• Journal of Microbiology and Biotechnology
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• 제4권1호
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• pp.63-67
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• 1994

A microorganism showing degradative activity towards benzene, toluene and ${\rho}-xylene$ (BTX) was isolated from an activated sewage sludge and was tentatively identified as Pseudomonas fluorescence BE103. This strain was found to utilize benzene and toluene as growth substrates, but to degrade ${\rho}-xylene$ in the obligate presence of a growth substrate. The metabolic product resulted from the cometabolism of ${\rho}-xylene$ was identified as 3, 6-dimethylpyrocatechol by LC/MS analysis, and the metabolic pathway was analyzed to be similar to the tod pathway. From the kinetic studies done regarding BTX biodegradation using Pseudomonas fluorescence BE103, it was revealed that the cometabolism of ${\rho}-xylene$ is significantly affected by the ratio of growth substrate concentration to biomass concentration, and that the cometabolism of ${\rho}-xylene$ initiates only when this ratio was about 0.03.

• Bulletin of the Korean Chemical Society
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• 제22권9호
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• pp.953-957
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• 2001

The specificity of conjugation site for coating ligands was investigated using toluene-bovine serum albumin (BSA) conjugates in which BSA was conjugated at the position of o-, m-, and ${\rho}-toluic$ acid. Toluene-BSA conjugated at ${\rho}-position$ showed a binding activity of about 89-95%, whereas, those conjugated at o- and m-position of toluene exhibited a binding activity of 5 and 11%, respectively. On the basis of the above result, coating ligands with various proteins (OVA, BSA, KLH) were compared by conjugating with $\rho-toluic$ acid, and toluene-KLH was considered as the best coating ligand for this ELISA. Indirect competitive ELISA method was developed using anti-toluene antibody and $\rho-position$ conjugated toluene-KLH. The dose-response curve constructed after kinetic and optimization studies showed a 1${\times}$10-4 - 1${\times}$102 mM detectable response range with 0.1 ${\mu}M$ detectability. In specificity test of the antibody, the binding capabilities of aromatic compounds substituted with nitro-, alkyl-, chloro-, and hydroxyl group were larger rather than those of aromatic compounds (benzene, toluene and xylene) themselves. Also, tests with soil and water samples that had been spiked with toluene resulted in 102.7-113.7% recovery.

• 한국진공학회지
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• 제14권4호
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• pp.195-200
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• 2005

For the longevity of OLEDs, passivation of OLEDs is an important process step since organic materials used in OLEDs are very vulnerable to moisture. In this work, the passivation effect of the plasma polymerized para-xylene (PP$\rho$X) layers was studied. The PPpX layers deposited by PECVD were formed on top of the cathode with various plasma powers of 50 - 90 W. Passivation effect of PP$\rho$X was significantly dependent upon the deposition plasma power of the PP$\rho$X film. The lifetime of OLEDs with the 70 W deposited PP$\rho$X passivation layer was about 5 times longer than that of the control device.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2000년도 춘계학술발표대회
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• pp.374-377
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• 2000

본 연구에 사용한 Pseudomonas sp. BCNU 154는 Gram 음성 toluene 내성세균으로 형태적${\cdot}$생리적 특성을 비교하여 보았을 때 Pseudomonas 속임이 확인되었다. 폭넓은 유기용매에 대한 내성한계를 가지고 있으며 Pseudomonas sp. BCNU 154 toluene 내성균주는 Modified Luria-Bertani(LBM) 배지에서 잘 자랐으며, $30^{\circ}C$에서 최적의 생육상태를 나타내었다. 최적 pH는 6에서 7로 나타났으며 1%의 toluene을 첨가하였을 경우에는 pH 2에서 8에 이르는 넓은 pH대에서 잘 자랐으며, cumene은 pH 6에서 10까지의 범위에서 좋은 성장을 보였다. Pseudomonas sp. BCNU 154 균주의 toluene, ethylbenzene, ${\rho}$ -xylene, cumene분해는 $1g/{\ell}$의 농도로 첨가시 toluene의 경우 97%이상이 분해되었고, ${\rho}$은 92%, ethylbenzene은 80%이며, cumene은 90% 이상이 분해되는 것으로 나타났다. 따라서 각 유기용매에 대해 대체로 12시간 내에 90%이상의 분해가 이루어졌으며, ethylbenzene의 경우에는 성장곡선과 마찬가지로 일정시간이 지난 후 성장과 분해가 둔화되다가 다시 성장과 분해가 일어나는 현상을 보였다.

• 한국산업보건학회지
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• 제19권1호
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• pp.73-79
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• 2009

This study was undertaken to investigate the effects of single and combined exposure of toluene (T) and xylene (X) on the cytochrome-450(CYP)-mediated metabolizing capacity, induction of CYP isozymes and the excretion of their metabolites in urine. Animal were adults male Sprague-Dawley (SD) rats and divided into 4 groups such as control, T (treated with 63.7 mg/body kg), X (treated with 65.9 mg/body kg) and TX(T=X). Organic solvents was administrated by intraperitoneal injection for 3 days. The contents of protein and CYP in liver microsomes of control group were $16.48{\pm}0.56 mg/m{\ell}$ and $0.744{\pm}0.025$ nmol/mg protein, respectively, and they contents were significantly lower than in derived from treated groups (p<0.01). The activities of PROD and ${\rho}NPH$ were significantly higher in single treated groups than in control and combined group (TX). When Western immunoblotting were carried out with two monoclonal antibodies (MAb 1-98-1 and MAb 2-66-3) which were specific against CYP2B1/2 and CYP2E1, respectively, a strong signal corresponding to CYP2B1/2 was observed in microsomes obtained from rats treated with X and TX. The color density against CYP2E1 was slightly increased in T and TX groups compared with C and X groups. The amounts of urinary hippuric acid in T single treated group was $3.29{\pm}1.97$ g/g creatinine and TX combined group was $2.91{\pm}1.76$ g/g creatinine, but was not significant. However, amount of urinary methy hippuric acid in X single treated group ($1.62{\pm}0.72$ g/g creatinine) was significantly higher than TX combined group ($0.93{\pm} 0.63$ g/g creatinine)(p<0.01). These results suggested that CYP2E1 isozyme might be responsible for the metabolism of T, and CYP2B1/2 isozyme is for X. And also, difference of metabolites level between single and combined group may be speculated that the intermediates of T and X interacted each other in the process of their metabolite formation reaction.