• Proceedings of the Korean Society of Life Science Conference
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• 2001.06a
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• pp.3-41
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• 2001

단백질의 부분 가수분해는 산성 음료에서의 용해도 증가, 환자들의 소화력과 알러지 내성의 개선, 다른 기능적 특성의 개발 등을 위하여 식품산업에 널리 이용되고 있다. 그러나 우유 단백질이나 대두 단백질과 같은 몇 가지 단백질들은 가수분해에 의하여 강한 쓴맛을 형성한다, 단백질 가수분해물의 쓴맛에 관한 연구는 1950년대 초에 시작되었으며, 여러 가지 원료로부터 쓴맛물질이 분리되었다. 이들 단백질 가수분해물의 쓴맛 물질은 올리고펩타이드로 알려져 있으며, 펩타이드 분자를 구성하는 소수성 아미노산의 존재와 밀접한 관계가 있는 것으로 보고되고 있다. 본 연구에서는 최근에 발달된 분석기술과 생명공학적 기법으로 E. coli에서 생산한 콩 단백질 단일 subunit를 이용하여 효소적 가수분해물의 분자구조를 확인하고자 하였다. 탈지대두박으로부터 115 glycinin와 E.coli떼서 발현된 proglycinin을 각각 90%, 97%의 정제도로 분리하여 이들 단백질을 trypsin으로 각각 가수분해하였다. 115 glycinin은 효소/기질 비 3%에서 4시간 가수분해에 의해 $14.0{\times}10^{-5}$ M quinine-HCI equivalent의 강한 쓴맛을 나타내었으며, 12%의 가수분해도(DH)를 나타내었다. 대두 단백질의 쓴맛 성분을 확인 위하여 이미 아미노산 서열이 밝혀진 11S glycinin과 proglycinin 가수분해물에서 GP-HPLC, $C_{18}$ RP-HPLC 등을 통하여 쓴맛 peptide들을 분리하였다. 각각의 분획은 다시 21개의 peptide로 분리되어 그 서열이 결정되었으며 이중 RP와 GI는 이미 알려진 쓴맛 dipeptide였고, LAGNQEQE, SAEFG, NALPE, KLHENIAR, GMIYPG 등이 주된 쓴맛 Peptide로 확인되었다. 이들은 11S glycinin의 5개의 subunit 중에서 그 위치가 확인되었다. Proglycinin 가수분해물에서도 11S glycinin과 같은 방법으로 7개의 쓴맛 peptide가 분리되었다. 이들은 $A_{1a}B_{1b}$의 아미노산 서열 중에서 37-42, 103-110, 164-167, 323-327, 367-373의 위치에 분포하고 있었으며, NALKPD, IYPGCPST, SlDT, HNIGQT, NAMFVPH의 서열을 나타내었다. 분리된 쓴맛 peptide 중에서 가장 쓴 두 분회의 peptide를 합성하여 관능 검사한 결과, NALPE는 매우 쓴맛을 내는 peptide로 확인되었다.

• Journal of the Korean Wood Science and Technology
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• v.34 no.6
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• pp.81-95
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• 2006

In order to investigate the possibility of waste logs after oak mushroom production as a source of an alternative energy and to obtain the fundamental data of supercritical water hydrolysis that has been paid attention as a new saccharification method of lignocellulosics, supercritical water hydrolysis of normal log woods (Quercus acutissima Carruth) and waste logs was carried out. With the increase of reaction time and temperature, the color of the degradation products has been dark and the degradation rate and the crystalline index increased. However the increase of reaction pressure affected the color of the degradation products and the degradation rate at only low reaction temperature. In the early stage of the reaction, the degradation of hemicellulose was progressed, while in the late stage, the cellulose was degraded. The increase of reaction time and reaction temperature (less than $415^{\circ}C$) improved the sugar yield, while at high temperature(more than $415^{\circ}C$), the sugar yield was decreased. Based on the result of the sugar yield, the optimal hydrolysis condition of Q. acutissima Carruth by supercritical water was determined to be $415^{\circ}C$, 60 seconds and 230 pressure bar with the sugar yield of 2.68% (w/w). At the optimal condition, the supercritical water hydrolysis of waste logs after the mushroom production was carried out and the sugar yield was increased to 358% (w/w). The major degradation products of waste logs by supercritical water hydrolysis were 1,1'-oxybis-benzene and 1,2-benzendicarboxylic acid by the GC-MS analysis. At the reaction condition with low degradation rate, the fatty acids such as pentadecanoic acid, 14-methyl-heptadecanoic acid were identified. With the increase of the reaction temperature and time, the amounts of phenol and benzene were increased, but the reaction pressure did not affect the kinds of degradation products. Holocellulose content was 60.6~79.2% in the water insoluble residue and the monosaccharide yield of the water insoluble residue was 49.2~675% by the acid hydrolysis. The monosaccharide yield of water-soluble portion was increased largely by the second hydrolysis using dilute acid.

