• Title/Summary/Keyword: 단백질 변성

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융합 페리틴의 요소 농도에 따른 재접힘 특성에 관한 연구

  • Kim, Hyeong-Won;Sin, Mi-Yeong;An, Eun-Gyeong;Kim, In-Ho
    • 한국생물공학회:학술대회논문집
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    • 2003.04a
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    • pp.480-483
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    • 2003
  • Fusion ferritin$(F_H+F_L)$, an iron-binding protein, was purified from recombinant E. coli by two-step sonications with urea. Unfolded ferritin was refolded by gel filtration chromatography with various concentration of urea. 50 mM Tris-HCl(pH 8.0) buffers with 1 M to 4 M urea were used in GFC. Objective was to characterize the structure change with urea concentration. Molecular weight was determined using GF-HPLC and RP-HPLC was used to quantify the unfolded and refolded proteins.

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Cryoprotectant Effects of Fructo-, Isomalto-, and Galacto-Oligosaccharides on Beef Protein (프락토, 이소말토 및 갈락토 올리고당들의 쇠고기단백질 냉동변성방지효과 연구)

  • 이경숙;이현규;양차범;박관화
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.30 no.3
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    • pp.565-568
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    • 2001
  • A study was conducted to investigate cryoprotectant effect of commercially produced oligosaccharides (IMO: isomalto-oligosaccharides, FO: fructo-oligosaccharides and GO: galacto-oligosaccharides) on beef protein and to compare their effectiveness to sucrose or a mixture of sucrose and sorbitol on freezing. The optimal addition level of cryoprotectants was determined by measuring $Ca^{2+}$-ATPase activity of sample treated with different concentration (0 to 12%) after freeze-thaw cycle. Since the stabilization effect was not dramatically increased above 8% sugar concentrations, the 8% was determined as an usage level. During frozen storage (at -18$^{\circ}C$ for 12 week), commercially produced oligosaccharides showed lower cryoprotection ability than sucrose but higher than sucrose+sorbitol as measured by protein solubilities and $Ca^{2+}$-ATPase activities.

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통닭의 포장형태가 저장기간 중 육질과 미생물에 미치는 영향

  • An, Jong-Nam;Chae, Hyeon-Seok;Yu, Yeong-Mo;Jo, Su-Hyeon;Park, Beom-Yeong;Kim, Jin-Hyeong;Kim, Yong-Gon;Choe, Yang-Il
    • Proceedings of the Korean Society for Food Science of Animal Resources Conference
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    • 2004.10a
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    • pp.266-269
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    • 2004
  • 저장기간 중 통닭의 포장형태에 따른 가열감량은 저장 3일과 저장 6일에는 벌크포장은 낮고 비닐포장에서는 높아 통계적인 유의차이(p<0.05)를 보였으며, 전단력은 저장 1일보다는저장 3일이후에 증가하는 경향을 나타내었다. 보수력은 저장 3일에는 벌크포장이 가장 높아 저장 1일의 보수력과는 반대의 결과를 보였다. 총균은 저장 1일에서 포장형태와 관계없이 총균이 모두 검출되었으나 저장 3일과 6일에는 비닐포장에서는 총균이 검출되지 않았으며, 저장 9일에는 비닐포장에서 가장 많이 검출되었다. Coliform는 포장형태와 저장기간에 관계없이 거의 검출되지 않았고, E.coli도 포장형태와 저장기간에 관계없이 거의 검출되지 않았다. 지방산패도(TBARS) 값은 포장형태에 따라 차이는 없었고, 단백질변성(VBN) 값은 저장 3일에서는 벌크포장이 랩트레이 포장과 비닐포장에서 높았다.

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닭고기 부분육의 포장형태가 저장기간 중 육질과 미생물에 미치는 영향

  • An, Jong-Nam;Chae, Hyeon-Seok;Yu, Yeong-Mo;Jo, Su-Hyeon;Park, Beom-Yeong;Kim, Jin-Hyeong;Lee, Jong-Mun;Choe, Yang-Il
    • Proceedings of the Korean Society for Food Science of Animal Resources Conference
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    • 2004.10a
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    • pp.274-277
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    • 2004
  • 저장기간 중 닭고기 부분육의 가열감량은 저장 1일과 저장 9일에서 포장형태에 따라 차이는 없었으나, 전단력은 저장 6일에 랩트레이 포장과 진공포장 간에 통계적인 유의차이(p<0.05)가 있었으며, 보수력은 저장 9일에 렙트레이 포장과 진공포장 닭고기에서 통계적인 유의차이(p<0.05)가 있었다. 총균은 저장 9일에 랩트레이 포장이 5.26으로 가장 많이 검출되었으며, Coliform은 벌크포장과 랩트레이 포장은 저장 1일과 3일, 6일에는 검출되지 않았다. 지방산패도(TBARS) 값은 저장 3일에는 각 포장형태에 따라 벌크포장이 0.10mgMA/kg, 랩트레이 0.08mgMA/kg, 비닐포장 0.07mgMA/kg으로 통계적인 유의차(p<0.05)가 있었으나, 단백질변성(VBN) 값은 차이가 거의 없었다.

