Open Access Open Access  Restricted Access Subscription Access

PGPR-Assisted Phytoremediation of Cadmium:An Advancement towards Clean Environment


Affiliations
1 Rhizosphere Biology Laboratory, Department of Environmental Microbiology, School for Environmental Sciences, Babasaheb Bhimrao Ambedkar University (A Central University), Lucknow 226 025, India
 

One of the major problems, that the world is facing today due to rapid industrialization is environmental pollution caused by several factors, including heavy metals. Among the heavy metals, cadmium is a hazardous carcinogenic element. From contaminated soil, cadmium enters the plants through the ischolar_mains and is accumulated in the harvestable (edible) parts, and thus gains entry into the food cycle. Phytoremediation plays a beneficial role in the remediation of cadmium contamination from soil, but becomes less effective with increasing toxicity. Even hyperaccumulator plants fail to perform under these conditions. Plant growth promoting rhizobacteria (PGPR), inhabitants of the plant rhizosphere, play a supporting role and promote bioremediation of soil by accumulation or transformation of contaminants, thereby enhancing plant growth and development. This article focuses on cadmium contamination and PGPR-assisted phyto-remediation of cadmium-contaminated soils.

Keywords

Cadmium, Phytoremediation, Plant Growth Promoting Rhizobacteria, Toxicity.
User
Notifications
Font Size

