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    • 91. 发明申请
    • ROTAVIRUS-LIKE PARTICLE PRODUCTION IN PLANTS
    • 在植物中的旋风样颗粒生产
    • US20150216961A1
    • 2015-08-06
    • US14398650
    • 2013-05-10
    • MEDICAGO INC.MITSUBISHI TANABE PHARMA CORPORATION
    • Marc-Andre D'AoustNathalie LandryPierre-Olivier LavoieMasaaki AraiNaomi AsaharaDavid Levi Rutendo MutepfaInga Isabel HitzerothEdward Peter Rybicki
    • A61K39/15C07K14/005C12N7/00
    • A61K39/15A61K39/12A61K2039/5258C07K14/005C12N7/00C12N7/02C12N15/8203C12N15/8214C12N15/8216C12N15/8218C12N15/8221C12N15/8258C12N2720/12334C12N2720/12351
    • A method of producing a virus-like particle (VLP) in a plant is provided. The method comprises introducing a first nucleic acid into the plant, or portion of the plant. The first nucleic acid comprising a first regulatory region active in the plant operatively linked to a nucleotide sequence encoding one or more rotavirus structural protein for example but not limited to rotavirus protein VP2. The nucleotide sequence may further comprise one or more than one amplification element and/or a compartment targeting sequence. A second nucleic acid might be introduced into the plant, or portion of the plant. The second nucleic acid comprises a second regulatory region active in the plant and operatively linked to a nucleotide sequence encoding one or more rotavirus structural protein, for example but not limited to rotavirus protein VP6. Optionally, a third nucleic acid and/or fourth nucleic acid might be introduced into the plant, or portion of the plant. The third nucleic acid comprises a third regulatory region active in the plant and operatively linked to a nucleotide sequence encoding one or more rotavirus structural protein, for example but not limited to rotavirus protein VP4. The fourth nucleic acid comprises a fourth regulatory region active in the plant and operatively linked to a nucleotide sequence encoding one or more rotavirus structural protein, for example but not limited to rotavirus protein VP7. The plant or portion of the plant is incubated under conditions that permit the expression of the nucleic acids, thereby producing the VLP.
    • 提供了一种在植物中生产病毒样颗粒(VLP)的方法。 该方法包括将第一核酸引入植物或植物的一部分。 所述第一核酸包含在植物中活性的第一调节区,其可操作地连接于编码一种或多种轮状病毒结构蛋白(例如但不限于轮状病毒蛋白VP2)的核苷酸序列。 核苷酸序列还可以包含一个或多于一个扩增元件和/或隔室靶向序列。 可以将第二种核酸引入植物或植物的一部分。 第二核酸包含在植物中有活性的第二调控区,并可操作地连接于编码一种或多种轮状病毒结构蛋白(例如但不限于轮状病毒蛋白VP6)的核苷酸序列。 任选地,第三核酸和/或第四核酸可以被引入植物或植物的一部分。 第三核酸包含在植物中活性的第三调节区,并且与编码一种或多种轮状病毒结构蛋白(例如但不限于轮状病毒蛋白VP4)的核苷酸序列可操作地连接。 第四核酸包含在植物中活性的第四调节区,并且可操作地连接于编码一种或多种轮状病毒结构蛋白(例如但不限于轮状病毒蛋白VP7)的核苷酸序列。 将植物或植物的一部分在允许核酸表达的条件下温育,从而产生VLP。
    • 92. 发明申请
    • PLANT TRANSFORMANT, TRANSFORMATION METHOD FOR PLANT, AND VECTOR USED IN SAID METHOD
    • 植物变异体,植物转化方法和用于确定方法的矢量
    • US20150101081A1
    • 2015-04-09
    • US14360379
    • 2012-11-22
    • National Institute of Agrobiological Sciences
    • Yutaka TabeiAyako Okuzaki
    • C12N15/82
    • C12N15/8238C12N15/8214
    • The present invention provides a method for transforming organelles having an own genomic DNA, the method enabling efficient production of highly homoplasmic plant cells, in which most of the organelles are transformed, and so forth. The method comprises the steps of: expressing in plant cells a fusion protein containing a function inhibiting factor of the organelles and a transit signal peptide to the organelles; introducing into the genomic DNA of the organelles of the plant cells an expression cassette comprising DNAs encoding a restoring factor of the organelles and a factor desired to be expressed in the organelles; and allowing the function inhibiting factor to destroy the organelles, in which the expression cassette is not introduced, in the plant cells.
