• Clean Technology
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• v.10 no.3
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• pp.131-137
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• 2004

Due to the low biodegradability of dyes, conventional biological wastewater treatment systems are inefficient in treating textile wastewater. In this study, white rot fungus, Trametes versicolor KCTC 16781, were investigated for the decolorization of Reactive black 5 solutions. This fungus was able to degrade the dye solutions by the ligninolytic enzymes (laccase and MnP) produced. The enzyme activity remained constant until the end of reaction. The combined process of biological treatment and ceramic membrane showed better efficiency for decolorization and TOC removal than each single process.

• Clean Technology
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• v.14 no.3
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• pp.211-217
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• 2008

We investigated the reduction of pollutants such as TOC (total organic carbon) and decolorization of Reactive Black 5 (RB5) by photocatalytic oxidation. The optimal values of major parameters for the reaction were obtained including the concentration of RB5, the amount of $TiO_2$ dosage and pH of solution. The values were 100 mg/L, 2 g/L and 4.9, respectively. As the concentration of oxygen increased, removal rate of pollutants increased. After $TiO_2$ was regenerated and used again by micro filtration (MF) ceramic membrane, the removal efficiency of color and removal rate of pollutants did not decrease significantly.

• The Korean Journal of Mycology
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• v.23 no.4 s.75
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• pp.298-304
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• 1995

Decolorization of poly R-478, congo red and methylene blue by 5 white rot fungi which were isolated in Korea has been carried out. Coriolus versicolor KR-11W and C. versicolor KR-65W gave the best results when they were grown under stationary culture. C. versicolor KR-11W decolorizes 100% of poly R-478 in 13 days, 100% of congo red in 7 days and 90% of methylene blue in 7 days. C. versicolor KR-65W decolorizes 100% of poly R-478 in 15 days, 85% of congo red in 7 days and 100% of methylene blue in 7 days. Phanerochaete chrysosporium IFO 31249, which was used as a control, decolorizes 35% of poly R-478 in 15 days, 85% of congo red in 7 days and 95% of methylene blue in 7 days.

• Restorative Dentistry and Endodontics
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• v.29 no.6
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• pp.498-503
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• 2004

The properties of ideal root canal sealers include the ability of sealing the total root canal system and no toxic effects to periradicular tissues. Cytotoxicity test using cell culture is a common screening method for evaluation of the biocompatibility of root canal sealers. The purpose of this study was to investigate the cytotoxic effect of newly developed resin-based sealer (Adseal 1, 2, and 3) comparing with those commercial resin-based sealers (AH26 and AH Plus), ZOE-based sealers (Tubliseal EWT, Pulp Canal Sealer EWT) and calcium hydroxide based sealer (Sealapex), An indirect contact test of cytotoxicity by agar diffusion was performed according to the international standard ISO 10993-5. L929 fibroblast cells were incubated at $37^{\circ}C$ in humidified 5% $CO_2-containing$ air atmosphere. The freshly mixed test materials were inserted into glass rings of internal diameter 5 mm and height 5 mm placed on the agar. After the 24 hrs incubation period, the decolorization zones around the test materials were assessed using an inverted microscope with a calibrated screen. A Decolorization Index was determined for each specimen. Adseal 1. 2, and 3 did not exert any cytotoxic effects, whereas AH26, AH Plus, Tubliseal EWT, Pulp Canal Sealer EWT, and Sealapex produced mild cytotoxicity.

• Journal of Korean Society on Water Environment
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• v.35 no.5
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• pp.418-424
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• 2019

In this study, $TiO_2$ nanotubes with different morphologies were prepared in the electrolyte consisting of ethylene glycol, ammonium fluoride($NH_4F$), and deionized water($H_2O$) by controlling the voltage and time in the anodization method. Thicknesses and pore sizes of these $TiO_2$ nanotubes were measured to interpret the relationship between anodization conditions and $TiO_2$ nanotube morphologies. Element contents in the $TiO_2$ nanotubes were detected for further analysis of $TiO_2$ nanotube characteristics. Photoelectrolyticdecolorization efficiencies of the $TiO_2$ nanotube plates with various morphologies were tested to clarify the morphology that a highly active $TiO_2$ nanotube plate should have. Influences of applied voltage in photoelectrolysis processes and sodium sulfate($Na_2SO_4$) concentration in wastewater on the decolorization efficiency were also studied. To save the equipment investment cost in photoelectrolysis methods, a two-photoelectrode system that uses the $TiO_2$ nanotube plates as photoanode and photocathode instead of adding other counter electrodes was studied. Compared with single-photoelectrode system that uses the $TiO_2$ nanotube plate as photoanode and titanium plate as cathode on the view of the treatment of dye wastewater containing different amounts of salt. As a result, a considerably suitable voltage was strictly needed for enhancing the photoelectrolyticdecolorization effect of the two-photoelectrode system but if salts exist in wastewater, an excellent increase in the decolorization efficiency can be obtained.

