• 한국식물생명공학회:학술대회논문집
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• 한국식물생명공학회 2002년도 추계학술대회
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• pp.49-58
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• 2002

Oxidative stress derived from reactive oxygen species (ROS) is one of the major damaging factors in plants exposed to environmental stress. In order to develop the platform technology to solve the global food and environmental problems in the 21s1 century, we focus on the understanding of the antioxidative mechanism in plant cells, the development of oxidative stress-inducible antioxidant genes, and the development of transgenic plants with enhanced tolerance to stress. In this report, we describe our recent results on industrial transgenic plants by the gene manipulation of antioxidant enzymes. Transgenic tobacco plants expressing both superoxide dismutase (SOD) and ascorbate peroxidase (APX) in chloroplasts were developed and were evaluated their protection effects against stresses, suggesting that simultaneous overexpression of both SOD and APX in chloroplasts has synergistic effects to overcome the oxidative stress under unfavorable environments. Transgenic tobacco plants expressing a human dehydroascorbate reductase gene in chloroplasts were showed the protection against the oxidative stress in plants. Transgenic cucumber plants expressing high level of SOD in fruits were successfully generated to use the functional cosmetic purpose as a plant bioreactor. In addition, we developed a strong oxidative stress-inducible peroxidase promoter, SWPA2 from sweetpotato (Ipomoea batatas). We anticipate that SWPA2 promoter will be biotechnologically useful for the development of transgenic plants with enhanced tolerance to environmental stress and particularly transgenic cell lines engineered to produce key pharmaceutical proteins.

• Journal of Crop Science and Biotechnology
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• 제10권2호
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• pp.112-116
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• 2007

Kinetin(KN) is an inducer of rice(Oryza sativa L.) defense/stress responses, as evidenced by the induction of inducible secondary metabolite and defense/stress protein markers in leaf. We show a novel light-dependent effect of KN-triggered defense stress responses in rice leaf. Leaf segments treated with KN(100 ${\mu}M$) show hypersensitive-like necrotic lesion formation only under continuous light illumination. Potent accumulation of two phytoalexins, sakuranetin and momilactone A(MoA) by KN that peaks at 48 h after treatment under continuous light is completely suppressed by incubation under continuous dark. Using two-dimensional gel electrophoresis we identified KN-induced changes in ribulose-1, 5-bisphosphate carboxylase/oxygenase, energy- and pathogenesis-related proteins(OsPR class 5 and 10 members) by N-terminal amino acid sequencing and mass spectrometry. These changes were light-inducible and could not be observed in the dark(and control). Present results provide a new dimension(light modulation/regulation) to our finding that KN has a potential role in the rice plant self-defense mechanism.

• 한국초지조사료학회지
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• 제37권3호
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• pp.223-230
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• 2017

Arabidopsis nucleoside diphosphate kinase 2 (AtNDPK2) is an upstream signaling molecule that has been shown to induce stress tolerance in plants. In this study, the AtNDPK2 gene, under the control of a stress-inducible SWPA2 promoter, was introduced into the genome of tall fescue (Festuca arundinacea Schreb.) plants. The induction of the transgene expression mediated by methyl viologen (MV) and NaCl treatments were confirmed by RT-PCR and northern blot analysis, respectively. Under salt stress treatment, the transgenic tall fescue plants (SN) exhibited lower level of $H_2O_2$ and lipid peroxidation accumulations than the non-transgenic (NT) plants. The transgenic tall fescue plants also showed higher level of NDPK enzyme activity compared to NT plants. The SN plants were survived at 300 mM NaCl treatment, whereas the NT plants were severely affected. These results indicate that stress-inducible overexpression of AtNDPK2 might efficiently confer the salt stress tolerance in tall fescue plants.

