Removal of sulfamethoxazole and diclofenac from water: strategies involving O3 and H2O2.

Diclofenac (DCF) and Sulfamethoxazole (SMX) are two of the most frequently detected pharmaceutical compounds in water and are hardly removed by biological treatment systems. The presence of H2O2 was investigated in the ozonation of these two compounds. Experiments were carried out with both using distilled water and secondary effluent from a municipal wastewater treatment plant spiked with pharmaceuticals. Chemical oxygen demand (COD) abatement rate improved when H2O2 was added at the beginning of the ozonation process and when the ozone inlet concentration increased, attaining a maximum value of 91% and simultaneously a lower ozone waste for a H2O2 initial concentration of 5 mM and an ozone inlet concentration of 20 g Nm-3. For these operation conditions, the water matrix has no significant impact on SMX and DCF removal, which were totally degraded in 45 and 60 min, respectively. Nevertheless, lower COD degradation and ozone usage were obtained when the secondary effluent was used. Inorganic ions such as chloride, sulphate and nitrate and short-chain organic compounds were detected as by-products of the SMX and DCF oxidation. Vibrio fischeri luminescence inhibition tests revealed that simultaneous use of ozone and H2O2 reduced acute toxicity.

Production of heterologous cutinases by E. coli and improved enzyme formulation for application on plastic degradation

Background: The hydrolytic action of cutinases has been applied to the degradation of plastics. Polyethylene terephthalate (PET) have long half-life which constitutes a major problem for their treatment as urban solid residues. The aim of this work was to characterize and to improve stable the enzyme to optimize the process of degradation using enzymatic hydrolysis of PET by recombinant cutinases. Results: The wild type form of cutinase from Fusarium solani pisi and its C-terminal fusion to cellulose binding domain N1 from Cellulomonas fimi were produced by genetically modified Escherichia coli. The maximum activity of cutinases produced in Lactose Broth in the presence of ampicillin and isopropyl β-D-1-thiogalactopyranoside (IPTG) was 1.4 IU/mL. Both cutinases had an optimum pH around 7.0 and they were stable between 30 and 50ºC during 90 min. The addition of glycerol, PEG-200 and (NH4)2SO4 to the metabolic liquid, concentrated by ultra filtration, stabilized the activity during 60 days at 28ºC. The treatment of PET with cutinases during 48 hrs led to maxima weight loss of 0.90%. Conclusions: Recombinant microbial cutinases may present advantages in the treatment of poly(ethylene terephthalate) PET through enzymatic treatments.