1. Introduction
Yeast is a heterotrophic microorganism that uses organic compounds as energy and carbon sources. Many yeasts have been discovered in waste that contain a high organic content. Cyberlindnera samutprakarnensis was reported as a novel ascomycetous yeast that was isolated from the wastewater of a cosmetic factory in Samutprakarn province, Thailand [1], while a novel genus of ascomycetous yeast, Allodekkera sacchari, was obtained from the waste of a sugar production plant in Nakhon Ratchasima province, Thailand [2]. The continuous reports of new yeast species suggest that organic waste in Thailand may be an attractive source to investigate yeast communities.
A grease trap is a chamber for separating fat from food waste. It consists of organic compounds and a high lipid content. For this reason, a sample from a grease trap was considered a good source to investigate yeast communities and also to discover a promising yeast that possesses the capability to produce lipase, which is an important enzyme in broad industrial applications. Lipase-producing yeasts have been continuously discovered and reported, for example Candida albicans, Candida cylindracea, Candida parapsilosis, Candida tropicalis, Saccharomyces cerevisiae, and Yarrowia lipolytica [3]. However, Candida rugosa is the most frequently used yeast for the production of commercial lipase. A novel cold active lipase, of which activity was retained by 70% at 10 °C as compared to the maximum value at 35 °C, was produced by Pichia lynferdii Y-7723 [4]. A halophilic yeast, Debaryomyces hansenii YLL29, isolated from dry-salted olives, showed 7.44 U/mL lipolytic activity [5]. Additionally, there has also been a report of lipase production in novel and undescribed yeasts. Limtongozyma siamensis DMKU-WBL1-3, a novel yeast genus isolated from a grease trap, was also shown to produce lipase [6], whereas Cryptococcus sp. S-2, an undescribed yeast species isolated from air, was reported to produce a lipase with 65.7 U/mL lipase activity at pH 7.0 and 37 °C, and the enzyme was shown to be stable between pH 5.0 and 9.0 and at temperatures up to 50 °C [7].
Beside lipase-producing ability, lipid accumulation is also a parallel character that has been found in lipase-producing yeasts [8]. Oleaginous yeasts or oily yeasts are yeast species that accumulate lipids in the range of 20%–70% of their cell dry biomass when cultivated under optimized conditions, while less than 10% of their cell dry biomass is accumulated in non-oleaginous yeasts [9]. The well-known typical oleaginous yeasts are in the genera Candida, Cryptococcus, Rhodotorula, Rhodosporidium and Yarrowia [10]. The presence of lipases in environment enables many yeasts to utilize lipids or other compounds with ester bonds as carbon sources. A triglyceride is a molecule that cannot pass through the cell membrane but has to be degraded into glycerol and free fatty acid prior to absorption [11]. The degradation process requires the activity of a lipolytic enzyme that is secreted into an environment where lipids are hydrolyzed. This may be the reason why many lipase-producing microorganisms have been isolated from lipid-rich environments, such as waste from the oil or fat industry [11]. Aside from being able to accumulate a high lipid content, various oleaginous yeasts also have the potential to present remarkable growth and accumulate lipids on waste and by-products of the agro-industry, such as sugar-enriched wastes or the hydrolysates of various products [12]. Thus, oleaginous yeasts have received great attention due to their potential for biotechnological applications [8]. Oleaginous yeasts usually accumulate intracellular lipids in an N-limited condition [13]. Under this condition, the excess carbon turns into fatty acid and is stored in the form of large lipid droplets (LD) in the cellular compartment. The fatty acid composition of a yeast lipids depends on many factors including species, environmental growth conditions, substrate used, and medium components. The general ratio of lipid composition was found to be C18:1 (oleic acid) > C16:0 (palmitic acid)> C18:2 (linoleic acid) = C18:0 (stearic acid), and C18:1 is one of the three main components in high-acid oil-biodiesel [14] Using an oleaginous yeast as a source of lipid production for biodiesel has several advantages compared to other oil sources, such as its high growth rate, its lesser requirement of space, and the fact that its oil production does not depend on climate change [15]. Hence, lipid production by oleaginous yeasts is considered a great alternative oil source for biodiesel production.
During the course of the yeast community study in the grease trap, the strains DMKU-JMGT1-45T and DMKU-JMGT4-14 were found. The multiple genes analysis showed that the two strains were identical but could not be placed onto any known taxonomic position. The closest species of both strains was Candida incommunis, which showed a weak relationship with the genus Yarrowia, which was classified into the family Trichomonascaceae [16]. Until now, 12 genera with published names have been recognized as members of the family Trichomonascaceae: Blastobotrys [17], Deakozyma [18], Diddensiella [19], Groenewaldozyma [20], Middelhovenomyces [18], Nadsonia [21], Spencermartinsiella [22], Starmerella [23], Sugiyamaella [24], Wickerhamiella [25], Yarrowia [26], and Zygoascus [27]. However, the strains DMKU-JMGT1-45T and DMKU-JMGT4-14 are unrelated to any described genera. We therefore propose the genus Limtongella gen. nov. to accommodate the novel species Limtongella siamensis. Additionally, we present the potential of lipase production with the preliminary experiment, as well as the intracellular lipid accumulation of the strain DMKU-JMGT1-45.
