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1. 发明申请

WO2012108630A3 Sbta gene derived from synechocystis sp. pcc6803 and use thereof 审中-公开
标题翻译： SBTA基因来源于SYNECHOCYSTIS SP。 PCC6803及其用途
公开(公告)号：WO2012108630A3
公开(公告)日：2012-12-27
申请号：PCT/KR2012000599
申请日：2012-02-03
申请人： KOREA RES INST OF BIOSCIENCE , LIU JANG RYOL , MIN SUNG RAN , JEONG WON JOONG , PARK YOUN IL , CHUNG HWA JEE , KIM JONG HYUN , PARK JI HYUN , LYU JAE IL , LEE JEONG HEE
发明人： LIU JANG RYOL , MIN SUNG RAN , JEONG WON JOONG , PARK YOUN IL , CHUNG HWA JEE , KIM JONG HYUN , PARK JI HYUN , LYU JAE IL , LEE JEONG HEE
IPC分类号： A01H5/00 , C12N15/82
CPC分类号： C07K14/415 , C12N15/8273
摘要： The present invention relates to: a method for enhancing salt tolerance of plants using a SbtA (Sodium dependent bicarbonate transporter) gene derived from Synechocystis sp. PCC6803; a method for preparing transgenic plants with enhanced salt tolerance using the SbtA gene; transgenic plants with enhanced salt tolerance prepared by the same method and seeds thereof; a method for increasing biomass of plants using the SbtA gene; a method for preparing the transgenic plants with increased biomass using the SbtA gene; and transgenic plants with increased biomass using the SbtA gene and seeds thereof.
摘要翻译：本发明涉及使用源自集胞藻属物种的SbtA（钠依赖性碳酸氢根转运蛋白）基因来提高植物耐盐性的方法。 6803; 使用SbtA基因制备具有改善的耐盐性的转基因植物的方法; 通过相同方法制备的具有改善的耐盐性的转基因植物及其种子; 使用SbtA基因增加植物生物量的方法; 使用SbtA基因制备具有增加的生物量的转基因植物的方法; 以及使用SbtA基因及其种子生物量增加的转基因植物。

2. 发明申请

WO2009066919A3 GPT GENE AS A MARKER FOR SELECTING PLANT TRANSFORMANT 审中-公开
公开(公告)号：WO2009066919A3
公开(公告)日：2009-05-28
申请号：PCT/KR2008/006784
申请日：2008-11-18
申请人： KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGY , JEON, Jae Heung , KIM, Hyun Soon , KIM, Yoon Sik , LEE, Yong Hwa , KIM, Mi Sun , MIN, Sung Ran , JEONG, Won Joong , KWON, Suk Yoon , JOUNG, Hyouk
发明人： JEON, Jae Heung , KIM, Hyun Soon , KIM, Yoon Sik , LEE, Yong Hwa , KIM, Mi Sun , MIN, Sung Ran , JEONG, Won Joong , KWON, Suk Yoon , JOUNG, Hyouk
IPC分类号： C12N15/11
摘要： The present invention relates to a marker consisting of GPT (UDP-Λ/-acetylgluco samine:dolichol phosphate-Λ/-acetylglucosamine-phosphotransferase) gene to select a transformed plant, a recombinant plant expression vector comprising GPT gene, plants that are transformed with said vector and seeds of the plants, a method of selecting a tr ansformed plant comprising steps of transforming a plant cell with said vector and selec ting a transformant in a medium comprising tunicamycin, and a method of producing a t ransformed plant comprising a step of transforming a plant cell with said vector.

