Industrial derivative of tallow: a promising renewable substrate for microbial lipid, single-cell protein and lipase production by Yarrowia lipolytica
Keywords: lipase, microbial lipids, single-cell protein, tallow, Yarrowia lipolytica.
aim of the present study was to assess the potential of valorisation
of a solid industrial derivative of tallow, composed of saturated
free-fatty acids (“stearin”), by fermentations carried out by the
yeast Yarrowia lipolytica ACA-DC
Current agricultural and industrial practice has led to an enormous generation of various low- or negative-cost crude fatty materials difficult to treat and valorise (e.g. tallow, waste-fats, soapstocks, rapeseed oil, grease-containing waste-waters, etc.) (Fickers et al. 2005a). Besides issues provided by the use of these substances as starting materials for bio-diesel production, biotechnological applications of fatty materials aiming at the synthesis of high-added value metabolites (e.g. single-cell protein, microbial lipids, organic acids, bio-surfactants, lipases) are of great economical and ecological significance (Adamczak and Bednarski, 1996; Čertik et al. 1997; Adamczak and Bednarski, 2000; Papanikolaou et al. 2001; Oswal et al. 2002; Papanikolaou and Aggelis, 2003; Fickers et al. 2004; Fickers et al. 2005a; Fickers et al. 2005b; Mantzouridou et al. 2006; Szczęsna-Antczak et al. 2006). Amongst fatty materials, widely available low-added ones are various animal fats and tallow or their industrial derivatives, which, while underused nowadays due to their replacement by vegetable oils, could become a competitive substrate for various microbial transformations. Nevertheless, few investigations dealing with the biotechnological valorisation of these low added-value materials have been conducted so far in the literature and are mainly referred to the production of sophorolipids, citric acid and enzymes by yeasts or moulds (Bednarski et al. 1994; Adamczak and Bednarski, 1996; Adamczak and Bednarski, 2000; Kamzolova et al. 2005).
The non-conventional dimorphic yeast Yarrowia (Candida-Saccharomycopsis) lipolytica has been efficiently cultivated on various hydrophobic substances producing many extra- or intra-cellular metabolites of industrial significance (Fickers et al. 2005a; Finogenova et al. 2005). Traditionally, the most widespread biotechnological application of strains belonging to this species has focused on the production of single-cell protein (microbial biomass) (Barth and Gaillardin, 1996; Musiał et al. 2004). In spite of the fact that species of the yeast Y. lipolytica were considered as good candidates for single-cell oil or lipase production (Hadeball, 1991; Ratledge, 1994), the production of these metabolites by Y. lipolytica strains has only recently been studied in detail. Wild or genetically engineered strains have recently been reported capable of storing huge quantities of intra-cellular lipid, located in lipid bodies, during growth on various hydrophobic materials (Papanikolaou et al. 2001; Papanikolaou and Aggelis, 2003; Mličková et al. 2004). The storage lipid was mainly composed of neutral fractions, i.e. triacylglycerols and to a lesser extent free-fatty acids and steryl-esters (Papanikolaou et al. 2001; Athenstaedt et al. 2006). Various studies have indicated that in Y. lipolytica strains, cell-bound or extra-cellular lipase production is stimulated by the presence into the culture medium of long-chain fatty acids, triacylglycerols and organic nitrogen (e.g. urea, peptone or yeast extract) (Adamczak and Bednarski, 1996; Pereira-Meirelles et al. 1997; Pereira-Meirelles et al. 2000; Dominguez et al. 2003; Fickers et al. 2004; Fickers et al. 2005a; Fickers et al. 2005b). Lipase production is also critically affected by the presence of surfactants and the aeration and the agitation of the culture medium, and with wild Y. lipolytica strains, quantities ranging from 1.0 up to 58.5 IU/ml (1 IU defined as the quantity of the enzyme required for the liberation of 1 µmol of fatty acid per min) have been achieved (Dominguez et al. 2003; Alonso et al. 2005; Kamzolova et al. 2005). Additionally, genetic engineering or mutagenesis have been employed in order to improve lipase production, and after extensive selection of new over-producing genetically engineered derivatives and optimisation of culture conditions, the concentrations have been remarkably ameliorated (Nicaud et al. 2002; Fickers et al. 2004; Fickers et al. 2005b).