  • Patorczyk-Pytlik, B. and Spiak, Z., Effect of liming on the availability of cadmium for plants. Zesz. Nauk. Kom. Człowiek i Srodowisko, PAN, 2000, 26, 219–225.
  • Gosh, S., Wetland macrophytes as toxic metal accumulators. Int. J. Environ. Sci., 2010, 1(4), 523–528.
  • Wagner, G. J., Accumulation of cadmium in crop plants and its consequences to human health. Adv. Agron., 1993, 51, 173–212.
  • Lima, A. I. G., Pereira, S. I. A., de Almeida Paula Figueira, E. M., Caldeira, G. C. N. and de Matos Caldeira, H. D. Q., Cadmium detoxification in ischolar_mains of Pisum sativum seedlings: relationship between toxicity levels, thiol pool alterations and growth. Environ. Exp. Bot., 2006, 55, 149–162.
  • Kabata Pendias, A. and Pendias, H., Trace Elements in Soils and Plants, CRC Press, Florida, USA, 2nd edn, 1992.
  • Baker, A. J., Reeves, R. D. and Hajar, A. S. M., Heavy metal accumulation and tolerance in British population of the metallophyte Thlaspi caerulescens J & C. Presel (Brassicaceae). New Phytol., 1994, 129, 61–68.
  • Khan, S. and Khan, N. N., Influence of lead and cadmium on the growth and nutrient concentration of tomato (Lycopersicon esculentum) and egg-plant (Solarium melongena). Plant Soil, 1983, 74, 387–394.
  • Prasad, M. N. V., Phytoremediation of metal–polluted ecosystems: hype for commercialization. Russ. J. Plant Phys., 2003, 50, 686–700.
  • Helmisaari, H.-S., Salemaa, M., Derome, J., Kiikkilä, O., Uhlig, C. and Nieminen, T. M., Remediation of heavy metal contaminated forest soil using recycled organic matter and native woody plants. J. Environ. Qual., 2007, 36, 1145–1153.
  • Glick, B. R., Plant growth-promoting bacteria: mechanisms and applications. Science, 2012, 2012, 15.
  • Ahemad, M., Implications of bacterial resistance against heavy metals in bioremediation: a review. Int. Integr. Omics. Appl. Biotechnol. J., 2012, 3, 39–46.
  • Ahemad, M. and Malik, A., Bioaccumulation of heavy metals by zinc resistant bacteria isolated from agricultural soils irrigated with wastewater. Bacteriol. J., 2011, 2, 12–21.
  • Hayat, R., Ali, S., Amara, U., Khalid, R. and Ahmed, I., Soil beneficial bacteria and their role in plant growth promotion: a review. Ann. Microbiol., 2010, 60, 579–598.
  • Rajkumar, M., Ae, N., Prasad, M. N. V. and Freitas, H., Potential of siderophore-producing bacteria for improving heavy metal phytoextraction. Trends Biotechnol., 2010, 28, 142–149.
  • World Health Organization, Evaluation of certain food additives and contaminants. Thirty-third Report of the Joint FAO/WHO Expert Committee on Food Additives. WHO Technical Report Series, 776, 1989.
  • International Agency for Research on Cancer, Beryllium, cadmium, mercury, and exposures in the glass manufacturing industry [M]. In Monographs on the Evaluation of Carcinogenic Risks to Humans, WHO Press, Lyon, France, 1994, vol. 58, p. 444.
  • Degraeve, N., Carcinogenic, teratogenic and mutagenic effects of cadmium. Mutat. Res., 1981, 86, 115–135.
  • Inaba, T. et al., Estimation of cumulative cadmium intake causing itai-itai disease. Toxicol. Lett., 2005, 159(2), 192–120.
  • FAO/WHO, 2011. JECFA cadmium evaluation, draft toxicological monograph, as submitted by WHO, to be published as: Safety evaluation of certain contaminants in food, 2011.
  • Gonick, H. C., Nephrotoxicity of cadmium and lead. Ind. J. Med. Res., 2008, 128, 335–352.
  • Ryu, D. Y., Lee, S. J., Park, D. W., Choi, B. S., Klassen, C. D. and Park, J. D., Dietary iron regulates intestinal cadmium absorption through iron transporters in rats. Toxicol. Lett., 2004, 152, 19–25.
  • McGrath, S. P., Effects of heavy metals from sewage sludge on soil microbes in agricultural ecosystems. In Toxic Metals Soil–Plant Systems (ed. Ross, S. M.), Wiley, New York, 1994, pp. 247–273.
  • Giller, K., Witter, E. and McGrath, S. P., Toxicity of heavy metals to microorganisms and microbial processes in agricultural soils: a review. Soil Biol. Biochem., 1998, 30, 1389–1414.
  • Salt, D. E., Blaylock, M., Kumar, N. P. B. A., Dushenkov, V., Ensley, D., Chet, I. and Raskin, I., Phytoremediation: a novel strategy for the removal of toxic metals from the environment using plants. Biotechnology, 1995, 13, 468–474.
