公开(公告)号：JP2020519239A

公开(公告)日：2020-07-02

申请号：JP2019556227

申请日：2018-04-16

申请人： トランスアクティヴァ エッセ エッレ エッレ

发明人： マルケッティ,ステファノ ,  パッティ,タマラ

IPC分类号： C12N15/84 ,  C12N1/21 ,  C12N5/10 ,  A01H5/00 ,  C12N15/82

摘要： 植物のタンパク質、特に穀物胚乳における組換え抗体全体の安定生産のための発現ベクターであって、遺伝子発現において同じ方向と同じ制御および調節要素を有する抗体のポリペプチド軽鎖(L)の発現カセットとポリペプチド重鎖(H)の発現カセットを含む。 【選択図】図2

公开(公告)号：JP4532413B2

公开(公告)日：2010-08-25

申请号：JP2005513158

申请日：2004-08-05

申请人： 日本たばこ産業株式会社

发明人： 祐二 石田

IPC分类号： A01H1/00 ,  C12N15/09 ,  C12N15/82 ,  C12N15/84

CPC分类号： C12N15/8205

公开(公告)号：JP2009106293A

公开(公告)日：2009-05-21

申请号：JP2008301075

申请日：2008-11-26

申请人： Univ Of Florida Research Foundation Inc ,  ユニバーシティ オブ フロリダ リサーチ ファンデーション、インク.

发明人： HANNAH L CURTIS ,  GREENE THOMAS W

IPC分类号： A01H5/00 ,  C12N15/09 ,  A01C1/00 ,  A01G7/06 ,  C12N5/10 ,  C12N9/10 ,  C12N9/12 ,  C12N15/29 ,  C12N15/82 ,  C12N15/84 ,  C12Q1/02 ,  C12Q1/68

CPC分类号： C12N9/1241 ,  C12N9/1051 ,  C12N15/8245 ,  C12N15/8271 ,  C12Y204/01021 ,  C12Y207/07027

摘要： PROBLEM TO BE SOLVED: To provide a starch biosynthesis enzyme having increased thermal stability to increase the yield of plants growing under thermal stress conditions. SOLUTION: A mutant polynucleotide molecule encoding enzymatic activity of maize endosperm ADP glucose pyrophosphorylase (AGP) and soluble starch synthase (SSS); a plant and a plant tissue bred to contain, or transformed with, the mutant polynucleotide, and expressing the polypeptide encoded by the polynucleotide; a method for isolating the polynucleotide and the polypeptide; and a method for increasing yield of plants growning under thermal stress conditions are provided. COPYRIGHT: (C)2009,JPO&INPIT

摘要翻译： 待解决的问题：提供具有增加的热稳定性以增加在热胁迫条件下生长的植物的产量的淀粉生物合成酶。 解决方案：编码玉米胚乳ADP葡萄糖焦磷酸化酶（AGP）和可溶性淀粉合成酶（SSS）的酶活性的突变体多核苷酸分子; 培育为含有或转化了突变多核苷酸并表达多核苷酸编码的多肽的植物和植物组织; 分离多核苷酸和多肽的方法; 并提供了一种提高在热应激条件下生长的植物产量的方法。 版权所有（C）2009，JPO＆INPIT

公开(公告)号：JP4099898B2

公开(公告)日：2008-06-11

申请号：JP12702599

申请日：1999-05-07

申请人： 王子製紙株式会社

发明人： 敬悟 土肥 ,  哲 河津 ,  啓子 近藤

IPC分类号： A01H1/00 ,  C12N15/09 ,  A01H4/00 ,  C12N5/10 ,  C12N15/82 ,  C12N15/84

CPC分类号： C12N15/8205 ,  A01H4/005

摘要： The present invention discloses a process for transforming mature trees of Eucalyptus plants comprising: inducing adventitious shoots from segments of the explant obtained from an adult tree of a Eucalyptus plant, preculturing the adventitious shoots in infection induction medium, infecting the adventitious shoots subjected to infection induction treatment with infection medium containing Agrobacterium tumefaciens, and rotary-culturing the infected explant segments in sterilization medium containing antibiotic; whereby sterilizing and forming transgenic calli, which regenerate transgenic plants by way of formation of shoot primordia by rotary-culturing under illumination.

公开(公告)号：JP2006508681A

公开(公告)日：2006-03-16

申请号：JP2004559306

申请日：2003-12-05

申请人： デル・モンテ・フレッシュ・プロデュース・カンパニー

发明人： エブラヒム・フィルーザバディー ,  トーマス・アール．・ヤング

IPC分类号： C12N15/09 ,  A01H5/00 ,  C12N5/10 ,  C12N9/00 ,  C12N15/29 ,  C12N15/31 ,  C12N15/82 ,  C12N15/84

CPC分类号： C12N15/825 ,  A01H4/008 ,  C12N15/8205

摘要： 本発明は形質転換細胞におけるカロテノイド蓄積を調節し、所定態様では前記細胞の着色を調節するカロテノイド生合成ポリペプチド発現レギュレーターによるパイナップル細胞及び植物体の形質転換方法を提供する。 本発明は形質転換細胞からのパイナップル植物体の再生も可能にする。 更に、本発明はカロテノイド生合成ポリペプチド発現レギュレーターを導入したパイナップル細胞及び植物体も提供する。

