Aasfar A, Bargaz A, Yaakoubi K, Hilali A, Bennis I, Zeroual Y, Meftah Kadmiri I (2021) Nitrogen-fixing Azotobacter species as potential soil biological enhancers for crop nutrition and yield stability. Front Microbiol. doi: 10.3389/fmicb.2021.628379
Abo-amer A, Abu-gharbia M, Soltan E, Abd El-Raheem W (2014) Isolation and molecular characterization of heavy metal-resistant Azotobacter chroococcum from agricultural soil and their potential application in bioremediation. Geomicrobiol J 31:551-561. doi: 10.1080/01490451.2013.850561
Abraham J, Silambarasan S (2016) Biodegradation of chlorpyrifos and its hydrolysis product 3,5,6-trichloro-2-pyridinol using a novel bacterium Ochrobactrum sp. JAS2: a proposal of its metabolic pathway. Pestic Biochem Phys 126:13-21. doi: 10.1016/j.pestbp.2015.07.001
Abraham J, Silambarasan, S (2018) Biodegradation of chlorpyrifos and 3,5,6-trichloro-2-pyridinol by fungal consortium isolated from paddy field soil. Environ Eng Manag J 17(3): 523–528. doi:10.30638/eemj.2018.052
Akbar S, Sultan S (2016) Soil bacteria showing a potential of chlorpyrifos degradation and plant growth enhancement. Braz Journal Microbiol 47(3): 563-570. doi: 10.1016/j.bjm.2016.04.009
Anderlei T, Büchs J (2001) Device for sterile online measurement of the oxygen transfer rate in shaking flasks. Biochem Eng J 7:157-162. doi: 10.1016/s1369-703x(00)00116-9
Anderlei T, Zang W, Papaspyrou M and Büchs J (2004) Online respiration activity measurement (OTR, CTR, RQ) in shake flasks. Biochem Eng J 17:187–194. doi: 10.1016/S1369-703X(03)00181-5
Anupama K, Paul S (2009) Ex situ and in situ biodegradation of lindane by Azotobacter chroococcum. J Environ Sci Health - B 45:58-66. doi: 10.1080/03601230903404465
Askar A, Khudhur M (2013) Effect of some pesticides on growth, nitrogen fixation and nif genes in Azotobacter chroococcum and Azotobacter vinelandii isolated from soil. J Toxicol Environ Health Sci 5:166-171. doi: 10.5897/jtehs12.029
Barman D, Haque M, Islam S, Yun H, Kim M (2014) Cloning and expression of ophB gene encoding organophosphorus hydrolase from endophytic Pseudomonas sp. BF1-3 degrades organophosphorus pesticide chlorpyrifos. Ecotoxicol Environ Saf 108:135-141. doi: 10.1016/j.ecoenv.2014.06.023
Bhosale H, Kadam T, Bobade A (2013) Identification and production of Azotobacter vinelandii and its antifungal activity against Fusarium oxysporum. J Environ Biol 34:177-182. http://www.jeb.co.in/journal_issues/201303_mar13/paper_06.pdf
Bose S, Kumar PS, N. Vo DV (2021) A review on the microbial degradation of chlorpyrifos and its metabolite TCP. Chemosphere 283: 131447. doi: 10.1016/j.chemosphere.2021.131447
Castillo J, Casas J, Romero E (2011) Isolation of an endosulfan-degrading bacterium from a coffee farm soil: persistence and inhibitory effect on its biological functions. Sci Total Environ 412-413:20-27. doi: 10.1016/j.scitotenv.2011.09.062
Castillo T, Flores C, Segura D, Espín G, Sanguino J, Cabrera E, Barreto J, Díaz-Barrera A, Peña C (2017) Production of polyhydroxybutyrate (PHB) of high and ultra-high molecular weight by Azotobacter vinelandii in batch and fed-batch cultures. J Chem Technol Biotechnol 92(7): 1809–1816. doi: 10.1002/jctb.5182
Castillo T, García A, Padilla-Córdova C, Díaz-Barrera A, Peña C (2020) Respiration in Azotobacter vinelandii and its relationship with the synthesis of biopolymers. Electron J Biotechnol 48:36-45. doi: 10.1016/j.ejbt.2020.08.001
Castillo T, Heinzle E, Peifer S, Schneider K, Peña M C (2013) Oxygen supply strongly influences metabolic fluxes, the production of poly(3-hydroxybutyrate) and alginate, and the degree of acetylation of alginate in Azotobacter vinelandii. Process Biochem 48:995-1003. doi: 10.1016/j.procbio.2013.04.014
