• 한국환경보건학회지
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• 제26권3호
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• pp.86-91
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• 2000

The purpose of this was to investigate the degradation efficiency of phenol compounds(catechol, ferulic acid, protocatechuic acid, syringic acid, vanillic acid) by Streptomyces halstedii scabies SAI-36, Streptomyces avendulas SA2-14, and Strptomyces badius(ATCC 39117, control group). The results were as follows: Catechol showed the degradation efficiency that is lower than 50% in three strains. Ferulic acid and vanillic acid showed high degradation efficiency of 98.8% and 94.5% respectively by Streptomyces lavendulas SA2-14. protocatechuic acid and syringicacid showed high degradation efficiency of 89.6% and 77.9%. The degradation efficiency of catechol by Streptomyces halstedii scabies SAI-36, Streptomyces lavendulas SA2-14 and Streptomyces badius(ATCC 39117) was low as 49.2%, 40.2% and 20.2% respectively. But the degradation of other phenolic compoumds except catechol by Streptomyces laven-dulas SA2-36 and Streptomyces badius(ATCC 39117). The results demonstrated that two experimental strains are superior ability to control group in degradation of phenol compounds and Streptomyces lavendulas SA2-14 was superior of two experimental strain. This results were consistent with previous research results that Streptomyces lavendulas SA2-14 was the best strain in degradation ability for lignin, decoloration abilities for variousdyes, and various enzyme production abilities. Therefore, it is suggested that lignin can be used as a indicator when selecting Actinomycetes for degradation of non-degradable materials such as phenol compounds.

• 한국미생물·생명공학회지
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• 제23권3호
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• pp.255-262
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• 1995

Intact cells of Acinetobacter sp. T5-7 completely degraded trichloroethylene (TCE) following growth with phenol. This strain could grow on at least eleven aromatic compounds, e.g., benzaldehyde, benzene, benzoate, benzylalochol, catechol, caffeic acid, 2.4-D, p-hydroxybenzoate, phenol, protocatechuate and salicylate, and did grow on alkane, such as octane. But except phenol, other aromatic compounds did not induced TCE degradation. Phenol biotransformation products, catechol was identified in the culture media. However, catechol-induced cells did not degrade TCE. So we assumed that phenol hydroxylase was responsible for the degradation of TCE. The isolate T5-7 showed growth in MM2 medium containing sodium lactate and catechol rather than phenol, but did not display phenol hydroxyalse activity, suggesting induction of enzyme synthesis by phenol. Phenol hydroxylase activity was independent of added NADH and flavin adenine dinucleotide but was dependent on NADPH addition. Degradation of phenol produced catechols which are then cleaved by meta-fission. We identified catechol-2.3-dioxygenase by active staining of polyacrylamide gel.

• 미생물학회지
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• 제36권1호
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• pp.58-63
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• 2000

공업단지 폐수로부터 benzoate에 대하여 분해능을 보이는 균주를 분리하여 생화학적 특성과 세포 지방산 분석을 실시하여 동정한 결과 Klebsiella oxytoca로 밝혀졌다. 따라서 이 균주를 Klebsiella oxytoca strain C3O2라 명명하였으며 여러 가지 방향족 탄화수소에 대한 분해특성을 알아본 결과, benzoate 외에 catechol, protocatechuate, 4-hydroxybenzoate에 대한 분해능이 우수하였으며, 특히 benzoate와 catechol에 대하여 높은 분해능을 보였다. Klebsiella oxytoca C3O2 균주의 catechol 분해능에 대한 환경요소의 영향을 실험한 결과, $30^{\circ}C$와 pH 7.0에서 그리고 0.5~1.0 mM의 농도에서 왕성한 생장과 분해능을 보였다.

• Journal of Microbiology and Biotechnology
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• 제7권5호
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• pp.345-351
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• 1997

An aqueous/organic two-phase reaction system was applied to the production of catechol using immobilized resting cells of Pseudomonas putida CY 400. Water/ethyl ether system was used because of high partition coefficient of catechol and thus to reduce the product inhibition and degradation. Among the tested immobilization carriers, polyacrylamide gel gave the highest catechol productivity. The immobilization seemed to protect the cells against solvent toxicity. From the simulation of reaction conditions based on two-phase models, it was found that there was an optimum acetate concentration at fixed benzoate and cell concentrations for the catechol productivity. A lower phase volume ratio (lower fraction of organic phase) gave a higher productivity. However, the substrate conversion was low at low phase volume ratio.

