Qualitative Screening of Yeast Biodiversity for Hydrolytic Enzymes Isolated from the Gastrointestinal Tract of a Coprophage “Gymnopleurus sturmi” and Dung of Ruminants

Abstract

In this study, thirty yeast strains isolated from the gut of coprophagous “Gymnopleurus sturmi” and twenty-four from the dung of ruminants were shown to be producers of cellulases. Cellulolytic yeast isolates could also produce other hydrolytic enzymes such as pectinase, lipase, β-glucosidase, catalase, inulinase, urease, gelatinase, and protease. The oroduction of amylase was present in only one isolate of dung of ruminants. On the other hand, the production of tannase was absent in these isolates. All the yeasts isolated from two sources could utilize various carbon sources, including sorbitol, sucrose, and raffinose, and withstand high concentrations of glucose (300 g/L), salt (100 g/L), and exogenous ethanol. They could grow in a wide pH range of 3 to 11. The growth was stable up to a temperature of 40 °C for isolates from the gut of coprophage and 37 °C for the yeast from the dung of ruminants. These activities and growing conditions were similar to the diet of coprophagous insects and the composition of ruminant manure, likely because the adaptation and distribution of these microorganisms depend on the phenology and trophic preferences of these insects.

1. Introduction

Yeasts are unicellular eukaryotic microorganisms with the ability to multiply rapidly because they are less demanding in nutrients. They are easily implemented in several farms, research, and industrial applications [1,2]. Indeed, they represent the largest group of exploited microorganisms compared to prokaryotes [3]. Yeasts play an essential role in recycling organic matter by drawing their energy from external carbon sources [4]. They can also cohabit in various environments where the living conditions are specific, such as acidic environments, tree bark, digestive tract, and insect dung [1,5,6,7,8]. Yeasts are widely used in food fermentation industry and making more progress in other industries [2,9]. They represent an important source to be exploited to develop new and very extensive biotechnological processes as they have a highly developed enzymatic system [10]. Indeed, yeasts can produce enzymes such as cellulases, ligninase, xylanase, pectinase, amylase, glucoamylase, and lipase (Table 1) [11] for applications in various industrial processes, which require the use of specific thermostable enzymes [12]. Several types of research have been reported on the ability of yeast strains to hydrolyze plant-derived substrates to provide an alternative to chemical hydrolysis for bioenergy production.

In this context, we have established a collection of yeasts isolated from various ecological niches; the digestive tract of a coprophagous beetle “G. sturmi” and ruminant dung, a food source for this insect. The choice of these sources is based on the fact that coprophagous beetles constitute a group of beetles well-adapted to grazed ecosystems [13], as they derive their food resources from the dung of large mammals [14]. This dung could be of carbohydrate origins, or lipid- or phenolic-dominant. The degradation of these compounds can be done through a system of enzymes secreted by the microorganisms colonizing the digestive tract of the animals or the microorganisms specific to the dung, in particular the cellulases to degrade the cellulose not transformed by the animals. These cellulases could be used for industrial applications due to their great biotechnological potential, and recycling of cellulosic biomass [15,16]. This research is focused on the isolation and screening of various yeast isolates from the gut and dung of coprophagous insect Gymnopleurus sturmi for biotechnological applications.

Table 1. Technological applications of yeast isolates.

Enzymes	Yeasts	Applications	References
Cellulases	Aureobasidium pullulans 98	Food, chemical, textile, paper, and biofuel industries	[17,18]
Pectinase	Kluveromyces marxianus Metschnikowia pulcherrima	Wine, cider, and fruit juice industries	[19,20]
Lipase	Aureobasidium pullulans HN2.3	Food, wastewater treatment, cosmetics, pharmaceuticals, leather processing, and biofuel industries	[21]
ß-glucosidase	Guehomyces pullulans 17-1	Food industry	[22]
Catalase	Saccharomyces cerevisiae	Food industry	[23]
Inulinase	Pichia guilliermondii	Food, beverage, and biofuel industries	[24]
Urease	Cryptococcus gattii	Diagnostic kits, beverages, and animal feed	[25]
Gelatinase	Trichosporon pullulans	Food, chemical, and medical industries	[26]
Protease	Rhodotorula mucilaginosa L7	Clinical applications, food, beverage, and leather processing industries	[27]
Amylase	Aureobasidium pullulans N13dSaccharomyces cerevisiae	Food, textile, paper, detergent industry, medical, and pharmaceutical industries	[28,29]
Tannase	Kluyveromyces marxianus	Feed, food, beverages, brewing, pharmaceutical, chemical, cosmetic, and leather industries	[30]

Table 1. Technological applications of yeast isolates.

