• KSBB Journal
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• v.14 no.1
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• pp.31-35
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• 1999

A biosorption of azo and reactive dyes into the intact and modified biomass of Penicillium janthinellum were investigated. Initial pH of medium affected the initial adsorption rate and decolorization. The initial optimum pH was found to be 2.0, and the maximum adsorption rates of dyes were $40^{\circ}C$. The reactive dyes called Apollocion Red 7EB, Apollofix Red SF-3B and Apollocion Red H-E3B showed the high initial adsorption rates as 0.06, 0.086 and 0.079 mg/g.min, respectively. A mixture of dyes containing azo and reactive dyes was adsorbed to the biomass of Pen. janthinellum and revealed that the initial adsorption rate was 0.084 mg/g.min. Both percent decolorization and the influence on the dye adsorption rate. Modified biomass of Pen. janthinellum was also investigated for the dye adsorption and the superior dye loading performance was observed compared with the ion-exchange/chelating resins used for removal of Apollocion Red 7EB.

• Journal of Life Science
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• v.18 no.10
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• pp.1331-1335
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• 2008

A Klebsiella pneumoniae WL-5 with the capability of decolorizing several recalcitrant dyes was isolated from activated sludge of an effluent treatment plant of a textile and dyeing industry. This strain showed a higher dye decolorization under static condition and color removal was optimal at pH 6-8 and $30-35^{\circ}C$. More than 90% of its color of Congo Red were reduced within 12 hr at $200\;{\mu}M$ dye concentration. Malachite Green, Brilliant Green and Reactive Black-5 lost over 85% of their colors at $10\;{\mu}M$ dye concentration, but the percentage decolorization of Reactive Red-120, Reactive Orange-16, and Crystal Violet were about 46%, 25%, and 13%, respectively. Decolorizations of Congo Red and triphenylmethane dyes, such as Malachite Green, Brilliant Green, and Crystal Violet were mainly due to adsorption to cells, whereas azo dyes, such as Reactive Black-5, Reactive Red-120, and Reactive Orange-16 seemed to be removed by biodegradation through unknown enzymatic processes.

• Korean Journal of Food Science and Technology
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• v.26 no.6
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• pp.787-790
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• 1994

An effective process manufacturing the decolorized chitin with high quality was established using shrimp shell powder. Ash and protein in shrimp shell powder were efficiently removed by 1.66% HCl and 3% NaOH treatments, respectively. A bleached chitin could be also obtained by 0.16% NaClO for 30 minutes, the treatment of which was much better than previously reported decolorization methods such as ethanol, acetone and $H_2O_2$ treatments. Since the pattern of IR spectrum of sample chitin was closely similar to those of commercially available chitins and the degree of deacetylation showed low value of 22.8%, it could be concluded that the bleached chitin obtained had highly-purified character as well as high quality of appearance.

• Journal of Microbiology and Biotechnology
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• v.12 no.4
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• pp.544-552
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• 2002

Several microorganisms from rat and human feces and lumen fluid of cows were screened for their ability to decolorize the synthetic dyes. Consequently, a novel dye-degrading strain AB&J was isolated. Taxonomic identification including 165 rDNA sequencing and phylogenetic analysis indicated that the isolate had 99.9% homology in its 165 rDNA base sequence with Clostridium perfringens. After 27 h Incubation with the strain, brilliant blue R, bromophenol blue, crystal violet, malachite green, methyl green, and methyl orange were decolorized by about 69.3%, 97.7%, 96.3%, 97.9%, 75.1%, and 97.2%, respectively. The triphenlmethane dye, bromophenol blue, was decolorized extensively by growing Clostridium perfringens AB&J cells in liquid cultures under anaerobic condition, although their growth was strongly inhibited in the initial stage of incubation. This group of dyes is toxic, depending on the concentration used. The dye was significantly decolorized at a relatively lower concentration of below 50 $\mu g \;ml^{-1}$, however, the growth of the cells was mostly suppressed at a dye concentration of 100 $\mu g \;ml^{-1}$. The decolorization activity in cell-free extracts was much higher in cytoplasm than in periplasm and cytoplasmic membrane. Therefore, the enzyme related uptake of bromophenol blue seemed to be localized in cytoplasm. The optimal pH and temperature of bromophenol blue uptake fur decolorization activities were 7.0 and 4$0^{\circ}C$, respectively.

• Applied Chemistry for Engineering
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• v.16 no.3
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• pp.366-371
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• 2005

In this study treatment efficiencies of methylene blue were evaluated in term of BOD, COD, TOC, absorbance and initial decolorization rates. Ozonation of the dye in distilled water was performed in a laboratory scale cylindrical batch reactor. The decolorization process of methylene blue was carried out by bubbling ozone at the bottom of a bubble column reactor containing the dye solution. Decolorization, determined by measuring the light absorbance at the maximum wavelength in the (${\lambda}_{max}$, 660 nm), was almost complete after 40 min with an ozone concentration of $50{\pm}10mg/L$. The $TOC/TOC_0$ ratio after ozonation was about 83.8%, the COD was diminished to 44.0% of the initial value. The $BOD_5/COD$ ratio was increased from 64.2% to about 90.8%, indicating an enhancement of biodegradable compounds in the ozonated solutions. The pseudo first-order rate constants of the ozonation was $3.30{\times}10^{-2}min^{-1}$ and the activation energy was $3.01kcal{\cdot}mol^{-1}$ at $30^{\circ}C$.

