• KSBB Journal
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• 제23권5호
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• pp.369-374
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• 2008

Rhdotorula glutinis epoxide hydrolase 유전자를 pColdI 벡터 와 pET-21b(+) 벡터에 재조합하여 제작한 E. coli를 생촉매로 사용하여 라세믹 styrene oxide에 대하여 회분식 가수분해 반응을 실시하였다. pET-21b(+)/RgEH 재조합 플라스미드 DNA를 가진 E. coli를 $15^{\circ}C$에서 저온 배양할 때 수용성 단백질 형태로 가장 많이 발현되었고, 입체선택적 가수분해 활성과 촉매 안정성이 가장 좋았다. 라세믹 styrene oxide 20 mM에 대하여 반응온도 $30^{\circ}C$에서는 반응시간 20분 동안에 수율 24.0%로 (S)-styrene oxide를 얻은 반면에, 반응온도를 $10^{\circ}C$로 낮추고 0.5% (w/v) Tween 20을 첨가하고 반응시키면 광학순도 99.0% ee 이상의 (S)-styrene oxide을 46.0%의 수율로 얻을 수 있었다. 최적조건에서 E 값은 6.68이었으며, 100 mM의 라세믹 styrene oxide에 대해서는 반응시간 50분에 이론 수율 50% 대비 40%의 높은 수율로 (S)-styrene oxide를 얻을 수 있었다.

• KSBB Journal
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• 제15권6호
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• pp.630-634
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• 2000

에폭사이드 가수분해효소 활성이 우수한 Aspergillus niger 를 생촉매로 이용하여 업체선택적 가수분해 반응을 통해 라세믹 styrene oxide 기질로부터 광학활성 (S)-styrene oxide를 생산하는 실험을 수행하였다. (R)-styrene oxide 이성질체에 대한 초기 가수분해 속도에 영향을 주는 실험인자들인 pH, 반응온도, cosolvent 첨가량 등에 대해 중심합성계획법을 이용한 반응표면 분석을 통해 가수분해반응 속도를 향상시킬 수 있는 최적 반응조건을 결정하였다. pH 7.78, 반응온도 2 $28.32^{\circ}C$ 및 cosolvent 첨가량 2.4% (v/v)의 조건에서 약 10시간 정도의 반응을 통해 ee 값이 100%인 광학적으로 순수한 (S)-styrene oxide를 35% 정도(이론수율 = 50%)의 높은 수율로 얻을 수 있었다.

• Archives of Pharmacal Research
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• 제17권2호
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• pp.76-79
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• 1994

The concentration of styrne in blood of the occupationally syrene-exposed workers was checked by gas chromatographic headspace analysis. Mandelic acd in urine, that is a major metabolite of styrene, and hippuric acid wre also analyzed by high performance liquid chromatography. For the biological monitoring of styrene-exposed workers, the routine method of the quantitative determination of styrene nad its metabolites in the biolgical samples were studied.

• 대한화학회지
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• 제21권3호
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• pp.161-170
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• 1977

Glycine (또는 glycino 음이온)과 styrene을 리간드로 하는 백금(II) 착물이 합성되었다. 적외선 분광법에 의하면 N-트란스 이성체에서는 킬레이트를 이루는 glycine음이온의 질소원자가 styrene에 대하여 트란스 위치에 있음이 확인되었다.

• 한국전기전자재료학회논문지
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• 제34권2호
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• pp.130-135
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• 2021

Wrinkle patterns were fabricated on styrene-butadiene-styrene (SBS) block copolymer substrates using ion-beam (IB) irradiation with various intensities. The wavelength of the wrinkle pattern increased as the IB intensity was increased from 800 to 1,600 eV. IB irradiation-induced changes in the surface properties that were confirmed via physicochemical surface analyses. X-ray photoelectron spectroscopy analysis revealed chemical surface reformation due to the IB irradiation, resulting in C-O/C=O bonds after IB irradiation that were not reported before. These results indicate that the surface chemical modification caused by IB irradiation is strongly related to the surface modulus, which is important when fabricating wrinkle patterns. Furthermore, a strong IB irradiation induced a strong compressive strain; thus the size of the wrinkle pattern was increased.

