Fitness for 1 genes in Synechocystis sp000284455 PCC 6803

Top 30 experiments (either direction), sorted by average fitness

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Group	Condition	SGL_RS06955
photoheterotrophic	growth in full media and 10 mM glucose= photoheterotrophic growth but diluted to prevent slight attenuation and replinshing of glucose	-6.8
nitrogen source	growth in full media and 10 mM glucose= photoheterotrophic growth	-5.8
photoheterotrophic	growth in full media and 10 mM glucose= photoheterotrophic growth	-5.8
nitrogen source	growth in full media and 10 mM glucose= photomixotrophic growth	-5.0
light_bubbling	high light; bubbling	-5.0
light_bubbling	high light; bubbling	-4.1
light_bubbling	high light; bubbling	-3.8
light_bubbling	high light; bubbling	-3.7
light_bubbling	high light; bubbling	-3.4
light_bubbling	high light; bubbling	-3.0
stress	D-Sorbitol 500 mM	-2.4
light_bubbling	medium light; bubbling	-2.3
stress	D-Sorbitol 500 mM	-2.2
light_bubbling	medium light; bubbling	-2.1
stress	D-Sorbitol 500 mM	-2.1
light_bubbling	medium light; bubbling	-0.7
carbon dioxide	growth in full media bubbled with ambient air	-0.6
light_bubbling	medium light; bubbling	-0.5
metal stress	growth in full media supplemented with 3 .M Cl2Co but diluted to prevent light attenuation	-0.3
stress	Zinc 20 uM	-0.3
	growth in full media	-0.3
nitrogen source	Ammonium chloride (N)	-0.2
metal stress	growth in full media supplemented with 5 .M Cl2Co but diluted to prevent light attenuation	-0.2
nitrogen source	Na NO3 10 mM as N source, buffered with TES 20 mM TES pH8 but diluted to prevent light attenuation	+0.2
carbon dioxide	growth in full media bubbled with air enriched in 5% CO2 but diluted to prevent light attenuation	+0.2
carbon dioxide	growth in full media bubbled with ambient air	+0.2
metal stress	growth in full media supplemented with 5 .M CuSO4 but diluted to prevent light attenuation	+0.2
carbon dioxide	growth in media lacking HCO3 buffered with 10 TES pH8 and bubbled with ambient air but diluted to prevent light attenuation	+0.2
nitrogen source	Inoculated in media lacking a N source and incubated for 1 week	+0.2
glucose	Na NO2 10 mM as N source, buffered with TES 20 mM TES pH8 but diluted to prevent light attenuation	+0.3
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