Experiment set1IT090 for Pseudomonas sp. RS175

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5-Aminovaleric acid carbon 10 mM

Group: carbon source
Media: MME_noCarbon + 5-Aminovaleric acid (10 mM), pH=7
Culturing: Pseudomonas_RS175_ML2, 96 deep-well microplate; 1.2 mL volume, Aerobic, at 30 (C), shaken=1200 rpm
By: Joshua Elmore on 1-Jul-22
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 9 genes in this experiment

For carbon source 5-Aminovaleric acid in Pseudomonas sp. RS175

For carbon source 5-Aminovaleric acid across organisms

SEED Subsystems

Subsystem #Specific
Polyamine Metabolism 2
Acetyl-CoA fermentation to Butyrate 1
Butanol Biosynthesis 1
Coenzyme A Biosynthesis 1
Orphan regulatory proteins 1
Polyhydroxybutyrate metabolism 1

Metabolic Maps

Color code by fitness: see overview map or list of maps.

Maps containing gene(s) with specific phenotypes:

MetaCyc Pathways

Pathways that contain genes with specific phenotypes:

Pathway #Steps #Present #Specific
phosphopantothenate biosynthesis I 4 4 1
phosphopantothenate biosynthesis III (archaea) 4 2 1
L-lysine degradation IV 5 4 1
(R)- and (S)-3-hydroxybutanoate biosynthesis (engineered) 5 4 1
glutaryl-CoA degradation 5 3 1
L-lysine degradation X 6 5 1
pyruvate fermentation to butanol II (engineered) 6 4 1
pyruvate fermentation to butanoate 7 3 1
pyruvate fermentation to butanol I 8 3 1
2-methylpropene degradation 8 2 1
superpathway of coenzyme A biosynthesis I (bacteria) 9 9 1
superpathway of Clostridium acetobutylicum acidogenic fermentation 9 5 1
superpathway of coenzyme A biosynthesis II (plants) 10 9 1
L-glutamate degradation V (via hydroxyglutarate) 10 6 1
methyl tert-butyl ether degradation 10 2 1
pyruvate fermentation to hexanol (engineered) 11 7 1
L-glutamate degradation VII (to butanoate) 12 3 1
superpathway of Clostridium acetobutylicum solventogenic fermentation 13 5 1
L-tryptophan degradation III (eukaryotic) 15 3 1
glycerol degradation to butanol 16 9 1
crotonate fermentation (to acetate and cyclohexane carboxylate) 16 4 1
superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation 17 7 1
benzoate fermentation (to acetate and cyclohexane carboxylate) 17 4 1
3-hydroxypropanoate/4-hydroxybutanate cycle 18 8 1
toluene degradation VI (anaerobic) 18 4 1
photosynthetic 3-hydroxybutanoate biosynthesis (engineered) 26 20 1
1-butanol autotrophic biosynthesis (engineered) 27 20 1
oleate β-oxidation 35 30 1
superpathway of L-lysine degradation 43 18 1