Aim of the present study was to evaluate the efficiency of fungal co-culture for the decolorization of synthetic brilliant green carpet industry dye. For this purpose two lignocellulolytic fungi Pleurotus florida (PF) and Rhizoctonia solani (RS) were employed. The study includes determination of enzyme profiles (laccase and peroxidase), dye decolorization efficiency of co-culture and crude enzyme extracts. Both fungi produced laccase and Mn peroxidase and successfully decolorized solutions of different concentrations (2.0, 4.0, 6.0, & 8.0(w/v) of dye. The co-culture resulted highest 98.54% dye decolorization at 2% (w/v) of dye as compared to monocultures (82.12% with PF and 68.89% with RS) during 12 days of submerged fermentation. The lower levels of dyes were rapidly decolorized, while higher levels in slow order as 87.67% decolorization of 8% dye. The promising achievement of the study was remarkable decolorizing efficiency of co-culture over monocultures. The direct treatment of the mono and co-culture enzyme extracts to dye also influenced remarkable. The highest enzymatic decolorization was through combined (PF and RS) extracts, while lesser by monoculture extracts. Based on the observations and potentiality of co-culture technology; further it can be exploited for the bioremediation of areas contaminated with hazardous environmental pollutants including textile and other industry effluents.
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http://dx.doi.org/10.1016/j.jenvman.2016.04.060 | DOI Listing |
Nat Prod Res
November 2024
National Research Center of Intercropping, The Islamia university of Bahwalpur, Bahwalpur, Pakistan.
often referred to as Cauliflower mushroom possess both medicinal and edibility values. In this research work, first time laccase purification and dye colourisation efficacy of 's purified laccase were assessed. Optimal laccase potential was noted after 12 day of incubation with 4 pH of medium at 45 °C.
View Article and Find Full Text PDFBraz J Microbiol
October 2024
Post Graduation Program of Biosciences of University of Latin American Integration (UNILA), Environmental Biotechnology Laboratory, Tarquínio Joslin dos Santos Av., 1000 Jd Universitário, Foz do Iguaçu, PR, Brazil.
We evaluated the bioremediation potential of petroleum-derived compounds using fungal strains isolated from marine samples collected on the coast of the states of Paraná, Brazil. About 75 isolated filamentous fungi were subjected to assays including decolorization of the synthetic dye Remazol Brilliant Blue R (RBBR), tolerance to diesel oil, production of bioemulsifying and degradation of pyrene. Nine isolates could decolorize RBBR between 3.
View Article and Find Full Text PDFMicrob Cell Fact
October 2024
Botany and Microbiology Department, Faculty of Science, Tanta University, Tanta, 31527, Egypt.
Background: Hazardous synthetic dye wastes have become a growing threat to the environment and public health. Fungal enzymes are eco-friendly, compatible and cost-effective approach for diversity of applications. Therefore, this study aimed to screen, optimize fermentation conditions, and characterize laccase from fungal endophyte with elucidating its ability to decolorize several wastewater dyes.
View Article and Find Full Text PDFData Brief
December 2024
Department of Chemistry, College of Science, De La Salle University, 2401 Taft Ave, Malate, Manila 1004, Metro Manila, Philippines.
Naphthol Green B (NGB) is a synthetic azo dye widely used in various industries, including textiles and leathers. NGB poses significant environmental and ecological concerns when released into natural water systems. This paper investigates the decolorization of NGB using UV/sulfite system.
View Article and Find Full Text PDFInt J Biol Macromol
September 2024
Henan Province Engineering Research Center of Innovation for Synthetic Biology, School of Life Sciences and Technology, Xinxiang Medical University, Xinxiang 453003, PR China. Electronic address:
rAzoR2326, an azoreductase derived from Roseibium sp. H3510, functions as an FMN-dependent homodimer utilizing NADH as cofactor. It demonstrated maximum activity at 45 °C and retained moderate activity above 50 °C, exhibiting stability from pH 7-10.
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