Microorganisms for n-Propanol Production
    1.
    发明申请
    Microorganisms for n-Propanol Production 审中-公开
    正丙醇生产微生物

    公开(公告)号:US20140134691A1

    公开(公告)日:2014-05-15

    申请号:US14118856

    申请日:2012-05-25

    Applicant: Novozymes A/S

    CPC classification number: C12P7/04 C12N1/20 C12P5/026

    Abstract: Described herein are host cells comprising lactate dehydrogenase activity, lactaldehyde dehydrogenase activity, lactaldehyde reductase activity, propanediol dehydratase activity, and/or n-propanol dehydrogenase activity, wherein the cells are capable of producing n-propanol. Also described are methods of producing n-propanol comprising (a) cultivating the host cells having lactate dehydrogenase activity, lactaldehyde dehydrogenase activity, lactaldehyde reductase activity, propanediol dehydratase activity, and/or n-propanol dehydrogenase activity in a medium under suitable conditions to produce n-propanol; and (b) recovering the n-propanol. Methods of producing polypropylene from the recombinant n-propanol are also provided.

    Abstract translation: 本文描述了包含乳酸脱氢酶活性,乳醛脱氢酶活性,乳醛还原酶活性,丙二醇脱水酶活性和/或正丙醇脱氢酶活性的宿主细胞,其中细胞能够产生正丙醇。 还描述了生产正丙醇的方法,其包括(a)在合适条件下培养具有乳酸脱氢酶活性,内醛脱氢酶活性,乳醛还原酶活性,丙二醇脱水酶活性和/或正丙醇脱氢酶活性的宿主细胞,以产生 正丙醇 和(b)回收正丙醇。 还提供了从重组正丙醇制备聚丙烯的方法。

    Bacterial Mutants with Improved Transformation Efficiency
    2.
    发明申请
    Bacterial Mutants with Improved Transformation Efficiency 有权
    具有改善转化效率的细菌突变体

    公开(公告)号:US20150125959A1

    公开(公告)日:2015-05-07

    申请号:US14397512

    申请日:2013-05-17

    Applicant: Novozymes A/S

    CPC classification number: C12N15/746 C12N9/1007 C12N9/22

    Abstract: Provided herein are Lactobacillus mutants having improved transformation efficiency, comprising a disruption to an endogenous gene encoding a restriction modification system protein. Also described are methods for producing the mutants, methods for generating transformants using the mutants, and methods for producing a polypeptide or fermentation product using the mutants.

    Abstract translation: 本文提供了具有改善的转化效率的乳杆菌突变体,其包含对编码限制性修饰系统蛋白质的内源基因的破坏。 还描述了用于产生突变体的方法,使用突变体产生转化体的方法,以及使用突变体产生多肽或发酵产物的方法。

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