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公开(公告)号：KR100654958B1
公开(公告)日：2006-12-08
申请号：KR1020040111623
申请日：2004-12-24
Applicant: 동아대학교 산학협력단
IPC: C07K14/415 , C12N15/29
Abstract: 본 발명은 벼에서 유래된 고친화성 인산운반체 유전자(
OsPT 8)에 관한 것으로, 더욱 자세하게는 벼에서 유래된 고친화성 인산운반체(OsPT8), 이를 코딩하는 유전자 및 상기 유전자로 형질전환된 인산결핍 스트레스 저항성 식물체에 관한 것이다.
본 발명에 의하면, 인산 결핍 스트레스를 보다 효율적으로 극복하는 새로운 식물체의 개발이 가능하여, 식물 자체의 양분흡수 및 수송능력을 향상시킴으로서 화학비료의 다량 사용으로 인한 토양과 수자원의 오염을 감소시켜서 생태계의 복원과 쾌적한 친환경적 농업의 발전과 나아가 작물의 생산량과 생산의 질을 높이는데 기여할 수 있다.
벼(Oryza sativa L.), 고친화성 인산운반체 유전자, 무기인산-
公开(公告)号：KR1020130051297A
公开(公告)日：2013-05-20
申请号：KR1020110116562
申请日：2011-11-09
Applicant: 동아대학교 산학협력단
Abstract: PURPOSE: A medium for inducing Echeveria callus, and a method for culturing a tissue are provided to quickly produce a plant, and to preserve and proliferate Echeveria plant resources. CONSTITUTION: A medium composition for inducing Echeveria callus contains 4mg/L of benzyladenine(BA) and 1mg/L of naphthalene acetic acid(NAA). Echeveria includes Echeveria Subrigida or Echeveria cante. A method for culturing an Echeveria tissue comprises: a step of placing an explant induced from Echeveria in the medium composition for inducing callus containing BA and NAA, and inducing the callus; and a step of culturing the callus in a medium and re-differentiating.
Abstract translation: 目的：提供诱导Echeveria愈伤组织的培养基和培养组织的方法，以快速生产植物，并保护和增殖Echeveria植物资源。 构成：诱导Echeveria愈伤组织的培养基组合物含有4mg / L的苄基腺嘌呤（BA）和1mg / L的萘乙酸（NAA）。 Echeveria包括Echeveria Subrigida或Echeveria cante。 培养Echeveria组织的方法包括：将从Echeveria诱导的外植体置于培养基组合物中用于诱导含有BA和NAA的愈伤组织并诱导愈伤组织的步骤; 以及在培养基中培养愈伤组织并重新分化的步骤。
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公开(公告)号：KR1020100045654A
公开(公告)日：2010-05-04
申请号：KR1020080104691
申请日：2008-10-24
Applicant: 동아대학교 산학협력단
IPC: C07K14/415 , C12N15/29 , C12N15/09 , C12N15/66
Abstract: PURPOSE: A rice plant-derived phosphatase OsPAP1(Oryza sativa purple acid phosphatase 1) is provided to enhance efficiency of phosphoric acid of a plant. CONSTITUTION: A rice plant-derived phosphatase OsPAP1(Oryza sativa purple acid phosphatase 1) comprises an amino acid of sequence number 2. A gene encoding the OsPAP1 protein comprises a sequence of sequence number 1. A phosphatase gene OsPAP1 encodes total 1195bp base sequences and 355 amino acids. A recombinant vector contains a gene encoding the OsPAP1 protein. A transgenic plant transformed by the recombinant vector is obtained under the phosphoric acid deficiency condition. The plant is vegetable, fruits, flowers, and feeds.