公开(公告)号：JP2002521006A

公开(公告)日：2002-07-16

申请号：JP2000560767

申请日：1999-07-21

IPC分类号： A01H5/00 ,  C07K14/415 ,  C07K16/40 ,  C12N1/15 ,  C12N1/19 ,  C12N1/21 ,  C12N5/10 ,  C12N9/12 ,  C12N15/09 ,  C12N15/29 ,  C12N15/82 ,  C12N15/84

公开(公告)号：JP2002511270A

公开(公告)日：2002-04-16

申请号：JP2000543618

申请日：1999-04-13

IPC分类号： A01H5/00 ,  C07K14/415 ,  C07K16/16 ,  C12N5/10 ,  C12N15/09 ,  C12N15/113 ,  C12N15/29 ,  C12N15/82 ,  C12N15/84

公开(公告)号：JP2000342256A

公开(公告)日：2000-12-12

申请号：JP15802599

申请日：1999-06-04

申请人： JAPAN TOBACCO INC

发明人： HIEI YOSHIHIRO ,  KASAOKA KEISUKE ,  ISHIDA YUJI

IPC分类号： C12N15/09 ,  A01H1/00 ,  C12N5/10 ,  C12N15/82 ,  C12N15/84

摘要： PROBLEM TO BE SOLVED: To improve the efficiency of gene transfer to a plant cell simply carried out through a bacterium of the genus Agrobacterium without damaging a tissue, to perform transformation and to better a breed by centrifuging a plant cell or a plant tissue. SOLUTION: A plant cell or a plant tissue of rice plant, maize, etc., is centrifuged at 100-250,000 G, preferably 500-200,000 G, more preferably 1,000-150,000 G centrifugal acceleration for 1 second to 4 hours, preferably for 5 minutes to 2 hours to improve the efficiency of gene transfer to a plant cell carried out through a bacterium of the genus Agrobacterium. Preferably the plant cell or plant tissue is derived from an angiosperm, a monocotyledon or a gramineous plant. Preferably after the plant cell or plant tissue is centrifuged, a gene transfer treatment is performed.

公开(公告)号：JP2000300254A

公开(公告)日：2000-10-31

申请号：JP2000089081

申请日：2000-03-28

申请人： STEPHEN A JOHNSTON ,  CORNELL RES FOUNDATION INC

发明人： JOHNSTON STEPHEN A ,  SANFORD JOHN C

IPC分类号： A01H1/02 ,  A01H1/00 ,  A01H5/00 ,  A01K67/027 ,  A01K67/033 ,  A61K38/00 ,  A61K48/00 ,  C07K14/005 ,  C12N1/00 ,  C12N1/15 ,  C12N1/19 ,  C12N1/20 ,  C12N1/21 ,  C12N5/00 ,  C12N5/10 ,  C12N15/00 ,  C12N15/09 ,  C12N15/113 ,  C12N15/33 ,  C12N15/84 ,  C12N15/85 ,  C12N15/87

摘要： PROBLEM TO BE SOLVED: To obtain a genetically inserted body capable of imparting resistance against a parasite to its host by adding a gene fraction or the like separated from the parasite and having a specific property. SOLUTION: This genetically inserted body contains a gene fraction separated from a parasite such as a virus, a DNA or RNA segment which is substantially homologous to a part of the gene fraction, or a DNA or RNA segment which is functionally equivalent to the gene fraction. Herein, these substances have each at least one property out of (i) the transcription of the gene fraction, or the DNA or RNA segment in a host such as a human proceeds in an antisense direction, (ii) the gene fraction, or the DNA or RNA segment is expressed in the host to produce a gene product, and the gene product has an ability to destroy an essential activity of the parasite, and (iii) the gene fraction, or the DNA or RNA segment acts as a bonding site which competes with the inherent bonding site of the parasite. Further, it is preferable that the gene fraction or the like is inserted into the host as a recombinant DNA vector.

公开(公告)号：JP2000300098A

公开(公告)日：2000-10-31

申请号：JP32098199

申请日：1999-11-11

申请人： BIOCEM

发明人： DE BOTH MICHIEL ,  BEN TAHAR SOPHIA ,  NOEL MARIANNE ,  PERRET JOEL

IPC分类号： A01H1/00 ,  A01H4/00 ,  A01H5/00 ,  A01H5/08 ,  C07K14/08 ,  C12N5/00 ,  C12N5/10 ,  C12N15/09 ,  C12N15/33 ,  C12N15/40 ,  C12N15/82 ,  C12N15/84

摘要： PROBLEM TO BE SOLVED: To obtain a transgenic plant capable of being regenerated from a transformed tissue in the species Cucumis melo and excellent in virus resistance by including a DNA sequence transduced through mediation of Agrobacterium tumefaciens. SOLUTION: This transgenic plant is a transgenic plant of the normal phenotype belonging to the species Cucumis melo and contains one or more DNA sequences transduced through mediation of Agrobacterium tumefaciens. Further, the transgenic plant of the normal phenotype belonging to the species Cucumis melo is preferably prepared by including one or more DNA sequences capable of imparting resistance to cucumber mosaic and having an encoding sequence represented by the formula or capable of encoding a capsid protein of the cucumber mosaic virus. The plant tissue is preferably a melon and the tissue is preferably a cotyledon obtained from an embryo germinated for 0-4 days or a shoot bud.