Experiment set21IT041 for Pseudomonas fluorescens SBW25-INTG

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m-Inositol 10 mM carbon source

Group: carbon source
Media: MME_noNitrogen_noCarbon + m-Inositol (10 mM) + Ammonium chloride (10 mM), pH=7
Culturing: PseudoSBW25_INTG_ML3, 96 deep-well microplate; 1.2 mL volume, Aerobic, at 30 (C), shaken=1200 rpm
By: Joshua Elmore on 8-Mar-22
Media components: 9.1 mM Potassium phosphate dibasic trihydrate, 20 mM 3-(N-morpholino)propanesulfonic acid, 4.3 mM Sodium 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 13 genes in this experiment

For carbon source m-Inositol in Pseudomonas fluorescens SBW25-INTG

For carbon source m-Inositol across organisms

SEED Subsystems

Subsystem #Specific
Inositol catabolism 10

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
myo-inositol degradation I 7 6 6
myo-, chiro- and scyllo-inositol degradation 10 6 6
β-alanine degradation II 2 2 1
β-alanine degradation I 2 1 1
propanoyl-CoA degradation II 5 4 1
acrylate degradation I 5 3 1
myo-inositol degradation II 5 1 1
2,4-dinitrotoluene degradation 7 3 1
L-valine degradation I 8 6 1
streptomycin biosynthesis 18 2 1