Partnering opportunities:
Genome Mass Transfer (GMT™) Strain engineering Technology


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Nuecleic Acid Vaccines and Gene Therapeutics Development | Genome Mass Transfer (GMT)Technology


Advanced Strains of Microorganisms for Biopharmaceutical and Industrial Production

GMT is a disruptive NTC technology, which facilitates orderly and predictable transfer of desirable traits between strains. The strategy is to directly transfer genomic DNA from a strain with a desired property into a recipient strain that expresses recombineering genes. It is not necessary to amplify or isolate DNA. GMT replaces older technology, such as phage P1 transduction. For example, genomic DNA becomes efficiently integrated into the recipient host genome through homologous recombination, after transfer, for example, by electroporation. In some cases, amplified DNA is transferred directly from cell lysates, dramatically simplifying the task of genome engineering. [Patent Ref: PCT/US08/06548]

E. coli cell
1) Cells are made competent for mass transfer

E. coli cell pre-transfection
2) Add DNA

E. coli cell electroporation
3) DNA is transfected into cells

E. coli cell foreign DNA assimilation
4) DNA associates with nucleoplasm

E. coli cell donor DNA recombination
5) Donor DNA integration and replication

E. coli cell Genome Mass Transfer (GMT) and septation
6) Assimilation and septation

E. coli cell division
7) Cell division

E. coli cell selection
8) Selection to grow out recombinant strains