This file contains the data of Figure 9.

Figure 9 shows the hydrophobicity percentage calculated from optical density measurements of cells suspended in 50 mM sodium acetate buffer overlaid with dodecane.
hydropbohic cells partition into the organic phase and the difference in optical density in the water phase can be calculated into a percentage indicating cell surface hydrophobicity.

The hydrophobicity assays were performed for the strains CEN.PK113-7D, IMK1061, IMX2897, IMX2912, IMX2913, IMX2914 and IMX2915.
All tests were done using biological duplicates.
CEN.PK113-7D was used as control for each experiment, resulting in a total of 16 biological replicates.
Hydrophobic partitioning assays were performed in technical duplicates. Ooptical density measurements were each performed in technical duplicates.

The data for each strain is found in a seperate tab.
In each tab, the data pertaining to the graph is seen at the top, with the values in light orange representing the data points used to generate the graph, while the values in blue represent the means and standard deviations depicted in the graph.

The raw data and calculations is marked in 5 steps. 

1. Raw OD660 measurements from samples taken from the aqueos phase hungate tubes after 10 minutes of vertical incubation. 
Each sample is measured in technical duplicates. These values are used to calculate Value A for the hydrophobicity formula.
The values measured are multiplied by 10 to factor for the dilution.

2. These are the Raw Optical density measurements of the cells after partitioning into the aqueous and organic phase. Each sample is measured in technical duplicates. 
These values are used to calculate Value C for the hydrophobicity formula.
The values measured are multiplied by 10 to factor for the dilution.

3. The hydrophobicity percentage is calculated using the values from step 1 and 2, and the formula: H = 100% x (A-C)/A
This is calculated per technical replicate of the partitioning assay.

4. The average hydrophobicity is calculated per biological replicate from the values obtained in step 3.