3. 发明申请

WO2009051289A1 PATATIN-FREE POTATO PLANT 审中-公开
标题翻译： PATATIN-POTATO植物
公开(公告)号：WO2009051289A1
公开(公告)日：2009-04-23
申请号：PCT/KR2007/006078
申请日：2007-11-29
申请人： KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGY , JEON, Jae Heung , KIM, Hyun Soon , KIM, Yoon Sik , LEE, Yong Hwa , KIM, Mi Sun , MIN, Sung Ran , JEONG, Won Joong , KWON, Suk Yoon , JOUNG, Hyouk
发明人： JEON, Jae Heung , KIM, Hyun Soon , KIM, Yoon Sik , LEE, Yong Hwa , KIM, Mi Sun , MIN, Sung Ran , JEONG, Won Joong , KWON, Suk Yoon , JOUNG, Hyouk
IPC分类号： C12N15/63 , C12N15/64 , C12N15/82 , A01H1/00
CPC分类号： C12N15/8218 , C12N15/8257
摘要： The present invention relates to a patatin-free potato plant. More specifically, the present invention relates to a recombinant vector comprising patatin gene that is ope ratively inserted to a vector for hairpin RNA interference (hpRNAi), a plant transformed with said vector, and a method of producing glycoproteins for treating conditions in hum ans comprising steps of expressing said glycoproteins in the above-described transgenic plant and isolating them therefrom. It is expected that the patatin-free or patatin-reduced potato plant of the present invention that is transformed with hpRNAi can be used as a host for producing various human therapeutic glycoproteins, due to plant-specific g lycosylation and reduction in glycoproteins.
摘要翻译：本发明涉及一种不含patatin的马铃薯植物。更具体地说，本发明涉及包含patatin基因的重组载体，该基因插入到发夹RNA干扰载体（hpRNAi），用所述载体转化的植物，以及生产糖蛋白的方法，所述方法包括：在上述转基因植物中表达所述糖蛋白并从其中分离的步骤。由于植物特异性g赖氨酰化和糖蛋白的还原，预期用hpRNAi转化的本发明的不含patatin的或patatin-reduced马铃薯植物可用作产生各种人类治疗性糖蛋白的宿主。

4. 发明申请

WO2012057465A3 SALT TOLERANCE SYGT GENE DERIVED FROM SYNECHOCYSTIS, AND USES THEREOF 审中-公开
标题翻译：来自细菌感染的盐耐受性致死基因及其用途
公开(公告)号：WO2012057465A3
公开(公告)日：2012-10-11
申请号：PCT/KR2011007605
申请日：2011-10-13
申请人： KOREA RES INST OF BIOSCIENCE , LIU JANG RYOL , KIM SUK WEON , KIM JONG HYUN , MIN SUNG RAN , JEONG WON JOONG , AHN MYUNG SUK , PARK YOUNG MIN , OH MYUNG JIN , PARK JI HYUN
发明人： LIU JANG RYOL , KIM SUK WEON , KIM JONG HYUN , MIN SUNG RAN , JEONG WON JOONG , AHN MYUNG SUK , PARK YOUNG MIN , OH MYUNG JIN , PARK JI HYUN
IPC分类号： A01H5/00 , C07K14/195 , C12N15/31 , C12N15/82
CPC分类号： C12N15/8271 , C07K14/195 , C12N9/1051 , C12N15/8273 , C12Y204/0108
摘要： The present invention relates to a method for increasing the salt tolerance of a plant, to a plant having increased salt tolerance prepared by the method, and to a seed of the plant, wherein the method comprises over-expressing SyGT by transforming a plant cell with a recombinant plant expression vector including a gene encoding Synechocystis PCC 6906-derived S SyGT protein and a SyGT gene.
摘要翻译：本发明涉及提高植物耐盐性的方法，通过所述方法制备的具有增强的耐盐性的植物，以及所述植物的种子，其中所述方法包括通过用植物细胞转化植物细胞来过表达SyGT 包含编码集胞藻PCC 6906衍生的S SyGT蛋白和SyGT基因的基因的重组植物表达载体。

