Scientifica / 2016 / Article

Review Article | Open Access

Volume 2016 |Article ID 1598325 |

Muhammad Kashif Javaid, Mehrban Ashiq, Muhammad Tahir, "Potential of Biological Agents in Decontamination of Agricultural Soil", Scientifica, vol. 2016, Article ID 1598325, 9 pages, 2016.

Potential of Biological Agents in Decontamination of Agricultural Soil

Academic Editor: Daniel Jun
Received05 Dec 2015
Accepted08 Mar 2016
Published03 May 2016


Pesticides are widely used for the control of weeds, diseases, and pests of cultivated plants all over the world, mainly since the period after the Second World War. The use of pesticides is very extensive to control harm of pests all over the globe. Persistent nature of most of the synthetic pesticides causes serious environmental concerns. Decontamination of these hazardous chemicals is very essential. This review paper elaborates the potential of various biological agents in decontamination of agricultural soils. The agricultural crop fields are contaminated by the periodic applications of pesticides. Biodegradation is an ecofriendly, cost-effective, highly efficient approach compared to the physical and chemical methods which are expensive as well as unfriendly towards environment. Biodegradation is sensitive to the concentration levels of hydrogen peroxide and nitrogen along with microbial community, temperature, and pH changes. Experimental work for optimum conditions at lab scale can provide very fruitful results about specific bacterial, fungal strains. This study revealed an upper hand of bioremediation over physicochemical approaches. Further studies should be carried out to understand mechanisms of biotransformation.

1. Introduction

A pesticide can be defined as any substance or mixture of substances intended for preventing, destroying, repelling, or mitigating any pest (insects, mites, nematodes, weeds, rats, etc.). Pesticides like insecticides, herbicides, fungicides, and various other substances are used to control pests [1]. In modern agriculture practices, the extensive use of pesticides is very frequent to fulfill higher yield requirements. Millions of tons of pesticides are applied annually all over the globe, which covers the billions of dollars’ market. The expenditures on pesticides were 35.8 billion in 2006 which rose up to 39.4 billion US dollars in 2007. Herbicides are most widely used in controlling of pests [2]. One of the primary concerns is to minimize harmful effects caused by the target organisms including viruses, bacteria, fungi, and insects [3]. The extensive use of pesticides causes serious environmental concerns, as only 5% or less from the applied pesticides reach the target organisms which resulted in contamination of soil and water bodies (major environmental problem of current age). The periodic use of pesticides makes the situation particularly perturbing. This repetition in the long term necessarily leads to an accumulation of pesticides and their residues in environment, endangering the entire population by their multifaceted toxicity [4]. There is a direct relationship between the contamination of pesticides and their residual detection [5]. In addition to causing toxic effects to humans, there is a high risk of contamination in ecosystem [6]. An enduring threat of volatilization of sprayed pesticides is present that usually hit (directly) nontarget vegetation. This leads towards contamination of air, soil, and nontarget plants [7]. There are chronic threats to human life, caused by long term, low dose exposure to pesticides. It can cause hormonal disruption, diminished intelligence, and reproductive abnormalities [8]. The constant mobility of applied pesticides through leaching, sorption, and volatilization results in contamination of different levels in the environment (Figure 1) [9, 10].

More than one kind of pesticide is applied for the control of different types of pests, as the classification of these substances can be accomplished on the basis of their use, mode of action, and chemical function. These include insecticides for insects control, fungicides against fungi, rodenticide for rodents, and defoliant for leaf harvesting. There are some classes to which pesticides are classified on the basis of their chemical nature, that is, organochlorides, organophosphates, pyrethroids, and so forth. In present age, more than 500 different formulations of pesticides are used mainly in agricultural tricks. These formulations are in general artificially synthesized substances which are nonbiodegradable and enhance environmental toxicity. These nonbiodegradable compounds persist in agricultural fields after application. About three million people are intoxicated per annum as a result of pesticides usage, reported by the World Health Organization (WHO) [6]. The degradation of persistent pesticides is very essential for decontaminating soil and water bodies [13].

The pesticides degradation processes are of different modes, involved in decontamination of various systems in variable efficiency. The rate of degradation of pesticides is influenced by several factors which include chemical structure of pollutants, pH of soil, concentration of hydrogen peroxide, and concentration of iron. The rate of degradation differs as the pathway of this process changes. Acceleration of degradation processes results in decontamination in short span of time. Thus, photocatalytic degradation, biodegradation, ozonation, and photo-Fenton reactions are commonly evaluated for pesticides removal studies [14]. Microorganisms are present on earth as an uncountable number of species. These microbes are very vital for the bioremediation of pesticides. Endosulfan (pesticide) can be removed from environment by applying strains of microbes (Aspergillus) [15]. The phenomenon of biotransformations is very common and sometimes very essential for the survival of microorganisms, responsible for biodegradation of applied pesticides. There is a natural balance in between microbial evolution and bioremediation [16]. Biodegradation can be approached via microbes and also augmenting this process by artificial means. This approach to environmental decontamination possesses a number of benefits; for example, there is minimum chance of environmental disruption, economical, and fewer chances of secondary exposure alongside not causing damage to ecosystem [17, 18]. The isolation and characterization of microbial strains capable of degrading pesticides and their residues are of interest for the last two decades. In these microbes bacteria and fungi are the major degraders. Molecular probes can be used for the isolation and identification of degrading potential of microbial strains [18]. Ultimately organic matter decomposes as a result of microbial action. There is mismatch in synthetic and natural occurring pesticides so degradation rate differs in both cases, which is slow in case of synthetic pesticides (due to structural variations and less compatibility with metabolic pathways of applied microbes) [19].

Biodegradation methodology is widely used for the treatment of xenobiotics such as pesticides in soil. It is employed in many countries due to its low cost and being ecofriendly [20, 21]. Conventional approaches like land filling, recycling, and incineration are not very efficient and cost-effective. Different types of toxic intermediates are also formed during these processes [22]. In the present review, different approaches for biological degradation of pesticides have been discussed, in addition to analyzing (on the basis of reported literature) various factors affecting these modes of bioremediation.

2. Different Approaches for Biodegradation

Although a number of techniques are available for biodegradation, the ones of utmost importance are discussed here:(i)Bacterial degradation.(ii) Fungal degradation.(iii) Enzymatic degradation.

2.1. Bacterial Degradation

The degradation of pesticides results in the production of carbon dioxide (CO2) and water (H2O) by the oxidation of parent compounds. The bacterium involves in the degradation process energy intake from these degradation products. The efficiency of degradation process depends upon optimum atmospheric conditions, that is, temperature, pH of soil, moisture contents, and so forth. The modifications of different bacterial specimens via genetic mutations also enhance effectiveness of applied microbes. The biodegradable removal of pesticides has positive effects on the fertility of agricultural soil. Chlorpyrifos has a massive effect on contaminating soil and water bodies. Microbial degradation is very useful for the detoxification of such (chloroorganic) pesticides. The specific genes and enzymes are very critical for the cleavage of specific functional groups of the pesticide. The optimization of environmental conditions and an effective microbial community in the contaminated site is very essential for the degradation of pesticides [23].