    • 本发明提供了一种用于转化具有自身基因组DNA的细胞器的方法,该方法能够高效地产生大多数细胞器被转化的高度均质的植物细胞,等等。 该方法包括以下步骤:在植物细胞中表达含有细胞器的功能抑制因子和转运信号肽至融合细胞器的融合蛋白; 向植物细胞的细胞器的基因组DNA中引入包含编码细胞器的恢复因子和期望在细胞器中表达的因子的DNA的表达盒; 并且允许功能抑制因子在植物细胞中破坏其中未引入表达盒的细胞器。
    • 100. 发明申请
    • MANIPULATION OF GENES OF THE MEVALONATE AND ISOPRENOID PATHWAYS TO CREATE NOVEL TRAITS IN TRANSGENIC ORGANISMS
    • 操纵梅毒基因和异常路径在转基因生物体系中创造新的条件
    • US20130203132A1
    • 2013-08-08
    • US13602723
    • 2012-09-04
    • Frederick M. HahnAdelheid R. Kuehnle
    • Frederick M. HahnAdelheid R. Kuehnle
    • C12P9/00
    • C12P9/00C12N9/90C12N15/52C12N15/8209C12N15/8214C12N15/8243
    • Disclosed are the uses of specific genes of the mevalonate and isoprenoid biosynthetic pathways, and of inactive gene sites (the pseudogene) to (1) enhance biosynthesis of isopentenyl diphosphate, dimethylallyl diphosphate and isoprenoid pathway derived products in the plastids of transgenic plants and microalgae, (2) create novel antibiotic resistant transgenic plants and microalgae, and (3) create a novel selection system and/or targeting sites for mediating the insertion of genetic material into plant and microalgae plastids. The specific polynucleotides to be used, solely or in any combination thereof, are publicly available from GeneBank and contain open reading frames having sequences that upon expression will produce active proteins with the following enzyme activities: (a) acetoacetyl CoA thiolase (EC 2.3.1.9), (b) 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) synthase (EC 4.1.3.5), (c) HMG-CoA reductase (EC 1.1.1.34), (d) mevalonate kinase (EC 2.7.1.36), (e) phosphomevalonate kinase (EC 2.7.4.2), (f) mevalonate diphosphate decarboxylase (EC 4.1.1.33), (g) isopentenyl diphosphate (IPP) isomerase (EC 5.3.3.2), and (h) phytoene synthase (EC 2.5.1.32).
    • 公开了甲羟戊酸和类异戊二烯生物合成途径的特定基因和无活性基因位点(假基因)的用途,以(1)增强转基因植物和微藻质体中异戊烯基二磷酸,二甲基烯丙基二磷酸和异戊二烯通路衍生产物的生物合成, (2)创建新的抗生素抗性转基因植物和微藻,(3)创建一个新的选择系统和/或靶向位点,用于介导遗传物质插入植物和微藻质体。 待使用的单独或以任何组合形式存在的特异性多核苷酸可从GeneBank公开获得并含有具有序列的开放阅读框,其表达将产生具有以下酶活性的活性蛋白:(a)乙酰乙酰辅酶A硫解酶(EC 2.3.1.9 ),(b)3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)合酶(EC 4.1.3.5),(c)HMG-CoA还原酶(EC 1.1.1.34),(d)甲羟戊酸激酶 (e)磷酸戊糖酸盐激酶(EC 2.7.4.2),(f)甲羟戊酸二磷酸脱羧酶(EC 4.1.1.33),(g)异戊烯基二磷酸(IPP)异构酶(EC 5.3.3.2)和(h) 合成酶(EC 2.5.1.32)。