Experiment set3IT061 for Pseudomonas sp. RS175

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4-Hydroxyphenylpropionic acid carbon source 2.5 mM

Group: carbon source
Media: MME_noCarbon + 4-Hydroxyphenylpropionic acid (2.5 mM), pH=7
Culturing: Pseudomonas_RS175_ML2, 24-well transparent microplate; Multitron, Aerobic, at 30 (C), shaken=700 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 30 genes in this experiment

For carbon source 4-Hydroxyphenylpropionic acid in Pseudomonas sp. RS175

For carbon source 4-Hydroxyphenylpropionic acid across organisms

SEED Subsystems

Subsystem #Specific
Arginine and Ornithine Degradation 4
ABC transporter dipeptide (TC 3.A.1.5.2) 3
Bacterial Chemotaxis 3
ABC transporter oligopeptide (TC 3.A.1.5.1) 2
Biogenesis of cytochrome c oxidases 1
Biotin biosynthesis 1
DNA-replication 1
DNA Repair Base Excision 1
Histidine Degradation 1
Lysine degradation 1
Polyhydroxybutyrate metabolism 1
Terminal cytochrome C oxidases 1
n-Phenylalkanoic acid degradation 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
ethanol degradation I 2 2 2
methanol oxidation to formaldehyde II 1 1 1
acetaldehyde biosynthesis I 1 1 1
long-chain fatty acid activation 1 1 1
pyruvate fermentation to ethanol I 3 2 2
pyruvate fermentation to ethanol III 3 2 2
L-threonine degradation IV 2 2 1
phytol degradation 4 3 2
linoleate biosynthesis II (animals) 2 1 1
arsenite to oxygen electron transfer 2 1 1
γ-linolenate biosynthesis II (animals) 2 1 1
pyruvate fermentation to ethanol II 2 1 1
ethanolamine utilization 5 5 2
acetylene degradation (anaerobic) 5 4 2
ethanol degradation II 3 3 1
L-isoleucine degradation II 3 2 1
2-aminoethylphosphonate degradation I 3 2 1
2-hydroxypenta-2,4-dienoate degradation 3 2 1
L-valine degradation II 3 2 1
2-deoxy-D-ribose degradation I 3 2 1
L-leucine degradation III 3 2 1
3-methyl-branched fatty acid α-oxidation 6 3 2
L-methionine degradation III 3 1 1
arsenite to oxygen electron transfer (via azurin) 3 1 1
oleate biosynthesis I (plants) 3 1 1
2-deoxy-α-D-ribose 1-phosphate degradation 3 1 1
alkane biosynthesis II 3 1 1
sulfoacetaldehyde degradation IV 3 1 1
L-histidine degradation I 4 4 1
aerobic respiration I (cytochrome c) 4 3 1
aerobic respiration II (cytochrome c) (yeast) 4 3 1
L-phenylalanine degradation III 4 2 1
salidroside biosynthesis 4 2 1
L-tyrosine degradation III 4 2 1
long chain fatty acid ester synthesis (engineered) 4 1 1
phosphatidylcholine acyl editing 4 1 1
wax esters biosynthesis II 4 1 1
superpathway of fermentation (Chlamydomonas reinhardtii) 9 5 2
sporopollenin precursors biosynthesis 18 4 4
L-histidine degradation II 5 5 1
octane oxidation 5 4 1
pyruvate fermentation to isobutanol (engineered) 5 4 1
sphingosine and sphingosine-1-phosphate metabolism 10 4 2
catechol degradation I (meta-cleavage pathway) 5 2 1
phenylethanol biosynthesis 5 2 1
(S)-propane-1,2-diol degradation 5 2 1
fatty acid salvage 6 6 1
stearate biosynthesis II (bacteria and plants) 6 5 1
L-histidine degradation III 6 4 1
stearate biosynthesis IV 6 4 1
methanol oxidation to carbon dioxide 6 3 1
Fe(II) oxidation 6 3 1
6-gingerol analog biosynthesis (engineered) 6 3 1
superpathway of pyrimidine deoxyribonucleosides degradation 6 3 1
triethylamine degradation 6 1 1
stearate biosynthesis I (animals) 6 1 1
noradrenaline and adrenaline degradation 13 8 2
superpathway of Clostridium acetobutylicum solventogenic fermentation 13 5 2
3-methylbutanol biosynthesis (engineered) 7 6 1
superpathway of purine deoxyribonucleosides degradation 7 5 1
serotonin degradation 7 4 1
capsaicin biosynthesis 7 4 1
catechol degradation II (meta-cleavage pathway) 7 3 1
ceramide degradation by α-oxidation 7 2 1
toluene degradation V (aerobic) (via toluene-cis-diol) 7 2 1
toluene degradation I (aerobic) (via o-cresol) 7 2 1
icosapentaenoate biosynthesis II (6-desaturase, mammals) 7 1 1
arachidonate biosynthesis III (6-desaturase, mammals) 7 1 1
icosapentaenoate biosynthesis III (8-desaturase, mammals) 7 1 1
L-histidine degradation VI 8 7 1
mixed acid fermentation 16 12 2
2-deoxy-D-ribose degradation II 8 4 1
3-phenylpropanoate and 3-(3-hydroxyphenyl)propanoate degradation 8 3 1
butanol and isobutanol biosynthesis (engineered) 8 3 1
ceramide and sphingolipid recycling and degradation (yeast) 16 4 2
p-cumate degradation 8 2 1
superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation 17 7 2
heterolactic fermentation 18 16 2
hexitol fermentation to lactate, formate, ethanol and acetate 19 14 2
meta cleavage pathway of aromatic compounds 10 3 1
suberin monomers biosynthesis 20 3 2
superpathway of fatty acid biosynthesis II (plant) 43 38 4
superpathway of N-acetylneuraminate degradation 22 15 2
p-cymene degradation 11 2 1
naphthalene degradation to acetyl-CoA 12 3 1
L-tryptophan degradation IX 12 2 1
L-tryptophan degradation XII (Geobacillus) 12 2 1
toluene degradation IV (aerobic) (via catechol) 13 4 1
L-tryptophan degradation V (side chain pathway) 13 1 1
palmitate biosynthesis II (type II fatty acid synthase) 31 29 2
cutin biosynthesis 16 1 1
superpathway of L-threonine metabolism 18 13 1
mandelate degradation to acetyl-CoA 18 7 1
superpathway of anaerobic sucrose degradation 19 15 1
superpathway of fatty acids biosynthesis (E. coli) 53 49 2
palmitate biosynthesis III 29 28 1
superpathway of aerobic toluene degradation 30 11 1
oleate β-oxidation 35 30 1
superpathway of aromatic compound degradation via 3-oxoadipate 35 13 1
superpathway of aromatic compound degradation via 2-hydroxypentadienoate 42 10 1