There is a vital advantage of microorganism usage for degradation of pesticides. This is due to the diversity, wide distribution, and adaptation of variable metabolic pathways. The gene clusters are involved in microbial degradation. The genetic manipulation and construction of gene engineering bacteria are also used for degradation of pesticides [24]. Microbial strain screening and isolation are very effective for degradation of carbendazim in mineral culture medium. Carbendazim is carbon source for the growth of this strain. The pH range, 5.1–8.1, and temperature range, 25–40°C, are optimum for maximum degradation efficiency, that is, up to 90% in nitrogen atmosphere [25]. Pesticide-degrading bacteria and Rhizobium meliloti coating on Medicago sativa seeds are effective for repairing soil, polluted by organic phosphorus pesticide. This approach is very efficient, possessing several advantages, that is, rapid soil repairing rate, simple operation, and high treating capability for removal of organic phosphorus pesticide [26, 27]. Sphingobium japonicum is a strain for degradation of chlorinated pesticides, that is, hexachlorocyclohexane. This strain (Sphingobium japonicum LZ-2) can completely decompose lindane 20 mg/L in 10 hours [28]. An aerobic bacterium (Burkholderia cepacia strain CH-9) can be used for degradation of imidacloprid and metribuzin. 69% degradation of imidacloprid and 86% degradation of metribuzin can be obtained in 20 days with initial dose of 50 mg/L in mineral salt medium [29]. Bifenthrin (BF) is a synthetic pesticide. It is degraded by pyrethroid bacteria (Acinetobacter calcoaceticus). The degradation rate could be achieved up to 56.4% with initial concentration of 100 mg/L with pH range of 6.0–8.0 and 5% inoculation [30].

Streptomycetes strains have enormous applications for degradation of chlorpyrifos (CP) pesticide. The degradation potential of these strains can be evaluated by performing study in agar medium. The pH alterations can affect the efficiency of degradation process [31]. Tert-Bu mercaptan (TMB) undergoes biodegradation in water under aerobic conditions. First-order kinetics are involved in biodegradation process. There is slight increase in rate of reaction by addition of TMB and slight decrease with addition of phenol [32]. Bacterial strains which are capable of degrading methomyl and carbofuran can be studied by high pressure liquid chromatography (HPLC) in biodegradation analysis. Acetonitrile and water were used as mobile phases. The closeness of carbofuran-degrading strains to the genera Flavobacterium and Alcaligenes and that of methomyl degrading strains to genera Pseudomonas and Alcaligenes were observable by using 16S rDNA sequence analysis [33, 34]. Photosynthetic bacterium (GJ-22) is capable of degrading cypermethrin (CMP). That CMP degradation by GJ-22 is very productive at 25–35°C and at pH of 7.0. By performing gas chromatography/mass spectrometry (GC-MS), metabolic products are detected. The degradation of CMP proceeds through oxidative or/and through hydrolytic pathways by GJ-22 yielding 5 metabolites [35]. The removal of organochlorine pesticides from soil is performed by microbial applications under optimum environmental conditions. Better results are obtained by addition of potassium humate for increasing concentration of microorganisms [36]. The strain of Pseudomonas putida and Pseudomonas mendocina has a great capacity of biodegrading permethrin and cypermethrin pesticides. Bioremediation up to 90% can be achieved with the help of these bacterial strains within the period of 15 days [37].

Acinetobacter sp. TW and Sphingomonas sp. TY strains are novel and very useful for the disposal of tobacco waste in the temperature range of 25–37°C and pH range of 7.0–8.0 [38]. The actinomycete strain HP-S-01 is isolated from activated sludge for its application to degrade deltamethrin. The degradation results in 3-phenoxybenzaldehyde as major hydrolysis product. This strain is highly efficient in degrading bifenthrin, fenvalerate, and fenpropathrin. This process undergoes first-order kinetics and provides an effective tool for bioremediation of environmental contamination from pesticides [39]. Diazinon degrading bacteria utilize it as a source of carbon and phosphorus under different culture conditions. The addition of carbon sources, as glucose or succinate, causes decrease in degradation rate [40]. Biodegradation of profenofos is conducted by bacterial strains isolated by enrichment technique. About 90% concentration of profenofos can be degraded in 90 hours [41]. Paracoccus sp. strain is applied for the biodegradation studies of pyridine. It was observed that, at the concentration of pyridine <0.9 mg/L, the rate of degradation is higher while at the concentration >0.9 mg/L the rate is lower [42]. A bacterial consortium which degrades tetrachlorvinphos is isolated from agricultural soil. It is composed of six pure strains. The study reveals that these strains have a potential to degrade organophosphate pesticides [43].

Lactic acid bacteria can degrade organophosphorous insecticides by fermentation. Lactic acid bacteria use organophosphate as a source of carbon and phosphorus [44]. An effective and specific method is bacterial degradation of pyrethroid (a pesticide). Highly efficient bacterial strain of Enterobacter aerogenes can degrade many other pesticides, that is, bifenthrin, cypermethrin, and so forth [45]. Acinetobacter johnsonii (MA-19) strain was used for degradation study of organophosphate pesticides, by enrichment culture method. Four additional compounds were added to enhance efficiency, out of which Na succinate was very effective; by increasing its concentration the rate of degradation of malathion increased [46]. The same methodology was applied to degrade para-nitrophenol by Rhodococcus bacteria. It is an efficient bacterial decomposition method for para-nitrophenol [47]. Similarly, organophosphate pesticides degradation is carried out by using strains Bacillus, Actinobacteria, and L-proteobacteria [48]. Bacterium Bacillus thuringiensis is effective in degrading malathion in minimum salt media. With the addition of glucose and yeast, the growth of bacteria increases up to 105-fold which degrades more than 99% malathion within 30 days. Residues were studied by HPLC and GC-MS [49]. Esbiothrin was degraded with much efficiency by immobilized Acinetobacter on magnetic polyurethane [50]. By using immobilized bacteria on Ca-alginate gel beads, organophosphate insecticide degradation was studied, along with hydrolyzed products [49].

Cyanobacteria and blue green algae convert fenamiphos into number of its stable, nontoxic components by using cultured technique [51]. Indigenous bacteria degrade sumithion OPs through anaerobic decomposition. They decompose them into CH4, N2, CO2, H2S, and so forth [52]. Beans of green coffee can be used for the support and growth of bacteria (Stenotrophomonas maltophilia) which degrade DDT and endosulfan. A medium amended with glucose is used as a supplement [53]. Pseudomonas bacterium can degrade endosulfan. Whenever it bioaccumulates in fishes (Cyprinus carpio), it uses endosulfan as a carbon source [54, 55]. Atrazine is degraded by Pseudomonas bacteria by two-phase biodegradation (unstable degradation products from first step further degrade to secondary components) [14]. Endosulfan is metabolized into endosulfan sulfate, which is the only product of endosulfan metabolism, by bacterial action. It resulted in 50% degradation of endosulfan within three days [56]. A Gram negative bacterial strain (Sphingomonas) possesses high potential for degrading DDT [57]. Microscopic organisms (3 bacterial strains) potentially degrade mefenacet and many other amide pesticides such as propanil and metolachlor by hydrolysis [58].

