/10.1007/978-3-319-33239-0_17
  • Tsutsumi M (1980) Intensification of As toxicity to paddy rice by hydrogen sulfide and ferrous iron. Soil Sci Plant Nutr 26:561–569. https://doi.org/10.1080/00380768.1980.10431243
  • Xi LC, Li FS, Yun S, Na JL, Yang LUX, Li HX (2007) Effects of As on seed germination and physiological activities of wheat seedlings. J Environ Sci 19:725–732. https://doi.org/10.1016/S1001-0742(07)60121-1
  • Zengin F (2015) Effects of exogenous salicylic acid on growth characteristics and biochemical content of wheat seeds under As stress. J Environ Biol 36:249–254
  • Zhang FQ, Wang YS, Lou ZP, Dong JD (2007) Effect of heavy metal stress on antioxidative enzymes and lipid peroxidation in leaves and roots of two mangrove plant seedlings (Kandelia candel and Bruguiera gymnorrhiza). Chemosphere 67:44–50. https://doi.org/10.1016/j.chemosphere.2006.10.007
  • Zhang WD, Liu DS, Tian JC, He FL (2009) Toxicity and accumulation of As in wheat (Triticum aestivum L.) varieties of China. Phyton (Buenos Aires) 78:147–154
  • Zhao FJ, Ma JF, Meharg AA, McGrath SP (2009) As uptake and metabolism in plants. New Phytol 181:777–794. https://doi.org/10.1111/j.1469-8137.2008.02716.x

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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