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    • 2. 发明申请
    • MICROBIOLOGICAL PRODUCTION OF 3-HYDROXYPROPIONIC ACID
    • 3-羟基丙酸的微生物制备
    • WO2007042494A2
    • 2007-04-19
    • PCT/EP2006067182
    • 2006-10-09
    • DEGUSSAFORSCHUNGSZENTRUM JUELICH GMBHMARX ACHIMWENDISCH VOLKER FRITTMANN DORISBUCHHOLZ STEFAN
    • MARX ACHIMWENDISCH VOLKER FRITTMANN DORISBUCHHOLZ STEFAN
    • C12N15/52C12P7/18C12P7/40C12P13/06
    • C12P7/40C12P7/42C12P7/44
    • The invention relates to a cell which is genetically modified in relation to a wild type and exhibits at least one following properties: a) the activity of an enzyme E 1 , which is used for catalysing the conversion of pyruvate into oxalacetate or of an enzyme E 1b for catalysing the conversion of phosphoenolpyruvate into oxalacetate, and which is greater than the wild type activity and b) the activity of an enzyme E 2 , which is used for catalysing the conversion of aspartate into beta-alanine and which is greater than the wild type activity, wherein the inventive cell, in addition to the a) and b) properties, is characterised in that it exhibits at least one following property: c) the genetically modified cell is capable to eject beta-alanine therefrom and d) the genetically modified cell is capable to convert the beta-alanine into the 3-hydrixypropionic acid. A method for producing a genetically modified cell, the genetically modified cells obtainable by said method, a method for producing the 3-hydrixypropionic acid, a method for producing an acrylic acid, a method for producing polyacrylates, a method for producing acrylic acid esters and the use of cells for producing the 3-hydrixypropionic acid are also disclosed.
    • 本发明涉及一种比其野生型遗传修饰的细胞,其包含的特征a)或b)至少一种的:相比于它的野生型,酶E 1 的,该方法包括使一) 催化丙酮酸成草酰乙酸,或酶E 图1b ,其催化磷酸烯醇丙酮酸转化成草酰乙酸的,b)相比,其野生型,酶E的 2 ,这 催化天冬氨酸向β-丙氨酸的转化,其中,除了a的属性)或b)由所述性质中的至少一种)或d)的特征在于c中的细胞:c)中经遗传修饰的细胞能够从β-丙氨酸 去除细胞; d)经遗传修饰的细胞能够将β-丙氨酸转化为3-羟基丙酸。 本发明还涉及一种用于制造经遗传修饰的细胞的方法,通过该方法获得的遗传修饰的细胞,产生3-羟基丙酸,为生产丙烯酸的过程中,聚丙烯酸酯的制备方法,用于Acrylsäureestern的制备方法的方法和 细胞用于生产3-羟基丙酸的用途。
    • 7. 发明申请
    • NUCLEOTIDE SEQUENCES ENCODING THE HEMD AND HEMB GENES
    • 编码HEMD和HEMB基因的核苷酸序列
    • WO0234775A2
    • 2002-05-02
    • PCT/EP0111705
    • 2001-10-10
    • DEGUSSA
    • FARWICK MIKEHUTHMACHER KLAUSPFEFFERLE WALTERSCHISCHKA NATALIEMARX ACHIM
    • C12N9/88C12P13/08C07K14/34C12N9/00C12N9/10C12N15/10C12N15/63C12Q1/68
    • C12P13/08C12N9/88C12Y402/01024C12Y402/01075
    • The invention relates to an isolated polynucleotide containing a polynucleotide sequence, selected from the group a) polynucleotide that is at least 70 % identical with a polynucleotide encoding a polypeptide that contains the amino acid sequence of SEQ ID No. 2, b) polynucleotide that is at least 70 % identical with a polynucleotide encoding a polypeptide that contains the amino acid sequence of SEQ ID No. 3, c) polynucleotide encoding a polypeptide that contains an amino acid sequence that is at least 70 % identical with the amino acid sequence of SEQ ID No. 2, d) polynucleotide encoding a polypeptide that contains an amino acid sequence that is at least 70 % identical with the amino acid sequence of SEQ ID No. 3, e) polynucleotide that is complementary to the polynucleotides of a), b), c) and d), and f) polynucleotide containing at least 15 consecutive nucleotides of the polynucleotide sequence of a), b), c), d) and e), and a method for the fermentative production of L-amino acids using coryneform bacteria, in which at least the hemD-gene and/or the hemB-gene is/are amplified, and the use, as Hybridization probes, of polynucleotides that contain the sequences according to the invention.
