IN VITRO METHODS FOR THE INDUCTION AND MAINTENANCE OF PLANT CELL LINES AS SINGLE SUSPENSION CELLS WITH INTACT CELL WALLS, AND TRANSFORMATION THEREOF
    1.
    发明申请
    IN VITRO METHODS FOR THE INDUCTION AND MAINTENANCE OF PLANT CELL LINES AS SINGLE SUSPENSION CELLS WITH INTACT CELL WALLS, AND TRANSFORMATION THEREOF 有权
    用于诱导和维持植物细胞系作为具有细胞壁的单个悬浮细胞的体外方法及其转化

    公开(公告)号:US20120034697A1

    公开(公告)日:2012-02-09

    申请号:US13206637

    申请日:2011-08-10

    IPC分类号: C12N5/04

    摘要: The subject invention provides simple and consistent methods to break suspension cell aggregates to single cells with intact primary cell walls. The subject invention relates in part to cell separation of suspension cell aggregates cultured in medium containing pectin-degrading enzymes or tubulin de-polymerizing compounds including colchicine. The subject invention also relates to novel uses of compounds for such purposes. Another aspect of the subject invention relates to transformation of the subject, isolated cells. Such processes simplify and integrate single-cell-based transformation and selection processes into transgenic and transplastomic event-generation work processes. The subject invention also removes technical constraints and produces marker-free and uniformly expressing transgenic lines in a high throughput fashion to support various needs of animal health, biopharma, and trait and crop protection platforms.

    摘要翻译: 本发明提供简单且一致的方法来将悬浮细胞聚集体破碎成具有完整原始细胞壁的单个细胞。 本发明部分涉及在包含果胶降解酶或包含秋水仙素的微管蛋白去聚合化合物的培养基中培养的悬浮细胞聚集体的细胞分离。 本发明还涉及化合物用于这些目的的新用途。 本发明的另一方面涉及受试者,分离的细胞的转化。 这样的过程简化并将基于单细胞的转化和选择过程整合到转基因和转基因组事件生成工作过程中。 本发明还消除了技术限制,并以高通量方式产生无标记和均匀表达的转基因品系,以支持动物健康,生物制药和性状和作物保护平台的各种需要。

    In vitro methods for the induction and maintenance of plant cell lines as single suspension cells with intact cell walls, and transformation thereof
    2.
    发明授权
    In vitro methods for the induction and maintenance of plant cell lines as single suspension cells with intact cell walls, and transformation thereof 有权
    诱导和维持作为具有完整细胞壁的单一悬浮细胞的植物细胞系的体外方法及其转化

    公开(公告)号:US08012752B2

    公开(公告)日:2011-09-06

    申请号:US11965543

    申请日:2007-12-27

    IPC分类号: C12N5/00 C12N5/02

    摘要: The subject invention provides simple and consistent methods to break suspension cell aggregates to single cells with intact primary cell walls. The subject invention relates in part to cell separation of suspension cell aggregates cultured in medium containing pectin-degrading enzymes or tubulin de-polymerizing compounds including colchicine. The subject invention also relates to novel uses of compounds for such purposes. Another aspect of the subject invention relates to transformation of the subject, isolated cells. Such processes simplify and integrate single-cell-based transformation and selection processes into transgenic and transplastomic event-generation work processes. The subject invention also removes technical constraints and produces marker-free and uniformly expressing transgenic lines in a high throughput fashion to support various needs of animal health, biopharma, and trait and crop protection platforms.

    摘要翻译: 本发明提供简单且一致的方法来将悬浮细胞聚集体破碎成具有完整原始细胞壁的单个细胞。 本发明部分涉及在包含果胶降解酶或包含秋水仙素的微管蛋白去聚合化合物的培养基中培养的悬浮细胞聚集体的细胞分离。 本发明还涉及化合物用于这些目的的新用途。 本发明的另一方面涉及受试者,分离的细胞的转化。 这样的过程简化并将基于单细胞的转化和选择过程整合到转基因和转基因组事件生成工作过程中。 本发明还消除了技术限制,并以高通量方式产生无标记和均匀表达的转基因品系,以支持动物健康,生物制药和性状和作物保护平台的各种需要。

    In vitro methods for the induction and maintenance of plant cell lines as single suspension cells with intact cell walls
    3.
    发明授权
    In vitro methods for the induction and maintenance of plant cell lines as single suspension cells with intact cell walls 有权
    用于诱导和维持植物细胞系作为具有完整细胞壁的单一悬浮细胞的体外方法

    公开(公告)号:US08206983B2

    公开(公告)日:2012-06-26

    申请号:US13206637

    申请日:2011-08-10

    IPC分类号: C12N5/00 C12N5/02

    摘要: The subject invention provides simple and consistent methods to break suspension cell aggregates to single cells with intact primary cell walls. The subject invention relates in part to cell separation of suspension cell aggregates cultured in medium containing pectin-degrading enzymes or tubulin de-polymerizing compounds including colchicine. The subject invention also relates to novel uses of compounds for such purposes. Another aspect of the subject invention relates to transformation of the subject, isolated cells. Such processes simplify and integrate single-cell-based transformation and selection processes into transgenic and transplastomic event-generation work processes. The subject invention also removes technical constraints and produces marker-free and uniformly expressing transgenic lines in a high throughput fashion to support various needs of animal health, biopharma, and trait and crop protection platforms.