5. 发明申请

WO2012057466A2 SALT TOLERANCE SYDBSP GENE DERIVED FROM SYNECHOCYSTIS, AND USES THEREOF 审中-公开
标题翻译：来自细菌感染的盐耐受SYDBSP基因及其用途
公开(公告)号：WO2012057466A2
公开(公告)日：2012-05-03
申请号：PCT/KR2011007606
申请日：2011-10-13
申请人： KOREA RES INST OF BIOSCIENCE , LIU JANG RYOL , KIM SUK WEON , KIM JONG HYUN , MIN SUNG RAN , JEONG WON JOONG , AHN MYUNG SUK , PARK YOUNG MIN , OH MYUNG JIN , PARK JI HYUN
发明人： LIU JANG RYOL , KIM SUK WEON , KIM JONG HYUN , MIN SUNG RAN , JEONG WON JOONG , AHN MYUNG SUK , PARK YOUNG MIN , OH MYUNG JIN , PARK JI HYUN
IPC分类号： A01H5/00 , C07K14/195 , C12N15/31 , C12N15/82
CPC分类号： C07K14/405 , C07K14/195 , C12N15/8273 , C12Q1/6895
摘要： The present invention relates to a method for increasing the salt tolerance of a plant, to a plant having increased salt tolerance prepared by the method, and to a seed of the plant, wherein the method comprises over-expressing SyDBSP by transforming a plant cell with a recombinant plant expression vector including a gene encoding Synechocystis PCC 6906-derived SyDBSP protein and a SyDBSP gene.
摘要翻译：本发明涉及提高植物耐盐性的方法，通过该方法制备的具有增强的耐盐性的植物，以及该植物的种子，其中该方法包括通过用包含编码集胞藻PCC 6906衍生的SyDBSP蛋白和SyDBSP基因的基因的重组植物表达载体。

6. 发明申请

WO2009054660A3 METHOD FOR INCREASING SALT TOLERANCE OF PLANT BY OVEREXPRESSING SYFBP/SBPASE GENE ISOLATED FROM SYNECHOCYSTIS AND PLANT PRODUCED BY THE SAME 审中-公开
标题翻译：通过超过SYMPBP / SBPASE基因分离的SYPBP / SBPASE基因和由其生产的植物增加植物耐盐性的方法
公开(公告)号：WO2009054660A3
公开(公告)日：2009-06-11
申请号：PCT/KR2008006215
申请日：2008-10-21
申请人： KOREA RES INST OF BIOSCIENCE , LIU JANG RYOL , MIN SUNG RAN , JEONG WON JOONG , CHUNG HWA JEE , KIM HYUN TAE , PARK JU YOUNG , KIM JONG HYUN
发明人： LIU JANG RYOL , MIN SUNG RAN , JEONG WON JOONG , CHUNG HWA JEE , KIM HYUN TAE , PARK JU YOUNG , KIM JONG HYUN
IPC分类号： C12N15/63
CPC分类号： C12N15/8273 , C12N9/16 , C12N15/8214
摘要： The present invention relates to a method for increasing salt tolerance of a plant by overexpressing SyFBP/SBPase gene isolated from Synechocystis, a plant and seed having increased salt tolerance ability that is produced by the same method, a composit ion for increasing salt tolerance of a plant in which gene encoding SyFBP/SBPase is comprised, and a recombinant vector for the transformation of chloroplasts in which gene encoding SyFBP/SBPase is comprised.
摘要翻译：本发明涉及一种通过过表达分离自Synechocystis的SyFBP / SBPase基因，通过相同方法生产的具有增加的耐盐能力的植物和种子的增加耐盐性的方法，用于增加耐盐性的复合离子包含编码SyFBP / SBPase的基因的植物和用于转化其中包含编码SyFBP / SBP酶的基因的叶绿体的重组载体。

