Process for preparing L-amino acids with corynebacteria with enhanced nucleotide sequences coding for pknD
    1.
    发明授权
    Process for preparing L-amino acids with corynebacteria with enhanced nucleotide sequences coding for pknD 有权
    用增强的编码pknD的核苷酸序列制备具有棒状杆菌的L-氨基酸的方法

    公开(公告)号:US07226763B2

    公开(公告)日:2007-06-05

    申请号:US11110837

    申请日:2005-04-21

    CPC分类号: C12N9/1205 C12R1/15

    摘要: An isolated polynucleotide which contains a polynucleotide sequence selected from the group comprising: (a) a polynucleotide which is at least 70% identical to a polynucleotide coding for a polypeptide containing the amino acid sequence of SEQ ID No. 2, (b) a polynucleotide coding for a polypeptide containing an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID No. 2, (c) a polynucleotide which is complementary to the polynucleotides of (a) or (b), and (d) a polynucleotide containing at least 15 consecutive nucleotides of the polynucleotide sequence of (a), (b), or (c), and a fermentation process for the preparation of L-amino acids using corynebacteria in which at least the pknD gene is amplified, and to the use, as hybridization probes, of polynucleotides containing the sequences according to the invention.

    摘要翻译: 一种分离的多核苷酸,其含有选自以下的多核苷酸序列:(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%的多核苷酸,(b) 编码含有与SEQ ID No.2的氨基酸序列至少70%相同的氨基酸序列的多肽,(c)与(a)或(b)的多核苷酸互补的多核苷酸和( 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,以及使用棒状杆菌制备L-氨基酸的发酵方法,其中至少pknD基因是 扩增和使用含有本发明序列的多核苷酸作为杂交探针。

    Nucleotide sequences coding for the pknD gene
    2.
    发明申请
    Nucleotide sequences coding for the pknD gene 有权
    编码pknD基因的核苷酸序列

    公开(公告)号:US20050255566A1

    公开(公告)日:2005-11-17

    申请号:US11110837

    申请日:2005-04-21

    CPC分类号: C12N9/1205 C12R1/15

    摘要: An isolated polynucleotide which contains a polynucleotide sequence selected from the group comprising: (a) a polynucleotide which is at least 70% identical to a polynucleotide coding for a polypeptide containing the amino acid sequence of SEQ ID No. 2, (b) a polynucleotide coding for a polypeptide containing an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID No. 2, (c) a polynucleotide which is complementary to the polynucleotides of (a) or (b), and (d) a polynucleotide containing at least 15 consecutive nucleotides of the polynucleotide sequence of (a), (b), or (c), and a fermentation process for the preparation of L-amino acids using corynebacteria in which at least the pknD gene is amplified, and to the use, as hybridization probes, of polynucleotides containing the sequences according to the invention.

    摘要翻译: 一种分离的多核苷酸,其含有选自以下的多核苷酸序列:(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%的多核苷酸,(b) 编码含有与SEQ ID No.2的氨基酸序列至少70%相同的氨基酸序列的多肽,(c)与(a)或(b)的多核苷酸互补的多核苷酸和( 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,以及使用棒状杆菌制备L-氨基酸的发酵方法,其中至少pknD基因是 扩增和使用含有本发明序列的多核苷酸作为杂交探针。

    Nucleotide sequences coding for the pknD gene

    公开(公告)号:US06927052B2

    公开(公告)日:2005-08-09

    申请号:US09949971

    申请日:2001-09-12

    CPC分类号: C12N9/1205 C12R1/15

    摘要: An isolated polynucleotide which contains a polynucleotide sequence selected from the group comprising: (a) a polynucleotide which is at least 70% identical to a polynucleotide coding for a polypeptide containing the amino acid sequence of SEQ ID No. 2, (b) a polynucleotide coding for a polypeptide containing an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID No. 2, (c) a polynucleotide which is complementary to the polynucleotides of (a) or (b), and (d) a polynucleotide containing at least 15 consecutive nucleotides of the polynucleotide sequence of (a), (b), or (c), and a fermentation process for the preparation of L-amino acids using corynebacteria in which at least the pknD gene is amplified, and to the use, as hybridization probes, of polynucleotides containing the sequences according to the invention.