Different types of pesticides (OPs, chlorinated pesticides, herbicides, and fungicides) are effectively degraded by the fermentation process carried out by Rhodobacter sphaeroides [58]. Screened bacteria are highly selective for the degradation of S-enantiomer of methylaxyl compared to its R-enantiomers at comparatively fast rate [59]. Vibrio and Shewanella bacteria can effectively degrade methyl parathion. Its biodegradation mechanism is entirely different from photocatalytic process [60]. Photosynthetic bacteria have capacity to degrade multiple types of pesticides (chlorpyrifos, phoxim, and triazophos) [61]. Ochrobactrum easily oxidize triazophos into its acidic form. It has the ability to degrade this pesticide up to 95% in crops [62]. Chlorinated pesticides can be degraded by using combination of aerobic-anaerobic decomposition with application of sugar solution. This is one of the very efficient methods for biodegradation of chlorinated pesticides [63]. Allethrin is a pyrethroid insecticide and its degradation is achieved by Acidomonas sp. [64]. Eight bacterial strains potentially degrade PCNP pesticide. Better results were obtained when all these strains were collectively used [65]. Two bacteria cad1 and cad2 degrade cadusafos in mineral salt medium with nitrogen (MSMN). They are also able to degrade ethoprophos nematicide completely [66].

Immobilized bacteria have capacity to degrade multiple pesticides (herbicides, fungicides, and carbamates) under different environmental conditions with different flow rates [67]. S-25 strain caused degradation (almost 100%) of 2,4-D organochlorine pesticide at optimum conditions, that is, temperature of 30°C and pH of 7.0 [68]. Aldrin (an organochlorine insecticide) is anaerobically degraded by microorganisms. These microorganisms used extracted yeast as carbon source [69]. Ethion (OPs) is anaerobically degraded by mesophilic bacteria. Other species are also capable of its degradation like Azospirillum and Pseudomonas [70]. Bacterial consortium, like Bacillus sp. and Chryseobacterium joostei, was used to compare biodegradation of lindane, methyl parathion, and carbofuran in individual and mixed pesticide enriched cultures by using biokinetic parameters. These bacteria use pesticide in their cometabolic pathways [71]. Psychrotrophic bacterium can degrade Me-parathion. This biodegradation is sensitive to pH and temperature variations [72]. Six genera are able to degrade organochloride pesticides, that is, endosulfan. Different genera have different potential to degrade them, from which Micrococcus and Pseudomonas were highly active compared to others [73]. Immobilized Escherichia coli (a well-known bacterium) could degrade organochlorine insecticide that contains ester bond [74].

The same bacterium is highly efficient in degrading a number of pesticides including BHC, DDT, endosulfan, HCH isomers, and 2,4-D [7580]. DLL-1 bacterial strain biologically degrades pesticide that is present in soil and plant system [81]. Growth promoting rhizobacteria (GPRB) strains are effective in degrading fungicide and herbicide compared to Azotobacter and bacilli. The purpose was to determine the capacity of different bacteria to effectively degrade fungicides and herbicides [82].

2.2. Fungal Degradation

Fungi, from natural sources, can be screened out as an effective tool for biodegradation of toxic organic chemicals. A fungal strain Fusarium verticillioides is able to use lindane as a carbon and energy source under aerobic conditions. This strain can be isolated from Agave tequilana leaves by enrichment techniques. In the presence of limited nitrogen and phosphorus atmosphere, the efficiency in terms of higher degradation is achieved. The environmental factors and concentration of lindane and yeast extract improved the efficiency of the biodegradation process [83, 84]. There is a great potential of fungal strains, that is, Fusarium oxysporum, Lentinula edodes, Penicillium brevicompactum, and Lecanicillium saksenae, for the biodegradation of the pesticides like terbuthylazine, difenoconazole, and pendimethalin in batch liquid cultures. These fungal strains are investigated to be valuable as active microorganisms for pesticides degradation [85]. Nonacclimated mixed culture of bacteria and white-rot fungus has applications for biodegradation of aldicarb, atrazine, and alachlor from the liquid phase, respectively. With incubation period of 14 days, mixed culture achieved 47, 98, and 62% removal, respectively. The removal of these pesticides is accompanied by phenomena of biosorption and biodegradation [86].

Methomyl and diazinon (pesticides) are biodegradable with the help of rot fungi isolates from contaminated soil. The optimum temperature for maximum efficiency is 28°C. The rate of degradation is higher by using mixture of fungal strains [87]. Different fungal strains are observed for their degradation ability of DDD pesticide. The accumulation of these strains shows characteristic pattern for degrading process [88]. Endosulfan-degrading, aerobic fungal strains are effective for soil contaminated with organochlorine pesticides. These strains (Mortierella sp. strains W8 and Cm1-45) resulted in 50–70% degradation in 28 days at 25°C. The diol formation of endosulfan firstly and then endosulfan lactone conversion take place during degradation. This enhances fertility of agriculture land [89]. On similar basis, there is possibility of degrading mixed insecticides (DDT and chlorpyrifos) by using mixed fungal strains. When low concentration of mixed insecticides was used, the efficiency of degradation is observed to be high. The efficiency is observed in 26.94% and 24.94% degradation of DDT and chlorpyrifos, respectively [90]. Under harsh conditions, Sphingomonas yanoikuyae strain can degrade carbamate and pyrethrin (OPs) with high efficiency in enrichment culture method, analyzed by gas chromatography [91]. Salt resistant actinomycete is capable of degrading carbofuran. One of seven actinomycetes, S. alanosinicus, is most effective and gives up to 95% degradation. It uses carbofuran as a carbon source and is applicable to saline soils for its efficiency [92].

Water body and soil that are affected by endosulfan can easily be bioremediated by fungal strain (Aspergillus niger). The chlorinated pesticide endosulfan is metabolized through various intermediates by this fungus [15]. More than 30 microorganisms are capable of degrading the pesticides, out of which Gliocladium genus has maximum activity for selectively degrading carbofuran [93]. Fungus uses chlorpyrifos as a carbon and energy source and causes its rapid degradation. Another fungus, basidiomycetes, degrades chlorpyrifos very effectively [94]. A fungus, C. elegans, degrades DEET, an insecticide, into different less toxic metabolites analyzed by HPLC-MS [95]. Phytopathogenic fungi easily degrade herbicides. This fungus easily grows up on organophosphonate herbicides and degrades them [96]. Trichoderma viride and T. harzianum have high potential to degrade pirimicarb. Degradation capacity increases when activated charcoal is added [97].

2.3. Enzymatic Degradation

Enzymes produced during different metabolic pathways in plants as well as in microbes present in soil are the key for bioremediation of pesticides. Optimum environmental conditions support fast rate of removal of toxic intermediates. The engineered bacteria were used to produce esterase gene which specifically act on substrate and degrade more than 65% methyl parathion within 3 hours [98]. Carbofuran, an insecticide present in contaminated soil, can be treated with Paracoccus sp. YM3, by MSM method, which enzymatically degrades carbofuran into its metabolites which were analyzed by HPLC. This bacterium uses carbofuran as sole source of carbon [99]. Genetically modified Escherichia coli enzymatically degrade methyl parathion and many other OPs, that is, PNP, which is detected by HPLC [100]. Micrococcus sp. has been found to have versatile ability to degrade OPs pesticide like cypermethrin by enzymatic action [101]. Lindane is degraded by fungus Conidiobolus through enzyme action. GC-ECD and GC/MS confirm that there is no metabolite; this proved that lindane is completely degraded by this fungus [102]. In a study of atrazine (AT) and alachlor (AL), their degradation by treating them with extracellular enzyme extracted from fungi was determined [103]. FDS-1 strain of Burkholderia sp. can degrade nitrophenyl enzymatically at 30°C and pH of 7.0 taken as optimized conditions [104]. Strains of genetically modified bacteria contain enzymes, which potentially can degrade number of pesticides including OPs, carbamates, and pyrethroids [105].