Abstract translation: 目的：提供水稻植物来源的磷酸酶OsPAP1（Oryza sativa紫色酸性磷酸酶1），以提高植物磷酸的效率。 构成：水稻植物来源的磷酸酶OsPAP1（水稻紫色酸性磷酸酶1）包含序列号2的氨基酸。编码OsPAP1蛋白的基因包含序列号1的序列。磷酸酶基因OsPAP1编码总共1195bp碱基序列， 355个氨基酸。 重组载体含有编码OsPAP1蛋白的基因。 在磷酸缺乏条件下获得由重组载体转化的转基因植物。 植物是蔬菜，水果，鲜花和饲料。
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公开(公告)号：KR100802135B1
公开(公告)日：2008-02-11
申请号：KR1020060138163
申请日：2006-12-29
Applicant: 동아대학교 산학협력단
Abstract: A transgenic plant prepared by using a novel gene encoding phosphatase derived from Oryza sp. is provided to increase the utilization efficiency of phosphoric acid by having the phosphoric acid-deficient stress resistance, thereby being useful for improving the productivity of crops. A gene coding phosphatase isolated from Oryza sp.(OsACP1) is described as an amino acid sequence of SEQ ID : NO. 1. An Arabidopsis thaliana is transformed by the gene or a recombinant vector including the gene. A method for preparing a phosphatase OsACP1 comprises the steps of: (a) culturing a microorganism transformed by the recombinant vector; and (b) recovering the phosphatase OsACP1 microorganism.
Abstract translation: 通过使用编码来自Oryza sp。的磷酸酶的新基因制备的转基因植物。 被提供以通过具有磷酸缺乏胁迫抗性来提高磷酸的利用效率，从而可用于提高作物的生产率。 从Oryza sp。（OsACP1）分离的编码磷酸酶的基因被描述为SEQ ID NO：1的氨基酸序列。 拟南芥被该基因或包含该基因的重组载体转化。 制备磷酸酶OsACP1的方法包括以下步骤：（a）培养由重组载体转化的微生物; 和（b）回收磷酸酶OsACP1微生物。
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Patent Agency Ranking6.发明授权
公开(公告)号：KR100701302B1
公开(公告)日：2007-03-29
申请号：KR1020040080587
申请日：2004-10-08
Applicant: 동아대학교 산학협력단
Abstract: 본 발명은 야생벼(
Oryza grandiglumis )로부터 분리한 식물병 저항성 유전자
OgPR1, 그 아미노산 서열 및 이를 이용한 형질전환체 식물에 관한 것으로, 더욱 상세하게는 상처 및 효모 추출물 스트레스 처리에 의해 야생벼로부터 분리한 것으로서, 자스몬산(jasmonic acid), 칸다리딘(cantharidin), 엔도살(endothall) 등의 호르몬 처리에 의해 그 발현이 증가하며, 토마토 풋마름병을 유발하는 슈도모나스 시린지(
Pseudomonas syringe ) 및 잿빛무늬곰팡이병을 유발하는 보트리티스 시네라(
Botrytis cinera ) 등의 진균성 병원균에 대해 저항성을 나타내는 신규한 식물병 저항성 유전자
OgPR1, 그 아미노산 서열 및 이를 이용한 형질전환체 식물에 관한 것이다. 본 발명은 상기 유전자를 제공함으로써, 외부 환경 스트레스 및 식물 병원균, 특히 슈도모나스 시린지(
Pseudomonas syringe ) 및 보트리티스 시네라(
Botrytis cinera )에 대한 식물병 저항성 작물을 새로이 개발, 육종할 수 있게 하므로 농산업 및 식물육종산업상 매우 유용한 발명이다.
야생벼(Oryza grandiglumis), 식물병 저항성 유전자 OgPR1, 슈도모나스 시린지, 보트리티스 시네라-
7.发明授权
公开(公告)号：KR101752728B1
公开(公告)日：2017-06-30
申请号：KR1020140145720
申请日：2014-10-27
Applicant: 동아대학교 산학협력단
Abstract: 본발명은식물체의개화시기를조절하는유전자및 이를이용한단일조건에서식물체의개화시기조절방법에관한것이다. 보다구체적으로, 스탠다드국화()의신마품종(Jinba) 유래의식물의개화시기를조절하는유전자와, 상기를포함하는재조합벡터, 상기재조합벡터에의하여형질전환된형질전환세포, 상기재조합벡터를이용하여단일조건에서식물체의개화시기를조절하는방법, 상기재조합벡터에의하여형질전환된형질전환식물체의제조방법및 이에의하여제조된형질전환식물체가개시된다.