• Journal of Microbiology and Biotechnology
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• v.25 no.9
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• pp.1433-1441
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• 2015

Pollution resulting from the discharge of textile dyes into water systems has become a major global concern. Because peroxidases are known for their ability to decolorize and detoxify textile dyes, the peroxidase activity of Vitreoscilla hemoglobin (VHb) has recently been studied. It is found that VHb and variants of this enzyme show great promise for enzymatic decolorization of dyes and may play a role in achieving their successful removal from industrial wastewater. The level of VHb peroxidase activity correlates with two amino acid residues present within the conserved distal pocket, at positions 53 and 54. In this work, sitedirected mutagenesis of these residues was performed and resulted in improved VHb peroxidase activity. The double mutant, Q53H/P54C, shows the highest dye decolorization and removal efficiency, with 70% removal efficiency within 5 min. UV spectral studies of Q53H/P54C reveals a more compact structure and an altered porphyrin environment (λ_Soret = 413 nm) relative to that of wild-type VHb (λ_Soret = 406), and differential scanning calorimetry data indicate that the VHb variant protein structure is more stable. In addition, circular dichroism spectroscopic studies indicate that this variant's increased protein structural stability is due to an increase in helical structure, as deduced from the melting temperature, which is higher than 90℃. Therefore, the VHb variant Q53H/P54C shows promise as an excellent peroxidase, with excellent dye decolorization activity and a more stable structure than wild-type VHb under high-temperature conditions.

• Journal of the Korean Wood Science and Technology
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• v.34 no.4
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• pp.46-53
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• 2006

This study was to screen white-rot fungi possesing strong lignin degrading enzymes, glucose-1 oxidase (GOD), laccase (LAC) and Mn-peroxidase (MnP), based on their decolorization activity of Remazol Brilliant Blue R (RBBR). In the midst of 20 tested fungi, 9 isolates were shown 4 kinds of activities such as RBBR decolorization, GOD, LAC and MnP. Relatively high active strains were identified as Phlebia radiata, Trametes versicolor, Abortiporus biennis, Gleophyllum odoratum and Cerrena unicolor. In particular, T. versicolor, G. odoratum, and C. unicolor, which have high activities of LAC, were used to confirm the optimal temperature and pH and to evaluate the effect of inducer, 2,5-xylidine on their LAC activity. The optimum temperatures for mycelial growth were $28^{\circ}C$ for T. versicolor and G. odoratum, and $25^{\circ}C$ for C. unicolor. The optimum pH for mycelial growth was 5.5. Three strains showed the increase of LAC enzyme activity by the addition of 2,5-xylidine. T. versicolor had the highest LAC activity of $22,700nkat/{\ell}$, corresponding to 11.3 times, G. odoratum $15,400nkat/{\ell}$, 9 times and C. unicolor $17,330nkat/{\ell}$, 5.5 times higher than those of the control.

• KSBB Journal
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• v.14 no.6
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• pp.718-723
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• 1999

In order to treat of alkaline dye-processing wastewater, alkalophilic strains biodegrading azo dye, Acid red 1, is isolated from natural system, and optimal culture conditions are examined using response surface analysis, statistical analysis system program. 15 different species which grow in alkaline culture media are isolated from the effluent and river soil discharged from wastewater treatment plant in dye industrial complex. One strain which has the best decolorization efficiency is chosen, and named as AR-1. The result of the examination of carbon, nitrogen and phosphorus sources which have influence on growth and decolorization reveals that optimum carbon, nitrogen and phosphorus sources are 1.0% fructose, 1.0% polypeptone, 1.0% yeast extract and 0.5% $K_2HPO_4$, respectively. In order to optimize of biodegradation conditions of dye by response surface analysis, the characteristics of decolorization and cell growth according to culture temperature and time are monitered. The result shows that the one is optimum 34.77$^{\circ}C$ for 12.97 hours; the other at 34.73$^{\circ}C$ for 12.96 hours. While, optimal conditions of culture that satisfy both cell growth and decolorization are the temperatures from 32.86$^{\circ}C$ to 36.36$^{\circ}C$ and the period of 10.96 to 15.75 hours, respectively.

• Journal of Life Science
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• v.14 no.1
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• pp.21-25
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• 2004

To identify genes involved in the decolorization of both crystal violet and malachite green, we isolated random mutants generated by transposon insertion in triphenylmethane-decolorizing bacterium, Citrobacter sp. The resulting mutant bank yielded 14 mutants with complete defect in color removal capability of both crystal violet and malachite green. Southern hybridization with a Tn5 fragment as a probe showed a single hybridized band in 5 mutants and these mutants appeared to have insertions at different sites of the chromosome. Tn5-inserted genes were isolated and the DNA sequence flanking Tn5 was determined. From comparison with a sequence database, putative protein products encoded by cmg genes were identified as follows. cmg 2 is MaIC protein in maltose transport system; cmg 6 is transcriptional regulator (LysR-type): cmg 12 is a putative oxidoreductase. The sequences deduced from two cmg genes, cmg 8 and cmg 11, showed no significant similarity to any protein with a known function. Therefore, these results indicate that these two cmg genes encode unidentified proteins responsible for decolorization of both crystal violet and malachite green.

• Proceedings of the Korean Society for Applied Microbiology Conference
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• 2004.06a
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• pp.212-212
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• 2004