Evaluation of both tenso-active and emulsifying activities indicated that a biosurfactant was produced by the newly isolated and promising strain Candida glabrata isolated from mangrove sediments. The extracellular water-soluble emulsifying agent was isolated and identified as a heteropolymer. The maximum of bioemulsifier production was observed when the strain was grown on soluble and insoluble substrates cotton seed oil plus glucose, reaching values of 10.0 g/l after 144 hrs at 200 rpm. The cell-free culture broth containing the examined agent lowered the surface tension of the medium to 31 mN/m. Stable and compact emulsions with emulsifying activity of 75% of cotton seed oil were detected. The emulsification capacity remained practically unaltered within a wide pH (2-12), temperature (4-80ºC) ranges and under NaCl concentrations up to 10%.

Surfactants and emulsifiers are indispensable components of daily life. They are widely used in the pharmaceutical, cosmetic, petroleum and food industries (Makkar and Cameotra, 1998; Lang, 2002). The surfactant industry now exceeds US$ 9 billion per year (Desai and Banat, 1997). Most of these compounds are of petroleum origin, which are not easily biodegradable and their manufacturing processes and by-products can be environmentally hazardous. Increased environmental awareness and strict legislation has made environmental compatibility of surfactants an important factor in their applications for various uses (Maier and Soberon-Chavez, 2000). Several different microbial products that exhibit surface-active properties have been identified in the past. These so called biosurfactants are produced by certain bacteria and by a number of yeasts and filamentous fungi. They include low-molecular-weight glycolipids, lipopeptides and high-molecular-weight lipid-containing polymers such as lipoproteins, lipopolyssacharide-protein complexes and polysaccharide-protein-fatty acid complexes (Ron and Rosenberg, 2001). Because biosurfactants are readly biodegradable and can be produced in large amounts by microorganisms and thus are not dependent on petroleum-derived products, they might well be able to replace, in some instances, the traditional synthetic surfactants (Banat et al. 2000).

The success of biosurfactant production depends on the development of cheaper processes and the use of low cost raw materials, which account for 10-30% of the overall cost. Most oils and fats produced in the world are used in the food industry, which generates great quantities of wastes, tallow, lard, marine oils and free fatty acids from the extraction of seed oils (Makkar and Cameotra, 1998; Makkar and Cameotra, 2002). The literature shows that a wide range of carbon sources, including agricultural renewable resources, like sugars and oils, are suitable carbon sources for production of ecologically safe biosurfactants with good properties. (Gallert and Winter, 2002). Optimal yields of bioemulsifier are usually obtained when carbohydrate and vegetable oil are used as substrate (Zhou and Kosaric, 1995).

Among yeasts, Candida species have been widely employed for insoluble substrates fermentation and have been reported to produce surface active agents (Sarubbo et al. 1999; Sarubbo et al. 2001). The objective of this work is to investigate the production of a biosurfactant by Candida glabrata isolated from mangrove sediments and to show the capacity of the emulsifying agent in stabilizing water-in-oil emulsions.

Organism

Candida glabrata UCP 1002 was isolated from mangrove sediment collected in the City of Rio Formoso, Pernambuco State, Brazil by Gomes et al. (2000). The isolation and identification of strain are according to O’Donnell (1979). The organism was kindly supplied from the Culture Collection of Nucleous of Resource in Environmental Sciences, Catholic University of Pernambuco, Recife, PE, Brazil. The culture was maintained at 5ºC on Yeast Mold Agar (YMA) slants containing (w/v): yeast extract (0.3%), malt extract (0.3%), tryptone (0.5%), D-glucose (1%) and agar (5%). Transfers were made to fresh agar slants each month to maintain viability.

Reagents

n-Hexadecane was obtained from Sigma Chemical Co. (St. Louis, MO); food grade cotton seed oil was kindly supplied from Bunge Alimentos S.A. (SC, Brasil). Other chemicals used were analytical grade.

Media and cultivation conditions

Cultures were grown on a mineral medium containing 0.1% NH₄NO₃,0.02% KH₂PO₄, 0.02% MgSO₄.7H₂O, 0.3% yeast extract and 7.5% cotton seed oil plus 5.0% glucose as substrates. The final pH of the medium was 5.7.

