Screening of Solid Food Wastes for Cultivation
The strain L3W grew on the pasteurized sake lees (Fig. 1) and although the growth after 72 h was lower than that in the control, this confirmed that the sake lees could be used as a substrate for growing the strain. In a previous study, S. aggregatum and Schizochytrium sp. TM02Bc were cultured on distillery lees for 15 d [25]. Although the amount of the distillery lees decreased after cultivation, the growth of these strains was not investigated further. The present study has directly confirmed that Aurantiochytrium sp. strain L3W can grow on sake lees and shown that a long cultivation period of 15 d may be unnecessary for thraustochytrids. Regarding the growth of the strain L3W after 72 h, the cell numbers were significantly higher when using 5 g/L of dried sake lees (p = 0.04). We therefore tested other food waste samples as a substrate for growing the strain L3W at this same concentration. As for the reason for less growth at 10 g/L, it might be due to the possible negative impact of the components of sake lees such as ethanol.
The growth of the strain L3W on pasteurized food waste after 72 h was normalized to that of the control experiment and then compared (Fig. 2). Of the seven waste samples, the sake lees and Japanese mustard spinach exhibited the highest growth of the strain L3W (p < 0.001), with the soy sauce residue and lemon peel as the next highest. In contrast, the strain L3W did not grow on the crown daisy and grape skin. These results confirmed that certain types of solid food waste can be used to cultivate thraustochytrids. Because the growth potential of the strain L3W depended on the type of food waste, we measured the elution of DOC and DN from the seven food wastes to characterize them.
Fig. 3 summarizes the relationship between the elution of DOC and DN from the pasteurized waste samples and the normalized growth of the strain L3W. Except for the Japanese mustard spinach (indicated by solid black circles), the eluted DOC and DN concentrations exhibited exponential relationships with the normalized growth values, thus indicating that elution of DOC and DN might be one of the factors dominating the growth of the strain L3W cultivated on solid food waste. Because the coefficient of determination for DOC was about ten times higher than that for DN, the elution of DN might affect the growth of strain L3W more than that of DOC.
The reason for exception of the Japanese mustard spinach may be the possible utilization of solid-state organic compounds by the strain L3W as the substrates. The Japanese mustard spinach eluted DOC and DN at only 53.2 and 2.33 mg/L, respectively, but exhibited the highest normalized growth of the seven waste samples. In contrast, the 790By+ medium exhibiting the normalized growth (100%) was reported to contain much higher DOC and DN values of 4200 and 350 mg/L, respectively [15, 16]. The biomass production of the strain L3W in the 790By+ medium was about 1600 mg/L [15, 16]. Because of the difficulty in separating the remaining Japanese mustard spinach and cells of the strain L3W, it was impossible to measure the biomass production of the strain L3W. However, the normalized growth based on cell numbers (Fig. 2) suggests that the biomass production on Japanese mustard spinach might be 59.4% of 1600 mg/L, i.e., 950 mg/L. The carbon and nitrogen contents of the biomass of strain L3W determined by the elemental analyzer were 60.5 ± 0.4% and 6.01 ± 0.09%, respectively, (n = 3). These values suggest that the carbon and nitrogen immobilized by the strain L3W might be about 60.5% and 6.01% of 950 mg/L, i.e., 575 and 57.1 mg/L, respectively. Because these estimated amounts of carbon and nitrogen were much higher than those for DOC and DN eluted from the Japanese mustard spinach, these results indicate the possible utilization of its solid-state carbon and nitrogen by the strain L3W.
Raghukumar et al. (1994) [26] reported that a thraustochytrid, Schizochytrium mangrovei produced cellulase using crystalline cellulose as a substrate. This thraustochytrid was recently reassigned to the genus Aurantiochytrium by Yokoyama and Honda (2007) [27]. However, a later study demonstrated the existence of extracellular cellulase in 14 of 19 strains of thraustochytrids but not in the five strains of Aurantiochytrium spp. using carboxymethylcellulose. Although the production of cellulase by the strain L3W was not investigated in the present study, one possible explanation for its growth on Japanese mustard spinach might be its ability to utilize dissolved and solid organic carbon and nitrogen. The crown daisy and grape skin exhibited the lowest DOC and DN elution, respectively, and crown daisy the second lowest DN elution, and the strain L3W did not grow on these types of food waste. As the possible reason for the lack of growth of the strain L3W (Fig. 2), less degradability of the food wastes and/or growth inhibitors, such as polyphenols in the grape skin, might also be considered. The present results provided evidence that the leachability of DOC and DN and the usability of solid-state organic carbon and nitrogen may be the factors determining the suitability of using particular types of solid food waste as substrates for cultivating thraustochytrids.