Enzymes	Yeasts	Applications	References
Cellulases	Aureobasidium pullulans 98	Food, chemical, textile, paper, and biofuel industries	[17,18]
Pectinase	Kluveromyces marxianus Metschnikowia pulcherrima	Wine, cider, and fruit juice industries	[19,20]
Lipase	Aureobasidium pullulans HN2.3	Food, wastewater treatment, cosmetics, pharmaceuticals, leather processing, and biofuel industries	[21]
ß-glucosidase	Guehomyces pullulans 17-1	Food industry	[22]
Catalase	Saccharomyces cerevisiae	Food industry	[23]
Inulinase	Pichia guilliermondii	Food, beverage, and biofuel industries	[24]
Urease	Cryptococcus gattii	Diagnostic kits, beverages, and animal feed	[25]
Gelatinase	Trichosporon pullulans	Food, chemical, and medical industries	[26]
Protease	Rhodotorula mucilaginosa L7	Clinical applications, food, beverage, and leather processing industries	[27]
Amylase	Aureobasidium pullulans N13dSaccharomyces cerevisiae	Food, textile, paper, detergent industry, medical, and pharmaceutical industries	[28,29]
Tannase	Kluyveromyces marxianus	Feed, food, beverages, brewing, pharmaceutical, chemical, cosmetic, and leather industries	[30]

2. Materials and Methods

2.1. Sampling

The coprophagous organisms and ruminant dung used for this study were collected in June 2015 and 2016 from two different regions of Fez, Morocco; Fez sais (33°54′14′′ N, 4°59′55′′ W), at 609 m of altitude, Ain Aicha (34°29′59′′ N, 4°42′01′′ W), at 246 m of altitude, Ain Aicha (34°29′59′′ N, 4°42′01′′ W), at 246 m of altitude, and Ain Beda (33°57′07.5′′ N, 4°53′59.9′′ W), at 579 m of altitude.

The isolation of the yeasts was carried out from the gastrointestinal tract of the coprophagous “Gymnopleurus sturmi” and the ruminate dung on Yeast Pepton Glucose (YPG) culture medium, comprised of Peptone (20 g/L), yeast extract (10 g/L), glucose (20 g/L), agar (20 g/L), and with two antibiotics, ampicillin (60 μg/mL) and kanamycin (60 μg/mL), used to prevent bacterial growth.

2.2. Qualitative Screening of Isolates for Hydrolytic Enzymes

The different yeast isolates were tested for their ability to produce hydrolytic enzymes.

2.2.1. Oxidation of Phenolic Substrates

The determination of the capacity of all the isolates to utilize and degrade phenolic substrates was carried out on the M9 culture medium, comprising of (g/L) Na₂HPO₄ (6 g), KH₂PO₄ (3 g), NH₄Cl (1 g), and NaCl (0.5 g) with 0.1% of catechol or pyrogallol. The positive result was visualized by a black coloration around the isolate, indicating assimilation of these substrates.

2.2.2. Cellulase Activity

This activity was determined using carboxymethylcellulose (CMC) agar medium as a source of carbon. The M9 buffer consists of (g/L) Na₂HPO₄ (6 g), KH₂PO₄ (3 g), NH₄Cl (1 g), and NaCl (0.5 g). The medium was autoclaved for 15 min at 120 °C. Then, 1 mL of 0.1 M CaCl₂ and 1 mL of MgSO₄ at 1 M were added. The cellulase medium was composed of carboxymethyl cellulose (CMC) or cellulose fiber (10 g), yeast extract (0.2 g), agar (20 g), and the M9 buffer. The final medium was autoclaved for 15 min at 110 °C [31]. The yeast was incubated on the prepared medium for 72 h at 30 °C. After that 1%, Congo red was flooded, which selectively binds to the polymers of cellulose. After 15 to 20 min, the dishes were washed several times with NaCl (1 M). The presence of a light halo around the colonies indicates the degradation of the CMC in the medium by the cellulase secreted from the isolates that were called “cellulase +” [32].

