m e d i ation b ie journal of o g l r a n r u o noitada ... · laccase, nitrilase, dehalogenase,...

3
Volume 4 • Issue 3 • 1000e132 J Bioremed Biodeg ISSN: 2155-6199 JBRBD, an open access journal Open Access Chen et al., J Bioremed Biodeg 2013, 4:3 DOI: 10.4172/2155-6199.1000e132 Open Access Editorial e increasingly anthropogenic release of toxic contaminants has led to the contamination of organic chemicals, such as phthalic esters (PAEs), Polycyclic Aromatic Hydrocarbons (PAHs), Polybrominated Diphenyl Ethers (PBDEs), Polychlorobiphenyls (PCBs), Petroleum Hydrocarbons (PHC), pesticides, etc [1]. Remediation of organic- polluted soils is becoming an increasing challenge worldwide [2]. Phytoremediation is an emerging technology that utilizes plants to clean up organic pollutants and toxic metals in water, sediments, or soils [3]. Phytoremediation has been accepted and utilized widely because it is a cost-effective and environmental friendly green technology with permanently removing the pollutants [4]. A large number of plant species have been found to be promising candidates for the phytoremediation of organic pollutants [5]. In general there are two approaches for the phytoremediation of organic-polluted soils based on the difference in remediative mechanism. First, organic pollutants can be taken up directly by plants, resulting in the sequestration or degradation of pollutants inside of plants [5], which is called phytoextraction. Second, organic pollutants can be degraded by plant-secreted enzymes or plant-modified microbial community in rhizosphere [5,6], which is called plant-assisted rhizoremediation. Phytoextraction depends on the absorption, translocation, and metabolism of organic pollutants in plants. Some organic compounds are able to enter into plant cells by penetrating cell membrane easily. Medicag osativa and Tagetes patula are potential candidates for the phytoremediation of soils contaminated with PAEs and PAHs [7- 9]. A field study indicates that M. osativa exhibits the largest Bio- Concentration Factors (BCFs) of PAEs comparing to other tested plant species, suggesting that the direct absorption and metabolism might be the main mechanisms for M. osativa-mediated phytoremediation of PAE-polluted soil [10]. Organic pollutants are artificial and thus lack membrane transporters in plant cells. e uptake of organic pollutants from soils by plant roots is mainly driven by simple diffusion based on their chemical properties and bioavailability [11]. e hydrophobicity of organic pollutants, evaluated by K ow , determines their efficiency of penetrating plant cell membrane [12]. To enhance the bioavailability of organic pollutants in soil, some amendments (e.g. Tween 80, citric and oxalic acids, biochar, and methylated-β-cyclodextrins) has been successfully applied in assisting phytoremediation of organic-polluted soils [13-15]. Aſter entering into root cells, organic pollutants could be further translocated and metabolized in plants. e diffusion of organic pollutants from root symplast into xylem apoplast is essential for their translocation from roots to shoots, which can be quantified by calculating the Transpiration Stream Concentration Factor (TSCF) [11,16]. Several detoxification enzymes are involved in the transformation and sequestration of organic pollutants in plants. Cytochrome P450 enzymes (CYP) play vital roles in the oxidative process for emulsifying highly hydrophobic pollutants [11,17]. Glutathione-S-transferases (GSTs) catalyze the conjugation between toxic organic pollutants and sulydryl (-SH) group of glutathione (GSH). GST-pollutants conjugates can be further transported and sequestrated from cytosol to vacuoles in plant cells [18]. Plant-assisted rhizoremediation refers to the