Production of DHA and EPA from Pasteurized Solid Food Waste
The FAs contents of the four types of food waste, sake lees, Japanese mustard spinach, soy sauce residue and lemon peel and of the resultant biomass mixtures and the biomass of strain L3W obtained in the control experiment were analyzed. Table 1 summarizes the four types of food waste that contained neither DHA nor EPA, whereas the pure biomass of strain L3W exhibited the highest DHA, EPA and total FAs contents. Because all biomass mixtures contained DHA and showed increase in total FAs contents, these results confirmed the feasibility of valorizing these four types of food waste regarding their DHA and/or EPA contents.
The sake lees was the only type of food waste from which both DHA and EPA were produced, at a ratio of DHA to EPA (20.6 : 1) similar to that in the pure biomass of strain L3W (29.1 : 1). Of the four types of food waste, the biomass mixture of sake lees exhibited the highest DHA and EPA contents. One possible explanation for this might be its composition of organic compounds. For example, Osada et al. (1994) [28] reported that three samples of sake lees contained not only glucose at 12.5%‑16.8% but also free amino acids at 1900‑3500 mg/g. Glucose is one of the carbon sources of the 790By+ medium to which polypeptone containing free amino acids was added. Although the glucose and free amino acids in the tested sake lees were not analyzed, it would be reasonable to expect that these might have promoted the growth of the strain L3W.
As shown in Fig. 2, the growth of strain L3W on the Japanese mustard spinach was higher than that on the sake lees. However, the DHA content of the former biomass mixture was about half that of the latter biomass mixture, possibly because the Japanese mustard spinach was an inadequate substrate for the production of DHA by the strain L3W. The growth of strain L3W on the Japanese mustard spinach may involve possible the utilization of its solid carbon and nitrogen (Fig. 3). The substrate composition may naturally affect the synthesis of organic compounds by microorganisms. For example, Quilodrán et al. (2009) [29] reported that the production of DHA by the two thraustochytrids depended on the carbon sources. Regarding Aurantiochytrium spp., previous studies confirmed that squalene can be produced as well as DHA by Aurantiochytrium mangrovei [30] and Aurantiochytrium sp. T66 [31] and that xanthophylls can be produced by Aurantiochytrium sp. KH105 [32]. In order to find the unknown additional value of the biomass mixture, further studies should analyze organic compounds adding to DHA and EPA produced by the strain L3W growing on the Japanese mustard spinach.
Table 1
Contents of DHA, EPA, and total FAs (mg/g) in the four types of raw pasteurized solid food waste and in the resultant biomass mixtures
|
Sake lees
|
Soy sauce cake
|
Japanese mustard spinach
|
Lemon peel
|
790 By+ med.b
(Control)
|
Raw
|
Mixture
|
Raw
|
Mixture
|
Raw
|
Mixture
|
Raw
|
Mixture
|
DHA (C22:6)
|
N.D.a
|
18.3
|
N.D.
|
2.88
|
N.D.
|
8.44
|
N.D.
|
8.04
|
103
|
EPA (C20:5)
|
N.D.
|
0.888
|
N.D.
|
N. D.
|
N.D.
|
N.D.
|
N.D.
|
N.D.
|
3.54
|
Total FAs
|
25.1
|
65.0
|
16.4
|
66.7
|
19.4
|
33.2
|
4.38
|
33.0
|
281.4
|
a Not detected (< 0.062 mg-DHA/g and < 0.011 mg/g-EPA).
b Pure biomass of the strain L3W.
