ISSN: 0973-7510
E-ISSN: 2581-690X
https://dx.doi.org/10.22207/JPAM.13.1.43 | © The Author(s). 2019
The present study reports the biodegradation studies of Monocrotophos in agricultural soils of Visakhapatnam district. Bacterial strains were isolated from agricultural soils of Visakhapatnam dist. The isolates based on their morphological, biochemical and molecular characteristics were identified as Bacillus aryabhatta Strain ENP 3, Bacillus drentensis strain ENA1, Bacillus firmus Strain EN5C, and Staphylococcus vitulinus Strain EN5F. These four strains were isolated for the first time in this region. The degradation potential of the organisms for Monocrotophos as the only carbon source were studied and also the influence of Cow dung manure and NPK fertilizer on the growth and degradation capacity of organisms were studied. Degradation potential in media for individual organism as well as consortia was studied using spectrophotometric analysis. LC-MS was used to detect the degradation potential of microbial consortia in soil and also know the intermediate metabolites formed during degradation. It was found that the bacterial consortium has the highest degradation potential compared to individual organisms and Bacillus aryabhattai strain ENP3 has higher is degradation potential for Monocrotophos compared to other organisms.
Biodegradation, Monocrotophos, Bacterial Isolates, Cow dung manure, NPK fertilizer, Spectrophotometric analysis, LC-MS.
India, despite its progress in various fields, is primarily considered as anagro based economy with more than 60% of its population depending mainly on agriculture for their subsistence. Due to pest infestation, more than 30%-40 % of the crop produce is damaged every year. In the process of development of an effective pest control strategy, deployment of pesticides has become inevitable, regardless of their known toxicity. Utilization of pesticides in India is about 3% of the total world consumption and is increasing at the rate of 2–5% per annum1. These pesticides are categorized into various groups such as, insecticides, fungicides, herbicides etc. About 98% of sprayed insecticides and 95% of herbicides reach a destination other than their target species including non-target species, air, water, bottom sediments, and food leading to food chain toxicity2. The use of these pesticides in many developing countries is not being regulated leading to accumulation of residues in various food which possess health hazards. Many studies have reported the presence of organophosphate insecticides as the main pesticide residue found in food chains3,4. Organophosphate insecticides such as Mono-crotophos, Parathion, Malathion, Methylpa-rathion are well known for their bioaccumulation and neurotoxic properties, because they act on the enzyme acetyl cholinesterase5.
Monocrotophos (MCP) (Dimethyl (E)-1-methyl-2 methyl carbamoyl vinyl phosphate) is a broad-spectrum organo phosphate (OP) insecticide and acaricide which works systemically and on contact. Monocrotophosis widely used in agriculture and house-hold, particularly effective against Lepidoptera, Homoptera, and certain Coleoptera. Mono-crotophos affects the central nervous system by inhibiting cholinesterase (AchE), which breaks down acetylcholine, a chemical that serves as neurotransmitters alongside other choline-based esters. Serious exposure may target the eyes, respiratory system, cardiovascular system and reproductive system6. Due to its toxicity to non- target organisms it is banned in many developed countries but is still widely used in developing countries like India. The widespread use of Monocrotophos is found to accumulate in soil and gets leached into water bodies, making the aquatic environment polluted and is found to be toxic to non-target organisms. It has been classified as extremely hazardous, with an LD50 value of 20 mg/kg for mammals7. The half-life of Monocrotophos in soil was reported to be 40–60 days8. Monocrotophos is easily soluble in water and therefore has potential to contaminate ground water. In the environment the degradation of Monocrotophos pathways are non-cholinesterase inhibiting and of low toxicity. Volatilization appears to be the major factor in the rapid loss of residues followed by hydrolysis and oxidation of Monocrotophos application. Monocrotophos and its metabolites are rapidly degraded in soil, mainly biologically, to complete mineralization. They will not accumulate in the environment under normal use conditions9.
The present study is focused on the degradation of Monocrotophos by bacterial isolates isolated from the agricultural soils of Visakhapatnam district. The degradation potential of both individual isolates as well as consortium has been studied; also the impact of cow dung manure and NPK on the growth of organisms was studied.
