• 제목/요약/키워드: Lowry method

검색결과 20건 처리시간 0.03초

감마선 조사에 의한 수산 자숙액의 단백질 함량 변화 (Changes of the Protein Contents of Seafood Cooking Drips by Gamma Irradiation)

  • 최종일;김현주;성낙윤;변의백;김재훈;전병수;안동현;조국연;변명우;이주운
    • KSBB Journal
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    • 제23권6호
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    • pp.489-493
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    • 2008
  • 수산가공 폐자원인 수산 자숙액의 산업적 활용 극대화 방안의 연구 일환으로 감마선 조사가 수산 자숙액 내 단백질 성분에 미치는 영향을 알아보기 위해 톳, 문어 및 참치 자숙액을 감마선 조사하여 단백질 정량 및 SDS-PAGE를 진행하였다. Lowry, BCA 및 Kjeldahl 법에 의한 단백질 정량 실험 결과 감마선 조사에 의해 수산 자숙액 단백질의 함량이 증가된 것으로 확인되었다. 또한 단백질 함량은 10 kGy이상에서는 선량에 따라 일정한 값을 가졌다. 이를 토대로 각각의 자숙액을 SDS-PAGE를 이용한 전기영동적 분리정도를 확인한 결과 감마선 조사에 의해 단백질의 응집과 저분자화가 관찰되었다. 이상의 결과를 볼 때 감마선 조사에 의해 수산 자숙액의 단백질 추출 효율이 증가한 것으로 판단되며 추후 감마선 조사에 의해 증가된 단백질의 동정 및 구조변화 등의 후속연구가 필요하다고 사료된다.

산란계(Dakalbwarren)의 연령에 따른 myeloperoxidase와 leukocyte peroxidase 활성에 관한 연구 (Activity of myeloperoxidase and leukocyte peroxidase according to ages in the hen(Dekalbwarren))

  • 전승기;강창원;이호일
    • 대한수의학회지
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    • 제34권3호
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    • pp.465-470
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    • 1994
  • This study was undertaken to measure the activity of myeloperoxidase and leukocyte peroxidase of hen. 70 hens were decapitated to observe the activity of enzymes according to ages. The activity of peroxidase by the Lowry's method with bovine serum albumin as standard. Gel filtration chromatography was carried out of sephacryl S-300 column. The results obtained were summarized as follows; 1. The mean of specific activity of myeloperoxidase and leukocyte peroxidase was 16.80(units/mg) and 15(units/mg), respectively. 2. The specific activity of myeloperoxidase in 35 days hen was significantly increased and showed almost the same level of activity to 350 days hen. 3. The specific activity of leukocyte peroxidase in 35 days hen was significantly increased and showed a little increased tendency from 210 days to 350 days hen. 4. On the sephacryl S-300 column chromatography, two separated peaks of myeloperoxidase activity were observed. The molecular weights of myeloperoxidase were 57,000 dalton and 13,700 dalton.

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Spin and shape analysis for the Mars-crossing asteroid 2078 Nanking

  • Choi, Jung-Yong;Kim, Myung-Jin;Choi, Young-Jun;Yoon, Tae Seog
    • 천문학회보
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    • 제40권1호
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    • pp.85.2-86
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    • 2015
  • The YORP effect is non-gravitational force that changes the spin-status of asteroid. So far this effect has been directly detected only from the Near-Earth asteroids (Taylor et al. 2007; Lowry et al. 2007, 2014; Breiter et al. 2011; Durech et al. 2008, 2012). Pravec at el. 2008 found the evidences for changing spin rate of small asteroids (3 - 15 km) by the YORP effect in the Main-Belt and Mars-crossing asteroids. The Mars-crossing asteroids (1.3 < q < 1.66 AU) are objects that cross orbit of the Mars. The Mars-crossing asteroids are regarded as one of the main sources for the Near-Earth asteroids. We expect that rotation of Mars-crossing asteroids would be influenced by the YORP effect. We try to search observational evidence of the YORP effect for the Mars-crossing asteroid. Our target 2078 Nanking is a population of the Mars-crossing asteroid. First light-curve of 2078 Nanking was obtained from Mohamed et al. 1994, and Warner et al. 2015 recently published new observational data. We observed this asteroid on 26th Nov. 2014 and 17th Jan. 2015 using SOAO (Sobaeksan Optical Astronomy Observatory) 0.61 m telescope with 4K CCD. Using light-curve inversion method (Kaasalainen & Torppa 2001; Kaasalainen et al. 2001), we try to determine the pole orientation and shape model of this asteroid based on the combination of our light-curve and literature photometric data. Knowing spin parameters, such as rotational period and spin axis, are essential for studying the YORP effect. In this presentation, we provide some preliminary results of our recent study: light-curve and processing of shape modeling of 2078 Nanking. We plan to find observational clue for the YORP effect on the Mars-crossing asteroids.