• 대한의생명과학회지
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• 제12권4호
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• pp.435-438
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• 2006

In eukaryotes, ER stress induces UPR (unfolded protein response) via IRE1 activation which sends a molecular signal for XBP1 mRNA splicing in the cytosol. During this mRNA splicing, 23 nt removed in which contains PstI site and then resulting XBP1 product is not digested with PstI restriction enzyme. In this study, using this XBP1 mRNA splicing mechanism, the effect of heat shock on thyrocytes is studied, because heat shock response in the thyrocytes needs more study to understand thyroid physiology under alternative environments. ER inducible drugs (tunicamycin, DTT, $Ca^{2+}$ ionopore A23187, BFA) induce ER stress in the thyrocytes. From 3 hours after heat shock, ER stress is induced and which is reversible when heat shock is without. While $Ca^{2+}$ ionopore A23187 is reversible from ER stress by washing out the drug, thapsigagin is irreversible. Other ER inducible drugs are not so sensitive to ER stress repairing. XBP1 mRNA splicing in a cell is very available method to detect ER stress. It needs only a small quantity of total RNA and processing also very easy.

• 한국작물학회:학술대회논문집
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• 한국작물학회 2006년도 Grop Science and Biotechnology in the 21st Century
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• pp.20-20
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• 2006

• Journal of Microbiology and Biotechnology
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• 제22권2호
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• pp.166-169
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• 2012

In several biotechnological applications of living bacterial cells with inducible gene expression systems, the extent of overexpression and the specificity to the inducer are key elements. In the present study, we established the concentration ranges of $Zn^{2+}$, $Ni^{2+}$, $Co^{2+}$, ${AsO_2}^-$, and $Cd^{2+}$ ions that caused significant activation of the respective promoters of Synechocystis sp. without concomitant unspecific stress responses. The low expression levels can be increased up to 10-100-fold upon treatments with $Cd^{2+}$, ${AsO_2}^-$, $Zn^{2+}$, and $Co^{2+}$ ions and up to 800-fold upon $Ni^{2+}$ treatment. These results facilitate the development of conditional gene expression systems in cyanobacteria.

• Journal of Microbiology and Biotechnology
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• 제33권7호
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• pp.955-963
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• 2023

Chlorella is a eukaryotic organism that can be used as an industrial host to produce recombinant proteins. In this study, a salt-inducible promoter (SIP) was isolated from the freshwater species Chlorella vulgaris PKVL7422 from the screening of genes that were upregulated after salt treatment. Several cis-acting elements, including stress response elements, were identified in the isolated SIP. Moreover, the Gaussia luciferase gene was cloned after the SIP and transformed into C. vulgaris to test the inducibility of this promoter. Reexamination of transcriptome of C. vulgaris revealed that genes involved in the synthesis of methyl jasmonic acid (MeJA), gibberellin (GA), and abscisic acid (ABA) were upregulated when C. vulgaris was treated with salt. Furthermore, the expression level of recombinant luciferase increased when the transformed C. vulgaris was treated with salt and MeJA, GA, and ABA. This study represents the first report of the C. vulgaris SIP and highlights how transformed microalgae could be used for robust expression of recombinant proteins.

• 한국식물생명공학회:학술대회논문집
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• 한국식물생명공학회 2002년도 춘계학술대회
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• pp.49-58
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• 2002

각종 환경스트레스에 의해 생체 내에서 과량으로 생성되는 독성의 활성산소종 (ROS)은 산화스트레스를 유발시켜 식물의 질병, 노화 및 세포사멸을 촉진시킨다. 연구팀은 21세기 당면한 지구규모의 환경, 식량 및 보건문제 해결에 기여할 수 있는 기발기술 (plateform technology)를 개발하기 위하여 식물 세포의 항산화기구 규명, 산화스트레스 유도성 항산화효소 유전자 개발, 스트레스 내성식물 개발에 관한 연구를 수행하고 있다. 여기에서는 항산화효소 유전자를 이용한 산업용식물체 개발에 관한 연구팀의 최근 연구결과를 중심으로 소개하였다. SOD와 APX 유전자를 엽록체에 동시에 발현시킨 담배식물체는 MV, 건조 등 여러 스트레스에 대한 내성을 나타내어, 복합 스트레스내성 농작물개발에 활용이 기대된다. 인체 DHAR 유전자를 엽록체에 도입시킨 담배식물체는 정상적으로 DHAR 유전자를 발현시켰으며, MV 등 여러 스트레스에 대한 내성을 나타내었다. 피부 노화방지 등에 관여하여 ROS를 제거하는 SOD를 과실에 과발현시킨 형질전환오이를 성공적으로 개발하여, SOD 오이는 기능성화장품의 용도로 제품개발이 기대된다. 또한 고구마에서 산화스트레스에 특이적으로 발현하는 POD (SWA2) promoter를 개발하였다. SWPAS2 Pormoter는 스트레스내성 및 의료용 단밸질 등 고부가가치 생리활성물질을 생산할 수 있는 산업용 형질전환 식물체 및 배양세포주 개발에 이용될 수 있을 것으로 기대된다.