    • 本发明涉及含有多核苷酸序列的分离的多核苷酸,所述多核苷酸序列选自:a)与编码含有SEQ ID No.2的氨基酸序列的多肽的多核苷酸至少70%相同的多核苷酸,b) 与编码含有SEQ ID No.3的氨基酸序列的多肽的多核苷酸至少70%相同,c)编码含有与SEQ ID No.3的氨基酸序列至少70%相同的氨基酸序列的多肽的多核苷酸 d)编码多肽的多核苷酸,所述多肽含有与SEQ ID No.3的氨基酸序列至少70%相同的氨基酸序列,e)与a)的多核苷酸互补的多核苷酸,b ),c)和d),和f)含有a),b),c),d)和e)的多核苷酸序列的至少15个连续核苷酸的多核苷酸,以及用于发酵生产L-氨基酸 ü 其中至少扩增hemD-基因和/或hemB-基因的棒状杆菌细菌,以及使用含有本发明序列的多核苷酸作为杂交探针。
    • 8. 发明申请
    • NOVEL NUCLEOTIDE SEQUENCES CODING FOR THE GLBO GENE
    • GLBO基因的新核苷酸序列编码
    • WO0194569A2
    • 2001-12-13
    • PCT/EP0104792
    • 2001-04-27
    • DEGUSSA
    • MOECKEL BETTINAMARX ACHIMPFEFFERLE WALTER
    • C07K14/34C07K14/805C12N1/21C12P13/04C12P13/08C12N15/00
    • C12P13/04C07K14/34C07K14/805C12P13/08
    • The present invention provides an isolated polynucleotide containing a polynucleotide sequence selected from the group a) polynucleotide which is at least 70% identical to a polynucleotide which codes for a polypeptide containing the amino acid sequence of SEQ ID no. 2, b) polynucleotide which codes for a polypeptide which contains an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID no. 2, c) polynucleotide which is complementary to the polynucleotides of a) or b), and d) polynucleotide containing at least 15 successive nucleotides of the polynucleotide sequence of a), b) or c), and a process for the fermentative production of L-amino acids with enhancement of the glbO gene which codes for the haemoglobin-like protein and the use of the above polynucleotides as a primer or hybridization probe.
