
NSF Org: |
CBET Division of Chemical, Bioengineering, Environmental, and Transport Systems |
Recipient: |
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Initial Amendment Date: | August 12, 2022 |
Latest Amendment Date: | August 12, 2022 |
Award Number: | 2225878 |
Award Instrument: | Standard Grant |
Program Manager: |
Steven Peretti
speretti@nsf.gov (703)292-4201 CBET Division of Chemical, Bioengineering, Environmental, and Transport Systems ENG Directorate for Engineering |
Start Date: | October 1, 2022 |
End Date: | September 30, 2025 (Estimated) |
Total Intended Award Amount: | $777,157.00 |
Total Awarded Amount to Date: | $777,157.00 |
Funds Obligated to Date: |
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History of Investigator: |
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Recipient Sponsored Research Office: |
200 UNIVERSTY OFC BUILDING RIVERSIDE CA US 92521-0001 (951)827-5535 |
Sponsor Congressional District: |
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Primary Place of Performance: |
900 UNIVERSITY AVE RIVERSIDE CA US 92521-9800 |
Primary Place of
Performance Congressional District: |
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Unique Entity Identifier (UEI): |
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Parent UEI: |
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NSF Program(s): |
Special Initiatives, Systems and Synthetic Biology |
Primary Program Source: |
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Program Reference Code(s): |
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Program Element Code(s): |
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Award Agency Code: | 4900 |
Fund Agency Code: | 4900 |
Assistance Listing Number(s): | 47.041, 47.074 |
ABSTRACT
Metabolism involves a complex set of reactions and control mechanisms. This makes microbial behavior difficult to understand and engineer. Machine learning (ML) identifies patterns and relationships in complex sets of data. A yeast will be subject to varied efforts to increase its yield of biochemicals and biofuels. Machine learning will help identify synthetic biology approaches that maximize production. Also, educational and training resources will be expanded for students in K-6 afterschool programs, in K-12 summer camps, and in a Data Science Academy for high school students.
The overall goal is to identify genes critical to driving high carbon flux to a desired central metabolite and product. A deep learning approach ? DeepGuide ? will be used to design optimized sgRNA libraries to generate genetic diversity. The build stage of the cycle will leverage efficient CRISPR-Cas9 technologies for gene disruption and regulation. A biosensor-driven approach to testing will enable high throughput analysis of the effect of host genetics on the production of malonyl-CoA, a key precursor to polyketides. The droplet microfluidics screening and analysis capabilities of the Agile BioFoundry (ABF) at Argonne National Laboratory will provide a wealth of additional information to link metabolite production with host genetics. The large datasets generated in the testing stage will be used as input for deep learning; a new algorithm linking genotypes to phenotypes ? DeepMetabolism ? will be used to predict a minimal set of genetic perturbations that maximize malonyl-CoA biosynthesis. This data-driven approach will advance both deep learning and high throughput approaches for microbial engineering and can be applied to other strategic metabolites.
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH
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