strategy of phytoremediation ex planta. Plant roots not only secrete enzymes degrading organic pollutants [19], but also improve the degrading ability of microorganisms in rhizosphere [20]. Plant enzymes with the role of degrading organic pollutants have been well reviewed by Gerhardt and Nwoko, respectively [5,11]. ese enzymes include laccase, nitrilase, dehalogenase, nitroreductase, etc. Although many microorganisms are capable of degrading organic compounds, microbial bioremediation approaches suffer a number of limitations for their widespread application [21]. Plants are able to improve the efficiency of microbial bioremediation of organic-polluted soils [22]. In a pot experiment, M. osativa improves soil microbial degradation ability to decrease benzo[a]pyrene concentration in soil rather than accumulates the pollutants inside of plant tissues [23]. Plant root exudates (e.g. organic acids, sugars, phenolics etc.) are commonly used as carbon and energy sources by soil microbes with the ability of degrading organic pollutants [24]. Aſter planting M. osativa in crude oil-contaminated soil, 731 and 379 functional genes related to organic remediation were detected by microarray in rhizosphere and non- rhizosphere, respectively. is study suggested that the rhizosphere with relatively high populations of heterotrophic bacteria and hydrocarbon-degrading bacteria selectively increases the abundance of these specific functional genes [25]. In addition, plant exudates may increase the water solubility of organic pollutants, which stimulates the bioavailability of pollutants for both plants and microbes [11]. In return, microbial community also provides beneficial compounds or enzymes for protecting plants from the toxicity induced by organic pollutants [26,27]. e effective degradation of organic pollutants in soil by mycorrhiza-plants system has been extensively documented [22,28- 30]. Actually, rhizoremediation is a complex degradation process with multiple fine interactions involving roots, rhizosphere soil, and microbes. e further understanding of the detailed mechanisms of these interactions is needed to better optimize the application of plant- assisted rhizoremediation. However, the capability of using single plant species for the phytoremediation of organic-polluted soils is limited. Intercropping systems with multiple plant species are able to remarkably increase the efficiency of phytoremediation [31]. e enhanced degradation of organic pollutants by intercropping multispecies may result from the accelerated degradation rate of some recalcitrant organic pollutants *Corresponding author: Fengxiang X Han, Department of Chemistry and Biochemistry, Jackson State University, 1400 John R Lynch Street Jackson, MS 39217, USA, E-mail: [email protected] Received March 01, 2013; Accepted March 04, 2013; Published March 06, 2013 Citation: Chen J, Xu QX, Su Y, Shi ZQ, Han FX (2013) Phytoremediation of Organic Polluted Soil. J Bioremed Biodeg 4: e132. doi:10.4172/2155-6199.1000e132 Copyright: © 2013 Chen J, et al. This is an open-a ccess article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Phytoremediation of Organic Polluted Soil Jian Chen 1 , Qing-Xuan Xu 2 , Yi Su 3 , Zhi-Qi Shi 1 and Fengxiang X Han 4 * 1 Institute of Food Quality and Safety, Jiangsu Academy of Agricultural Sciences, Nanjing, China 2 College of Plant Protection, Yunnan Agriculture University, Kunming, China 3 Institute for Clean Energy Technology, Mississippi State University, Oktibbeha County, Mississippi, USA 4 Department of Chemistry and Biochemistry, Jackson State University, Jackson, Mississippi, USA Journal of Bior emediation & Biodegradation J o u r n a l o f B i o r e m e d i a ti o n & B i o d e g r a d a t i o n ISSN: 2155-6199