The Candida glabrata was grown in solid medium at 27ºC for 48-72 hrs; then, a loopful of the cream coloured culture was transferred to Erlenmeyer flasks of 250 ml containing 50 ml of the liquid medium, Yeast Mold Broth (CYM) and incubated for one day at 27ºC on an orbital shaker (200 rpm). The CYM culture contained 10⁴ cells/ml and was used to initiate growth in mineral medium using a 10% vol/vol inoculum. The production of the emulsifier was carried out in Erlenmeyer’s flasks of 500 ml containing 100 ml of the production medium and shaking at 200 rpm for 144 hrs at 27ºC. The pH of the media was not adjusted during cultivation. Growth of the culture was monitored by counts on Neubauer Camera and plate YMA. The fermentation’s was monitored by aseptically removing of samples until the end of the experiment. All analyses were performed in triplicate and did not vary more than 5%.

Emulsification activity

Emulsification activity was measured using the method described by Cooper and Goldenberg (1987) whereby 6 ml of n-hexadecane or cotton seed oil was added to 4 ml of the culture broth free of cells in a graduated screwcap test tube and vortexed at 3000 rpm for 2 min. The emulsion stability was determined after 24 hrs, and the emulsification index was calculated by dividing the measured height of the emulsion layer by the mixture's total height and multiplying by 100.

Efficiency studies

The efficiency of the biosurfactant as an emulsifying agent was measured on the cell-free broth. Variations between volumes of the oil phase (n-hexadecane or cotton seed oil) and aqueous phase were prepared for water in oil emulsions.

Stability studies

Stability studies were done using the cell-free broth obtained centrifuging the cultures at 10000 x g for 15 min. 4 ml of the culture broth free of cells were heated at 80ºC, and cooled to room temperature, after which the emulsification activity was measured. The emulsification capacity of culture broth free of cells was also determined after exposure at lower temperature (0-4ºC). To study the pH stability of the cell-free broth, the pH of the cell-free broth was adjusted to different pH values (2 to 12) and the emulsification activity was measured. The culture liquid pH was adjusted with 1 M NaOH. The effect of NaCl concentrations (2 to 10%) on the emulsification capacity of the culture broth free of cells was also determined.

Surface activities

Surface tension and critical micellar concentration (CMC) were determined on cell-free broth obtained by centrifuging the cultures at 10000 x g for 15 min with a Tensiometer model Sigma 70 (KSV Instruments LTD - Finland) using the Du Nouy ring method at room temperature. The CMC was determined by measuring the surface tensions of dilutions of cell-free broth in distilled water up to a constant value of surface tension. Measurements of surface tension from distilled water and from the mineral medium were used as controls.

Isolation of biosurfactant

The 144-h culture was refrigerated for 24 hrs to solidify the remaining oil and to effect yeast settling. The culture was filtered through Whatman no. 1 filter paper and centrifuged at 10000 x g for 15 min. The cell-free broth was concentrated (500 ml) by freeze drying and extracted three times with chloroform (1:1, by vol.) in a separatory funnel at 28ºC.

Analytical methods

Protein concentration in the isolated bioemulsifier was determined by the Lowry method (Lowry et al. 1951) using Bovine serum albumin as a standard. Carbohydrates were determined by the phenol-sulphuric acid method, using D-glucose as a standard (Hanson and Phillips, 1981). The lipid composition of the crude bioemulsifier was determined according to Manocha et al. (1980).

Growth kinetics and extracellular bioemulsifier production

Figure 1 shows the biomass concentration, pH and emulsification index of Candida glabrata cultivation in mineral medium containing 7.5% of cotton seed oil plus 5% of glucose. Maximum biomass concentration was achieved after 72 hrs. After 48 hrs of growth, a diauxic behaviour was observed, probably due to the consumption of other substrate used in the fermentation. During the exponential growth phase, culture medium pH gradually decreased from 5.7 to 2.6, after which it remained around 3.0. The profile of emulsification activity production was observed in three independently run fermentations. Emulsification of cotton seed oil increased with increasing biomass formation, reaching its optimum nearly at about 24 hrs, and after 48 hrs of growth it showed with constant values around 75% until the end of cultivation. Conversely, the emulsification of n-hexadecane started after the microorganism entered the stationary growth phase, with maximum activity of 67% after 96 hrs of cultivation.

Bioemulsifier properties

For the measurements of surface tension of distilled water after different dilutions of the cell-free broth after 144 hrs of cultivation, it was found that the emulsifier agent obtained from glucose plus cotton seed oil could lower the surface tension of water (air-water interface) from 68 mN/m to 31 mN/m (CMC), which shows that it is a good surfactant (Figure 2). This result is similar to others surfactants produced by yeast from carbohydrate and vegetal oil as substrates (Davila et al. 1992; Zhou and Kosaric, 1995; Garcia-Ochoa and Casas, 1999).