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동결농축유의 일반성분 및 이화학적 특성에 관한 연구

  • Lee, Su-Jeong;Hwang, Ji-Hyeon;Park, Heung-Sik;Min, Sang-Gi;Gwak, Hae-Su
    • Proceedings of the Korean Society for Food Science of Animal Resources Conference
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    • 2005.05a
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    • pp.303-306
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    • 2005
  • 본 연구는 개발한 batch type 동결농축장치를 이용하여 제조한 동결농축유의 일반성분 분석 및 이화학적 특성을 분석하고, 진공농축유와 비교하여 동결농축유의 우수성을 입증하기위하여 실시되었다. 동결농축유와 진공농축유는 농축방법에 따라 차이가 나타났으며, 전기영동 실험결과 진공농축유에 비하여 동결농축유의 band가 뚜렷하게 나타나 열처리한 진공농축유가 열변성이 된 것을 확인할 수 있었다. 열처리시에는 Maillard반응이 일어나거나 유효성 lysine함량이 감소되며, 유청내 용해성 칼슘이 인산이나 변성된 단백질과 결합하여 한외여과성칼슘(calcium ions in milk ultrafiltrates)함량이 감소되며, 비타민 손실, 유당의 이성체화, 휘발성 황화합물 생성에 의해 가열취가 발생될 수 있다. 따라서 전기영동 실험결과 batch type 동결농축장치를 이용하여 제조한 동결농축유의 우수성을 확인할 수 있었다.

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전자파와 인체세포의 생리

  • 강위생
    • The Proceeding of the Korean Institute of Electromagnetic Engineering and Science
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    • v.8 no.2
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    • pp.22-28
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    • 1997
  • 세포는 생명체의 가장 기본단위이다. 식물은 태양 에너지를 변환하여 화학에너지의 형태로 축적한다. 모든 생물은 이 화학에너지를 변환하여 생명을 유지하고 있다. 인체 세포는 이 화학에너지 를 변환하여 세포 자체의 구조를 유지하면서 체온을 유지하고, 근육수축과 같은 기계적인 일과 신경 전달과 같은 전기적인 일도 한다. 또 세포는 새로운 화학물질을 합성하기도 한다. 세포에 이상이 생기면 조직이나 기관의 이상이 따르게 되고 결국 병적인 상태에 이르게 된다.외 부 환경이 세포의 기능에 영향을 미치는 것 중의 중요한 요인이다. 세포에 대한 외부환경은 세포를 둘러 싸고 있는 세포외액과 몸밖에서 들어오는 방사선이나 열과 같은 물리적 에너지로 대별된다. 영양의 불균형이나 섭취한 물질은 세포외액의 항상성 유지를 방해한다. 방사선, 특히 이온화 방사선은 직접 세포속에서 중요한 분자를 분해시키기도 하고 새로운 분자를 합성하기도 하여 세포를 죽이기도 하고 세포의 기능을 비정상적으로 바꾸기도 하고 드물게는 암세포로 바꾸기도 한다. 열은 단백질의 변성 을 촉진한다.

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Significant Attenuation of Aden-associate Virus Gene Expression by Catechol-conjugated Heparin Surface Coating (카테콜기가 도입된 헤파린의 표면고정화에 의한 아데노연관바이러스의 발현 억제에 관한 연구)

  • Do, Minjae;Lee, Slgirim;Jang, Jae-Hyung;Lee, Haeshin
    • Journal of Adhesion and Interface
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    • v.17 no.4
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    • pp.149-154
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    • 2016
  • In this study, natural polymer-based virus neutralizing agent was developed in an attempt to replace the conventional sterilization method for mammalian cell culture. A catechol conjugated heparin was synthesized by using EDC chemistry, and it show unique binding ability to virus which has heparin affinity (adenovirus, adeno-associated virus). To evaluate neutralization ability of catechol conjugated heparin, adeno-associated virus was used for test model, instead of using a pathogenic virus. The catechol conjugated heparin exhibited resistance to high concentration of salt and complete inactivation of adeno-associated virus. The result suggests that the catechol conjugated heparin, which is biocompatible and efficiency, may replace conventional sterilization method for mammalian cell culture.