Upload: doandang

Post on 12-May-2018

214 views

Category:

Documents


0 download

TRANSCRIPT

Volume 4 • Issue 3 • 1000e132J Bioremed Biodeg ISSN: 2155-6199 JBRBD, an open access journal

Open Access

Chen et al., J Bioremed Biodeg 2013, 4:3 DOI: 10.4172/2155-6199.1000e132

Open Access

Editorial

The increasingly anthropogenic release of toxic contaminants has led to the contamination of organic chemicals, such as phthalic esters (PAEs), Polycyclic Aromatic Hydrocarbons (PAHs), Polybrominated Diphenyl Ethers (PBDEs), Polychlorobiphenyls (PCBs), Petroleum Hydrocarbons (PHC), pesticides, etc [1]. Remediation of organic-polluted soils is becoming an increasing challenge worldwide [2]. Phytoremediation is an emerging technology that utilizes plants to clean up organic pollutants and toxic metals in water, sediments, or soils [3]. Phytoremediation has been accepted and utilized widely because it is a cost-effective and environmental friendly green technology with permanently removing the pollutants [4]. A large number of plant species have been found to be promising candidates for the phytoremediation of organic pollutants [5]. In general there are two approaches for the phytoremediation of organic-polluted soils based on the difference in remediative mechanism. First, organic pollutants can be taken up directly by plants, resulting in the sequestration or degradation of pollutants inside of plants [5], which is called phytoextraction. Second, organic pollutants can be degraded by plant-secreted enzymes or plant-modified microbial community in rhizosphere [5,6], which is called plant-assisted rhizoremediation.

Phytoextraction depends on the absorption, translocation, and metabolism of organic pollutants in plants. Some organic compounds are able to enter into plant cells by penetrating cell membrane easily. Medicag osativa and Tagetes patula are potential candidates for the phytoremediation of soils contaminated with PAEs and PAHs [7-9]. A field study indicates that M. osativa exhibits the largest Bio-Concentration Factors (BCFs) of PAEs comparing to other tested plant species, suggesting that the direct absorption and metabolism might be the main mechanisms for M. osativa-mediated phytoremediation of PAE-polluted soil [10]. Organic pollutants are artificial and thus lack membrane transporters in plant cells. The uptake of organic pollutants from soils by plant roots is mainly driven by simple diffusion based on their chemical properties and bioavailability [11]. The hydrophobicity of organic pollutants, evaluated by Kow, determines their efficiency of penetrating plant cell membrane [12]. To enhance the bioavailability of organic pollutants in soil, some amendments (e.g. Tween 80, citric and oxalic acids, biochar, and methylated-β-cyclodextrins) has been successfully applied in assisting phytoremediation of organic-polluted soils [13-15]. After entering into root cells, organic pollutants could be further translocated and metabolized in plants. The diffusion of organic pollutants from root symplast into xylem apoplast is essential for their translocation from roots to shoots, which can be quantified by calculating the Transpiration Stream Concentration Factor (TSCF) [11,16]. Several detoxification enzymes are involved in the transformation and sequestration of organic pollutants in plants. Cytochrome P450 enzymes (CYP) play vital roles in the oxidative process for emulsifying highly hydrophobic pollutants [11,17]. Glutathione-S-transferases (GSTs) catalyze the conjugation between toxic organic pollutants and sulfhydryl (-SH) group of glutathione (GSH). GST-pollutants conjugates can be further transported and sequestrated from cytosol to vacuoles in plant cells [18].

Plant-assisted rhizoremediation refers to the strategy of phytoremediation ex planta. Plant roots not only secrete enzymes degrading organic pollutants [19], but also improve the degrading ability of microorganisms in rhizosphere [20]. Plant enzymes with the role of degrading organic pollutants have been well reviewed by Gerhardt and Nwoko, respectively [5,11]. These enzymes include laccase, nitrilase, dehalogenase, nitroreductase, etc. Although many microorganisms are capable of degrading organic compounds, microbial bioremediation approaches suffer a number of limitations for their widespread application [21]. Plants are able to improve the efficiency of microbial bioremediation of organic-polluted soils [22]. In a pot experiment, M. osativa improves soil microbial degradation ability to decrease benzo[a]pyrene concentration in soil rather than accumulates the pollutants inside of plant tissues [23]. Plant root exudates (e.g. organic acids, sugars, phenolics etc.) are commonly used as carbon and energy sources by soil microbes with the ability of degrading organic pollutants [24]. After planting M. osativa in crude oil-contaminated soil, 731 and 379 functional genes related to organic remediation were detected by microarray in rhizosphere and non-rhizosphere, respectively. This study suggested that the rhizosphere with relatively high populations of heterotrophic bacteria and hydrocarbon-degrading bacteria selectively increases the abundance of these specific functional genes [25]. In addition, plant exudates may increase the water solubility of organic pollutants, which stimulates the bioavailability of pollutants for both plants and microbes [11]. In return, microbial community also provides beneficial compounds or enzymes for protecting plants from the toxicity induced by organic pollutants [26,27]. The effective degradation of organic pollutants in soil by mycorrhiza-plants system has been extensively documented [22,28-30]. Actually, rhizoremediation is a complex degradation process with multiple fine interactions involving roots, rhizosphere soil, and microbes. The further understanding of the detailed mechanisms of these interactions is needed to better optimize the application of plant-assisted rhizoremediation.

