• 산업식품공학
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• 제21권2호
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• pp.103-109
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• 2017

DEAE sephacel anion chromatography 및 SP sepharose cation chromatography에 의해 Streptomyces violaceoruber 유래 alginate lyase의 정제를 수행하여 비활성 14.59 units/mL 정제배율 40.64배를 나타내었다. Tricine SDS-PAGE에 의한 단일밴드를 확인하였고, 분자량은 23.3 kDa으로 결정되었다. 정제효소에 의해 sodium alginate를 가수분해하여 1차 activated carbon column chromatography와 2차 bio gel P-2 gel filtration에 의해 당가수분해물을 분리 회수하여 TLC와 FACE를 통해 중합도를 확인하고 Timell's method에 의해 hetero type M/G-oligosaccharide 중합도 6, 8로 결정되었다. B. animalis, B. bifidum, B. breve, B. infantis, B. longum와 L. acidophilus, L. casei, L. reuteri에 생육활성에 대한 중합도 6, 8의 영향을 검토하기 위하여 modified-MRS media에 탄소원으로 중합도 6, 8를 대체하여 생육활성을 비교한 결과 B. longum에서는 D.P. 6 M/G-oligosaccharide를 탄소원으로 대체한 경우 표준 MRS배지와 비교하여 4.25배, D.P. 8에서 6.44배의 상대활성을 나타내어 가장 우수한 생육활성을 나타내었으며, B. bifidum의 경우에서도 D.P. 6에서 3.27배, D.P. 8에서 5.4배의 상대활성을 나타내었다. 이외에도 B. animalis, B. breve그리고 L. casei에 있어서도 D.P. 8의 경우 3배의 상대활성을 나타내었으나, L. reuteri에 대한 D.P. 8의 경우에서는 표준 MRS media와 비교하여 0.29배로 감소하였다. 결과적으로 D.P. 8의 올리고당이 D.P. 6의 올리고당보다 생육활성에 크게 기여하는 것으로 나타났다.

• 멤브레인
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• 제22권2호
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• pp.95-103
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• 2012

본 연구에서는 생활오수, 산업폐수, 축산폐수 등에서 발생하는 질산성화합물 및 난분해성 화합물을 효과적으로 처리하기 위해 막분리법과 다공 전극형 전기분해법을 조합한 하 폐수의 고도처리 기술을 제안하였고 제안 시스템의 효율성을 검토하였다. 제안하는 시스템은 활성슬러지 공정, 막분리 공정, 다공 전극형 전기분해공정의 3단계로 구성하였다. 본 연구에서 구성되는 막분리 공정은 부유물질을 제거해줌으로써 전기분해공정의 부하를 최소화할 수 있는 역할을 담당할 수 있게 하여 시스템을 안정하게 운전할 수 있도록 하였다. 전기분해 하이브리드 공정에 있어서는 다공성 전극으로 구성함으로써 비표면적의 확대로 인한 전극의 효율성을 높였다. 아울러 외부전압을 인가함에 따라 처리제의 공급 없이 장치에 유입된 물을 분해시킴으로써 산화 환원 반응을 유도하였다. 즉 중간체로서 수소 자유전자 라디칼과 산소원자 라디칼이 발생되어 난분해성 유기물을 산화 분해하는 역할을 담당하도록 하였다. 이는 전극 내에서 발생하는 중간체를 폐용질의 분해에 사용하기 때문에 친환경적 처리공법이었다. 실험결과들은 제안공정이 활성슬러지공법에 비하여 우수한 공정임을 보여 주었다. SS제거율은 제안공정, 막분리공정, 활성슬러지 단독공정에서 각각 약 100%, 약 100%, 약 90%였고 COD 제거효율은 제안공정 약 92%, 막분리공정 약 84%, 활성슬러지 단독공정 약 75%였으며 T-N의 제거효율은 제안공정 약 88%, 막분리공정 약 67% 활성슬러지 단독공정 약 58%였다. 이결과는 SS의 제거에 있어서 막분리 하이브리드 공정만으로도 부유물질이 충분히 제거됨을 나타내고 있었다. COD의 제거에 있어서 막분리 하이브리드 공정은 SS분의 제거를 통한 COD와 SS이외의 유기물질이 소량제거 되었음을 보였고 전기분해 하이브리드 공정에 있어서는 유기물질의 산화반응을 통한 분해로 높은 제거효율을 보였다. T-N의 제거에 있어서는 막분리 하이브리드 공정은 SS분에 포함된 부분과 소량의 유기물에 포함된 부분이 제거되고 있는 반면 전기분해 공정에 있어서는 유기물질의 산화분해반응으로 인한 높은 제거효율을 나타내고 있었다.

