IP Library Granted Patent US 8,457,941
Granted Patent B2
US 8,457,941 · App. 13/210,484 · Granted Jun 4, 2013

Method for determining gene knockouts

Inventors: Costas D. Maranas (Port Matilda, PA); Anthony R. Burgard (State College, PA); Priti Pharkya (State College, PA)
Assignee: The Penn State Research Foundation
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 8,457,941
App. No.
13/210,484
Granted
Jun 4, 2013
Kind
B2
Abstract

A method for determining candidates for gene deletions and additions using a model of a metabolic network associated with an organism, the model includes a plurality of metabolic reactions defining metabolite relationships, the method includes selecting a bioengineering objective for the organism, selecting at least one cellular objective, forming an optimization problem that couples the at least one cellular objective with the bioengineering objective, and solving the optimization problem to yield at least one candidate.

Claims (30)

1. A method for determining candidates for gene deletions and additions using a model of a metabolic network associated with an organism comprising:

providing a model in a computer comprising an electronic representation of a plurality of metabolic reactions defining metabolite relationships;

selecting at least one bioengineering objective function for the organism;

selecting at least one cellular objective function;

forming an optimization problem that couples the at least one cellular objective function with the at least one bioengineering objective function, and

executing commands in a suitably programmed computer for solving the optimization problem to yield at least one gene candidate for deletion or addition.

2. The method of claim 1 further comprising using the at least one candidate to genetically modify the organism.

3. The method of claim 1 wherein the bioengineering objective function is overproduction of a chemical.

4. The method of claim 1 wherein the bioengineering objective function is underproduction of a chemical.

5. The method of claim 1 wherein the cellular objective function growth.

6. The method of claim 1 wherein the cellular objective is minimization of metabolic adjustment.

7. The method of claim 1 wherein the candidate is a candidate for gene deletion, and the optimization problem includes a binary value for specifying if reaction flux is active or inactive.

8. The method of claim 1 wherein the optimization problem is a bilevel optimization problem.

9. The method of claim 1 wherein the optimization problem is a mixed-integer optimization problem.

10. The method of claim 1 wherein the optimization problem includes at least one stoichiometric constraint.

11. The method of claim 1 wherein the optimization problem includes at least one chemical uptake constraint.

12. The method of claim 1 wherein the step of forming an optimization problem includes quantifying the cellular objective function as an aggregate reaction flax.

13. The method of claim 1 further comprising evaluating performance limits of the metabolic network with the at least one candidate based on ability of the network to meet the at least one cellular objective function.

14. The method of claim 1 wherein the cellular objective function is selected from the group consisting of maximizing a growth rate, maximizing ATP production, minimizing metabolic adjustment, minimizing nutrient uptake, minimizing redox production, minimizing a Euclidean norm, and combinations thereof.

15. The method of claim 1 wherein the bioengineering Objective is overproduction of glycerol and at least one candidate is for gene deletion and comprising genes coding for the enzymes fructose-1,6-hisphosphatase, fructose-1,6-bisphosphatase aidolase, phosphoglycerate kinase, glyceraldehydes-3-phosphate dehydrogenase, phosphoenolpyravate synthase, NADH dehydrogenase I, phosphogluconate dehydratase, 2-keto-3-deoxy-6-phosphofluconate aldolase, triosphosphate isomerase, glucose 6-phosphate-1-dehydrogenase, 6-phosphogluconolactonase-, deoxyribose-phosphate aldolase, aldehyde dehydrogenase, or combinations thereof.

16. The method of claim 1 wherein the bioengineering objective is overproduction of 1,3-propanediol and at least one candidate is for gene deletion and comprising genes coding for the enzymes fructose-1,6-bisphosphatase, fructose-1,6-bisphosphatase aldolase, phosphoglycerate kinase, glyceraldehyde-3-phosphate dehyrogonase, triosphosphate isomerase, glucose 6-phosphate-1-dehydrogenase, 6-phosphogluconolactonase, deoxyribose-phosphate aldolase, aldehyde dehydrogenase, or combinations thereof.

17. The method of claim 1 wherein the bioengineering objective is overproduction of succinate and at least one candidate is for gene deletion and comprising genes coding for the enzymes pyruvate formate lyase, acetaldehyde dehydrogenase, pyruvate kinase, FOF1-ATPase, NADH dehydrogenase I, fumarase, D-Lactate dehydrogenase, pyridine nucleotide transhydrogenase, phosphotransacetylase, acetate kinase, phosphotransferase, or combinations thereof.

18. The method of claim 1 wherein the bioengineering objective function is overproduction of lactate and at least one candidate is for gene deletion and comprising genes coding for the enzymes phosphotransacetylase, acetate kinase, phosphofructokinase, fructose-1,6-bisphosphatase aldolase, triosphosphate isomerase, acetaldehyde dehyrogenase, glucokinase, or combinations thereof.

19. A computer-based method for determining candidates for gene deletions and additions using a. model of a metabolic network associated with an organism, comprising:

providing a model in a computer comprising an electronic representation of a plurality of metabolic reactions defining metabolite relationships;

inputting at least one bioengineering objective function;

receiving as input at least one cellular objective function;

forming an optimization problem that quantifies the at least one cellular objective function as an aggregate reaction flux and couples the at least one cellular objective function with the at least one bioengineering objective function;

executing commands in a suitably programmed computer for solving the optimization problem to yield at least one gene candidate for deletion or addition; and

outputting the at least one gene candidate.

Assignments (1)
CONFIRMATORY LICENSE Recorded Dec 27, 2011
From: THE PENNSYLVANIA STATE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 027449/0833 →
Continuity (5)
Continuation 10616659 · Jul 9, 2003
Provisional Application 60395763 · Jul 10, 2002
Provisional Application 60417511 · Oct 9, 2002
Provisional Application 60444933 · Feb 3, 2003
Related Publication 20110301930A1 · Dec 8, 2011