• 공업화학
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• 제32권1호
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• pp.61-67
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• 2021

본 연구에서는 천연 오일인 시벅턴 오일의 천연 자외선 흡수제로의 사용 가능성을 알아보기 위하여 시벅턴 원유에 대한 흡착 탈색공정을 수행하고, 이를 CCD-RSM (central composite design model-response surface methodology)을 이용하여 최적화하였다. CCD-RSM의 반응치로는 탈색과정의 탈색효과, 탈색 후 정제유의 산가 및 290 nm에서의 자외선흡광도로 설정하였으며, 독립변수로는 탈색제의 첨가량, 탈색온도, 탈색시간으로 설정하였다. CCD-RSM에 의한 통계학적 최적화 결과와 수학적 최적화 결과를 비교한 결과 3가지 반응치를 동시에 만족하는 최적조건으로 탈색제의 첨가량(4.32 wt.%), 탈색온도(134.9 ℃) 및 탈색시간(19.8 min)으로 나타났다. 이 최적 조건하에서 예측된 반응치 중 탈색과정의 탈색효과는 94.78%, 탈색 후 정제유의 산가는 2.08 mg/g KOH, 그리고 290 nm에서의 자외선 흡광도는 2.91로 나타났으며, 오차율은 2% 이하로 낮게 나타났다. 따라서 CCD-RSM을 시벅턴 원유의 흡착 탈색공정에 적용할 경우 매우 높은 수준의 만족하는 결과를 얻을 수 있음을 확인하였으며 천연 식물성 오일인 시벅턴 오일을 천연 자외선 흡수제로서 사용 가능함을 확인하였다.

• 한국미생물·생명공학회지
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• 제26권3호
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• pp.269-274
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• 1998

Triphenylmethane계 염료 탈색균인 E. cloacae MG 82를 이용한 crystal violet의 탈색 특성을 조사하였다. 배지내의 용존산소의 양이 많을수록 crystal violet의 탈색과 E. cloacae MG82의 균생장이 좋았다. 균생장 중기의 세포 군에서 crystal violet의 탈색능이 가장 활발하였고 염료의 농도가 높아짐에 따라 균생장과 탈색능이 억제되었으며, 균생장이 가능한 crystal violet의 최고 농도치는 375 $\mu$M이었다. E. cloacae MG82는 crystal violet을 유일한 탄소원으로 이용할 수 없었고, 균생장 및 염료의 탈색에 또 다른 에너지원을 필요로 하였다.

• 한국염색가공학회지
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• 제12권1호
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• pp.25-31
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• 2000

In order to decolorize disperse dyes by using biological treatment process, a strain which has potential ability to degrade disperse dyes was isolated from natural system. To increase the removal efficiency of decolorization in the aqueous solutions, the optimal condition of decolorization by this strain was investigated, and continuous plant test was also developed. The optimal culture conditions of temperature and pH were found to be 4$0^{\circ}C$ and 8.5~9, respectively. When yeast extract was mixed with polypeptone at the mixing ratio of 1:1 as a nitrogen source, decolorization efficiency was highest(93%) among the nitrogen sources. The strain to be screened was excellent to adjust to pH, and it seems to be have ability to control pH needed to growth. The optimal culture conditions in concentration of $MgSO_4\cdot{7H}_2O$ and $KH_2PO_4$ were 0.1%(w/v) and 0.2%(w/v). The result of continuous plant process using wastewater was as following : $COD_{Mn}$ removal efficiency was over than 50%, and this strain was very excellent in decolorization-efficiency for the wastewater of Taegu dyeing complex.

• Journal of the Korean Wood Science and Technology
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• 제27권4호
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• pp.72-79
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• 1999

The ability of several wood rotting fungi for decolorization of two anthracene derivatives, Carminic acid (CA) and Remazol brilliant blue R (RBBR), and hardwood KP bleaching liquor (BL) as well as laccase activities in these fungi were studied. The enzyme activity appeared exclusively in fungi destaining RBBR and CA, but in the case of BL, such relationship was not observed. The laccase enzyme was released into the decolorization media and its inducible (but not constitutive) forms shown destaining activity. The purified inducible forms of Kuehneromyces mutabilis and Pleurotus ostreatus laccase destained CA. Thus the possible differentiation between specificity of particular LAC forms was confirmed. In addition the nitrogen starvation induced both laccase and CA destaining activities, but the increase was higher for decolorization of CA than LAC activity. Probably LAC would be only partly responsible for decolorization of this dye. This results suggested that purified LACs decolorize CA, however its destaining activities were considerably lower than the activities on syringaldazine.

• Journal of Microbiology and Biotechnology
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• 제15권1호
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• pp.221-225
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• 2005

A Staphylococcus sp. EY-3 with the capability of decolorizing Congo Red was isolated from soil at an effluent treatment plant of a textile and dyeing industry. This strain was able to almost completely decolorize a high concentration of Congo Red in 48 h under aerobic conditions. Optimal color removal (more than 96%) was achieved at 30- 40oC, and no noticeable effects of different pH values (5.5- 8.0) on decolorization were observed. This strain also exhibited a remarkable decolorization capability against azo dyes under aerobic conditions, even at a high concentration (dyes 1 g/l) of dye. The metabolic product of Congo Red degradation by this strain was identified by gas chromatography with mass selective detection (GC/MSD) to be an amine derivative benzidine.