Application of Unsterilized Solid Food Waste for Production of DHA and EPA
Fig. 4 shows the growth curves of strain L3W on pasteurized and unsterilized Japanese mustard spinach samples. With no pasteurization, the growth of the strain L3W was suppressed at an initial pH of 7 (p = 0.0007). However, by adjusting the initial pH to 4, the growth increased significantly (p = 0.0035), possibly because of the inactivation of the contaminating microorganisms by the pH-shock load, even though the strain L3W is resistant to the acidic pH of 4 [10].
Fig. 5 compares the normalized growth of strain L3W between pasteurized and unsterilized food waste, where any reduction due to unsterile conditions was insignificant at an initial pH of 4, not only for the sake lees (p = 0.89) but also for unsterilized lemon peel at an initial pH of 4 where the growth was higher than that on the pasteurized lemon peel (p = 0.354). The growth of strain L3W on unsterilized Hiroshima pickle at an initial pH of 4 was higher than that at a pH of 7 (p = 0.049), similar to that on Japanese mustard spinach. These results confirmed that adjusting the pH is a promising method for improving the growth of the strain L3W under unsterile conditions. When lemon peel was used, the normalized maximum growth at the initial pH of 4 under unsterile conditions was, surprisingly, higher than that under pasteurized conditions, possibly because of the hydrolysis of organic compounds to produce hydrolysates available for the strain L3W and/or the suppression of the autoxidation of antioxidants such as ascorbic acid and polyphenols contained in the lemon peel [33]. It has been reported that the autoxidation of polyphenols may induce an anti-algal effect through the production of radicals [34], as the suppression of autoxidation by ascorbic acid and polyphenols under acidic condition is well-known.
Table 2 summarizes the DHA, EPA, and total FAs contents in the biomass mixtures produced using the four types of unsterilized solid food waste. Except for the DHA in the sake lees mixture at a pH of 4, the DHA, EPA, and total FAs contents in the biomass mixtures of sake lees, the Japanese mustard spinach and lemon peel exhibited lower values under unsterile conditions than under pasteurized conditions (Table 1). However, the biomass mixtures of these three food wastes did contain DHA. The biomass mixture of sake lees also contained EPA. The Hiroshimana old pickle also contained DHA, but its raw material did not (Fig. 6). The reason for the higher content of DHA in the sake lees mixture at an initial pH of 4 might be due to the possible degradation by the contaminating microorganisms. These results clearly showed that valorizing solid food waste containing DHA and/or EPA can be achieved by cultivating the strain L3W without pasteurization.
Table 2
DHA, EPA, and total FAs content (mg/g) in biomass mixtures produced using unsterilized solid food waste.
|
Sake lees
|
Japanese mustard spinach
|
Lemon peel
|
Hiroshimana old pickle
|
pH4
|
pH7
|
pH4
|
pH7
|
pH4
|
pH7
|
pH4
|
pH7
|
DHA
(C22:6)
|
26.9
|
13.1
|
4.91
|
2.40
|
5.23
|
7.00
|
2.23
|
1.16
|
EPA
(C20:5)
|
0.155
|
0.205
|
N. D.
|
N.D.
|
N. D.
|
N.D.
|
N.D.
|
N.D.
|
Total FAs
|
59.0
|
54.4
|
25.2
|
18.4
|
27.4
|
15.7
|
33.5
|
29.9
|
The growth of strain L3W is critical for increasing the contents of DHA (C22:6n3) and EPA (C20:5n3) in the biomass mixtures, and the three most abundant FAs were DHA, palmitic (C16:0) and docosadienoic (C22:2) acids in the biomass of strain L3W (Fig. 6). These FAs formed the majority of the total FAs content in the resultant biomass mixtures of sake lees obtained under pasteurized and unsterile conditions at an initial pH of 4, where the normalized growth of the strain L3W was about 50% (Fig. 5). Under unsterile conditions, the growth of L3W on the sake lees at an initial pH of 7 was suppressed (Fig. 5), and the proportion of oleic acid increased (Fig. 6), possibly due to contaminating microorganisms. These three FAs were found in the biomass mixtures of Japanese mustard spinach and lemon peel obtained under pasteurized conditions. However, the proportion of palmitic acid was highest under pasteurized conditions, possibly because of the different substrate compositions. On lemon peel, the growth of strain L3W at an initial pH of 4 under unsterile conditions was greater than that under pasteurized. conditions (Fig. 5). However, under unsterile conditions, the proportion of the other FAs increased (Fig. 6), possibly because of the greater production of FAs from the lemon peel caused by hydrolysis and/or the activity of contaminating microorganisms. Under unsterile conditions, the normalized growth values of strain L3W on the Japanese mustard spinach at an initial pH of 7 and on the Hiroshimana old pickle at an initial pH of 4 and 7 were the three lowest (Fig. 5), and therefore the proportion of DHA in the biomass mixtures was also lowest (Fig. 6).