• KSBB Journal
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• 제10권2호
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• pp.131-136
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• 1995

본 실험에서는 인간 전과립 세포를 회분배양 조건 에서 10%의 혈청을 포함하는 배지로 배양하였다. 이 와같은 조건에서 세포의 비성장율은 0.374C1/day) 이고 세포내 존재하는 살균활성을 가진 목적 단백질 의 생산성은 0.435(mg/10' viable cells)으로 나타났 다. 세포내 존재하는 목척 단백질의 순수 분리를 위 해 sephadex G-75, sephadex G-100, Bio→Rex70 을 이용해 분리하였다. 정제된 목적 단백질은 감수성 균주, E. coli IFO 13168과 St. aureus IFO 3060 을 표준 균주로 살균 측정을 하였을 때, 기존의 항생 물질은 균주에 대해 40~701땅1m!에서 활성을 나타 낸 반면, 정제된 목적 단백질은 G(+)균(St. aureus IFO 3060)에서는 $0.5\mu\textrm{g}$/ml이고, G(-)균(E. coli IFO 13168)에서는 $0.4\mu\textrm{g}$/ml에서 살균 활성을 보였다. 따라서 AMF가 기존 항생물질보다 살균 활성이 강력한 단백질임을 알 수 있다. 해당 분자량을 측정 하기 위해 SDS-PAGE로 측정한 결과 약 15,000 Dalton의 분자량을 갖고 있음이 확인됐다.

• 한국수산과학회지
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• 제55권2호
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• pp.91-101
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• 2022

In this study, we analyzed the compositional characteristics of Melosira nummuloides mass-cultured using Jeju lava seawater. M. nummuloides showed the highest growth rate when cultured for 14 days at 17-20℃ and 15,000 lx. Proximate composition of raw-material (RM) and freeze-dried M. nummuloides (FM) showed high ash content (65-72%), while ethanol-extracted M. nummuloides (EM) had low ash and high lipid contents. The predominantly occurring mineral, Si, was 334 g/kg in RM and 269 g/kg in FM, but EM contained only 1.97 g/kg. The ratio of essential amino acids was similar in RM (38.93%) and FM (36.89%) lower in EM (17.83%), but branched chain amino acids required for muscle metabolism was high (63.40%). The polyunsaturated fatty acids of EM (34.74%) was 11% more than that in RM (23.81%), and the ratio of omega-6 to omega-3 fatty acids was 1:3.6. Furthermore, the concentration of total chlorophyll was higher by 5.15 times (62.32 mg/g) and that of fucoxanthin by 7.06 times (11.02 mg/g) in EM than in RM (12.11, 1.56 mg/g, respectively). The mass cultivation and filtration of M. nummuloides using lava seawater has high prospects of commercialization as a competitive bio silica, cosmetic and healthy functional food material.

• 한국식품저장유통학회지
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• 제15권1호
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• pp.155-160
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• 2008

본 연구는 대구 무형문화재 제11호인 하향주의 품질 우수성을 규명하고자 향기성분 분석 후 랫드에 대한 알코올 대사 특성을 조사하였다. GC/MS 분석시, 하향주는 iso-butyl alcohol과 iso-amyl alcohol 등을 포함하여 17가지의 향기성분이 분석되었고 여과에 의해 acetaldehyde와 ethylacetate의 농도는 낮아짐을 확인하였다. 하향주와 동일한 농도인 17% 알코올을 SD계 랫드에 단회 경구 투여시 혈중 알코올 농도와 acetaldehyde 농도가 하향주 투여군이 낮았으며, 5시간 뒤 간조직에서 alcohol dehyogenase와 acetaldehyde dehyogenase의 농도는 하향주 투여군이 17% 알코올 투여군보다 높았다. 따라서 하향주는 동일농도의 17% 알코올 투여군보다 알코올 대사를 촉진시켜 숙취를 감소시킴을 확인하였다.

• Journal of Biosystems Engineering
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• 제30권1호
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• pp.17-24
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• 2005

An efficient microbial control system was introduced into a garlic peeling system using pressurized water in order to improve the quality and the shelf-life of peeled garlic. High microbial density of the spoiled peeled garlic and the water used for peeling and washing indicated that an efficient microbial control system is necessary far the peeling system. Though Pseudomonas spp. and Penicillium spp. were closely related to the spoilage of peeled garlic, the spoilage of peeled garlic was thought to be caused mainly by nonspecific increase in microbial density. The shelf-life of the garlic peeled by pressurized water was longer than that of the garlic peeled by pressurized air, and the degree of damage had great effect on the shelf-life of peeled garlic. Ozonated water was effective in decreasing the microbial contamination and in increasing the shelf-life of peeled garlic. Based on the findings of the study, following improvements were made to the garlic peeling system using pressurized water; 1) the water circulation system was modified in order to completely separate the water for washing from the water for garlic peeling, 2) filtration and cooling equipments were introduced into the circulation system of the water for peeling, and 3) an ozone generator which could continuously supply ozonated water (dissolved ozone concentration of 0.4 ppm) was attached to the circulation system of the water for washing.

