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    • 2. 发明申请
    • CO-EXPRESSION OF ZEIN PROTEINS
    • IN蛋白的共表达
    • WO02086077A2
    • 2002-10-31
    • PCT/US0212646
    • 2002-04-18
    • UNIV NEW MEXICO STATE TECH TRAKEMP JOHN DRANDALL JENNIFER J
    • KEMP JOHN DRANDALL JENNIFER J
    • C07K14/425C12N15/62C12N15/82C12N
    • C12N15/62C07K14/425C07K2319/02C12N15/8251
    • Methods and constructs for transformed plants and plant tissues that are capable of expressing high levels of stable proteins localized as protein bodies within the plant cell. Transformed plants co-expressing high levels of both the 15 kD and 10 kD zein proteins are disclosed which accumulate to high levels as protein bodies in the vegetative tissue of the plant. Transformed plants co-expressing the 15 kD and 10 kD zein proteins are useful for providing forage crops containing increased levels of sulfur containing amino acids, such as methionine, in the diet of animals that normally feed on such crops. In one embodiment, a stable protein body is expressed in a plant or plant tissue as a fusion protein comprising both the 15 kD and 10 kD zein proteins operably linked by a polypeptide or peptide linker. The protein bodies provided in the present invention are resistant to rumin digestion or environmental degradation.
    • 能够表达高水平的稳定蛋白质的转化植物和植物组织的方法和构建体,其定位为植物细胞内的蛋白质体。 公开了共表达高水平的15kD和10kD玉米醇溶蛋白的转化植物,其在植物的营养组织中作为蛋白质体累积到高水平。 共同表达15kD和10kD玉米醇溶蛋白的转化植物可用于在通常饲养这种作物的动物的饮食中提供含有含量高的含硫氨基酸(例如甲硫氨酸)的饲料作物。 在一个实施方案中,稳定的蛋白质体在作为融合蛋白的植物或植物组织中表达,所述融合蛋白包含通过多肽或肽接头可操作地连接的15kD和10kD的玉米醇溶蛋白。 在本发明中提供的蛋白质体对抗紫苏消化或环境降解是有抗性的。
    • 7. 发明申请
    • AZOLE NUCLEOSIDES AND USE AS INHIBITORS OF RNA AND DNA VARIAL POLYMERASES
    • 单核苷酸和用作RNA和DNA多肽的抑制剂
    • WO2008067002A3
    • 2008-11-06
    • PCT/US2007078139
    • 2007-09-11
    • SOUTHERN RES INSTUNIV NEW MEXICOARTERBURN JEFFREY BJONSSON COLLEEN BPARKER WILLIAM B
    • ARTERBURN JEFFREY BJONSSON COLLEEN BPARKER WILLIAM B
    • A01N43/04A61K31/70C07H5/04C07H5/06C07H19/044C07H19/056
    • C07H5/04C07H5/06C07H19/044C07H19/056
    • Azole nucleosides represented by the formulae (I) and (II); wherein A = C or N B = C or N X = H; C 1 -C 6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo, halogen such as F, C1, Br and I; OH, NH 2 , NH-(C 1 -C 6 alkyl, cycloalkyl, aryl, or heterocyclo); Z = H; C 1 -C 6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo, halogen such as F, Cl, Br, I; OH, NH 2 , NH-(C 1 -C 6 alkyl, cycloalkyl, aryl, or heterocyclo; E= (CH 2 )HONHR 1 ; n is an integer from 0-6 and more typically 0-3; R 1 = aryl or heterocyclo; each of W, Y, R is individually selected from the group consisting of H; C 1 -C 6 alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclo; halogen such as F, Cl, Br, and I; O, OH, Oalkyl, Oaryl, NH 2 , NH-(C 1 -C 6 alkyl, cycloalkyl, aryl, or heterocyclo); provided that at least one of W, Y, and R is other than H and wherein both W and Y together can be =O; and each D individually is OH, Oalkyl, Oaryl, Fl and H;pharmaceutically acceptable salts thereof, prodrugs thereof and mixtures thereof are provided. Compounds of this disclosure are useful as inhibitors of viral RNA and DNA polymerases such as, but not limited to, Influenza, Hantaan Virus, Crimean Congo hemorrhagic fever virus, hepatitis B, hepatitis C, Polio, Coxsackie A and B, Rhino, Echo, orthopoxvirus (small pox), HIV, Ebola, and West Nile virus polymerases; and especially orthopoxvirus, HIV, and hepatitis B.
    • 由式(I)和(II)表示的唑类核苷; 其中A = C或N B = C或N X = H; C 1 -C 6烷基,环烷基,烯基,环烯基,炔基,芳基,杂环基,卤素如F,Cl,Br和I; OH,NH 2,NH-(C 1 -C 6烷基,环烷基,芳基或杂环); Z = H; C 1 -C 6烷基,环烷基,烯基,环烯基,炔基,芳基,杂环基,卤素如F,Cl,Br,I; OH,NH 2,NH-(C 1 -C 6烷基,环烷基,芳基或杂环; E =(CH 3) 2 HONHR 1; n是0-6,更典型地0-3的整数; R 1 =芳基或杂环; W,Y R 1独立地选自H; C 1 -C 6烷基,环烷基,烯基,环烯基,炔基,芳基,杂环;卤素如F, Cl,Br和I; O,OH,O烷基,芳基,NH 2,NH-(C 1 -C 6烷基,环烷基 ,芳基或杂环基);条件是W,Y和R中的至少一个不是H,并且其中W和Y一起可以是= O;并且每个D分别是OH,O烷基,芳基,F 1和H; 本公开的化合物可用作病毒RNA和DNA聚合酶的抑制剂,例如但不限于流感,汉坦病毒,克里米亚刚果出血热病毒,乙型肝炎,肝炎 C,脊髓灰质炎, 柯萨奇A和B,犀牛,回声,正痘病毒(小痘),HIV,埃博拉和西尼罗病毒聚合酶; 尤其是正痘病毒,艾滋病毒和乙型肝炎。