In recent investigations, Y. lipolytica strain ACA-DC 50109 has been cultivated on industrial free fatty acids and produced notable quantities of reserve lipid that presented a composition similar to that of cocoa-butter (Papanikolaou et al. 2001). The present investigation aims to use this organism to valorise an industrial derivative of tallow, generated in abundant quantities, in order to produce microbial lipid (single-cell oil), lipases and microbial biomass (single-cell protein). Bio-kinetic interpretations of the experimental data are considered and discussed.
Y. lipolytica was isolated and identified in the Laboratory of General and Agricultural Microbiology - Agricultural University of Athens and obtained the code LGAM S(7)1. Then the strain was deposited in the Greek Coordinated Collections of Microorganisms obtaining the official reference number ACA-DC 50109. The microorganism was maintained on potato dextrose agar (Fluka) at T = 5 ± 1ºC. The salt composition of the medium has been described in previous investigations (Papanikolaou et al. 2001). Nitrogen sources used were (NH4)2SO4 (Fluka) (at various concentrations as indicated in the text) and yeast extract (Fluka) (at 2.0 mg/ml). The initial medium pH was 6.0 ± 0.1. Stearin [an industrial solid fat composed of 100% (wt/wt) free-fatty acids] purchased by the Hellenic Chemical Industry PAPOUTSANIS A.S., was used as the sole carbon source. The fatty acid composition of stearin was as follows (%, wt/wt): C12:0 10; C14:0 10; C16:0 25; C18:0 52; Δ9C18:1 2; Δ9,12C18:2 < 0.5. Tween 80 (Fluka) and PEG 20000 (Fluka) at 10% (wt/wt fat) of each were added as emulsifiers. An Ultra Turrax homogeniser (T25 basic) (Janke and Kunkel, Germany) allowed the dispersion of fat particles into the aqueous phase.
All experiments were performed in batch mode. Cultures were done
in either 250 ml conical flasks or a
In the bioreactor experiments, the fermentor with an initial fermentation
In flask experiments, dissolved oxygen (D.O.) was determined off-line with the aid of a selective electrode (oxi200 Sensodirect, Lovinbod). Before harvesting, the shaker was stopped and the probe was placed into the flask. Then, the shaker was switched on and the measurement was taken after D.O. equilibration (usually within 10 min). pH was measured using a Jenway 3020 pH-meter. In the bioreactor cultures, pH was adjusted to 6.0 ± 0.1 and was automatically controlled by addition of 1M NaOH, while the levels of dissolved oxygen were determined on-line by a selective electrode (Adi 1020, Applikon).
Cells were harvested by centrifugation (Heraeus Sepatech Suprafuge-22
apparatus) at 7000 x g/20 min and washed successively with ethanol
and hexane (Papanikolaou et al. 2001). Biomass concentration was determined
from the dry weight (drying at 85 ±
In all trials, yeast morphology was checked by light microscopic observations made by a Zeiss (Axioscop 40, Germany) microscope. Photographed cells were stained with crystal violet and viewed at x 100.
