IP Library Granted Patent US 8,067,239
Granted Patent B2
US 8,067,239 · App. 12/341,882 · Granted Nov 29, 2011

Reagents for recombinogenic engineering and use thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,067,239
App. No.
12/341,882
Granted
Nov 29, 2011
Kind
B2
Abstract

The present invention features homologous recombination methods and systems. The methods and systems promote highly efficient homologous recombination in cells (e.g., in prokaryotic cells). The methods and systems are useful, for example, in pharmaceutical drug development, vaccine development and cloning.

Claims (47)

1. A method of producing an attenuated pathogenic microorganism, comprising:

(a) introducing a vector into a pathogenic microorganism, the vector comprising

(i) a λ exo and a λ bet nucleotide sequences encoding bacteriophage λ Red recombinase;

(ii) a λ gam nucleotide sequence encoding bacteriophage anti-RecBCD;

(iii) a Ptac promoter sequence operably linked to the nucleotide sequence of (i) and (ii); and

(iv) a nucleotide sequence encoding Lad operably linked to its native promoter; and

(v) at least one origin of replication sequence which confers low copy number on the vector;

(b) introducing a substrate into the pathogenic microorganism, wherein the substrate comprises recombination segments comprising nucleotide sequences homologous to a gene required for pathogenicity or surrounding native sequences; and

(c) culturing the microorganism under conditions such that recombination between the substrate and the gene sequences or surrounding native sequences occurs;

such that the gene required for pathogenicity is mutated, thereby producing an attenuated pathogenic microorganism, and

wherein the pathogenic microorganism is a strain of Escherichia coli which is pathogenic to humans, animals, or plants.

2. A method of producing an attenuated pathogenic microorganism, comprising:

(a) introducing a vector into a pathogenic microorganism, the vector comprising

(i) a λ exo and a λ bet nucleotide sequences encoding bacteriophage λ Red recombinase;

(ii) a λ gam nucleotide sequence encoding bacteriophage anti-RecBCD;

(iii) a Ptac promoter sequence operably linked to the nucleotide sequence of (i) and (ii); and

(iv) a nucleotide sequence encoding Lad operably linked to its native promoter; and

(v) at least one origin of replication sequence which confers low copy number on the vector;

(b) introducing a substrate into the pathogenic microorganism, wherein the substrate comprises recombination segments comprising nucleotide sequences homologous to a gene required for pathogenicity or surrounding native sequences; and

(c) culturing the microorganism under conditions such that recombination between the substrate and the gene sequences or surrounding native sequences occurs;

such that the gene required for pathogenicity is mutated, thereby producing an attenuated pathogenic microorganism, and

wherein the pathogenic organism is enterohemorrhagic E. coli (EHEC) or enteropathogenic E. coli (EPEC).

3. A method of producing an attenuated pathogenic microorganism, comprising:

(a) introducing a vector into a pathogenic microorganism, the vector comprising

(i) a λ exo and a λ bet nucleotide sequences encoding bacteriophage λ Red recombinase;

(ii) a λ gam nucleotide sequence encoding bacteriophage anti-RecBCD;

(iii) a Ptac promoter sequence operably linked to the nucleotide sequence of (i) and (ii); and

(iv) a nucleotide sequence encoding Lad operably linked to its native promoter; and

(v) at least one origin of replication sequence which confers low copy number on the vector;

(b) introducing a substrate into the pathogenic microorganism, wherein the substrate comprises recombination segments comprising nucleotide sequences homologous to a gene required for pathogenicity or surrounding native sequences; and

(c) culturing the microorganism under conditions such that recombination between the substrate and the gene sequences or surrounding native sequences occurs;

such that the gene required for pathogenicity is mutated, thereby producing an attenuated pathogenic microorganism, and

wherein the pathogenic microorganism is of the genus Pseudomonas.

4. A method of producing an attenuated pathogenic microorganism, comprising:

(a) introducing a vector into a pathogenic microorganism, the vector comprising

(i) a λ exo and a λ bet nucleotide sequences encoding bacteriophage λ Red recombinase;

(ii) a λ gam nucleotide sequence encoding bacteriophage anti-RecBCD;

(iii) a Ptac promoter sequence operably linked to the nucleotide sequence of (i) and (ii); and

(iv) a nucleotide sequence encoding Lad operably linked to its native promoter; and

(v) at least one origin of replication sequence which confers low copy number on the vector;

(b) introducing a substrate into the pathogenic microorganism, wherein the substrate comprises recombination segments comprising nucleotide sequences homologous to a gene required for pathogenicity or surrounding native sequences; and

(c) culturing the microorganism under conditions such that recombination between the substrate and the gene sequences or surrounding native sequences occurs;

such that the gene required for pathogenicity is mutated, thereby producing an attenuated pathogenic microorganism, and

wherein the pathogenic microrganism is of the genus Mycobacterium.

5. The method of claim 3 , wherein the pathogenic microorganism is Pseudomonas aeruginosa.

6. The method of claim 4 , wherein the pathogenic microorganism is Mycobacterium tuberculosis.

7. The method of claims 1 , 2 , 3 or 4 , wherein at least one origin of replication sequence is temperature sensitive.

Assignments (4)
CONFIRMATORY LICENSE Recorded Dec 20, 2011
From: UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027414/0773 →
CONFIRMATORY LICENSE Recorded Dec 20, 2011
From: UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027414/0829 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2009
From: MURPHY, KENAN C.
To: UNIVERSITY OF MASSACHUSETTS
Reel/Frame 023425/0503 →
CONFIRMATORY LICENSE Recorded Mar 18, 2009
From: UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022411/0837 →