Biodecolorization of Metanil Yellow by Serratia marcescens MM06 Under Variable Environmental Conditions for Soil and Water Remediation

Authors

  • Ibrahim Alhaji Sabo Department of Microbiology, Faculty of Pure and Applied Sciences, Federal University Wukari, P.M.B. 1020 Wukari, Taraba State Nigeria.
  • Motharasan Manogaran Malaysia Genome and Vaccine Institute (MGVI) National Institute of Biotechnology Malaysia (NIBM) Jalan Bangi, 43000 Kajang, Selangor, Malaysia.
  • Mohd Izuan Effendi Halmi Department of Land Management, Faculty of Agriculture, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
  • Mohd Yunus Shukor Department of Biochemistry, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, D.E, Malaysia.

DOI:

https://doi.org/10.54987/jemat.v13i2.1149

Keywords:

Biodecolorization, Metanil Yellow, Serratia marcescens, Salinity tolerance, Soil and water remediation

Abstract

Metanil Yellow is a common pollutant coming from the dyeing industry. Its removal using decolorizing bacteria offers a sustainable approach to remediate polluted soils and water bodies. This research examines the impact of several parameters, such as initial dye concentration, temperature, pH, and NaCl concentration, on the decolorization efficacy of Serratia marcescens strain MM06 for the dye Metanil Yellow. The percentage of decolorization studied across different dye concentrations from 100 to 700 mg/L shows the highest decolorization at dye concentrations of between 100 and 300 mg/L. The decolorization was highest at 25°C. The effect of pH on the decolorization showed that the best decolorization occurred between pH 7 and 8. The effect of salinity on the decolorization for future coastal areas remediation showed that the best decolorization (90–100%) happened at NaCl levels up to 15 g/L. The decolorization effectiveness decreased as the NaCl concentration increased, reaching 10% at 30 g/L. Decolorization was severely inhibited by mercury, silver, and copper at 1 mg/L, which shows that chelating or sequestering agents may need to be added to the contaminated soil or water bodies before decolorization can take place. Gaining a thorough understanding of the decolorization characteristics is an important preliminary study before field studies are carried out to understand the limitations of the decolorization bacterium.

References

Abba O, Anyaoha V, Obianom A, Chisom A, Odibo F. Isolation and Characterization of Keratinase Producing Organisms from Fish Scale Dumpsite at Gusau Dam, Gusau, Zamfara State, Nigeria. Int. J. Res. Innov. Appl. Sci. 2024;IX:745–55. https://doi.org/10.51584/IJRIAS.2024.908067

Jayam J, K.J.Sharmila. Characterization And Biodegradation Potential of Bacillus Cereus B66 Isolated from Deliming Effluent. Afr. J. Biomed. Res. 2024;27:210–24. https://doi.org/10.53555/AJBR.v27i2S.1404

Oberemok V, Laikova K, Andreeva O, Gal’chinsky N. Biodegradation of insecticides: oligonucleotide insecticides and double-stranded RNA biocontrols paving the way for eco-innovation. Front. Environ. Sci. 2024;12:1430170. https://doi.org/10.3389/fenvs.2024.1430170

Dome R, Hazra S, Ghosh D, Ghosh S. Beneficial Effects of Ethanolic Leaf Extract of Coriandrum Sativum on Metanil Yellow induced alteration in activity of Catalase and Level of Lipid Peroxidation in Hercine Cardiac tissue In Vitro. Int. J. Pharm. Pharm. Sci. 2017;9. https://doi.org/10.22159/ijpps.2017v9i5.17331

Guo G, Hao J, Tian F, Liu C, Ding K, Zhang C, et al. Decolorization of Metanil Yellow G by a halophilic alkalithermophilic bacterial consortium. Bioresour. Technol. 2020;316. https://doi.org/10.1016/j.biortech.2020.123923

Ramlan MAM, Azizan NA, Han BH, Kim LC, Mohamad SE, Ibrahim Z. Decolourisation of reactive black 5 by azoreductase produced by Brevibacillus panacihumi ZBI. J. Teknol. Sci. Eng. 2012;59:11–6. https://doi.org/10.11113/jt.v59.1571

Issayeva A, Syzdykova M, Akhmet A, Bakhov Z, Ospanova Z, Chingisbayev B, et al. Use of Acidithiobacillus ferrooxidans for Decontamination of Explosive Waste from Oil Refineries. J. Ecol. Eng. 2023;24:19–24. https://doi.org/10.12911/22998993/163250

Dubovik V, Ratnaweera H, Markevich R, Issayeva A, Maletskyi Z, Sorogovets V. Inhibition effects of petroleum products on nitrogen and phosphorous removal. IOP Conf. Ser. Earth Environ. Sci. 2022;981:042008. https://doi.org/10.1088/1755-1315/981/4/042008