Chen S, Liu S, Peng C, Liu H, Hu M, Zhong G (2012) Biodegradation of chlorpyrifos and its hydrolysis product 3,5,6-trichloro-2-pyridinol by a new fungal strain Cladosporium cladosporioides Hu-01. PloS One 7: 1-12. doi: 10.1371/journal.pone.0047205
Chennappa G, Adkar-Purushothama C, Naik M, Suraj U, Sreenivasa M (2014a) Impact of pesticides on PGPR activity of Azotobacter sp. isolated from pesticide flooded paddy soils. Greener J Agric Sci 4:117-129. doi: 10.15580/gjas.2014.4.010314003
Chennappa G, Adkar-Purushothama C, Suraj U, Tamilvendan K, Sreenivasa M (2013) Pesticide tolerant Azotobacter isolates from paddy growing areas of northern Karnataka, India. World J Microbiol Biotechnol 30:1-7. doi: 10.1007/s11274-013-1412-3
Chennappa G, Adkar-Purushothama CR, Suraj U, Tamilvendan K, Sreenivasa MY (2014b) Pesticide tolerant Azotobacter isolates from paddy growing areas of northern Karnataka, India. World J Microbiol Biotechnol 30(1):1–7. doi: 10.1007/s11274-013-1412-3
Chennappa G, Naik MK, Adkar-Purushothama CR, Amaresh YS, Sreenivasa MY (2016). PGP potential, abiotic stress tolerance, and antifungal activity of Azotobacter strains isolated from paddy soils. Indian J Exp Biol 54 5, 322-31. http://nopr.niscair.res.in/handle/123456789/34155
Chennappa G, Naik MK, Amaresh YS, Nagaraj H, Sreenivasa MY (2018a) Azotobacter - A potential bio-fertilizer and bio inoculants for sustainable agriculture. In: Panpatte D (ed) Microorganisms for green revolution Springer Nature, Singapore, pp 78–87.
Chennappa G, Sreenivasa M, Nagaraja H (2018b) Azotobacter salinestris: A novel pesticide-degrading and prominent biocontrol PGPR bacteria. In: Naveen Kumar A (ed) Microorganisms for sustainability 23-43. doi: 10.1007/978-981-10-7146-1_2
Chennappa G, Udaykumar N, Vidya M, Nagaraja H, Amaresh Y, Sreenivasa M (2019) Azotobacter—a natural resource for bioremediation of toxic pesticides in soil ecosystems. New and future developments in microbial biotechnology and bioengineering 267-279. doi: 10.1016/b978-0-444-64191-5.00019-5
Chitara M, Chauhan S, Singh R (2021) Bioremediation of polluted soil by using plant growth-promoting rhizobacteria. Microbial rejuvenation of polluted environment 203-226. doi: 10.1007/978-981-15-7447-4_8
Chobotarov A, Volkogon M, Voytenko L, Kurdish I (2017) Accumulation of phytohormones by soil bacteria Azotobacter vinelandii and Bacillus subtilis under the influence of nanomaterials. J Microbiol Biotechnol Food Sci 7:271-274. doi: 10.15414/jmbfs.2017/18.7.3.271-274
Cycoń M, Żmijowska A, Wójcik M, Piotrowska-Seget Z (2013) Biodegradation and bioremediation potential of diazinon-degrading Serratia marcescens to remove other organophosphorus pesticides from soils. J Environ Manage 117:7-16. doi: 10.1016/j.jenvman.2012.12.031
Deng S, Chen Y, Wang D, Shi T, Wu X, Ma X, Li X, Hua R, Tang X, Li QX (2015) Rapid biodegradation of organophosphorus pesticides by Stenotrophomonas sp. G1. J. Hazard Mater., 297: 17-24. doi: 10.1016/j.jhazmat.2015.04.052
Díaz-Barrera A, Aguirre A, Berrios J and Acevedo F (2011) Continuous cultures for alginate production by Azotobacter vinelandii growing at different oxygen uptake rates. Process Biochem 46:1879–1883. doi: 10.1016/j.procbio.2011.06.022
Díaz-Barrera A, Peña C, Galindo E (2007) The oxygen transfer rate influences the molecular mass of the alginate produced by Azotobacter vinelandii. Appl Microbiol Biotechnol 76:903–910. doi: 10.1007/s0025 3-007-1060-3
Díaz-Barrera A, Sanchez-Rosales F, Padilla-Córdova C, Andler R, Peña C (2021) Molecular weight and guluronic/mannuronic ratio of alginate produced by Azotobacter vinelandii at two bioreactor scales under diazotrophic conditions. Bioprocess Biosyst Eng 44:1275-1287. doi: 10.1007/s00449-021-02532-8
