45 research outputs found

    Production of chlorella vulgaris biomass on uv-treated wastewater as an alternative for environmental sustainability on high-mountain fisheries

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    The sustained expansion of agricultural industry in Colombian high-mountain has led to an increased size of residues, especially untreated wastewater. This untreated water is an urgent matter for public and environmental health, not only by its nutrient concentration (composed especially of food residuals and feces) but also the presence of pathogens (virus, bacteria, etc.) which are discharged to the environment. The overall objective of this work is to evaluate the effect of UV-treated wastewater from a high-mountain fishery as culture media for the production of Chlorella vulgaris as a sustainable method for nutrient and water recirculation on the fishery production system. The UV-canal efficiency was evaluated by the implementation of an experimental factorial design (time, distance of the UV-lamps towards the canal, number of UV-lamps and the sample concentration) using STATISTICA 7.0 software. Results shown that time (3 to 5 minutes) and the number of lamps (3-4) of 15 Watts eliminate completely coliforms from the samples. After UV-treatment the resulting water was test as culture media for C. vulgaris production by the adjustment of C/N ratio (Sodium Carbonate/potassium nitrate) by the implementation of an experimental 23 factorial design. Results shown that higher nitrate concentrations (>0,22 g/L) and moderate carbonate concentrations (1 g/L) increase the final biomass concentration up to 4g/L in 20 days

    Removal of cationic pollutants from water by xanthated corn cob: optimization, kinetics, thermodynamics, and prediction of purification process

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    The removal of Cr(III) ions and methylene blue (MB) from aqueous solutions by xanthated corn cob (xCC) in batch conditions was investigated. The sorption capacity of xCC strongly depended of the pH, and increase when the pH rises. The kinetics was well fitted by pseudo-second order and Chrastil’s model. Sorption of Cr(III) ions and MB on xCC was rapid during the first 20 min of contact time and, thereafter, the biosorption rate decrease gradually until reaching equilibrium. The maximum sorption capacity of 17.13 and 83.89 mg g-1 for Cr(III) ions and MB, respectively was obtained at 40 °C, pH 5 and sorbent dose 4 g dm-3 for removal of Cr(III) ions and 1 g dm-3 for removal of MB. The prediction of purification process was successfully carried out and the verification of theoretically calculated amounts of sorbent was confirmed by using packed-bed column laboratory system with recirculation of the aqueous phase. The wastewater from chrome plating industry was successfully purified, i.e. after 40 min concentration of Cr(III) ions was decreased lower than 0.1 mg dm-3. Also, removal of MB from the river water was successfully carried out and after 40 min removal efficiency was about 94 %

    Structural basis of non-canonical transcriptional regulation by the A-bound iron-sulfur protein WhiB1 in M. tuberculosis

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    WhiB1 is amonomeric iron–sulfur cluster-containing transcription factor in the WhiB-like family that is widely distributed in actinobacteria including the notoriously persistent pathogen Mycobacterium tuberculosis (M. tuberculosis). WhiB1 plays multiple roles in regulating cell growth and responding to nitric oxide stress inM. tuberculosis, but its underlying mechanism is unclear. Here we report a 1.85 A° -resolution crystal structure of the [4Fe–4S] cluster-bound (holo- )WhiB1 in complex with the C-terminal domain of the 70-family primary sigma factor A of M. tuberculosis containing the conserved region 4 (A 4). Region 4 of the 70-family primary sigma factors is commonly used by transcription factors for gene activation, and holo-WhiB1 has been proposed to activate gene expression via binding to A 4. The complex structure, however, unexpectedly reveals that the interaction between WhiB1 and A 4 is dominated by hydrophobic residues in the [4Fe–4S] cluster binding pocket, distinct from previously characterized canonical 70 4-bound transcription activators. Furthermore, we show that holo-WhiB1 represses transcription by interaction with A 4 in vitro and that WhiB1 must interact with A 4 to perform its essential role in supporting cell growth in vivo. Together, these results demonstrate that holo-WhiB1 regulates gene expression by a non-canonical mechanism relative to well-characterized A 4-dependent transcription activators
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