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Bio-Mineralization of Organophosphorous Insecticide-Chlorpyrifos and its Hydrolyzed Product 3,5,6-Trichloro-2-Pyridinol by Staphylococcus Sp. ES-2

M. Supreeth1*and N. S. Raju1

DOI:http://dx.doi.org/10.12944/CWE.11.2.17

毒死蜱在农业领域的应用to protect crops against pests results in accumulation of it in soil and other environmental samples. The insecticide transform into3,5,6-Trichloro-2-Pyridinol (TCP) through hydrolysis in soil, which has got antimicrobial property and hence resists its degradation in natural condition. In the current findings, a bacterial isolate capable of mineralizing Chlorpyrifos without accumulation of TCP was isolated from agricultural soil by enrichment method. Based on Morphological, Biochemical Characterization and with Bergey’s Manual comparision, the isolate was identified asStaphylococcus sp. The isolate was found to metabolize chlorpyrifos completely in Mineral salt medium with chlorpyrifos as the sole carbon source. No metabolites of chlorpyrifos were detected in Liquid Chromatography-Mass Spectroscopy (LC-MS) analysis after 7 days of incubation. The novelty of the outcome of the experiment relies onStaphylococcussp.ES-2 in complete mineralization of chlorpyrifos which can be used as a potential bioaugmenting agent in the chlorpyrifos contaminated sites.


Biomineralization; Chlorpyrifos; 3; 5; 6-Trichloro-2-Pyridinol; Staphylococcus Sp.ES-2

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Supreeth M, Raju N. S. Bio-Mineralization of Organophosphorous Insecticide-Chlorpyrifos and its Hydrolyzed Product 3,5,6-Trichloro-2-Pyridinol by Staphylococcus Sp. ES-2. Curr World Environ 2016;11(2) DOI:http://dx.doi.org/10.12944/CWE.11.2.17

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Supreeth M, Raju N. S. Bio-Mineralization of Organophosphorous Insecticide-Chlorpyrifos and its Hydrolyzed Product 3,5,6-Trichloro-2-Pyridinol by Staphylococcus Sp. ES-2. Curr World Environ 2016;11(2). Available from://www.a-i-l-s-a.com/?p=14198


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Article Publishing History

Received: 2016-04-18
Accepted: 2016-05-13

Introduction

Large quantities of pesticides are used in agriculture throughout the world and most of them are toxic to both humans and animals. Once the pesticide is applied in agricultural field, it remains in the soil for longer periods and sometimes it gets transformed into various byproducts. These byproducts may impact on Environment

Organophosphorus (OPPs) pesticides are beeing widely used in agricultural practice for more than 40 years. The toxic accumulation of OPPs is achieved by inhibiting acetylcholinesterase, an enzyme necessary for normal nerve impulse transmission. Most of the OPPs have similar general structure, containing three phosphoester linkages, and hydrolysis of one of the phosphor ester bonds dramatically reduce the toxicity of the pesticides by eliminating their acetylcholinesterase-inactivating properties.1

OPPs accounts Ë‚34% or world’s total pesticide application for controlling pests of various crops in different countries. Application of OPPs in the fields or accidental release leads to contamination of surface and ground water. These compounds are being highly mammalian toxicity, has to be removed from the environment.2

Chlorpyrifos(CP) O, O-diethyl O-(3,5,6 – trichloro -2n pyridyl phosphorothioate) is a crystalline organophosphate insecticide. It was discovered by Dow chemical company in 1965. CP hydrolyses rapidly in soil into its primary metabolite 3,5,6 trichloro-2-pyridinol (TCP)3and this TCP has antimicrobial property, which prevents the degradation of CP by soil microorganisms.4的studies on the fate of TCP and its degradation in environment are very much limited

CP is the second most detected insecticide in food and water because of its broad usage in agriculture on various crops. This has raised public concern demand to remove it from the contaminated sites.5

Removal of CP in Environment through biotic degradation is one of the most viable option. Several researchers have focused on microbial degradation of CP.6-14

Fig. 1: Structure of Chlorpyrifos and its hydrolyzed metabolite 3,5,6-trichloro-2-pyridinol


Figure 1: Structure of Chlorpyrifos and its hydrolyzed
metabolite 3,5,6-trichloro-2-pyridinol

Click here to View figure


Despite several papers reporting biodegradation of chlorpyrifos by microbial cultures, only few isolates have capable of degrading both chlorpyrifos and its hydrolysis product 3,5,6 trichloro-2-pyridinol. In this context, we framed objective to isolate and degrade both these compounds by enrichment technique.

