Patent EP0190921A2 successfully refreshed from Google Patents.
← Back to Patent Explorer
EP0190921A2 Expired / Lapsed EP ⏱️ 0.0 years remaining

Method for the overproduction of amino acids

Assignee: Engenics Inc
•
Filing: 1986-02-04
•
Granted: —
•
Expires: 2006-02-04
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract A method is provided for overexpressing an amino acid in a microorganism comprising the step of altering the chromosomal DNA of host microorganisms or transforming the host microorganisms with at least one expression vector such that the resultant microorganism will overexpress certain operons and be inactive with respect to the other operons in the biosynthetic pathway of the amino acid, whereby overexpression of the amino acid will occur.

Inventors

  • 👤 Carol Talkington

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-11-09 08:45
CPC Classifications
C; C12; C12P; C12P13/00; C12P13/04; C12N; C12N15/00; C12N15/09; C12N15/11; C12N15/52; C12N15/63; C12N15/70; C12P13/22

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 101 words
A method for overexpressing an amino acid in a microorganism comprising the step of altering the chromosomal DNA of said microorganism and/or transforming said microorganism with at least one expression vector wherein said alterations or vector causes (a) overexpression of at least one enzyme necessary for the biosynthesis of said amino acid; (b) elimination of feedback inhibition of expression of said amino acid by mutation of at least one gene necessary for the biosynthesis of said amino acid; and (c) inactivation of at least one gene which produces a product which inhibits or represses expression of said enzyme in step (a).
Claim 2
Independent Claim 101 words
A method for overexpressing an amino acid in a microorganism comprising the step of altering the chromosomal DNA of said microorganism and/or transforming said microorganism with at least one expression vector wherein said alterations or vector causes (a) overexpression of at least one enzyme necessary for the biosynthesis of said amino acid; (b) elimination of feedback inhibition of expression of said amino acid by mutation of at least one gene necessary for the biosynthesis of said amino acid; and (c) inactivation of at least one gene which produces a product which inhibits or represses expression of said enzyme in step (a).
Claim 3
Dependent Claim 11 words
A method according to claim 1 wherein said microorganism comprises bacteria.
Claim 4
Dependent Claim 24 words
A method according to claim 1 or claim 2 wherein said bacteria are selected from the group consisting of Escherichia, Bacillus, Corynebacteria and Brevibacteria.
Claim 5
Dependent Claim 12 words
A method according to claim 3 wherein said bacteria comprise Escherichia coli.
Claim 6
Dependent Claim 30 words
A method according to claim 4 wherein said overexpression is performed by subcloning the aroF operon or the pheA onto a multicopy plasmid and transforming said plasmid into E. coli.
Claim 7
Dependent Claim 24 words
A method according to claim 4 wherein said elimination of feedback inhibition is performed by a mutant pheA gene and/or a mutant aroF gene.
Claim 8
Dependent Claim 27 words
A method according to claim 4 wherein said overexpression is performed by excising the attenuator region and performing site-directed mutagenesis on the pheA operon to overproduce phenylalanine.
Claim 9
Dependent Claim 20 words
A method according to claim 5 wherein the pheA gene is subcloned onto the muticopy plasmid containing the aroF gene.
Claim 10
Dependent Claim 26 words
A method according to claim 4 wherein said inactivation is performed by mutagenizing E. coli host chromosomal DNA by transposon mutagenesis to inactivate the tyrA gene.
Claim 11
Independent Claim 17 words
A method according to any one of claims 1 to 9 wherein said amino acid comprises phenylalanine.

References Cited (Backward Citations)

No citation records indexed.

USPTO Annuity & Maintenance Windows

Maintenance schedule is calculated for granted US utility patents.

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag