• 제목/요약/키워드: Protein X

검색결과 1,445건 처리시간 0.032초

Proteome analysis between diverse phenotypes of Salmonella enterica subspecies enterica serovar Typhimurium (S. Typhimurium)

  • Shin, Gee-Wook;Cha, In-Seok;Lee, Woo-Won;Nho, Seong-Won;Park, Seong-Bin;Jang, Ho-Bin;Kim, Yong-Hwan;Jung, Tae-Sung
    • 대한수의학회지
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    • 제50권4호
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    • pp.285-295
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    • 2010
  • Protein expression patterns in Salmonella enterica subspecies enterica serovar Typhimurium (S. Typhimurium) strains with diverse phenotypes, such as phage type, antibiotic resistance pattern and plasmid profiles were examined. For detailed analysis of proteins expressed by different S. Typhimurium strains, protein fractions were divided into detergent-rich phase (DP) and aqueous phase (AP) using triton X-114 detergent. The two phases were subjected to two-dimensional gel electrophoresis (2-DE), followed by protein identification using peptide mass fingerprinting (PMF). In the results, PMF showed that DP fractions consisted mainly of outer membrane proteins, whereas the AP fractions included cytosolic proteins. Comparison of 2-DE profiles of DP did not show any distinct protein spots which could be correlated with phage type, antibiotic resistance pattern or plasmid profile. However, comparisons of 2-DE profiles of the AP revealed differences in the protein spots, which could be correlated with the plasmid profile and phage types. Among these protein spots, flagellin was specific for strains containing a 90 kb plasmid. Compared to DT193 phage type, three protein spots in the range of pI 5.0-5.5 and MW 8-15 kDa of AP 2-DE profiles were absent in the DT104 phage types. Additionally, a protein spot with PI in the range of 4.5-5.0 and molecular weight (MW) between 51-69 kDa was specific for phage type DT104, while a protein spot with pI in the range of 4.0-4.8 and MW between 18-20 kDa was specific for DT193 phage type. These protein spots may be useful for discriminating phage types of S. Typhimurium.

반응표면분석법을 이용한 쌀 단백질 초고압 추출조건 최적화 (Optimization of the High-Pressure Condition for Rice Protein Extracting Using Response Surface Methodology (RSM))

  • 라하나;박사라;김하윤;조용식;김경미
    • 한국식생활문화학회지
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    • 제34권6호
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    • pp.779-784
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    • 2019
  • The purpose of this study was to optimize the rice protein extracted using a response surface methodology. The experiment was designed based on a CCD (Central Composite Design), and the independent variables were the high pressure (X1, 0-400 MPa) and processing time (X2, 0-10 minutes). The results of the extraction content (Y1), residue content (Y2), and recovery yield (Y3) were fitted to a response surface methodology model (R2= 0.92, 0.92, and 0.93, respectively). Increasing the pressure and processing time has a positive effect on the extraction content (Y1), residue content (Y2), and recovery yield (Y3). Therefore, these high-pressure conditions (independent variables) can significantly affect the improvement in rice protein extraction efficiency. Thus, the optimal conditions of X1 and X2 were 400 MPa and 10 min., respectively. Under these optimal conditions, the predicted values of Y1, Y2, and Y3 were 62.93, 57.53 mg/g, and 91.76%, respectively.

Amoeba proteus에 있어서 박테리아 감염에 의한 변이주 특이성 단백질의 손실 (Loss of a Strain-Specific Protein by Bacterial Infection in Amoeba proteus)