In the first part of the investigation, the effects of nitrogen and substrate fat availability upon microbial growth, lipid accumulation and lipase secretion were studied. In this series of experiments, the initial concentration of stearin, S0, was first adjusted to 10 mg/ml and the concentration of (NH4)2SO4 ranged from 0.5 to 10.0 mg/ml (kinetics carried out with 0.5, 1.0, 2.0, 4.0, 5.0, 6.0 and 10.0 mg/ml). In all of the cultures and regardless of the extra-cellular nitrogen availability of the medium, significant biomass and lipid quantities were produced (Xmax = 8.0 ± 0.5 mg/ml, Lmax = 3.9 ± 0.5 mg/ml) (Figure 1a). Fat was removed from the culture medium with comparable rates regardless of the available nitrogen quantity in the medium (kinetics not presented). Total cellular lipid was produced in significant quantities regardless of the nitrogen availability into the medium [lipid from 25 to 44% (wt/wt) in dry weight] with the higher quantities produced when low initial nitrogen media were employed, while at the stationary growth phase significant quantities of substrate fat remained unconsumed [around 25 ± 6% (wt/wt) of the initial fat quantity] (see cases with S0 = 10 mg/ml in Figure 1a). To further investigate the effect of nitrogen availability of the medium upon microbial growth experiments, an initial stearin concentration S0 = 20 mg/ml and (NH4)2SO4 concentrations 1.0, 2.0, 3.0, 4.0 and 5.0 mg/ml were used. Xmax and Lmax values significantly increased despite variations in the nitrogen concentration in the medium (X = 16.0 ± 0.9 mg/ml, L = 7.1 ± 0.8 mg/ml) while, as in the previous trials lipid production was favoured at low nitrogen concentration media (see cases with S0 = 20 mg/ml in Figure 1a). Significant quantities of extra-cellular substrate fat, higher than in the trials with S0 = 10 mg/ml, remained unconsumed in the medium at the end of the fermentation [Sr = 6.5 ± 0.5 mg/ml corresponding to around 32 ± 4% (wt/wt) of the initial fat quantity] (Figure 1a). The highest amount of cellular lipid produced was 7.9 mg/ml [corresponding to 52.0% (wt/wt) in dry weight] and was observed in the culture with the ratio (S)/(NH4)2SO4 10/0.5 g/g (= 20/1.0 g/g), while in all cases and regardless of substrate fat or (NH4)2SO4 concentration in the medium, the yield YX/S presented remarkable values of 1.10 ± 0.10 g/g.
Extra-cellular lipase was produced regardless of the substrate fat or the nitrogen concentration in the medium, and occurred during primary anabolic activity. Enzyme production was clearly enhanced with increases in (NH4)2SO4 and S concentrations (Figure 1b); when S0 = 10 mg/ml, the Lipmax value obtained was 1.41 IU/ml in the medium with (NH4)2SO4 at 10 mg/ml while the respective value when the initial (NH4)2SO4 quantity was adjusted to 0.5 mg/ml was 0.88 IU/ml (Figure 1b). Increases in both substrate fat and (NH4)2SO4 concentrations significantly increased the concentration of produced lipase, with the Lipmax value 2.50 IU/ml obtained when S0 = 20 mg/ml and the initial (NH4)2SO4 concentration was 5.0 mg/ml (Figure 1b). In all cultures and regardless of the initial fat or (NH4)2SO4 concentration in the culture medium, lipase concentration decreased during the stationary growth phase (Figure 1b).
D.O. concentrations of the growth medium in the flask fermentations ranged in values between 20 and 60% (v/v) of the saturation for the period 0-100 hrs after inoculation, before increasing to values higher than 65% at the end of fermentation (after 100 hrs), indicating that full aerated conditions were employed. It is also noted that in spite of the fact that some of the trials were conducted in nitrogen-limited conditions [e.g. S0 = 20 mg/ml, (NH4)2SO4 1.0 mg/ml], the pH of the medium dropped very little (pH drop of the medium around 0.5 ± 0.1 units). Low quantities of organic acids were produced (total amount of organic acids up to 1.4 ± 0.3 g/l, main organic acids detected by H.P.L.C. analysis were acetic and citric acid).
