Experiment set1IT024 for Pseudomonas sp. RS175

Compare to:

D-Mannose carbon 10 mM

Group: carbon source
Media: MME_noCarbon + D-Mannose (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 14 genes in this experiment

For carbon source D-Mannose in Pseudomonas sp. RS175

For carbon source D-Mannose across organisms

SEED Subsystems

Subsystem #Specific
Ribitol, Xylitol, Arabitol, Mannitol and Sorbitol utilization 6
Fructose utilization 2
Mannitol Utilization 2
Fructose and Mannose Inducible PTS 1
Sialic Acid 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
N-acetylneuraminate and N-acetylmannosamine degradation II 3 1 1
D-fructuronate degradation 4 3 1
sulfoquinovose degradation III 4 1 1
mannitol cycle 5 4 1
sulfoquinovose degradation I 5 1 1
sulfoquinovose degradation VI 5 1 1
superpathway of β-D-glucuronosides degradation 7 4 1
sulfoquinovose degradation V 7 3 1
superpathway of hexuronide and hexuronate degradation 10 4 1
superpathway of microbial D-galacturonate and D-glucuronate degradation 31 14 1