The efficiency of the bioemulsifier containing cell-free broth is shown in Figure 3. The results showed that the biosurfactant form Candida glabrata was efficient in emulsificating the cotton seed oil once no significant variation in the emulsification index was observed for this substrate, however, for n-hexadecane emulsification, the reduction of cell-free broth volume decreased the emulsification capacity.

The effect of added NaCl concentrations on n-hexadecane and cotton seed oil emulsification capacity of the cell-free broth is summarized in Figure 4. A reduction of approximately 20% of emulsification activity was observed with the addition of up to 10% (w/v) sodium chloride for both substrates, showing a relative tolerance over these salt concentrations. Once the salinity decreases the viscosity, it is possible that the increase of NaCl concentration had influenced the quality of the emulsion, thus reducing the emulsification capacity. Reductions in emulsification activity were also reported for other surfactants of microorganisms as Candida lipolytica grown in n-hexadecane (Cirigliano and Carman, 1984) and a mixed culture cultivated in molasses (Ghurye et al. 1994).

The effect of thermal treatment on the emulsifier activity of Candada glabrata culture showed that no appreciable changes in emulsification capacity occurred, if the cell-free broth was heated, once only 10% of activity was lost at 80ºC. The lost of emulsifier activity could be explained by the denaturation of proteinaceous compounds of the bioemulsifier during heating. There was no significant change at lower temperature (4ºC). Liposan from Candida lipolytica found to be relatively stable between 30 and 90ºC, but lost 60% of its activity after boiling for 1 hr (Cirigliano and Carman, 1984).

The pH of the cell-free broth was varied from 2 to 12 to test the effect of pH on emulsification capacity. No appreciable effect on activity was observed along the pH range, although it was observed an increase at pH 12, especially for cotton seed oil emulsification. Extremes of pH could possibly transform less surface-active species into more active emulsifiers by increased ionization. The activity of the biosurfactant produced by Bacillus subtillis was also pH stable (Makkar and Cameotra, 1998), while the effectiviness of liposan as emulsifier was limited to the acid to neutral pH (Cirigliano and Carman, 1984).

Bioemulsifier isolation

The examined agent was isolated from the culture filtrate of Candida glabrata. The precipitate collected in the aqueous phase recovered 100% of the emulsification activity of n-hexadecane that was present in the culture filtrate, while the emulsification activity of the cotton seed oil increased 25%. The average yield of precipitate in the aqueous phase was approximately 10.0 g/l.Bioemulsifier production by yeast Candida utilis varied from 0.26 to 0.93 g/l and depended on process conditions (Shepherd et al. 1995), while the extracellular emulsifying agent from Curvularia lunata yielded 2.6 g/l (Paraszkiewicz et al. 2002). The emulsification activity of both the isolated biosurfactant and the cell-free remained stable for a reasonable period (more than 4 weeks) under low temperature and upon sterilization.

Preliminary chemical characteristics of bioemulsifier

Bioshyntesis of biosurfactants from a variety of bacteria and yeasts has been reported (Davila et al. 1992; Zhou and Kosaric, 1995; Daniel et al. 1999; Lang and Wullbrandt, 1999), most commonly involving rhamno-lipids, trehalose and sophorose-lipids. These usually contain various hydroxy fatty acids and carbohydrates and are characterized by unique surfactant properties (Ron and Rosenberg, 2001). Preliminary analysis of the bioemulsifier produced by the new strain Candida glabrata indicated that it was a heteropolymer, which consisted of 45% protein, 20% lipid and 10% carbohydrate. Liposan, an extracellular emulsifier synthesized by Candida lipolytica was composed of 93% carbohydrate and 7% protein (Cirigliano and Carman, 1984). Other polymeric emulsifiers containing proteins, carbohydrates and lipids were also produced by Candida lipolytica when grown in babassu vegetal oil (Sarubbo et al. 1999) or glucose (Sarubbo et al. 2001) as the sole carbon sources.

The results obtained in this work show that this new strain of Candida glabrata represents a valuable source of new compounds with surface-active properties, with potential of application in different industries. Work is in progress to improve the production process of these compounds by using industrial wastes as substrates.

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