Experiment set3IT018 for Cupriavidus basilensis FW507-4G11

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L-Phenylalanine nitrogen source

Group: nitrogen source
Media: RCH2_defined_noNitrogen + L-Phenylalanine (20 mM), pH=7
Culturing: cupriavidus_4G11_ML11, 24 deep-well microplate; Multitron, Aerobic, at 30 (C), shaken=750 rpm
By: Jayashree on 3/3/2015
Media components: 0.1 g/L Potassium Chloride, 0.6 g/L Sodium phosphate monobasic monohydrate, 20 mM Sodium D,L-Lactate, 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)

Specific Phenotypes

For 3 genes in this experiment

For nitrogen source L-Phenylalanine in Cupriavidus basilensis FW507-4G11

For nitrogen source L-Phenylalanine across organisms

SEED Subsystems

Subsystem #Specific
Homogentisate pathway of aromatic compound degradation 2
Aromatic amino acid degradation 1
Pterin 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-phenylalanine degradation I (aerobic) 1 1 1
3-(4-hydroxyphenyl)pyruvate biosynthesis 1 1 1
L-tyrosine biosynthesis IV 1 1 1
L-phenylalanine biosynthesis III (cytosolic, plants) 2 2 1
atromentin biosynthesis 2 1 1
L-tyrosine degradation II 2 1 1
L-tyrosine degradation I 5 5 2
L-tyrosine biosynthesis I 3 3 1
L-phenylalanine biosynthesis I 3 3 1
L-phenylalanine degradation II (anaerobic) 3 2 1
L-phenylalanine degradation V 3 2 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
superpathway of plastoquinol biosynthesis 5 2 1
4-hydroxybenzoate biosynthesis I (eukaryotes) 5 1 1
L-tyrosine degradation V (reductive Stickland reaction) 5 1 1
L-phenylalanine degradation VI (reductive Stickland reaction) 5 1 1
superpathway of aromatic amino acid biosynthesis 18 18 2
L-phenylalanine degradation IV (mammalian, via side chain) 9 6 1
superpathway of L-phenylalanine biosynthesis 10 10 1
superpathway of L-tyrosine biosynthesis 10 10 1
rosmarinic acid biosynthesis I 10 2 1
(S)-reticuline biosynthesis I 11 3 1
tropane alkaloids biosynthesis 11 1 1
superpathway of rosmarinic acid biosynthesis 14 2 1
superpathway of hyoscyamine (atropine) and scopolamine biosynthesis 16 3 1
anaerobic aromatic compound degradation (Thauera aromatica) 27 7 1
superpathway of chorismate metabolism 59 45 2