Materials and Methods

Sample Collection and Chemicals

的soil samples were collected from sugar cane and rice field area of Hosahalli, Haniyambadi village, Mandya Taluk, Karnataka. The collected soil samples were air dried, sieved through a 2mm mesh and stored at 4⁰ C until further use. Analytical grade chlorpyrifos was obtained from Sigma-Aldrich Co., USA. Stock solution (100 ppm) of CP was prepared in HPLC grade Acetonitrile by weighing approximately 1mg of compound into a 10ml volumetric flask and diluting into a volume. Stock standard solutions were stored in the dark at -20⁰C. Working solutions were prepared as and when required.15

Enrichment and Isolation of Chlorpyrifos Degrading Bacterial Strain

的bacterial strain was screened from soil samples by enrichment technique. For isolation, 1g of soil sample was inoculated into 250ml Erlenmeyer flask containing 100 ml of MSM medium (Table-1) and 100 mg L-1chlorpyrifos as sole carbon source at pH 7 and kept for incubation at 120 rpm in shaker at 37⁰C for 7 days. After 7 days of incubation, 35mL culture aliquot was taken in 50ml centrifuge tube and centrifuged at 10,000 rpm for 5min. later the supernatant was taken in separate flask and extracted using equal volume of acetonitrile by shake flask method and the organic aqueous layer was separated. The solvent was evaporated by rotary evaporator. The residues was then dissolved in HPLC grade acetonitrile and analyzed by TLC followed by LC-MS.

Table: 1: Composition of MSM Medium In 1000 ml distilled water, pH=7.6

Ingredients

Quantity

Dipotassium hydrogen phosphate(K2HPO4)

1.5 g

Monopotassium phosphate (KH2PO4)

0.5 g

Ammonium sulphate (NH4)2SO4

0.5 g

Sodium chloride (Nacl)

0.5 g

Magnesium Sulphate (MgSO4)

0.2 g

Calcium chloride (CaCl2)

0.05 g

Ferrous sulphate (FeSO4)

0.02 g


Identification of the Isolated Chlorpyrifos Degrading Bacterial Strain

的potent strain isolated was characterized Morphologically and Biochemically and compared with Bergey’s manual of systematic bacteriology.

LC-MS Analysis

After 07 days of incubation, 35mL culture aliquot was taken in 50ml centrifuge tube and centrifuged at 10,000 rpm for 5min. later the supernatant was taken in separatory flask and extracted using equal volume of acetonitrile by shake flask method and the organic aqueous layer was separated. The solvent was evaporated by rotary evaporator. The residue was then dissolved in HPLC grade acetonitrile and analyzed using liquid chromatography-mass spectroscopy (LC-MS) (Acquity Waters, USA)according to.16的LC-MS was equipped with a BEHC 181.7µm column (10 x 50mm) with auto injector. The cartridges were conditioned with acetonitrile and washed with deionized water containing 0.1 % formic acid. Mass spectroscopy (MS) was performed using a Synapt G2 HPMS MS (Waters, USA) equipped with Electron spray ionization (ESI) detector. The operating condition was Capillary (kV)-3.00, Sampling Cone-40.00, Extraction Cone-4.00, Source Temperature (⁰C)-100, Desolvation Temperature (⁰C)-200, and Desolvation Gas flow (L/Hr)-500.0.

Results and Discussions

Isolation of Chlorpyrifos Degrading Bacteria

In the present study, selective enrichment method was used to isolate chlorpyrifos-degrading bacteria from paddy field. Eight soil samples were screened for isolating potent bacterial strain. From eight samples, three distinct strains were obtained, and among which bacterial strain designated ES-2 was chosen for analysis due to its highest tolerance to chlorpyrifos (100 mg L-1) as the sole carbon source on Mineral salt agar medium plates.