A study revealed that different enzymes specifically degrade different pesticides (OPs) in wheat kernels [106]. Thirty fungal strains were used to investigate degradation rate of Diuron and pyrithiobac-sodium. Results suggested that the highest degrading rate was by ligninolytic enzymes [107]. Enterobacter enzymatically degrades chlorpyrifos and many other OPs. It degrades them and uses them as carbon and phosphorus source (sole source) [108]. Some Gram negative bacteria have ability to degrade dimethoate. They use it as a sole source of carbon. Bacteria hydrolyze insecticide by using different enzymes, namely, phosphatases and esterases [109]. More than 15 fungal strains were capable of degrading different OPs up to 96% by enzyme catalyzed pathways [110]. Enzymes for the degradation of organochlorinated pesticide are mainly dehydrochlorination enzymes, hydrolytic enzymes, and dehydrogenases. The genes related are Lin family genes with typical functional codes. Further research could be an effective tool for removal of these pesticides [111]. The amino acid sequence of phosphotriesterase mutant is very effective for the application in organophosphorus pesticide degradation [112].

3. Conclusion

Decontamination, caused by pesticides usage, of polluted areas is the need of modern age. The applications of conventional means, that is, physicochemical methods, for the degradation of toxic chemicals are not very efficient. These methods are expensive and also not friendly to ecosystem. For the degradation of pesticides and ultimate decontamination of polluted areas, biodegradation is becoming a method of choice. For the removal of hazardous chemicals from environment, the usage of biological agents (bacteria, fungi, and enzymes) is very efficient as they are cost-effective as well as ecofriendly. These biological agents have a potential to decompose pesticides into their less toxic byproducts. There is a need of further study for the investigation of mechanisms of microorganisms and their enzymes during degradation process. The understanding of enzymatic actions, especially concepts related to pesticides mechanism of action, resistance, selectivity, tolerance, and environmental fate, has a vital impact on the knowledge of pesticide science and biological applications.

Competing Interests

The authors declare that there are no competing interests regarding the publication of this paper.

Authors’ Contributions

Muhammad Kashif Javaid, Mehrban Ashiq, and Muhammad Tahir contributed equally to this publication.


The authors wish to thank Dr. Muhammad Danish and Dr. Muhammad Waseem Mumtaz for their valuable support, University of Gujrat for providing lab facilities, and Higher Education Commission of Pakistan for Scholarship, PIN: 117-5254-PS7-150.


