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公开(公告)号：KR1020130025426A
公开(公告)日：2013-03-11
申请号：KR1020130020839
申请日：2013-02-27
Applicant: 충남대학교산학협력단
IPC: C12N15/113 , C12N15/63
Abstract: PURPOSE: BrMiR 156f, a novel miRNA, which is isolated from Brassica rapa and is one of 109 Brassica rapa mRNAs belonging to total 47 family is provided to understand post-transcription regulation which is a function of Brassica rapa genome, such as plant differentiation and metabolism. CONSTITUTION: BrMiR 156f, a novel miRNA isolated from Brassica rapa has a base sequence of sequence number 3 or a complementary sequence thereof.
Abstract translation: 目的：提供BrMiR 156f，一种从芸苔属中分离出来的miRNA，是属于总共47个家族的109种芸苔属之一，用于了解转录后调控，其是芸苔属芸苔基因组的功能，如植物分化和 代谢。 构成：BrMiR 156f是从芸苔属分离的新型miRNA具有序列号3的碱基序列或其互补序列。
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公开(公告)号：KR1020110001312A
公开(公告)日：2011-01-06
申请号：KR1020090058795
申请日：2009-06-30
Applicant: 충남대학교산학협력단
CPC classification number: C12N15/8281
Abstract: PURPOSE: A plant with enhanced pest injury resistance, which expresses pinIISP-aii fusion gene is provided to enhance soft rot resistance to use in plant industry. CONSTITUTION: A recombinant plant expression vector contains a signal peptide coding gene of potato-derived PinII(protease inhibitor II) and Bacillus sp. GH02-derived aii(autoinducer inactivation) gene. The signal peptide comprises an amino acid sequence of sequence number 1. The aii gene comprises a base sequence of sequence number 2. The vector is pCAMBIA1302. A plant with enhanced pest injury resistance is obtained by transforming the plant with the recombinant plant expression vector.
Abstract translation: 目的：提供具有增强的抗病虫害性的植物，其表达pinIISP-aii融合基因，以提高耐腐蚀性，用于植物工业。 构成：重组植物表达载体含有马铃薯衍生的PinII（蛋白酶抑制剂II）和芽孢杆菌属的信号肽编码基因。 GH02衍生的aii（自动诱导失活）基因。 信号肽包含序列号1的氨基酸序列.aii基因包含序列号2的碱基序列。载体是pCAMBIA1302。 通过用重组植物表达载体转化植物获得具有增强的害虫损伤抗性的植物。
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公开(公告)号：KR100998863B1
公开(公告)日：2010-12-08
申请号：KR1020080053510
申请日：2008-06-09
Applicant: 충남대학교산학협력단
CPC classification number: Y02A50/351
Abstract: 본 발명은 살충 활성을 갖는 균주 페니실리움 왁스마니(
Penicillium
waksmanii )를 유효성분으로 포함하는 식물 해충 및 식물병 방제용 살균 및 살충 조성물 및 상기 조성물을 이용한 식물 해충 및 식물병 방제 방법에 관한 것으로서, 보다 자세하게는 살충 활성을 갖는 균주 페니실리움 왁스마니(
Penicillium waksmanii )
, 아트로보트리스 브로초파가(
Arthrobotrys brochopaga ), 아트로보트리스 무시포미스(
Arthrobotrys musiformis ), 은행잎 추출물, 은행 열매 추출물, 커피 추출물, 마늘 추출물, 고추 추출물을 주성분으로 하는 소나무 재선충을 비롯한 식물 해충 및 식물병 방제용 살균 및 살충 조성물 및 상기 조성물을 이용한 식물 해충 및 식물병 방제 방법에 관한 것이다.
소나무 재선충, 삼림 해충, 농작물 해충, 페니실리움 왁스마니, 아트로보트리스 브로초파가, 아트로보트리스 무시포미스, 방제용 조성물-
公开(公告)号：KR100744760B1
公开(公告)日：2007-08-01
申请号：KR1020060052177
申请日：2006-06-09
Applicant: 충남대학교산학협력단
Abstract: A lateral suppressor-like(DgLsL) gene isolated from Dendranthema grandiflorum Kitamura is provided to reduce the time and labor for removing lateral branching of Dendranthema grandiflorum Kitamura. The lateral suppressor-like(DgLsL) gene isolated from Dendranthema grandiflorum Kitamura 95B1-49 has the nucleotide sequence of SEQ ID NO:1 and is obtained by cloning cDNA(complementary DNA) of lateral suppressor-like gene from Dendranthema grandiflorum Kitamura 95B1-49 and analyzing the whole sequence of the cloned cDNA through RACE(Rapid amplification of cDNA ends). A protein encoded by the lateral suppressor-like(DgLsL) gene isolated from Dendranthema grandiflorum Kitamura 95B1-49 has the amino acid sequence of SEQ ID NO:2.
