감마선 조사에 의한 고온내성 김 변이체 및 이의 선발 방법
    2.
    发明公开
    감마선 조사에 의한 고온내성 김 변이체 및 이의 선발 방법 有权
    由伽马射线辐照获得的吡虫啉的耐高温突变体及其选择方法

    公开(公告)号:KR1020160097487A

    公开(公告)日:2016-08-18

    申请号:KR1020150019176

    申请日:2015-02-09

    CPC classification number: C12N15/01 A23L17/60 A23V2002/00 C12N1/12 C12N13/00

    Abstract: 본발명은김()에감마선을조사하여수득된고온내성의김 변이체(기탁번호: KCTC12719BP), 김에방사선을조사하여돌연변이체를유도하는단계를포함하는고온내성의김 변이체의제조방법, 상기고온내성의김 변이체를배양하는단계를포함하는고온내성의김 생산방법, 상기생산방법에의해생산된고온내성의김 및상기김을이용하여제조된김 가공식품을제공한다.

    Abstract translation: 提供:通过γ射线照射获得的耐高温Pyropia yezoensis突变体(登录号:KCTC12719BP); 一种制备耐高温Pyropia yezoensis突变体的方法,包括通过用辐射照射Pyropia yezoensis诱导突变体的步骤; 包括高温抗性Pyropia yezoensis突变体培养步骤的耐高温Pyropia yezoensis的方法。 通过生产方法生产的耐高温Pyropia yezoensis; 和Pyropia yezoensis加工食品通过使用Pyropia yezoensis生产。 本发明的焦螨属(Pyropia yezoensis)突变体可以在各种温度条件下生长,从而能够有效地用作适宜提高白芍的生产率的Pyropia yezoensis。

    대장균 유래 TPSP 유전자를 이용한 고온 스트레스 내성 형질전환 식물체의 제조방법 및 그에 따른 식물체
    7.
    发明公开
    대장균 유래 TPSP 유전자를 이용한 고온 스트레스 내성 형질전환 식물체의 제조방법 및 그에 따른 식물체 有权
    用于生产具有耐高温胁迫的转基因植物的方法,该方法使用来自欧洲花椰菜的TPSP基因及其植物

    公开(公告)号:KR1020140042339A

    公开(公告)日:2014-04-07

    申请号:KR1020120108982

    申请日:2012-09-28

    CPC classification number: C12N15/8271 C07K14/245 C12N15/8205 C12N15/8216

    Abstract: The present invention relates to a method for producing a transgenic plant having resistance to high temperature stress without a growth and development inhibition phenomenon or morphological transformation comprising a step of transforming plant cells with a recombinant vector comprising a trehalose-6-phosphate synthase/phosphatase fusion (TPSP) gene derived from Escherichia Coli and a transgenic plant having enhanced resistance to high temperature stress without a growth and development inhibition phenomenon or morphological transformation manufactured by the same method. A TPSP overexpressing transgenic plant of the present invention is expected to greatly contribute to improve productivity and yield under high temperature stress environment.

    Abstract translation: 本发明涉及一种具有抗高温胁迫而没有生长发育抑制现象或形态转化的转基因植物的方法,其包括用包含海藻糖-6-磷酸合酶/磷酸酶融合物的重组载体转化植物细胞的步骤 (TPSP)基因和具有增强的抗高温胁迫抗性的转基因植物,而没有生长发育抑制现象或通过相同方法制造的形态转化。 预期本发明的过度表达转基因植物的TPSP将有助于在高温胁迫环境下提高生产率和产量。

    MDH 유전자의 색소체 형질전환을 통한 식물체의광합성량 또는 바이오매스 증대 방법
    10.
    发明授权
    MDH 유전자의 색소체 형질전환을 통한 식물체의광합성량 또는 바이오매스 증대 방법 失效
    通过马来酸脱氢酶的PLASTID转化提高植物光合作用和生物量的方法

    公开(公告)号:KR100813150B1

    公开(公告)日:2008-03-17

    申请号:KR1020060109550

    申请日:2006-11-07

    CPC classification number: C12N15/8214 C12N9/0004 C12N15/8261 Y02A40/146

    Abstract: An MDH plastid transgenic plant is provided to show significantly increased growth rate, area of leaves, diameter of stem and bio-mass compared with a control plant, thereby being usefully used for increasing the photosynthesis amount or biomass of the plant. A transgenic C3 plant is characterized in that an MDH(malate dehydrogenase) gene derived from prokaryote such as Corynebacterium glutamicum, Rhodococcus, Oceanobacillus, Aspergillus, Methanothermus, Chaetomium, Methanopyrus, Bacillus, Methanocaldococcus, Magnaporthe, Phaeosphaeria, Gibberella, Desulfitobacterium, coccidioides, Thermus, Candidatus, Pyrococcus, Solibacter, Aurantimonas, Syntrophus, Enterococcus, Methanosphaera, Anopheles, Entamoeba, Yersinia, Mesorhizobium, Tribolium, Salmonella, Aurantimonas, Amycolatopsis, Escherichia coli, Apis, Burkhoderia, Bordetella, Pseudomonas and Aedes is inserted into plastid genome of the C3 plant. A method for preparing the transgenic plant comprises the steps of: (a) inserting the MDH gene sequence into a transforming vector to prepare an MDH plastid transforming vector; (b) introducing the MDH plastid transforming vector into a C3 plant or a culture cell of the C3 plant to prepare a transgenic body; (c) culturing the transgenic body; and (d) redifferentiating the cultured transgenic body through tissue culturing.

    Abstract translation: 提供MDH质体转基因植物以显示与对照植物相比显着增加的生长速率,叶面积,茎直径和生物质量,从而有效地用于增加植物的光合作用量或生物量。 转基因C3植物的特征在于,从原核生物如谷氨酸棒杆菌,红球菌,海洋芽孢杆菌,曲霉,甲烷热原,毛壳菌,甲烷us us,芽孢杆菌,甲烷球菌,马鞭草,Ph ia,赤霉菌,脱硫杆菌,球虫,栖热菌中的MDH(苹果酸脱氢酶) ,Candidatus,Pyrococcus,Solibatus,Aurantimonas,Syntrophus,Enterococcus,Methanosphaera,按蚊,阿米巴,耶尔森氏菌,中生根瘤菌,Tribolium,沙门氏菌,Aurantimonas,Amycolatopsis,大肠杆菌,Apis,Burkhoderia,博德特氏菌,假单胞菌和Aedes被插入质体基因组 C3植物。 制备转基因植物的方法包括以下步骤:(a)将MDH基因序列插入转化载体中以制备MDH质体转化载体; (b)将MDH质体转化载体导入C3植物或C3植物的培养细胞以制备转基因体; (c)培养转基因体; 和(d)通过组织培养重新分化培养的转基因体。

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