Abstract translation: 本发明涉及调节植物开花时间的基因和使用该基因在单一条件下控制植物开花时间的方法。 更特别地，标准菊（）uisin镇品种和（金霸）基因控制植物衍生的，重组载体的开花时间，由该重组载体转化的转化细胞，含有该重组载体的 公开了在单一条件下调节植物开花时间的方法，产生用该重组载体转化的转基因植物的方法，以及由此产生的转基因植物。
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公开(公告)号：KR1020140046740A
公开(公告)日：2014-04-21
申请号：KR1020120112763
申请日：2012-10-11
Applicant: 동아대학교 산학협력단
CPC classification number: C07K14/415 , C12N9/1051 , C12N15/8205 , C12N15/8243 , C12N15/8257 , C12Y204/01
Abstract: The present invention relates to: recombinant glycosyltransferase UGT72E3/2 protein formed of an amino acid sequence in the sequence number 2; a gene encoding the protein; a recombinant vector including the gene; and a method of increasing the syringin synthesis in a plant compare to a wild plant by transforming plant cells using the recombinant vector. Through the present invention, a user can effectively mass-produce syringin which is confirmed to have an excellent effect on treating diabetes and depression, the most concerned problems of health of modern city people and is expanding the applicability in a plant body, thereby allowing the development of agrobiological material industry with high value.
Abstract translation: 本发明涉及：由序列号2的氨基酸序列形成的重组糖基转移酶UGT72E3 / 2蛋白; 编码蛋白质的基因; 包含该基因的重组载体; 以及通过使用重组载体转化植物细胞，与野生植物相比，增加植物中的丁香素合成的方法。 通过本发明，用户可以有效地批量生产出已被证实对治疗糖尿病和抑郁症具有优异作用的戒毒素，这是现代城市人最健康的健康问题，并且正在扩大植物体内的适用性，从而允许 发展具有高价值的农业物资产业。
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公开(公告)号：KR1020100122175A
公开(公告)日：2010-11-22
申请号：KR1020090041087
申请日：2009-05-12
Applicant: 동아대학교 산학협력단
Abstract: PURPOSE: A high affinity phosphate transporter gene OsPT2(Oryza sativa phosphate transporter 2) isolated from rice plant is provided to enhance growth of plant. CONSTITUTION: An OsPT2 gene comprises a nucleotide sequence encoding a polypeptide having an amino acid sequence of sequence number 2. The gene isolated from rice plant. The gene is expressed under phosphate depletion. A method for manufacturing a plant transformed by OsPT2 gene comprises: a step of constructing a recombinant vector having OsPT2 gene; a step of transforming the plant with a recombinant vector; and a step of redifferentiating the transformed plant.
Abstract translation: 目的：提供从水稻植物中分离的高亲和力磷酸转运蛋白基因OsPT2（Oryza sativa phosphate transporter 2），以增强植物的生长。 构成：OsPT2基因包含编码具有序列号2的氨基酸序列的多肽的核苷酸序列。从水稻植物分离的基因。 该基因在磷酸盐消耗下表达。 用于制备由OsPT2基因转化的植物的方法包括：构建具有OsPT2基因的重组载体的步骤; 用重组载体转化植物的步骤; 以及重新分化转化植物的步骤。
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公开(公告)号：KR100925798B1
公开(公告)日：2009-11-11
申请号：KR1020080051031
申请日：2008-05-30
Applicant: 동아대학교 산학협력단
IPC: A01H1/00
CPC classification number: B09C1/105 , C02F3/327 , C02F2103/007 , C07K14/415 , C12N15/8259 , C12N15/8261
Abstract: PURPOSE: A rice plant transformant with enhanced absorption of phosphoric acid is provided to remove phosphate which excessively exists in a river and prevent eutrophication of soil or river. CONSTITUTION: A rice plant transformant with enhanced absorption of phosphoric acid overexpresses OsPT1 which is a phosphoric acid carrier gene of rice plant of the sequence number 1. The OsPT1 always expresses in all tissues of rice plant regardless of variation of phosphoric acid concentration.
Abstract translation: 目的：提供一种具有增加磷酸盐吸收性的水稻转化体，以去除过量存在于河流中的磷酸盐，防止土壤或河流富营养化。 构成：磷酸吸收增加的水稻转化株过表达OsPT1，它是序列1的水稻植物的磷酸载体基因。OsPT1总是在水稻植株的所有组织中表达，不管磷酸浓度如何变化。
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