Given that the higher quantity of cellular lipid was produced in the medium containing initial stearin (S0) at 20 mg/ml and (S)/(NH4)2SO4 ratio 20 g/g, growth was carried out in a bioreactor experiment with these culture conditions. The culture pH was adjusted and maintained at the value of 6.0 ± 0.1, and a higher agitation rate, than that used in the shake flask studies, was employed (650 against 180 rpm). The oxygenation in the culture medium was higher compared with the 250-ml flask culture experiments; in the period 0-140 hrs after inoculation the D.O. ranged between 45 and 70% (v/v) of the saturation level. Higher agitation and oxygenation rates seemed to critically influence the metabolism of Y. lipolytica; significantly higher quantities of biomass (Xmax = 30.5 mg/ml) and lower quantities of total lipid [L = 2.5-4.0 mg/mlcorresponding to 7-16% (wt/wt) of lipid in dry weight] were produced compared with the respective fermentation carried out in 250-ml flasks. Likewise, in the bioreactor experiment, extra-cellular lipase activity was remarkably lower compared with the equivalent flask trial (maximum activity 0.95 against 1.42 IU/ml). These differences were attributed to the different aeration and agitation conditions between the 250-ml flask and the bioreactor culture.
A numerical model capable of quantifying the production of biomass and the biosynthesis and subsequent degradation of lipase by Y. lipolytica cultivated on stearin in the bioreactor trial was developed. The equations of the model are presented below:
From the above equation it can be assumed that Lip activity was considered as a primary anabolic activity, while its hydrolysis rate was considered to be quantitatively related to the biomass concentration (X) in the growth medium (proteases were considered as cell-bounded enzymes).
It can be deduced, hence, that μ was either governed by the maximum attainable culture density (Xmax-carrying capacity of the system), or it linearly decreased with the diminution of the available quantity of substrate fat used as the sole carbon source.
Differential equations were integrated by using the Runge-Kutta 4th order integration method, while the parameters for optimisation were maximum specific growth rate (μmax), maximum biomass achieved (Xmax), biomass yield on fat consumed (YX/S), α (parameter related with the production of lipase as primary anabolic product) and KD (parameter related with the degradation of lipase). The parameters were optimised using the least squares method, while the Marquardt iterative search algorithm (initial λ = 10-3) was used to determine the parameter values that minimised the residual sum of squares. Both models fitted well on the experimental data (Figure 2a and Figure 2b) while comparison between the optimised-predicted parameter values and those experimentally measured were satisfactory, indicating the validity of the proposed models (Table 1). If various constraints were imposed (e.g. change of the initial values of the parameters), the models converged always towards the optimised parameter values. Furthermore, attempt to introduce the term of the energy of maintenance coefficient (mS) in Equation  was not successful given that during optimisation process mS tended to achieve almost negligible values [e.g. values of around 1.2 x 10-12 g/(g x h)].
Yeast morphology and fatty acid composition of cellular and extra-cellular fat were studied during all of the experimental runs. In all trials and despite variations in the quantity of fat or nitrogen utilised in the culture medium or the mode of culture (cultivation in either flasks or bioreactor), Y. lipolytica was present primarily in its mycelial form with few single cells observed. True mycelium development was observed even at the very early stages of fermentation and this morphology was maintained until the end of the culture (up to 250-300 hrs after inoculation). A characteristic photographic picture of the morphology of Y. lipolytica cultivated on stearin is shown in Figure 3.
In all trials and regardless of the nitrogen availability and the agitation and aeration rate employed, the remaining fat was notably richer in C18:0 (around 75% (wt/wt) of total lipid) and less rich in C12:0, C14:0 and C16:0 compared with the initial composition of the fatty mixture. Also, the microorganism had the tendency to produce a highly saturated cellular lipid; cellular C18:0 presented the value of 78 ± 3%, wt/wt, of total lipids. C16:0 presented the value of 17 ± 2%, wt/wt, of total lipids, while cellular Δ9C18:1 was produced in quite small quantities (5 ± 2%, wt/wt, of total cellular lipids). It was noted that higher quantities of oleic acid were obtained in the highly aerated bioreactor experiment, in which lipid accumulation was not dominant (cellular Δ9C18:1 around 6-7% (wt/wt) in the bioreactor trial against 2.0-3.5% (wt/wt) in flask trials).