• 한국생물공학회:학술대회논문집
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• 2003.04a
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• pp.374-377
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• 2003

The purpose of this study was to investigate the characteristics of anaerobic methane fermentation using several organic wastes. The substrates used in this study were food wastes, vegetable wastes, and cow manure. The substrates were mixed with inocula (mixed methanogenic fluid) at a ratio of 1:1, and several parameters such as TS, VS, sCOD, and biogas production have been monitored. Anaerobic degradation of food wastes were occurred in the intial stage of cultivation, whereas that of vegetable wastes were occurred in the late stage. However, in case of cow manure, the degradation was occurred two times both in the intial and the late stage of reaction.

• KSBB Journal
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• v.18 no.6
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• pp.479-484
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• 2003

34 strains were isolated from dyeing wastewater in order to improve treatment efficiency of dyeing wastewater containing PVA. Two strains of them were finally selected through the PVA degrading test, and identified as Microbacterium barkeri LCa and Paenibacillus amylolyticus LCb. As a result, optimal conditions for microbial growth and PVA degradation were 30$^{\circ}C$, neutral pH, starch as a carbon source, and peptone as a nitrogen source. And it was concluded that these two strains have good ability for PVA degradation. And 90% over PVA was degraded by single culture as well as a mixed culture of 2 different strains.

• Korean Chemical Engineering Research
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• v.49 no.6
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• pp.851-856
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• 2011

In this study, char was produced via pyrolysis of sewage sludge and the effects of reaction conditions(temperature, heating rate, reaction time) on characteristics of char were investigated. As temperature increased from $300^{\circ}C$ to $800^{\circ}C$, the surface area of sludge char increased in general but decreased at $700^{\circ}C$ temporarily. The effect of heating rate on specific surface area and pore volume of char was not large. Meanwhile, specific surface area and pore volume increased with reaction time but average pore diameter decreased.

• Applied Biological Chemistry
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• v.28 no.3
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• pp.162-166
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• 1985

Three isozymes of Carboxymethyl Cellulase $(FI^*,\;FII^*,\;FIII)$ and two fractious of ${\beta}-1,4-D-Cellobiohydrolase$(CI, CIl) from Aspergillus niger were purified by Sephadex G-150, DEAE-Sephadex and Sephadex G-75 column chromatography. From the results of enzymatic hydrolysis and X-ray diffraction, ${\beta}-1,4-D-Cellobiohyarolase$ has a high activity toward highly crystalline cellulose such as filter paper and acts synergistically with Cx enzyme.

• Applied Biological Chemistry
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• v.32 no.3
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• pp.315-320
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• 1989

Bacteria utilizing naphthalene as a sole carbon source for growth were isolated and identified and code named as Acinetobacter calcoaceticus R-88, Pseudomonas testosteroni R-87 and Pseudomonas putida R-89. Among these isolates, A. calcoaceticus R-88 found most effective in utilizing naphthalene. The optimal pH, temperature and concentration of naphthalene was 7.0, $30^{\circ}C$ and 10mM, respectively. The strain degraded naphthalene to salicylic acid as an intermediate. And the strain showed to be resistant to ampicillin, tetracyclin, chloramphenicol and kanamycin. A. calcoaceticus R-88 harbored plasmid DNA which was believed to be involved in naphthalene degradation.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.6 no.4
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• pp.337-341
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• 2005

