Development of pyrF- Based Genetic System for Targeted Gene Deletion in Clostridium thermocellum and Creation of a pta Mutant

Author:

Tripathi Shital A.12,Olson Daniel G.132,Argyros D. Aaron12,Miller Bethany B.12,Barrett Trisha F.12,Murphy Daniel M.12,McCool Jesse D.12,Warner Anne K.12,Rajgarhia Vineet B.12,Lynd Lee R.132,Hogsett David A.12,Caiazza Nicky C.12

Affiliation:

1. Mascoma Corporation, 67 Etna Rd., Suite 300, Lebanon, New Hampshire 03755

2. BioEnergy Science Center (BESC), Oak Ridge National Laboratory, P.O. Box 2008, Oak Ridge, Tennessee 37831

3. Thayer School of Engineering, Dartmouth College, 8000 Cummings Hall, Hanover, New Hampshire 03755

Abstract

ABSTRACT We report development of a genetic system for making targeted gene knockouts in Clostridium thermocellum , a thermophilic anaerobic bacterium that rapidly solubilizes cellulose. A toxic uracil analog, 5-fluoroorotic acid (5-FOA), was used to select for deletion of the pyrF gene. The Δ pyrF strain is a uracil auxotroph that could be restored to a prototroph via ectopic expression of pyrF from a plasmid, providing a positive genetic selection. Furthermore, 5-FOA was used to select against plasmid-expressed pyrF , creating a negative selection for plasmid loss. This technology was used to delete a gene involved in organic acid production, namely pta , which encodes the enzyme phosphotransacetylase. The C. thermocellum Δ pta strain did not produce acetate. These results are the first examples of targeted homologous recombination and metabolic engineering in C. thermocellum , a microbe that holds an exciting and promising future in the biofuel industry and development of sustainable energy resources.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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