2.2.3. Amylase Activity

Yeast isolates with amylase activity were detected by cultivation on a starch agar medium. This culture media was comprised (g/L) of peptone (2 g), MgSO₄7H₂O (0.5 g), CaCl₂ (0.2 g) NaCl (0.5 g), and starch (1 g). Isolates possessing the amylase enzyme were able to degrade the starch present in the agar, thus developing a clear zone around the colonies. The evidence of starch degradation by the secreted enzyme was confirmed after adding Lugol and rinsing with distilled water [33].

2.2.4. Inulinase Activity

Inulinase production by the isolated yeasts was detected on a medium containing inulin (2 g), yeast extract (0.5 g), KH₂PO₄ (3 g), agar (20 g), and distilled water (1 L). Inulin was used as the only carbon source in this medium; yeast growth after 4 days of incubation at 30 °C showed the presence of inulinase activity [34].

2.2.5. β-Glucosidase Activity

The β-glucosidase activity was carried out in a medium containing (g/L) yeast extract (1 g), peptone (1 g), ferric ammonium citrate (0.01 g), esculin (0.3 g), and agar (20 g). The Petri dishes inoculated with yeast cultures were incubated at 30 °C for 24 to 48 h. The presence of enzymatic activity was visualized as a dark halo surrounding yeast growth [35].

2.2.6. Pectinase Activity

To check the pectinase activity of the isolates, yeast cultures were grown on a medium based on (g/L) pectin (2.5 g), yeast extract (5 g), (NH₄)₂SO₄ at 10% (5 mL), 1 M MgSO₄ (0.5 mL), 50% glycerol (5 mL), and agar (20 g). The pH of the culture medium was adjusted to 8.0. The medium was autoclaved at 120 °C for 15 min [36]. The pectinase secretion was detected by adding lugol (selectively binding to the pectin polymers) and a successive rinsing of the dishes with distilled water after 10–15 min. “The pectinase +” isolates were characterized by the presence of a clear halo around colonies [12].

2.2.7. Lipase Activity

Lipase activity was carried out on a culture medium based on olive oil and rhodamine B. This method was based on the emission of fluorescence by the colonies, which was due to the interaction of rhodamine B with the fatty acids released during the enzymatic hydrolysis of the olive oil. The medium consisted of (g/L) NaHPO₄ (12 g), KH₂PO₄ (2 g), MgSO₄ 7H₂O (0.3 g), CaCl₂ (0.25 g), (NH₄) SO₄ (2 g), and pH was adjusted to 7.0. After sterilization, the medium was mixed with olive oil (31.25 mL) and rhodamine B 10 mL (1 mg/mL). Colonies with lipase activity develop a fluorescence after exposure of the Petri dishes to UV radiation (350 nm) [37].

2.2.8. Gelatinase Activity

The detection of gelatinase activity was carried out on a gelatin-based culture medium: (g/L) gelatin (15 g), peptone (4 g), yeast extract (1 g), meat extract (1 g), agar (15 g). While the medium showed an opaque appearance on the proteinaceous substrate, having a clear zone around the colonies indicates the hydrolysis of gelatin substrate [38].

2.2.9. Urease Activity

The medium Christensen was used to reveal urease activity in the yeasts studied. This enzyme converts urea to ammonia, which increases the pH that changes the color indicator. After 2 days of incubation at 30 °C, a pink to violet coloration in the culture media indicated positive results [39].

