Halophilic Alkaline Protease Enzyme on Biodegradation of Contaminants in Raw Textile Effluent

IJEP 42(2): 142-148 : Vol. 42 Issue. 2 (February 2022)

A. Yogeeswaran1, R. Raja Jeya Sekar1*, S. Uma Maheswari2, S.M. Vijila3 and T. Vijaya Kumar4

1. S.T. Hindu College, P.G. and Research Department of Zoology, Nagercoil – 629 002, Tamil Nadu, India
2. Manonmaniam Sundaranar University, Department of Biotechnology, Tirunelveli – 627 012, Tamil Nadu, India
3. Pioneer Kumaraswamy College, Department of Zoology, Nagercoil – 629 003, Tamil Nadu, India
4. Delhi Technological University, Department of Environmental Engineering, New Delhi, India

Abstract

Textile effluent is composed of pollutants, such as dyes, dissolved solids, suspended solids and toxic materials. If this effluent is discharged without any process of treatment either into the water bodies or into the surface of the land will lead to the alteration of physico-chemical parameters of water and the soil. The present investigation revealed how the alkaline protease enzyme secreted from the halophilic bacterial strain Bacillus cereus RRJS2 was used to reduce the contaminants in textile wastewater. The bacterial strains were optimized at different pH, temperatures, NaCl concentrations and incubation times to produce alkaline protease enzyme. The extracted alkaline protease enzyme was used to treat the raw textile effluent. The physico-chemical parameters of both the raw textile effluent and treated effluent were compared. The results indicated that alkaline protease treated effluent recorded the reduction of physico-chemical parameters, such as pH 9.2%, temperature 4.69%, BOD 43%, COD 44%, TDS 66%, TH 44% and chlorides 46% in 5 days of degradation study. The FTIR analysis of raw and alkaline protease treated textile effluent revealed the disappearance of amine, sulphate and alkene groups of compounds and the appearance of hydroxyl, amine and aromatic groups of compounds. Thus, the alkaline protease showed a promising effect on the degradation of contaminants in the textile effluent.

