Microaerophilic biodegradation of raw textile effluent by synergistic activity of bacterial community DR4

Treatment of raw textile effluent (RTE) is very difficult, due to its inherent heterogeneous, low-biodegradable and toxic compositions. Pure and mixed microbial cultures have limited metabolic capabilities in effective mineralization of complex RTE. Therefore, in this study a novel bacterial community DR4 was enriched directly into a complex RTE consisting of 27 different dyes using textile dye polluted soil as an inoculum. The rigorous enrichment process resulted in acclimatization of a taxonomically distinct bacterial population, with an abundance of the genus Comamonas in the bacterial community DR4 as compared to the abundance of Pseudomonas in the RTE respectively, as revealed by high-throughput 16S rRNA gene (V3-V4 region) sequencing. Microaerophilic treatment of RTE by enriched bacterial community DR4, in the presence of optimized electron donor (sucrose) and nitrogen source (yeast extract) resulted in 88% of American Dye Manufacturer's Institute (ADMI) removal and 98% of Chemical oxygen demand (COD) reduction within 32 hat 37 degrees C. In silico prediction of the functional genes within bacterial community DR4 was made by Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) analysis. The PICRUSt analysis revealed high abundance of xenobiotic degradation and metabolism genes. The predicted functional genes and textile dye degradation pathways were further validated using Ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared (FFIR) spectroscopy and High Resolution Liquid Chromatography coupled with Mass Spectrometry (HR-LCMS) based characterization of textile dye degradation metabolites. The activity of azoreductases in the cellfree extracts (CFE) of the enriched bacterial community DR4 was induced by 1.83-7.81 folds in the presence of representative textile dyes as compared to uninduced samples, which confirmed their role in textile effluent decolourization. The degradation of four representative azo dyes present in RTE such as Disperse orange 30, Reactive red 152, Direct blue 2 and Acid brown 15 depicted symmetric degradation of azo bonds by bacterial community DR4.