In order to validate the experimental findings, all of the experiments
were done at least in duplicate. Furthermore, an additional experiment
was conducted, in which a flask culture of Y. lipolytica was
carried out at S0 = 10 mg/ml and initial (NH4)2SO4
0.5 mg/ml. Flasks were simultaneously collected 72 hrs after inoculation,
assay of extra-cellular lipase was carried out while biomass from
each flask was collected and dried and microbial lipid was extracted.
Also residual substrate fat was extracted from the culture medium.
The obtained result for 8 individual flasks showed the following feature:
for total biomass (X) maximum and minimum values were 7.0 and
7.8 mg/ml respectively, with a mean value of 7.40 mg/ml, an obtained
standard deviation of
Y. lipolytica was cultivated on an inexpensive solid and saturated industrial derivative of tallow, as the sole carbon source, and presented impressive cell growth. Despite the physico-chemical characteristics of the substrate fat (solid in ambient temperature), this substrate was rapidly removed from the cultivation medium. However, significant quantities of fat remained unconsumed at the stationary growth phase, regardless of the initial fat or nitrogen concentration in the growth medium or the culture configuration (growth on bioreactor or flasks). Tan and Gill (1985) considered that yeast strains did not grow sufficiently well on solid fats due to inadequate dispersion of these substrates into the liquid medium. While liquid fats are dispersed with moderate agitation, solid fats require considerable agitation (e.g. 1200 rpm) for dispersal in the growth medium. Similarly, cultivation of yeasts and fungi (strains belonging to Y. lipolytica, Mucor miehei and Geotrichum candidum) on animal-waste fats for relatively long fermentation times resulted in limited fat removal from the growth medium, while the more the fat was saturated (and hence solid) the more the quantity of remaining substrate was high at the end of fermentation. For instance, fermentations carried out by various Y. lipolytica strains resulted in removal of 18 ± 4% (wt/wt) of beef tallow while the respective values for poultry fat was 36 ± 4% (wt/wt) (Bednarski et al. 1994). However, in at least one case, cultivation of a newly isolated Y. lipolytica strain on beef tallow, resulted in fat removal of 75% (wt/wt) at optimum fermentation conditions (fat removal values near to our study) (Davin and Quilty, 2001). In contrast, cultivation of various moulds resulted in almost complete lipid removal [95 ± 5% (wt/wt) of the initial fat quantity] when growth was carried out on liquid fats (Čertik et al. 1997; De Felice et al. 1997; Mantzouridou et al. 2006; Szczęsna-Antczak et al. 2006). In general, limited substrate removal on solid fats, is not only due to the physico-chemical condition of the substrate but also to the biochemical composition of the substrate. The selective uptake of fatty acids by Y. lipolytica has preciously been reported (Papanikolaou et al. 2001; Papanikolaou and Aggelis, 2003). In general, Y. lipolytica strains cultivated on fatty materials tended to metabolise the poly-unsaturated fatty acids and to accumulate the mono-unsaturated and saturated ones (Aggelis et al. 1997; Kamzolova et al. 2005). Likewise, other yeast strains (e.g. S. lipolytica ATCC 8661 and Apiotrichum curvatum ATCC 20509) presented restricted growth when cultivated on media rich in C18:0 (Tan and Gill, 1985; Lee et al. 1993).