Keywords

Alkaline protease, Bacillus cereus RRJS2, Textile effluent

References

  1. Pearce, C.J., J.R. Llyod and J.T. Guthrie. 2003. Review : The removal of colour from textile wastewater using whole bacterial cells. Dyes Pigments. 58:179-196.
  2. Schleiphake, K., et al. 2000. Transformation and degradation of the disazo dye Chicago Sky Blue by a purified laccase from Pycnoporous cinnabarinus. Enzyme microbila. Tech., 27:100-107.
  3. Verma, P. and D. Madamwar. 2002. Decolo-urization of synthetic textile dyes by lignin peroxidase of Phanecrochaete chrysosporium. Folia Microbiol., 47:283-286.
  4. Keharia, H. and D. Madamwar. 2003. Biorem-ediation concepts for treatment of dye containing wastewater : A review. Indian J. Expt. Biol., 41: 1068-1075.
  5. Nigam, P., et al. 1996. Microbial process for the decolourization of textile effluent containing azo, diazo and reactive dyes. Proc. Biochem., 31:435-442.
  6. Banat, I.M., et al. 1996. Microbial decolourization of textile dye containing effluents : A review. Bioresour. Tech., 58:217-227.
  7. McMullan, G., et al. 2001. Microbial decolourization and degradation of textile dyes. Appl. Microbiol. Biotech., 56:81-87.
  8. Garcha, S., N. Verma and S.K. Brar. 2016. Isolation, characterization and identification of microorganisms from unorganized diary sector wastewater and sludge samples and evaluation of their biodegradability. Water Resour. Ind., 16:19-28.
  9. Asad, S., et al. 2007. Decolourization of textile azo dyes by newly isolated halophilic and halotolerant bacteria. Bioresour. Tech., 98:2082-2088.
  10. Asgher, M., et al. 2008. Recent development in biodegradation of industrial pollutants by white rot fungi and their enzyme system. Biodegrad., 19:771-783.
  11. Kalme, S., et al. 2009. Textile dye degradation laccase from Pseudomonas desmolyticurn NCIM 2112. Enzyme Microbial Tech., 44:65-71.
  12. Joo, H.S., et al. 2003. Oxidant and SDS-stable alkaline protease from Bacillus clausii 1-52 : Production and some properties. J. Appl. Microbiol., 5:267-272.
  13. Shamasehar, Abdulhameed. 2011. Extracellular alkaline protease by a newly isolated halophilic Bacillus sp. Global J. Biotech. Biochem., 6:142-148.
  14. Johnvely, B., B.R. Manjunath and G.R. Naik. 2002. Pigeon pea waste as a novel, inexpensive, substrate for production of a thermostable alkaline protease from thermo alkalophilic Bacillus sp. JP-99. Bioresour. Tech., 82:61-64.
  15. Naseimento, W.C.A. and M.L.L. Martins. 2004. Production and properties of an extracellular protease from thermophilic Bacillus sp. Brazilian J. Microbiol., 3:591-596.
  16. Campos, R., et al. 2001. Indigo degradation with purified laccases from Trametes hirsuta and sclerotium rolfsii. J. Biotech., 89:131-139.
  17. Agarry, S.E. and O. Ayobami. 2011. Evaluation of microbial systems for biotreatment of texile waste effluents in Nigeria : Biodecolourization and biodegradation of textile dye. J. Appl. Sci. Env. Manage., 15:79-86.
  18. Suzuki, T., et al. 2001. Correlation of aerobic biodegradability of sulphonated azo dyes with the chemical structure. Chemosphere. 45:1-9.
  19. Robinson, T., et al. 2001. Remediation of dyes in textile effluent : A critical review on current treat ment technologies with a proposed alternative. Bioresour. Tech., 77:247-255.
  20. Maier, J., et al. 2004. A new alkali-thermostable azo reductase from Bacillus sp. strain SF. Appl. Env. Microbiol., 70:837-844.
  21. Bergey, D.H. and J.G. Holt. 2000. Bergey’s mannual of determinative bacteriology (9th edn). Lippincott Williams and Wilkins, Philadelphia.
  22. Salwan, R., A. Gulati and R.C. Kasana. 2010. Phylogenetic diversity of alkaline protease producing psychrotrophic bacteria from glacier and cold environments of Lahual and Spiti, India. J. Basic Microbiol., 50:150-159.
  23. Anson, M.L. 1938. The estimation of pepsin, tryp-sin, papain and cathepsin with hemoglobin. J. Gen. Physiol., 22:79-89.
  24. Bakri, Y., M. Magali and P. Thonart. 2009. Isolation and identification of a new fungal strain for amylase biosynthesis. Polish J. Microbiol., 58:269-273.
  25. APHA. 2005. Standard methods for the examination of water and wastewater (21st edn). American Public Health Association, Washington D.C.
  26. Goodacre, R., et al. 2000. Detection of the dipico-linic acid biomarker in Bacillus spores using Curie-point pyrolysis mass spectrometry and Fourier transform infrared spectroscopy. Anal. Chem., 72:119-127.
  27. Jeyachandra, S., et al. 2012. Characterization of extracellular hydrolytic enzyme producing extremely halophilic bacterium Virgibacillus sp. JS5. World J. Sci. Tech., 2:23-26.
  28. Moreno, M.L. et al. 2013. Halophilic bacteria as a source of novel hydrolytic enzymes. Life. 3:38-51.
  29. Annapura, S., et al. 2013. Isolation and molecular characterization of alkaline protease producing Bacillus thuringiensis. Cell. Biochem. Biophy., 66:45-51.
  30. Olajuyigbe, F.M. and J.O. Ajele. 2005. Production dynamics of extracellular protease from Bacillus species. African J. Biotech., 4:776-779.
  31. Abdelnasser, S.S., et al. 2015. Production of extracellular protease by new halotolerant alkaliphilic Bacillus sp. NPST-AK15 isolated from hypersaline soda lakes. Electronic J. Biotech., 18:236-243.
  32. Suganthi, C., et al. 2013. Screening and optimization of protease production from a halotolerant Bacillus licheniformis isolated from saltern sediments. J. Gen. Eng. Biotech., 11:47-52.
  33. Lokhande, R.S., P.U. Singare and D.S. Pimple. 2011. Toxicity study of heavy metal pollutants in wastewater effluent collected from Taloja, industrial estate of Mumbai, India. Resour. Env., 1:13-19.
  34. Benzina, O., et al. 2012. Enhanced decolourization of the azo dye Sirius rose BB by laccase-HBT system. 3 Biotech., 2:149-157.
  35. Devi, V.M., et al. 2012. Dye decolourization using fungal laccase. Bull. Env. Pharmacol. Life Sci., 1:67-71.
  36. Prasad, S.S. and K. Aikat. 2014. Study of biodegradation and biodecolourization of azo dye by Enterobacter sp. SXCR. Env. Tech., 35:956-965.
  37. Sarkar, S., et al. 2017. Degradation of synthetic azo dyes of textile industry : A sustainable approach using microbial enzymes. Water conser. Sci. Eng., 2:121-131.
  38. Soune, N. and A. Garode. 2018. Isolation characterization and identification of extracellular enzyme producer Bacillus licheniformis from municipal wastewater and evaluation of their biodegradability. Biotech. Res. Innovation. 2:37-41.
  39. Shin, K.S. 2004. The role of enzymes produced by white rot fungus Irpex lacteus in the decolourization of the textile industry effluent. Microbiol., 42:37-41.
  40. Pourbabaee, A., et al. 2006. Aerobic decolourization and detoxification of a disperse dye in textile effluent by a new isolate of Bacillus sp. Biotech. Bioeng., 93:631-635.
  41. Husain, Q. 2006. Potential applications of the oxido-reactive enzymes in the decolourization and detoxification of textile and other synthetic dyes from polluted water : A review. Critical Reviews Biotech., 26:201-221.
  42. Khilfi, R., et al. 2010. Decolourization and detoxification of textile industry wastewater by the lacca-se-mediator system. J. Hazard. Mater., 175:802-808.
  43. Bento, R.M.F., M.R. Almeida and P. Bharmoria. 2020. Improvements in the enzymetic degradation of textile dyes using ionic liquid-based surfactants. Sep. Purif. Tech., 235:1-7.