  • Ahn, Tae-In;Park, Eui-Yul
    • 한국동물학회지
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    • 제28권1호
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    • pp.21-30
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    • 1985
  • Amoeba proteux xD strain에서 추출한 공생박테리아를 tD strain에 감염시키고, 숙주의 박테리아 감염으로 인한 변이주 특이성 단백질의 손실을 2차원 전기영동에 의해 탐지하였다. 유도 식작용에 의한 실험감염 50일 만에 숙주인 아메바는 tD strain 특이성 단백질을 손실하였며, 이는 $27^\\circC$ 배양에 의해 감염 박테리아 및 xD strain 특이성 단백질을 제거한 후에도 재합성되지 못하였다. 이 시기면 숙주인 아메바는 박테리아에 완전히 의존한 것으로 판명되었다. 이상의 결과 및 Lorch Jeon (1981, Science 221:549)의 결과를 볼 때 감염된 숙주핵이 감염되지 않은 아메바 원형질과 양립하지 못하는 것이나 숙주의 박테리아에 대한 의존 유발은 박테리아 감염에 의해 세포 특이성 유전인자의 비가역적인 불활성화 또는 솔실로 인한 것이 분명하다.

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Neuronal function and dysfunction of CYFIP2: from actin dynamics to early infantile epileptic encephalopathy

  • Zhang, Yinhua;Lee, Yeunkum;Han, Kihoon
    • BMB Reports
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    • 제52권5호
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    • pp.304-311
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    • 2019
  • The cytoplasmic FMR1-interacting protein family (CYFIP1 and CYFIP2) are evolutionarily conserved proteins originally identified as binding partners of the fragile X mental retardation protein (FMRP), a messenger RNA (mRNA)-binding protein whose loss causes the fragile X syndrome. Moreover, CYFIP is a key component of the heteropentameric WAVE regulatory complex (WRC), a critical regulator of neuronal actin dynamics. Therefore, CYFIP may play key roles in regulating both mRNA translation and actin polymerization, which are critically involved in proper neuronal development and function. Nevertheless, compared to CYFIP1, neuronal function and dysfunction of CYFIP2 remain largely unknown, possibly due to the relatively less well established association between CYFIP2 and brain disorders. Despite high amino acid sequence homology between CYFIP1 and CYFIP2, several in vitro and animal model studies have suggested that CYFIP2 has some unique neuronal functions distinct from those of CYFIP1. Furthermore, recent whole-exome sequencing studies identified de novo hot spot variants of CYFIP2 in patients with early infantile epileptic encephalopathy (EIEE), clearly implicating CYFIP2 dysfunction in neurological disorders. In this review, we highlight these recent investigations into the neuronal function and dysfunction of CYFIP2, and also discuss several key questions remaining about this intriguing neuronal protein.

사료내 조단백질 수준이 진도성견의 질소균형에 미치는 영향 (Effects of Crude Protein Levels on Nitrogen Balance in Adult Jindo Dog)