• Journal of Microbiology and Biotechnology
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• 제13권5호
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• pp.700-705
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• 2003

Pseudomonas sp. S-47 is capable of degrading benzoate and 4-chlorobenzoate as well as catechol and 4-chlorocatechol via the meta-cleavage pathway. The three enzymes of 2-oxopenta-4-enoate hydratase (OEH), acetaldehyde dehydrogenase (acylating) (ADA), and 2-oxo-4-hydroxypentonate aldolase (HOA) encoded by xylJQK genes are responsible for the three steps after the meta-cleavage of catechol. The nucleotide sequence of the xylJQK genes located in the chromosomal DNA was cloned and analyzed. GC content of xylJ, xylQ, and xylK was 65% and consisted of 786, 924, and 1,041 nucleotides, respectively. The deduced amino acid sequences of xylJ, xylQ, and xylK genes from Pseudomonas sp. S-47 showed 93%, 99%, and 99% identity, compared with those of nahT, nahH, and nahI in Pseudomonas stutzeri An10. However, there were only about 53% to 85% identity with xylJQK of Pseudomonas putida mt-2, dmpEFG of P. putida CF600, aphEFG of Comamonas testosteroni TA441, and ipbEGF of P. putida RE204. On the other hand, the xylLTEGF genes located upstream of xylJQK in the strain S-47 showed high homology with those of TOL plasmid from Pseudomonas putida mt-2. These findings suggested that the xylLTEGFIJQK of Pseudomonas sp. S-47 responsible for complete degradation of benzoate and then catechol via the meta-pathway were phylogenetically recombinated from the genes of Pseudomonas putida mt-2 and Pseudomonas stutzeri An10.

• Journal of Microbiology
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• 제37권2호
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• pp.73-79
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• 1999

Pseudomonas sp. NGK1, isolated by naphthalene enrichment culture technique, is capable of degrading anthracene as a sole source of carbon and energy. The organism degraded anthracene through the intermediate formation of 1,2-dihydroxyanthracene, 2-hydroxy-3-naphthoic acid, salicylate, and catechol. The intermediates were isolated and characterized by TLC, spectrophotometry, and HPLC analysis. The cell free extract of anthracene-grown cells showed activities of anthracene dioxygenase, 2-hydroxy-3-naphthylaldehyde dehydrogenae, 2-hydroxy-3-naphthoate hydroxylase, salicylate hydroxylase and catechol 2,3-dioxygenase. The formed catechol as a metabolite is degraded through meta-cleavage with the formation of ${\alpha}$-hydroxymuconic semi-aldehyde.

• 한국환경과학회:학술대회논문집
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• 한국환경과학회 2002년도 봄 학술발표대회 발표논문집
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• pp.209-212
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• 2002

본 연구는 방향족 화합물질 중 페놀폐수에 대한 생물학적 처리를 위해 본 실험실에서 분리한 페놀분해능이 우수한 Rhodococrus sp. EL-GT를 이용하여 catechol 분해 catechol 1,2-dioxygenase 분해활성을 측정하였고, 이것이 ortho-pathway임을 확인할 수 있었다. 또한 다른 연구에서 보고된 Rhodococcus rhodochrous NCIMB 13259 균주의 catechol 1,2 dioxygenase를 기초로한 primer를 이용하여 PCR을 수행하였으며 이 분해 유전자의 cloning실험을 수행 중이다. 이들 실험을 통하여 Rhodococcus sp.의 페놀분해균의 유전적 구조 및 특성을 검토하고 밝혀지는 단백질 정보를 이용하여 방향족 화합물의 분해능이 보다 우수한 균주의 개발을 시도하고자 한다.