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Sodium Fluoride가 조골세포주 MC3T3-E1의 제 1 형 ${\alpha}2$ 교원질 mRNA에 미치는 영향에 관한 연구 (THE EFFECTS OF SODIUM FLUORIDE ON TYPE I $\alpha$ 2 COLLAGEN RIBONUCLEIC ACID (mRNA) LEVEL IN MURIN OSTEOBLAST LIKE (MC3T3-E1) CELLS)

  • 황정빈;정규림;박영국
    • 대한치과교정학회지
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    • 제23권3호
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    • pp.415-425
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    • 1993
  • Fluoride is one of the most potent stimulators of bone formation in vivo. But its direct effects on osteoblast is not yet clear This study was to investigate the effects of Sodium fluoride on alkaline phosphatase(ALP) activity, cAMP formation responsive to parathormone(PTH) and type I $\alpha$ 2 collagen ribonucleic acid (mRNA) level in Murin osteoblast-like (MC3T3-E1) cells. The cells were cultured in $\alpha-Minimal$ essential medium $(\alpha-MEM)$ supplemente with $10\%$ fetal bovine serum (FBS) and then changed to $0.1\%$ FBS with various concentration of Sodium fluoride. The ALP activity was assayed by the method of Lowry with disodium phenyl phosphated as substrate. cAMP formation was measured by Radioimmuno Assay(RIA). Type I $\alpha$ 2 collagen ribonucleic acid(mRNA) expression was studied by Nothern blot analysis. The results were as follows: 1. cAMP level was increased by PTH in MC3T3-E1 cells. 2. Sodium fluoride showed the tendency of inhibitory effects on cAMP responsiveness to PTH in MC3T3-E1 cells. 3. Sodium fluoride increased ALP activity at cocentration of $2{\mu}M,\;4{\mu}M,\;and\;10{\mu}M$ significantly different from control at the 0.001 level. ALP activity revealed maximum value at $10{\mu}M$ in this study. 4. Nothern blot analysis of Sodium fluoride treated cells, using Type I $\alpha$ 2 collagen prove, revealed significant increase at $10{\mu}M$ in MC3T3-E1 cells.

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Ether 및 Halothane 전신마취(全身麻醉)가 가토폐(家兎肺) 및 간조직(肝組織)의 단백량(蛋白量)에 미치는 영향(影響) (Effect of Ether and Halothane Anesthesia on Protein Contents of the Lung and Liver in Rabbits)

  • 이석강;신현국;조중환;이기석
    • The Korean Journal of Physiology
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    • 제5권1호
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    • pp.11-14
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    • 1971
  • In an attempt to observe possible effects of ether and halothane anesthesia on the protein contents of the lung and liver of rabbits, the animal was subjected to the moderato anesthesia with either ether or halothane by non-rebreathing system for one hour, and the protein content of the lung and liver was measured by the method of Lowry et at. using Folin-phenol reagent. The comparison was made with the protein content from the normal rabbits, and the following results were obtained. l) The protein contents of the lung and liver of the normal rabbit were $45.0{\sim}11.5\;mg/gm$ wet wt. and $100.4{\sim}15.1\;mg/gm$ wet wt. respectively. 2) In the ether or halothane anesthesized group, the protein contents of the lung were $57.2{\sim}13.3\;and\;60.3{\sim}7.2$ respectively. 3) In the anesthesia groups with ether and halothane, the protein contents of the liver were $103.4{\sim}10.0\;and\;90.1{\sim}13.0$ respectively. 4) No significant difference in the protein contents of the lung and liver was observed after ether or halothane anesthesia comparing with the normal.