  1. EPA, “What is a Pesticide,” April 2015, View at: Google Scholar
  2. EPA, “Pesticides industry, sales and usage,” April 2015, View at: Google Scholar
  3. Y.-H. Liu, Y.-C. Chung, and Y. Xiong, “Purification and characterization of a dimethoate-degrading enzyme of Aspergillus niger ZHY256, isolated from sewage,” Applied and Environmental Microbiology, vol. 67, no. 8, pp. 3746–3749, 2001. View at: Publisher Site | Google Scholar
  4. M. Bouziani, “L'usage immodéré des pesticides. De graves conséquences sanitaires,” Le Guide de la Médecine et de la Santé, Santémaghreb, 2007. View at: Google Scholar
  5. A. Calderbank, “The occurrence and significance of bound pesticide residues in soil,” Reviews of Environmental Contamination and Toxicology, vol. 108, pp. 71–103, 1989. View at: Google Scholar
  6. M. M. Veiga, D. M. Silva, L. B. E. Veiga, and M. V. de Castro Faria, “Pesticide pollution in water systems in a small rural community in Southeast Brazil,” Cadernos de Saúde Pública, vol. 22, no. 11, pp. 2391–2399, 2006. View at: Publisher Site | Google Scholar
  7. J. Johnson and W. G. Ware, Pesticide Litigation Manual 1992 Edition, Clark Boardman Callaghan Environmental Law Series, New York, NY, USA, 1992.
  8. P. K. Gupta, “Pesticide exposure—Indian scene,” Toxicology, vol. 198, no. 1–3, pp. 83–90, 2004. View at: Publisher Site | Google Scholar
  9. V. Andreu and Y. Picó, “Determination of pesticides and their degradation products in soil,” TrAC—Trends in Analytical Chemistry, vol. 23, no. 10-11, pp. 772–789, 2004. View at: Publisher Site | Google Scholar
  10. A. Nawab, A. Aleem, and A. Malik, “Determination of organochlorine pesticides in agricultural soil with special reference to γ-HCH degradation by Pseudomonas strains,” Bioresource Technology, vol. 88, no. 1, pp. 41–46, 2003. View at: Publisher Site | Google Scholar
  11. M. Ashiq, M. Danish, and M. W. Mumtaz, “Particulate matter as potential outdoor pollutant of ambient environment,” Journal of Environmental Monitoring, vol. 12, no. 7-8, pp. 4–9, 2012. View at: Google Scholar
  12. M. W. Bashir, M. Ashiq, M. Y. Saddique, M. F. Mukhtar, A. Hassan, and S. U. Islam, “Indoor particulate matter and its characteristics challenging for environmental remediation,” International Journal of Ecological Science and Environmental Engineering, vol. 2, no. 6, pp. 48–51, 2015. View at: Google Scholar
  13. G. Hodaifa, L. M. Nieto, and M. S. Casanova, “Elimination of pesticide residues from virgin olive oil by ultraviolet light: preliminary results,” Journal of Hazardous Materials, vol. 168, no. 1, pp. 555–559, 2009. View at: Publisher Site | Google Scholar
  14. A. Wyss, J. Boucher, A. Montero, and I. Marison, “Micro-encapsulated organic phase for enhanced bioremediation of hydrophobic organic pollutants,” Enzyme and Microbial Technology, vol. 40, no. 1, pp. 25–31, 2006. View at: Publisher Site | Google Scholar
  15. T. S. Bhalerao and P. R. Puranik, “Biodegradation of organochlorine pesticide, endosulfan, by a fungal soil isolate, Aspergillus niger,” International Biodeterioration and Biodegradation, vol. 59, no. 4, pp. 315–321, 2007. View at: Publisher Site | Google Scholar
  16. E. Hodgson, R. M. Roe, D. K. S. Goh, G. C. Rock, and R. L. Rose, “Insect cytochrome P-450: metabolism and resistance to insecticides,” Biochemical Society Transactions, vol. 21, no. 4, pp. 1060–1065, 1993. View at: Publisher Site | Google Scholar
  17. R. E. Hinchee, D. B. Anderson, F. B. Metting Jr., and G. D. Sayles, Applied Biotechnology for Site Remediation, Lewis, Chelsea, Mich, USA, 1994.
  18. G. R. Chaudhry, Biological Degradation and Bioremediation of Toxic Chemicals, Dioscorides Press, Warsaw, Poland, 1994.
  19. R. M. Surekha, P. K. L. Lakshmi, and D. Suvarnalatha, “Isolation and characterization of a chlorpyrifos degrading bacterium from agricultural soil and its growth response,” African Journal of Microbiology, vol. 2, pp. 26–31, 2008. View at: Google Scholar
  20. G. Enrica, “The role of Microorganisms in environmental decontamination,” in Contaminants in the Environment: A Multidisciplinary Assessment of Risks to Man and Other Organisms, A. Renzoni, Ed., vol. 25, pp. 235–246, Lewis Publishers, Boca Raton, Fla, USA, 1994. View at: Google Scholar
  21. B. E. Ritmann, D. E. Jacson, and S. L. Storck, “Potential for treatment of hazardous organic chemicals with biological Process,” Biotreatment Systems, vol. 3, pp. 15–64, 1988. View at: Google Scholar
  22. G. S. Sayler, S. W. Hooper, A. C. Layton, and J. M. H. King, “Catabolic plasmids of environmental and ecological significance,” Microbial Ecology, vol. 19, no. 1, pp. 1–20, 1990. View at: Publisher Site | Google Scholar
  23. Z. Chishti, S. Hussain, K. R. Arshad, A. Khalid, and M. Arshad, “Microbial degradation of chlorpyrifos in liquid media and soil,” Journal of Environmental Management, vol. 114, pp. 372–380, 2013. View at: Publisher Site | Google Scholar
  24. Z.-l. Cui, L.-x. Cui, Y. Huang, X. Yan, J. He, and S.-p. Li, “Advances and application of microbial degradation in pesticides pollution remediation,” Nanjing Nongye Daxue Xuebao, vol. 35, no. 5, pp. 93–102, 2012. View at: Google Scholar
  25. L. S. Tian and F. Chen, “Biological characteristics and degradation performance of a degrading strain,” Yangzhou Daxue Xuebao, vol. 33, no. 1, pp. 86–90, 2012. View at: Google Scholar
  26. J. Jiang, B. Yang, F. Fan et al., “Method for using alfalfa-organophosphorus pesticide degradation bacteria to jointly renovate organophosphorus pesticide contaminated soil,” Faming Zhuanli Shenqing, CN 102755991 B, 2012. View at: Google Scholar
  27. P. Zhao, Q. Wen-jing, Y. Wang et al., “Isolation and identification of two strains capable of degrading of organophosphorus pesticides and their biodegradation abilities,” Lanzhou LigongDaxue Xuebao, vol. 36, no. 3, pp. 86–90, 2012. View at: Google Scholar
  28. Z. Liu, C. Yang, and Ch.-L. Qiao, “Biodegradation of p-nitrophenol and 4-chlorophenol by Stenotrophomonas sp,” FEMS Microbiology Letters, vol. 277, no. 2, pp. 150–156, 2007. View at: Publisher Site | Google Scholar
  29. G. Madhuban, D. Debashis, and S. K. Das, “Biodegradation of imidacloprid and metribuzin by Burkholderia cepacia strain CH9,” Pesticide Research Journal, vol. 23, no. 1, pp. 36–40, 2011. View at: Google Scholar
  30. L. Tingting, D. Kunming, L. Miao et al., “Isolation, identification and biodegradation characteristics of a bacterial strain able to degrade bifenthrin,” Nongye Huanjing KexueXuebao, vol. 31, no. 6, pp. 1147–1152, 2012. View at: Google Scholar
  31. G. Briceño, M. S. Fuentes, G. Palma, M. A. Jorquera, M. J. Amoroso, and M. C. Diez, “Chlorpyrifos biodegradation and 3,5,6-trichloro-2-pyridinol production by actinobacteria isolated from soil,” International Biodeterioration and Biodegradation, vol. 73, pp. 1–7, 2012. View at: Publisher Site | Google Scholar
  32. R. Karthikeyan and S. L. Hutchinson, “Biodegradation of tertiary butyl mercaptan in water,” Journal of Bioremediation and Biodegradation, vol. 3, no. 6, p. 156, 2012. View at: Publisher Site | Google Scholar