2.2.10. Protease Activity

Protease production was determined according to the method of Strauss et al. [40] by plating yeast colonies on a medium containing (g/L) yeast extract (0.5 g), NaNO₃ (1 g), K₂HPO₄ (2 g), KCl (1 g), MgSO₄ (0.5 g), agar (20 g), and milk powder (10 g). Incubation was carried out at 30 °C for 7 days. The proteolytic activity was revealed by the presence of a clear zone around the colony.

2.2.11. Catalase Activity

The catalase activity was evaluated using the method described by Whittenbury [41] by directly adding 3% (v/v) hydrogen peroxide to a 48 h yeast culture. Catalase activity was evidenced by the presence of oxygen bubbles.

2.2.12. Tannase Activity

The tannase activity in the different yeast isolates was detected on YPG media supplemented with 10 mL of a tannic acid (20%) solution. The yeasts that have a Tannase activity showed a clear halo, reflecting the decomposition of tannic acid, gallic acid, and glucose.

2.3. Study of Physiological Characteristics of Cellulolytic Isolates

2.3.1. Thermotolerance

The thermotolerance of the isolate temperatures was evaluated on YPG agar and M9-CMC medium, after incubation for 48 h at different temperatures: 30, 37, 40, 42, 44, 46, and 48 °C.

2.3.2. pH Tolerance

The pH tolerance of the isolates was carried out on a YPG agar medium at different pH values: 3, 4, 5, 6, 8, 9, 10, 11, and incubated at 30 °C for 48 h.

2.3.3. Utilization of Carbon Sources

The digestion of carbon sources by these isolates was carried out on a minimal medium of M9 agar supplemented with 1% of each source, CMC [42], cellobiose, cellulose, sorbitol, sucrose, raffinose, maltose, ribose, xylose, galactose, arabinose, fructose, casein, mannitol, lactose, dextrin, glycine, and glycerol. The growth of isolates was noted after incubation at 30 °C for 48 h.

2.3.4. Glucose Tolerance of Yeasts

The growth of the isolates at different glucose concentrations—50, 100, 150, 200, 250, and 300 (g/L)—was evaluated to investigate the yeast’s tolerance. The isolates were incubated on a YPG agar medium, properly supplemented with different concentrations of glucose. Next, the culture plates were incubated at 30 °C for 48 h.

2.3.5. Tolerance to Ethanol

We tested the isolate’s tolerance for exogenous ethanol on YPG agar medium that was supplemented with different concentrations of ethanol: 1, 5, 6, 8, 10, and 12%. Then, the plate was incubated at 30 °C for 48 h.

2.4. Molecular Identification

Cellulolytic isolates were cultured in test tubes containing 5 mL of YPG medium. Incubation was carried out at 30 °C for 24 h. DNA extraction from yeast isolates was carried out by the classic method [43]. 1.5 mL of yeast suspension were centrifuged for 10 min at 12,000 rpm, and the pellet was suspended in 200 µL of lysis buffer (2% Triton X-100, 1% SDS, 100 mM NaCl, 10 mM Tris-HCl at pH 8, 1 mM EDTA at pH 8). The mixture was placed at −20 °C for 2 min and then at 95 °C for 1 min. This step was repeated twice to create a thermal shock and promote cell bursting. Next, the DNA was extracted with phenol/chloroform. The amplification by PCR of the sequence ITS1 (TCCGTAGGTGAACCTGCGG) ITS4 (TCCTCCGCTTATTGATATGC) was carried out according to the method of White et al. [44]. The reaction was carried out in a final volume of 25 µL, containing primers (final concentration 10 pm, each), dNTPs (200 µM final concentration), MgCl₂ (1.5 mM final concentration), 10 µL 1× PCR buffer, Taq polymerase (0.5 U), pure H₂O, and extracted DNA. PCR conditions were as follows: initial denaturation at 95 °C for 2 min and 30 cycles of denaturation at 95 °C for 45 s, primer annealing at 55 °C for 1 min, and extension at 72 °C for 1 min. A final extension was completed at 72 °C for 10 min. Sanger sequencing was performed at the pastor institute (Casablanca-Morocco) using an ABI PRISM 3130XL Genetic Analyzer, Applied Biosystems. Preliminary identifications were performed based on sequence assembly and by searching in the NCBI ITS RefSeq Fungi database using command line interface.