• 한국산업보건학회지
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• 제17권3호
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• pp.235-244
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• 2007

By comparing the proteins from the workers exposed to styrene with the ones from controls, it may be possible to identify proteins that play a role in the occurrence and progress of occupational disease and thus to study the molecular mechanisms of occupational disease. In order to find the biomarkers for assessing the styrene effects early, before clinical symptoms develop and to understand the mechanisms of adverse health effects, we surveyed 134 employees, among whom 52 workers(30 male and 22 female) were chronically exposed to styrene in 10 glass-reinforced plastic boat manufacturing factories in Korea and 82 controls had never been occupationally exposed to hazardous chemicals including styrene. The age and drinking habits and serum biochemistry such as total protein, BUN and serum creatinine in both groups were significantly different. Exposed workers were divided into three groups according to exposure levels of styrene(G1, below 1/2 TLV; G2, 1/2 TLV to TLV; G3, above TLV). The mean concentration of airborne styrene in G1 group was $10.93{\pm}11.33ppm$, and those of urinary mandelic acid(MA) and phenylglyoxylic acid(PGA) were $0.17{\pm}0.21$ and $0.13{\pm}0.11g/g$ creatinine, respectively. The mean concentration of airborne styrene in G2 and G3 groups were $47.54{\pm}22.43$ and $65.33{\pm}33.47ppm$, respectively, and levels of urinary metabolites such as MA and PGA increased considerably as expected with the increase in exposure level of styrene. The airborne styrene concentration were significantly correlated to the urinary concentration of MA(r=0.784, p=0.000) and PGA(r=0.626, p<0.001). In the 2D electrophoresis, the concentration of five proteins including complement C3 precursor, alpha-1-antitrypsin(AAT), vitamin D binding protein precursor(DBP), alpha-1-B-glycoprotein(A1BG) and inter alpha trypsin inhibitor(ITI) heavy chain-related protein were significantly altered in workers exposed to styrene compared with controls. While expression of complement C3 precursor and AAT increased by exposure to styrene, expression of DBP, A1BG and ITI heavy chain-related protein decreased. These results suggest that the exposure of styrene might affects levels of plasma proteinase, carriers of endogenous substances and immune system. In particular, increasing of AAT with the increase in exposure level of styrene can explain the tissue damage and inflammation by the imbalance of proteinase/antiproteinase and decrease of DBP, A1BG and ITI heavy chain-related protein in workers exposed to styrene is associated with dysfunction and/or declination in immune system and signal transduction

• 폴리머
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• 제26권4호
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• pp.415-421
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• 2002

E-beam 전조사법을 이용하여 HPP-g-styrene 공중합체와 술폰화 반응을 통한 술폰화 HPP-g-styrene 섬유이온교환체를 합성하였다. 그라프트율은 스티렌 단량체 농도가 증가함에 따라 증가하였으며 스티렌 단량체 농도가 80%에서 그라프트율이 128%로 최대를 나타냈다. 술폰화율은 그라프트율이 증가함에 따라 증가하는 경향을 나타내었으며, 그라프트율이 100%일 때 13.4%로 최대값을 나타내었다. 술폰화 HPP-g-styrene 섬유이온교환체의 이온교환용량은 약 3.42 meq/g으로써 흡착 성능이 매우 우수한 소재임을 확인하였다. BET 분석결과 술폰화 HPP-g-styrene의 비표면적은 62.54 $m^2/g$, 기공크기는 25 $\AA$으로 반응전보다 비표면적은 감소하였고 기공크기는 약간 증가하는 경향을 보였다. 또한 Bovine Serum Albumin (BSA) 흡착 실험 결과 술폰화도가 증가함에 따라 BSA 흡착 용량이 증가하는 경향을 나타내었으며, 술폰화도 13.4%에서 BSA 흡착용량 3.8 mg/g으로 최대를 나타내었다. 따라서 본 연구에서 합성한 섬유이온교환체가 BSA 흡착.분리에 적합한 소재임을 확인하였다.