Abstract translation: 从Dendranthema grandiflorum Kitamura中分离出一种横向抑制物样（DgLsL）基因，以减少去除菊花Dendranthema grandiflorum Kitamura侧枝的时间和劳力。 从Dendranthema grandiflorum Kitamura 95B1-49中分离的横向抑制物样（DgLsL）基因具有SEQ ID NO：1的核苷酸序列并且通过克隆来自Dendranthema grandiflorum Kitamura 95B1-49的横向抑制物样基因的cDNA（互补DNA） 并通过RACE（cDNA末端的快速扩增）分析克隆cDNA的全部序列。 由从Dendranthema grandiflorum Kitamura 95B1-49分离的横向抑制物样（DgLsL）基因编码的蛋白质具有SEQ ID NO：2的氨基酸序列。
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公开(公告)号：KR1020070002581A
公开(公告)日：2007-01-05
申请号：KR1020050058177
申请日：2005-06-30
Applicant: 충남대학교산학협력단
IPC: A01H4/00
CPC classification number: A01H4/008 , A01C1/08 , A01H4/001 , A01H4/005 , C12N5/0025 , C12N2501/30
Abstract: A method for regenerating the plants by using inbred line of Chinese cabbage is provided to increase efficiency of genetic transformation of plants mediated by Agrobacterium, and enhance regeneration rate of plants. The method for regenerating the plants comprises the steps of: (a) sterilizing the inbred seeds of Chinese cabbage; (b) germinating the sterilized seeds for 2-5 days; (c) obtaining the cotyledon or hypocotyl explants from the germinated seeds; (d) culturing the cotyledon or hypocotyl explants in MS medium containing 0.1-5 mg/L of BA(6-benzylaminopurine) and 0.1-0.5 mg/L of NAA(alpha-naphthaleneacetic acid) for 10-30 days to induce shoots; (e) orientating the shoots in MS medium containing NAA to induce root development; and (f) transplanting the root developed young plant to a pot and raising it.
Abstract translation: 提供了通过使用大白菜近交系再生植物的方法，以提高农杆菌介导的植物的遗传转化效率，提高植物的再生率。 植物再生方法包括以下步骤：（a）对白菜的近交种子进行灭菌; （b）将灭菌的种子发芽2-5天; （c）从发芽种子获得子叶或下胚轴外植体; （d）在含有0.1-5mg / L BA（6-苄基氨基嘌呤）和0.1-0.5mg / L NAA（α-萘乙酸）的MS培养基中培养子叶或下胚轴外植体10-30天以诱导芽; （e）使含有NAA的MS培养基中的嫩芽定向以诱导根发育; 和（f）将根发育的幼苗移植到盆中并提高它。
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Patent Agency Ranking
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公开(公告)号：KR102116428B1
公开(公告)日：2020-05-28
申请号：KR1020180172078
申请日：2018-12-28
Applicant: 충남대학교산학협력단
IPC: C12Q1/6895
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公开(公告)号：KR101854350B1
公开(公告)日：2018-05-03
申请号：KR1020160183556
申请日：2016-12-30
Applicant: 충남대학교산학협력단
IPC: C12Q1/68
Abstract: 본발명은배추글루코시놀레이트함량조절인자기반의 SNP 마커및 이의용도에관한것이다. 본발명에따른 SNP 마커를배추작물에적용하면, 배추의글루코시놀레이트함량을효율적으로판별및 육성할수 있어육종에소요되는시간, 비용및 노력을절감하는데매우유용할것으로기대된다. 또한, 본발명의방법으로육성한글루코시놀레이트고함량배추품종의보급은재배농가및 소비자에게도고품질의배추생산및 공급을가능하게할 것으로기대된다.
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公开(公告)号：KR101704382B1
公开(公告)日：2017-02-08
申请号：KR1020150155782
申请日：2015-11-06
Applicant: 충남대학교산학협력단
IPC: C12Q1/68
Abstract: 본발명은배추뿌리혹병저항성품종을특이적으로판별하기위한프라이머세트및 이의용도에관한것으로, 본발명을통해배추뿌리혹병저항성품종에대해특이적판별이쉽고빠르게수행될수 있으므로, 배추의뿌리관련내병성품종육성시 효율적으로품종이나계통들의뿌리관련특성과병 저항성을평가함으로써배추의뿌리관련내병성품종육종에유용하게이용될수 있다.
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公开(公告)号：KR101602536B1
公开(公告)日：2016-03-10
申请号：KR1020130137237
申请日：2013-11-12
Applicant: 충남대학교산학협력단
Abstract: 본발명은 KACC98014P, KACC98016P, KACC98017P, KACC98018P 및 KACC98019P로이루어진군에서선택되는종자수탁번호로기탁된배추()인, 글루코나스튜틴(gluconasturtiin)의함량이증가된식물체및 이의육종방법에관한것이다. 본발명에따른식물체, 즉배추품종은글루코나스튜틴의함량이기존의배추에비해현저히높은바, 일상적으로다량섭취하는배추를통해글루코나스튜틴의항암효과를얻을수 있도록하는데 중요하게응용될수 있을것으로기대된다. 또한, 본발명에따른육종방법을통해글루코나스튜틴함량이크게향상된고기능성, 고부가가치의배추품종의개발이가능한바, 농가의수익창출에도크게기여할수 있을것으로기대된다.
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