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    • 1. 发明专利
    • Fertilization production of solid-state nonvolatile microorganism metabolic product
    • 固态非挥发性微生物代谢产物的生产
    • JP2013048625A
    • 2013-03-14
    • JP2012223174
    • 2012-10-05
    • Basf Seビーエーエスエフ ソシエタス・ヨーロピアBasf Se
    • POMPEJUS MARKUSFREYER STEPHANLOHSCHEIDT MARKUSZELDER OSKARBOY MATTHIASSCHOLTEN EDZARD
    • C12P19/14C12P39/00
    • C12P13/08A23K10/12A23L7/104C12P7/46C12P13/02C12P13/10C12P13/12C12P13/14C12P13/24C12P19/14
    • PROBLEM TO BE SOLVED: To provide a method for producing at least one nonvolatile microorganism metabolic product by performing micororganism-fertilization based on sugar.SOLUTION: In the method, a microorganism culture which produces a desired metabolic product is cultivated by using a sugar-containing liquid culture medium containing a monosaccharide content exceeding 20 wt.% on the basis of the total weight of the liquid culture medium, most of volatile components of fertilization liquids are removed, and the pickles are produced by (a1) a step of powdering a starch supply raw material selected from grains, and (a2) a step of liquefying the powdered material in an aqueous liquid under the existence of at least one starch liquefied enzyme, then saccharifying the material by using saccharified enzyme, adding a partial amount of a crushed raw material to the aqueous liquid continuously or in a batch manner, and performing the liquefaction. Related to a solid preparation of the obtained nonvolatile microorganism metabolic product, the method uses the solid preparation as an additive or a supplementary agent to the food of human beings or animals, or fabric, leather, cellose, paper, or for treating the surface the product.
    • 待解决的问题:提供通过基于糖进行微生物施肥来生产至少一种非挥发性微生物代谢产物的方法。 解决方案:在该方法中,通过使用含有超过20重量%的单糖含量的含糖液体培养基,基于液体培养基的总重量培养产生所需代谢产物的微生物培养物 去除受精液体的大部分挥发性成分,并且通过(a1)粉碎选自谷物的淀粉供给原料的工序来制造泡菜,(a2)在水溶液中粉化材料的液化步骤 存在至少一种淀粉液化酶,然后通过使用糖化酶对材料进行糖化,连续地或间歇地向水性液体中分批加入一部分破碎的原料,并进行液化。 与所获得的非挥发性微生物代谢产物的固体制剂相关,该方法使用固体制剂作为人或动物的食物或织物,皮革,纤维素,纸或用于处理表面的添加剂或补充剂 产品。 版权所有(C)2013,JPO&INPIT
    • 4. 发明专利
    • Psod expression unit
    • Psod表达单位
    • JP2008212154A
    • 2008-09-18
    • JP2008095699
    • 2008-04-02
    • Basf Seビーエーエスエフ ソシエタス・ヨーロピアBasf Se
    • KROEGER BURKHARDZELDER OSKARKLOPPROGGE CORINNASCHROEDER HARTWIGHAEFNER STEFAN
    • C12N15/09C12N1/15C12N1/19C12N1/21C12N5/10C12N9/02C12N15/77C12P13/08C12R1/15
    • C12N15/77
    • PROBLEM TO BE SOLVED: To provide the use of a nucleic acid sequence for controlling the transcription and expression of a gene, to provide a new promoter and expression unit itself, to provide a method for modifying or inducing the transcription rate and/or the expression rate of the gene, to provide an expression cassette comprising the expression unit, to provide a genetically modified microorganism having the modified or induced transcription rate and/or expression rate and to provide a method for producing a biosynthetic product by culturing the genetically modified microorganism. SOLUTION: There is provided the use of (A) a specific nucleic acid sequence, (B) a sequence induced from the specific nucleic acid sequence by substitution, insertion or deletion of a nucleotide and having at least 90% homogeneity to the sequence at the nucleic acid level, (C) a nucleic acid sequence hybridizing to the nucleic acid sequence under stringent conditions or (D) a nucleic acid comprising a fragment functionally equivalent to the sequence (A), (B) or (C) and having a promoter activity. COPYRIGHT: (C)2008,JPO&INPIT
    • 待解决的问题:提供用于控制基因的转录和表达的核酸序列的用途,以提供新的启动子和表达单元本身,以提供修饰或诱导转录速率和/ 或基因的表达速率,以提供包含表达单元的表达盒,以提供具有修饰或诱导的转录速率和/或表达率的遗传修饰微生物,并提供通过遗传培养生产生物合成产物的方法 修饰微生物。 提供(A)特定核酸序列的用途,(B)通过取代,插入或缺失核苷酸并且具有至少90%同一性的特异性核酸序列诱导的序列 (C)在严格条件下与核酸序列杂交的核酸序列或(D)包含与(A),(B)或(C)和(B)的序列功能等同的片段的核酸和 具有启动子活性。 版权所有(C)2008,JPO&INPIT
    • 9. 发明专利
    • Pgro EXPRESSION UNIT
    • Pgro表达单位
    • JP2008237218A
    • 2008-10-09
    • JP2008095696
    • 2008-04-02
    • Basf Seビーエーエスエフ ソシエタス・ヨーロピアBasf Se
    • KROEGER BURKHARDZELDER OSKARKLOPPROGGE CORINNASCHROEDER HARTWIGHAEFNER STEFAN
    • C12N15/09C07K14/34C12N1/15C12N1/19C12N1/21C12N9/00C12N15/77C12P13/08
    • C12P13/08C07K14/34C12N15/77
    • PROBLEM TO BE SOLVED: To provide the use of nucleic acid sequences for regulating gene transcription and expression, a novel promoter and an expression unit itself, a method for modifying or inducing the gene transcription rate and/or expression rate, an expression cassette containing the expression unit, genetically modified microorganism having a modified or induced transcription rate and/or expression rate, and a method for producing biosynthetic products by culturing the genetically modified microorganism. SOLUTION: The use of a nucleic acid having promotor activity containing (A) a specific nucleic acid sequence for transcribing the gene, (B) a sequence having at least 90% homology and derived by substitution, insertion or deletion of nucleotides from the (A) sequence, (C) a nucleic acid sequence hybridizing under stringent conditions with the (A) sequence or (D) a functionally equivalent fragment of the sequence (A), (B) or (C) is provided. COPYRIGHT: (C)2009,JPO&INPIT
    • 待解决的问题:提供用于调节基因转录和表达的核酸序列的使用,新型启动子和表达单元本身,修饰或诱导基因转录速率和/或表达率的方法,表达 含有表达单位的盒,具有修饰或诱导的转录速率和/或表达率的遗传修饰微生物,以及通过培养经遗传修饰的微生物生产生物合成产物的方法。 解决方案:使用具有启动子活性的核酸,其含有(A)用于转录该基因的特异性核酸序列,(B)具有至少90%同源性并通过其核苷酸取代,插入或缺失衍生的序列 (A)序列,(C)在严格条件下与(A)序列杂交的核酸序列或(D)序列(A),(B)或(C)的功能等同片段的核酸序列。 版权所有(C)2009,JPO&INPIT