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    • 3. 发明申请
    • NOVEL ENGINEERED MICROORGANISM PRODUCING HOMO-SUCCINIC ACID AND METHOD FOR PREPARING SUCCINIC ACID USING THE SAME
    • 生产同型酸的新型工程化微生物及其制备方法
    • US20090203095A1
    • 2009-08-13
    • US12359322
    • 2009-01-25
    • Sang Yup LEESung Won LIMHyohak SONG
    • Sang Yup LEESung Won LIMHyohak SONG
    • C12P7/46C12N1/21C12N15/87
    • C12P7/46C12N1/20C12N9/0006C12N9/1029C12N9/1217C12N15/902C12Y203/01054Y02P20/52
    • The present invention relates to a mutant microorganism, which is selected from the group consisting of genus Mannheimia, genus Actinobacillus and genus Anaerobiospirillum, producing homo-succinic acid and a method for producing homo-succinic acid using the same, and more particularly to a mutant microorganism producing succinic acid at a high concentration while producing little or no other organic acids in anaerobic conditions, which is obtained by disrupting a gene encoding lactate dehydrogenase (ldhA), a gene encoding phosphotransacetylase (pta), and a gene encoding acetate kinase (ackA), without disrupting a gene encoding pyruvate formate lyase (pfl), as well as a method for producing succinic acid using the same. The inventive mutant microorganism has the property of having a high growth rate and succinic acid productivity while producing little or no organic acids, as compared to the prior strains producing succinic acid. Thus, the inventive mutant microorganism is useful to produce succinic acid for industrial use.
    • 本发明涉及一种突变体微生物,其选自人嗜血杆菌属(Mannheimia),放线杆菌属(Actinobacillus)和放线虫属(Anaerobiospirillum)属,产生同型琥珀酸,以及使用其制备均琥珀酸的方法,更具体地说,涉及突变体 通过破坏编码乳酸脱氢酶(ldhA)的基因,编码磷酸转乙酰酶(pta)的基因和编码乙酸激酶(ackA)的基因而获得的在厌氧条件下产生很少或不存在其它有机酸的微生物,产生高浓度的琥珀酸 ),而不破坏编码丙酮酸甲酸裂合酶(pfl)的基因,以及使用其生产琥珀酸的方法。 与生产琥珀酸的现有菌株相比,本发明的突变微生物具有生长速度快和琥珀酸生产率少的特性,同时产生很少或不含有机酸。 因此,本发明的突变微生物可用于生产用于工业用途的琥珀酸。
    • 4. 发明申请
    • Recombinant cells that highly express chromosomally-integrated heterologous genes
    • 高度表达染色体整合的异源基因的重组细胞
    • US20070172937A1
    • 2007-07-26
    • US11725728
    • 2007-03-20
    • Lonnie IngramKazuyoshi OhtaBrent Wood
    • Lonnie IngramKazuyoshi OhtaBrent Wood
    • C12N1/21C12N15/74
    • C12N15/67C12N9/1029C12N15/74C12Y203/01054
    • Recombinant host cells are obtained that comprise (A) a heterologous, polypeptide-encoding polynucleotide segment, stably integrated into a chromosome, which is under transcriptional control of an endogenous promoter and (B) a mutation that effects increased expression of the heterologous segment, resulting in enhanced production by the host cells of each polypeptide encoded by that segment, relative to production of each polypeptide by the host cells in the absence of the mutation. The increased expression thus achieved is retained in the absence of conditions that select for cells displaying such increased expression. When the integrated segment comprises, for example, ethanol-production genes from an efficient ethanol producer like Zymomonas mobilis, recombinant Escherichia coli and other enteric bacterial cells within the present invention are capable of converting a wide range of biomass-derived sugars efficiently to ethanol.
    • 获得重组宿主细胞,其包含(A)编码染色体的异源,编码多肽的多核苷酸片段,其在内源性启动子的转录控制下(B)产生异源片段表达增加的突变,导致 在不存在突变的情况下,通过宿主细胞增强由该片段编码的每种多肽的产生,相对于宿主细胞每种多肽的产生。 在没有选择用于显示这种增加的表达的细胞的条件的情况下,保留了如此实现的增加的表达。 当整合片段包括例如来自有效乙醇生产​​者的乙醇生产基因如运动发酵单胞菌,本发明中的重组大肠杆菌和其它肠道细菌细胞能够将大范围的生物质衍生的糖有效转化为乙醇。
    • 5. 发明授权
    • Recombinant cells that highly express chromosomally-integrated heterologous gene
    • 高度表达染色体整合的异源基因的重组细胞
    • US07192772B1
    • 2007-03-20
    • US09620060
    • 2000-07-21
    • Lonnie O. IngramKazuyoshi OhtaBrent E. Wood
    • Lonnie O. IngramKazuyoshi OhtaBrent E. Wood
    • C12N15/00C12N1/20C07H21/04
    • C12N15/67C12N9/1029C12N15/74C12Y203/01054
    • Recombinant host cells are obtained that comprise (A) a heterologous, polypeptide-encoding polynucleotide segment, stably integrated into a chromosome, which is under transcriptional control of an endogenous promoter and (B) a mutation that effects increased expression of the heterologous segment, resulting in enhanced production by the host cells of each polypeptide encoded by that segment, relative to production of each polypeptide by the host cells in the absence of the mutation. The increased expression thus achieved is retained in the absence of conditions that select for cells displaying such increased expression. When the integrated segment comprises, for example, ethanol-production genes from an efficient ethanol producer like Zymomonas mobilis, recombinant Escherichia coli and other enteric bacterial cells within the present invention are capable of converting a wide range of biomass-derived sugars efficiently to ethanol.
    • 获得重组宿主细胞,其包含(A)编码染色体的异源,编码多肽的多核苷酸片段,其在内源性启动子的转录控制下(B)产生异源片段表达增加的突变,导致 在不存在突变的情况下,通过宿主细胞增强由该片段编码的每种多肽的产生,相对于宿主细胞每种多肽的产生。 在没有选择用于显示这种增加的表达的细胞的条件的情况下,保留了如此实现的增加的表达。 当整合片段包括例如来自有效乙醇生产​​者的乙醇生产基因如运动发酵单胞菌,本发明中的重组大肠杆菌和其它肠道细菌细胞能够将大范围的生物质衍生的糖有效转化为乙醇。