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A Pilot Study Exploring Temporal Development of Gut Microbiome/Metabolome in Breastfed Neonates during the First Week of Life

  • Imad Awan;Emily Schultz;John D. Sterrett;Lamya'a M. Dawud;Lyanna R. Kessler;Deborah Schoch;Christopher A. Lowry;Lori Feldman-Winter;Sangita Phadtare
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제26권2호
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    • pp.99-115
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    • 2023
  • Purpose: Exclusive breastfeeding promotes gut microbial compositions associated with lower rates of metabolic and autoimmune diseases. Its cessation is implicated in increased microbiome-metabolome discordance, suggesting a vulnerability to dietary changes. Formula supplementation is common within our low-income, ethnic-minority community. We studied exclusively breastfed (EBF) neonates' early microbiome-metabolome coupling in efforts to build foundational knowledge needed to target this inequality. Methods: Maternal surveys and stool samples from seven EBF neonates at first transitional stool (0-24 hours), discharge (30-48 hours), and at first appointment (days 3-5) were collected. Survey included demographics, feeding method, medications, medical history and tobacco and alcohol use. Stool samples were processed for 16S rRNA gene sequencing and lipid analysis by gas chromatography-mass spectrometry. Alpha and beta diversity analyses and Procrustes randomization for associations were carried out. Results: Firmicutes, Proteobacteria, Bacteroidetes and Actinobacteria were the most abundant taxa. Variation in microbiome composition was greater between individuals than within (p=0.001). Palmitic, oleic, stearic, and linoleic acids were the most abundant lipids. Variation in lipid composition was greater between individuals than within (p=0.040). Multivariate composition of the metabolome, but not microbiome, correlated with time (p=0.030). Total lipids, saturated lipids, and unsaturated lipids concentrations increased over time (p=0.012, p=0.008, p=0.023). Alpha diversity did not correlate with time (p=0.403). Microbiome composition was not associated with each samples' metabolome (p=0.450). Conclusion: Neonate gut microbiomes were unique to each neonate; respective metabolome profiles demonstrated generalizable temporal developments. The overall variability suggests potential interplay between influences including maternal breastmilk composition, amount consumed and living environment.

누액 단백질 침착에 의한 소프트콘택트렌즈의 굴절력 변화 (The Change in Refractive Powers of Soft Contact Lenses Caused by the Deposition of Tear Proteins)