However, the capability of using single plant species for the phytoremediation of organic-polluted soils is limited. Intercropping systems with multiple plant species are able to remarkably increase the efficiency of phytoremediation [31]. The enhanced degradation of organic pollutants by intercropping multispecies may result from the accelerated degradation rate of some recalcitrant organic pollutants

*Corresponding author: Fengxiang X Han, Department of Chemistry and Biochemistry, Jackson State University, 1400 John R Lynch Street Jackson, MS 39217, USA, E-mail: [email protected]

Received March 01, 2013; Accepted March 04, 2013; Published March 06, 2013

Citation: Chen J, Xu QX, Su Y, Shi ZQ, Han FX (2013) Phytoremediation of Organic Polluted Soil. J Bioremed Biodeg 4: e132. doi:10.4172/2155-6199.1000e132

Copyright: © 2013 Chen J, et al. This is an open-a ccess article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Phytoremediation of Organic Polluted SoilJian Chen1, Qing-Xuan Xu2, Yi Su3, Zhi-Qi Shi1 and Fengxiang X Han4*1Institute of Food Quality and Safety, Jiangsu Academy of Agricultural Sciences, Nanjing, China2College of Plant Protection, Yunnan Agriculture University, Kunming, China3Institute for Clean Energy Technology, Mississippi State University, Oktibbeha County, Mississippi, USA4Department of Chemistry and Biochemistry, Jackson State University, Jackson, Mississippi, USA

Journal of Bior emediation & Biodegradation Jo

urna

l of B

iorem

ediation & Biodegradation

ISSN: 2155-6199

Citation: Chen J, Xu QX, Su Y, Shi ZQ, Han FX (2013) Phytoremediation of Organic Polluted Soil. J Bioremed Biodeg 4: e132. doi:10.4172/2155-6199.1000e132

Volume 4 • Issue 3 • 1000e132J Bioremed BiodegISSN: 2155-6199 JBRBD, an open access journal

Page 2 of 3

and the elevated soil microbial biomass, microbial functional diversity, and degrading enzymes activities [10,32-34].

With the rapid development of biotechnology, transgenic modification of plants is becoming a powerful tool for enhancing the efficiency of phytoremediation of organic-polluted soil [35-37]. The genetically modified strategies are supposed to achieve the goals of enhancing the degrading rates of pollutants in planta or enhancing the release of degrading enzymes from roots leading to the accelerated degradation of pollutants ex planta [37]. The genes coding for CYP and GSTs are the usually modified targets for stimulating the degradation of organic pollutants in plants [38-40]. A recent study suggested that transgenic M. osativa plants co-expressing GST and human CYP2E1 showed great potential for phytoremediation of organic pollutants [41]. Many degrading genes can be introduced and over-expressed in plants to improve the degradation of organic pollutants ex planta. For instance, two laccase genes from cotton and Coriolus versicolor were over expressed in Arabidopsis thaliana and tobacco, respectively. The two transgenic plants showed increased secretory laccase activity resulting in the enhanced degradation of trichlorophenol and pentachlorophenol, respectively [42,43]. The over expression of other genes coding for degrading enzymes (e.g. peroxidases and nitroreductases) in plants can stimulate the degradation of organic pollutants in rhizoshphere as well [44-46]. However, the invasive risk of releasing transgenic plants into the environmental on biodiversity should be regulatory concerned.