2.5. Multiple Sequence Alignment and Phylogenetic Tree

ITS sequences from all the isolates were used to perform BLASTN, and the top 5 hits were retrieved to find close relatives to the isolates. Sequences from all isolates were subjected to multiple sequence alignment using MUSCLE v3.8.31 with default parameters. A phylogenetic tree was constructed using FastTree v2.1.10 with –nt –gtr parameters. The phylogenetic tree was visualized with ggtree v3.4.0 in RStudio and R v4.2.0.

3. Results and Discussion

3.1. Distribution of Isolated Yeasts

The yeasts isolated from the gut of coprophagous “Gymnopleurus sturmi” revealed a large load of 79 × 10⁸ CFU/g and 65.24 × 10⁸ CFU/g in June 2015 and 2016, respectively. The ruminant manure contained 16.8 × 10⁶ CFU/g and 11 × 10⁶ CFU /g in 2015 and 2016, respectively (

Table 2. Percentage of isolates screened for cellulase activity.

Isolation Medium	Sampling Period	Total Counts of Yeasts (CFU/g)	Number of Isolates
Isolates from GGS	2015	7.9 × 109	24
	2016	6.52 × 109	31
Isolates from DR	2015	16.8 × 106	19
	2016	11 × 106	22

). In addition, yeast biodiversity was different among the four samples. The collection consists of 96 isolates, of which 57.29% were isolated from gut Gymnopleurus sturmi (GGS) and 42.71% were isolated from the dung of ruminants (DR).

3.2. Oxidation of Phenolic Substrates

The isolated yeasts were tested to demonstrate their degradation potential of phenolic lignin by-product compounds (pyrogallol and catechol), essential components of the plant cell wall. Results showed (

Table 3. Percentage of isolates capable of degrading lignin by-products.

Isolation Medium	Positive Isolates	Total Number of Isolates
Isolates from GGS	22 (40%)	55
Isolates from DR	17 (41.5%)	41

) that 40% of the isolates from GGS and 41.5% of the isolates from DR were able to degrade these compounds. These yeasts were isolated from media with a high concentration of phenolic products after the degradation of plants rich in ligninolytic products by the mammals and the assimilation of these products by the clean microflora of the dung and the microflora of the coprophages feeding this dung [45]. Indeed, the phenolic compounds are always liable to be degraded by the enzymes produced by microorganisms [46,47,48,49]. Other studies have shown that fungi such as Aspergillus terreus [49] and yeasts such as Candida tropicalis [50] have a great ability to degrade phenolic products.

3.3. Screening of Cellulolytic Isolates

One of the main objectives of this study was to determine the ability of isolated yeasts to produce cellulase enzymes. Therefore, two different substrates (CMC and cellulose fiber) were used for the screening of cellulolytic isolates. Only isolates that showed a positive result in both substrates were considered cellulolytic. This has enabled us to build a library of isolates capable of producing our enzyme of interest from which 30 isolates (54.54%) were collected from GGS and 24 isolates (58.54%) from DR. The degradation time of two substrates varies between isolates (Figure 1A,B). For the GGS isolates, the hydrolysis zone of CMC varied between 6 to 25 mm, and the hydrolysis of the cellulose fiber varied between 3 to 15 mm (Figure 1A). For the DR isolates, the zone of hydrolysis for CMC was noted from 2 to 16 mm and 3 to 7 mm for cellulose fiber (Figure 1B). Thongekkaew and Kongsanthia [18] showed that 45 yeast isolates, obtained from various samples (soil, tree bark, and insect excrement), can hydrolyze cellulose.

