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      Ecofriendly biodegradation of Reactive Black 5 by newly isolated Sterigmatomyces halophilus SSA1575, valued for textile azo dye wastewater processing and detoxification

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          Abstract

          A total of seven yeast strains from 18 xylanolytic and/or xylose-fermenting yeast species isolated from the wood-feeding termite Reticulitermes chinenesis could efficiently decolorize various azo dyes under high-salt conditions. Of these strains, a novel and unique azo-degrading and halotolerant yeast, Sterigmatomyces halophilus SSA1575, has been investigated in this study. This strain could significantly decolorize four combinations of a mixture of dyes. It showed a high capability for decolorizing Reactive Black 5 (RB5) even at 1,500 mg L −1. The strain SSA1575 still showed a high capability for decolorizing a 50 mg L −1 RB5 with a salt mixing at a NaCl concentration of up to 80 g L −1. It also exhibited significant ability to decolorize repeated additions of dye aliquots, with a reduction in time of up to 18 h. Most of the tested carbon and nitrogen sources could significantly enhance a RB5 decolorization. However, this process was inhibited by the addition of sucrose and sodium nitrate. NADH-dichlorophenol indophenol (NADH-DCIP) reductase and lignin peroxidase were determined as the key reductase and oxidase of S. halophilus SSA1575. Finally, strain SSA1575, can effectively detoxify RB5 into non-toxic products. Overall, S. halophilus SSA1575, might be a promising halotolerant yeast valued for the treatment of various textile effluents with high salinity.

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          Decolorization of textile azo dyes by newly isolated halophilic and halotolerant bacteria.

          Studies were carried out on the decolorization of textile azo dyes by newly isolated halophilic and halotolerant bacteria. Among the 27 strains of halophilic and halotolerant bacteria isolated from effluents of textile industries, three showed remarkable ability in decolorizing the widely utilized azo dyes. Phenotypic characterization and phylogenetic analysis based on 16S rDNA sequence comparisons indicate that these strains belonged to the genus Halomonas. The three strains were able to decolorize azo dyes in a wide range of NaCl concentration (up to 20%w/v), temperature (25-40 degrees C), and pH (5-11) after 4 days of incubation in static culture. They could decolorize the mixture of dyes as well as pure dyes. These strains also readily grew in and decolorized the high concentrations of dye (5000 ppm) and could tolerate up to 10,000 ppm of the dye. UV-Vis analyses before and after decolorization and the colorless bacterial biomass after decolorization suggested that decolorization was due to biodegradation, rather than inactive surface adsorption. Analytical studies based on HPLC showed that the principal decolorization was reduction of the azo bond, followed by cleavage of the reduced bond.
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            Biodegradation of synthetic dyes of textile effluent by microorganisms: an environmentally and economically sustainable approach

            Due to its overall environmental impact, the residual dye in the wastewater from the synthetic dye manufacturing and textile industries is a global concern. The discharge contains a high content of pigments and other additives, possessing complex structures. As per the requirement for dyed clothing, dyestuff in the effluent is less susceptible to acids, bases, and oxygen. Thus, conventional physical and chemical methods are not always efficient in degrading the dyes. Some microorganisms growing in an area affected with textile effluent have the capability to utilize the dyes as a source of carbon or nitrogen or both. As a very clean, inexpensive, and sufficient alternative, bioremediation of textile wastewater using these microorganisms has gained major popularity. This review primarily centers the contribution of bacteria in this sector and the isolation of such bacteria from textile effluent. A secondary focus is discussing the factors which influence the performance by different bacteria.
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              Decolorization and detoxification of sulfonated azo dye methyl orange by Kocuria rosea MTCC 1532.

              Kocuria rosea (MTCC 1532) showed 100% decolorization of methyl orange (50 mg l(-1)) under static condition. The optimum pH and temperature for dye decolorization was 6.8 and 30 degrees C, respectively. The K. rosea (MTCC 1532) showed maximum decolorization of methyl orange when growth medium containing yeast extract as compared to other substrates. The culture exhibited significant ability to decolorize repeated additions of dye, with reduction in time up to 12 h at eighth dye aliquot addition. Significant induction of reductases (NADH-DCIP reductase and azoreductase) suggests its involvement in decolorization of methyl orange. The metabolites formed after decolorization of methyl orange, such as 4-amino sulfonic acid and N,N'-dimethyl p-phenyldiamine were characterized using FTIR and MS. Phytotoxicity and microbial toxicity study showed the methyl orange was toxic and metabolites obtained after its decolorization was nontoxic for experimental plants (Triticum aestivum and Phaseolus mungo) and bacteria (K. rosea, Pseudomonas aurugenosa and Azatobacter vinelandii). 2009 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                jzsun1002@ujs.edu.cn
                samh@ujs.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                23 July 2020
                23 July 2020
                2020
                : 10
                : 12370
                Affiliations
                [1 ]ISNI 0000 0001 0743 511X, GRID grid.440785.a, Biofuels Institute, School of the Environment and Safety Engineering, , Jiangsu University, ; Xuefu Rd. 301, Zhenjiang, 212013 China
                [2 ]ISNI 0000 0000 9477 7793, GRID grid.412258.8, Department of Home Economic, Faculty of Specific Education, , Tanta University, ; Tanta, Egypt
                [3 ]ISNI 0000 0000 9477 7793, GRID grid.412258.8, Polymer Research Group, Department of Chemistry, Faculty of Science, , Tanta University, ; Tanta, 31527 Egypt
                [4 ]ISNI 0000 0000 9477 7793, GRID grid.412258.8, Botany Department, Faculty of Science, , Tanta University, ; Tanta, 31527 Egypt
                Article
                69304
                10.1038/s41598-020-69304-4
                7378048
                31913322
                c5088ae2-304f-4112-a383-5eef8b44f1f6
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 January 2020
                : 10 July 2020
                Funding
                Funded by: National Key R
                Funded by: National Natural Science Foundation of China
                Award ID: 31772529
                Award ID: 31772529
                Award ID: 31772529
                Award Recipient :
                Funded by: Priority of Academic Program Development of Jiangsu Higher Education Institutions
                Award ID: PAPD 4013000011
                Award ID: PAPD 4013000011
                Award ID: PAPD 4013000011
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                biological techniques,microbiology,environmental sciences
                Uncategorized
                biological techniques, microbiology, environmental sciences

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