Abstract
Azo dyes are extensively used in textile processing industry, which are resistant to degradation and persist in soil for long time due to its fused aromatic structure. Aim of this study was to identify the azo dye compound accumulated in soil and screening of native azo dye degrading microorganisms. Azo dyes present in the soil sample were identified using high performance liquid chromatography (HPLC). Selective isolation of azo dye degrading microorganism was done using the minimal medium supplemented with azo dye (50 mg/L). The isolates were identified and tested as individual and as mixed cultures for azo dye decolourisation and degradation. Azo dye degradation pathway by the fungal cultures were assessed through GC–MS. HPLC analysis of soil samples indicated the presence of various azo dyes such as congored, methylred and reactive dyes. Dichotomomyces cejpii MRCH 1-2 plus Phoma tropica MRCH 1-3 exhibited maximum congored (48.7 ± 0.66 mg/L out of 50 mg/L), methylred (43.57 ± 1.07 mg/L out of 50 mg/L) and reactive blue (45.3 ± 2.7 mg/L out of 50 mg/L) degradation compared to other treatments. Response surface methodology analysis was used to optimise the culture condition for effective azo dye degradation. The possible azo dye degradation pathway by the fungal mixed culture and enzyme involved was illustrated in this study. Fungal mixed culture Dichotomomyces cejpii MRCH 1-2 and Phoma tropica MRCH 1-3 may be recommended for azo dye decolourisation as well as degradation in the textile industrial effluent.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.