Trametes hirsuta and a purified laccase from this organism were able to degrade triarylmethane, indigoid, azo, and anthraquinonic dyes. Initial decolorization velocities depended on the substituents on the phenolic rings of the dyes. Immobilization of the T. hirsuta laccase on alumina enhanced the thermal stabilities of the enzyme and its tolerance against some enzyme inhibitors, such as halides, copper chelators, and dyeing additives. The laccase lost 50% of its activity at 50 mM NaCl while the 50% inhibitory concentration (IC 50 ) of the immobilized enzyme was 85 mM. Treatment of dyes with the immobilized laccase reduced their toxicities (based on the oxygen consumption rate of Pseudomonas putida) by up to 80% (anthraquinonic dyes). Textile effluents decolorized with T. hirsuta or the laccase were used for dyeing. Metabolites and/or enzyme protein strongly interacted with the dyeing process indicated by lower staining levels (K/S) values than obtained with a blank using water. However, when the effluents were decolorized with immobilized laccase, they could be used for dyeing and acceptable color differences (⌬E*) below 1.1 were measured for most dyes.It is known that 90% of reactive textile dyes entering activated sludge sewage treatment plants will pass through unchanged and will be discharged to rivers (34). Not all dyes currently used could be degraded and/or removed with physical and chemical processes, and sometimes the degradation products are more toxic (40). The traditional textile finishing industry consumes about 100 liters of water to process about 1 kg of textile materials. New closed-loop technologies such as the reuse of microbially or enzymatically treated dyeing effluents could help to reduce this enormous water consumption.Several combined anaerobic and aerobic microbial treatments have been suggested to enhance the degradation of textile dyes (5, 23, 32). However, under anaerobic conditions, azo-reductases usually cleave azo dyes into the corresponding amines, many of which are mutagenic and/or carcinogenic (10,11,32). Furthermore, azo reductases have been shown to be very specific enzymes, thus cleaving only azo bonds of selected dyes (50, 51). By contrast, laccases act oxidatively and less specifically on aromatic rings, thus having potential to degrade a wider range of compounds (43).Laccases are involved in the biodegradation of lignins, which constitute the main noncarbohydrate component in wood and are among the most abundant groups of biopolymers in the biosphere. A great number of white-rot fungi have been reported to produce the lignin-degrading enzymes laccase, lignin peroxidases, and manganese peroxidases, or at least one of these enzymes (15,16,44).Laccases (benzenediol:oxygen oxidoreductase, EC 1.10.3.2) have very broad substrate specificity with respect to the electron donor. They catalyze the removal of a hydrogen atom from the hydroxyl group of ortho-and para-substituted monoand polyphenolic substrates and from aromatic amines by one-electron abstraction to form free radicals...

Bacteria often colonize in-dwelling medical devices and grow as complex biofilm communities of cells embedded in a self-produced extracellular polymeric matrix, which increases their resistance to antibiotics and the host immune system. During biofilm growth, bacterial cells cooperate through specific quorum-sensing (QS) signals. Taking advantage of this mechanism of biofilm formation, we hypothesized that interrupting the communication among bacteria and simultaneously degrading the extracellular matrix would inhibit biofilm growth. To this end, coatings composed of the enzymes acylase and α-amylase, able to degrade bacterial QS molecules and polysaccharides, respectively, were built on silicone urinary catheters using a layer-by-layer deposition technique. Multilayer coatings of either acylase or amylase alone suppressed the biofilm formation of corresponding Gram-negative Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus. Further assembly of both enzymes in hybrid nanocoatings resulted in stronger biofilm inhibition as a function of acylase or amylase position in the layers. Hybrid coatings, with the QS-signal-degrading acylase as outermost layer, demonstrated 30% higher antibiofilm efficiency against medically relevant Gram-negative bacteria compared to that of the other assemblies. These nanocoatings significantly reduced the occurrence of single-species (P. aeruginosa) and mixed-species (P. aeruginosa and Escherichia coli) biofilms on silicone catheters under both static and dynamic conditions. Moreover, in an in vivo animal model, the quorum quenching and matrix degrading enzyme assemblies delayed the biofilm growth up to 7 days.

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This study attempted to introduce the bio-processes in the conventional scouring and bleaching preparation of cotton. The scouring with two types of pectinases, acting under acidic and alkaline conditions respectively, was as efficient as the chemical process in terms of obtained adequate water absorbency of the fabrics. The necessity of surfactants application in scouring was outlined. Bleaching of the fabrics was performed with hydrogen peroxide, which was enzymatically produced by glucose oxidase during oxidation of glucose. The aeration plays an important role in the enhancement of the enzyme reaction, so that the quantity of generated peroxide is sufficient to overcome the stabilizing effect of the glucose and protein in the subsequent bleaching. A closed-loop process reusing starch containing desizing baths in a single step scouring/bleaching operation with enzyme-generated peroxide was performed.

Catheter associated urinary tract infections are common during hospitalization due to the formation of bacterial biofilms on the indwelling device. In this study, we report an innovative biotechnology-based approach for the covalent functionalization of silicone catheters with antifouling zwitterionic moieties to prevent biofilm formation. Our approach combines the potential bioactivity of a natural phenolics layer biocatalytically conjugated to sulfobetaine-acrylic residues in an enzymatically initiated surface radical polymerization with laccase. To ensure sufficient coating stability in urine, the silicone catheter is plasma-activated. In contrast to industrial chemical methods, the methacrylate-containing zwitterionic monomers are polymerized at pH 5 and 50 °C using as an initiator the phenoxy radicals solely generated by laccase on the phenolics-coated catheter surface. The coated catheters are characterized by X-ray photoelectron spectroscopy (XPS), Fourier transformed infrared (FTIR) analysis, atomic force microscopy (AFM), and colorimetrically. Contact angle and protein adsorption measurements, coupled with in vitro tests with the Gram-negative Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus in static and dynamic conditions, mimicking the operational conditions to be faced by the catheters, demonstrate reduced biofilm formation by about 80% when compared to that of unmodified urinary catheters. The zwitterionic coating did not affect the viability of the human fibroblasts (BJ-5ta) over seven days, corresponding to the extended useful life of urinary catheters.