3.4. Hydrolytic Enzymes

Yeasts have the potential to contribute to the development of biotechnological processes with specific applications [51,52]. To characterize the different isolates biochemically, different substrates were tested. The choice of these substrates was related to the composition of the dung [45] and the food requirement of the insect studied [53], which contains a large number of complex substrates. The qualitative tests revealing the production of hydrolytic enzymes in the cellulosic isolates tested made it possible to select efficient isolates. Figure 2 shows that all DR isolates were capable of producing the β-glucosidase and catalase. For GGS, 93.33% of isolates were β-glucosidase-positive and 96.67% were catalase-positive. In addition, the hydrolysis of olive oil by the lipase was noted in 86, 67% of the GGS isolates and 95.83% of the DR isolates. On the other hand, the considerable production of pectinase was detected in 80% GGS isolates and 50% DR isolates. Protease was also more prevalent in 87% of GGS and 75% of DR isolates. In addition, 63.33% of GGS, and 29.17% of DR isolates were positive for Inulinase. Gelatinase synthesis was detected for many of the 56.67% GGS and 4% DR isolates. Most isolates had urease activity, of which 50% were isolated from GGS and 66.67% from DR. Tannase activity was absent in all isolates considered in this study. The amylase activity was present only in one isolate of DR out of a total of 24 isolates, which was 4% (Figure 2). In previous studies, (

Table 4. Enzymatic activity of isolated yeast a: Isolates from GGS, b: Isolates from DR, 1: Bautista-G et al. [54], 2: Strauss et al. [40], 3: Lilao et al. [27], 4: Romo-Sánchez et al. [11], 5: Hernandez et al. [41].

Enzyme	Current Study		1	2	3	4	5
	a	b
Cellulase	30	24	-	11	-	38	-
Pectinase	24	12	-	9	62	4	23
Lipase	26	23	4	-	134	-	6
β-glucosidase	28	24	10	-	142	13	-
Catalase	29	24	16	-	-	-	41
Inulinase	19	7	-	-	-	-	-
Urease	15	16	-	-	-	-	-
Gelatinase	17	1	-	-	-	-	-
Protease	26	18	6	10	49	-	-
Amylase	0	1	-	9	-	-	-
Tannase	0	0	-	-	-	-	-
Number of isolates	30	24	30		216	42	83

) [11,27,40,41,54], the isolated various strains exhibited the ability to produce interesting enzymes, with interesting technological applications (Table 4).

3.5. Study of Physiological Characteristics

3.5.1. Temperature

The effect of temperature on the yeast growth showed that the growth was stable up to a temperature of 40 °C in GGS isolates and 37 °C for the DR isolates (Figure 3). The percentage of isolates capable of tolerating these temperatures decrease with increasing temperature (Figure 3). Aissam et al. [55] reported an optimum temperature of 37 °C for yeast strains. Babavalian et al. [56] showed that most yeasts isolated from soil cannot withstand a temperature above 37 °C, while complete inhibition of their growth is observed at 45 °C.

3.5.2. Exogenous Ethanol

All cellulosic isolates from DR were able to support up to 8% of ethanol and 52% of isolates were able to grow in a 12% ethanol culture medium. However, isolates from the GGS only supported a 5% concentration of exogenous ethanol. While increasing the concentration of ethanol, the percentage of these isolates, which grow in the medium, decreases (Figure 4). Arguably, the DR isolates support a higher concentration of ethanol than GGS isolates. This type of behavior has also been observed in strains S. cerevisiae C2 and TA, Saccharomyces cerevisiae K2, Saccharomyces rosinii S1 and S2, Rhodotorula minuta S3, and Saccharomyces exiguus K1 [57].

3.5.3. Utilization of Carbon Sources

Figure 5 shows that the yeast isolates (GGS and DR) had a great ability to assimilate several types of carbon sources. These results corroborate with those of Gao et al. [34], who showed that isolated yeasts of marine origin could grow on several sources of carbon.

3.5.4. Osmotolerance

The osmotolerance test showed that all the isolates of the digestive tract and ruminant dung were osmotolerant and could survive a culture medium with 30% glucose and 10% NaCl (

Table 5. Osmotolerance of isolates for glucose and NaCl.

	Glucose Concentration (g/L)						NaCl Concentration (g/L)
Concentration	50	100	150	200	250	300	100
Isolates from (GGS) (%)	100	100	100	100	100	100	100
Isolates from (DR) (%)	100	100	100	100	100	100	95.83

). In 2005, Milala et al. [58] reported that the sugar tolerance was 20% for the two strains of S. cerevisiae TA and C, 15% for S. cerevisiae MTCC 170, and 10% for the two strains Saccharomyces rosinii S1 and S2, as well as the strain Rhodotorula minuta S3.