Collection of soil samples
Soil samples were collected from four agriculture practicing villages of Visakhapatnam District, Andhra Pradesh, India. Control sample was taken from an area where agriculture is no longer practiced. All the sample sites were dry fields. The Soil samples were collected in quadrilateral method from a depth of 0-15cm in sterile sealed plastic bags. Each sample bag was labelled properly with soil type and location. The experimental samples were stored in cool and moist place for the purpose of microbial survival. The soil samples were dried in shade for 24 hrs, the clods were crushed and the entire quantity is passed through 2mm stainless steel sieve. The physico-chemical properties of the soil such as pH, EC, soil texture and soil moisture were determined using UF/IFAS methods10. Nitrogen was estimated using Kjeldahl11; Phosphorus was determined by Bray and Kurtz method12and Potassium was estimated by the method asreported by Black13. Table 1 show the GPS location of the soil sample locations and Table 2 depicts the physico-chemical properties of the soil samples collected.
Table (1):
GPS Location of the soil samples collected
Place |
GPS Location |
|---|---|
1 (Control) Sample 1 |
17°36’58.71″N 83°04’52.19″N |
2 Sample 2 |
17°37’19.86″N 83°04’43.61″N |
3 Sample 3 |
17°33’05.85″N 83°58’44.22″N |
4 Sample 4 |
17°47’28.85″N 83°06’51.07″N |
5 Sample 5 |
17°47’39.82″N 83°11’46.29″N |
Table (2):
Physico – Chemical Properties of soil samples
| Samples | pH | EC
µs/cm |
Soil texture | Soil Moisture | Available (Kg/ha) | |||
|---|---|---|---|---|---|---|---|---|
| N | P | K | ||||||
| Sample 1 | 7.8 | 197 | Sandy soil | 3.7 | 165.2 | 21.2 | 270.0 | |
| Sample 2 | 7.3 | 220 | Sandy soil | 5.8 | 186.3 | 29.3 | 340.0 | |
| Sample 3 | 7.1 | 207 | Sandy soil | 5.7 | 196.2 | 32.4 | 320.2 | |
| Sample 4 | 7.5 | 217 | Sandy soil | 6.2 | 207.0 | 39.2 | 370.7 | |
| Sample 5 | 7.9 | 244 | Sandy soil | 6.8 | 170.3 | 31.5 | 283.2 | |
Isolation of bacteria
Isolation of bacteria was done using serial dilution plate technique and subsequent dilutions were made up to 107 times. Each diluted sample was spread over the surface of nutrient agar plates in duplicate and incubated at 37°C for72 hours. The strains of bacteria were selectively isolated from the mixed population of microbes growing on the nutrient agar medium by single colony isolation. Isolates were selected based on their morphological characteristics such as colour, margin, elevation, and optical features of the colonies, shape and arrangements of the vegetative cells14. Streak plate method was employed to isolate pure cultures and maintained for further studies. Biochemical analyses of all the isolates were carried out according to Bergey’s Manual of Determinative Bacteriology15. Confirmation of the genus and species level was done using 16s rRNA sequencing and molecular analysis was done using 16s rDNA technique using universal primer 27 F AGAGTTTGATCMTGG CTCAG 20, 1492 R TACGGYTACCTTGTTA CGACTT2′.
Chemicals
Commercial grade insecticide Mono-crotophos (50% E.C)andNPK fertilizer having a ratio of 19:19:19 was obtained from Sri Sai Agrochemicals Visakhapatnam. Dried cow dung manure was collected from Simhachalam Goshala, a dedicated unit for the protection of cows. All other chemicals and reagents used in this experiment were of analytical grade and procured from Hi-Media. Double distilled water was used throughout the experiment.
Enrichment of isolates
Nutrient medium supplemented with Monocrotophos was used to grow the Isolates and incubated for 24 hrs. 1% of the cultures were transferred to minimal salt media (MSM) containing 0.5 g of K2HPO4,0.04 g of KH2PO4, 0.1 g of (NH4)2SO4, 0. 05 g of MgSO4, 0.01 g of FeSO4 and0.5 g of NaCl/ litre at pH 7.0 containing Monocrotophos as the sole source of carbon. The cultures grown on MSM were used for further studies.
Optimization of pH, Temperature and Pesticide concentration
Pesticide concentration
The Isolates were streaked in MSM agar containing 10 – 500 ppm of Monocrotophos, The isolated organisms were grown in MSM at different pHof 6.0, 7.0 and 8.0 and temperature of 25°C, 37°C and 45°C in MSM containing 200mgL-1 of Monocrotophos. The plates were incubated at room temperature for 24hours and growth was observed. MSM without Monocrotophos, served as control.