Identification and Characterization of Myxobacteria from Korean Soil (국내토양에서 분리한 점액세균의 동정및 특성)

  • 김재헌;손승렬
    • Korean Journal of Microbiology
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    • v.37 no.4
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    • pp.239-244
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    • 2001
  • We isolated a Myxobacteria strain from a soil sample obtained from Mt. Daedoon located in Choongnam, Korea. This strain, ARJ, secreted slime while swarmed on the surface of CT medium. It produced greenish yellow pigment in liquid or solid media, and the swarming edge showed green florescence under U. V. at 366 nm. It formed fruiting bodies when nutrient was exhausted, which is one of the most imkportant characteristics of Myxobacteria. The fruiting bodies did not have a stalk and consisted of naked myxospores when examined under the scanning electron microscope. These traits lead us to believe that this strain is very close to Myxococcus virescens. It showed antimicrobial activity, especially against Gram positive bacteria. Culture filtrate showed the activity but this was not due to protein. The culture filtrate also had proteolytic activity in which at least two enzymes are involved.

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Separation of Soybean Protein by Free-flow Electrophoresis (자유유동 전기이동법에 의한 대두단백질 분리)

  • 한재갑;류화원
    • KSBB Journal
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    • v.10 no.1
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    • pp.63-70
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    • 1995
  • The effect of operating conditions on separation of soybean proteins in a home-made free-flow electrophoresis apparatus was investigated. Measurement of the pH, conductivity, and UV-absorbance(280 nm) were carried out at each run and the purity of the sample was tested with SDS-PAGE analysis. The soybean extract pretreated with Tris and boric acid was mixed with the amino acids composed of glutamic acid, histidine, arginine, glycine(1 mM each) with glycyl-glycine(2mM) and KCl(1mM). When the cellulose acetate was used as a compartment between the electrode and the buffer solution in the cell, pH distribution in the separation cell varied from 3.0 at the anodic side to 8.0 at the cathodic side and had two inflection point. The applied voltage was from 300V to 1000V and the separation was better at a higher voltage but the voltage was limited by the capability of the cooling system due to Joule heat. The proteins focused near the middle of the channel. From the change of pH and conductivity it was found that the ions in the channel moved out to the electrodes through the membrane. In the case when the concentration of the buffer solution was increased 5 times, proteins were focused at 300V. We could not increase up to the ten times of the concentration since the temperature difference between inlet and outlet was more than $25^{\circ}C$ and denaturation of proteins was expected. When ion-exchange membranes were used U-type pH distribution was set up due to the ionic polarization near the membrane. The commercial ampholytes, instead of the mixed amino acids showed not much improvements in purity of the separated sample.

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Dystrophin Degradation in Skeletal Muscles with Lipid Enrichment in Cattle (지방 침착률이 높은 식용소에서 나타난 골격근의 디스트로핀 소실)

  • Jeon, Sung-Hwan;Kim, Ah-Young;Lee, Eun-Mi;Lee, Eun-Joo;Hong, Il-Hwa;Hwang, Ok-Kyung;Jeong, Kyu-Shik
    • Journal of Life Science
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    • v.26 no.5
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    • pp.592-602
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    • 2016
  • This study investigated the muscular dystrophin levels in freely moving Australian cattle mainly fed grass, freely moving Korean cattle fed mainly a grain diet, and Korean cattle fed a grain diet but housed in a relatively limited space of a cow house. The total skeletal muscle specimens of 244 cattle were collected and immediately fixed in 10% neutral formalin. The same area was biopsied from the cattle in both countries. The findings showed that fatty infiltration is highly correlated with membrane-associated protein degradation in skeletal muscle, and that among several membrane-associated proteins, dystrophin showed the most significant reduction in expression in the cattle with fatty infiltration. Similarly, CD36 was more highly expressed in the cattle with fatty infiltration of skeletal muscle. Various breeding factors, such as oxidative stress; the presence of oxidized lipids in the diet; and environmental factors such as exercise, temperature and amount of time spent, may have critical effects on the degradation of normal cytoskeleton proteins, which are required for maintaining normal skeletal muscle architecture. Among the sarcolemma membrane-associated proteins, dystrophin is the most sensitive membrane protein that is involved muscular dystrophy and muscular degeneration. Thus, the present findings may be useful for studies on muscular dystrophy in humans or the pathogenesis of muscular diseases in animal models.