3.5.5. Effect of pH

The effect of pH shows that all isolates were able to grow over a wide range from pH = 5 to pH = 8 (Figure 6), but from a pH equalling 9, the percentage of isolates that could endure the medium decreased. The results showed that cellulosic isolates have interesting technological properties for their application in the course. This species was well-adapted to the environmental conditions that govern fermentations, such as low pH and high concentrations of NaCl [59]. However, in other studies on volcanic yeasts, the optimum pH for growth for all isolates was between 3.5 and 5.5 [60].

3.6. Molecular Identification

Taxonomic characterization of the 21 cellulosic isolates was carried out after morphological examination under a microscope (Figure 7). The sequence homology search was carried out using the BLASTN algorithm on the command line using ITS RefSeq Fungi database. The latter confirmed that the isolates studied belong to the genus Trichosporon (

Table 6. Results of yeast identification by rDNA internal transcribed spacer (ITS).

Coded	Biotope	Homologous Strains	Accession Numbers
Mor-L1	GGS	Trichosporon insectorum	ON810624.1
Mor-L2a	GGS	Trichosporon insectorum	ON810627.1
Mor-L3b	GGS	Trichosporon insectorum	ON810628.1
Mor-L4a	GGS	Trichosporon japonicum	ON810629.1
Mor-L5	GGS	Trichosporon insectorum	ON810630.1
Mor-L5a	GGS	Trichosporon insectorum	ON862731.1
Mor-L11a	GGS	Trichosporon insectorum	ON810622.1
Mor-L11 (1)	GGS	Trichosporon insectorum	ON862728.1
Mor-L11 (2)	GGS	Trichosporon insectorum	ON862729.1
Mor-L11C	GGS	Trichosporon insectorum	ON810621.1
Mor-L14	GGS	Trichosporon insectorum	ON810623.1
Mor-L14 (1)	GGS	Trichosporon insectorum	ON862731.1
Mor-L14 (3)	GGS	Trichosporon insectorum	ON862732.1
Mor-L23b	GGS	Trichosporon insectorum	ON810625.1
Mor-L23C	GGS	Trichosporon insectorum	ON810626.1
Mor-L30a	GGS	Trichosporon coremiiforme	ON810631.1
Mor-B13	DR	Trichosporon insectorum	ON810633.1
Mor-B25	DR	Trichosporon insectorum	ON810632.1
Mor-B13a	DR	Trichosporon insectorum	ON862726.1
Mor-B25a	DR	Trichosporon insectorum	ON862727.1
Mor-B5	DR	Trichosporon insectorum	ON862730.1

). All the identified sequences of strains showed high similarity with Trichosporon insectorum, Trichosporon faecale, and Trichosporon coremiiforme. All except L4a showed a high similarity with Trichosporon asahii. Many of the strains showed high similarity to Trichosporon aquatile. However, biotype DR also had high similarity with Trichosporon japonicum. The top hit of L30a was with Trichosporon coremiiforme with only 90.6% sequence identity. Details of the top 5 hits are shown in Figure 8, along with a phylogenetic tree. In order to understand the phylogenetic relationship of the strains, the sequences of the top hits were combined with the ITS sequences of the strains to build a phylogenetic tree. It is evident that the strains from the biotype DR are more closely related to Trichosporon sp. (top hits of the BLAST) as compared to biotype GGS, except B5, which shares a clade with GGS strains. All the strains were split into 4 clades, while L11C and L11a were different from other clades (Figure 9).

4. Conclusions

Microbial resources represent natural and real assets. Their exploitation was conducted under rigorous environmental conditions, and the exploitation of their potential was oriented towards targeted biotechnological applications. The gut of coprophagous insects and the dung of ruminants are abundant and culminate an important richness of the yeasts. Purified isolates show interesting enzymatic activities. They are therefore highly desirable biomolecules in the enzyme market, and their quantification and various biotechnological applications are by far the most promising and could be explored in future studies.