  • Lehoczky, E., Marth., P., Szabados, I., Palkovics, M. and Lukacs, P., Influence of soil factors in the accumulation of cadmium by lettuce. Commun. Soil Sci. Plant Anal., 2000, 31, 11–14.
  • Sanità di Toppi, L. and Gabbrielli, R., Response to cadmium in higher plants. Environ. Exp. Bot., 1999, 41, 105–130.
  • Van Assche, F., Cardinaels, C. and Clijsters, H., Induction of enzyme capacity in plants as a result of heavy metal toxicity; dose–response relations in Phaseolus vulgaris L., treated with zinc and cadmium. Environ. Pollut., 1988, 52, 103–115.
  • Guo, J., Dai, X., Xu, W. and Ma, M., Over expressing GSHI and AsPCSI simultaneously increases the tolerance and accumulation of cadmium and arsenic in Arabidopsis thaliana. Chemosphere, 2008, 72, 1020–1026.
  • Alcantara, E., Romera, F. J., Canete, M. and De La Guardia, M. D., Effects of heavy metals on both induction and function of ischolar_main Fe(III) reductase in Fe-deficient cucumber (Cucumis sativus L.) plants. J. Exp. Bot., 1994, 45, 1893–1898.
  • Hernandez, L. E., Carpena-Ruiz, R. and Garate, A., Alterations in the mineral nutrition of pea seedlings exposed to cadmium. J. Plant Nutr., 1996, 19, 1581–1598.
  • Mathys, W., Enzymes of heavy metal-resistant and non-resistant populations of Silenecu cubalus and their interactions with some heavy metals in vitro and in vivo. Physiol. Plant, 1975, 33, 161–165.
  • Balestrasse, K. B., Benavides, M. P., Gallego, S. M. and Tomaro, M. L., Effect on cadmium stress on nitrogen metabolism in nodules and ischolar_mains of soybean plants. Funct. Plant Biol., 2003, 30, 57–64.
  • Costa, G. and Morel, J. L., Water relations, gas exchange and amino acid content in Cd-treated lettuce. Plant Physiol. Biochem., 1994, 32, 561–570.
  • Fodor, A., Szabo-Nagy, A. and Erdei, L., The effects of cadmium on the fluidity and H?-ATPase activity of plasma membrane from sunflower and wheat ischolar_mains. J. Plant Physiol., 1995, 14, 787–792.
  • De Filippis, L. F. and Ziegler, H., Effect of sublethal concentrations of zinc, cadmium and mercury on the photosynthetic carbon reduction cycle of Euglena. J. Plant Physiol., 1993, 142, 167–172.
  • Turan, M., and Esringu, A., Phytoremediation based on canola (Brassica napus L.) and Indian mustard (Brassica juncea L.) planted on spiked soil by aliquot amount of Cd, Cu, Pb and Zn. Plant Soil Environ., 2007, 53, 7–15.
  • Hayes, W. J., Chaudhry, R. T., Buckney, R. T. and Khan, A. G., Phytoaccumulation of trace metals at the Sunny Corner mine, New South Wales, with suggestions for a possible remediation strategy. Aust. J. Ecotoxicol., 2003, 9, 69–82.
  • Gupta, A., K., Verma, S. K., Khan, K. and Verma, R. K., Phytoremediation using aromatic plants: a sustainable approach for remediation of heavy metals polluted sites. Environ. Sci. Technol., 2013, 47, 10115–10116.
  • Gomes, H. I., Phytoremediation for bioenergy: challenges and opportunities. Environ. Technol. Rev., 2012, 1(1), 59–66.
  • Zhang, S., Chen, M., Li, T., Xu, X. and Deng, L., A newly found cadmium accumulator Malva sinensis Cavan. J. Hazard. Mater., 2010, 173, 705–709.
  • Visoottiviseth, P., Francesconi, K. and Sridokchan, W., The potential of Thai indigenous plant species for the phytoremediation of arsenic contaminated land. Environ. Pollut., 2002, 118, 453–461.
  • Baker, A. J. M. and Brooks, R. R., Terrestrial higher plants which hyperaccumulate metallic elements: a review of their distribution, ecology and phytochemistry. Biorecovery, 1989, 1, 81–126.
  • Ghosh, M. and Singh, S., A review on phytoremediation of heavy metals and utilization of its byproducts. Asian J. Energy Environ., 2005, 3, 214–231.
  • Begonia, M. T., Begonia G. B., Ighoavodha, M. and Gilliard, D., Lead accumulation by tall fescue (Festuca arundinacea Schreb) grown on a lead contaminated soil. Int. J. Environ. Res. Public Health, 2005, 2, 228–233.
  • Oh, K., Hu, X. F., He, C. Q., Yonemochi, S. and Shi, F., Perspective on application of phytoremediation technology in remediation of contaminated soils. In Proceedings of the 2011 World Congress on Engineering and Technology, Shanghai, China, 2011, pp. 532–535.
  • Wenzel, W. W., Adriano, D. C., Salt, D. and Smith, R., Phytoremediation: a plant–microbe-based remediation system. In Bioremediation of Contaminated Soils (eds Adriano, D. C. et al.), Madison, WI: ASA, CSSA and SSSA, Agronomy Monographs 37, 1999, pp. 457–508.