  33. O. K. Mbogo, G. Magoma, K. Ngamau et al., “Characterization of methomyl and carbofuran degrading-bacteria from soils of horticultural farms in Rift Valley and Central Kenya,” African Journal of Environmental Science and Technology, vol. 6, no. 2, pp. 104–114, 2012. View at: Google Scholar
  34. S. Kumar, A. Anthonisamy, and S. Arunkumar, “Biodegradation of methyl parathion and endosulfan using: Pseudomonas aeruginosa and Trichodermaviridae,” Journal of Environmental Science and Engineering, vol. 53, no. 1, pp. 115–122, 2011. View at: Google Scholar
  35. L. Yin, X. Li, Y. Liu, D. Zhang, S. Zhang, and X. Luo, “Biodegradation of cypermethrin by rhodopseudomonas palustris GJ-22 isolated from activated sludge,” Fresenius Environmental Bulletin A, vol. 21, no. 2, pp. 397–405, 2012. View at: Google Scholar
  36. A. Soromotin, L. Ogurtsova, T. Morozova, and E. B. Zhdanova, “Method of microbiological degradation of organochlorine pesticides,” Russian Patent 2448786, 2012. View at: Google Scholar
  37. J. C. Mendoza, Y. Perea, and J. A. Salvador, “Bacterial biodegradation of permetrina and cipermetrina pesticides in a culture assemblage,” Avances en Ciencias e Ingenieria, vol. 2, no. 3, pp. 45–55, 2011. View at: Google Scholar
  38. M. Wang, G. Yang, X. Wang, Y. Yao, H. Min, and Z. Lu, “Nicotine degradation by two novel bacterial isolates of Acinetobacter sp. TW and Sphingomonas sp. TY and their responses in the presence of neonicotinoid insecticides,” World Journal of Microbiology and Biotechnology, vol. 27, no. 7, pp. 1633–1640, 2011. View at: Publisher Site | Google Scholar
  39. S. Chen, K. Lai, Y. Li, M. Hu, Y. Zhang, and Y. Zeng, “Biodegradation of deltamethrin and its hydrolysis product 3-phenoxybenzaldehyde by a newly isolated Streptomyces aureus strain HP-S-01,” Applied Microbiology and Biotechnology, vol. 90, no. 4, pp. 1471–1483, 2011. View at: Publisher Site | Google Scholar
  40. A. E. Abo-Amer, “Biodegradation of diazinon by Serratia marcescens DI101 and its use in bioremediation of contaminated environment,” Journal of Microbiology and Biotechnology, vol. 21, no. 1, pp. 71–80, 2011. View at: Publisher Site | Google Scholar
  41. S. Malghani, N. Chatterjee, H. X. Yu, and Z. Luo, “Isolation and identification of profenofos degrading bacteria,” Brazilian Journal of Microbiology, vol. 40, no. 4, pp. 893–900, 2009. View at: Publisher Site | Google Scholar
  42. L. Qiao and J. Wang, “Biodegradation characterization of a pyridine-degrading strain,” Qinghua Daxue Xuebao, vol. 50, no. 6, pp. 869–872, 2010. View at: Google Scholar
  43. M. Ortiz-Hernandez and E. Sanchez-Salinas, “Biodegradation of the organophosphate pesticide tetrachlorvinphos by bacteria isolated from agricultural soil in Mexico,” Revista Internacional de Contaminacion Ambiental, vol. 26, no. 1, pp. 27–38, 2010. View at: Google Scholar
  44. C. M. Kye, M. Reukaradhya, K. Islam et al., “Biodegradation of chlorpyrifos by lactic acid bacteria during kimchi fermentation,” Journal of Agriculture and Food Chemistry, vol. 57, no. 5, pp. 1882–1889, 2009. View at: Publisher Site | Google Scholar
  45. M. Lio and X. Xie, “Application of enterobacteraerogenes in degrading pyrethroid pesticide residue, and preparation with enterobacteraerogenes,” Faming Zhuanli Shenqing, CN102021135 A, 2009. View at: Google Scholar
  46. S. Xie, J. Liu, L. Li, and C. Qiao, “Biodegradation of malathion by Acinetobacter johnsonii MA19 and optimization of cometabolism substrates,” Journal of Environmental Sciences, vol. 21, no. 1, pp. 76–82, 2009. View at: Publisher Site | Google Scholar
  47. J. Zhang, Z. Sun, Y. Li, X. Peng, W. Li, and Y. Yan, “Biodegradation of p-nitrophenol by Rhodococcus sp. CN6 with high cell surface hydrophobicity,” Journal of Hazardous Materials, vol. 163, no. 2-3, pp. 723–728, 2009. View at: Publisher Site | Google Scholar
  48. A. Sabdono and O. K. Radjasa, “Phylogenetic diversity of organophosphorous pesticide-degrading coral bacteria from Mid-West Coast of Indonesia,” Biotechnology, vol. 7, no. 4, pp. 694–701, 2008. View at: Publisher Site | Google Scholar
  49. K. Zeinat, A. H. Nashwa, and M. Ibrahim, “Biodegradation and detoxification of malathion by of bacillus thuringiensis MOS-5,” Australian Journal of Basic and Applied Sciences, vol. 2, no. 3, pp. 724–732, 2008. View at: Google Scholar
  50. J. Ha, C. R. Engler, and J. R. Wild, “Biodegradation of coumaphos, chlorferon, and diethylthiophosphate using bacteria immobilized in Ca-alginate gel beads,” Bioresource Technology, vol. 100, no. 3, pp. 1138–1142, 2009. View at: Publisher Site | Google Scholar
  51. T. P. Cáceres, M. Megharaj, and R. Naidu, “Biodegradation of the pesticide fenamiphos by ten different species of green algae and cyanobacteria,” Current Microbiology, vol. 57, no. 6, pp. 643–646, 2008. View at: Publisher Site | Google Scholar
  52. P. W. Savadogo, A. Savadogo, A. S. Ouattara, M. P. Sedogo, and A. S. Traoré, “Anaerobic biodegradation of sumithion an organophosphorus insecticide used in Burkina Faso agriculture by acclimatized indigenous bacteria,” Pakistan Journal of Biological Sciences, vol. 10, no. 11, pp. 1896–1905, 2007. View at: Publisher Site | Google Scholar
  53. B. E. Barragán-Huerta, C. Costa-Pérez, J. Peralta-Cruz, J. Barrera-Cortés, F. Esparza-García, and R. Rodríguez-Vázquez, “Biodegradation of organochlorine pesticides by bacteria grown in microniches of the porous structure of green bean coffee,” International Biodeterioration and Biodegradation, vol. 59, no. 3, pp. 239–244, 2007. View at: Publisher Site | Google Scholar
  54. V. Prabakaran and A. Peterson, “Effect of Pseudomonas on biodegradation of pesticide in the fish Cyprinus carpio,” Journal of Ecotoxicology and Environmental Monitoring, vol. 16, no. 5, pp. 475–479, 2006. View at: Google Scholar
  55. V. Prabakaran and A. Peterson, “Effect of Pseudomonas on biodegradation of pesticide in the fish Cyprinus carpio,” Journal of Ecotoxicology and Environmental Monitoring, vol. 16, no. 5, pp. 459–464, 2006. View at: Google Scholar
  56. H. M. Shivaramaiah and I. R. Kennedy, “Biodegradation of endosulfan by a soil bacterium,” Journal of Environmental Science and Health Part B: Pesticides, Food Contaminants, and Agricultural Wastes, vol. 41, no. 6, pp. 895–905, 2006. View at: Publisher Site | Google Scholar
  57. L. Shunpeng and Z. Mingxing, “Sphingomonas strain for degrading chlorophenothane pesticide residue and bacteria agent containing this strain,” Faming Zhuanli Shenqing Gongkai Shuomingshu, 2006. View at: Google Scholar
  58. N. Harada, K. Takagi, A. Harazono, K. Fujii, and A. Iwasaki, “Isolation and characterization of microorganisms capable of hydrolysing the herbicide mefenacet,” Soil Biology and Biochemistry, vol. 38, no. 1, pp. 173–179, 2006. View at: Publisher Site | Google Scholar
  59. C. Shengwen, L. Weiping, and Z. Anping, “Enantioselective biodegradation of metalaxyl by sewage sludge and screening bacteria,” in Proceedings of the 231st ACS National Meeting, Abstracts of Papers, Atlanta, Ga, USA, March 2006. View at: Google Scholar