Based on the current reports, phytoremediation is emerging as a potential approach for remediating organic-polluted soils. More field application of phytoremediation is much needed. First, the identification of plant species with the ability of hyper accumulating specific organic pollutants will be desired. Second, the understanding of the detailed mechanisms for the degradation of organic pollutants in plants and rhizosphere is essential for improving the efficiency of phytoremedation and avoiding the secondary contamination of the possibly toxic metabolites from the degradation of parent organic pollutants. Third, more quantitative experimental data analyses about the effect of intercropping or plant-microbe interaction on the efficiency of organic phytoremediation are useful for constructing models for the usage of plants in remediating organic-polluted soils. Finally, regulatory requirements, site assessment, and risk evaluation are indispensable for the field application of phytoremediation for organic pollutants.

References

1. Harmens H, Foan L, Simon V, Mills G (2013) Terrestrial mosses as biomonitors of atmospheric POPs pollution: a review. Environ Pollut 173: 245-254.

2. Weber R, Watson A, Forter M, Oliaei F (2011) Review Article: Persistent organic pollutants and landfills - a review of past experiences and future challenges. Waste Manag Res 29: 107-121.

3. Cherian S, Oliveira MM (2005) Transgenic plants in phytoremediation: recent advances and new possibilities. Environ Sci Technol 39: 9377-9390.

4. Chen J, Shiyab S, Han FX, Monts DL, Waggoner CA, et al. (2009) Bioaccumulation and physiological effects of mercury in Pteris vittata and Nephrolepis exaltata. Ecotoxicology 18: 110-121.

5. Gerhardt KE, Huang X-D, Glick BR, Greenberg BM (2009) Phytoremediation and rhizoremediation of organic soil contaminants: Potential and challenges. Plant Sci 176: 20-30.

6. Alkorta I, Garbisu C (2001) Phytoremediation of organic contaminants in soils. Bioresour Technol 79: 273-276.

7. Hamdi H, Benzarti S, Aoyama I, Jedidi N (2012) Rehabilitation of degraded soils containing aged PAHs based on phytoremediation with alfalfa (Medicago sativa L.). Int Biodeterior Biodegrad 67: 40-47.

8. Sun Y, Zhou Q, Xu Y, Wang L, Liang X (2011) Phytoremediation for co-contaminated soils of benzo[a]pyrene (B[a]P) and heavy metals using ornamental plant Tagetes patula. J Hazard Mater 186: 2075-2082.

9. Fu D, Teng Y, Luo Y, Tu C, Li S, et al. (2012) Effects of alfalfa and organic fertilizer on benzo[a]pyrene dissipation in an aged contaminated soil. Environ Sci Pollut Res Int 19: 1605-1611.

10. Ma T, Luo Y, Christie P, Teng Y, Liu W (2012) Removal of phthalic esters from contaminated soil using different cropping systems: A field study. Eur J Soil Biol 50: 76-82.

11. Nwoko CO (2010) Trends in phytoremediation of toxic elemental and organic pollutants. Afr J Biotechnol 9: 6010-6016.

12. Schröder P, Collins C (2002) Conjugating enzymes involved in xenobiotic metabolism of organic xenobiotics in plants. Int J Phytoremediat 4: 247-265.

13. Beesley L, Moreno-Jiménez E, Gomez-Eyles JL (2010) Effects of biochar and greenwaste compost amendments on mobility, bioavailability and toxicity of inorganic and organic contaminants in a multi-element polluted soil. Environ Pollut 158: 2282-2287.

14. Mitton FM, Gonzalez M, Peña A, Miglioranza KS (2012) Effects of amendments on soil availability and phytoremediation potential of aged p,p’-DDT, p,p’-DDE and p,p’-DDD residues by willow plants (Salix sp.). J Hazard Mater 203-204: 62-8.