Y. lipolytica cultivated on saturated free-fatty acids produced some quantities of extra-cellular lipase. The simultaneous production of microbial lipid and lipase has rarely been reported (Szczęsna-Antczak et al. 2006). A wide range of microorganisms has been reported capable of producing lipases with different enzymological properties and substrate specificities (Hadeball, 1991; Dalmau et al. 2000; Sharma et al. 2001; Montesinos et al. 2003; Szczęsna-Antczak et al. 2006). Among them, various Y. lipolytica strains have been tested, with secretion of extra-cellular lipase being stimulated by the presence of long-chain fatty acids or triacylglycerols as carbon source and organic nitrogen (i.e. urea, peptone, yeast extract) as nitrogen source in the growth medium (Fickers et al. 2004; Fickers et al. 2005a; Fickers et al. 2005b). In the present study, the simultaneous increase of carbon and nitrogen concentrations notably increased lipase yield (Lipmax = 2.50 IU/ml). In accordance with our findings, Montesinos et al. (2003) studying the effect of nitrogen limitation upon lipase secretion by Candida rugosa ATCC found that Lip secretion was almost completely suppressed in nitrogen-limited media. Pereira-Meirelles et al. (1997) reported maximum lipase concentrations around 2.5-3.0 IU/ml by a wild C. lipolytica strain cultivated on media containing olive oil and peptone, while higher quantities of total (extra-cellular and cell-bound) lipase were obtained in media enriched with both yeast extract and peptone (5.0-8.5 IU/ml) (Pereira-Meirelles et al. 2000). Additionally, lipase production was lowered when the agitation rate in the medium increased (Alonso et al. 2005). Kamzolova et al. (2005) screened a huge number of Y. lipolytica strains and reported lipase activities ranging from 1.8-45.5 IU/ml. Results for other wild Candida species showed a lipase production of the same magnitude with the present investigation (e.g. concentrations 2-15 IU/ml for various carbon sources used) (Dalmau et al. 2000; Montesinos et al. 2003). In order to obtain increased lipase production by Y. lipolytica strains, combinations of genetic engineering and mutagenesis methods have been employed. An expression system has been developed and strains containing multi-copy integration of the expression cassettes carrying the LIP2 gene expressed under the control of the oleic acid-inducible POX2 promoter were obtained, by using ura3d4 as selection marker gene (Pignede et al. 2000). Optimisation of the growth parameters in fed-batch cultivation resulted in very high lipase (60000 IU/ml) and biomass (100 mg/ml) production (Nicaud et al. 2002). Further selection of overproducing derivatives and use of olive oil and tryptone as substrates yielded the considerable activity of 158246 IU/ml after 80 hrs of culture (Fickers et al. 2005b).
In the present study, growth of Y. lipolytica on solid fats was accompanied by a µmax value lower compared with those reported in the literature for strains grown on liquid fats (Aggelis et al. 1997; Mličková et al. 2004; Kamzolova et al. 2005). Very satisfactory values of YX/S were obtained during cultivation in flasks (1.1 ± 0.1 g/g), while in bioreactor trials the respective value was excellent (1.5 ± 0.1 g/g). The above findings support the potential of the microorganism for the biotechnological valorisation of saturated waste fats and the production of single-cell protein from fatty materials. In the literature, it is suggested that yield YX/S values of around 0.9 ± 0.2 g/g are very satisfactory for single-cell protein fermentation from fatty substrates (Aggelis et al. 1997; Alonso et al. 2005) with lower YX/S values (e.g. 0.5-0.7 g/g) obtained for high-lipase producing wild Y. lipolytica strains (Dominguez et al. 2003; Kamzolova et al. 2005). Additionally, cellular lipid production appeared to be critically influenced by the nitrogen quantity, the agitation and the aeration rate of the growth medium. In the flask cultures (that presented lower oxygen saturation) accumulated lipids were produced in some quantities regardless of the nitrogen availability of the medium (25-52% (wt/wt) in dry matter), but this process was clearly favoured in low-nitrogen concentration media. Cells of Y. lipolytica were saturated with fat at high-stearin and low (NH4)2SO4 media (Lmax = 7.9 mg/ml), resulting in the cessation of carbon source assimilation, as indicated by the large amounts of the fat remaining unconsumed in the growth