Experiment set4IT083 for Acidovorax sp. GW101-3H11

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L-Phenylalanine nitrogen source

Group: nitrogen source
Media: RCH2_defined_Glucose_noNitrogen + L-Phenylalanine (20 mM), pH=7
Culturing: acidovorax_3H11_ML3a, 24 deep-well microplate; Multitron, Aerobic, at 30 (C), shaken=750 rpm
Growth: about 5.4 generations
By: Mark on 6/10/2015
Media components: 0.1 g/L Potassium Chloride, 0.6 g/L Sodium phosphate monobasic monohydrate, 20 mM D-Glucose, 30 mM PIPES sesquisodium salt, Wolfe's mineral mix (0.03 g/L Magnesium Sulfate Heptahydrate, 0.015 g/L Nitrilotriacetic acid, 0.01 g/L Sodium Chloride, 0.005 g/L Manganese (II) sulfate monohydrate, 0.001 g/L Cobalt chloride hexahydrate, 0.001 g/L Zinc sulfate heptahydrate, 0.001 g/L Calcium chloride dihydrate, 0.001 g/L Iron (II) sulfate heptahydrate, 0.00025 g/L Nickel (II) chloride hexahydrate, 0.0002 g/L Aluminum potassium sulfate dodecahydrate, 0.0001 g/L Copper (II) sulfate pentahydrate, 0.0001 g/L Boric Acid, 0.0001 g/L Sodium Molybdate Dihydrate, 0.003 mg/L Sodium selenite pentahydrate), Wolfe's vitamin mix (0.1 mg/L Pyridoxine HCl, 0.05 mg/L 4-Aminobenzoic acid, 0.05 mg/L Lipoic acid, 0.05 mg/L Nicotinic Acid, 0.05 mg/L Riboflavin, 0.05 mg/L Thiamine HCl, 0.05 mg/L calcium pantothenate, 0.02 mg/L biotin, 0.02 mg/L Folic Acid, 0.001 mg/L Cyanocobalamin)
Growth plate: Nplate1 C6

Specific Phenotypes

For 8 genes in this experiment

For nitrogen source L-Phenylalanine in Acidovorax sp. GW101-3H11

For nitrogen source L-Phenylalanine across organisms

SEED Subsystems

Subsystem #Specific
Aromatic amino acid degradation 2
Homogentisate pathway of aromatic compound degradation 2
Plastoquinone Biosynthesis 1
Pterin biosynthesis 1
Tocopherol Biosynthesis 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
L-tyrosine biosynthesis IV 1 1 1
L-phenylalanine degradation I (aerobic) 1 1 1
3-(4-hydroxyphenyl)pyruvate biosynthesis 1 1 1
L-tyrosine degradation I 5 3 3
L-phenylalanine biosynthesis III (cytosolic, plants) 2 2 1
L-tyrosine degradation II 2 1 1
atromentin biosynthesis 2 1 1
superpathway of plastoquinol biosynthesis 5 2 2
L-phenylalanine biosynthesis I 3 3 1
L-phenylalanine degradation V 3 3 1
L-tyrosine biosynthesis I 3 3 1
L-phenylalanine degradation II (anaerobic) 3 2 1
plastoquinol-9 biosynthesis I 3 1 1
L-tyrosine degradation IV (to 4-methylphenol) 3 1 1
L-tyrosine degradation III 4 2 1
L-phenylalanine degradation III 4 2 1
4-hydroxy-2-nonenal detoxification 4 1 1
L-phenylalanine degradation IV (mammalian, via side chain) 9 4 2
pentachlorophenol degradation 10 4 2
L-phenylalanine degradation VI (reductive Stickland reaction) 5 1 1
L-tyrosine degradation V (reductive Stickland reaction) 5 1 1
4-hydroxybenzoate biosynthesis I (eukaryotes) 5 1 1
vitamin E biosynthesis (tocopherols) 7 1 1
glutathione-mediated detoxification I 8 3 1
superpathway of aromatic amino acid biosynthesis 18 18 2
gliotoxin biosynthesis 9 1 1
glutathione-mediated detoxification II 9 1 1
superpathway of L-tyrosine biosynthesis 10 10 1
superpathway of L-phenylalanine biosynthesis 10 10 1
rosmarinic acid biosynthesis I 10 3 1
(S)-reticuline biosynthesis I 11 1 1
tropane alkaloids biosynthesis 11 1 1
indole glucosinolate activation (intact plant cell) 12 3 1
camalexin biosynthesis 12 2 1
superpathway of rosmarinic acid biosynthesis 14 4 1
superpathway of hyoscyamine (atropine) and scopolamine biosynthesis 16 4 1
anaerobic aromatic compound degradation (Thauera aromatica) 27 6 1
superpathway of chorismate metabolism 59 44 2