  60. J. Liu, L. Wang, L. Zheng, X. Wang, and F. S. C. Lee, “Analysis of bacteria degradation products of methyl parathion by liquid chromatography/electrospray time-of-flight mass spectrometry and gas chromatography/mass spectrometry,” Journal of Chromatography A, vol. 1137, no. 2, pp. 180–187, 2006. View at: Publisher Site | Google Scholar
  61. D. Zhang, T. Xinqiu, and L. Xiangwen, “Isolation of photosynthetic bacteria HP-1 with degradation of organicphosphorus insecticides and studies on its biodegradation ability and capacity of increasing growth,” Shengming Kexue Yanjiu, vol. 9, no. 3, pp. 247–253, 2005. View at: Google Scholar
  62. L. Shunpeng and L. Z. Shen, “Pseudomonas putida and its bacterial products for degrading organophosphorus pesticide residues,” Faming Zhuanli Shenqing Gongkai Shuomingshu, 2005. View at: Google Scholar
  63. D. K. Li and K. W. Rutherford, “In situ anaerobic-aerobic process for the biodegradation of chlorinated pesticides in soil: in situ and on-site bioremediation,” in Proceedings of the 8th International In Situ and On-Site Bioremediation Symposium, Baltimore, Md, USA, June 2005. View at: Google Scholar
  64. M. Paingankar, M. Jain, and D. Deobagkar, “Biodegradation of allethrin, a pyrethroid insecticide, by an Acidomonas sp.,” Biotechnology Letters, vol. 27, no. 23-24, pp. 1909–1913, 2005. View at: Publisher Site | Google Scholar
  65. L. Ning, C. Jing-ying, and L. Li, “Isolation and selection of strains used to degrade organic PCNB pesticides and their application effects,” Jilin Nongye Daxue Xuebao, vol. 27, no. 2, pp. 205–208, 2005. View at: Google Scholar
  66. D. G. Karpouzas, A. Fotopoulou, U. Menkissoglu-Spiroudi, and B. K. Singh, “Non-specific biodegradation of the organophosphorus pesticides, cadusafos and ethoprophos, by two bacterial isolates,” FEMS Microbiology Ecology, vol. 53, no. 3, pp. 369–378, 2005. View at: Publisher Site | Google Scholar
  67. A. Pattanasupong, H. Nagase, M. Inoue et al., “Biodegradation of persistent pesticides by immobilized microbial consortia for use in paddy fields,” Biotechnology for Sustainable Utilization of Biological Resources in the Tropics, vol. 17, pp. 421–425, 2004. View at: Google Scholar
  68. A. Pattanasupong, H. Nagase, M. Inoue et al., “Ability of a microbial consortium to remove pesticide, carbendazim and 2,4-dichlorophenoxyacetic acid,” World Journal of Microbiology and Biotechnology, vol. 20, no. 5, pp. 517–522, 2004. View at: Publisher Site | Google Scholar
  69. W. Guohui, Selection of High Efficient Degrading Strains and Study on Its Degrading Capability, vol. 8, Huanjing Baohu, Beijing, China, 2004.
  70. X. Zhang, W. Wu, Y. Zhang et al., “Screening of efficient hydrocarbon-degrading strains and study on influence factors of degradation of refinery oily sludge,” Industrial and Engineering Chemistry Research, vol. 46, no. 26, pp. 8910–8917, 2007. View at: Publisher Site | Google Scholar
  71. L. J. R. Foster, B. H. Kwan, and T. Vancov, “Microbial degradation of the organophosphate pesticide,” FEMS Microbiology Letters, vol. 240, no. 1, pp. 49–53, 2004. View at: Publisher Site | Google Scholar
  72. K. R. Krishna and L. Philip, “Biodegradation of mixed pesticides by mixed pesticide enriched cultures,” Journal of Environmental Science and Health—Part B: Pesticides, Food Contaminants, and Agricultural Wastes, vol. 44, no. 1, pp. 18–30, 2009. View at: Publisher Site | Google Scholar
  73. H. Li, W. Liang, X. Wu, and Y. Liu, “Research on biodegradation of organophosphorus insecticide by a novel psychrotrophic bacterium SA-8,” Zhongshan Daxue Xuebao, Ziran Kexueban, vol. 43, no. 3, pp. 131–132, 2004. View at: Google Scholar
  74. A. Singh, J. A. Ranjit, P. Dhasarathan et al., “Isolation and characterization of pesticide metabolizing bacteria from groundnut soil system,” Asian Journal of Microbiology, Biotech and Environmental Science, vol. 5, no. 3, pp. 323–332, 2003. View at: Google Scholar
  75. C.-L. Qiao, Y.-C. Yan, H. Y. Shang, X. T. Zhou, and Y. Zhang, “Biodegradation of pesticides by immobilized recombinant Escherichia coli,” Bulletin of Environmental Contamination and Toxicology, vol. 71, no. 2, pp. 370–374, 2003. View at: Publisher Site | Google Scholar
  76. U. S. Gupta, “Biodegradation of chlorinated hydrocarbon insecticide by Pseudomonas species,” Himalayan Journal of Environmental and Zoology, vol. 19, no. 1, pp. 1–10, 2005. View at: Google Scholar
  77. L. Shun-Peng, Z. Ruifu, J. Jian-Dong et al., “Ochrobactrum MP-4 and its products for degrading residues of triazophos-based pesticide,” in Faming Zhuanli Shenqing Gongkai Shuomingshu, 2005. View at: Google Scholar
  78. P. Chaudhary, M. Kumar, B. S. Khangarot, and A. Kumar, “Degradation and detoxification of hexachlorocyclohexane isomers by Pseudomonas aeruginosa ITRC-5,” International Biodeterioration and Biodegradation, vol. 57, no. 2, pp. 107–113, 2006. View at: Publisher Site | Google Scholar
  79. G. Santacruz, E. R. Bandala, and L. G. Torres, “Chlorinated pesticides (2,4-D and DDT) biodegradation at high concentrations using immobilized Pseudomonas fluorescens,” Journal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes, vol. 40, no. 4, pp. 571–583, 2005. View at: Publisher Site | Google Scholar
  80. W. Xue-Dong, O. Xiao-Ming, W. Hui-Li et al., “Optimized cultivation of highly-efficient bacterial strains and their biodegradation ability towards imazapyr,” Nongye Huanjing Kexue Xuebao, vol. 22, no. 1, pp. 102–105, 2003. View at: Google Scholar
  81. L. Yu-Suo, X. Yi-Gang, S. Li-Li et al., “Study on biodegradation and removal of pesticide residue in soil and plant system,” Nongye Huanjing Kexue Xuebao, vol. 22, no. 2, pp. 221–223, 2003. View at: Google Scholar
  82. M. Atia, N. M. Awad, and A. Z. Turky, “Associative action of growth promoting Rhizobacteria and phytoremediationon the biodegradation of certain pesticides in soil,” Bulletin of the National Research Centre Egypt, vol. 27, no. 4, pp. 469–480, 2002. View at: Google Scholar
  83. F. D. M. Guillén-Jiménez, E. Cristiani-Urbina, J. C. Cancino-Díaz, J. L. Flores-Moreno, and B. E. Barragán-Huerta, “Lindane biodegradation by the Fusarium verticillioides AT-100 strain, isolated from Agave tequilana leaves: kinetic study and identification of metabolites,” International Biodeterioration and Biodegradation, vol. 74, pp. 36–47, 2012. View at: Publisher Site | Google Scholar
  84. A. P. Pinto, C. Serrano, T. Pires et al., “Degradation of terbuthylazine, difenoconazole and pendimethalin pesticides by selected fungi cultures,” Science of the Total Environment, vol. 435-436, pp. 402–410, 2012. View at: Publisher Site | Google Scholar
  85. F. I. Hai, O. Modin, K. Yamamoto, K. Fukushi, F. Nakajima, and L. D. Nghiem, “Pesticide removal by a mixed culture of bacteria and white-rot fungi,” Journal of the Taiwan Institute of Chemical Engineers, vol. 43, no. 3, pp. 459–462, 2012. View at: Publisher Site | Google Scholar
