Inhibitory Effect of High Concentrations of Furfural on Industrial Strain of Saccharomyces cerevisiae

Bioethanol made from lignocelluloses biomass resources, provides unique environmental, economic and strategic benefits, when compared to gasoline as automobile fuel. To be able to substitute gasoline by bioethanol, one should over come many obstacles, including the production of furfural and hydroxyl-methyl furfural, which are produced when cellulosic materials are treated in the presence of acids in high temperature and pressure to produce simple sugars. These inhibitory compounds have a profound negative effect on the growth of ethanol producing yeasts and their ethanol production. Saccharomyces cerevisiae Lalvin EC1118™, an industrial ethanologenic strain, was used in media with high concentrations of furfural (i.e. 4, 5 and 6 g/L) to study the tolerance it shows against this compound. Results showed that both the amount of growth and ethanol production were decreased when furfural was present in the media. The amount of decrease was higher in the concentration of 6 g/L of furfural than 4 and 5 g/L

Isolation and production of biosurfactant from Pseudomonas aeruginosa isolated from Iranian southern wells oil

In this study one hundred and fifty two bacterial strains were isolated from oil contaminated. Hemolysis was used as a criterion for the primary isolation of biosurfactant producing-bacteria. Fifty five strains had haemolytic activity, among -them twelve strains were good biosurfactant producers by measuring surface tension and emulsification activity. Two microorganisms showed the highest biosurfactant production when grown on paraffin and glycerol as sole carbon source. As a result of biosurfactant synthesis the surface tension of the medium were reduced from 73 mN/m to values below 32 mN/m.A rhamnolipid producing bacterium, P.aeruginosa isolate from oil wells in the southern of Iran. Isolated strain was identified by morphological, biochemical, physiological. The identified Pseudomonas aeruginosa   confirmed by Persian type culture collection. Glycolipid production by isolated bacterium using different carbon (gasolin, paraffin oil, glycerol, whey) and nitrogen sources (NaNO3, (NH4)2SO4 and CH4N2O) was studied. Biosurfactant production was quantified by surface tension reduction, critical micelle dilution (CMD), emulsification capacity (EC), and ThinLayerChromatogeraphy. The best result were obtained when using glycerol as a C/N ratio of 55/1 and use of sodium nitrate as nitrogen source resulted in higher production of the rhamnolipid, expressed by rhamnose (4.2 g/l) and by the yield in relation to biomass (Yp/x = 0.65 g/g). Additionally, physical-chemical characteristics of the spent broth with and without cells were studied, providing a low critical micelle concentration of 19 mg/l and surface tension was reduced to 20 mN/m (%)

Environmental importance of rhamnolipid production from molasses as a carbon source

Rhamnolipid has been known as biosurfactant which is produced by Pseudomonas aeruginosa   in fermentation process. Several carbon sources such as ethanol, glucose, vegetable oil and hydrocarbon have been used to produce rhamnolipid. In this study, we are trying to use molasses which is a waste product from sugar industry as carbon source to produce rhamnolipid. The bacterium which was previously isolated from Iranian oil over years Glycolipid production by isolated bacterium using sugar beet molasses as a carbon and energy source was investigated. Result from the study showed that the growth of the bacteria using molasses as carbon sources is growth-associated. The specific production rate of rhamnolipid with 2%, 4%, 6%, 8% and 10% of molasses are 0.00065, 4.556, 8.94, 8.85, and 9.09 respectively. The yield of rhamnolipid per biomass with 2%, 4%, 6%, 8% and 10% molasses are 0.003, 0.009, 0.053, 0.041 and 0.213 respectively. The production of rhamnolipid (0.0531 g. rhamnolipid/g biomass) is higher compare to the culture grown in aerobic condition (0.04 g. rhamnolipid/g biomass). These studies indicate that renewable, relatively inexpensive and easily available resources can be used for important biotechnological processes

Emulsan Analysis Produced by Locally Isolated Bacteria and Acinetobacter Calcoaceticus RAG-1

Growth of previously isolated bacteria from Iranian oil reservoirs on different carbon and energy sources and under varying conditions have been used to produce a class of extracellular microbial protein-associated lipopolysaccharides named emulsan.Several Bacteria were previously isolated from Iranian oil reservoirs and designated as; Ilam-1 and Paydar-4. In present study, the isolated strains were compared with standard sample of Acinetobacter Calcoaceticus RAG-1 from Persian Type Culture Collection (PTCC 1641), IROST. Among the isolated strains, two strains were found to produce an extracellular, emulsifying agent when grown in Mineral Salt Medium containing soya oil, ethanol or local crude oil. The isolated bacteria were cultured and further analysed using protein estimation, reducing sugar analysis, hemolytic activity, surface tension and emulsification activity tests. The crude emulsifier of RAG-1, PAYDAR-4 and ILAM-1 were concentrated from the cell-free culture fluid by ammonium sulfate precipitation to yield 1.89g, 1.78g and 1.69g of bioemulsan respectively. Emulsifying activity was observed over the entire production process. These investigations showed that emulsan produced by isolated Iranian crude oil reservoir were comparable with Acinetobacter Calcoaceticus RAG-1 which is made of carbohydrate backbone as its hydrophilic part (N-acetyl-D-galactoseamine, N-acetylgalactoseamine uronic acid, diamino-6-deoxy-D-glucose) and fatty acid chain as its hydrophobic portion