Dilly O (2001) Microbial respiratory quotient during basal metabolism and after glucose amendment in soils and litter. Soil Biol Biochem 33:117-127. doi: 10.1016/s0038-0717(00)00123-1
Dilly O (2003). Regulation of the respiratory quotient of soilmicrobiota by availability of nutrients. FEMS Microbiol Ecol 43(3): 375–381. doi: 10.1111/j.1574-6941.2003.tb01078.x
Farhan M, Ahmad M, Kanwal A Butt ZA, Khan QF, Raza SA, Qayyum H, Wahid A (2021) Biodegradation of chlorpyrifos using isolates from contaminated agricultural soil, its kinetic studies. Sci Rep 11: 10320. doi: 10.1038/s41598-021-88264-x
Feng Y, Minard R, Bollag J (1998) Photolytic and microbial degradation of 3, 5, 6-trichloro-2-pyridinol. Environ Toxicol Chem 17: 814–819. doi: 10.1002/etc.5620170508
Fishel FM (2013) EPA's endocrine disruptor screening program (EDSP). doi: 10.32473/edis-pi227-2013
García A, Ferrer P, Albiol J, Castillo T, Segura D, Peña C (2018) Metabolic flux analysis and the NAD(P)H/NAD(P)+ ratios in chemostat cultures of Azotobacter vinelandii. Microb Cell Fact. doi: 10.1186/s12934-018-0860-8
Gilani RA, Rafique M, Rehman A, Munis MFH, Rehman SU, Chaudhary HJ (2016) Biodegradation of chlorpyrifos by bacterial genus Pseudomonas. J Basic Microbiol 56(2):105–119. doi: 10.1002/jobm.201500336
Gilani S, Ageen M, Shah H, Raza S (2010) Chlorpyrifos degradation in soil and its effect on soil microorganisms. J Anim Plant Sci 20: 99–102. http://www.thejaps.org.pk/docs/20-2-2010/
Giri K, Rai J (2012) Biodegradation of endosulfan isomers in broth culture and soil microcosm by Pseudomonas fluorescens isolated from soil. Int J Environ Stud 69:729-742. doi: 10.1080/00207233.2012.702480
Gómez-Pazarín K, Flores C, Castillo T, Büchs J, Galindo E, Peña C (2015) Molecular weight and viscosifying power of alginates produced in Azotobacter vinelandii cultures in shake flasks under low power input. J Chem Technol Biotechnol 91:1485-1492. doi: 10.1002/jctb.4747
Gurikar C, Naik MK, Sreenivasa MY (2016) Azotobacter: PGPR activities with special reference to effect of pesticides and biodegradation. In: Singh D, Singh H, Prabha R (eds) Microbial inoculants in sustainable agricultural productivity. Springer, New Delhi. doi: 10.1007/978-81-322-2647-5_13
Hernández-Ruíz GM, Álvarez-Orozco NA, Ríos-Osorio LA (2017) Biorremediación de organofosforados por hongos y bacterias en suelos agrícolas: revisión sistemática. Cienc Tecnol Agropecuaria 18(1): 139-159. https://www.redalyc.org/articulo.oa?id=449949161008
Jabeen H, Iqbal S, Anwar S (2015) Biodegradation of chlorpyrifos and 3, 5, 6-trichloro-2-pyridinol by a novel rhizobial strain Mesorhizobium sp. HN3. Water Environ J. doi: 10.1111/wej.12081
Jayasri Y, Naidu MD, Mallikarjuna M (2014) Review article microbial degradation of chlorpyrifos. Int J Recent Sci Res 5: 1444-1450. http://recentscientific.com/sites/default/files/1678.pdf
John EM, Shaike JM (2015) Chlorpyrifos: pollution and remediation. Environ Chem Lett 13:269–291. 2015). doi: 10.1007/s10311-015-0513-7
Kahraman B, Altın A (2020) Evaluation of different approaches for respiratory quotient calculation and effects of nitrogen sources on respiratory quotient values of hydrocarbon bioremediation. Water Air Soil Pollut 231, 38.1doi: 10.1007/s11270-020-04763-z
Klimek J, Ollis D (1980) Extracellular microbial polysaccharides: kinetics of Pseudomonas sp., Azotobacter vinelandii, and Aureobasidium pullulans batch fermentations. Biotechnol Bioeng 22:2321-2342. doi: 10.1002/bit.260221109
Kumar A, Singh VK, Tripathi V, Singh PP, Singh AK (2018) Chapter 16 - Plant growth-promoting rhizobacteria (PGPR): perspective in agriculture under biotic and abiotic stress. In: Prasad R, Gill SS, Tuteja N (Eds) Crop improvement through microbial biotechnology, Elsevier, 333-342 pp. doi: 10.1016/B978-0-444-63987-5.00016-5.