  • Kuiper, I., Lagendijk, E. L., Bloemberg, G. V. and Lugtenberg, B. J., Rhizoremediation: a beneficial plant–microbe interaction. Mol. Plant–Microbe Interact., 2004, 17, 6–15.
  • Belimov, A. A. et al., Characterization of plant growth-promoting rhizobacteria isolated from polluted soils and containing 1-aminocyclopropane1-carboxylate deaminase. Can. J. Microbiol., 2001, 47, 642–652.
  • Belimov, A. A. and Dietz, K.-J., Effect of associative bacteria on element composition of barley seedlings grown in solution culture at toxic cadmium concentrations. Microbiol. Res., 2000, 155, 113–121.
  • Glick, B. R., Phytoremediation: synergistic use of plants and bacteria to clean up the environment. Biotechnol. Adv., 2003, 21, 383.
  • Gadd, G. M., Heavy metal accumulation by bacteria and other microorganisms. Experientia, 1990, 46, 834–840.
  • Amico, E. D., Cavalca, L. and Andreoni, V., Analysis of rhizobacterial communities in perennial Graminaceae from polluted water meadow soil, and screening of metal-resistant, potentially plant growth-promoting bacteria. FEMS Microbiol. Ecol., 2005, 52, 153–162.
  • Walker, T. S., Bais, H. P., Grotewols, E. and Vivanco, J. M., Root exudation and rhizosphere biology. Plant Physiol., 2003, 132(1), 44–51.
  • Erkovan, I., Giillap, M. K., Dasci, M. and Koc, A., Effects of phosphorus fertilizer and phosphorus solubilizing bacteria application on clover dominant meadow: yield and botanical composition. Turk. J. Field Crops, 2010, 15(1), 12–17.
  • Egamberdiyeva, D. and Hoflich, G., Influence of growth promoting bacteria on the growth of wheat at different soil and temperatures. Soil Biol. Biochem., 2003, 35, 973–978.
  • Glick, B., Bacteria with ACC deaminase can promote plant growth and help to feed the world. Microbiol. Res., 2014, 169(1), 30–39.
  • Upadhyay, S. K., Singh, J. S. and Singh, D. P., Exopolysaccharide producing plant growth promoting rhizobacteria under salinity condition. Pedosphere, 2011, 21(2), 214–222.
  • Mulligan, C. N., Recent advances in the environmental applications of biosurfactants. Curr. Opin. Colloid Interface Sci., 2009, 14, 372–378.
  • Ma, Q. Y., Traina, S. J., Logan, T. J. and Ryan, J. A., Effects of aqueous Al, Cd, Cu, Fe(II), Ni, and Zn on Pb immobilization by hydroxyapatite. Environ. Sci. Technol., 1994, 28, 1219–1228.
  • Hernandez, A. N., Hernandez, A. and Heydrich, M., Seleccion de rizobacterias asiciadas al cultivo del maiz. Cultivos Trop., 1995, 16, 5–8.
  • Belimov, A. A., Hontzeas, N., Safronova, V. I., Demchinskaya, S. V., Piluzza G., Bullitta, S. and Glick, B. R., Cadmium-tolerant plant growth-promoting bacteria associated with the ischolar_mains of Indian mustard (Brassica juncea L. Czern.). Soil Biol. Biochem., 2005, 37, 241.
  • Redon, P. O., Béguiristain, T. and Leyval, C., Influence of Glomus intraradiceson Cd partitioning in a pot experiment with Medicago truncatula in four contaminated soils. Soil Biol. Biochem., 2008, 40, 2710–2712.
  • Idris, R. et al., Bacterial communities associated with flowering plants of the Ni hyperaccumulator Thalspi goesingense. Appl. Environ. Microbiol., 2004, 70, 2667–2677.
  • Wu, C.H., Wood, T. K., Mulchandani, A. and Chen, W., Engineering plant–microbe symbiosis for rhizoremediation of heavy metals. Appl. Environ. Microbiol., 2006, 72, 1129–1134.
  • Biswas, B., Sarkar, B., Mandal, A. and Naidu, R., Heavy metalimmobilizing organoclay facilitates polycyclic aromatic hydrocarbon biodegradation in mixed-contaminated soil. J. Hazard Mater., 2015, 298, 129–137.
  • Khan, A. G., Kuek, C., Chaudhry, T. M., Khoo, C. S. and Hayes, W. J., Role of plants, mycorrhizae and phytochelators in heavy metal contaminated land remediation. Chemosphere, 2000, 41, 197–207.
  • Neubauer, U., Furrer, G., Kayser, A. and Schulin, R., Siderophores, NTA, and citrate: potential soil amendments to enhance heavy metal mobility in phytoremediation. Int. J. Phytoremediat, 2000, 2, 353–368.
  • Kiss, T. and Farkas, E., Metal-binding ability of desferrioxamine B. J. Inclus. Phenom. Mol., 1998, 32, 385–403.
  • Burd, G. I., Dixonand, D. G. and Glick, B. R., A plant growth promoting bacterium that decreases nickel toxicity in seedlings. Appl. J. Environ. Microbiol., 1998, 64, 3663.
