• Biotechnology and Bioprocess Engineering:BBE
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• 제9권4호
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• pp.274-277
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• 2004

Production of green fluorescent protein (GFP) as a model foreign protein using different culture scales under co-expression of Vitreoscilla hemoglobin (VHb) in the industrial Escherichia coli strain W3110 (a K12 derivative), was examined. It was found that the VHb co-expressing W3110, exhibited an exceptional and sustained production ability during cell cultures using different scales, while the VHb non-expressing strain showed variable production levels. This high and sustained production ability indicates that the VHb co-expressing E. coli W3110, could be successfully employed for practical large-scale production cultures without the need for serious consideration of scale-up problems.

• 한국경영과학회:학술대회논문집
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• 한국경영과학회/대한산업공학회 2003년도 춘계공동학술대회
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• pp.800-807
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• 2003

Decomposition of tasks in the ordinary manufacturing systems is usually based on the predefined goal of the system. To achieve the high-level-goals (e.g., factory goal or company goal), several sub-goals should be achieved in advance. However, goals can change along with the current status of the system and the external environmental situations. Thus, a manufacturing system should support the goal-formations which can be bearable these changes for efficient and effective operations. Therefore, it IS necessary to develop a systematic methodology for the goal-formations in a manufacturing system. Especially, the formation and/or change of goals in real-time should be possible for distributed and dynamic systems including the fractal manufacturing system (FrMS). In this paper, a threefold methodology is proposed for the goal-formation process (GFP) in the FrMS; 1) a goal­generating process (GGP) to make and propagate fuzzy goals, 2) a goal-harmonizing process (GHP) to eliminate or reduce conflicts and interferences of goals by using a mobile agent- based negotiation scheme, and 3) a goal-balancing process (GBP) to make a compromise between goals by using quantifiable indicators of the manufacturing system.

• 대한수의학회지
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• 제46권1호
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• pp.13-19
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• 2006

Generally known psittacosis or ornithosis is a disease of birds caused by the bacterium Chlamydia psittaci. Humans are accidential hosts and are most commonly infected from avian sources. It raises hepatitis or neurosis. As major outer membrane protein (MOMP) of Chlamydia psittaci has been known to play a role in the avoidance of host immune defenses, research on developing a Chlamydia vaccine has focused on the MOMP. In this study, the gene encoding the major outer membrane protein (MOMP) of the Chlamydia psittaci strain 6BC was cloned and expressed in Escherichia coli strain M-15. The recombinant DNA was cloned by fusion prokaryotic expression vector pQE30-GFPII. Expression of the recombinant protein was performed in E. coli and was induced by IPTG. The size of expressed recombinant protein is 74.220 kDa (MOMP, 43.260 kDa; GFP expression region, 30 kDa; $6{\times}His$ tag, 960Da). This protein was purified by using his-tagging-inclusion body. Recombinant protein was reconfirmed through ELISA test and western blot with antibody against pQE30-GFPII. It will be useful antibody development.

• 한국어병학회지
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• 제33권2호
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• pp.103-109
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• 2020

In order to use nervous necrosis virus (NNV) virus-like particles (VLPs) as a delivery tool for heterologous antigens or plasmids, we attempted to produce red-spotted grouper nervous necrosis virus (RGNNV) VLPs displaying a partial region of viral hemorrhagic septicemia virus (VHSV) glycoprotein at the surface and VLPs that are harboring DNA vaccine plasmids within the VLP. A peptide encoding 105 amino acids of VHSV glycoprotein was genetically inserted in the loop region of NNV capsid gene, and VLPs expressing the partial part of VHSV glycoprotein were successfully produced. However, in the transmission electron microscope analysis, the shape and size of the partial VHSV glycoprotein-expressing NNV VLPs were irregular and variable, respectively, indicating that the normal assembly of capsid proteins was inhibited by the relatively long foreign peptide (105 aa) on the loop region. To encapsulate by simultaneous transformation with both NNV capsid gene expressing plasmids and DNA vaccine plasmids (having an eGFP expressing cassette under the CMV promoter), NNV VLPs containing plasmids were produced. The encapsulation of plasmids in the NNV VLPs was demonstrated by PCR and cells exposed to the VLPs encapsulating DNA vaccine plasmids showed fluorescence. These results suggest that the encapsulation of plasmids in NNV VLPs can be done with a simple one-step process, excluding the process of disassembly-reassembly of VLPs, and NNV VLPs can be used as a delivery tool for DNA vaccine vectors.