• Journal of Plant Biotechnology
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• 제29권2호
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• pp.69-77
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• 2002

각종 환경스트레스에 의해 생체 내에서 과량으로 생성되는 독성의 활성산소종 (ROS)은 산화스트레스를 유발시켜 식물의 질병, 노화 및 세포사멸을 촉진시킨다. 연구팀은 21세기 당면한 지구규모의 환경, 식량 및 보건문제 해결에 기여할 수 있는 기반기술 (plateform technology)를 개발하기 위하여 식물세포의 항산화기구 규명. 산화스트레스 유도성 항산화효소 유전자 개발. 스트레스 내성식물 개발에 관한 연구를 수행하고 있다. 여기에서는 항산화효소 유전자를 이용한 산업용식물체 개발에 관한 연구팀의 최근 연구결과를 중심으로 소개하였다. SOD와 APX 유전자를 엽록체에 동시에 발현시킨 담배 식물체는 MV, 건조 등 여러 스트레스에 대한 내성을 나타내어, 복합 스트레스내성 농작물개발에 활용이 기대된다 인체 DHAR 유전자를 엽록체에 도입시킨 담배식물체는 정상적으로 DHAR 유전자를 발현시켰으며, MV 등 여러 스트레스에 대한 내성을 나타내었다. 피부 노화방지 등에 관여하여 ROS를 제거하는 SOD를 과실에 과발현시킨 형질전환오이를 성공적으로 개발하여. SOD 오이는 기능성화장품의 용도로 제품개발이 기대된다. 또한 고구마에서 산화스트레스에 특이적으로 발현하는 POD (SWPA2.) promoter를 개발하였다. SWPA2 promoter는 스트레스내성 및 의료용 단백질 등 고부가가치 생리활성물질을 생산할 수 있는 산업용 형질전환 식물체 및 배양세포주 개발에 이용될 수 있을 것으로 기대된다.

• Journal of Plant Biotechnology
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• 제4권4호
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• pp.143-150
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• 2002

A strong oxidative stress-inducible peroxidase promoter (referred to as SWPA2 promoter) was cloned from tell cultures of sweetpotato (Ipomoea batatas) and characterized in transgenic tobacco cultured cells in terms of biotechnological applications. Employing a transient expression assay in tobacco protoplasts, with five different 5'-deletion mutants of the SWPA2 promoter fused to the $\beta$-glucuronidase (GUS) reporter gene, the 1314 bp deletion mutant showed approximately 30 times higher GUS expression than the CaMV 35S promoter. The expression of GUS activity in suspension cultures of transgenic cells derived from transgenic tobacco leaves containing the -1314 bp SWPA2 promoter-GUS fusion was strongly expressed following 15 days of subculture compared to other deletion mutants, suggesting that the 1314 bp SWPA2 promoter will be biotechnologically useful for the development of transgenic cell lines engineered to produce key pharmaceutical proteins. In this respect, we developed transgenic cell lines such as tobacco (Nicotiana tabacum L. BY-2), ginseng (Panax ginseng) and Siberian ginseng (Acanthopanax senticosus) using a SWPA2 promoter to produce a human lactoferrin (hLf) and characterized the hLf production in cultured cells. The hLf production monitored by ELISA analysis in transgenic BY-2 cells was directly increased proportional to cell growth and reached a maximal level (up to 4.3% of total soluble protein) at the stationary phase in suspension cultures. The SWPA2 promoter should result in higher productivity and increased applications of plant cultured cells for the production of high-value recombinant proteins.