  • 최진용;박재성;김소라;박미정
    • 한국안광학회지
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    • 제16권4호
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    • pp.383-390
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    • 2011
  • 목적: 본 연구에서는 소프트콘택트렌즈를 착용하였을 때 렌즈에 부착되는 누액 단백질에 의하여 굴절력의 변화가 유발되는 지를 알아보고자 하였다. 방법: -1.00 D, -3.00 D, -5.00 D 및 -7.00 D의 굴절력을 가지는 etafilcon A, hilafilcon A 및 comfilcon A 재질 렌즈를 인공누액에 각각 1일, 3일, 5일, 7일 및 14일 동안 배양시킨 후 자동렌즈미터를 이용하여 wet cell 방법으로 굴절력을 측정하였으며, 렌즈에 침착된 단백질 양을 Lowry 방법으로 정량하였다. 결과: 세 종류의 렌즈 가운데 이온성인 etafilcon A 재질 렌즈에서 가장 많은 단백질이 침착되어 굴절력의 변화 가 크게 나타남을 확인하였다. 즉, 인공누액에 1일 동안 배양시킨 후에는 모든 디옵터의 렌즈에서 굴절력이 크게 감소하였으나, 배양 기간이 증가할수록 굴절력이 다시 점차적으로 증가하였다. 모든 디옵터의 etafilcon A 렌즈에서 관찰된 굴절력 변화는 소프트콘택트렌즈의 기준오차범위를 벗어나는 큰 변화였으며 이러한 변화는 저굴절력 렌즈에서의 더 크게 나타났다. 반면, 비이온성의 hilafilcon A 렌즈는 etafilcon A 재질 렌즈의 약 20%에 해당하는 단백질 이 침착되었으며, 인공누액에서의 배양기간이 증가할수록 지속적으로 유의한 굴절력의 증가를 보였다. Hilafilcon A 재질 렌즈의 굴절력 역시 인공누액에 배양하게 되면 기준오차범위를 벗어나는 변화가 나타났으며 저굴절력 렌즈에서 더 큰 굴절력의 변화가 나타났다. 실리콘 하이드로겔 재질인 comfilcon A 렌즈의 경우는 침착되는 단백질의 양이 가장 적어 etafilcon A 렌즈의 약 10%에도 미치지 못하였으며, 이에 따른 굴절력 변화도 적어 모든 디옵터에서 기준 오차범위 내의 변화를 보였다. 결론: 본 연구에서는 렌즈에 침착된 누액 단백질에 의해 렌즈 재질에 따라서는 기준오차범위를 벗어날 정도의 큰 굴절력 변화가 나타남을 밝혔다. 이로써 소프트콘택트렌즈의 긴 착용 시간으로 유발되는 시야흐림 현상의 원인 중의 하나가 누액 단백질 침착에 의한 것임을 알 수 있었으며, 많은 침착 단백질 양을 가지는 콘택트렌즈 착용자의 경우 적절한 재질의 렌즈 선택이 필요하다는 것을 알 수 있었다.

관리 용품에 따른 RGP 렌즈의 세척효과 및 습윤성 차이 (The Difference of the Cleaning and Wettability-maintaining Efficacy of Lens Care Solution to RGP Lens)

  • 김명혜;박미정
    • 한국안광학회지
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    • 제11권1호
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    • pp.27-34
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    • 2006
  • 본 논문에서는 RGP 렌즈에 부착된 누액 성분의 세척효과 및 RGP 렌즈의 습윤성 유지에 대한 RGP 렌즈 관리용액, 소프트콘택트렌즈(SCL) 관리용액, RGP 렌즈-SCL 겸용관리용액 및 생리식염수의 작용의 차이를 알아 보았다. 단백질 세척력을 알아보기 위해 Lowry protein assay와 주사현미경 관찰을 하였으며, 지질 세척력을 알아보기 위해 High Pressure Liquid Chromatology(HPLC)를 사용하였고, 습윤성은 water-in-air 방법으로 접촉각을 측정하여 알아 보았다. RGP 렌즈관리용액으로 RGP 렌즈를 세척 및 보관하였을 때 부착된 단백질의 62%가 제거되었으며, 이러한 단백질 부착물 세척력은 생리식염수나 겸용 관리용액에 비해 약 4배 우수한 것일 뿐만 아니라 SCL 관리용액에 비해 2배 우수한 것이었다. 이러한 결과는 소프트 콘택트렌즈에서의 SCL 관리용액의 단백질 세척력이 가장 우수하다는 것과 상이한 결과로, 세척 효과가 단순히 계면활성제의 활성만의 차이에 의해 나타나는 것은 아니며 RGP 렌즈 관리용액에 들어있는 점성증가제와 같은 성분들이 RGP 렌즈와 용액의 접촉을 증가시켜 세척효과가 강화되는 것과 같이 다른 요인들이 작용하여 나타나는 결과로 여겨진다. RGP 렌즈에 부착되어 있는 지질 또한 RGP 렌즈 관리용액이 가장 우수한 지질세척 효과를 가져 렌즈에 잔존하는 cholesterol의 양이 50%로 감소하였다. RGP 렌즈의 편안한 착용감을 위한 중요한 평가 지료인 렌즈 표면의 습윤성은 RGP 렌즈 관리용액에 의해 가장잘 유지되었다. 겸용 관리용액의 경우 세척력 및 습윤성 유지력이 모두 RGP 렌즈 용액에 못 미쳤다.