• 한국동물생명공학회지
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• 제36권1호
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• pp.17-24
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• 2021

In this study, the potential toxicity of isoprocarb was demonstrated using zebrafish embryos. We treated isoprocarb (0, 29, and 58 mg/L) to the zebrafish embryos for 72 h then, we estimated morphological changes and apoptotic cell numbers. The increasing extent of apoptosis from the anterior to posterior region of developing zebrafish larvae was correlated with toxicity in the overall development process, including growth and normal organ formation. The appearance of abnormalities in the isoprocarb-treated groups in comparison to normal developing zebrafish larvae was verified using quantitative image analysis based on ImageJ software program. The vascular system comprising a complex interconnection of blood vessels was visualized in vessel-fluorescent transgenic zebrafish (fli1:eGFP). The main vasculature was malformed on isoprocarb treatment, and this was also related to cardiac defects. Taken together, normal embryonic development in zebrafish was interrupted owing to the acute toxicity of isoprocarb.

• 한국동물생명공학회지
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• 제37권3호
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• pp.176-182
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• 2022

Norflurazon is widely used on agricultural lands and has a high potential to pollute water sources. However, its effects on fish have not been fully elucidated. The purpose of our study was to determine whether norflurazon adversely affects the developmental stage of zebrafish, which are frequently used as a model system to evaluate the environmental impact of pollutants. Norflurazon interfered with the hatching of zebrafish embryos and induced several sublethal deformities including body length reduction, increased yolk sac volume, and enlargement of the pericardial region. We further examined the cardiotoxicity of norflurazon in the flk1:eGFP transgenic zebrafish line. The vascular network, mainly in the brain region, was significantly disrupted in norflurazon-exposed zebrafish. In addition, due to the failure of cardiac looping, norflurazon-exposed zebrafish had an abnormal cardiac structure. These developmental abnormalities were related to the apoptotic process triggered by norflurazon. Overall, the present study demonstrated the non-target toxicity of norflurazon by analyzing the hazardous effects of norflurazon on developing zebrafish.

• 한국식품영양과학회지
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• 제32권5호
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• pp.752-757
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• 2003

홍삼으로부터 홍삼알콜 추출물을 제조하고 부산물로 생성된 홍삼추출잔사로부터 한외 여과를 이용하여 홍삼산성다당체(RGAP, red ginseng acidic polysaccharide)를 대량으로 분리할 수 있는 방법을 개발하였다. 본 방법으로 홍삼추출잔사로부터 분리된 RGAP의 수율은 20.9%이었고, RGAP로부터 지표성분인 활성성분(GFP)의 분리수율은 39.4%이었다. 분리된 RGAP는 macrophage에 의한 NO(nitric oxide)를 생성하여 암세포를 사멸시키는 것으로 나타났다. RGAP를 BALB/c 마우스에 복강투여한 후 분리된 복강 macrophage를 P815 암세포(mastocytoma)와 함께 배양하였을 때 배지내의 NO 농도는 대조군에서 4.3 $\mu\textrm{m}$이었으나, RGAP 100, 300 mg/kg 투여군에서는 각각 9.8 및 25.3$\mu\textrm{m}$로 증가하는 경향을 나타내었다. 아울러 암세포인 P8l5세포의 사멸율도 정상대조군일 경우 7.3%이었으나 RGAP 100, 300 mg/kg 투여군에서는 각각 22.7 및 31.8%로 증가하는 경향을 나타내었다. RGAP을 2M의 TFA로 10$0^{\circ}C$에서 1시간 가수분해한 후 당 표준품과 TLC로 비교한 결과 당 표준품과 Rf치 및 발색 색깔이 일치하는 4개의 spot, 즉 rhamnose(Rf 0.78, 노란색 ), glucose(Rf 0.61, 녹색), galactose(Rf 0.56, 녹색), glucuronic acid(Rf 0.36, 황갈색)를 관찰할 수 있었다. 가수분해된 RGAP 분해산물을 Gl(glucose)부터 G7(maltoheptaose)까지의 당류와 함께 TLC를 행한 결과 진한 색상을 나타내는 spot은 Rf 0.56~0.61로 G2(maltose, Rf 0.46) 이상의 단당류(monosaccharide)인 것으로 나타났다. RGAP의 일부 이화학적 특성을 조사한 결과 pH는 4.74, 건조감량은 4.72%, 조단백질 함량은 3.30%, 회분은 4.74%이었고 중금속인 Pb는 2.30 ppm이었다.

