RESUMEN
Attachment and separation of sulfate-reducing bacteria (SRB) biofilm on stainless steel (SS) in simulated cooling water with and without different sterilization treatments was investigated by calculation of surface energy, theoretical work of adhesion and analysis of Scanning Electron Microscope/Energy Dispersive Spectrometer. Two types of biocides, glutaraldehyde and Polyhexamethylene guanidine (PHMG), and electromagnetic treatment were used in this paper. The results show that PHMG had the best bactericidal performance, followed by glutaraldehyde, and electromagnetic treatment was the lowest one. The theoretical work of adhesion was used to quantitatively evaluate the adhesion of biofilm on the surface of the metal. Theoretical work of adhesion between biofilm and SS in simulated cooling water increased with time. The theoretical adhesion work and adhesive capacity of biofilm to SS surface increased after treating with glutaraldehyde while decreasing after treating with PHMG and electromagnetic field. As the theoretical adhesion work decreased, the biofilm was gradually removed from the stainless steel surface. On the contrary, the biofilm adhered more firmly. The results of SEM were also consistent with the calculation results of theoretical adhesion work. The results obtained indicated that electromagnetic treatment had the lowest effect in sterilization but the best in biofilm separation.
Asunto(s)
Desinfectantes , Acero Inoxidable , Adhesión Bacteriana , Biopelículas , Desinfección , Propiedades de SuperficieRESUMEN
The real alkaline cleaning wastewater (ACW) was treated by a process consisting of neutralization, NaClO oxidation and aluminum sulfate (AS) coagulation, and a novel response surface methodology coupled nonlinear programming (RSM-NLP) approach was developed and used to optimize the oxidation-coagulation process under constraints of relevant discharge standards. Sulfuric acid neutralization effectively removed chemical oxygen demand (COD), surfactant alkylphenol ethoxylates (OP-10) and silicate at the optimum pH of 7.0, with efficiencies of 62.3%, >82.7% and 94.2%, respectively. Coagulation and adsorption by colloidal hydrated silica formed during neutralization were the major removal mechanisms. NaClO oxidation achieved almost complete removal of COD, but was ineffective for the removal of surfactant OP-10. AS coagulation followed by oxidation can efficiently remove OP-10 with the formation of Si-O-Al compounds. The optimum conditions for COD ≤100 mg/L were obtained at hypochlorite to COD molar ratio of 2.25, pH of 10.0 and AS dosage of 0.65 g Al/L, with minimum cost of 9.58 $/m3 ACW. This study shows that the integrative RSM-NLP approach could effectively optimize the oxidation-coagulation process, and is attractive for techno-economic optimization of systems with multiple factors and threshold requirements for response variables.
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Eliminación de Residuos Líquidos , Aguas Residuales , Análisis de la Demanda Biológica de Oxígeno , Polietilenglicoles , Contaminantes Químicos del AguaRESUMEN
The presence of multidrug-resistant bacteria has challenged the clinical treatment of bacterial infection. There is a real need for the development of novel biocompatible materials with broad-spectrum antimicrobial activities. Antimicrobial hydrogels show great potential in infected wound healing but are still being challenged. Herein, broad-spectrum antibacterial and mechanically tunable amyloid-based hydrogels based on self-assembly and local mineralization of silver nanoparticles are reported. The mineralized hydrogels are biocompatible and have the advantages of sustained release of silver, prolonged antimicrobial effect, and improved adhesion capacity. Moreover, the mineralized hydrogels display a significant antimicrobial effect against both Gram-positive and Gram-negative bacteria in cells and mice by inducing membrane damage and reactive oxygen species toxicity in bacteria. In addition, the mineralized hydrogels can rapidly accelerate wound healing by the synergy between their antibacterial activity and intrinsic improvement for cell proliferation and migration. This study provides a modular approach to developing a multifunctional protein hydrogel platform based on biomolecule-coordinated self-assembly for a wide range of biomedical applications.
Asunto(s)
Antibacterianos , Proliferación Celular , Hidrogeles , Plata , Cicatrización de Heridas , Plata/química , Plata/farmacología , Animales , Hidrogeles/química , Hidrogeles/farmacología , Cicatrización de Heridas/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Ratones , Antibacterianos/química , Antibacterianos/farmacología , Nanopartículas del Metal/química , Humanos , Especies Reactivas de Oxígeno/metabolismo , Pruebas de Sensibilidad Microbiana , Antiinfecciosos/farmacología , Antiinfecciosos/química , Materiales Biocompatibles/química , Materiales Biocompatibles/farmacologíaRESUMEN
Carbohydrate utilization is critical to microbial survival. The phosphotransferase system (PTS) is a well-documented microbial system with a prominent role in carbohydrate metabolism, which can transport carbohydrates through forming a phosphorylation cascade and regulate metabolism by protein phosphorylation or interactions in model strains. However, those PTS-mediated regulated mechanisms have been underexplored in non-model prokaryotes. Here, we performed massive genome mining for PTS components in nearly 15,000 prokaryotic genomes from 4,293 species and revealed a high prevalence of incomplete PTSs in prokaryotes with no association to microbial phylogeny. Among these incomplete PTS carriers, a group of lignocellulose degrading clostridia was identified to have lost PTS sugar transporters and carry a substitution of the conserved histidine residue in the core PTS component, HPr (histidine-phosphorylatable phosphocarrier). Ruminiclostridium cellulolyticum was then selected as a representative to interrogate the function of incomplete PTS components in carbohydrate metabolism. Inactivation of the HPr homolog reduced rather than increased carbohydrate utilization as previously indicated. In addition to regulating distinct transcriptional profiles, PTS associated CcpA (Catabolite Control Protein A) homologs diverged from previously described CcpA with varied metabolic relevance and distinct DNA binding motifs. Furthermore, the DNA binding of CcpA homologs is independent of HPr homolog, which is determined by structural changes at the interface of CcpA homologs, rather than in HPr homolog. These data concordantly support functional and structural diversification of PTS components in metabolic regulation and bring novel understanding of regulatory mechanisms of incomplete PTSs in cellulose-degrading clostridia.