7. 发明申请

WO2008056915A1 THE METHOD FOR ENHANCEMENT OF PHOTOSYNTHESIS AND BIOMASS OF PLANT BY PLASTID TRANSFORMATION OF MALATE DEHYDROGENASE 审中-公开
标题翻译：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：WO2008056915A1
公开(公告)日：2008-05-15
申请号：PCT/KR2007/005529
申请日：2007-11-02
申请人： KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGY , LIU, Jang Ryol , CHUNG, Hwa-Jee , MIN, Sung Ran , JEONG, Won Joong , KIM, Hyun Tae , PARK, Ju Young , HUR, Jung He
发明人： LIU, Jang Ryol , CHUNG, Hwa-Jee , MIN, Sung Ran , JEONG, Won Joong , KIM, Hyun Tae , PARK, Ju Young , HUR, Jung He
IPC分类号： A01H1/00
CPC分类号： C12N15/8214 , C12N9/0004 , C12N15/8261 , Y02A40/146
摘要： The present invention relates to a method for enhancement of photosynthesis and biomass of a plant by plastid transformation with MDH gene, more precisely a method for enhancement of photosynthesis and biomass of C3 plant by plastid transformation system with MDH gene. The MDH plastid transgenic plant prepared by the method of the present invention exhibits not only increased photosynthesis efficiency but also increased growth rate, leaf area, stem diameter and biomass of the plant, compared with the control plant. Therefore, the plastid transformed C3 plant prepared by C4 type gene introduction can be effectively used for enhancing photosynthesis and biomass of the plant.
摘要翻译：本发明涉及通过MDH基因质体转化来提高植物的光合作用和生物量的方法，更准确地说是通过具有MDH基因的质体转化系统增强C3植物的光合作用和生物量的方法。通过本发明方法制备的MDH质体转基因植物与对照植物相比不仅具有增加的光合作用效率，而且显示植物的增长速率，叶面积，茎直径和生物量的增加。因此，通过C4型基因导入制备的质体转化的C3植物可以有效地用于提高植物的光合作用和生物量。

8. 发明申请

WO2003060137A1 METHOD FOR RECOMBINATING PLASTID USING PROCARYOTIC RECOMBINASE GENE 审中-公开
标题翻译：使用过程重组蛋白酶基因重组PLASTID的方法
公开(公告)号：WO2003060137A1
公开(公告)日：2003-07-24
申请号：PCT/KR2002/002506
申请日：2002-12-31
申请人： KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGY , LIU, Jang-Ryol , JEONG, Won-joong , MIN, Sung-ran , JEONG, Seok-won , HAN, Su-kyoung
发明人： LIU, Jang-Ryol , JEONG, Won-joong , MIN, Sung-ran , JEONG, Seok-won , HAN, Su-kyoung
IPC分类号： C12N15/82
CPC分类号： C12N15/8214 , C12N15/8213
摘要： The objective of this invention is to enhance the efficiency of plastid transformation using nuclear transformed plants in which the microbial recombinase A( recA ) is to target to (or expressed in) the plastid. This invention will be better explained by the following detailed descriptions. A plant is transformed with a nuclear transformation vector containing the microbial recA gene added with a plastid targeting sequence. In this nuclear transformed plant, the frequency of plastid transformation is enhanced greater than two-folds due to increased homologous recombination between the plastid transformation vector carrying genes of interest (or target genes) and the plastid genome. In addition, because plastid transformation is accomplished through a gradual process, adventitious shoots selected after being subjected to plastid transformation should be cut into explants, and then shoots regenerated from the explants are to be reselected until all of the plastids in the shoots are uniformly transformed. However, when the nuclear transformed plant is used, the number of reselection is reduced to 1/2 to 1/3 due to increased homologous recombination.
摘要翻译：本发明的目的是使用核转化植物提高质体转化的效率，其中微生物重组酶A（recA）靶向（或表达于）质体。以下的详细说明将更好地说明本发明。用含有质体靶向序列的微生物recA基因的核转化载体转化植物。在这种核转化植物中，质体转化的频率由于携带感兴趣的基因（或靶基因）的质体转化载体和质体基因组之间的同源重组增加而增加了大于2倍。另外，由于质体转化是通过逐步过程完成的，因此应将外来物质切割后进入质体转化后的不定芽进行切割，然后重新选择从外植体中再生的枝条，直到枝条中的所有质体均匀转化为止。然而，当使用核转化植物时，由于增加的同源重组，重选次数减少到1/2至1/3。

