Experiment set5IT037 for Klebsiella michiganensis M5al

Compare to:

a-Cyclodextrin carbon source

Group: carbon source
Media: RCH2_defined_noCarbon + a-Cyclodextrin (20 mM), pH=7
Culturing: Koxy_ML2, 24-well transparent microplate; Multitron, Aerobic, at 30 (C), shaken=700 rpm
By: Adam on 27-Mar-17
Media components: 0.25 g/L Ammonium chloride, 0.1 g/L Potassium Chloride, 0.6 g/L Sodium phosphate monobasic monohydrate, 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: 1764 B4

Specific Phenotypes

For 51 genes in this experiment

For carbon source a-Cyclodextrin in Klebsiella michiganensis M5al

For carbon source a-Cyclodextrin across organisms

SEED Subsystems

Subsystem #Specific
Maltose and Maltodextrin Utilization 8
Glycogen metabolism 2
Potassium homeostasis 2
Bacterial Chemotaxis 1
Entner-Doudoroff Pathway 1
Glutathione-regulated potassium-efflux system and associated functions 1
Glycolysis and Gluconeogenesis 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
glycogen degradation I 8 8 5
starch degradation III 4 4 2
trehalose degradation I (low osmolarity) 2 2 1
trehalose degradation II (cytosolic) 2 2 1
starch degradation V 4 3 2
glycogen degradation II 6 4 3
sucrose biosynthesis II 8 6 3
starch degradation IV 3 2 1
GDP-α-D-glucose biosynthesis 3 2 1
trehalose degradation V 3 2 1
trehalose degradation IV 3 1 1
sucrose degradation III (sucrose invertase) 4 4 1
lipid IVA biosynthesis (P. gingivalis) 9 9 2
glucose and glucose-1-phosphate degradation 5 5 1
lipid IVA biosynthesis (P. putida) 6 6 1
lipid IVA biosynthesis (E. coli) 6 6 1
lipid IVA biosynthesis (generic) 6 6 1
lipid IVA biosynthesis (H. pylori) 6 6 1
lipid IVA biosynthesis (Vibrio cholerae serogroup O1 El Tor) 6 6 1
lipid IVA biosynthesis (2,3-diamino-2,3-dideoxy-D-glucopyranose-containing) 6 5 1
UDP-N-acetyl-D-glucosamine biosynthesis II 6 4 1
UDP-N-acetyl-D-galactosamine biosynthesis II 7 4 1
chitin derivatives degradation 8 4 1
1,3-propanediol biosynthesis (engineered) 9 7 1
chitin biosynthesis 9 6 1
starch degradation II 9 1 1
glycolysis III (from glucose) 11 11 1
homolactic fermentation 12 12 1
Bifidobacterium shunt 15 13 1
superpathway of (Kdo)2-lipid A biosynthesis 17 17 1
heterolactic fermentation 18 16 1
superpathway of Kdo2-lipid A biosynthesis 25 18 1