  • 강태일;맹원재;김명화;이상락
    • Journal of Animal Science and Technology
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    • 제51권2호
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    • pp.155-162
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    • 2009
  • 본 연구는 진도성견의 단백질 급여수준이 질소균형에 미치는 영향을 조사하여 단백질 급여 표준을 설정하기 위한 기초 자료를 얻기 위하여 실시하였다. 진도견 성견초기(생후 36~38주령)와 성견후기(생후 45~49주령)의 암컷 12두를 대상으로 단백질 수준을 17, 19 및 21%로 설정한 실험사료를 급여하여 체중, 사료섭취량 및 분뇨 배설량을 측정하였다. 성견초기의 일당 증체량은 조단백질 함량 17, 19 및 21%구에서 각각 -38.33, -16.25 및 -12.71g으로 나타났으며 17% 조단백질 사료급여구가 19 및 21% 급여구에 비하여 유의하게 낮았다(p<0.05). 축적된 질소량은 각각 -0.29, -0.04 및 -0.03g/kg$BW^{.75}$/d로 계산되었으며 조단백질 17% 급여구가 19 및 21% 급여구에 비하여 유의하게(p<0.05) 낮은 결과를 나타내었다. 질소섭취량(x)과 질소축적량(y)간에 y = 0.7484x-1.18 ($R^2$ = 0.9923)의 회귀식이 도출되었으며, 이 식으로부터 성견초기의 유지 조단백질 요구량은 9.85g/kg$BW^{.75}$/d로 추정되었다. 진도견 성견후기의 일당 증체량은 실험구 별로 각각 -34.05, -28.71 및 -28.28g으로 17% 단백질 사료급여구가 다른 구에 비하여 낮게 나타났으나 유의한 차이는 아니었다. 축적된 질소량은 각각 -0.33, -0.06 및 -0.09g/kg$BW^{.75}$/d로 계산되었으며 17% 조단백질 급여구가 19 및 21% 급여구에 비하여 유의하게(p<0.05) 낮은 결과를 나타내었다. 질소섭취량(x)과 질소축적량(y)간에 y = 0.8823x-1.0894 ($R^2$ = 0.9982)의 회귀식이 도출되었으며 이식을 이용하여 계산한 결과 성견후기의 유지 조단백질 요구량은 7.72g/kg$BW^{.75}$/d로 추정되었다. 본 연구는 우리나라에서 진도견을 대상으로 한 영양소 요구량을 설정하기 위한 최초의 연구로 생각되며 연구의 결과는 진도견의 단백질 요구량을 설정하는데 기초 자료가 될 것으로 생각된다. 그러나 진도견의 단백질 요구량을 최종적으로 설정하기 위해서는 전 생애에 걸쳐서 성별 및 사육환경에 따른 영양소 요구량에 대한 추가적인 연구가 필요하다고 사료된다.

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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구름버섯 배양액으로부터 단백다당류의 추출 및 정제방법 (Extraction and Separation of Protein-bound Polysaccharide Produced by Coriolus versicolor (Fr) Quel)

  • 박경숙;이재양;이상직;김선희;이재성
    • 한국균학회지
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    • 제20권1호
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    • pp.72-76
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    • 1992
  • 고등균류의 배양액 및 균사체로부터 항암작용이 있는 단백다당류의 추출 및 정제방법에 관한 실험을 구름버섯 균사배양체를 이용하고 실시하였다. 실온에서 비이온성 계면활성제인 2% Triton X-100과 함께 교반시키면서 추출했을 때 얻어진 단백다당류의 함량이 이미 사용되어 온 $100^{\circ}C$ 열수에 의한 추출방법을 통해 얻을 수 있는 것보다 더 좋았다. 그러나 4 N NaCl을 포함한 2% Triton-X-100 용액으로 처리했을 때는 추출 후 ethanol 침전과정에서 단백다당류의 침전물을 얻을 수 없었다. 열수추출과 ethanol 침전과정에서 얻어진 단백다당류의 순도를 높이기 위해 chromatography를 이용한 정제실험을 하였다. alumina와 DEAE-Cellulose, DEAE-Sephadex를 각각 충전제로 하여 시료를 전개시키고 280nm에서의 흡광도를 기준으로 단백질 성분의 용출을 확인하고 이들 분획에 대하여 anthrone정색반응과 625nm에서의 흡광도를 측정함으로써 단백다당류를 분리, 정제하였다. 단백다당류의 정제는 alumina를 충전제로 사용하는 것보다 DEAE-Cellulose와, DEAE-Sephadex를 충전제로 한 chromatography에 의하여 더 효율적으로 정제되었다.

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Effect of Nitrogen Fertilizer Application on Yield and Quality of Korean Soft Wheat Cultivar 'Goso'

