Abstract
Dye-decolorizing peroxidases (DyPs) are recently identified superfamily of heme-containing peroxidases which has received much attention for its potential application in dye decolourization. In the current research, six bacterial colonies (SDB1-6) showing lignolytic activity were isolated from forest soils of SBR using a minimal salt medium supplemented with alkali lignin and screened for DyP activity using brilliant green dye supplemented luria bertani agar medium. The highest DyP activity showing bacterium was identified using biochemical and 16SrRNA sequencing and was identified as Achromobacter insolitus. A. insolitus was found to be an efficient strain showing the highest DyP activity of 2.7 U/mL/ml at un-optimized condition. The RSM optimization was conducted to increase the DyP enzyme activity. A. insolitus demonstrated DyP activity of 6.20 U/mL/min with an increase of 2.29 times of enzyme activity in optimal condition of pH 7.0, temperature 25 °C, H2O2 concentration 0.1 mM, and time 24 h. The bacterium was further screened for dye decolorization taking crystal violet, methyl orange, methylene blue, brilliant green and methyl red dyes supplemented in LB medium. The bacterium showed maximum brilliant green degradation ability was analyzed using UV-Vis and FTIR analyses to characterize the degraded product. The highest brilliant green degradation activity of the A. insolitus in the present study could be exploited for bioremediation of brilliant green contaminated industrial effluents in a ecofriendly and cost effective way.
Acknowledgments
The authors extend their thanks to the Head of the Department of Biotechnology at Maharaja Sriram Chandra Bhanja Deo University, Baripada, Odisha, India, for supplying the necessary infrastructure facilities for the ongoing study. Furthermore, the authors express their gratitude to the Department of Applied Geology (AGL), IIT (ISM) Dhanbad (http://www.iitism.ac.in), for performing FTIR analyses and supplying visualizations for this research. The authors are also appreciative of AGL, IIT (ISM), Dhanbad, for allowing access to equipment, providing technical support, and offering laboratory facilities through the DST-FIST Level-II Program [No. SR/FST/ESII-014/2012(C)].
Authors’ contributions
SD and SR wrote all the parts of this research paper with related previous review works, and contributed original manuscript and formatting. SD and SR conducted major part of experiments, investigated the results, analyzed data, validated the results with related previous works. Whereas, AS helped in doing some of experiments like biochemical analysis. HT supervised the whole work, conceptualized the research, and guided the writing & editing of the manuscript. All authors have read and approved the manuscript
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Disclosure statement
No potential conflict of interest was reported by the author(s).
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Data availability statement
All data generated or analyzed during this study are included in this article.