9. 发明申请

WO2012108630A2 Sbta gene derived from synechocystis sp. pcc6803 and use thereof 审中-公开
标题翻译： GENE SBTA衍生集胞藻。 6803和使用
公开(公告)号：WO2012108630A2
公开(公告)日：2012-08-16
申请号：PCT/KR2012000599
申请日：2012-02-03
申请人： KOREA RES INST OF BIOSCIENCE , LIU JANG RYOL , MIN SUNG RAN , JEONG WON JOONG , PARK YOUN IL , CHUNG HWA JEE , KIM JONG HYUN , PARK JI HYUN , LYU JAE IL , LEE JEONG HEE
发明人： LIU JANG RYOL , MIN SUNG RAN , JEONG WON JOONG , PARK YOUN IL , CHUNG HWA JEE , KIM JONG HYUN , PARK JI HYUN , LYU JAE IL , LEE JEONG HEE
IPC分类号： A01H5/00 , C12N15/82
CPC分类号： C07K14/415 , C12N15/8273
摘要： The present invention relates to: a method for enhancing salt tolerance of plants using a SbtA (Sodium dependent bicarbonate transporter) gene derived from Synechocystis sp. PCC6803; a method for preparing transgenic plants with enhanced salt tolerance using the SbtA gene; transgenic plants with enhanced salt tolerance prepared by the same method and seeds thereof; a method for increasing biomass of plants using the SbtA gene; a method for preparing the transgenic plants with increased biomass using the SbtA gene; and transgenic plants with increased biomass using the SbtA gene and seeds thereof.
摘要翻译：本发明涉及用于改良植物的耐盐性与来自集胞藻来源的基因SBTA（钠依赖性碳酸氢根转运）的步骤。 6803; 具有用于制备使用所述SBTA基因提高耐盐性的方法的转基因植物; 具有增强的转基因植物的耐受性通过相同的方法和它们的种子制备的盐; 为增加与SBTA基因植物生物量的方法; 具有使用该SBTA基因增加的生物量的转基因植物的制备方法; 并且具有与所述SBTA基因和它们的种子增加的生物量的转基因植物。

10. 发明申请

WO2007091756A1 PLASTID TRANSFORMATION SYSTEM TO PREVENT THE INTRAMOLECULAR RECOMBINATION OF TRANSGENE 审中-公开
标题翻译： PLASTID转化系统，以防止转移子的分子内重组
公开(公告)号：WO2007091756A1
公开(公告)日：2007-08-16
申请号：PCT/KR2006/004377
申请日：2006-10-25
申请人： KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGY , LIU, Jang Ryol , JEONG, Won Joong , CHUNG, Hwa-Jee , MIN, Sung Ran , PARK, Ju Young
发明人： LIU, Jang Ryol , JEONG, Won Joong , CHUNG, Hwa-Jee , MIN, Sung Ran , PARK, Ju Young
IPC分类号： C12N15/05 , C12N15/64 , C12N15/82
CPC分类号： C12N15/8214
摘要： The present invention relates to a plastid transformation system capable of preventing second recombination events of heterologous genes inserted into plastid genomes. More specifically, this invention relates to a plastid transformation vector carrying a promoter and a terminator derived from organisms other than tobacco. The inventive recombinant expression vector for plastid transformation is capable of mass-producing exogenous proteins on a level par with conventional vectors carrying promoter/terminator couples of tobacco origin. At the same time, it is capable of preventing second recombination events within plastids. Thus, the vector of this invention is greatly useful in producing transgenic plants since it can effect a secure introduction of heterologous genes and support normal transformation and heterologous gene expression.
摘要翻译：本发明涉及能够防止插入到质体基因组中的异源基因的第二重组事件的质体转化系统。更具体地，本发明涉及携带启动子的质体转化载体和源自烟草以外的生物体的终止子。本发明的用于质体转化的重组表达载体能够以与产生烟草来源的启动子/终止子对的常规载体水平相当的量产生外源蛋白质。同时，它能够防止质体内的第二次重组事件。因此，本发明的载体在生产转基因植物中是非常有用的，因为它能够有效地引入异源基因并支持正常转化和异源基因表达。

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