Vijayasree VP, Abdul Manan NS. Bio-inspired magnetic chitosan/Iron oxide macromolecules for multiple anionic dyes adsorption from aqueous media. Int. J. Biol. Macromol. 2024;277. https://doi.org/10.1016/j.ijbiomac.2024.134103

Pal A, Paul SR, Debnath A. An Experimental Study of Metanil Yellow Dye Remediation Using Fe-Mn Bimetal Oxide Composites. Springer Proc. Earth Environ. Sci. 2023;Part F1447:141–52. https://doi.org/10.1007/978-3-031-37596-5_11

Kulkarni K, Manujendra Kumar P, Kulkarni A, Satpute S. Bioremediation of hazardous Metanil yellow dye by using Trichoderma and Azotobacter biofertilizers. Acta Ecol. Sin. 2023. https://doi.org/10.1016/j.chnaes.2023.11.007

Sivashankar R, Sivasubramanian V, Anand Kishore K, Sathya AB, Thirunavukkarasu A, Nithya R, et al. Metanil Yellow dye adsorption using green and chemical mediated synthesized manganese ferrite: An insight into equilibrium, kinetics and thermodynamics. Chemosphere 2022;307. https://doi.org/10.1016/j.chemosphere.2022.136218

Sarkar R, Ghosh AR. Metanil yellow, a food additive induces the responses at cellular and sub-cellular organisations of stomach, intestine, liver, and kidney of heteropneustes fossilis (bloch). EM Int. 2010;29:453–60

Sarkar R, Ghosh A, Bengal W. Metanil yellow - an azo dye induced histopathological and ultrastructural changes in albino rat (Rattus norvegicus). The Bioscan 2012;7:427–32

Nath PP, Sarkar K, Mondal M, Paul G. Metanil yellow impairs the estrous cycle physiology and ovarian folliculogenesis in female rats. Environ. Toxicol. 2016;31:2057–67. https://doi.org/10.1002/tox.22205

Nagaraja TN, Desiraju T. Effects of chronic consumption of metanil yellow by developing and adult rats on brain regional levels of noradrenaline, dopamine and serotonin, on acetylcholine esterase activity and on operant conditioning. Food Chem. Toxicol. Int. J. Publ. Br. Ind. Biol. Res. Assoc. 1993;31:41–4. https://doi.org/10.1016/0278-6915(93)90177-z

Ramchandani S, Das M, Joshi A, Khanna SK. Effect of oral and parenteral administration of metanil yellow on some hepatic and intestinal biochemical parameters. J. Appl. Toxicol. 1997;17:85–91. https://doi.org/10.1002/(sici)1099-1263(199701)17:1%253C85::aid-jat394%253E3.0.co;2-k

Manogaran M, Yasid NA, Othman AR, Gunasekaran B, Halmi MIE, Shukor MYA. Biodecolourisation of Reactive Red 120 as a Sole Carbon Source by a Bacterial Consortium—Toxicity Assessment and Statistical Optimisation. Int. J. Environ. Res. Public. Health 2021;18:2424. https://doi.org/10.3390/ijerph18052424

Rizvi M, Tiwari N, Mishra A, Gupta R. Kinetic and Computational Study of Degradation of Two Azo Dyes, Metanil Yellow and Orange II, by Iron Oxide Nanoparticles Synthesized Using Hylocereus undatus. ACS Omega 2022;7. https://doi.org/10.1021/acsomega.2c00966

Anjaneya O, Souche SY, Santoshkumar M, Karegoudar TB. Decolorization of sulfonated azo dye Metanil Yellow by newly isolated bacterial strains: Bacillus sp. strain AK1 and Lysinibacillus sp. strain AK2. J. Hazard. Mater. 2011;190:351–8. https://doi.org/10.1016/j.jhazmat.2011.03.044

Khalid A, Koh SH, Halmi MIE, Syed MA, Shamaan NA. Characterization of a Metanil Yellow-decolorizing Pseudomonas strain Isolated from the Juru Industrial Park. Bull. Environ. Sci. Sustain. Manag. E-ISSN 2716-5353 2023;7:49–57. https://doi.org/10.54987/bessm.v7i2.917

Lal N, Chand S. Decolorization of Sulphonated Azodye Metanil Yellow by Newly Isolated Bacterial Strain: Bacillus -3330. J. Environ. Sci. Eng. 2014;56:341–6

Mansur R, Gusmanizar N, Roslan MAH, Ahmad SA, Shukor MY. Isolation and characterisation of a molybdenum-reducing and Metanil yellow dye-decolourising Bacillus sp. strain Neni-10 in soils from West Sumatera, Indonesia. Trop. Life Sci. Res. 2017;28:69–90. https://doi.org/10.21315/tlsr2017.28.1.5

