USE OF MULTIPLE TRANSFORMATION ENHANCER SEQUENCES TO IMPROVE PLANT TRANSFORMATION EFFICIENCY
    34.
    发明申请
    USE OF MULTIPLE TRANSFORMATION ENHANCER SEQUENCES TO IMPROVE PLANT TRANSFORMATION EFFICIENCY 审中-公开
    使用多变换增强子序列来提高植物转化效率

    公开(公告)号:US20170009246A1

    公开(公告)日:2017-01-12

    申请号:US15258901

    申请日:2016-09-07

    CPC classification number: C12N15/8205 C12N15/8202

    Abstract: The present invention relates to methods and compositions for improving the efficiency of Agrobacterium- and Rhizobium-mediated plant cell transformation by use of additional transformation enhancer sequences, such as overdrive or TSS sequences, operably linked to a T-DNA border sequence on a recombinant construct that comprises T-DNA.

    Abstract translation: 本发明涉及通过使用与重组构建体上的T-DNA边界序列有效连接的其它转化增强子序列(例如过度驱动或TSS序列)来提高农杆菌和根瘤土壤介导的植物细胞转化效率的方法和组合物 其包含T-DNA。

    VECTORS AND METHODS FOR IMPROVED PLANT TRANSFORMATION EFFICIENCY
    35.
    发明申请
    VECTORS AND METHODS FOR IMPROVED PLANT TRANSFORMATION EFFICIENCY 审中-公开
    改进植物转化效率的方向和方法

    公开(公告)号:US20150232865A1

    公开(公告)日:2015-08-20

    申请号:US14642674

    申请日:2015-03-09

    CPC classification number: C12N15/8205

    Abstract: Methods and compositions for improved bacterial-mediated plant transformation are provided. The methods generally allow plant transformation with reduced vector backbone integration and a high frequency of low-copy transformation events. Vectors for achieving these results are described, as are methods for their use.

    Abstract translation: 提供了用于改善细菌介导的植物转化的方法和组合物。 这些方法通常允许具有减少的载体骨架整合和高频率的低拷贝转化事件的植物转化。 描述了用于实现这些结果的载体,以及它们使用的方法。

    METHODS FOR PLASTID TRANSFORMATION
    38.
    发明申请

    公开(公告)号:US20230057290A1

    公开(公告)日:2023-02-23

    申请号:US17818913

    申请日:2022-08-10

    Abstract: Methods and compositions for plastid transformation and regeneration or development of transplastomic plants are provided. Embryo explants may be excised from seeds, and their meristematic tissue may be transformed directly without initiation of any callus phase before and/or after transformation. The present methods may be performed with fewer culturing steps relative to conventional methods, thereby enabling more rapid and efficient production of targeted transplastomic events in plants.

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