SBIR-STTR Award

Computer-Assisted Strain Construction And Development Engineering (CASCADE)
Award last edited on: 4/3/2008

Sponsored Program
SBIR
Awarding Agency
DOD : CBD
Total Award Amount
$818,530
Award Phase
2
Solicitation Topic Code
CBD06-107
Principal Investigator
Tom Fahland

Company Information

Genomatica Inc

4757 Nexus Center Drive
San Diego, CA 92121
   (858) 824-1771
   info@genomatica.com
   www.genomatica.com
Location: Single
Congr. District: 52
County: San Diego

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2006
Phase I Amount
$69,010
The recent advances of modern high-throughput genomic technologies have resulted in a large number of fully sequenced microbial organisms. The construction of these comprehensive metabolic models serves many purposes including encapsulating all the data and allowing for in silco experiments to be performed that can drive experimental work and aid in strain development and optimization. The creation of a full metabolic reconstruction requires a significant amount of manual work; an automated procedure for rapidly developing metabolic models would be extremely valuable for the biotechnology field. We intend to develop a fully automated procedure for creating the metabolic reconstruction based on sequence data analysis and develop an automated analysis to determine growth and substrate utilization and protein production capability. The combination of automating the sequenced based metabolic reconstruction and downstream analysis of chemical production capabilities will rapidly produce fully functioning metabolic models with predictive power. These models will significantly increase productivity and decrease the time and effort required for strain design and aid in bioprocessing and chemical production.

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
2007
Phase II Amount
$749,520
The recent advances of modern high-throughput genomic technologies have resulted in a large number of fully sequenced microbial organisms. The construction of these comprehensive metabolic models serves many purposes including encapsulating all the data and allowing for in silco experiments to be performed that can drive experimental work and aid in strain development and optimization. The creation of a full metabolic reconstruction requires a significant amount of manual work; an automated procedure for rapidly developing metabolic models would be extremely valuable for the biotechnology field. We intend to use our recently developed automated metabolic model construction system and apply this to build a complete predictive model of Pichia pastoris for use in recombinant protein production. We will perform dedicated experiments to complete and validate the in silico metabolic model of Pichia pastoris and use this model to develop metabolic intervention strategies and optimize the process feed strategy to increase production of a protein of interest to the DOD. This combined computational and experimental methodology takes advantage of the simulation and predictive powers of the complete genome-scale metabolic model to drive experimentation and create rational-based metabolic intervention changes and process development changes.

Keywords:
Computational Biology, Metabolism, Microbial Systems, Bioinformatics, Protein Production.