Kumar V, Singh S, Upadhyay N (2019) Effects of organophosphate pesticides on siderophore producing soils microorganisms. Biocatal Agric Biotechnol 21:101359. doi: 10.1016/j.bcab.2019.101359.
Lamy E, Tran TC, Mottelet S, Pauss A, Schoefs O (2013) Relationships of respiratory quotient to microbial biomass and hydrocarbon contaminant degradation during soil bioremediation. Int Biodeter Biodegradation 83: 85–91. doi: 10.1016/j.ibiod.2013.04.015
Lenart A (2012) In vitro effects of various xenobiotics on Azotobacter chroococcum strains isolated from soils of southern Poland. J Environ Sci Health B 47:7-12. doi: 10.1080/03601234.2012.601942
Li X, He J, Li S (2007) Isolation of chlorpyrifos degrading bacterium, Sphingomonas sp. strain Dsp-2, and cloning of the mpd gene. Res Microbiol.158:143–149. doi:10.1016/j.resmic.2006.11.007
Liu ZY, Chen X, Shi Y, Su ZC. 2011. Bacterial degradation of chlorpyrifos by Bacillus cereus. Adv Mater Res 356–360: 676-680. doi: 10.4028/www.scientific.net/AMR.356-360.676
Lowry O, Rosebrough N, Farr A, Randall R (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193:265-275. doi: 10.1016/s0021-9258(19)52451-6
Lozano E, Galindo E. Peña CF (2011) Oxygen transfer rate during the production of alginate by Azotobacter vinelandii under oxygen-limited and non-oxygen-limited conditions. Microb Cell Fact 10 (13). doi: 10.1186/1475-2859-10-13
Mac-Rae IC, Celo JS (1974) The effects of organo-phosphorus pesticides on the respiration of Azotobacter vinelandii. Soil Biol Biochem 6(2):109–111. doi: 10.1016/0038-0717(74)90068-6
Maya K, Singh RS, Upadhyay SN, Dubey SK (2011) Kinetic analysis reveals bacterial efficacy for biodegradation of chlorpyrifos and its hydrolyzing metabolite TCP. Process Biochem 46(11): 2130–2136. doi: 10.1016/j.procbio.2011.08
Menon P, Gopal M, Prasad R (2004) Influence of two insecticides, chlorpyrifos and quinalphos, on arginine ammonification and mineralizable nitrogen in two tropical soil types. J Agric Food Chem 52:7370-7376. doi: 10.1021/jf049502c
Miller G (1959) Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal Chem 31:426-428. doi: 10.1021/ac60147a030
Moneke A, Okpala G, Anyanwu C (2010) Biodegradation of glyphosate herbicide in vitro using bacterial isolates from four rice fields. Afr J Biotechnol 9:4067–4074.