15. Shen C, Tang X, Cheema SA, Zhang C, Khan MI, et al. (2009) Enhanced phytoremediation potential of polychlorinated biphenyl contaminated soil from e-waste recycling area in the presence of randomly methylated-beta-cyclodextrins. J Hazard Mater 172: 1671-1676.

16. Verkleij JAC, Golan-Goldhirsh A, Antosiewisz DM, Schwitzguébel J-P, Schröder P (2009) Dualities in plant tolerance to pollutants and their uptake and translocation to the upper plant parts. Environ Exp Bot 67: 10-22.

17. Page V, Schwitzguébel JP (2009) The role of cytochromes P450 and peroxidases in the detoxification of sulphonated anthraquinones by rhubarb and common sorrel plants cultivated under hydroponic conditions. Environ Sci Pollut Res Int 16: 805-816.

18. Cummins I, Dixon DP, Freitag-Pohl S, Skipsey M, Edwards R (2011) Multiple roles for plant glutathione transferases in xenobiotic detoxification. Drug Metab Rev 43: 266-280.

19. Gianfreda L, Rao MA (2004) Potential of extra cellular enzymes in remediation of polluted soils: a review. Enzyme Microb Technol 35: 339-354.

20. Kuiper I, Lagendijk EL, Bloemberg GV, Lugtenberg BJ (2004) Rhizoremediation: a beneficial plant-microbe interaction. Mol Plant Microbe Interact 17: 6-15.

21. Megharaj M, Ramakrishnan B, Venkateswarlu K, Sethunathan N, Naidu R (2011) Bioremediation approaches for organic pollutants: a critical perspective. Environ Int 37: 1362-1375.

22. Wenzel W (2009) Rhizosphere processes and management in plant-assisted bioremediation (phytoremediation) of soils. Plant Soil 321: 385-408.

23. Ding KQ (2012) Phytoremediation of benzo[a]pyrene-contaminated soil by alfalfa (Medicago sativa L.). Adv Mat Res 518-523: 5559-5564.

24. Chaudhry Q, Blom-Zandstra M, Gupta S, Joner EJ (2005) Utilising the synergy between plants and rhizosphere microorganisms to enhance breakdown of organic pollutants in the environment. Environ Sci Pollut Res Int 12: 34-48.

25. Zhong Y, Wang J, Song Y, Liang Y, Li G (2012) Microbial community and functional genes in the rhizosphere of alfalfa in crude oil-contaminated soil. Front Environ Sci Eng 6: 797-805.

26. Hontzeas N, Zoidakis J, Glick BR, Abu-Omar MM (2004) Expression and characterization of 1-aminocyclopropane-1-carboxylate deaminase from the rhizobacterium Pseudomonas putida UW4: a key enzyme in bacterial plant growth promotion. Biochim Biophys Acta 1703: 11-19.

27. Dams RI, Paton GI, Killham K (2007) Rhizoremediation of pentachlorophenol by Sphingobium chlorophenolicum ATCC 39723. Chemosphere 68: 864-870.

28. Teng Y, Luo Y, Sun X, Tu C, Xu L, et al. (2010) Influence of arbuscular mycorrhiza and Rhizobium on phytoremediation by alfalfa of an agricultural soil contaminated with weathered PCBs: a field study. Int J Phytoremediation 12: 516-533.

29. Joner E, Leyval C (2009) Phytoremediation of organic pollutants using mycorrhizal plants: a new aspect of rhizosphere interactions. In: Sustainable

Citation: Chen J, Xu QX, Su Y, Shi ZQ, Han FX (2013) Phytoremediation of Organic Polluted Soil. J Bioremed Biodeg 4: e132. doi:10.4172/2155-6199.1000e132

Volume 4 • Issue 3 • 1000e132J Bioremed BiodegISSN: 2155-6199 JBRBD, an open access journal

Page 3 of 3

Agriculture. Lichtfouse E, Navarrete M, Debaeke P, Véronique S, Alberola C (Eds). Springer Netherlands. 885-894.

