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1.
Chinese Journal of Biotechnology ; (12): 3685-3695, 2021.
Article in Chinese | WPRIM | ID: wpr-921457

ABSTRACT

Biological denitrification is the most widely used technology for nitrate removal in wastewater treatment. Conventional denitrification requires long hydraulic retention time, and the nitrate removal efficiency in winter is low due to the low temperature. Therefore, it is expected to develop new approaches to enhance the denitrification process. In this paper, the effect of adding different concentrations of Fe₃O₄ nanoparticles on the denitrification catalyzed by Pseudomonas stutzeri was investigated. The maximum specific degradation rate of nitrate nitrogen improved from 18.0 h⁻¹ to 23.7 h⁻¹ when the concentration of Fe₃O₄ increased from 0 mg/L to 4 000 mg/L. Total proteins and intracellular iron content also increased along with increasing the concentration of Fe₃O₄. RT-qPCR and label-free proteomics analyses showed that the relative expression level of denitrifying genes napA, narJ, nirB, norR, nosZ of P. stutzeri increased by 55.7%, 24.9%, 24.5%, 36.5%, 120% upon addition of Fe₃O₄, and that of denitrifying reductase Nap, Nar, Nir, Nor, Nos increased by 85.0%, 147%, 16.5%, 47.1%, 95.9%, respectively. No significant difference was observed on the relative expression level of denitrifying genes and denitrifying reductases between the bacteria suspended and the bacteria adhered to Fe₃O₄. Interestingly, the relative expression level of electron transfer proteins of bacteria adhered to Fe₃O₄ was higher than that of the bacteria suspended. The results indicated that Fe₃O₄ promoted cell growth and metabolism through direct contact with bacteria, thereby improving the denitrification. These findings may provide theoretical support for the development of enhanced denitrification.


Subject(s)
Aerobiosis , Denitrification , Nitrates , Nitrogen , Pseudomonas stutzeri/genetics
2.
Braz. j. microbiol ; 49(1): 38-44, Jan.-Mar. 2018. tab, graf
Article in English | LILACS | ID: biblio-889215

ABSTRACT

ABSTRACT Discharge of coke-oven wastewater to the environment may cause severe contamination to it and also threaten the flora and fauna, including human beings. Hence before dumping it is necessary to treat this dangerous effluent in order to minimize the damage to the environment. Conventional technologies have inherent drawbacks however, biological treatment is an advantageous alternative method. In the present study, bacteria were isolated from the soil collected from the sites contaminated by coke-oven effluent rich in phenol and cyanide. Nucleotides sequence alignment and phylogenetic analysis showed the identity of the selected phenol and cyanide degrading isolates NAUN-16 and NAUN-1B as Pseudomonas putida and Pseudomonas stutzeri, respectively. These two isolates tolerated phenol up to 1800 mg L-1 and cyanide up to 340 mg L-1 concentrations. The isolates were immobilized on activated charcoal, saw dust and fly ash. The effluent was passed through the column packed with immobilized cells with a flow rate of 5 mL min-1. The isolates showed degradation of phenol up to 80.5% and cyanide up to 80.6% and also had the ability to reduce biological oxygen demand, chemical oxygen demand and lower the pH of effluent from alkaline to near neutral. The study suggests the utilization of such potential bacterial strains in treating industrial effluent containing phenol and cyanide, before being thrown in any ecosystem.


Subject(s)
Cyanides/metabolism , Phenol/metabolism , Pseudomonas putida/metabolism , Pseudomonas stutzeri/metabolism , Waste Disposal, Fluid/methods , Wastewater/microbiology , Biodegradation, Environmental , Cells, Immobilized/classification , Cells, Immobilized/metabolism , Coke/analysis , Cyanides/analysis , Industrial Waste/analysis , Phenol/analysis , Phylogeny , Pseudomonas putida/classification , Pseudomonas putida/genetics , Pseudomonas putida/isolation & purification , Pseudomonas stutzeri/classification , Pseudomonas stutzeri/genetics , Pseudomonas stutzeri/isolation & purification , Wastewater/analysis
3.
Braz. j. microbiol ; 46(2): 377-387, Apr-Jun/2015. tab, graf
Article in English | LILACS | ID: lil-749728

ABSTRACT

Three bacterial isolates identified as Alcanivorax borkumensis SK2, Rhodococcus erythropolis HS4 and Pseudomonas stutzeri SDM, based on 16S rRNA gene sequences, were isolated from crude oil enrichments of natural seawater. Single strains and four bacterial consortia designed by mixing the single bacterial cultures respectively in the following ratios: (Alcanivorax: Pseudomonas, 1:1), (Alcanivorax: Rhodococcus, 1:1), (Pseudomonas: Rhodococcus, 1:1), and (Alcanivorax: Pseudomonas: Rhodococcus, 1:1:1), were analyzed in order to evaluate their oil degrading capability. All experiments were carried out in microcosms systems containing seawater (with and without addition of inorganic nutrients) and crude oil (unique carbon source). Measures of total and live bacterial abundance, Card-FISH and quali-, quantitative analysis of hydrocarbons (GC-FID) were carried out in order to elucidate the co-operative action of mixed microbial populations in the process of biodegradation of crude oil. All data obtained confirmed the fundamental role of bacteria belonging to Alcanivorax genus in the degradation of linear hydrocarbons in oil polluted environments.


Subject(s)
Alcanivoraceae/metabolism , Petroleum/metabolism , Pseudomonas stutzeri/metabolism , Rhodococcus/metabolism , Alcanivoraceae/classification , Alcanivoraceae/genetics , Alcanivoraceae/isolation & purification , Biotransformation , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Microbial Consortia , Molecular Sequence Data , Phylogeny , Pseudomonas stutzeri/classification , Pseudomonas stutzeri/genetics , Pseudomonas stutzeri/isolation & purification , /genetics , Rhodococcus/classification , Rhodococcus/genetics , Rhodococcus/isolation & purification , Sequence Analysis, DNA , Seawater/microbiology
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