• Journal of Microbiology and Biotechnology
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• v.30 no.4
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• pp.615-621
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• 2020

Laccases are multicopper oxidases with important industrial value. In the study, a novel laccase gene (mco) in a Staphylococcus haemolyticus isolate is identified and heterologously expressed in Escherichia coli. Mco shares less than 40% of amino acid sequence identities with the other characterized laccases, exhibiting the maximal activity at pH 4.0 and 60℃ with 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt (ABTS) as a substrate. Additionally, the Mco is tolerant to a wide range of pH, heavy metal ions and many organic solvents, and it has a high decolorization capability toward textile dyes in the absence of redox mediators. The characteristics of the Mco make this laccase potentially useful for industrial applications such as textile finishing. Based on BLASTN results, mco is found to be widely distributed in both the bacterial genome and bacterial plasmids. Its potential role in oxidative defense ability of staphylococci may contribute to the bacterial colonization and survival.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.16 no.5
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• pp.222-226
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• 2006

Effects of a carboxylated styrene-butadiene-based liquid additive on the microstructure, mechanical strength and decolorization resistance of inorganic pigment layer in the color block have been examined. More dense inorganic pigment layer characterized by lower apparent porosity, lower water absorption and uniform pigment distribution has been achieved by incorporation of a liquid additive. Also significant enhancements in the mechanical strength and decolorization resistance have been observed.

• Journal of Environmental Science International
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• v.18 no.1
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• pp.61-72
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• 2009

Fabrication and oxidants production of 3 or 4 components metal oxide electrode, which is known to be so effective to destruct non-biodegradable organics in wastewater, were studied. Five electrode materials (Ru as main component and Pt, Sn, Sb and Gd as minor components) were used for the 3 or 4 components electrode. The metal oxide electrode was prepared by coating the electrode material on the surface of the titanium mesh and then thermal oxidation at $500^{\circ}C$ for 1h. The removed RhB per 2 min and unit W of 3 components electrode was in the order: Ru:Sn:Sb=9:1:1 > Ru:Pt:Gd=5:5:1 > Ru:Sn=9:1 > Ru:Sn:Gd=9:1:1 > Ru:Sb:Gd=9:1:1. Although RhB decolorization of Ru:Sn:Sb:Gd electrode was the highest among the 4 components electrode, the RhB decolorization and oxidants formation of the Ru:Sn:Sb=9:1:1 electrode was higher than that of the 3 and 4 components electrode. Electrogenerated oxidants (free Cl and $ClO_2$) of chlorine type in 3 and 4 components electrode were higher than other oxidants such as $H_2O_2\;and\;O_3$. It was assumed that electrode with high RhB decolorization showed high oxidant generation and COD removal efficiency. OH radical which is electrogenerated by the direct electrolysis was not generated the entire 3 and 4 components electrode, therefore main mechanism of RhB degradation by metal oxide electrode based Ru was considered indirect electrolysis using electrogenerated oxidants.

• Journal of Korean Society on Water Environment
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• v.24 no.5
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• pp.537-542
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• 2008

Textile industry has been recognized as an important pollution source due to its consumption of large volumes of water and chemicals. Textile wastewater contains very diverse chemicals in types and composition, among them the presence of dyes is highly visible and undesirable. In spite of these problems, there has not been a proper control for the wastewater because many dyes are difficult to be degraded or decolorized due to their complex structure and synthetic characteristics. This study has been progressed to evaluate more easily the potential decolorization of advanced treatment processes. It has been surveyed with the Y textile complex wastewater treatment plant, the raw wastewater has appeared very difficult biodegradability by 4.7 of $CODcr/BOD_5$ and 1,158.9 degree of color. In view of CODcr fractions, biodegradable COD portion was 46.4%, colloidal COD and real soluble COD was 45.3% and 31.5% each others. From research on unit processes, the degradable coefficient (k) became from 0.065 to $0.125d^{-1}$ by the processes, the decolorization appeared best efficiency by 30.1% (458.4 degree) in pre-ozone process. On the effluent from the biological process, the filterable CODcr became 129.3 mg/L, the biodegradable portion appeared 64.7% (83.6 mg/L), and the fixed dissolved solid (FDS), non-reactivity (NR), appeared very heavy portion by 80.5% (1,659.0 mg/L).

• Journal of Microbiology and Biotechnology
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• v.24 no.4
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• pp.545-555
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• 2014

It has been previously demonstrated that laccases exhibit great potential for use in several industrial and environmental applications. In this paper, two laccase isoenzyme genes, lccB and lccC, were cloned and expressed in Pichia pastoris GS115. The sequence analysis indicated that the lccB and lccC genes consisted of 1,563 and 1,584 bp, and their open reading frames encoded 520 and 527 amino acids, respectively. They had 72.7% degree of identity in nucleotides and 86.7% in amino acids. The expression levels of LccB and LccC were up to 32,479 and 34,231 U/l, respectively. The recombinant laccases were purified by ultrafiltration and $(NH_4)_2SO_4$ precipitation, showing a single band on SDS-PAGE, which had a molecular mass of 58 kDa. The optimal pH and temperature for LccB were 2.0 and $55^{\circ}C$ with 2,2'-azinobis-[ 3-ethylbenzthiazolinesulfonic acid (ABTS) as a substrate, whereas LccC exhibited optimal pH and temperature at 3.0 and $60^{\circ}C$. The apparent kinetic parameters of LccB were 0.43 mM for ABTS with a $V_{max}$ value of 51.28 U/mg, and the Km and $V_{max}$ values for LccC were 0.29 mM and 62.89 U/mg. The recombinant laccases were able to decolorize five types of dyes. Acid Violet 43 (100 g/ml) was completely decolorized by LccB or LccC (2 U/ml), and the decolorization of Reactive Blue KN-R (100 g/ml) was 91.6% by LccC (2 U/ml). Thus, the study characterizes useful laccase isoenzymes from T. versicolor that have the capability of being incorporated into the treatment of similar azo and anthraquinone dyes from dyeing industries.