    Process for the production of L-amino acids by fermentation using coryneform bacteria with an attenuated mqo gene
    4.
    发明授权
    Process for the production of L-amino acids by fermentation using coryneform bacteria with an attenuated mqo gene 有权
    使用具有减毒mqo基因的棒状细菌通过发酵生产L-氨基酸的方法

    公开(公告)号:US07049106B2

    公开(公告)日:2006-05-23

    申请号:US10118325

    申请日:2002-04-09

    IPC分类号: C12P13/04

    CPC分类号: C12N9/0036 C12P13/08

    摘要: A process for the production of an L-amino acid wherein coryneform bacteria (e.g. Coryneform glutamicum) in which expression of the mqo gene coding for malate quinone oxidoreductase is attenuated are fermented to produce a desired amino acid, and the amino acid is concentrated in the medium or cells and isolated. Optionally, further genes in the biosynthetic pathway of the desired amino acid are enhanced, and/or metabolic pathways that reduce formation of the amino acid are suppressed.

    摘要翻译: 其中生产L-氨基酸的方法,其中将其中编码苹果酸醌氧化还原酶的mqo基因的表达减弱的棒状细菌(例如谷氨酸棒杆菌)被发酵以产生所需的氨基酸,并且氨基酸浓缩在 培养基或细胞分离。 任选地,所需氨基酸的生物合成途径中的其它基因被增强,和/或减少氨基酸形成的代谢途径被抑制。

    Nucleotide sequences coding for the pknB gene
    7.
    发明申请
    Nucleotide sequences coding for the pknB gene 有权
    编码pknB基因的核苷酸序列

    公开(公告)号:US20050130277A1

    公开(公告)日:2005-06-16

    申请号:US10940606

    申请日:2004-09-15

    摘要: An isolated polynucleotide which contains a polynucleotide sequence selected from the group comprising: (a) a polynucleotide which is at least 70% identical to a polynucleotide coding for a polypeptide containing the amino acid sequence of SEQ ID No. 2, (b) a polynucleotide coding for a polypeptide containing an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID No. 2, (c) a polynucleotide which is complementary to the polynucleotides of (a) or (b), and (d) a polynucleotide containing at least 15 consecutive nucleotides of the polynucleotide sequence of (a), (b) or (c), and a fermentation process for the preparation of L-amino acids using corynebacteria in which at least the pknB gene is amplified, and to the use, as hybridization probes, of polynucleotides containing the sequences according to the invention.

    摘要翻译: 一种分离的多核苷酸,其含有选自以下的多核苷酸序列:(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%的多核苷酸,(b) 编码含有与SEQ ID No.2的氨基酸序列至少70%相同的氨基酸序列的多肽,(c)与(a)或(b)的多核苷酸互补的多核苷酸和( 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,以及使用其中至少pknB基因被扩增的棒状杆菌制备L-氨基酸的发酵方法 以及使用含有本发明序列的多核苷酸作为杂交探针。

    Nucleotide sequences coding for the sigM gene
    8.
    发明授权
    Nucleotide sequences coding for the sigM gene 失效
    编码sigM基因的核苷酸序列

    公开(公告)号:US06995000B2

    公开(公告)日:2006-02-07

    申请号:US09942935

    申请日:2001-08-31

    IPC分类号: C12P13/04

    CPC分类号: C07K14/34 C12P13/08

    摘要: The invention relates to an isolated polynucleotide from Corynebacterium glutamicum having a polynucleotide sequence which encodes the sigma factor M (sigM) gene, and a host-vector system having a coryneform host bacterium in which the sigM gene is present in enhanced form and a vector which carries at least the sigM gene according to SEQ ID No 1, and the use of polynucleotides which comprise the sequences according to the invention as hybridization probes.

    摘要翻译: 本发明涉及具有编码σ因子M(sigM)基因的多核苷酸序列的谷氨酸棒杆菌分离的多核苷酸,以及具有其中sigM基因以增强形式存在的棒状细胞宿主细菌的宿主 - 载体系统和载体, 至少携带根据SEQ ID No 1的sigM基因,以及使用包含根据本发明的序列的多核苷酸作为杂交探针。

    Nucleotide sequences coding for the pknB gene

    公开(公告)号:US06939692B2

    公开(公告)日:2005-09-06

    申请号:US09949970

    申请日:2001-09-12

    IPC分类号: C12N9/12 C12P13/04

    摘要: An isolated polynucleotide which contains a polynucleotide sequence selected from the group comprising: (a) a polynucleotide which is at least 70% identical to a polynucleotide coding for a polypeptide containing the amino acid sequence of SEQ ID No. 2, (b) a polynucleotide coding for a polypeptide containing an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID No. 2, (c) a polynucleotide which is complementary to the polynucleotides of (a) or (b), and (d) a polynucleotide containing at least 15 consecutive nucleotides of the polynucleotide sequence of (a), (b) or (c), and a fermentation process for the preparation of L-amino acids using corynebacteria in which at least the pknB gene is amplified, and to the use, as hybridization probes, of polynucleotides containing the sequences according to the invention.