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    • 1. 发明授权
    • FC binding protein and method for manufacturing same
    • FC结合蛋白及其制造方法
    • US09453066B2
    • 2016-09-27
    • US13583550
    • 2011-03-10
    • Kouta HatayamaYoshiharu AsaokaToru TanakaTeruhiko Ide
    • Kouta HatayamaYoshiharu AsaokaToru TanakaTeruhiko Ide
    • C07K1/00A23J1/00C07K14/735C07K1/22C07K17/08C07K16/00
    • C07K14/70535C07K1/22C07K17/08C07K2319/21
    • Disclosed are: an Fc binding protein having increased stability with respect to heat, acid, and/or alkalinity compared with the wild type; a method for producing same; and a method for specifically isolating protein containing an Fc binding protein binding site using said Fc binding protein as a ligand for affinity chromatography.An Fc binding protein was obtained having increased stability with respect to heat, acid, and/or alkalinity compared with the wild-type human Fc receptor by means of substituting at least one specific amino acid residue in the extracellular domain of the wild-type human Fc receptor with another amino acid residue. The Fc binding protein is useful as a ligand for affinity chromatography for example by immobilizing in a solid phase. Also, when the Fc binding protein is expressed using a host that has been transformed with an expression vector containing a polynucleotide coding for said protein, the amount of produced protein is increased compared with using a wild-type human Fc receptor.
    • 获得了与野生型人Fc受体相比,通过用野生型人细胞外结构域中的至少一个特定氨基酸残基取代的具有相对于热,酸和/或碱度的稳定性增加的Fc结合蛋白质 Fc受体与另一个氨基酸残基。 Fc结合蛋白可用作亲和层析的配体,例如通过固定在固相中。 此外,当使用已经用含有编码所述蛋白质的多核苷酸的表达载体转化的宿主来表达Fc结合蛋白时,与使用野生型人Fc受体相比,产生的蛋白质的量增加。
    • 2. 发明申请
    • FC BINDING PROTEIN AND METHOD FOR MANUFACTURING SAME
    • FC结合蛋白及其制造方法
    • US20130079499A1
    • 2013-03-28
    • US13583550
    • 2011-03-10
    • Kouta HatayamaYoshiharu AsaokaToru TanakaTeruhiko Ide
    • Kouta HatayamaYoshiharu AsaokaToru TanakaTeruhiko Ide
    • C07K14/735C07K17/08C07K1/22
    • C07K14/70535C07K1/22C07K17/08C07K2319/21
    • Disclosed are: an Fc binding protein having increased stability with respect to heat, acid, and/or alkalinity compared with the wild type; a method for producing same; and a method for specifically isolating protein containing an Fc binding protein binding site using said Fc binding protein as a ligand for affinity chromatography.An Fc binding protein was obtained having increased stability with respect to heat, acid, and/or alkalinity compared with the wild-type human Fc receptor by means of substituting at least one specific amino acid residue in the extracellular domain of the wild-type human Fc receptor with another amino acid residue. The Fc binding protein is useful as a ligand for affinity chromatography for example by immobilizing in a solid phase. Also, when the Fc binding protein is expressed using a host that has been transformed with an expression vector containing a polynucleotide coding for said protein, the amount of produced protein is increased compared with using a wild-type human Fc receptor.
