Metabolic gene–deletion strains of Escherichia coli evolve to computationally predicted growth phenotypes
By Stephen S. Fong, Bernhard O. Palsson. Nature Genetics, 2004
314 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/fe51bbde261528df0b97bea94a7f81b395f4b747
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- Jennie L. Reed
- Adam M. Feist
- Bernhard O. Palsson
- Nathan D. Price
- Natali Gulbahce
- Costas D. Maranas
- Prit Pharkya
- Scott A. Becker
In Molecular Biology
- Bernhard O. Palsson
- Adam M. Feist
- Costas D. Maranas
- Markus J. Herrgård
- Jason A. Papin
- Nathan D. Price
- Prit Pharkya
- Jennie L. Reed
Citations in the corpus
- Using Genome-Scale Models to Predict Biological Capabilities (2015, unknown): “A total of 78% of strains tested reached the metabolic model predicted optimal growth rate after adaptive laboratory evolution after 40 days of passage (Fong and Palsson, 2004).”
- Systems biotechnology for strain improvement. (2005, unknown): “Palsson and colleagues demonstrated the usefulness of constraints-based flux analysis to predict the effects of genetic modifications on cellular metabolic characteristics [ 36 ].”
- Interpreting Expression Data with Metabolic Flux Models: Predicting Mycobacterium tuberculosis Mycolic Acid Production (2009, methodology): “FBA has been used to successfully predict the metabolic phenotype of gene knockouts [1– 3], and the use of metabolic modeling in this case has the advantage of predicting nutrient-dependent phenotypes.”
- Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox v2.0 (2007, unknown): “The Matlab functions to perform batch simulations and to plot the results are: model 1⁄4 readCbModel(‘Ec_iJR904_GlcMM’); model 1⁄4 changeRxnBounds(model, {‘EX_glc(e)’,‘EX_o2(e)’},y [ 10 18], ‘l’); substrateRxns 1⁄4 {‘EX_glc(e)’}; initConcentrations 1⁄4 10; initBiomass 1⁄4 .”
- Basic and applied uses of genome-scale metabolic network reconstructions of Escherichia coli (2013, background): “Constraint-based modeling with GEMs (Palsson, 2006) has allowed researchers to rapidly predict growth phenotypes in various genetic (Fong and Palsson, 2004) and environmental (Ibarra et al , 2002) conditions, explore different objectives of microbial metabolism (Schuetz et al , 2007; Ow et al ,…”
- Applications of genome-scale metabolic reconstructions (2009, background): “Some studies have examined the phenomenon of shortterm adaptive evolution, and have shown that as a particular strain adapts to media it is grown in, its growth characteristics will converge toward the FBA-predicted optimal solution (Fong and Palsson, 2004; Fong et al, 2005).”
- Network Medicine: A Network-based Approach to Human Disease (2011, background): “Given the relative accuracy of metabolic maps ( Box 1 ) and the ability to predict flux changes that are induced by drug-altered enzymatic activity in bacteria using flux balance analysi”
- Modular epistasis in yeast metabolism (2005, methodology): “For the deletion of gene X , fitness was defined as W x = V ΔX growth / V wild–type growth (refs”
- Network-based prediction of human tissue-specific metabolism (2008, background): “, and a strong correlation between gene expression and measure”
- An optimization framework for identifying reaction activation/inhibition or elimination candidates for overproduction in microbial systems. (2006, background): “In the case of biomass maximization, this leads to, under certain situations , a highly desirable coupling of biomass formation to targeted biochemical production enabling the use of adaptive evolution for strain design (Ibarra et al., 2002; Fong and Palsson, 2004).”
- Context-Specific Metabolic Networks Are Consistent with Experiments (2008, methodology): “The gene expression data used to construct the models consists of CEL files containing the data described in [17], normalized using GCRMA [14].”
- Genome-scale models of microbial cells: evaluating the consequences of constraints (2004, background): “If a knockout strain is suboptimal,it can be evolved to achieve optimal functions 88 .”