• KSBB Journal
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• 제8권2호
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• pp.115-121
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• 1993

호르몬이 결여되고 polyamine이 농도별로 처리된 M MS배지에서 10일 동안 발아생장(light, 16hrs: d dark, 8hrs) 시켜서 얻은 벼 잎 절편에서 엽록소 함 량은 polyamine 처리구가 대조구에 비해 높았으며, s spermine(O.OlmM, O.lmM, ImM) 이 가장 효과적이였다. 한편 chloroplast peroxidase의 활성은 polyamine 처리구가 대조구에 비해 전반적으로 높았으며, 특히 1mM spermidine 처리구는 약 100% 정도 활성을 증가시켰다. SDS-PAGE에 의해 chloroplast thylakoid membrane protein의 band를 조사한 결과 polyamine 처리구와 대조구에서 56, 2 25Kd의 major band를 얻었으며 이 band들의 total a area는 polyamine 처리구가 대조구 보다 더 높았다. 이러한 결과들은 벼 유식물에서 엽록체 발달에 p polyamine이 중요한 인자로 작용한 것으로 사료된다.

• 한국잡초학회지
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• 제8권3호
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• pp.250-257
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• 1988

Bensulfuron에 대표적인 내성군(耐性群)(UCP-28, Chinsurah Boro II, Fukunohama, Fadehpur-2, IR 14252-13-2-2-5)과 감수성품종군(感受性品種群)(HP93(3) FA, HP94(9) FA, Padilabou Alumbis. KH-17854, IR 1846-2841-1)을 공시(供試)하여 종실(種實) 단백질(蛋白質)(SDS-PAGE)과 유묘(幼苗) 동위효소(同位酵素)(malate dehydrogenase, acid phosphatase, peroxidase, esterase: 7% PAGE)의 전기영동(電氣泳動) profile을 분석(分析)하고, bensulfuron 0, $10^{-6}$, $10^{-5}$, $3{\times}10^{-5}M$ 용액에서 생장(生長)한 두 대표 품종(品種)(cv. Chinsurah Boro II와 cv. IR 1846)의 5 일령(日齡) 유묘(幼苗)의 동위효소(同位酵素) profile 변화양상(變化樣相)을 비교(比較)하므로써, bensulfuron에의 내성차이(耐性差異)와 이들 전기영동(電氣泳動) profile 차이(差異)가 갖는 연관성(聯關性)을 알고저 하였다. 결과(結果)를 요약(要約)하면 다음과 같다. 1. 종실단백(種實蛋白)의 전기영동(電氣泳動)으로 16개(個) band를 확인(確認)할 수 있었고, 이를 근거(根據)로 clustering한 결과(結果), 내성(耐性)에서의 M, O, P band가 높게 나타났고 또한 전체 peak 면적(面積)이 크다는 특이성(特異性)에 기인(起因)하여 두 품종군간(品種群間)에 비유사성(非類似性)이 인정(認定)되는 정도(程度)로 분류(分類)되었다. 2. 무처리(無處理)된 유묘(幼苗)의 동위효소(同位酵素) 가운데, peroxidase로는 4개(個) band가 얻어졌고, 내성군(耐性群)의 특이성(特異性)은 D band에서의 활성(活性)이 높은 데 있었다. Malate dehydrogenase는 3개(個) band로 분리(分離)되었고, 내성군(耐性群)만이 A band를 나타내며 B 및 C band도 내성군(耐性群)에서 선명하였다. Esterase는 3~4개(個) band로 구분(區分)되었고 내성군(耐性群)이 A 및 B band에서 높은 활성(活性)을 보였다. Acid phosphatase는 하나의 major band와 2~3개(個)의 minor band로 나타났으며 내성군(耐性群)만은 B band를 갖는 경향(傾向)이었다. 3. Bensulfuron의 처리농도(處理濃度)에 따라, 동위효소(同位酵素) 가운데 peroxidase는 감수성(感受性)에서만 C band의 생성(生成)과 D band의 소실현상(消失現象)이 야기(惹起)되었고, 내성품종(耐性品種)에서는 C band가 나타나지 않았으며, 다른 band에서의 변화(變化)도 없었다. Malate dehyrogenase의 경우, major band인 D, E, F는 감수성(感受性)에서 활성(活性)이 컸고 변화(變化)는 없었으며, minor band인 A, B, C는 감수성(感受性)에서만 민감(敏感)하게 소실(消失)되었다. Esterase는 5개(個) band로 표현(表現)되었으며 내성(耐性)에서는 A, B, C, D 감수성(感受性)에서는 A, B, C, E만 나타났으며, 약처리농도증가(藥處理濃度增加)로 감수성품종(感受性品種)은 A, C, E band의 활성(活性)이 민감(敏感)하게 소실(消失)되었다.

