Surface expression method of peptides P5 and Anal3 using the...

Drug – bio-affecting and body treating compositions – Whole live micro-organism – cell – or virus containing – Genetically modified micro-organism – cell – or virus

Reexamination Certificate

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C435S320100, C435S252330, C435S252300

Reexamination Certificate

active

10789164

ABSTRACT:
The present invention relates to a method for expressing each of peptide antibiotics P5 3 and Ana13 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 fromBacillussp. 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 Ana13 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 Ana13 35.

REFERENCES:
patent: 10-2000-0078615 (2002-06-01), None
patent: 10-2001-0057837 (2003-03-01), None
patent: WO 03/014360 (2003-02-01), None
Boman et al., FEB Letts. vol. 259, (1): 103-106, 1989.
Cintas, L.M. et al., “Enterocins L50A and L50B, Two Novel Bacteriocins fromEnterococcus faeciumL50, Are Related to Staphylococcal Hemolysins,” Journal of Bacteriology, Apr. 1998, vol. 180, No. 8, 1988-1994.
Bevins, C.L. and Zasloff, M., “Peptides from Frog Skin,” Annu. Rev. Biochem, 1990, 59:395-414.
Miyasaki, K.T. and Lehrer, R. I., “β-sheet Antibiotic Peptides as Potential Dental Therapeutics,” International Journal of Antimicrobial Agents 9, 1998, 269-280.
Boman, H.G., “Antibacterial Peptides: Key Components Needed in Immunity,” Cell, vol. 65, 205-207, Apr. 19, 1991.
Boman, H.G., “Peptide Antibiotics and Their Role in Innate Immunity,” Annu. Rev. Immunol, 1995, 13:61-92.
Boman, H.G., et al., “Antibacterial and Antimalarial Properties Peptides that are Cecropin-melittin Hybrids,” Federation of European Biochemical Societies, vol. 259, No. 1, 103-106, Dec. 1989.
Wade, D. et al., “Antibacterial Peptides Designed as Analogs or Hybrids of Cecropins and Melittin,” Int. J. Peptide Protein Res. 40, 1992, 429-436.
Putsep, K. et al., “Antibacterial Peptide fromH. pylori,” Nature, vol. 398, Apr. 22, 1999.
Charbit, A., et al., “Presentation of Two Epitopes of the preS2 Region of Hepatitis B Virus on Live Recombinant Bacteria,” The Journal of Immunology, 1987, The American Association of Immunologists, vol. 139, 1658-1664, No. 5, Sep. 1, 1987.
Agterberg, M. et al., “Outer Membrane PhoE Protein ofEscherichia colias a Carrier for Foreign Antigenic Determinants: Immunogenicity of Epitopes of Foot-and-Mouth Disease Virus,” Vaccine, vol. 8, Feb. 1990, Butterworth & Co. Ltd.
Felici, F. et al., “Section of Antibody Ligands from a Large Library of Oligopeptides Expressed on a Multivalent Exposition Vector,” J.Mol. Biol. 1991, 222, 301-310.
Fuchs, P. et al., “Targeting Recombinant Antibodies to the Surface ofEscherichia coli: Fusion to a Peptidoglycan Associated Lipoprotein,” Bio/Technology, vol. 9, Dec. 1991.
Francisco, J.A.., et al., “Transport and Anchoring of β-lactamase to the External Surface ofEscherichia coli.” Proc. Natl. Acad. Sci. USA, vol. 89, pp. 2713-2717, Apr. 1992.
Hedegaard, L. et al., “Type 1 Fimbriae ofEscherichia colias Carriers of Heterologous Antigenic Sequences,” Gene, 85, 1989, 115-124.
Jung, H.C., et al., “Surface Display ofZymomonas mobilisLevansucrase by Using the Ice-nucleation Protein ofPseudomonasSyringae,” Nature Biotechnology, vol. 16, Jun. 1998.
Jung, H.C., et al., “Expression of Carboxymethylcellulase on the Surface ofEscherichia coliUsingPseudomonasSyringae Ice Nucleation Protein,” Enzyme and Microbial Technology 22:348-354, 1998, New York, USA.
Lee, J.S., et al., “Surface-displayed Viral Antigens onSalmonellaCarrier Vaccine,” Nature Biotechnology, vol. 10, Jun. 2000.
Kornacker, M.G. and Pugsley, A.P., “The normally periplasmic enzyme β-lactamase is Specifically and Efficiently Translocated through theEscherichia coliOuter Membrane when it is Fused to the Cell-surface Enzyme Pullulanase,” Molecular Microbiology, 1990, 4(7), 1101-1109.
Klauser, T., et al., “Extracellular Transport of Cholera Toxin B Subunit Using Neisseria IgA Protease β-domain: Conformation-dependent Outer Membrane Translocation,” The EMBO Journal, vol. 9, No. 6, pp. 1991-1999, 1990.

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