Browsing by Author "Carvalho, M. F."
Now showing 1 - 10 of 15
Results Per Page
Sort Options
- 2-Fluorophenol degradation by aerobic granules in a sequencing batch reactorPublication . Duque, A. F.; Bessa, V. S.; Carvalho, M. F.; De Kreuk, M. K.; Loosdrecht, M. C. M. van; Castro, P. M. L.
- 4-Chlorophenol degradation by a bacterial consortium: development of a granular activated carbon biofilm reactorPublication . Caldeira, M.; Heald, S. C.; Carvalho, M. F.; Vasconcelos, I.; Bull, A. T.; Castro, P. M. L.A bacterial consortium that can degrade chloro- and nitrophenols has been isolated from the rhizosphere of Phragmitis communis. Degradation of 4-chlorophenol (4-CP) by a consortium attached to granular activated carbon (GAC) in a biofilm reactor was evaluated during both open and closed modes of operation. During the operation of the biofilm reactor, 4-CP was not detected in the column effluent, being either adsorbed to the GAC or biodegraded by the consortium. When 4-CP at 100 mg l−1 was fed to the column in open mode operation (20 mg g−1 GAC total supply), up to 27% was immediately available for biodegradation, the rest being adsorbed to the GAC. Biodegradation continued after the system was returned to closed mode operation, indicating that GAC bound 4-CP became available to the consortium. Biofilm batch cultures supplied with 10–216 mg 4-CP g−1 GAC suggested that a residual fraction of GAC-bound 4-CP was biologically unavailable. The consortium was able to metabolise 4-CP after perturbations by the addition of chromium (Cr VI) at 1–5 mg l−1 and nitrate at concentrations up to 400 mg l−1. The development of the biofilm structure was analysed by scanning electron microscopy and confocal laser scanning microscopy (CLSM) techniques. CLSM revealed a heterogeneous structure with a network of channels throughout the biofilm, partially occupied by microbial exopolymer structures.
- 4-fluorocinnamic acid biodegradation by a rhodococcus strainPublication . Amorim, Catarina L.; Carvalho, M. F.; Afonso, C. M. M.; Castro, Paula M. L.
- Bacterial degradation of moxifloxacin in the presence of acetate as a bulk substratePublication . Carvalho, M. F.; Maia, A. S.; Tiritan, M. E.; Castro, P. M. L.Fluoroquinolones constitute a group of emerging pollutants and their occurrence in different environmental compartments is becoming object of increasing public concern due to their ecotoxicological effects and the potential to develop resistant bacteria. This study aimed to investigate the biodegradation of moxifloxacin (MOX), for which studies in the literature are very scarce. An activated sludge (AS) consortium and three bacterial strains able to degrade fluoroaromatic compounds e strains F11, FP1 and S2 e were tested. Biodegradation studies were conducted using acetate as a bulk carbon source. Strain F11 showed the highest biodegradation capacity, being able to completely consume and dehalogenate 7.5 mM of the target antibiotic when daily co-supplemented with acetate present as a readily degradable organic substrate in wastewaters. MOX could be used by strain F11 as a sole nitrogen source but the presence of an external nitrogen source in the culture medium was essential for complete biodegradation. Strain F11 was capable of completely consuming MOX in a range between 2 and 11 mM, although stoichiometric fluoride release was not obtained for the highest tested concentration. The antibacterial activity of residual MOX and of the metabolic products potentially resultant from the biodegradation process was investigated by agar diffusion tests, demonstrating that MOX biodegradation is associated with the elimination of the antibacterial properties of the target antibiotic and of the produced metabolites, which is an important result, as the activity of antibiotics and/or their metabolites in the environment, even at low levels, may lead to the development of resistant bacterial strains. Overall, the results obtained in this study suggest that strain F11 is a promising microorganism for the treatment of waters contaminated with MOX, where it could be used for bioaugmentation/bioremediation purposes. To the best of our knowledge, this is the first study reporting complete removal and dehalogenation of MOX by a single microorganism.
- Bioaugmentation of a rotating biological contactor with a bacterial strain able to degrade fluorinated phenolsPublication . Duque, A. F.; Bessa, Vânia S.; Carvalho, M. F.; Castro, P. M. L.
- Biodegradation of 2-fluorophenol in a rotating biological contactorPublication . Duque, A. F.; Bessa, V. S.; Franco, A. R.; Carvalho, M. F.; Castro, P. M. L.
- Biological treatment of a contaminated gaseous emission from a leather industry in a suspended-growth bioreactorPublication . Carvalho, M. F.; Duque, A. F.; Moura, S. C.; Amorim, Catarina L.; Ferreira Jorge, R. M.; Castro, Paula M. L.A suspended-growth bioreactor (SGB) was operated for the treatment of a gaseous stream mimicking emissions generated at a leather industrial company. The main volatile organic compounds (VOCs) present in the gaseous stream consisted of 1-methoxy-2-propanol, 2,6-dimethyl-4-heptanone, 2-butoxyethanol, toluene and butylacetate. A microbial consortium able to degrade these VOCs was successfully enriched. A laboratory- scale SGB was established and operated for 210-d with an 8 h cycle period and with shutdowns at weekends. Along this period, the SGB was exposed to organic loads (OL) between 6.5 and 2.3 £ 102 g h¡1 m¡3. Most of the compounds were not detected at the outlet of the SGB. The highest total VOC removal efficiency (RE) (ca 99%) was observed when an OL of 1.6 £ 102 g h¡1 m¡3 was fed to the SGB. The maximum total VOC elimination capacity (1.8 £ 102 g h¡1 m¡3) was achieved when the OL applied to the SGB was 2.3 £ 102 g h¡1 m¡3. For all the operating conditions, the SGB showed high levels of degradation of toluene and butylacetate (RE t 100%). This study also revealed that recirculation of the gaseous effluent improved the performance of the SGB. Overall, the SGB was shown to be robust, showing high performance after night and weekend shutdown periods.
- Cloning, nucleotide sequence and expression of Fluorobenzene Dioxygenase from Labrys portucalensis strain F11Publication . Moreira, I. S.; Kirschner, A.; Carvalho, M. F.; Castro, P. M. L.; Janssen, D. B.
- Degradation of difluorobenzenes by the wild strain Labrys portucalensisPublication . Moreira, I. S.; Carvalho, M. F.; Amorim, Catarina L.; Janssen, D. B.; Castro, Paula M. L.
- Degradation of difluorobenzenes by the wild strain Labrys portucalensisPublication . Moreira, I.S.; Carvalho, M. F.; Amorim, Catarina L.; Janssen, D. B.; Castro, Paula M. L.