• BMB Reports
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• 제39권2호
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• pp.216-222
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• 2006

In the present study, we compared six different solubilization buffers and optimized two-dimensional electrophoresis (2-DE) conditions for human lymph node proteins. In addition, we developed a simple protocol for 2-D gel storage. Efficient solubilization was obtained with lysis buffers containing (a) 8M urea, 4% CHAPS (3-[(3-cholamidopropyl) dimethylammonio]-1-propanesulfonate), 40 mM Tris base, 65 mM DTT(dithiothreitol) and 0.2% carrier ampholytes; (b) 5M urea, 2M thiourea, 2% CHAPS, 2% SB 3-10 (N-decyl-N, N-dimethyl-3-ammonio-1-propanesulfonate), 40mM Tris base, 65 mM DTT and 0.2% carrier ampholytes or (c) 7M urea, 2M thiourea, 4% CHAPS, 65 mM DTT and 0.2% carrier ampholytes. The optimal protocol for isoelectric focusing (IEF) was accumulated voltage of 16,500 Vh and 0.6% DTT in the rehydration solution. In the experiments conducted for the sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), best results were obtained with a doubled concentration (50 mM Tris, 384 mM glycine, 0.2% SDS) of the SDS electrophoresis buffer in the cathodic reservoir as compared to the concentration in the anodic reservoir (25 mM Tris, 192 mM glycine, 0.1% SDS). Among the five protocols tested for gel storing, success was attained when the gels were stored in plastic bags with 50% glycerol. This is the first report describing the successful solubilization and 2D-electrophoresis of proteins from human lymph node tissue and a 2-D gel storage protocol for easy gel handling before mass spectrometry (MS) analysis.

• 한국미생물·생명공학회지
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• 제28권5호
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• pp.251-257
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• 2000

Serratia marcescens purine nucleoside phosphorylase (PNP) was purfied to homogeneity by streptomycin sulfate treatment, Sephacry HR S-200 gel filtration chromatography and AMP-agarose affinity chromatography. The specific activity of the enzyme was increased 49-fold during purification with an overall yield of 7.0%. The molecular weight was 168kD as estimated by Sephadex G-150 gel filtration chromatography. The S. marcescens enzyme was composed of six identical subunits with subunit molecular weight of 28kD, as estimated by SDS-PAGE. The Km values of S. marcescens enzyme for inosine and deoxyinsoine were 0.38 and 1.20 mM, respectively. The ph optimum was near 8.0, and the enzyme was relatively heat-stable protein. The enzyme was inactivated com-pletely by 0.5 mM of $Cu^{ 2+}$.

• 대한화장품학회지
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• 제25권1호
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• pp.107-119
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• 1999

3 Kinds of PEG-hEGF conjugate, PEG5-hEGF, PEG5-hEGF, PEG10-hEGF, were synthesized. Major fractions containing 2 chains of PEG were separated by preparative GPC. Molecular weight was estimated by GPC-MALLS, TOF-Mass and SDS-PAGE, and the data were well corresponding to calculated one. The cell proliferation effect of the conjugates was evaluated, Indicating that the conjugate bound to longer chain PEG exhibits lower activity. Selective modification of hEGF and activity preservation of PEG-hEGF conjugate are undergoing.

• 한국식물병리학회지
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• 제12권1호
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• pp.99-108
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• 1996

3종의 빙핵세균 Peudomonas syringae 8401, Pseudomonas fuorescens 8701, Erwinia herbicola 8701의 세포 외막으로부터 아무런 변성제도 사용치 않고 sucrose density gradient centrifugation, Sephacryl gel filtration chromatography, DEAE-cellulose ion exchange chromatography, non-denaturing buffer를 이용한 PAGE, electroelution, SDS-PAGE를 통해 빙핵활성 단백질을 고도로 정제할 수 있었다. P. suringae와 P. fluorescens에서는 각각 3종류(155 kD, 75 kD, 50 kD)의 빙핵활성 단백질이, E. herbicola에서는 155 kD를 제외한 2종류(75 kD, 50 kD)의 빙핵활성 단백질은 이 연구를 통해 처음 밝혀진 것으로 , 지금까지 보고된 빙핵활성 단백질(150 KD 이상)보다는 훨씬 작은 것이다. 이는 빙핵활성을 나타내는 단백질의 기본단위는 이 실험의 결과만에 의하면 최대 50 kD임을 시사한다. 이들 단백질은 그 유래된 세균의 종류나 또는 단백질 분자량의 크기에 관계없이 모두 -5.5~7.5$^{\circ}C$에서 물을 동결시키는 높은 빙핵활성을 갖고 있었다. 이는 지금까지 보고된 어느 정제단백질의 빙핵활성보다 높은 것이다. 정제된 단백질의 빙핵활성은 trypsin 처리에 의해 상실되었고, pH6~8범위에서는 안정하였으며, pH5이하, pH9이상에서는 활성을 상실하였다. 보존온도에 대한 영향은 3$0^{\circ}C$이상이 되면 점차 활성이 감소하는 경향을 보이다 37$^{\circ}C$이상에서는 활성이 완전히 상실되었다. 금속이온으로서 Hg\ulcorner이온과 SDS에 의해 활성이 상실되었으나 phosphatidylinositol의 첨가에 의해서는 활성이 약간 증가(-1$^{\circ}C$)하였다.