Cleaning Oil-Contaminated Vessel By Emulsan Producers (Autochthonous Bacteria)

In a process for cleaning hydrocarbonaceous residues, including residual petroleum from laboratory made oil-contaminated vessels, several previously isolated bacteria from Ilam and Paydar oil reservoirs, were used. The isolated strains were compared with the standard sample of Acinetobacter calcoaceticus PTCC 1318 from Persian Type Culture Collection (PTCC). This gram-negative bacterium grows on a variety of different substrates as sole carbon and energy sources, including crude oil, soy oil and ethanol. It is oxidase-negative, non-motile and strictly aerobic. Among the isolated strains, two autochthonous strains were found to produce an extracellular emulsifying agent when grown in Mineral Salt Medium containing soy oil, ethanol or local crude oil. The crude emulsifier of PTCC1318, Paydar-4 and Ilam-1 were concentrated from the cell-free culture fluid by ammonium sulfate precipitation to yield 1.89 g, 1.78 g and 1.69 g of bioemulsan, respectively. Although measuring the surface tension (ST) is not very applicable procedure in case of bioemulsan, but in order to prove this theory, ST was conducted.Further analysis of purified emulsion was performed to prove the molecular structure by Carbon13 Nuclear Magnetic Resonance, Proton1Nuclear Magnetic Resonance and Fourier Transform Infrared Radiation methods. These investigations showed that the molecular weight of emulsion produced by species isolated from Ilam and Paydar crude oil reservoirs are comparable with Acinetobacter calcoaceticus PTCC 1318

Ability of indigenous Bacillus licheniformis and Bacillus subtilis in microbial enhanced oil recovery

Microbially produced lipopeptide have been isolated and studied for microbial enhanced oil recovery. About 60 gram positive bacteria isolated from soil contaminated with crude oil, near the crude oil storage tank in Tehran Refinery, Tehran, Iran. However, most of these studies have produced lipopeptide by one of the pure-culture microbes isolated in a laboratory. Among the isolates, heamolytic tests revealed two biosurfactant producers. The isolated strains were designated as C2, E1. By using morphological, biochemical and molecular biology tests (16 SrRNA), the strains identified as Bacillus licheniformis and Bacillus subtitlis, respectively. Emulsification activity and measurement of surface tension indicated that, the isolates were high producers of biosurfactant. The product of C2 and E1 is mainly lipopeptide. This product reduce surface tension from 65 to 30 mN/m. Emulsified activity of crude oil was 92% for C2 and 90 % in case of E1. This is the first report of indigenous Bacillus licheniformis and Bacillus subtilis from a soil contaminated with oil in an Iranian refinery with ability to produce biosurfactant

Isolation of biosurfactant producing bacteria from oil reservoirs

Biosurfactants or surface-active compounds are produced by microoaganisms. These molecules reduce surface tension both aqueous solutions and hydrocarbon mixtures. In this study, isolation and identification of biosurfactant producing bacteria were assessed. The potential application of these bacteria in petroleum industry was investigated. Samples (crude oil) were collected from oil wells and 45 strains were isolated. To confirm the ability of isolates in biosurfactant production, haemolysis test, emulsification test and measurement of surface tension were conducted. We also evaluated the effect of different pH, salinity concentrations, and temperatures on biosurfactant production. Among importance features of the isolated strains, one of the strains (NO.4: Bacillus .sp) showed high salt tolerance and their successful production of biosurfactant in a vast pH and temperature domain and reduced surface tension to value below 40 mN/m. This strain is potential candidate for microbial enhanced oil recovery. The strain4 biosurfactant component was mainly glycolipid in nature

Optimization Of Reactive Blue 19 Decolorization By Ganoderma Sp. Using Response Surface Methodology

Synthetic dyes are extensively used in different industries. Dyes have adverse impacts such as visual effects, chemical oxygen demand, toxicity, mutagenicity and carcinogenicity characteristics. White rot fungi, due to extracellular enzyme system, are capable to degrade dyes and various xenobiotics. The aim of this study was to optimize decolorization of reactive blue 19 (RB19) dye using Ganoderma sp. fungus. Response Surface Methodology (RSM) was used to study the effect of independent variables, namely glycerol concentration (15, 20 and 25 g/L), temperature (27, 30 and 33 oC) and pH (5.5, 6.0 and 6.5) on color removal efficiency in aqueous solution. From RSM-generated model, the optimum conditions for RB19 decolorization were identified to be at temperature of 27oC, glycerol concentration of 19.14 mg/L and pH=6.3. At the optimum conditions, predicted decolorization was 95.3 percent. The confirmatory experiments were conducted and confirmed the results by 94.89% color removal. Thus, this statistical approach enabled to improve reactive blue 19 decolorization process by Ganoderma sp. up to 1.27 times higher than non-optimized conditions