    摘要翻译: 本发明提供简单且一致的方法来将悬浮细胞聚集体破碎成具有完整原始细胞壁的单个细胞。 本发明部分涉及在包含果胶降解酶或包含秋水仙素的微管蛋白去聚合化合物的培养基中培养的悬浮细胞聚集体的细胞分离。 本发明还涉及化合物用于这些目的的新用途。 本发明的另一方面涉及受试者,分离的细胞的转化。 这样的过程简化并将基于单细胞的转化和选择过程整合到转基因和转基因组事件生成工作过程中。 本发明还消除了技术限制,并以高通量方式产生无标记和均匀表达的转基因品系,以支持动物健康,生物制药和性状和作物保护平台的各种需要。

    In Vitro Methods for the Induction and Maintenance of Plant Cell Lines as Single Suspension Cells With Intact Cell Walls, and Transformation Thereof
    4.
    发明申请
    In Vitro Methods for the Induction and Maintenance of Plant Cell Lines as Single Suspension Cells With Intact Cell Walls, and Transformation Thereof 有权
    植物细胞系诱导和维持作为具有完整细胞壁的单一悬浮细胞的体外方法及其转化

    公开(公告)号:US20100159598A1

    公开(公告)日:2010-06-24

    申请号:US11965543

    申请日:2007-12-27

    IPC分类号: C12N15/82 C12N5/04 C12N5/10

    摘要: The subject invention provides simple and consistent methods to break suspension cell aggregates to single cells with intact primary cell walls. The subject invention relates in part to cell separation of suspension cell aggregates cultured in medium containing pectin-degrading enzymes or tubulin de-polymerizing compounds including colchicine. The subject invention also relates to novel uses of compounds for such purposes. Another aspect of the subject invention relates to transformation of the subject, isolated cells. Such processes simplify and integrate single-cell-based transformation and selection processes into transgenic and transplastomic event-generation work processes. The subject invention also removes technical constraints and produces marker-free and uniformly expressing transgenic lines in a high throughput fashion to support various needs of animal health, biopharma, and trait and crop protection platforms.

    摘要翻译: 本发明提供简单且一致的方法来将悬浮细胞聚集体破碎成具有完整原始细胞壁的单个细胞。 本发明部分涉及在包含果胶降解酶或包含秋水仙素的微管蛋白去聚合化合物的培养基中培养的悬浮细胞聚集体的细胞分离。 本发明还涉及化合物用于这些目的的新用途。 本发明的另一方面涉及受试者,分离的细胞的转化。 这样的过程简化并将基于单细胞的转化和选择过程整合到转基因和转基因组事件生成工作过程中。 本发明还消除了技术限制,并以高通量方式产生无标记和均匀表达的转基因品系,以支持动物健康,生物制药和性状和作物保护平台的各种需要。

    PLANT PEPTIDE GAMMA-ZEIN FOR DELIVERY OF BIOMOLECULES INTO PLANT CELLS
    10.
    发明申请
    PLANT PEPTIDE GAMMA-ZEIN FOR DELIVERY OF BIOMOLECULES INTO PLANT CELLS 有权
    用于将生物分子植入植物细胞的植物肽GAMMA-ZEIN

    公开(公告)号:US20110247100A1

    公开(公告)日:2011-10-06

    申请号:US13042565

    申请日:2011-03-08

    CPC分类号: C12N15/8206

    摘要: A method of introducing a molecule of interest into a plant cell having a cell wall includes interacting a gamma-zein peptide with a molecule of interest to form a gamma-zein linked structure. The gamma-zein linked structure is then placed in contact with the plant cell having a cell wall, and allowing uptake of the gamma-zein linked structure into the plant cell. Alternatively, a gene of interest can be expressed in a plant cell having an intact cell wall by interacting a gamma-zein peptide with the gene of interest to form a gamma-zein linked gene structure, allowing uptake of the gamma-zein linked gene structure into the plant cell, and expressing the gene of interest in the plant cell and its progeny.

    摘要翻译: 将感兴趣的分子引入具有细胞壁的植物细胞中的方法包括将γ-玉米醇溶蛋白肽与感兴趣的分子相互作用以形成γ-玉米醇溶蛋白连接的结构。 然后将γ-玉米醇溶蛋白连接的结构与具有细胞壁的植物细胞接触,并允许将γ-玉米醇溶蛋白连接的结构摄取到植物细胞中。 或者,通过将γ-玉米醇溶蛋白肽与感兴趣的基因相互作用以形成γ-玉米醇溶蛋白连接的基因结构,可以在具有完整细胞壁的植物细胞中表达感兴趣的基因,从而允许γ-玉米醇溶蛋白连接的基因结构 进入植物细胞,并在植物细胞及其后代中表达感兴趣的基因。