    • 公开了:与野生型相比,相对于热,酸和/或碱度具有增加的稳定性的Fc结合蛋白; 其制造方法; 以及使用所述Fc结合蛋白作为亲和层析的配体来特异性分离含有Fc结合蛋白结合位点的蛋白质的方法。 获得了与野生型人Fc受体相比,通过用野生型人细胞外结构域中的至少一个特定氨基酸残基取代的具有相对于热,酸和/或碱度的稳定性增加的Fc结合蛋白 Fc受体与另一个氨基酸残基。 Fc结合蛋白可用作亲和层析的配体,例如通过固定在固相中。 此外,当使用已经用含有编码所述蛋白质的多核苷酸的表达载体转化的宿主来表达Fc结合蛋白时,与使用野生型人Fc受体相比,产生的蛋白质的量增加。
    • 6. 发明申请
    • NOVEL MICROORGANISM AND METHOD FOR PRODUCING CAROTENOID USING THE SAME
    • 新型微生物及其制造方法
    • US20100285524A1
    • 2010-11-11
    • US12095511
    • 2006-10-19
    • Toru TanakaTeruhiko Ide
    • Toru TanakaTeruhiko Ide
    • C12P23/00C12N1/20C12N1/21
    • C12R1/01C12P23/00
    • [Object] To provide a canthaxanthin selective producing bacterium being able to easily extract and purify canthaxanthin, which is one of carotenoids, and a method for producing canthaxanthin by a culture method.[Solving Means] A carotenoid producing bacterium belonging to the genus Paracoccus is provided which selectively produces canthaxanthin so that the amount thereof is not less than 90 percent by weight of the total amount of produced carotenoids including β-carotene, β-cryptoxanthin, echinenone, canthaxanthin, 3-hydroxyechinenone, 3′-hydroxyechinenone, zeaxanthin, phoenicoxanthin, adonixanthin, and astaxanthin. In addition, a method for producing canthaxanthin is provided which has the steps of culturing the above bacterium, and then collecting carotenoids from bacterial cells or a culture solution after the culturing.
    • 本发明提供能够容易地提取和纯化作为类胡萝卜素的角黄素的角黄素选择性生产菌,以及通过培养方法制备角黄素的方法。 [解决方案]提供属于副球菌属的类胡萝卜素生产细菌,其选择性地产生角黄素,其量不小于包含“胡萝卜素”,“副霉黄素”的生产的类胡萝卜素总量的90重量% 海参酮,角黄素,3-羟基喹喔啉酮,3'-羟基喹喔啉酮,玉米黄质,磷酸黄嘌呤,亚二黄素和虾青素。 此外,提供了一种生产角黄素的方法,其具有培养上述细菌的步骤,然后在培养后从细菌细胞或培养液中收集类胡萝卜素。
    • 8. 发明申请
    • METHOD FOR PRODUCTION OF CAROTENOID-SYNTHESIZING MICROORGANISM AND METHOD FOR PRODUCTION OF CAROTENOID
    • US20090226582A1
    • 2009-09-10
    • US12089486
    • 2006-09-25
    • Teruhiko IdeToru Tanaka
    • Teruhiko IdeToru Tanaka
    • A23L1/30C12P23/00C12N15/11C12N15/00C12N1/21
    • C12P23/00A23K20/179A23L5/44C12N15/743
    • A microorganism is provided which allows carotenoid production in industrial production scale. A method of preparing a carotenoid includes: culturing a cell transformed with a DNA chain having a DNA sequence selected from the group consisting of the following (a) to (f) or a cell transformed with a vector having a DNA sequence selected from the group consisting of the following (a) to (f) in an appropriate culture condition, and isolating carotenoid from the cell or a culture medium: (a) DNA sequence encoding a polypeptide having such an enzymatic activity of Paracoccus sp. Strain MBIC1143 that converts a methylene group at 4 position in β-ionone ring into a keto group (crtW), described in SEQ ID NO: 2, or a substantially homologous DNA sequence thereof; (b) DNA sequence encoding a polypeptide having such an enzymatic activity of Paracoccus sp. Strain MBIC1143 that adds one hydroxyl group to a carbon at 3-position of 4-keto-β-ionone ring and/or at 3-position of β-ionone ring (crtZ), described in SEQ ID NO: 3, or a substantially homologous DNA sequence thereof; (c) DNA sequence encoding a polypeptide having such an enzymatic activity of Paracoccus sp. Strain MBIC1143 that converts lycopene into β-carotene (crtY), described in SEQ ID NO: 4, or a substantially homologous DNA sequence thereof; (d) DNA sequence encoding a polypeptide having such an enzymatic activity of Paracoccus sp. Strain MBIC1143 that converts phytoene into lycopene (crtI), described in SEQ ID NO: 5, or a substantially homologous DNA sequence thereof; (e) DNA sequence encoding a polypeptide having prephytoene synthase activity of Paracoccus sp. Strain MBIC1143 (crtB), as described in SEQ ID NO: 6, or a substantially homologous DNA sequence thereof; and (f) DNA sequence encoding a polypeptide having geranylgeranyl diphosphate synthase activity of Paracoccus sp. Strain MBIC1143 (crtE), as described in SEQ ID NO: 7, or a substantially homologous DNA sequence thereof.