  • Reed, M. and Glick, B., Growth of canola (Brassica napus) in the presence of plant growth-promoting bacteria and either copper or polycyclic aromatic hydrocarbons. Can. J. Microbiol., 2005, 51, 1061–1069.
  • Vivas, A., Vorosm, A., Biro, B., Barea, J. M., Ruiz-Lozano, J. M. and Azcon, R., Beneficial effects of indigenous Cd-tolerant and Cd-sensitive Glomus mosseae associated with a Cd-adapted strain of Brevi bacillus sp. in improving plant tolerance to Cd contamination. Appl. Soil Ecol., 2003, 24, 177–186.
  • Kumar, K. V., Srivastava, S., Singh, N. and Behl, H. M., Role of metal resistant plant growth promoting bacteria in ameliorating fly ash to the growth of Brassica juncea. J. Hazard. Mater., 2009, 170, 51–57.
  • Ma, Y., Rajkumar, M. and Freitas, H., Improvement of plant growth and nickel uptake by nickel resistant-plant-growth promoting bacteria. J. Hazard. Mater., 2009, 166, 1154–1161.
  • He, C. Q. et al., Effect of Zn-tolerant bacterial strains on growth and Zn accumlation in Orychophragmus violaceus. Appl. Soil Ecol., 2010, 44, 1–5.
  • Sheng, X., He, L., Wang, Q., Ye, H. and Jiang, C., Effects of inoculation of biosurfactant-producing Bacillus sp. J119 on plant growth and cadmium uptake in cadmium-amended soil. J. Hazard. Mater., 2008, 155, 17–22.
  • Rodriguez, H., Vessely, S., Shah, S. and Glick, B. R., Isolation and characterization of nickel resistant Pseudomonas strains and their effect on the growth of non-transformed and transgenic canola plants. Curr. Microbiol., 2008, 57, 170–174.
  • Kumar, K. V., Singh, N., Behl, H. M. and Srivastava, S., Influence of plant growth promoting bacteria and its mutant on heavy metal toxicity in Brassica juncea grown in fly ash amended soil. Chemosphere, 2008, 72, 678–683.
  • Zaidi, S., Usmani, S., Singh, B. R. and Musarrat, J., Significance of Bacillus subtilis SJ-101 as a bioinoculant for concurrent plant growth promotion and nickel accumulation in Brassica juncea. Chemosphere, 2006, 64, 991–997.
  • Hussein, H. S., Optimization of plant–bacteria complex for phyto-remediation of contaminated soils. Int. J. Bot., 2008, 4, 437–443.
  • Farwell, A. J. et al., The use of transgenic canola (Brassica napus) and plant growth-promoting bacteria to enhance plant biomass at a nickel-contaminated field site. Plant Soil, 2006, 288, 309–318.
  • Tripathi, M., Munot, H., Shouche, Y., Meyer, J. M. and Goel, R., Isolation and functional characterization of siderophore-producing lead- and cadmium-resistant Pseudomonas putida KNP9. Curr. Microbiol., 2005, 50, 233–237.
  • Safranova, V. I., Stepanok, V. V., Engqvist, G. L., Alekseyev, Y. V. and Belimov, A. A., Root-associated bacteria containing 1-aminocyclopropane-1-carboxylate deaminase improve growth and nutrient uptake by pea genotypes cultivated in cadmium supplemented soil. Biol. Fertil. Soils, 2006, 42, 267–272.
  • Sheng, X.-F. and Xia, J.-J., Improvement of rape (Brassica napus) plant growth and cadmium uptake by cadmium-resistant bacteria. Chemosphere, 2006, 64, 1036–1042.
  • Ike, A., Sriprang, R., Ono, H., Murooka, Y. and Yamashita, M., Bioremediation of cadmium contaminated soil using symbiosis between leguminous plant and recombinant rhizobia with the MTL4 and the PCS genes. Chemosphere, 2007, 66, 1670–1676.
  • Li, W. C., Ye, Z. H. and Wong, M. H., Effects of bacteria on enhanced metal uptake of the Cd/Zn hyperaccumulating plant, Sedum alfredii. J. Exp. Bot., 2007, 58, 4173–4182.
  • Sheng, X.-F., Xia, J.-J., Jiang, C.-Y., He, L.-Y. and Qian, M., Characterization of heavy metal-resistant endophytic bacteria from rape (Brassica napus) ischolar_mains and their potential in promoting the growth and lead accumulation of rape. Environ. Pollut., 2008, 156, 1164–1170.
  • Ganesan, V., Rhizoremediation of cadmium soil using a cadmiumresistant plant growth-promoting rhizopseudomonad. Curr. Microbiol., 2008, 56, 403–407.
  • He, L.-Y., Chen, Z.-J., Ren, G.-D., Zhang, Y.-F., Qian, M. and Sheng, X.-F., Increased cadmium and lead uptake of a cadmium hyperaccumulator tomato by cadmium-resistant bacteria. Exotoxicol. Environ. Saf., 2009, 72, 1343–1348.
  • Dimpka, C. O., Merten, D., Svatos, A., Büchel, G. and Kothe, E., Siderophores mediate reduced and increased uptake of cadmium by Streptomyces tendae F4 and sunflower (Helianthus annuus), respectively. J. Appl. Microbiol., 2009, 107, 1687–1696.