  • Han-yong Jeong;Yulim Kim;Chuloh Cho;Jinhee Park;Chon-Sik Kang;Jong-Min Ko;Jiyoung Shon
    • 한국작물학회:학술대회논문집
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    • 한국작물학회 2022년도 추계학술대회
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    • pp.63-63
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    • 2022
  • Wheat flour can be categorized into bread, all-purpose, cake flour according to its protein content. Since optimal wheat flour protein content is different for each end use, it is necessary to diversify the nitrogen fertilizer methods depending on the end use and cultivar. Optimal wheat flour protein content of soft wheat (for cake flour) is lowest (<=10%) among all end use, it is necessary to develop nitrogen fertilizer methods for high yield and low protein content. In order to analyze the yield and quality changes of soft wheat as nitrogen fertilizer amount and splitting timing, soft wheat cultivar 'goso' was sown on paddy soil in jeunju, Republic of Korea ('21.10). the amount of nitrogen fertilizer was divided into 4 levels by adjusting 2kg/10a increments from 5.1 to ll.lkg/lOa, and in the N 7.1 and 9.1 kg/1 Oa(standard) treatment, N amount divided into sowing date:regrowing stage=3:7,4:6(standard), 5:5. In regrowing stage, Tiller number and N fertilizer amount at sowing date showed a correlation; y=-121.14x2+792.66x-525.41 (R2=0.77*, y: Tiller number/m2, x: N amount at sowing date(kg/10a)). Tiller number in regrowing stage was the highest when the nitrogen fertilizer amount at sowing date was 3.23kg/10a. spike number per m2 was the highest when N fertilizer was divided into sowing date:regrowing stage=3:7(N amount: 9.1kg/10a). If N fertilizer amount was fixed, grain yield was also the highest when N fertilizer was divided into sowing date :regrowing stage=3:7. Also, N amount at sowing date and grain yield showed no correlation, but N amount at regrowing stage and grain yield showed significant correlation. As N amount increased, protein content also showed a tendency to increase.

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Zinc finger RING-H2 protein관련 Ac/Ds전이인자 삽입 변이체 Oszinc626 유전자의 특성 분석 (Characterization of Oszinc626, knock-out in zinc finger RING-H2 protein gene, in Ac/Ds mutant lines of rice(Oryza sativar L.))

  • 박슬아;정유진;안병옥;윤도원;지현소;박용환;은무영;서석철;이순열;이명철
    • Journal of Plant Biotechnology
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    • 제35권3호
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    • pp.177-183
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    • 2008
  • 본 연구는 동진벼 유래의 Ac/Ds 삽입변이집단의 GUS 분석을 통하여 뿌리 및 미숙종자에서 강하게 GUS가 발현한 개체를 선발하여 FST(flanking sequence tag) 분석 한 결과 Ds 전이 인자가 3번 염색체 zinc finger RING-H2 관련 Oszinc626 유전자의 첫 번째 exon 부위에 single copy로 삽입되어 있었으며, 선발변이체는 뿌리 및 종자 발달이 정상인 동진벼에 비해 매우 낮은 것으로 나타났다. Oszinc626 유전자는 RING-H2 type(C3-H2-C3)으로 $Cys-X_2-Cys-X_{28}-Cys-X-His-X_2-His-X_2-Cys-X_{14}-Cys-X_2-Cys$ 배열이 C-terminus 가장 말단에 위치하며, 49 kDa의 분자량을 가지고 있다. 또한 Southern blot 분석에서 Oszinc626 유전자는 벼 게놈상에 single copy로 존재하였다. RT-PCR을 통한 돌연변이 유전자의 발현분석 결과 250 mM의 염과, $4^{\circ}C$ 저온등과 같은abiotic stress에 의해 발현이 증가함을 보였고, 호르몬처리에 있어서 ABA와 IAA의 식물호르몬을 처리했을 경우 24시간까지 계속해서 발현양이 증가하는 것을 보이는 반면, 2,4-D 처리의 경우 30분 후에 발현이 일시적으로 증가되었으나 이후 발현이 급속히 감소한 것을 보였다. 벼의 조직 별 발현 검정에서 미성숙한 종자, 뿌리 분열조직 및 신초 등 주로 생장점 부위에서 강하게 발현되는 것을 보임에 따라 Oszinc626 유전자의 경우 식물의 생장에 관여하는 주동 유전자의 하나로 판단된다.