Shekhar B. Jadhav

Communal action of microbial cultures for Red HE3B degradation.

The consortium PMB11 consisting of three bacterial species, originally isolated from dye contaminated soil was identified as Bacillus odysseyi SUK3, Morganella morganii SUK5 and Proteus sp. SUK7. The consortium possessed the ability to decolorize various textile dyes as well as mixtures of dyes. PMB11 could decolorize Red HE3B (50 mg l(-1)) with 99% of decolorization within 12 h in nutrient broth, while in mineral medium it could decolorize up to 97% within 24h. Induction in the activities of various oxidative and reductive enzymes indicates the involvement of these enzymes in decolorization. Biodegradation of the dye was monitored using UV-vis spectroscopy, HPLC and FTIR analysis. The Red HE3B degradation pathway was proposed by GC-MS analysis. Various metabolites formed after the degradation were identified as 2,5-diaminobenzene 6-aminotriazine, aniline 2-sulfate, aniline 3-sulfate, 2-amino 5-chlorotriazine and naphthalene. Phytotoxicity studies revealed that metabolites formed after degradation were significantly less toxic in nature.

Optimization of l‐DOPA production by Brevundimonas sp. SGJ using response surface methodology

l‐DOPA (3,4‐dihydroxyphenyl‐l‐alanine) is an extensively used drug for the treatment of Parkinsons disease. In the present study, optimization of nutritional parameters influencing l‐DOPA production was attempted using the response surface methodology (RSM) from Brevundimonas sp. SGJ. A Plackett–Burman design was used for screening of critical components, while further optimization was carried out using the Box–Behnken design. The optimized levels of factors predicted by the model were pH 5.02, 1.549 g l−1 tryptone, 4.207 g l−1 l‐tyrosine and 0.0369 g l−1 CuSO4, which resulted in highest l‐DOPA yield of 3.359 g l−1. The optimization of medium using RSM resulted in a 8.355‐fold increase in the yield of l‐DOPA. The anova showed a significant R2 value (0.9667), model F‐value (29.068) and probability (0.001), with insignificant lack of fit. The highest tyrosinase activity observed was 2471 U mg−1 at the 18th hour of the incubation period with dry cell weight of 0.711 g l−1. l‐DOPA production was confirmed by HPTLC, HPLC and GC‐MS analysis. Thus, Brevundimonas sp. SGJ has the potential to be a new source for the production of l‐DOPA.