• 환경생물
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• 제18권3호
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• pp.307-313
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• 2000

석유화학 공업으로부터 생산되는 방향족 탄화수소 화합물질들은 여러 가지 산업과정에서 널리 활용되고 있으나, 자연계에 오염될 때에는 쉽게 분해되지 않는다는 점에서 환경 오염물질로 주목받고 있다. 방향족 탄화수소 물질의 미생물 분해는 산화반응에 의한 benzene고리의 개환으로부터 시작되기 때문에 이 개환 작용을 갖는 미생물의 분리와 함께 그 분해 기능을 연구하는 것은 매우 중요한 일이다. 본 연구에서는 여천 화학공업단지 폐수로부터 benzoate와 catechol 등의 방향족 탄화수소에 대하여 분해능이 우수한 균주를 분리하여 생화학적 특성과 세포 지방산 분석에 의하여 동정한 결과 Pseudomonas putida로 밝혀졌다. 따라서 이 균주를 Pseudomonas putida Z104라 명명한 후, benzoate와 catechol의 분해과정을 검토하였다. Pseudomonus putida Z104의 catechol분해능에 대하여 환경요소의 영향을 실험한 결과, 3$0^{\circ}C$와 pH 7.0 그리고 0.5mM의 농도에서 왕성한 세포의 생장과 catechol의 분해능을 보였으다. 그러므로 Z104 균주는 benzoate를 연속적으로 완전분해시키는 유전자를 모두 가지고 있다는 점에서 활용가치가 있는 균주라고 판단된다.

• 미생물학회지
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• 제35권2호
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• pp.139-145
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• 1999

방향족 탄화수소 화학물질들은 자연계에 오염되면 미생물에 의한 분해가 미미하여 장기 축적됨으로써 생명체에 독성을 나타낸다. 이러한 방향족 탄화수소가 준치사 수준의 농도로 미생물에 노출되면 stress-shock 단백질을 합성하거나 세포 구성물질에 생화학적 변화가 일어나 적응현상이 나타나게 된다. 본 연구에서는 Pseudomonas sp. DJ-12를 여러 가지 농도의 catechol 로 처리했을 때 나타나는 stress-shock 단백질의 합성양상과 함께 세포의 형태와 생존을 위한 내성의 변화를 연구하였다. Pseudomonas sp. DJ-12는 0.5~1mM 의 catechol 이 6시간 배양 후 60% 이상이 분해되었으나, 3mM 도는 그 이상의 농도에서는 전혀 분해되지 않앗고 생존 세포수는 30시간 처리 했을 때부터 \10^2$ cell/ml 또는 그 이상이 사멸되었다. DnaK는 1mM 이상의 catechol 로 10분간 처리할 때 유도 생성되었고, GroEL은 0.5 mM 이상에서 생성되었다. 10mM 의 catechol로 처리한 Pseudomonas sp. DJ-12 의 세포는 세포벽에 구멍이 생겼으며 간균의 형태가 일그러지는 변화가 관찰되었다. 준치사 농도인 1mM의 catechol 이나 benzoate 또는 4-chlorobenzoate 로 전처리한 Pseudomonas sp. DJ-12는 stress-shock 단백질이 합성되었을 뿐 아니라, 치사 농도인 10mM 의 catechol에서 tolerance를 나타내었다.

• Journal of Microbiology and Biotechnology
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• 제11권1호
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• pp.112-117
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• 2001

A nonconventional yeast strain Y103 capable of degrading several aromatic hydrocarbons was isolated from the wastewater of the Yocheon industrial complex. The strain Y103 was identified as Yarrowia lipolytica on the basis of its unique dimorphic and biochemical characteristics as determined by a Biolog test. Y. lipolytica Y103 was found to degrade phenol and 4-chlorophenol to produce catechol. The catechol then will be further degraded to produce 2-hydroxymuconic semialdehyde via meta-cleavage. These results indicate that strain Y103 degrades 4-chlorophenol, phenol, and catechol through a consecutive reaction to produce 2-hydroxymuconic semialdehyde. The most active degradation of phenol by Y. lipolytica Y103 occurred with a 0.5 mM phenl concentration in an MM2 medium at $30^{\circ}C$ and pH 7.0.