R. Rathour, Vaishali Sharma, Nidhi Rana, R. Bhatia, A. Bhatt
{"title":"Bioremediation of Simulated Textile Effluent by an Efficient Bio-catalyst Purified from a Novel Pseudomonas fluorescence LiP-RL5","authors":"R. Rathour, Vaishali Sharma, Nidhi Rana, R. Bhatia, A. Bhatt","doi":"10.2174/2212796814666200406100247","DOIUrl":null,"url":null,"abstract":"\n\nMicrobial degradation of highly stable textile dyes, using lignin peroxidase,\nis an eco-friendly, less expensive and much advantageous in comparison to the\nchemical method.\n\n\n\nBiodegradation potential of lignin peroxidase (LiP), from Pseudomonas fluorescens\nLiP-RL5, was enhanced after optimization and purification so as to use it as a potential\nbioresource for the treatment of textile effluent.\n\n\n\n LiP producing bacterial isolate was primarily screened by methylene blue assay\nfollowed by LiP assay. The standard protocol was used for purification of lignin peroxidase\nand purified LiP was finally used for degradation of textile dyes.\n\n\n\n57 bacterial isolates were screened for lignin peroxidase activity. Isolate LiP-RL5\nshowed maximum activity (19.8 ±0.33 %) in terms of methylene blue reduction in comparison\nto others. Biochemical and molecular characterization of LiP-RL5 showed 99 % similarity\nwith P. fluorescens. Lignin peroxidase activity was increased by 50 % after optimization\nof cultural conditions. Maximum enhancement in the activity was achieved when peptone\nwas used as a nitrogen source. LiP from P. fluorescens LiP-RL5 was further purified up to 2\nfolds. SDS-PAGE analysis revealed a single protein band of approximately 40 kDa. Enzyme\nalso showed high catalytic efficiency with Km= 6.94 mM and Vmax= 78.74 μmol/ml/min. Purified\nenzyme was able to decolorize the simulated textile effluent up to 45.05 ±0.28 % after\n40 minutes.\n\n\n\n: High catalytic efficiency of purified LiP from P. fluorescens LiP-RL5 suggests\nits utility as a potential candidate for biodegradation of toxic dyes in the industrial effluent,\nwhich could be successfully utilized for wastewater treatment at commercial level.\n","PeriodicalId":10784,"journal":{"name":"Current Chemical Biology","volume":"32 1","pages":"128-139"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Chemical Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2212796814666200406100247","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Microbial degradation of highly stable textile dyes, using lignin peroxidase,
is an eco-friendly, less expensive and much advantageous in comparison to the
chemical method.
Biodegradation potential of lignin peroxidase (LiP), from Pseudomonas fluorescens
LiP-RL5, was enhanced after optimization and purification so as to use it as a potential
bioresource for the treatment of textile effluent.
LiP producing bacterial isolate was primarily screened by methylene blue assay
followed by LiP assay. The standard protocol was used for purification of lignin peroxidase
and purified LiP was finally used for degradation of textile dyes.
57 bacterial isolates were screened for lignin peroxidase activity. Isolate LiP-RL5
showed maximum activity (19.8 ±0.33 %) in terms of methylene blue reduction in comparison
to others. Biochemical and molecular characterization of LiP-RL5 showed 99 % similarity
with P. fluorescens. Lignin peroxidase activity was increased by 50 % after optimization
of cultural conditions. Maximum enhancement in the activity was achieved when peptone
was used as a nitrogen source. LiP from P. fluorescens LiP-RL5 was further purified up to 2
folds. SDS-PAGE analysis revealed a single protein band of approximately 40 kDa. Enzyme
also showed high catalytic efficiency with Km= 6.94 mM and Vmax= 78.74 μmol/ml/min. Purified
enzyme was able to decolorize the simulated textile effluent up to 45.05 ±0.28 % after
40 minutes.
: High catalytic efficiency of purified LiP from P. fluorescens LiP-RL5 suggests
its utility as a potential candidate for biodegradation of toxic dyes in the industrial effluent,
which could be successfully utilized for wastewater treatment at commercial level.
期刊介绍:
Current Chemical Biology aims to publish full-length and mini reviews on exciting new developments at the chemistry-biology interface, covering topics relating to Chemical Synthesis, Science at Chemistry-Biology Interface and Chemical Mechanisms of Biological Systems. Current Chemical Biology covers the following areas: Chemical Synthesis (Syntheses of biologically important macromolecules including proteins, polypeptides, oligonucleotides, oligosaccharides etc.; Asymmetric synthesis; Combinatorial synthesis; Diversity-oriented synthesis; Template-directed synthesis; Biomimetic synthesis; Solid phase biomolecular synthesis; Synthesis of small biomolecules: amino acids, peptides, lipids, carbohydrates and nucleosides; and Natural product synthesis).