Influence of fermented tannery solid waste on morphological, biochemical, yield and nutritional responses of tomato plants.

The non-tanned proteinaceous tannery solid waste animal fleshing (ANFL), containing high nutritive value, was hydrolyzed using bacteria Selenomonas ruminantium HM000123 through submerged (SmF) and solid-state (SSF) fermentation processes. In addition, the effects of ANFL fermentative hydrolysate on growth, yield and biochemical properties of tomato plants were investigated. The treatments included T1 (SmF-ANFL), T2 (SSF-ANFL), T3 (recommended dose of NPK fertilizers) and a control without any amendment. Hydrolysates of both SmF-ANFL and SSF-ANFL treatments increased the biomass and yield as evidenced by plant height, stem girth, number of leaves and fruit yield when compared with both NPK and control plants. In this 90-day study, significant (p ≤ 0.05) changes were observed in SSF-ANFL treated plants compared to the other treatments. Protein profile analyzed through SDS-PAGE indicates the expression of a high molecular weight protein (205 kDa) and other proteins in the leaves of the SSF-ANFL treated plants. Overall results revealed that SSF-ANFL can be successfully utilized as a fertilizer particularly for cultivating tomato plants.

Production of prodigiosin using tannery fleshing and evaluating its pharmacological effects.

AIM: The focal theme of present investigation includes isolation of prodigiosin producing fish gut bacteria, enhancing its production using tannery solid waste fleshing, and evaluation of its pharmacological effect. METHODS: Optimization of fermentation conditions to yield maximum prodigiosin, and instrumental analysis using FTIR, NMR, ESI-MS, TGA, and DSC. RESULTS: The optimum conditions required for the maximum prodigiosin concentration were achieved at time 30 h, temperature 30°C, pH 8, and 3% substrate concentration. The secondary metabolite was analyzed using ESI-MS, FTIR, and NMR. Therapeutic efficacy was assessed by in vitro anticancer studies. Among the pathogenic bacteria Pseudomonas aeruginosa was most susceptible at the lowest concentration followed by Salmonella typhi. IC50 concentration was cell line specific (HeLa cells: 4.3 µM, HEp2: 5.2 µM, and KB cells: 4.8 µM) and remains nontoxic up to the concentration of 25 µM on normal Vero cells suggesting that cancerous cells are more susceptible to the prodigiosin at lower concentration. CONCLUSION: Maximum prodigiosin production was obtained with tannery fleshing. The potency of the fish gut bacterial secondary metabolite prodigiosin as a therapeutic agent was confirmed through in vitro antimicrobial and anticancer studies.