Screening methods | Advantages | Disadvantages | References |
---|---|---|---|
Emulsification Index |
Simple to use Gives indication of biosurfactant presence |
Low stability of emulsion Surface activity and emulsification capacity do not always correlate |
( |
Surface tension test |
Precise Simple Reliable |
Concurrent measurements present difficulties Variation prone |
( |
Oil displacement/Oil spreading test |
High precision Small sample volume Low quantity of biosurfactant detected No need for specialized equipment Rapid |
Amount of oil used influences detection |
( |
Drop collapse assay |
Simple Rapid No need for specialized equipment Small sample volume |
Low sensitivity |
( |
Penetration assay |
Used for screening large number of samples |
Qualitative |
( |
Optical distortion grid assay |
Easy Rapid Sensitive Small sample volume Suitable for automated high throughput screening |
Rough Only qualitative |
( |
BATH assay |
Simple Inexpensive |
Indirect Only qualitative |
( |
Tilted glass slide test |
Simple Easy |
Preliminary If negligible amount of surfactant is present, false results are given |
( |
Hydrocarbon overlay agar test |
Direct Efficient |
Cannot be used if microbe does not degrade hydrocarbons |
( |
Atomized oil assay |
Surface enhanced biosurfactant production is shown |
Many strains only produce biosurfactant in liquid media |
( |
Blood hemolysis test |
Preliminary screening method Also predicts surface activity of producer |
Dubious results (lytic enzymes can also cause hemolysis) Hydrophobic substrates cannot be used as sole carbon source Diffusion restriction can inhibit zone formation |
( |
Blue agar plate test |
Semi-quantitative Allows various culture conditions |
Specific for anionic biosurfactants Inhibits growth of some microbes |
( |