• 한국동물학회지
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• 제34권1호
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• pp.44-53
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• 1991

Distribution of the antigens during the cell cycle of amoebae was followed by immunof-luorescence microscopy using a monoclonal antibody against the nucleus as a probe. While the cells were in the interphase, the antigen was localized on the nucleus membrane. But it was dispersed all over the cytoplasm during mitosis and cytokinesis. The molecular weights of the immunoreacted antigens were 210 KD and 190 KD as determined by SDS PAGE and western blotting of the purified nuclei. The antigens were not soluble in non-ionic detergent, but were released from the nucleus by incubation with 0.05 M sodium carbonate, pH 10.6 or with 8 M urea at serial chemical extraction. Thus the antigens appeared to be peripheral proteins of the nurBeus envelope. The isoelectic point of both antigens was 7.64 as determined by 2 D PAGE and transfer blotting. Considering the peiipherd association with the nucleus membrane and the dispersed distribution during mitosis, the antigens could be lamin like proteins. Hourever, it appears also possible that they are the component molecules of the unusually structured aurous lamina of amoeba nucleus since they have the large molecular weight and the basic pl.

• Journal of Applied Biological Chemistry
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• 제54권2호
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• pp.94-100
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• 2011

Bacillus licheniformis로 부터 phospholipase D (PLD)로 추정되는 유전자를 PCR 기술을 이용하여 분리하여 pGEM-T easy 운반체에 cloning 하였다. 분리된 유전자는 His6가 붙은 pET-21 운반체를 이용하여 E. coli BL21 (DE3)에서 발현시켰다. 재 조합된 PLD는 nikel-nitrilotriacetic acid (Ni-NTA) resin을 갖는 column을 이용하여 affinity chromatography로 분리하였다. SDS-PAGE 분석 결과 PLD로 추정되는 단백질은 약 44 kDa의 주요 단일밴드를 나타내었다. 분리된 효소의 최적 활성도는 pH 7.0에서 나타났으며 이 조건에서 또한 효소가 제일 안정되었다. 효소활성에 미치는 최적 온도는 $40-45^{\circ}C$의 온도에서 형성되어 비교적 높은 온도를 나타내었으며 비교적 넓은 범위의 온도에서 상당히 높은 효소 활성도를 나타내었다. 여러 가지 detergent 중에서 Triton X-100을 0.6 mM까지 첨가할 경우 PLD의 효소활성도는 점진적으로 증가하여 대조구 대비 최대 181%의 효소 활성도를 나타내었다.

• Journal of Microbiology and Biotechnology
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• 제11권2호
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• pp.242-250
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• 2001

A Gram-positive bacterium (strain JB-13) that was isolated from soil as a producer of cyclodextrin glucanotransferase (CGTase) [EC 2.4.1.19] was identified as Panibacillus sp. JB-13. This CGTase could catalyze the transglucosylation reaction from soluble starch to L-ascorbic acid (AA). A main product formed by this enzyme with ${\alpha}-glucosidase$ was identified as $2-O-{\alpha}-D-glucopyranosyl{\;}_{L}-ascorbic$ acid (AA-2G) by the HPLC profile and the elemental analysis. CGTase was purified to homogeneity using ammonium sulfate fractionation, ion-exchange chromatography on DEAE-Seohadex A-50, and gel chromatography on Sephacryl S-200HR. The molecular weight was determined to be 66,000 by both gel chromatography and SDS-PAGE. The isoelectric point of the purified enzyme was 5.3. The optimum pH and temperature was PH 7.0 and $45^{\circ}C$ respectively. The enzyme was stable in the range of pH 6-9 and at temperatures of $75{\circ}C$ or less in the presence of 15 mM ${CaCl_2}.\;{Hg^2+},\;{Mn^+2},{Ag^+},\;and\;{Cu^2+}$ all strongly inhibited the enzyme's activity.

• Archives of Pharmacal Research
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• 제19권4호
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• pp.275-279
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• 1996

To study the functional roles of dopamine receptors, we decided to raise antibodies against these proteins. To make antigen, we expressed the whole 3rd cytoplasmic loop of dopamine receptors in a fusion protein with glutathione-S-transferase (GST). $For D_2\; and\; D_3$ receptors, it was successful to express and purify fusion proteins for the whole 3rd cytoplasmic loops. However, we could not express the fusion protein for the whole 3rd cytoplasmic loop of $D_4$ dopamine receptor in the bacteria. To study the causes that prevent the bacterial expression of the GST-fusion protein of the 3rd cytoplasmic loop of $D_4$ dopamine receptor, we conducted more detailed studies on $D_4$ dopamine receptor. To locate the region which prevents bacterial expression, we made sequential constructs in the 3rd cytoplasmic loop decreasing the size step by step, and confirmed their expressions in the SDS PAGE. It was found that certain regions of 3rd cytoplasmic loop of $D_4$ dopamine receptor, located in N-terminal side of the 3rd cytoplasmic loop of $D_4$ dopamine receptor suppress the bacterial expression of fusion protein.