Growth kinetics
Turbid metric method was used to determine the growth kinetics. The organisms selected were grown in sterile nutrient broth containing Monocrotophos as the sole carbon source. The effects of NPK and cow dung on the growth pattern of the organisms were studied. Individual sterile broth containing inoculates without the addition of carbon source, NPK and Cow dung manure was set as control.
Bioremediation studies in media
The bioremediation efficacy of the selected organisms was observed by growing the four organisms in nutrient broth containing Monocrotophos (500mgL-1) in 500 ml Erlenmeyer flask. After 24h of incubation, about 1% of culture was transferred to minimal salt media (MSM). Monocrotophos was used as the sole carbon source and incubated on a rotary shaker at 150 rpm for 7 days at room temperature. Samples from culture flasks were centrifuged at 3,500 rpm for 15 min to obtain cell free extract. Spectrophotometric readings of the cell free extract were taken on daily basis/ 24h for 7 days.
Bioremediation studies of the selected bacterial consortium along with addition of NPK fertilizer and cow dung manure (CDM).
The selected Bacterial consortium was grown in an erlynmayer flask (500ml) containing nutrient broth with Chlorpyrifos (500mgL-1) as sole carbon source. After 24h of incubation about 1% of culture is transferred to another erlynmayer flask (500ml) containing minimal salt media (MSM) with Chlorpyrifos. About 2.5gms of NPK 19-19-19 was taken and diluted thoroughly in distilled water and added to MSM. To another flask about 50gms of sterilized and dried cow dung manure16 was taken and diluted thoroughly in distilled water and added to MSM. The flask is incubated on a rotary shaker at 150 rpm for 7 days at room temperature. Media containing Chlorpyrifos and NPK and Chlorpyrifos and Cow dung manure without addition of inoculates were set as control. Samples from culture flask were centrifuged at 4,200 rpm for 15 min to obtain cell free extract. Spectrophotometric readings of the cell free extract were taken on daily bases or 24h for 7 days. All the experiments were carried out in triplicates.
In soil
The soils collected from agricultural fields, were subjected to three-fold autoclaving at 15lbs pressure & 121°C for 30 min for sterilization before analysis. 500 g of these sterilized soils were taken into plastic bags. Monocrotophos (500 mg/kg) was added to each soil bag and the soil was thoroughly mixed to ensure uniform concentration of pesticides. Bacterial isolates were grown in nutrient broth medium. After 24 h incubation, the organisms were transferred to individual MSM with pesticides. The organisms were inoculated with the contaminated soilsat 1×108cfu/g. Soil samples (15 g) were recovered and extracted with acetonitrile solvent. Each of the extract was analysed by LC–MS for every 4 days. Pesticide contaminated soils without organisms were kept as controls.
LC-MS
Soil samples were collected from each bag for pesticide analysis. 15 grams of soil samples were weighed into a 250-ml Erlenmeyer flask and 20 ml of HPLC grade acetonitrile was successively added with continuous shaking for 30 min on a rotary shaker at 120 rpm. Then, the samples were allowed until the soil had settled and the clear supernatant liquid was used to determine the pesticide concentration by LC-MS as per the following conditions: column: Agilent C20 (230 x 5.4 mm), detector: programmable variable wave length UV detector, flow rate: 1 mL/min, mobile phase: acetonitrile + ammonium acetate (90:10), pH 5.5 and injection volume: 50µL.
LC-MS determination was done to identify the intermediates and final degradation compounds.
Identification of bacterial isolates
The morphological and biochemzical characterization of soil bacteria has identified a total of 24 bacterial isolates out of which four bacterial isolates showed distinct morphological features. Further, biochemical results of these strains using 16s rDNA sequence analysis against BLAST search showed that the bacterial isolates were Bacillus aryabhatta Strain ENP 3, Bacillus drentensis strain ENA1, Bacillus firmus Strain EN5C, and Staphylococcus vitulinus Strain EN5FThese organisms were isolated for the first time in Visakhapatnam district. The sequence of the four isolates was submitted to gene bank and the following accession numbers KY399763, KY399764, KY399766, KY399767 were obtained.
