IT8421612A0 - CLONING VECTOR, PROCEDURE FOR ITS CONSTRUCTION AND PROCEDURE FOR CONCENTRATION AND PURIFICATION OF PRODUCED PROTEINS, FORMED BY THE CLONING VECTOR. - Google Patents

CLONING VECTOR, PROCEDURE FOR ITS CONSTRUCTION AND PROCEDURE FOR CONCENTRATION AND PURIFICATION OF PRODUCED PROTEINS, FORMED BY THE CLONING VECTOR.

Info

Publication number
IT8421612A0
IT8421612A0 IT8421612A IT2161284A IT8421612A0 IT 8421612 A0 IT8421612 A0 IT 8421612A0 IT 8421612 A IT8421612 A IT 8421612A IT 2161284 A IT2161284 A IT 2161284A IT 8421612 A0 IT8421612 A0 IT 8421612A0
Authority
IT
Italy
Prior art keywords
procedure
cloning vector
purification
concentration
construction
Prior art date
Application number
IT8421612A
Other languages
Italian (it)
Other versions
IT1178489B (en
Inventor
Gordon L Williams
Original Assignee
Biovec Technology Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Biovec Technology Inc filed Critical Biovec Technology Inc
Publication of IT8421612A0 publication Critical patent/IT8421612A0/en
Application granted granted Critical
Publication of IT1178489B publication Critical patent/IT1178489B/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/70—Vectors or expression systems specially adapted for E. coli
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/62—DNA sequences coding for fusion proteins
    • C12N15/625—DNA sequences coding for fusion proteins containing a sequence coding for a signal sequence
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/74—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora
    • C12N15/75—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora for Bacillus
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/035—Fusion polypeptide containing a localisation/targetting motif containing a signal for targeting to the external surface of a cell, e.g. to the outer membrane of Gram negative bacteria, GPI- anchored eukaryote proteins
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/61—Fusion polypeptide containing an enzyme fusion for detection (lacZ, luciferase)
IT21612/84A 1983-06-29 1984-06-26 CLONANT VECTOR, PROCEDURE FOR ITS CONSTRUCTION AND CONCENTRATION AND PURIFICATION PROCEDURE OF PRODUCED PROTEINS, FORMED BY THE CLONANT VECTOR IT1178489B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US50839183A 1983-06-29 1983-06-29

Publications (2)

Publication Number Publication Date
IT8421612A0 true IT8421612A0 (en) 1984-06-26
IT1178489B IT1178489B (en) 1987-09-09

Family

ID=24022578

Family Applications (1)

Application Number Title Priority Date Filing Date
IT21612/84A IT1178489B (en) 1983-06-29 1984-06-26 CLONANT VECTOR, PROCEDURE FOR ITS CONSTRUCTION AND CONCENTRATION AND PURIFICATION PROCEDURE OF PRODUCED PROTEINS, FORMED BY THE CLONANT VECTOR

Country Status (5)

Country Link
EP (1) EP0148845A1 (en)
JP (1) JPS60501688A (en)
AU (1) AU2860384A (en)
IT (1) IT1178489B (en)
WO (1) WO1985000185A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1177378B (en) * 1984-12-11 1987-08-26 Anic Spa PSM112 PLASMIDIC VECTOR FOR EXPRESSION IN BACILLUS SUBTILIS

Also Published As

Publication number Publication date
AU2860384A (en) 1985-01-25
EP0148845A1 (en) 1985-07-24
JPS60501688A (en) 1985-10-11
WO1985000185A1 (en) 1985-01-17
IT1178489B (en) 1987-09-09

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