Biosurfactant Production by Pseudomonas fluorescens NCIM 2100 Forming Stable Oil-in-Water Emulsions

Author(s):  
Neha Panjiar ◽  
Shashwati Ghosh Sachan ◽  
Ashish Sachan
2008 ◽  
Vol 35 (11) ◽  
pp. 1303-1308 ◽  
Author(s):  
Mahmoud Abouseoud ◽  
Aziza Yataghene ◽  
Abdeltif Amrane ◽  
Rachida Maachi

2009 ◽  
Vol 64 (1-2) ◽  
pp. 96-102 ◽  
Author(s):  
Emilia Stoimenova ◽  
Evgenia Vasileva-Tonkova ◽  
Anna Sotirova ◽  
Danka Galabova ◽  
Zdravko Lalchev

The indigenous strain Pseudomonas fluorescens, isolated from industrial wastewater, was able to produce glycolipid biosurfactants from a variety of carbon sources, including hydrophilic compounds, hydrocarbons, mineral oils, and vegetable oils. Hexadecane, mineral oils, vegetable oils, and glycerol were preferred carbon sources for growth and biosurfactant production by the strain. Biosurfactant production was detected by measuring the surface and interfacial tension, rhamnose concentration and emulsifying activity. The surface tension of supernatants varied from 28.4 mN m-1 with phenanthrene to 49.6 mN m-1 with naphthalene and heptane as carbon sources. The interfacial tension has changed in a narrow interval between 6.4 and 7.6 mN m-1. The emulsifying activity was determined to be highest in media with vegetable oils as substrates. The biosurfactant production on insoluble carbon sources contributed to a signifi cant increase of cell hydrophobicity and correlated with an increased growth of the strain on these substrates. Based on these results, a mechanism of biosurfactant-enhanced interfacial uptake of hydrophobic substrates could be proposed as predominant for the strain. With hexadecane as a carbon source, the pH value of 7.0 - 7.2 and temperature of (28 ± 2) °C were optimum for growth and biosurfactant production by P. fluorescens cells. The increased specific protein and biosurfactant release during growth of the strain on hexadecane in the presence of NaCl at contents up to 2% could be due to increased cell permeability. The capability of P. fluorescens strain HW-6 to adapt its own metabolism to use different nutrients as energy sources and to keep up relatively high biosurfactant levels in the medium during the stationary phase is a promising feature for its possible application in biological treatments.


2017 ◽  
pp. 41-54
Author(s):  
Aderonke K. Akintokun ◽  
Seun O. Adebajo ◽  
Caroline A. Akinremi

merging multiple opportunities for industrial production and environmental applications have focused increasing research attention on biosurfactants in recent years. Hydrocarbon-polluted soils have proved a major source of biosurfactant-producing bacteria. In this study an alternative method of producing biosurfactants was established, based on pharmaceutical effluents. Pharmaceutical effluents are a rich source of complex organic compounds with potential as a substrate for micro-bial biosurfactant production. A successful biosurfactant screening assay is achieved when a com-bination of different methods are employed. Biosurfactant producing bacteria were isolated from pharmaceutical effluent and identified by biochemical methods. The best biosurfactant producer was identified by a molecular method. The biosurfactant screening techniques employed were drop collapse assay, haemolytic assay, oil spreading assay, bacteria adhesion to hydrocarbon assay and emulsification assay. Analysis of haemolytic activity indicated that 35 isolates (44.30%) produced beta-haemolysis, 12 isolates (15.19%) produced gamma-haemolysis, while 32 isolates (40.51%) produced alpha-haemolysis. The highest zone of clearance was 42.0± 1.73 by isolate DF7 and lowest zone of clearance was obtained from isolate GC5 of 12.0± 0.73. Screening of the 35 isolates using the oil spreading test showed that 28 isolates (80.0%) were positive, while 7 isolates (20.0%) were negative. The highest zone of clearance for the oil in water was 19.0±0.1 by DF1 while the lowest zone was 4.3±0.33 by MB3. The drop collapse test revealed that 22 isolates (78.57%) were positive and 6 isolates (21.43%) were negative. At 0h, the highest emulsification percentage was 74.4% by Bacillus licheniformis and the lowest was 42.5% by Arthrobacter globiformis. After 24h, the highest emulsification value (69.23%) was obtained for Bacillus clausis, while the lowest value (30.84%) was obtained for Arthrobacter globiformis. The findings demonstrated the ability of the isolates to produce biosurfactant, and confirmed the capacity of Bacillus clausis isolated from pharmaceutical effluents as a potential bacteria for biosurfactant production.


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