Bio-remediation studies
Biodegradation of Monocrotophos was studied using the four organisms; Bacillus aryabhattai, Bacillus drentensis, Bacillus firmus, and Staphylococcus vitulinus which were isolated from the agricultural soils for the first time in Visakhapatnam district. Initially the organisms were enriched by growing them in MSM containing Monocrotophos as the sole source of carbon. The influence of varying pH and temperatures on the organisms were determined (Fig. 1 a & b) and it was observed that all the isolates have shown fair growth at pH 7 and between 20 -350C temperature range. Table 3 depicts the tolerance levels of these four organisms for Monocrotophos from 10ppm to 500ppm. The data shows that Bacillus aryabhattai was able to grow actively up to 300ppm, Bacillusdrentensis and Bacillus firmus up to100ppm while Staphylococcusvitulinus can grow up to 60ppmof pesticide concentration. The average degradation potential of the organisms is shown in Table 4. Growth kinetics of the selected organisms (Fig. 2 a-d) in the presence and absence of Monocrotophos shows that the organisms are able to utilize Monocrotophos as the carbon source. Also the ability of Cow dung manure and NPK on the growth of organisms indicate that the organisms can grow well utilizing both NPK and Cow dung manure but the maximum growth is observed with NPK and this may be attributed to direct availability of large amount of extra nutrient source. The degradation potential studies of individual isolates and consortium for Monocrotophos (Fig. 3) and the degradation efficacy on the addition of Cow Dung Manure (Fig. 4) and NPK (Fig. 5) shows that all organisms can degrade the pesticide at a higher rate when NPK is added to the medium. Besides, the control sample containing Cow dung manure and Monocrotophos without the addition of consortia has shown 15 % degradation capacity and this may be due to the indigenous organisms present in cow dung manure. Among the individual isolates studied for the degradation of Monocrotophos B.aryabhattai is able to degrade Monocrotophos faster followed by B.drentensis, B. firmus and S.vitulinus. The degradation potential in consortium of these isolates is found to be faster compared to individual organisms.
Table (3):
Tolerance of Monocrotophos concentration by the four isolates
Conc in PPM |
B. drentensis strain ENA1 |
B.aryabhattai strain ENP3 |
B.firmus strain EN5C |
S. vitulinus strain EN5F |
|---|---|---|---|---|
10 ppm |
+ + |
+ + |
+ + |
+ + |
20 ppm |
+ + |
+ + |
+ + |
+ + |
40 ppm |
+ + |
+ + |
+ + |
+ + |
60 ppm |
+ + |
+ + |
+ + |
+ + |
80 ppm |
+ + |
+ + |
+ + |
+ + |
100 ppm |
+ + |
+ + |
+ + |
+ + |
200 ppm |
+ |
+ + |
+ |
+ + |
300 ppm |
+ |
+ + |
+ |
+ |
400 ppm |
+ |
+ |
+ |
+ |
500 ppm |
+ |
+ |
+ |
+ |
+ + Active growth, + slight growth.
Table (4):
Degradation efficacy of the Isolates for Monocrotophos obtained by Enrichment culture
ENA1 |
0.430 ±0.083 |
|---|---|
EN5C |
0.426 ±0.102 |
EN5F |
0.593 ±0.093 |
ENP3 |
0.496 ±0.091 |
Consortia |
0.184 ±0.153 |
Mean and SD of OD are value of three experiments.
Fig. 1. a) Growth of organisms at different pH containing Monocrotophos, b) Growth of organisms at different temperature containing Monocrotophos
Fig. 2. Growth kinetics of organisms in the presence of Monocrotophos, without Monocrotophos, with addition of NPK, and Cow Dung Manure (CDM). a) ENP3; b) ENA1; c) EN5C; d)EN5F.
Fig. 3. Degradation potential of individual Isolates and Consortium for Monocrotophos.