• Biotechnology and Bioprocess Engineering:BBE
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• 제11권6호
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• pp.530-537
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• 2006

Recently isolated, Pseudomonas putida SN1 grows on styrene as its sole carbon and energy source through successive oxidation of styrene by styrene monooxygenase (SMO), styrene oxide isomerase (SOI), and phenylacetaldehyde dehydrogenase. For the production of (S)-styrene oxide, two knockout mutants of SN1 were constructed, one lacking SOI and another lacking both SMO and SOI. These mutants were developed into whole-cell biocatalysts by transformation with a multicopy plasmid vector containing SMO genes (styAB) of the SN1. Neither of these self-cloned recombinants could grow on styrene, but both converted styrene into an enantiopure (S)-styrene oxide (e.e. > 99%). Whole-cell SMO activity was higher in the recombinant constructed from the SOI-deleted mutant (130 U/g cdw) than in the other one (35 U/g cdw). However, the SMO activity of the former was about the same as that of the SOI-deleted SN1 possessing a single copy of the styAB gene that was used as host. This indicates that the copy number of styAB genes is not rate-limiting on SMO catalysis by whole-cell SN1.

• Journal of Microbiology and Biotechnology
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• 제15권6호
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• pp.1207-1213
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• 2005

In a search for bacteria capable of degrading styrene better than previously isolated strains, bacterium IS-3 was isolated from activated sludge and found to be most closely related to Pseudomonas sp. Styrene degradation by this strain was tested in liquid cultures and polyurethane-packed biofilters. In liquid cultures, the rate of styrene degradation by this bacterium increased from 24.93 to $76.53\;{\mu}mol\;g^{-1}\;DCW\;H^{-1}$ for an initial mass range from 8.7 to $34.8{\mu}mol$. The maximum styrene elimination capacity was 580-635 $g/m^{3}\cdot$h at a space velocity (SV) of 50-200/h. The critical elimination capacities guaranteeing $95\%$ removal of the input styrene were determined to be 635, 170, and 38 $g/m^{3}\cdot$h, respectively, at SVs of 50, 100, and 200/h. Kinetic analysis revealed that the maximum styrene elimination velocity ($V_{m}$) for this biofilter was 1,000 g/m$\cdot$h, and the saturation constant ($K_{m}$) was 454 ppmv. Together, these results suggest that a polyurethane biofilter containing Pseudomonas sp. IS-3 could have potential practical applications for the effective removal of styrene gas.

• 생명과학회지
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• 제12권5호
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• pp.584-588
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• 2002

Apergillus niger LK의 epoxide hydrolase 활성을 이용하여 chiral styrene oxide를 제조할 수 있는 hollow-fiber 반응기 기반의 비대칭 분할 시스템을 개발하였다. 라세믹 styrene oxide 기질을 dodecane 유기용매에 용해시켜 hollow-fiber 반응기의 lumen 부위로 공급하였으며, 생촉매인 A. niger LK 미세분말은 shell 부위로 공급함으로써 막 표면에서 비대칭 분할 반응을 수행하였다. 반응 산물로 생성되는 phenyl-1,2-ethandiol에 의한 epoxide hydrolase 활성 저해효과를 감소시키기 위하여 2번째 hollow-fiber 반응기에서 완충용액을 이용하여 diol을 추출하여 제거시켰다. 2성분 용매를 사용한 cascade형 hollow-fiber 반응기 시스템을 이용하여 광학적으로 순수한 (ee > 99%) (5)-styrene oxide를 19.5% (이론 수율 대비 39%)의 수율로 얻을 수 있었다.