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급성(急性) 기아(饑餓)마우스의 간단백질(肝蛋白質), 핵산(核酸) 및 Guanine Deaminase 활성(活性)에 관(關)한 연구(硏究) (A Study on The Content of Liver Protein, Nucleic Acids, and Guanine Deaminase Activity of Mouse During Acute Starvation)

  • 박승희;김승원
    • Journal of Nutrition and Health
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    • 제1권2호
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    • pp.107-115
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    • 1968
  • Number of aspects, not only nutritional but social as well as political involved in human starvation pose nowadays global problems. In order to help establish the minimum nutritional requirements in the daily life of a man and to free people as well from either undernourishment, malnutrition or even starvation many workers have devoted themselves so far on the research programs to know what and how number of metabolic events take place in animals in vivo. It is the purpose of the present paper to examine in effect to what extent both of the protein and nucleic acids (DNA & RNA) together with an enzyme, guanine deaminase, which converts guanine into xanthine and in turn ends up to uric acid as an end product, undergo changes, quantitatively during acute starvation, using the mouse as an experimental animal. The mouse was strictly inhibited from taking foods except drinking water ad libitum and was sacriflced 24, 48, and 72 hours following starvation thus acutely induced. The animals consisted of two experimental groups, one control and another starvation groups, each being consisted of 6-24 mice of whose body weights ranged in the vicinity of 10 g. The animals were sacriflced by a blow on the head, followed by immediate excision of their livers into ice-cold distilled water, washing adherent blood and other contaminant tissues. The liver was minced foramin, by an all-glass homogenizer immersing it in an ice-bath, followed by subsequent fractionatin of the homogenate (10% W/V in 0.25M sucrose solution made up with 0.05M phosphate buffer of pH 7.4). For the liver protein and guanine deaminase assay, the 10% homogenate was centrifuged at 600 x g for 10 minutes to eliminate the nuclear fraction; and for the estimation of DNA and RNA, the homogenate was prepared by the addition of 10% trichloroacetic acid in order to free the homogenate from the acid-soluble fraction, the remaining residue being delipidate by the addition of alcohol and dried in vacuo for later KOH (IN) hydrolysis. The changes in body and liver wegihts during acute starvation were checked gravimetrically. Protein contents in the liver were monitored by the method of Lowry et al; and guanine deaminase activities were followed by the assay of liberated ammonia from the substrate utilizing the Caraway's colorimetry. The extraction of both DNA and RNA was performed by the Schmidt-Thannhauser's method, which was followed by Marmur's method of purification for DNA and by Chargaff's method of purification for RNA. The determinations of both DNA and RNA were carried out by the diphenylamine reaction for the former and by the orcinol reaction for the latter. The following resume was the results of the present work. 1. It was observed that the body as well as liver weights fall abruptly during starvation, and that the loss of body weight showed no statistical correlation with the decreases in the content of liver protein. 2. The content of liver protein and activity of liver guanine deaminase activity as well decline dramatically, and the specific activities of the enzyme (activity/protein), however, decreased gradually as starvation proceeded. 3. Both of the nucleic acids, DNA and RNA, showed decrements in the liver of mouse during acute starvation; the latter, however, being more striking in the decline as compared to the former. 4. The decreases in the liver protein content as resulted from the acute starvation had no statistically significant correlation with the decrements of DNA in the same tissue, but had regressed with a significant statistical correlation with the fall of RNA in the tissue. 5. The decrease in the activity of guanine deaminase in the liver of mouse during acute starvation was functionally more proportional to the decrease in RNA than DNA, and moreover correlated with the changes in the content of the liver protein. 6. The possible mechanisms involved during in this acute starvation as bring the decreases in the contents of DNA, protein, and guanine deaminase were discussed briefly.