• 미생물학회지
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• 제26권2호
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• pp.73-81
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• 1988

$\alpha$-Amylase (EC.3.2.1.1) of Neurospora crassa (ATCC9279) was cloned in E. coli HB101 using shotgun method, and the enzymes isolated from both N. crassa and E. coli were compared. Chromosomal DNA isolated from the spores of N. crassa was partially digested with PstI restriction endonuclease and rejoined to pBR322 which had been digested with the same enzyme. The resulting recombinant DNA were introduced into E. coli HB101 which had competancy by treating with $CaCl_{2}$. As the result, about 8000 colonies which showed tetracycline resistance were selected and two of the colonies which had 13.5Kb recombinant plasmid exhibit starch degrading activity on starch-containing plate when treated with D-cycloserine. $\alpha$-Amylases from both N.crassa and E. coli were isolated by using ammonium sulfate precipitation, DEAE-cellulose ion exchange column chromatography and Bio-Gel P150 gel foltration column. As the result, about 81.3 fold and 5.6 fold purifications in specific activities were obtained respectively, and specific activities of the gel filtrates were 6.1u/mg and 85u/mg respectively. The properties of both enzymes were compared and they showed quite the similar patterns in optimal temperature, optimal pH and had same molecular weight about 100,000 daltons on gel filtration method. Optimal temperatures for both enzymes were $70^{\circ}C$ and optimal pH were about 6 and 10.

• BMB Reports
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• 제32권6호
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• pp.579-584
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• 1999

Mantis egg fibrolase (MEF-3) was purified from the egg cases of Tenodera sinensis using ammonium sulfate fractionation, gel filtration on Bio-Gel P-60, DEAE Affi-Gel blue gel affinity chromatogragphy, and MONO-Q anion-exchange chromatography. This protease had a molecular weight of 35,600 Da as determined by SDS-polyacrylamide gel electrophoresis under reducing conditions and its isoelectric point was 6.0. The N-terminal amino acids sequence was Ala-Thr-Gln-Asp-Asp-Ala-Pro-Pro-Gly-Leu-Ala-Arg-Arg. This sequence was 80% homologous to the serine protease from Tritirachium album. MEF-3 readily digested the ${\alpha}$-and ${\beta}$-chains of fibrinogen and more slowly the ${\gamma}$-chains. It showed strong proteolytic and fibrinolytic activities. Phenylmethanesulfonyl fluoride and chymostatin inhibited its proteolytic activity, while EDTA, EGTA, cysteine, ${\beta}$-mercaptoethanol, elastinal, tosyl-lysine chloromethylketone, and tosyl-amido-2-phenylethyl chloromethyl ketone did not affect its proteolytic activity. Among the chromogenic protease substrates, the most sensitive one to the hydrolysis of MEF-3 was benzoyl-Phe-Val-Arg-p-nitroanilide. Based on these experimental results, we speculated that MEF-3 is a serine protease with a strong fibrin(ogen)olytic activity.

• Journal of Microbiology and Biotechnology
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• 제13권6호
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• pp.853-858
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• 2003

Helicobacter pylori specifically adhere to host cells through a number of putative receptors and ligands, mainly based on carbohydrate-protein interactions. Polysaccharide fractions isolated from the leaves of Artemisia capillaris showed different inhibitory activities against H. pylori adhesion by using hemagglutination assay. Among these fractions, an acidic polysaccharide fraction FlA showed highly effective inhibitory activity, and its minimum inhibition concentration was 0.63 mg/ml. The inhibition results by the hemagglutination assay were consistent with those obtained by the enzymelinked glycosorbent assay, which was developed by the conjugation of horseradish peroxidase with fetuin, a sialic acid-containing glycoprotein which was specific to H. pylori adhesion. FlA contained the highest carbohydrate content among polysaccharide fractions, and no protein was detectable when further purified by gel filtration FPLC. Sugar composition analysis using GC revealed the highest amount of galacturonic acid among sugars, which suggests that FlA contains essentially acidic polysaccharides. Our data suggest that acidic polysaccharides may play an important role in the inhibition of H. pylori adhesion to host cells.

• Journal of Microbiology and Biotechnology
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• 제23권11호
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• pp.1554-1559
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• 2013

A protease produced by Bacillus polyfermenticus SCD was purified and characterized as a new detergent material. The protease was purified from supernatant produced by B. polyfermenticus SCD, by ammonium sulfate precipitation, ion-exchange chromatography on a DEAE-Sephadex A-50, and finally gel filtration chromatography on Sephadex G-50. The molecular mass of this enzyme was 44 kDa based on SDS-PAGE. The optimum temperature and pH were $50^{\circ}C$ and pH 8.0. The ranges of its stability to the pH and temperature were 7.0 to 9.0 and under $40^{\circ}C$, respectively. The enzyme was highly stable in the presence of the surfactants like Triton X-100 (0.1%), showing a 2-fold increase in its proteolytic activity. However, the enzyme was slightly inhibited by the chelating agent EDTA (1 mM). The enzyme has a maximum activity at $50^{\circ}C$ and the activity can be increased by surfactants such as Triton X-100 and Tween 80.