Experiment set47S226 for Pseudomonas putida KT2440
mixed carbon sources Trisodium citrate dihydrate 10 mM and 3-Chloro-L-tyrosine 10 mM
Group: mixed carbon sourceMedia: MME_noCarbon + Trisodium citrate dihydrate (10 mM) + 3-Chloro-L-tyrosine (10 mM)
Culturing: Putida_ML5_PNNL, 96 deep well, Aerobic, at 30 (C), shaken=1200 rpm
By: Andrew Frank on 11/17/23
Media components: 9.1 mM Potassium phosphate dibasic trihydrate, 20 mM 3-(N-morpholino)propanesulfonic acid, 4.3 mM Sodium Chloride, 10 mM Ammonium chloride, 0.41 mM Magnesium Sulfate Heptahydrate, 0.07 mM Calcium chloride dihydrate, MME Trace Minerals (0.5 mg/L EDTA tetrasodium tetrahydrate salt, 2 mg/L Ferric chloride, 0.05 mg/L Boric Acid, 0.05 mg/L Zinc chloride, 0.03 mg/L copper (II) chloride dihydrate, 0.05 mg/L Manganese (II) chloride tetrahydrate, 0.05 mg/L Diammonium molybdate, 0.05 mg/L Cobalt chloride hexahydrate, 0.05 mg/L Nickel (II) chloride hexahydrate)
Specific Phenotypes
For 10 genes in this experiment
For mixed carbon source Trisodium citrate dihydrate in Pseudomonas putida KT2440
For mixed carbon source Trisodium citrate dihydrate across organisms
SEED Subsystems
Metabolic Maps
Color code by fitness: see overview map or list of maps.
Maps containing gene(s) with specific phenotypes:
- Ubiquinone and menaquinone biosynthesis
- Tyrosine metabolism
- Ascorbate and aldarate metabolism
- Phenylalanine metabolism
- Phenylalanine, tyrosine and tryptophan biosynthesis
- Glutathione metabolism
- Nucleotide sugars metabolism
- Glycosaminoglycan degradation
- Styrene degradation
- Metabolism of xenobiotics by cytochrome P450
- Drug metabolism - cytochrome P450
- Biosynthesis of phenylpropanoids
- Biosynthesis of alkaloids derived from shikimate pathway
- Biosynthesis of plant hormones
MetaCyc Pathways
Pathways that contain genes with specific phenotypes:
Pathway | #Steps | #Present | #Specific |
---|---|---|---|
3-dehydroquinate biosynthesis I | 2 | 2 | 1 |
L-tyrosine degradation I | 5 | 5 | 2 |
plastoquinol-9 biosynthesis I | 3 | 1 | 1 |
gentisate degradation I | 3 | 1 | 1 |
4-hydroxy-2-nonenal detoxification | 4 | 1 | 1 |
pentachlorophenol degradation | 10 | 4 | 2 |
superpathway of plastoquinol biosynthesis | 5 | 2 | 1 |
5-nitroanthranilate degradation | 6 | 2 | 1 |
chorismate biosynthesis I | 7 | 7 | 1 |
vitamin E biosynthesis (tocopherols) | 7 | 1 | 1 |
glutathione-mediated detoxification I | 8 | 3 | 1 |
L-phenylalanine degradation IV (mammalian, via side chain) | 9 | 6 | 1 |
gliotoxin biosynthesis | 9 | 2 | 1 |
glutathione-mediated detoxification II | 9 | 1 | 1 |
superpathway of L-phenylalanine biosynthesis | 10 | 10 | 1 |
superpathway of L-tyrosine biosynthesis | 10 | 10 | 1 |
3-phenylpropanoate degradation | 10 | 4 | 1 |
indole glucosinolate activation (intact plant cell) | 12 | 3 | 1 |
camalexin biosynthesis | 12 | 2 | 1 |
superpathway of L-tryptophan biosynthesis | 13 | 13 | 1 |
superpathway of aromatic amino acid biosynthesis | 18 | 18 | 1 |
superpathway of chorismate metabolism | 59 | 42 | 1 |