• 한국미생물·생명공학회지
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• 제36권4호
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• pp.260-267
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• 2008

단백질의 산업적 생산을 위해 발현벡터의 선정이 중요하지만 이용 가능한 프로모터가 극히 제한적이며 많은 경우 과발현되는 특성과 함께 불용성 응집체가 형성되는 단점을 지닌다. 따라서 다양한 생물로부터 유래된 잠재성이 큰 유전자원(metagenome)에서의 프로모터 발굴과 한정된 숙주를 해결하려는 노력이 요구된다. 선행연구에서 발굴한 metagenome 유래의 항시발현 프로모터를 이용해 대장균의 일반적인 배양조건에서 세포생리에 영향이 적은 신규 항시발현 벡터를 제작하였다. 이를 위해 예측된 프로모터 서열과 MCS를 포함하는 합성 primer를 제작한 후 PCR로 증폭해 발현벡터를 구성한 후, 프로모터 구동여부와 단백질 발현양상 등을 관찰하였다. 인위적으로 도입된 MCS에 GFP, esterase, $\beta$-glucosidase를 클로닝해 단백질 발현양과 가용성을 분석한 결과, 안정적으로 전체단백질의 $2{\sim}3%$ 정도로 발현되며 80% 이상의 높은 가용성을 지닌 단백질의 발현이 유도되는 것으로 확인되었다. 이와 같은 결과는 잠재적인 생물자원의 보고로서 metagenome의 활용가능성을 제시하고 있다. 따라서 다양한 숙주에서 작동하는 프로모터의 발굴 및 발현벡터의 제작을 시도할 경우 단백질의 생산이나 대사공학에 의한 균주개량에 유용하게 활용할 수 있을 것이다.

• Asian Pacific Journal of Cancer Prevention
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• 제13권9호
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• pp.4435-4439
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• 2012

Purpose: This study aimed to explore the role of the Twist gene in the epithelial-mesenchymal transition of ovarian cancer. Methods: An RNA interference plasmid expressing a small interfering RNA (siRNA)-targeting Twist (Twist siRNA vector) was designed, constructed, and transfected into the human ovarian cancer cell line A2780. Transfection efficiency was assessed under a fluorescence microscope. Changes in the expression of Twist mRNA in A2780 after transfection with the pGenesil Twist shRNA plasmid were analyzed through RT-PCR. MTT assays and adhesion experiments were applied to determine changes in proliferation and adhesion ability of A2870 after transfection with the Twist shRNA plasmid. Changes in the expression of the E-cadherin and N-cadherin proteins in A2780 after transfection with the Twist shRNA plasmid were analyzed using Western blotting. Result: The restructuring plasmid pGenesil-Twist shRNA was constructed successfully. After 48 h of culture, 80% of the cells expressed high-intensity GFP fluorescence and stability. The expression of Twist decreased significantly after the transfection of the Twist shRNA plasmid (P<0.05). Proliferation of the transfected Twist shRNA cells showed no difference with that of the A2780-nontransfection or A2780-si-control groups (P>0.05) but the adhesion ability of A2780 decreased dramatically (P<0.05). Expression of the E-cadherin protein increased, whereas that of the N-cadherin protein decreased compared with that in the A2780-nontransfection or A2780-si-control groups (P<0.05). Conclusion: Twist is essential for epithelial-mesenchymal transition, invasion, and metastasis of ovarian cancer.

• Journal of Microbiology
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• 제42권3호
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• pp.169-173
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• 2004

Enterobacter cloacae (strain PR2/7), a genetically modified endophyte(GME) in citrus plants, carrying different plasmids (pEC3.0/18, pCelE, pEglA and pGFP), was inoculated into Citrus sinensis seedlings under greenhouse conditions. The impact of this on the indigenous bacterial endophytic community was studied by analyses of 2 different morphologic groups. The germination rates of inoculated seeds were evaluated in greenhouse, and plasmid stability under in vitro conditions. Results demonstrated a great and diverse endophytic community inside plants, and specialization in tissue colonization by some bacterial groups, in different treatments. Shifts in seed germination rate were observed among treatments: in general, the PR2/7 harboring pEglA bacterial- clone significantly reduced seed germination, compared to the PR2/7 harboring pEC3.0/18 clone. This suggests that the presence of the pEglA plasmid changes bacteria-seed interactions. The endophytic community of citrus seedlings changed according to treatment. In seedlings treated with the PR2/7 with pEglA clone, the population of group II decreased significantly, within the context of the total endophytic community. These results indicate that the application of GMEs induces shifts in the endophytic bacterial community of citrus seedlings.