• 생명과학회지
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• 제10권4호
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• pp.333-339
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• 2000

To identify genes involved in the decolorization of crystal violet, we isolated random mutants generated by transponson insertion in crystal violet-declorizing bacterium, Citrobacter sp. The resulting mutant bank yielded mutants with six distinct phenotypes, and Southern hybridization with a Tn5 fragment as a probe showed a single hybridized with six distinct phenotypes, and Southern hybridization with a Tn5 fragment as a probe showed a single hybridized band in the mutants Ctg 2, 5 an 6, whereas two and three bands were detected in Ctg1, 4 and 3, respectively. Tn5-inserted genes were isolated and the DNA sequence flanking Tn5 was determined. From comparison with a sequence database, putative protein product encoded by ctg 5 was identified as E. coli maltose transproter(Mal G) homolog, whereas the deduced amino acid sequence of the other ctg genes did not show any significant similarity with any DNA or protein sequency. Therefore, these results indicate that the other ctg genes except ctg 5 encode new proteins responsible for decolorization of crystal violet.

• Mycobiology
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• 제41권4호
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• pp.214-220
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• 2013

This study was conducted in order to perform efficient extraction of lignocellulolytic enzymes amylase (EC 3.2.1.1), cellulase (EC 3.2.1.4), laccase (EC 1.10.3.2), and xylanase (EC 3.2.1.8) from spent mushroom compost (SMC) of Pleurotus ostreatus, P. eryngii, and P. cornucopiae. Optimal enzyme recovery was achieved when SMCs were extracted with 50 mM sodium citrate (pH 4.5) buffer at $4^{\circ}C$ for 2 hr. Amylase, cellulase, and xylanase activities showed high values in extracts from P. ostreatus SMC, with 2.97 U/g, 1.67 U/g, and 91.56 U/g, respectively, whereas laccase activity and filter paper degradation ability were highest in extracts from P. eryngii SMC, with values of 9.01 U/g and 0.21 U/g, respectively. Enzymatic activities varied according to the SMCs released from different mushroom farms. The synthetic dyes remazol brilliant blue R and Congo red were decolorized completely by the SMC extract of P. eryngii within 120 min, and the decolorization ability of the extract was comparable to that of 0.3 U of commercial laccase. In addition, laccase activity of the SMC extract from P. eryngii was compared to that of commercial enzymes or its industrial application in decolorization.

• Korean Chemical Engineering Research
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• 제53권3호
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• pp.327-332
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• 2015

A large amount of dye wastewater poses a threat to environmental safety. Disperse blue, an anthraquinone dye that is widely used in textile dyes, is difficult to degrade in wastewater. In this work, one fungus was screened according to the decolorization rate of disperse blue. The fungus was identified and named Aspergillus XJ-2 on the basis of its morphological characteristics and 18s rDNA. Response surface method was used to optimize culture conditions for A. XJ-2. The optimum values of obtained responses were as follows: temperature, $35^{\circ}C$; pH, 5.2; carbon-to-nitrogen ratio, 30:5.5; and rotation ratio, $175r{\cdot}min^{-1}$. Under optimized conditions, the decolorization rate of A. XJ-2 was up to 94.8% in 48 h.

• Journal of Microbiology
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• 제42권2호
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• pp.139-142
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• 2004

To identify genes involved in the decolorization of brilliant green, we isolated random mutants generated by transposon insertion in brilliant green-decolorizing bacterium, Citrobacter sp. The resulting mutant bank yielded 19 mutants with a complete defect in terms of the brilliant green color removing ability. Southern hybridization with a Tn5 fragment as a probe showed a single hybridized band in 7 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. By comparing these with a sequence database, putative protein products encoded by bg genes were identified as follows: bg 3 as a LysR-type regulatory protein; bg 11 as a MalG protein in the maltose transport system; bg 14 as an oxidoreductase; and bg 17 as an ABC transporter. The sequences deduced from the three bg genes, bg 2, bg 7 and bg 16, showed no significant similarity to any protein with a known function, suggesting that these three bg genes may encode unidentified proteins responsible for the decolorization of brilliant green.

• 생명과학회지
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• 제13권4호
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• pp.511-515
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• 2003

대표적인 azo계 반응성 염료인 Remazol Black B에 대한 탈색능이 우수한 신규 백색부후균인 Phanerochaete sp. EJ-31L의 탈색 특성을 평가해 보았다. 보조 탄소원 농도, 질소원, pH 등의 배양조건이 염료 탈색율에 미치는 영향을 분석한 결과, 3%(w/v)의 sucrore, 0.05%(w/v)의 $(NH_4)_2SO_4$를 첨가한 배지에서 pH 6.5의 조건에서 탈색능이 우수하였다. 혐기적 조건에서는 호기적 조건 대비 27% 수준의 탈색 효율을 보였으며, 진탕배양에서의 탈색율이 정치배양 대비 2배이상 높아 Phanerochaete sp. EJ-31L은 호기적 조건에서 탈색능이 우수함을 알 수 있었다. 초기 Remazol Black B 농도 50 ppm에 대한 회분식 처리시 약 95% 이상의 탈색율을 보여 향후 azo계 염료 처리용 생물공정에 백색부후균인 Phanerochaete sp. EJ-31L을 활용할 수 있을 것으로 기대된다.