Moral ÇK, Ertesvåg H, Sanin FD (2016) Guluronic acid content as a factor affecting turbidity removal potential of alginate. Environ Sci Pollut Res 23:22568–22576. doi: 10.1007/s11356-016-7475-6
Mousa N, Adham A, Merzah N, Jasim S (2021) Azotobacter spp. bioremediation chemosate. Asian J Water Environ Pollut 18:103-107. doi: 10.3233/ajw210034
Muttawar AS,
Wadhai VS (2014) Isolation of pesticide tolerant Azotobacter species from rhizospheric region of the crop. Int J Res Biosci Agric Techn. doi: 10.29369/ijrbat.2014.03.iii.0006
Nagaraja H, Chennappa G, Rakesh S, Naik M, Amaresh Y, Sreenivasa M (2016) Antifungal activity of Azotobacter nigricans against trichothecene-producing Fusarium species associated with cereals. Food Sci Biotechnol 25:1197-1204. doi: 10.1007/s10068-016-0190-8
Noar J, Bruno-Bárcena J (2018) Azotobacter vinelandii: the source of 100 years of discoveries and many more to come. Microbiology 164:421-436. doi: 10.1099/mic.0.000643
Noguez R, Segura D, Moreno S, Hernandez A, Juarez K, Espín G (2007) Enzyme INtr, NPr, and IIANtr are involved in regulation of the poly-𝛽-hydroxybutyrate biosynthetic genes in Azotobacter vinelandii. J Mol Microbiol Biotechnol 15:244-254. doi: 10.1159/000108658
Omar SA, Abd-Alla MH (1992) Effect of pesticides on growth, respiration, and nitrogenase activity of Azotobacter and Azospirillum. World J Microbiol Biotechnol 8:326–328 doi: 10.1007/BF01201891
Pant R, Pandey P, Kotoky R (2016) Rhizosphere mediated biodegradation of 1, 4-dichlorobenzene by plant growth-promoting rhizobacteria of Jatropha curcas. Ecol Eng 94:50–56. doi: 10.1016/j.ecoleng.2016.05.079
Peña C, Campos N, Galindo E (1997) Changes in alginate molecular mass distributions, broth viscosity and morphology of Azotobacter vinelandii cultured in shake flasks. Appl Microbiol Biotechnol 48:510-515. doi: 10.1007/s002530051088
Peña C, Galindo E, Büchs J (2011) The viscosifying power, degree of acetylation and molecular mass of the alginate produced by Azotobacter vinelandii in shake flasks are determined by the oxygen transfer rate. Process Biochem 46:290-297. doi: 10.1016/j.procbio.2010.08.025
Peña C, Peter CP, Büchs J, Galindo E (2007) Evolution of the specific power consumption and oxygen transfer rate in alginate-producing cultures of Azotobacter vinelandii conducted in shake flasks. Biochem Eng J 36(2) 73-80. doi: 10.1016/j.bej.2007.02.019.
Plunkett M, Knutson C, Barney B (2020) Key factors affecting ammonium production by an Azotobacter vinelandii strain deregulated for biological nitrogen fixation. Microb Cell Fact. doi: 10.1186/s12934-020-01362-9
Praveen Kumar G, Mir Hassan Ahmed S, Desai S, Leo Daniel Amalraj E, Rasul A (2014) In vitro screening for abiotic stress tolerance in potent biocontrol and plant growth-promoting strains of Pseudomonas and Bacillus spp. Int J Bacteriol 2014:1-6. doi: 10.1155/2014/195946
Rani R, Kumar V (2017) Endosulfan degradation by selected strains of plant growth-promoting rhizobacteria. Bull Environ Contam Toxicol 99:138-145. doi: 10.1007/s00128-017-2102-x
Rani R, Kumar V, Gupta P, Chandra A (2019) Effect of endosulfan tolerant bacterial isolates (Delftia lacustris IITISM30 and Klebsiella aerogenes IITISM42) with Helianthus annuus on remediation of endosulfan from contaminated soil. Ecotoxicol Environ Saf 168:315-323. doi: 10.1016/j.ecoenv.2018.10.059
Rayu S, Nielsen UN, Nazaries L, Singh BK (2017) Isolation and molecular characterization of novel chlorpyrifos and 3,5,6-trichloro-2-pyridinol-degrading bacteria from sugarcane farm soils. Front. Microbiol 8:1-16. doi: 10.3389/fmicb.2017.00518
Revillas J, Rodelas B, Pozo C, Martínez-Toledo M, González-López J (2000) Production of B-group vitamins by two Azotobacter strains with phenolic compounds as sole carbon source under diazotrophic and adiazotrophic conditions. J Appl Microbiol 89:486-493. doi: 10.1046/j.1365-2672.2000.01139.x
