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Fitness for 5 genes in
Pseudomonas putida KT2440
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Top 30 experiments (either direction), sorted by average fitness
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500 nt
PP_0837 and PP_0838 are separated by 168 nucleotides
PP_0838 and PP_0839 are separated by 151 nucleotides
PP_0839 and PP_0840 are separated by 3 nucleotides
PP_0840 and PP_0841 are separated by 179 nucleotides
PP_0837: PP_0837 - putative regulator of flagellation, at 974,609 to 975,151
_0837
PP_0838: PP_0838 - inositol monophosphatase / glycerol-2-phosphatase, at 975,320 to 976,138
_0838
PP_0839: PP_0839 - tRNA Cm32/Um32 methyltransferase, at 976,290 to 977,045
_0839
PP_0840: PP_0840 - serine acetyltransferase, at 977,049 to 977,834
_0840
PP_0841: PP_0841 - DNA-binding transcriptional dual regulator 2Fe-2S cluster IscR, at 978,014 to 978,505
_0841
Group
Condition
PP
_0837
PP
_0838
PP
_0839
PP
_0840
PP
_0841
agar plate interaction control
Parafilmed volatile agar plate with no fungus
-0.3
N.D.
-0.1
-1.1
-1.2
pH
Growth at pH6 and (C) D-Glucose
+0.2
N.D.
-0.7
-0.6
-1.5
stress
R2A with Fusaric 240 ug/mL
-0.4
N.D.
-0.6
+0.2
-1.9
pH
Growth at pH6 and (C) Trisodium citrate
+0.1
N.D.
-2.1
+0.3
-0.9
temperature shift
Temperature shift 10_to_30
-0.3
N.D.
-1.0
-0.2
-0.7
carbon source
carbon source 4-vinylphenol 0.1 mM
+0.0
N.D.
-0.8
+0.6
-1.6
nitrogen source
nitrate (N)
-0.5
N.D.
-1.3
-0.5
+0.5
phage
P. putida PUT10 MOI 10
+0.4
N.D.
-1.4
+0.5
-1.1
temperature shift
Temperature shift 30_to_25; with MOPS
+0.2
N.D.
+0.3
-1.0
-1.0
phage
P. putida PUT10 MOI 10
+0.3
N.D.
-1.1
+0.3
-0.8
carbon source
carbon source 2-Deoxy-D-glucose 50 mM
-0.1
N.D.
+0.6
-0.9
-0.9
phage
P. put South MOI 1
+0.1
N.D.
-1.0
+0.4
-0.8
carbon source
carbon source D-Glucose 55.5 mM
-0.1
N.D.
+0.6
-0.5
-1.2
reactor
72hr timepoint from 1L M9/1% dextrose BATCH fermentation in 2L Sartorius Biostat reactor kept at 10% DO.
+0.2
N.D.
-1.4
+0.4
-0.3
pH
Growth at pH6 and (C) Trisodium citrate
-0.3
N.D.
+0.2
+0.5
-1.4
pH
Growth at pH7 and (C) Trisodium citrate
+0.1
N.D.
-1.3
+0.5
-0.4
soil
Soil=PNNL_Prosser_PlotA_B_20191220; Sterility=sterile; Collection=outgrowth_in_LB; SoilTreatment=coldshock; SoilTreatmentTime=288_hrs
+0.6
N.D.
-0.8
+0.4
-1.2
carbon source
D-Glucose (C); with MOPS
+0.1
N.D.
-1.9
+0.5
+0.4
mixed carbon source
mixed (C)s Trisodium citrate 10 mM and L-Meta-tyrosine 10 mM
+0.2
N.D.
+0.4
+0.3
-1.8
soil
Soil=PNNL_Prosser_PlotA_B_20191220; Sterility=nonsterile; Collection=outgrowth_in_LB_2hrs_then_extra_outgrowth_in_LB; SoilTreatment=coldshock; SoilTreatmentTime=72_hrs
-0.3
N.D.
-0.2
-1.3
+1.0
carbon source
butyrate (C)
+0.2
N.D.
-0.2
+0.5
-1.3
pH
pH 8
-0.5
N.D.
+0.4
+0.5
-1.0
pH
Growth at pH7 and (C) Trisodium citrate
+0.3
N.D.
-1.4
+0.6
+0.3
in planta
Plant=Zea_mays; PlantTreatment=34_degrees_celsius; Sample=rhizosphere; GrowthSubstrate=sand_vermiculite_perlite_mix; Collection=16_outgrowth_LB; Time=7_days
+0.6
N.D.
+0.0
+0.6
-1.2
phage
PUT 8 MOI 1
+0.3
N.D.
-1.2
+0.7
+0.3
in planta
Plant=Zea_mays; PlantTreatment=34_degrees_celsius; Sample=rhizosphere; GrowthSubstrate=sand_vermiculite_perlite_mix; Collection=16_outgrowth_LB; Time=7_days
-0.1
N.D.
+0.2
+1.1
-1.1
micoeukaryotes
Acanthamoeba sp., muxed culture-2
-0.1
N.D.
-1.0
-0.2
+1.4
nitrogen source
NAG (N); with MOPS
+0.4
N.D.
-1.2
+0.5
+0.6
agar plate interaction
Parafilmed volatile agar plate with Trichoderma atroviridae IMI dcr2mutant
+0.5
N.D.
+1.0
-0.4
+0.4
temperature shift
Temperature shift 30_to_21; with MOPS
+0.6
N.D.
+0.8
+0.9
+0.3
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