30. Yu XZ, Wu SC, Wu FY, Wong MH (2011) Enhanced dissipation of PAHs from soil using mycorrhizal ryegrass and PAH-degrading bacteria. J Hazard Mater 186: 1206-1217.

31. Wei S, Pan S (2010) Phytoremediation for soils contaminated by phenanthrene and pyrene with multiple plant species. J Soils Sediments 10: 886-894.

32. Sun M, Fu D, Teng Y, Shen Y, Luo Y, Li Z, et al. (2011) In situ phytoremediation of PAH-contaminated soil by intercropping alfalfa (Medicago sativa L.) with tall fescue (Festuca arundinacea Schreb.) and associated soil microbial activity. J Soils Sediments 11: 980-989.

33. Meng L, Qiao M, Arp H (2011) Phytoremediation efficiency of a PAH-contaminated industrial soil using ryegrass, white clover, and celery as mono- and mixed cultures. J Soils Sediments 11: 482-490.

34. Ma TT, Teng Y, Luo YM, Christie P (2012) Legume-grass intercropping phytoremediation of phthalic acid esters in soil near an electronic waste recycling site: a field study. Int J Phytoremediat 15: 154-167.

35. Kawahigashi H (2009) Transgenic plants for phytoremediation of herbicides. Curr Opin Biotechnol 20: 225-230.

36. Van Aken B (2009) Transgenic plants for enhanced phytoremediation of toxic explosives. Curr Opin Biotechnol 20: 231-236.

37. James CA, Strand SE (2009) Phytoremediation of small organic contaminants using transgenic plants. Curr Opin Biotechnol 20: 237-241.

38. Abhilash PC, Jamil S, Singh N (2009) Transgenic plants for enhanced biodegradation and phytoremediation of organic xenobiotics. Biotechnol Adv 27: 474-488.

39. Kumar S, Jin M, Weemhoff JL (2012) Cytochrome P450-mediated phytoremediation using transgenic plants: a need for engineered cytochrome P450 enzymes. J Pet Environ Biotechnol 3: 1000127.

40. Shimazu S, Inui H, Ohkawa H (2011) Phytomonitoring and phytoremediation of agrochemicals and related compounds based on recombinant cytochrome P450s and aryl hydrocarbon receptors (AhRs). J Agric Food Chem 59: 2870-2875.

41. Zhang Y, Liu J (2011) Transgenic alfalfa plants co-expressing glutathione S-transferase (GST) and human CYP2E1 show enhanced resistance to mixed contaminates of heavy metals and organic pollutants. J Hazard Mater 189: 357-362.

42. Wang GD, Li QJ, Luo B, Chen XY (2004) Ex planta phytoremediation of trichlorophenol and phenolic allelochemicals via an engineered secretory laccase. Nat Biotechnol 22: 893-897.

43. Sonoki T, Kajita S, Ikeda S, Uesugi M, Tatsumi K, et al. (2005) Transgenic tobacco expressing fungal laccase promotes the detoxification of environmental pollutants. Appl Microbiol Biotechnol 67: 138-142.

44. Limura Y, Yoshizumi M, Sonoki T, Uesugi M, Tatsumi K, Horiuchi K-i, et al. (2007) Hybrid aspen with a transgene for fungal manganese peroxidase is a potential contributor to phytoremediation of the environment contaminated with bisphenol A. J Wood Sci 53: 541-544.

45. Oller ALW, Agostini E, Talano MA, Capozucca C, Milrad SR, et al. (2005) Overexpression of a basic peroxidase in transgenic tomato (Lycopersicon esculentum Mill. cv. Pera) hairy roots increases phytoremediation of phenol. Plant Sci 169: 1102-1111.

46. Van Dillewijn P, Couselo JL, Corredoira E, Delgado A, Wittich RM, et al. (2008) Bioremediation of 2,4,6-trinitrotoluene by bacterial nitroreductase expressing transgenic aspen. Environ Sci Technol 42: 7405-7410.