  86. W. O. Nyakundi, G. Magoma, J. Ochora, and A. B. Nyende, “Biodegradation of diazinon and methomyl pesticides by white rot fungi from selected horticultural farms in rift valley,” Journal of Applied Technology in Environmental Sanitation, vol. 1, no. 2, pp. 107–124, 2011. View at: Google Scholar
  87. V. Sagar and D. P. Singh, “Biodegradation of lindane pesticide by non white- rots soil fungus Fusarium sp,” World Journal of Microbiology and Biotechnology, vol. 27, no. 8, pp. 1747–1754, 2011. View at: Publisher Site | Google Scholar
  88. S. N. Ortega, M. Nitschke, A. M. Mouad et al., “Isolation of Brazilian marine fungi capable of growing on DDD pesticide,” Biodegradation, vol. 22, no. 1, pp. 43–50, 2011. View at: Publisher Site | Google Scholar
  89. R. Kataoka, K. Takagi, and F. Sakakibara, “A new endosulfan-degrading fungus, Mortierella species, isolated from a soil contaminated with organochlorine pesticides,” Journal of Pesticide Science, vol. 35, no. 3, pp. 326–332, 2010. View at: Publisher Site | Google Scholar
  90. G. Kulshrestha and A. Kumari, “Simultaneous degradation of mixed insecticides by mixed fungal culture isolated from sewage sludge,” Journal of Agricultural and Food Chemistry, vol. 58, no. 22, pp. 11852–11856, 2010. View at: Publisher Site | Google Scholar
  91. Z. C. Ouyang, Y. H. Wang, X. N. Li et al., “Test of pesticide degradability by Sphingomonas yanoikuyae XJ strain,” Huanan Nongye Daxue Xuebao, vol. 29, no. 2, pp. 47–49, 2008. View at: Google Scholar
  92. V. V. Chougale and A. M. Deshmukh, “Biodegradation of carbofuran pesticide by saline soil actinomycetes,” Asian Journal of Microbiology, Biotechnology and Environmental Sciences, vol. 9, no. 4, pp. 1057–1061, 2007. View at: Google Scholar
  93. M. Slaoui, M. Ouhssine, E. Berny, and M. Elyachioui, “Biodegradation of the carbofuran by a fungus isolated from treated soil,” African Journal of Biotechnology, vol. 6, no. 4, pp. 419–423, 2007. View at: Google Scholar
  94. Y. L. Yu, H. Fang, X. Wang, X. M. Wu, M. Shan, and J. Q. Yu, “Characterization of a fungal strain capable of degrading chlorpyrifos and its use in detoxification of the insecticide on vegetables,” Biodegradation, vol. 17, no. 5, pp. 487–494, 2006. View at: Publisher Site | Google Scholar
  95. J. Seo, Y.-G. Lee, S.-D. Kim, C.-J. Cha, J.-H. Ahn, and H.-G. Hur, “Biodegradation of the insecticide N,N-diethyl-m-toluamide by fungi: identification and toxicity of metabolites,” Archives of Environmental Contamination and Toxicology, vol. 48, no. 3, pp. 323–328, 2005. View at: Publisher Site | Google Scholar
  96. J. Lipok, I. Dombrovska, P. Wieczorek et al., “The ability of fungi isolated from stored carrot seeds to degrade organophosphonate herbicides,” in Pesticide in Air, Plant, Soil and Water System, Proceedings of the 12th Symposium Pesticide Chemistry, Piacenza, Italy, June 4–6, 2003, pp. 575–580, La Goliardica Pavese, 2003. View at: Google Scholar
  97. A. A. A. Romeh, “Biodegradation of carbosulfan, pirimicarb and diniconazole pesticides by Trichoderma spp,” Journal of Environmental Research, vol. 3, pp. 162–172, 2001. View at: Google Scholar
  98. B. Z. Li-Qing, J. Hong-Xia, Y. Yan-Chun et al., “Degradation of organophosphorus pesticide by engineered bacteria and immobilized cell,” Huanjing Kexue Yu Jishu, vol. 31, no. 5, pp. 45–48, 2008. View at: Google Scholar
  99. X. Peng, J. S. Zhang, Y. Y. Li, W. Li, G. M. Xu, and Y. C. Yan, “Biodegradation of insecticide carbofuran by Paracoccus sp. YM3,” Journal of Environmental Science and Health B, vol. 43, no. 7, pp. 588–594, 2008. View at: Publisher Site | Google Scholar
  100. H. Zhang, C. Yang, C. Li, L. Li, Q. Zhao, and C. Qiao, “Functional assembly of a microbial consortium with autofluorescent and mineralizing activity for the biodegradation of organophosphates,” Journal of Agricultural and Food Chemistry, vol. 56, no. 17, pp. 7897–7902, 2008. View at: Publisher Site | Google Scholar
  101. P. N. Tallur, V. B. Megadi, and H. Z. Ninnekar, “Biodegradation of Cypermethrin by Micrococcus sp. strain CPN 1,” Biodegradation, vol. 19, no. 1, pp. 77–82, 2008. View at: Publisher Site | Google Scholar
  102. V. Nagpal, M. C. Srinivasan, and K. M. Paknikar, “Biodegradation of γ-hexachlorocyclohexane (Lindane) by a non-white rot fungus conidiobolus 03-1-56 isolated from litter,” Indian Journal of Microbiology, vol. 48, no. 1, pp. 134–141, 2008. View at: Publisher Site | Google Scholar
  103. A. E. M. Chirnside, W. F. Ritter, and M. Radosevich, “Bioremediation strategies for pesticide-contaminated Soil: IV. Biodegradation using a selected microbial consortium following pretreatment with fungal Enzymes,” in Proceedings of the 9th International In Situ and On-Site Bioremediation Symposium, pp. 1233–1240, Baltimore, Md, USA, May 2007. View at: Google Scholar
  104. W. S. Lan, J. D. Gu, J. L. Zhang et al., “Coexpression of two detoxifying pesticide-degrading enzymes in a genetically engineered bacterium,” International Biodeterioration and Biodegradation, vol. 58, no. 2, pp. 70–76, 2006. View at: Publisher Site | Google Scholar
  105. Z. Liu, Q. Hong, J.-H. Xu, W. Jun, and S.-P. Li, “Construction of a genetically engineered microorganism for degrading organophosphate and carbamate pesticides,” International Biodeterioration and Biodegradation, vol. 58, no. 2, pp. 65–69, 2006. View at: Publisher Site | Google Scholar
  106. K. Yoshii, Y. Tonogai, H. Ueno, and K. Nakamuro, “Malathion residue in wheat kernels is degraded by thion organophosphorus pesticide-specific carboxylesterase,” Journal of Health Science, vol. 52, no. 3, pp. 221–227, 2006. View at: Publisher Site | Google Scholar
  107. M. A. Gondim-Tomaz, T. T. Franco, and L. R. Durrant, “Biodegradation of diuron and pyruthiobac-sodium by white-rot and soil fungi,” Contaminated Soils, Sediments and Water, vol. 9, pp. 21–32, 2005. View at: Publisher Site | Google Scholar
  108. B. K. Singh, A. Walker, J. A. W. Morgan, and D. J. Wright, “Biodegradation of chlorpyrifos by Enterobacter strain B-14 and its use in bioremediation of contaminated soils,” Applied and Environmental Microbiology, vol. 70, no. 8, pp. 4855–4863, 2004. View at: Publisher Site | Google Scholar
  109. T. A. Kadam, V. D. Jadhav, and G. Gyananath, “Microbial degradation of dimethoate by gram negative soil isolates from cotton field,” Pollution Research, vol. 22, no. 3, pp. 443–445, 2003. View at: Google Scholar
  110. J. Jauregui, B. Valderrama, A. Albores, and R. Vazquez-Duhalt, “Microsomal transformation of organophosphorus pesticides by white rot fungi,” Biodegradation, vol. 14, no. 6, pp. 397–406, 2003. View at: Publisher Site | Google Scholar
  111. F. Y. Zhang, Y. A. Jiao, and Y. Guangyu, “Sequence of Geobacillus phosphotriesterase mutant and its uses in decomposing organophosphorus pesticide,” Faming Zhuanli Shenqing, 2012. View at: Google Scholar
  112. L. Xiang-Ming and C. Ping-Ping, “Progress in degradation of organo-chlorinated pesticides by microorganism,” Huanjing Kexue Yu Jishu, vol. 35, no. 6, pp. 89–93, 2012. View at: Google Scholar

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