Identification of ES-2

的bacterial strain ES-2 was identified as gram-positive facultatively anaerobic coocci. The bacterial strain is non-motile, Catalase positive, oxidasde negative and exhibited creamish white colony morphology. According to the Bergey’s Manual of Systematic Bacteriology, the bacterium comes under orderBacillales, familyStaphylococcaceaeand genusStaphylococcus. Biochemical test results (Table-1) show the close relatedness of strain ES-2 with genusStaphylococcus.

Table 2: Biochemical tests results

Test

Results

Catalase

+

Urease

+

Starch hydrolysis

-

Mannitol salt agar

+

Glucose

+

Lactose

-

Sucrose

-


Biodegradation Ability ofStaphylococcussp. ES-2

的biodegradation of chlorpyrifos (100 mg L-1) was assessed usingStaphylococcussp ES-2. Thin Layer Chromatography (TLC) followed by LC-MS was used to monitor the disappearance of chlorpyrifos and TCP. The result of TLC analyses revealed the formation of unknown metabolites. The LC-MS analysis showed that the bacteria was able to efficiently degrade chlorpyrifos without formation of TCP (based onm/zvalue obtained). The current findings suggest that the isolate used this compound as carbon and energy source for its growth by forming polar metabolites. In most of the research outcomes on biodegradation of CP, the microorganisms hydrolysis it into TCP, which accumulates in the culture medium or soil and avoids further degradation of the same because of its antimicrobial property.17-19Environmental Protection Agency (EPA) of USA has found, TCP has been associated with estrogenic activity and has been listed as potential endocrine disrupting chemical.

Fig-2: Chlorpyrifos standard obtained by LC-MS analysis and its Total Ion Chromatogram (TIC)


Figure 2: Chlorpyrifos standard obtained by LC-MS
analysis and its Total Ion Chromatogram (TIC)

Click here to View figure

Fig-3: m/z values of LC-MS analysis of chlorpyrifos and its metabolites obtained from Staphylococcus sp. ES-2 culture grown from Mineral medium after 7 days of incubation


Figure 3:m/zvalues of LC-MS analysis of chlorpyrifos and its metabolites obtained fromStaphylococcussp. ES-2 culture grown from Mineral medium after 7 days of incubation
Click here to View figure


Pseudomonas putidawas reported to metabolize Chlorpyrifos after the strain immobilized with calcium alginate, the products of degradation detected by LC-MS was found to be TCP and Chlorpyrifos oxon.19TCP was accumulated during the degradation process of 100 mg L-1of Chlorpyrifos bySphingomonas sp,减缓退化过程。19

的Mechanism of chlorpyrifos degradation in bacteria is fairly understood and a number of degradation products such as diethylthiophosphoric acid, TCP, Chlorodihydro-2-pyridone and Maleamide semialdehyde have been identified.21In the present study, it was found that the bacterial isolate ES-2 was able to degrade chlorpyrifos with complete mineralization. The occurrence of unidentified peaks in chromatogram of present study may be byproducts of one of the above said products, which need further investigation.

Conclusions

Bioremediation, biodegradation and bioaugmentation based techniques are gaining popularity for the purpose of ecological restoration. Potential indigenous microbial strain, isolated from the area where contamination has occurred over a years can be used as successful bioaugmenting agent to remove toxic contaminants. These indigenous microbe give duel benefit, first they detoxify the contaminant and secondly do not pose any serious threat to other native flora and fauna. Many biotic and abiotic factors significantly influence the process of biodegradation. Results from the present study confirm that the isolated chlorpyrifos-degrading bacterium could be successfully implemented for removal of chlorpyrifos contaminated sites.

Acknowledgment

的authors thank Department of Science and Technology (DST)-Science and Engineering Research Board (SERB), Government of India, for grant received to carry out this work and Institution of Excellence (IOE), University of Mysore, Mysuru, for providing Liquid Chromatography-Mass spectroscopy (LC-MS).

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