Mass Cultivation for Producing Sources of DHA and EPA
The strain L3W grew successfully on a mixture of sake lees and Hiroshimana old pickle (Fig. 7a). The time to achieve maximum growth was 96 h, whereas 48 h was sufficient for growth on sake lees at 25°C and pH 4 during flask-scale cultivation under unsterile conditions. This was not surprising because the temperature for mass cultivation was between 16 and 21 °C (Fig. 7b), and the optimal temperature for the growth of strain L3W is between 20 and 25°C [10]. The strain L3W is an obligate aerobe, and during the first 24 h of cultivation, the DO was less than 3 mg/L (Fig. 7b), which was lower than that during the flask-scale cultivation of more than 6 mg/L. The resultant biomass mixture collected after 120 h contained DHA and EPA at 12.6 and 0.217 mg/g, respectively, thus confirming the valorization of solid food waste in terms of DHA and EPA contents on the mass scale unsterile cultivation. These values were expected because the biomass mixtures of sake lees produced in the flask-scale cultivation contained DHA at 26.9 mg/g (pH 4) and 13.1 mg/g (pH 7) and EPA at 0.155 mg/g (pH 4) and 0.205 mg/g (pH 7) (Table 2), whereas the DHA content in the biomass mixture of Hiroshimana old pickle was 2.23 mg/g (pH 7) and 1.16 mg/g (pH 4), respectively (Table 2).
Utilization of the Biomass Mixture as a Source of DHA and EPA
The biomass mixture of sake lees and Hiroshima old pickle produced in the mass cultivation tank contained DHA and EPA at 12.6 and 0.217 mg/g, 1500 times and 37 times higher, respectively, than those in the samples of commercial poultry feed (DHA, 0.0084 mg/g; EPA, 0.0058 mg/g), thus indicating that the biomass mixtures are potentially usable as an additive in poultry feed to produce DHA and EPA-enriched products such as eggs. In contrast, the commercial fish feed contained DHA and EPA at 5.73 and 2.13 mg/g, respectively. Although the three sake lees biomass mixtures contained DHA at levels of 26.9, 13.1 and 12.6 mg/g, more than twice that of commercial fish feed, a higher margin may be necessary because the biomass mixtures cannot serve as a complete fish feed but only as an additive for fish feed. The EPA contents of the biomass mixtures (0.155, 0.205 and 0.217 mg/g) were lower than those of the commercial fish feed. This means that a greater enrichment of DHA and EPA contents in the biomass mixtures would be necessary for use as an additive in fish feed.
Optimizing the operational parameters for cultivating the strain L3W is one option for increasing the production of DHA and EPA. Jakobsen et al. (2008) [35] found that limiting O2 increased the DHA content of the biomass of Aurantiochytrium sp. T66 as well as decreasing the palmitic acid content, which suggested that O2 limitation hindered the O2-dependent desaturase(s) and favored the O2-independent polyunsaturated fatty acid synthase. In terms of energy consumption for cultivation, it is also reasonable to optimize the aeration time. A later study based on a fermentation strategy for producing DHA by Aurantiochytrium limacinum SR21 used intermittent oxygen feeding in a fed-batch culture system [36]. An increase in the DHA content in the biomass of A. limacinum SR21was associated with a decrease in its C16:0 content [35]. As well as the DO, pH may also affect the production of DHA and EPA by the strain L3W [10]. However, the value set for the pH may depend on the type of food waste in real applications because of the possible influence of pH on the utilization of the food waste and the activities of contaminating microorganisms in the biomass and FAs production (Fig. 5, Table 1). Future research should focus on optimizing the cultivation processes or thraustochytrids using food waste to increase the DHA and EPA contents of the resultant biomass mixture.