Abstract Views: 459

PDF Views: 126




  • PGPR-Assisted Phytoremediation of Cadmium:An Advancement towards Clean Environment

Abstract Views: 459  |  PDF Views: 126

Authors

Chhaya Verma
Rhizosphere Biology Laboratory, Department of Environmental Microbiology, School for Environmental Sciences, Babasaheb Bhimrao Ambedkar University (A Central University), Lucknow 226 025, India
Amar Jyoti Das
Rhizosphere Biology Laboratory, Department of Environmental Microbiology, School for Environmental Sciences, Babasaheb Bhimrao Ambedkar University (A Central University), Lucknow 226 025, India
Rajesh Kumar
Rhizosphere Biology Laboratory, Department of Environmental Microbiology, School for Environmental Sciences, Babasaheb Bhimrao Ambedkar University (A Central University), Lucknow 226 025, India

Abstract


One of the major problems, that the world is facing today due to rapid industrialization is environmental pollution caused by several factors, including heavy metals. Among the heavy metals, cadmium is a hazardous carcinogenic element. From contaminated soil, cadmium enters the plants through the ischolar_mains and is accumulated in the harvestable (edible) parts, and thus gains entry into the food cycle. Phytoremediation plays a beneficial role in the remediation of cadmium contamination from soil, but becomes less effective with increasing toxicity. Even hyperaccumulator plants fail to perform under these conditions. Plant growth promoting rhizobacteria (PGPR), inhabitants of the plant rhizosphere, play a supporting role and promote bioremediation of soil by accumulation or transformation of contaminants, thereby enhancing plant growth and development. This article focuses on cadmium contamination and PGPR-assisted phyto-remediation of cadmium-contaminated soils.

Keywords


Cadmium, Phytoremediation, Plant Growth Promoting Rhizobacteria, Toxicity.

References





DOI: https://doi.org/10.18520/cs%2Fv113%2Fi04%2F715-724