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X-선(線) 조사(照射)가 Ehrlich 암세포(癌細胞)의 용적(容積), 단백양(蛋白量) 및 수종(數種) Sulfhydryl 기(基)에 미치는 영향(影響)에 관(關)하여 (Effect of X-Irradiation on the Levels of some Sulfhydryl Groups, Protein and Cell Volume of Ehrlich Ascites Tumour Cells)

  • 유춘식;주영은
    • The Korean Journal of Physiology
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    • 제3권2호
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    • pp.9-16
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    • 1969
  • It is well known that a number of -SH and -SS containing substances afford a certain measure of protection against radiation effects in many biological systems, and it is conceivable that inherent -SH levels in Ehrlich ascites tumour (ELD)cells may be of decisive improtance with respect to the development of cellular radiation injury. So far, little effort has been directed to elucidate the changes in levels of different -SH and -SS groups in ELD cells when the tumour-bearing whole animal was subjected to the sublethal dose of X-irradiation. The present study was designed to bring some lights in the possible changes of and relationship between various sulfhydryl levels, such as P-SH, NP-SH and NP-SS, as well as the content of protein and cell volume of ELD cells, after subjecting the ELD mice to 1,200 r of X-irradiation. The animals used in this experiment were all mixed bred mice of $20{\sim}25\;gm$ in body weight (approximately 2 months old) irrespective of sex. 12 mice in one experiment were inoculated intraperitoneally with 0.2 ml of ascites tumour cells $(2{\times}10^6\;cells)$, and on the 7th day of the tumour growth, they were X-irradiated with 1,200 r, using the conventional X-ray machine under the following conditions: 200 Kv at 15 mA, 0.5 mm Cu filter, target-skin distance: 50 cm. Radiation dose was measured with the the Philip integrating dosimeter. At 24, 36, 48 and 60 hours after the X-irradiation, the mice were killed by cervical dislocation, and the tumours were taken out. Freshly withdrawn ascites tumours were placed in ice, and immediately the cell concentration was measured with the Coulter Cell Counter (Model B), and the hematocrit of the tumour cells were also determined. Cell volume was thus calculated by the cell concentration and hematocrit value. P-SH content of ELD cells was measured potentiometrically according to the method of Calcutt & Doxey, and NP-SH and NP-SS contents were measured spectrophotometrically by the method described by Ellman. Protein content of ELD cells was determined with the Folin phenol reagent by Lowry et al. Altogether, 48 experimental mice were used, and 12 mice with the only exception of X-irradiation were used as the control. Results obtained indicate that the contents of all the cellular sulfhydryl groups as well as cell volume and protein content of the ELD cells increase significantly as time progresses after the sub-lethal X-ray dose of 1,200 r was given and that all the increase is in a lineal fashion. The regression lines of the relative values, (i. e., taking each control value as 1) of all the values obtained, and the regression lines of cell volume, protein and NP-SH are identical, whereas those of NP-SS and P-SH appear to be widely seperated. However, the difference of those two lines (NP-SS & P-SH) were found to be not significant statistically (p>0.05). Therefore, it can be concluded from the above results that all the values examined increase in a lineal fashion with no statistically significant difference among them. Also, with the radiation dose of 1,200 r, the ELD cell becomes enlarged and swollen progressively up to 60 hours post-irradiation and it becomes more than two times of the original normal size at 60 hours after the irradiation, and up to this stage, it seems apparent that the cell division has been slow due to the X-irradiation applied in this experiment. It is well understandable that the contents of NP-SH, NP-SS, P-SH and protein of the ELD cells increase in parallel with the increase of the cell volume by the X-ray does used, but it also seems interesting to note that all the cellular substances tested show no appreciable difference in the pattern of increase.

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