The degradation of IPA according to coating conditions was examined by $TiO_2/P-25-coated$ POF. In the photoactivity of $TiO_2-coated$ POF, ethanol solvent was higher activity than other solvents. Inorganic(KR-400), organic(A-9540) and inorganic$\cdot$organic hybrid(GPTMS, TMOS) resins were used as binder. Organic binder(A-9540) showed the highest activity for degradation of IPA, but organic binder was decomposed by $TiO_2$. Inorganic binder had lower binder ability than others, and lower adhesive than organic binders. In TMOS as inorganic · organic hybrid binder, activity of IPA degradation was decreased by addition of TMOS when the ratio of TMOS and P-25 was changed from 0.05 to 1.

• Journal of Korea Soil Environment Society
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• v.4 no.3
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• pp.95-104
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• 1999

Comparative biodegradation studies of liquid and solid alkanes and of two different solid alkanes were conducted by an isolated Acinetobacter sp., which degraded crude oil alkanes simultaneously. for the determination of degradation mechanism of hydrophobic crude oil constituents. Also a model oil experimental system composed of a solid alkane. heneicosane, as a substrate and a non-degradable non-aqueous phase liquid. pristane, as an oil matrix was established and studied. It was proposed that the Acinefobacter sp. utilized hydrophobic substrates directly on the surface of them with no difference in the degradation rates between the liquid and solid alkanes. On the basis of the results from the heneicosane/pristane system which imitates crude oil matrix containing solid constituents. the crude oil matrix was considered to reduce the bioavailability of contained substrates by reducing the specific surface area of substrates to contact with microorganisms.

• 한국신재생에너지학회:학술대회논문집
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• 2005.11a
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• pp.638-641
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• 2005

수소는 자원이 무한하고 청결한 에너지이다. 수소는 무공해 청정 대체연료로 사용될 수 있을 뿐만 아니라 풍부한 자원으로부터 얻을 수 있다. 수소에너지는 물을 분해하여 얻거나 화석연료를 수증기개질 또는 부분산화 시킴으로써 얻을 수가 있다. 수소에너지는 1차 에너지를 변환시켜 얻을 수 있는 2차 에너지로서 환경에 대한 부하가 거의 없어 향후 화석연료를 대체할 수 있는 가장 가능성이 높은 에너지이며, 연료전지의 상용화를 앞두고 있어 중요성이 더욱 증대되고 있다. 수소를 생산하는 방법 중 가장 이상적인 방법으로는 물분해함으로써 수소를 제조하는 방법이 있다. 그러나 물분해에 의한 수소생산은 제조비용이 비싸 경제성이 떨어진다는 점과 수소의 대량생산에 필요한 기술확보가 여의치 않아 어렵다. 그러므로 수소를 저 비용으로 대량 생산할 수 있는 수소 제조 기술의 확보가 선행되어야 할 것이다. 현재 상용화되어 있는 수소제조방법은 거의 석유나 천연가스의 수증기 개질에 의한 수소 제조 방법이다. 그러나 이러한 방법은 유해 환경 물질인 CO나 $CO_2$를 배출하는 단점을 지니고 있다. 이러한 단점을 보완키 위한 수소 제조공정의 대안 중 하나는 탄화수소연료의 수소와 탄소로의 직접분해에 의한 수소생산이다. 이 중 원하는 생성물인 수소 외에 부산물이 카본이 동시에 얻을 수 있는 메탄분해에 의한 수소생산방법은 생산된 수소의 약 15%만 연소시킴으로서 필요한 에너지를 공급할 수 있으며, 동시에 지구온난화의 주범인 CO 또는 $CO_2$가 생성되지 않는 장점이 있다. 하지만 메탄을 분해하기 위해서는 매우 높은 에너지가 필요로 하게 된다. 이에 반해 프로판은 메탄보다 낮은 열원에서 분해할 수 있는 장점을 지니고 있다. 본 연구에서는 메탄보다 분해하기 쉬운 프로판을 직접 분해하여 수소를 생산하고자 하였다. 프로판 직접분해반응는 $500\sim750^{\circ}C$의 온도 범위에서 이루어 졌으며, 촉매로서는 국내에서 생산되는 상용촉매인 카본블랙을 이용하였다.