Rokade KB, Mali GV (2013) Biodegradation of chlorpyrifos by Pseudomonas desmolyticum NCIM 2112. Int J Pharma Bio Sci 4(2):(B)609–616. http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.302.2334&rep=rep1&type=pdf
Roy T, Das N, Majumdar S (2020) Pesticide tolerant rhizobacteria: paradigm of disease management and plant growth promotion. In: Varma A, Tripathi S, Prasad R (eds) Plant-microbe symbiosis. Springer, Cham 221-239. doi: 10.1007/978-3-030-36248-5_12
Santos MS, Rondina ABL, Nogueira MA, Hungria M (2020) Compatibility of Azospirillum brasilense with pesticides used for treatment of maize seeds. Int J Microbiol ID 8833879. doi:10.1155/2020/8833879
Sethi S, Gupta S (2013) Impact of pesticides and biopesticides on soil microbial biomass carbon. Univers J Environ 3(2):326-330. http://web.a.ebscohost.com/ehost/pdfviewer/pdfviewer?vid=1&sid=bd5623b9-c38a-4afd-b9ea-d316a3f69789%40sdc-v-sessmgr01
Shahgholi H, Ahangar A (2014) Factors controlling degradation of pesticides in the soil environment: a review. Agric Sci Dev 3(8): 273-8. https://www.semanticscholar.org
Shahid M, Zaidi A, Ehtram A, Khan M (2019) In vitro investigation to explore the toxicity of different groups of pesticides for an agronomically important rhizosphere isolate Azotobacter vinelandii. Pestic Biochem Phys 157:33-44. doi: 10.1016/j.pestbp.2019.03.006
Shi T, Fang L, Qin H, Chen Y, Wu X, Hua R (2019) Rapid biodegradation of the organophosphorus insecticide chlorpyrifos by Cupriavidus nantongensis x1T. Int J Environ Res Publ Health 16(23): 4593. doi: 10.3390/ijerph16234593
Singh DP, Khattar JIS, Nadda, J, Singh Y, Garg A, Kaur N, Gulati A (2011) Chlorpyrifos degradation by the cyanobacterium Synechocystis sp. strain PUPCCC 64. Environ Sci Pollut Res 18:1351–1359. doi: 10.1007/s11356-011-0472-x
Strobel S, Allen K, Roberts C, Jimenez D, Scher H, Jeoh T (2018) Industrially-scalable microencapsulation of plant beneficial bacteria in dry cross-linked alginate matrix. Ind Biotechnol 14:138-147. doi: 10.1089/ind.2017.0032
Sumbul A, Ansari R, Rizvi R, Mahmood I (2020) Azotobacter: a potential bio-fertilizer for soil and plant health management. Saudi J Biol Sci 27:3634-3640. doi: 10.1016/j.sjbs.2020.08.004
Tejera N, Lluch C, Martìnez-Toledo M, Gonzàlez-López J (2005) Isolation and characterization of Azotobacter and Azospirillum strains from the sugarcane rhizosphere. Plant Soil 270:223-232. doi: 10.1007/s11104-004-1522-7
Then C, Wai O, Elsayed E, Mustapha W, Othman N, Aziz R, Wadaan M, Enshsay H (2016) Comparison between classical and statistical medium optimization approaches for high cell mass production of Azotobacter vinelandii. J Sci Ind Res 75:231-238.
Vidya Lakshmi C, Kumar M, Khanna S (2009) Biodegradation of chlorpyrifos in soil enriched cultures. Curr Microbiol 58:35-38. doi: 10.1007/s00284-008-9262-1
Vijayalakshmi P, Usha MS (2012) Degradation of chlorpyrifos by free cells and calcium-alginate immobilized cells of Pseudomonas putida. Adv Appl Sci Res 3:2796–2800. https://www.cabdirect.org/cabdirect/abstract/20123377370
Walvekar V, Bajaj S, Singh D, Sharma S (2017) Ecotoxicological assessment of pesticides and their combination on rhizospheric microbial community structure and function of Vigna radiata. Environ Sci and Pollut R 24:17175-17186. doi: 10.1007/s11356-017-9284-y
Wu X, Xu J, Dong F, Liu X, Zheng Y (2014) Responses of soil microbial community to different concentration of fomesafen. J Hazard Mater 273:155-164. doi: 10.1016/j.jhazmat.2014.03.041
Yang L, Zhao YH, Zhang BX, Yang CH, Zhang X (2005) Isolation and characterization of a chlorpyrifos and 3,5,6-trichloro-2- pyridinol degrading bacterium. FEMS Microbiol Lett 251(1): 67-73. doi: 10.1016/j.femsle.2005.07.031
Zhu J, Zhao Y, Ruan H (2019) Comparative study on the biodegradation of chlorpyrifos-methyl by Bacillus megaterium CM-Z19 and Pseudomonas syringae CM-Z6. An Acad Bras Cienc 91(3). doi: 10.1590/0001-3765201920180694