Muliadi FNA, Halmi MIE, Wahid SBA, Gani SSA, Zaidan UH, Mahmud K, et al. Biostimulation of Microbial Communities from Malaysian Agricultural Soil for Detoxification of Metanil Yellow Dye; a Response Surface Methodological Approach. Sustainability 2021;13:138. https://doi.org/10.3390/su13010138

Vijaykumar MH, Vaishampayan PA, Shouche YS, Karegoudar TB. Decolourization of naphthalene-containing sulfonated azo dyes by Kerstersia sp. strain VKY1. Enzyme Microb. Technol. 2007;40:204–11. https://doi.org/10.1016/j.enzmictec.2006.04.001

Jadhav SU, Kalme SD, Govindwar SP. Biodegradation of Methyl red by Galactomyces geotrichum MTCC 1360. Int. Biodeterior. Biodegrad. 2008;62:135–42. https://doi.org/10.1016/j.ibiod.2007.12.010

Hafshejani MK, Ogugbue CJ, Morad N. Sequential microaerophilic-oxic phase mineralization of Azo dyes by a monoculture of Pseudomonas aeruginosa strain AWF isolated from textile wastewater. Water. Air. Soil Pollut. 2013;224. https://doi.org/10.1007/s11270-013-1672-4

Ogugbue CJ, Sawidis T, Oranusi NA. Bioremoval of chemically different synthetic dyes by Aeromonas hydrophila in simulated wastewater containing dyeing auxiliaries. Ann. Microbiol. 2012;62:1141–53. https://doi.org/10.1007/s13213-011-0354-y

Wong PK, Yuen PY. Decolorization and biodegradation of methyl red by Klebsiella pneumoniae RS-13. Water Res. 1996;30:1736–44

El Ahwany AMD. Decolorization of Fast red by metabolizing cells of Oenococcus oeni ML34. World J. Microbiol. Biotechnol. 2008;24:1521–7. https://doi.org/10.1007/s11274-007-9640-z

Song XY, Liu FJ, Zhou HB, Yang HL. Biodegradation of Acid Scarlet 3R by a New Salt-tolerant Strain Alcaligenes faecalis LJ-3: Character, Enzyme and Kinetics Analysis. Chem. Biochem. Eng. Q. 2018;32:371–81. https://doi.org/10.15255/CABEQ.2018.1410

Gao F, Ding H, Feng Z, Liu D, Zhao Y. Functional display of triphenylmethane reductase for dye removal on the surface of Escherichia coli using N-terminal domain of ice nucleation protein. Bioresour. Technol. 2014;169:181–7. https://doi.org/10.1016/j.biortech.2014.06.093

Pathak H, Madamwar D. Biosynthesis of indigo dye by newly isolated naphthalene-degrading strain pseudomonas sp. HOB1 and its application in dyeing cotton fabric. Appl. Biochem. Biotechnol. 2010;160:1616–26

Chen G, An X, Feng L, Xia X, Zhang Q. Genome and transcriptome analysis of a newly isolated azo dye degrading thermophilic strain Anoxybacillus sp. Ecotoxicol. Environ. Saf. 2020;203:111047. https://doi.org/10.1016/j.ecoenv.2020.111047

Guo G, Li X, Tian F, Liu T, Yang F, Ding K, et al. Azo dye decolorization by a halotolerant consortium under microaerophilic conditions. Chemosphere 2020;244. https://doi.org/10.1016/j.chemosphere.2019.125510

Beydilli MI, Pavlostathis SG. Biodecolorization of the Azo Dye Reactive Red 2 by a Halotolerant Enrichment Culture. Water Environ. Res. 2007;79:2446–56. https://doi.org/10.2175/106143007X212166

Asad S, Amoozegar MA, Pourbabaee AA, Sarbolouki MN, Dastgheib SMM. Decolorization of textile azo dyes by newly isolated halophilic and halotolerant bacteria. Bioresour. Technol. 2007;98:2082–8

Johari WLW, Ghazali N, Shukor MY. Biodecolorization of azo dyes by microorganisms isolated from Serdang and Merambong soils. Bioremediation Sci. Technol. Res. 2014;2:5–8. https://doi.org/10.54987/bstr.v2i1.62

Othman AR, Ahmad SA, Baskaran G, Halmi MIE, Shamaan NA, Syed M, et al. River monitoring of mercury using a novel molybdenum-reducing enzyme assay. Bull. Environ. Sci. Manag. 2014;2:30–5. https://doi.org/10.54987/bessm.v2i1.121

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Published

12.12.2025

How to Cite

Sabo, I. A., Manogaran, M. ., Halmi, M. I. E., & Shukor, M. Y. (2025). Biodecolorization of Metanil Yellow by Serratia marcescens MM06 Under Variable Environmental Conditions for Soil and Water Remediation. Journal of Environmental Microbiology and Toxicology, 13(2), 24–29. https://doi.org/10.54987/jemat.v13i2.1149

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