Fig. 4. Degradation potential of individual isolates and consortium with Cow dung manure for Monocrotophos
Fig. 5. Degradation potential of individual isolates and consortium with NPK for Monocrotophos
LC-MS analysis of soil sample
The LC-MS spectra of soil sample spiked with Monocrotophos at 0h (Fig. 6a) showed a major peak at m/z 223.6 with a retention time of 3.3 min, indicating the presence of maximum conc. of Monocrotophos. After 4 days, the LC-MS data for the same soil sample (Fig. 6b) showed a major peak at m/z 209.2 with a retention time of 2.9minPeak followed by another peak at m/z 223.6with a retention time of 3.3 min with an intensity of about 43%. This clearly shows that after 4 days, 57% of the pesticide got degraded indicating the presence of less amount of Monocrotophos. The LC-MS spectra for the same soil sample after 8 days (Fig. 6c) showed a major peak at m/z 170.0 with a retention time of 2.4 min. but the Monocrotophos peak appeared with an intensity of about 17%only. This shows that after 8 days 83% of the pesticide got degraded. After 12 days (Fig. 6d), the LC-MS data showed a major peak at m/z 126.2 with a retention time of 1.8 min. The mass 126.2 shows that the pesticide has degraded to Di methyl phosphoric acid17. No semblance of m/z 223.6 is observed indicating complete degradation of the pesticide. The soil sample after 16 days (Fig. 6e) showed a major peak at m/z 96.0 with a retention time of 1min. It is also observed that there are two major peaks at m/z 114 and m/z 126.2 with retention times of 1.3 min and 1.7 min. respectively. Mass numbers 114 and 126 indicate the degradation of the pesticide to N-methyl acetoacetamide18, 19, 20 and Di methyl phosphoric acid. The LC-MS spectra for the control soil sample after 16 days (Fig. 6f) showed a peak at m/z 223.0 with a retention time of 3.1 min. and the intensity is around 73%. This may be due to abiotic degradation of the compound.
Fig. 6. LC-MS analysis of the degradation study of Moocrotophos a. 0th h, b. 4th days, c. 8th days, d. 12th days, e. 16th day, f. 16th day Control soil.
To isolate potential Monocrotophos degrading organism bacterial consortium was developed from agricultural soil by selective enrichment technique by providing Mono-crotophos as the sole source of carbon. Degradation of Monocrotophos by consortium was found to be effective, this could be due to the synergistic effect of various bacterial isolates than degradation by individual organisms.
Bioremediation of Monocrotophos has been extensively studied and many potential bacterial strains have been isolated for the degradation of Monocrotophos. Organisms like Pseudomonas aeruginosa F10B and Clavibacter-michiganensessp. insidiosum SBL 1121 have shown to utilize Monocrotophos as a phosphorus source but not as a carbon source. Bacillus sp. Isolated from previously treated soil 22 with Pseudomonas mendocina23is studied to be the most efficient Monocrotophos degrader and its degrading capability is plasmid based. Pseudomonas sps, Arthrobactersps, B. megatherium, Arthro-bacteratrocyaneus24 can utilize Monocrotophos as a sole source of carbon.
In the present study four organism sBacillus aryabhatta Strain ENP 3, Bacillus drentensis strain ENA1, Bacillus firmus Strain EN5C, and Staphylococcus vitulinus Strain EN5F were studied for their degradation capacities for Monocrotophos. In MSM media, the degradation potential of B. aryabhatta is found to be 74% followed by B. drentensis is 69% B. firmus, 59%,and S. vitulinus 38%. The degradation potential of B. aryabhattai B. drentensis and B. firmus and S. vitulinus increased by 10% on the addition of Cow dung manure and the degradation potential increased by 20 -25 % for B.drentensis, B.firmus, B. aryabhattai and S. vitulinus by the addition of NPK. Moreover the degradation potential of the consortium was found to be higher at about 70% and degradation potential increased for about 10% when Cow dung manure is added and 25% when NPK is added to the media. LC-MS analysis of soil sample suggests that the consortia were able to completely degrade Monocrotophos within 12 days. Intermediate compounds like N-methyl acetoacetamide and Di methyl phosphoric acid were detected. Degradation rate of the consortia in soil sample was observed to be nearly 80%. The present study reveal that the degradation potential of the isolates follow in the order Bacillusaryabhatta Strain ENP 3> Bacillus drentensis strain ENA1> Bacillus firmus Strain EN5C > Staphylococcus vitulinus Strain EN5F The results of the present study reveal that these organisms have the potential to degrade pesticide Mono-crotophos. Further studies will throw more credible information on the practical application of these isolated organisms in degrading Monocrotophos in soil.
One of the authors Miss Sri Lakshmi Balakrishnan is grateful to Department of Science and Technology (DST), Govt. of India for extending financial support in the form of Women Scientist Program. Thanks are due to DST-Promotion of University Research and Scientific Excellence programme and Department of Environmental Sciences of Andhra University for providing infrastructural facilities.
The authors declare no conflict of interest.
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