发明授权
US08080402B2 Surface expression method of peptides P5 and Anal3 using the gene encoding poly-gamma-glutamate synthetase
有权
使用编码聚-γ-谷氨酸合成酶的基因的肽P5和Anal3的表面表达方法
- 专利标题: Surface expression method of peptides P5 and Anal3 using the gene encoding poly-gamma-glutamate synthetase
- 专利标题(中): 使用编码聚-γ-谷氨酸合成酶的基因的肽P5和Anal3的表面表达方法
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申请号: US11622158申请日: 2007-01-11
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公开(公告)号: US08080402B2公开(公告)日: 2011-12-20
- 发明人: Moon-Hee Sung , Seung-Pyo Hong , Jong-Su Lee , Chang-Min Jung , Kyung-Soo Hahm , Dong-Gun Lee , Yoon Kyung Park , Chul-Joong Kim , Ha-Ryoung Poo
- 申请人: Moon-Hee Sung , Seung-Pyo Hong , Jong-Su Lee , Chang-Min Jung , Kyung-Soo Hahm , Dong-Gun Lee , Yoon Kyung Park , Chul-Joong Kim , Ha-Ryoung Poo
- 申请人地址: KR Daejon KR Daejon KR Gwangji
- 专利权人: Bioleaders Corporation,Korea Research Institute of Bioscience and Biotechnology,Chosun University
- 当前专利权人: Bioleaders Corporation,Korea Research Institute of Bioscience and Biotechnology,Chosun University
- 当前专利权人地址: KR Daejon KR Daejon KR Gwangji
- 代理机构: Moore & Van Allen PLLC
- 代理商 Tristan A. Fuierer; Andrew D. Gerschutz
- 主分类号: C12N15/00
- IPC分类号: C12N15/00 ; C12N1/21 ; A61K48/00
摘要:
The present invention relates to a method for expressing each of peptide antibiotics P5 3 and Anal3 35 having amphiphilicity and showing antibacterial, antifungal and anticancer activities 61, 63, 65, 67, 69, 71, on the microbial surface, using a vector containing outer membrane protein genes (pgsBCA) that are derived from Bacillus sp. strains and involved in the synthesis of poly-gamma-glutamate. Moreover, the present invention relates to lactic acid-forming bacteria having each of the peptide antibiotics P5 15 and Anal3 43 expressed on their surface, and the use thereof. According to the present invention, the peptide antibiotics can be expressed on the surface of various microorganisms transformed with the surface expression vectors. The inventive method for the surface expression of the peptide antibiotics allows the peptide antibiotics to be mass-produced without a purification process. Thus, the inventive method has very high industrial applicability. Further, the present invention can be applied to other peptide antibiotics besides P5 3 and Anal 3 35.
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