medium. Therefore, the total lipid content of 52.0% (wt/wt) should be considered as the upper limit of fat accumulation for this strain. In contrast, in the bioreactor trial, in which higher aeration and agitation were observed, total cellular lipids of only 7-16% (wt/wt) in dry matter were produced, and a metabolic shift favouring the production of lipid-free material was observed (higher YX/S value compared with flask trials). Degradation of hydrophobic materials in Y. lipolytica strains is a multi-step process requiring different enzymatic activities by acyl-coenzyme A oxidases (Aox) (Luo et al. 2002; Mličková et al. 2004; Fickers et al. 2005a). Aox3p is specific for short chain acyl-CoAs, Aox2p preferentially oxidises long-chain acyl-CoAs while Aox1p, Aox4p and Aox5p do not appear of being sensitive in the chain length of the aliphatic acyl-CoA chain (Mauersberger et al. 2001; Luo et al. 2002; Fickers et al. 2005a). Presumably at higher aeration and agitation conditions short-chain acyl-CoA oxidases (Aox3p and probably Aox1p, Aox4p and Aox5p) show increased activity, the carbon flow consequently is directed towards the synthesis of acetyl-CoA and, hence, towards lipid-free biomass formation instead of that of reserve lipophilic materials.
Y. lipolytica ACA-DC 50109 underwent a morphological transition from single-cell to true mycelial form rapidly after its cultivation on solid fat materials. Development of the microorganism principally under its filamentous form was enhanced by the presence of saturated free-fatty acids and occurred regardless of the initial concentrations of fat or (NH4)2SO4 into the medium, or the cultivation in flasks or bioreactor. Given that during growth on stearin used as substrate for the production of total biomass, the accumulation of storage lipid, the removal of substrate aliphatic chains from the medium and the secretion of lipase the organism was critically affected by the culture conditions used (see previous paragraphs), it may be assumed that the response of the organism was not linked with the morphology of the strain but was related only with the supplied carbon source used. The same strain cultured in nitrogen-limited cultures with glucose or industrial glycerol used as individual substrates or co-substrates developed only into its single-cell form while almost no mycelia were observed (Papanikolaou et al. 2002). In contrast, during cultivation on unsaturated free-fatty acids used as substrates, although storage lipid production was not favoured (Papanikolaou et al. 2001), growth with a mycelium morphology was equally enhanced. In a similar manner, Y. lipolytica NCIM 3589 growing on palm-oil mill effluent (a fat-rich residue) considerably decreased C.O.D. and B.O.D. values while a true mycelium morphology occurred, presumably due to morphological transition in response with the presence of fat into the medium (Oswal et al. 2002). In contrast with results obtained in this study, the cultivation of Y. lipolytica strains on hydrophobic materials other that fats (e.g. alkanes) favour the development of the microorganism in its yeast form (Zinjarde et al. 1998), while in others reports, cultivation of strains of the aforementioned species on hydrophilic materials (e.g. glucose, citric acid etc) mycelium formation was triggered (Perez-Campo and Dominguez, 2001; Ruiz-Herrera and Sentandreu, 2002).
In conclusion, Y. lipolytica ACA-DC 50109 presented efficient cell growth on media containing a solid fat composed of free-fatty acids used as sole carbon source. Fat was efficiently removed from the growth medium, although non-negligible quantities of substrate, rich in stearic acid, remained unconsumed. In flask cultures, considerable quantities of microbial lipids were accumulated inside the yeast cells, while to a lesser extent extra-cellular lipase was also produced. Lipid accumulation was favoured in relatively high carbon excess conditions in contrast with the secretion of lipase. In bioreactor trials lower quantities of cellular lipids and extra-cellular lipase were produced, while biomass, in terms of both final concentration and yield per fat consumed, was produced in significant quantities. All these findings support the potential of waste fatty material utilisation for the production of useful metabolites by Y. lipolytica strains.
Special thanks are addressed to the unknown referees for kindly revising the language of the manuscript.
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