    • 本发明提供了一种分离的多核苷酸,其含有多核苷酸序列,该多核苷酸序列选自a)多核苷酸,该多核苷酸与编码含有SEQ ID NO:1的氨基酸序列的多肽的多核苷酸具有至少70%的相同性。 2,b)编码多肽的多核苷酸,其含有与SEQ ID No:1的氨基酸序列至少70%相同的氨基酸序列。 2,c)与a)或b)的多核苷酸互补的多核苷酸,以及d)包含a),b)或c)的多核苷酸序列的至少15个连续核苷酸的多核苷酸,以及d)发酵生产 具有编码血红蛋白样蛋白质的glbO基因增强的L-氨基酸和使用上述多核苷酸作为引物或杂交探针。
    • 9. 发明申请
    • NUCLEOTIDE SEQUENCES CODING FOR THE CHRS GENE
    • 核糖体序列编码CHRS基因
    • WO0220572A2
    • 2002-03-14
    • PCT/EP0109096
    • 2001-08-07
    • DEGUSSA
    • BATHE BRIGITTESCHISCHKA NATALIEMARX ACHIMPFEFFERLE WALTER
    • C07K14/34C12N9/12C12N15/54C12P13/08C07K14/195
    • C12N9/1223A01K2217/075C07K14/34C12P13/08
    • The invention provides an isolated polynucleotide containing a polynucleotide sequence chosen from the group consisting of a) a polynucleotide which is at least 70% identical to a polynucleotide which codes for a polypeptide which contains the amino acid sequence in SEQ ID No. 2, b) a polynucleotide which codes for a polypeptide which contains an amino acid sequence which is at least 70% identical to the amino acid sequence in SEQ ID No. 2, c) a polynucleotide which is complementary to the polynucleotides in a) or b), and d) a polynucleotide containing a sequence of at least 15 consecutive nucleotides from the polynucleotide sequence in a), b) or c),and a process for the fermentative preparation of L-amino acids using coryneform bacteria in which at least the chrS gene present is attenuated, and the use of polynucleotides which contain sequences according to the invention as hybridization probes.
    • 本发明提供了一种分离的多核苷酸,其含有多核苷酸序列,所述多核苷酸序列选自a)与编码含有SEQ ID No.2所示氨基酸序列的多肽的多核苷酸至少70%相同的多核苷酸,b) 编码多肽的多核苷酸,其含有与SEQ ID No.2中的氨基酸序列至少70%相同的氨基酸序列,c)与a)或b)中的多核苷酸互补的多核苷酸,以及 d)含有a),b)或c)中多核苷酸序列至少15个连续核苷酸序列的多核苷酸,以及使用至少存在chrS基因的棒状细菌发酵制备L-氨基酸的方法 并且使用含有根据本发明的序列的多核苷酸作为杂交探针。
    • 10. 发明申请
    • NUCLEOTIDE SEQUENCES WHICH CODE FOR THE GORA GENE
    • 核苷酸序列,其代码为GORA基因
    • WO0222666A3
    • 2002-07-25
    • PCT/EP0109314
    • 2001-08-11
    • DEGUSSA
    • FARWICK MIKEHUTHMACHER KLAUSPFEFFERLE WALTERMARX ACHIM
    • C12N9/02C12P13/08C12N15/53C12N5/10C12P13/04C12Q1/68C12R1/15
    • C12N9/0036C12P13/08
    • The invention relates to an isolated polynucleotide comprising a polynucleotide sequence chosen from the group consisting of a) polynucleotide which is identical to the extent of at least 70% to a polynucleotide which codes for a polypeptide which comprises the amino acid sequence of SEQ ID No. 2, b) polynucleotide which codes for a polypeptide which comprises an amino acid sequence which is identical to the extent of at least 70% to the amino acid sequence of SEQ ID No. 2, c) polynucleotide which is complementary to the polynucleotides of a) or b), and d) polynucleotide comprising at least 15 successive nucleotides of the polynucleotide sequence of a), b) or c), and a process for the fermentative preparation of L-amino acids using coryneform bacteria in which at least the gorA gene is present in attenuated form, and the use of polynucleotides which comprise the sequences according to the invention as hybridization probes.
    • 本发明涉及一种分离的多核苷酸,其包含多核苷酸序列,所述多核苷酸序列选自a)多核苷酸,其与编码多肽的多核苷酸的程度相同,所述多核苷酸包含SEQ ID No的氨基酸序列 2,b)编码多肽的多核苷酸,其包含与至少70%与SEQ ID No.2的氨基酸序列相同程度的氨基酸序列,c)多核苷酸,其与 )或b),和d)包含a),b)或c)的多核苷酸序列的至少15个连续核苷酸的多核苷酸,以及使用棒状细菌发酵制备L-氨基酸的方法,其中至少gorA 基因以减毒形式存在,并且使用包含根据本发明的序列的多核苷酸作为杂交探针。