Table 1

Strains	Access Number	Hemolysis activities onto 2% sheep red blood cell plate and incubated for 48 h		Surface tension+/-STD mN/m		Ionic charge of the rinsing solution
Strains	Access Number	Growth at 8°C	Growth at 17°C	Growth at 8°C	Growth at 17°C	Growth at 8°C	Growth at 17°C
PfA7B	GQ334362	β ++	β ++	27.0+/-0.0	26.7+/-0.0	anionic	anionic
Pf1 Vis-	GQ334362	-	-	71.2+/-0.1	60.9+/-0.7	non ionic	non ionic
CTS38	GQ334368	β +	β +	63.8+/-1.2	31.1+/-0.3	anionic	anionic
CTS50	GQ334367	β ++	β +	27.5+/-0.1	27.2+/-0.1	anionic	anionic
CTS117	GQ334368	β ++	β ++	35.9+/-0.7	29.6+/-1.1	anionic	anionic
DR54	GQ334370	β +	β +	38.2+/-0.9	34.6+/-1.4	non ionic	non ionic
DSS73	GQ334363	α +	α +	32.1+/-0.9	33.2+/-0.1	anionic	anionic
DSS73-15C2	GQ334363	-	-	69.8 +/-0.9	70.8+/-0.3	non ionic	non ionic
CTS22	GQ334364	α +	α +	57.1+/-2.3	33.2+/-0.2	anionic	anionic
CTS70	GQ334365	α +	α +	31.4+/-0.1	30.1+/-0.0	anionic	anionic
CTS193	GQ334369	α +	α +	37.6+/-1.4	35.2+/-0.1	anionic	anionic

Table 1: Registration number of sequenced 16S rRNA fragments and surfactant production evaluated by hemolytic phenotype, surface tension and ionic charge of the bacterial rinsing solution for the 11 strains. Hemolysis on plate at 8°C and 17°C was realized as described in materials and methods. α corresponds to opaque lysis areas and β to transparent lysis areas. - : absence of clearing zone; + : lysis area≤1mm; ++: lysis area > 1mm. Surface tension of bacterial rinsing was determined as indicated in materials and methods at either 8°C or 17°C after four days (triplicate). The ionic charge determination was made with the rinsing solution of bacteria grown at either 8°C or 17°C as described in materials and methods.