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    • 36. 发明申请
    • Low-cost production of peptides
    • 低成本生产肽
    • US20050227321A1
    • 2005-10-13
    • US10971444
    • 2004-10-22
    • Joseph KrebsPaul ZornerIan Tomlinson
    • Joseph KrebsPaul ZornerIan Tomlinson
    • C07H21/04C07K5/06C07K14/47C12N1/21C12N9/48C12N15/74C12P21/04C12P21/06
    • C07K14/4723C07K2319/35C07K2319/50
    • The subject invention relates to a low cost method of producing peptides, including antimicrobial peptides (AMPs), by using microbes. The subject methods enable greatly improved yields of the peptide/AMP as compared to those heretofore known in the art. The subject methods also surprisingly enable the use of Pseudomonas fluorescens to produce AMPs and other peptides. There are several components of the subject invention, which can be used alone or in combination. The subject invention provides for the production of peptides/AMPs in concatemeric precursors. The subject invention also provides novel methods of assembling monomers into multimers, and of cleaving the multimers to yield active monomers. The subject invention also relates to the use of these multimers fused to carrier peptides to produce fusion proteins. Preferably, both the multimers and the fusion proteins (multimers with the carrier polypeptides) lack charge balancing. It has been surprisingly determined that it is not necessary to offset the positive charges of multiple copies of AMPs in multimeric constructs. Thus, the subject invention enables the use of a wider range of multimers and carrier peptides.
    • 本发明涉及通过使用微生物生产肽(包括抗微生物肽(AMP))的低成本方法。 与本领域已知的方法相比,本发明方法能够大大提高肽/ AMP的产率。 本发明的方法也令人惊奇地使得能够使用荧光假单胞菌来产生AMP和其他肽。 本发明的几个组分可单独使用或组合使用。 本发明提供了在并联前体中生产肽/ AMP。 本发明还提供了将单体组装成多聚体的新方法,以及裂解多聚体以产生活性单体。 本发明还涉及这些与载体肽融合的多聚体产生融合蛋白的用途。 优选地,多聚体和融合蛋白(携带多肽的多聚体)都缺乏电荷平衡。 已经令人惊讶地确定,不需要在多聚体构建体中抵消多个拷贝的AMP的正电荷。 因此,本发明使得能够使用更宽范围的多聚体和载体肽。