2. Materials and Methods
2.1. Strains and Isolation Procedures
Grease samples were collected from grease traps in Kasetsart University, Thailand. Five milliliters of the sample was suspended in 45 mL of sterile water in a 250 mL Erlenmeyer flask and shaken on a rotary shaker at 30 ± 2 °C for 1 h to detach the cells. The samples were serially diluted, and then 100 µL of the diluted sample were spread onto yeast extract peptone dextrose (YPD) agar supplemented with 0.025% sodium propionate and 0.02% chloramphenicol to prevent filamentous fungal and bacterial growth, respectively. The culture was incubated at 30 ± 2 °C until colonies appeared. Strains that possessed different colony morphologies were collected and cross streaked on YPD agar until the pure culture was obtained. For preservation, a single colony was cultivated in a yeast extract malt extract (YM) broth for 18 h. After incubation, the yeast culture was centrifuged, and cell pellets were washed and resuspended with a fresh YM medium. After that, the purified yeast was preserved in a YM broth supplemented with sterile 30% (v/v) glycerol in a freezer at −80 °C. The new discovered species has also been kept at China General Microbiological Culture Collection Center (CGMCC), CGMCC 2.680; NITE Biological Resource Center (NBRC), NBRC 114140; Portuguese Yeast Culture Collection (PYCC), PYCC 8358, and Thailand Bioresource Research Center (TBRC), TBRC 10242.
2.2. Screening of Lipase Production on Tween 80 Agar
Lipase production was estimated on Tween 80 agar. The yeast isolate was activated in the YM broth for 18 h. Then, each isolate was pointed onto Tween 80 agar. The petri dishes were incubated for 5 days. The lipase activity index (LI) was calculated as follows:
(1)
2.3. Study of Lipase Production in Liquid Medium
The yeast inoculum was cultured in the YM broth and incubated at 30 ± 2 °C for 18 h on a rotary shaker at 170 rpm and was transferred to 50 mL of the YM broth and the YM broth with 1% olive oil in a 250 mL Erlenmeyer flask for 5 days under the same culture conditions. At the end of incubation, the culture was centrifuged at 8200× g, 4 °C. A cell-free supernatant was used as crude enzyme for a quantitative analysis of lipase production, which was estimated, on the basis of olive oil hydrolysis, via the titrimetric method [28]. One milliliter of cell-free supernatant was mixed with assay substrate containing 10 mL of 10% homogenized olive oil in 10% gum acacia, 2 mL of a 0.6% CaCl2 solution, and 5 mL of a phosphate buffer. The mixture was incubated on a rotary shaker at 200 rpm and 30 °C for 1 h. To stop the reaction, 20 mL of a alcohol:acetone (1:1) mixture was added. The released fatty acids were titrated against 0.1N NaOH by using phenolphthalein as an indicator. The end point was the appearance of a pink color. A lipase activity unit is defined as the amount of enzyme that releases 1 mmol of fatty acids in 1 min under specified assay conditions.
2.4. Examination of Intracellular Lipid Accumulation
Lipid accumulation was investigated by Nile red staining under a fluorescence microscope. Yeast was cultivated in a nitrogen-limited medium II broth containing 70 g/L of glucose as a sole carbon source, 0.75 g/L of yeast extract, 0.55 g/L of (NH4)2SO4, 0.4g/L of KH2PO4 and 2g/L of MgSO4, and incubated on a rotary shaker at 150 rpm and 28 °C for 72 h. Lipid accumulation was investigated by staining cells in 40 μL of a culture broth with 10 μL of a Nile red solution (10 μg/L) [29]. Yeast cells were observed with a fluorescence microscope, under which the lipid content showed a strong yellow–gold emission. Fatty acids composition was analyzed by using the Sherlock Microbial Identification System (MIDI) version 6.1 at the Biodiversity Research Centre, Thailand Institute of Scientific and Technological Research (TISTR).
2.5. Phenotypic Characterization of Yeast
The morphology, biochemistry and physiology of the strain DMKU-JMGT1-45T were characterized according to the standard methods described by Yarrow [30]. Morphological studies were performed in a YM broth and YM agar at 25 °C for 3 days. After incubation, cell morphology was studied by using a phase-contrast microscope. A study of pseudohyphae formation was performed via slide culture on potato dextrose agar (PDA) at 25 °C. Growth at various temperatures was determined by cultivation yeast on YM agar incubated at 15, 25, 30, 35, 37, 40 and 45 °C. Ascospore formation was examined for individual strains, and the culture was mixed at weekly intervals for three months on YM agar, YPD agar, PDA agar, corn meal agar (CMA), 5% malt extract agar, Gorodkowa agar, and Fowell’s acetate agar [31] at 25 °C. The assimilation of carbon and nitrogen compounds was investigated in a liquid medium.
2.6. Molecular Genetic Characterization of Yeast
For molecular taxonomic identification, genomic DNA was extracted from yeast cells grown in the YM broth at the exponential phase. The D1/D2 domain of the large subunit (LSU) rRNA gene was used to identify all yeast isolates with NL1/NL4 primers [32]. For the strain DMKU-JMGT1-45T, small subunit rRNA (SSU), large subunit rRNA (LSU), internal transcribed spacer (ITS), translation elongation factor-1α (EF-1α), RNA polymerase II, subunits 1 (RPB1) and 2 (RPB2) genes were amplified with the primer pairs SSU1f/SSU4r, SSU3f/SSU2r, LSU3f/LSU4r, LSU5f/LSU2r [33], NS7A/NL5A [34], YTEF-1F/YTEF-6AR, EF1-1577F/YTEF-6AR, YRPB1-2F/YRPB1-12R, YRPB2-2F/YRPB2-8R and YRPB2-4F/YRPB2-6FR [18], respectively. PCR products were confirmed by agarose gel electrophoresis and purified with a FavorPrepTM Gel/PCR Purification Mini Kit (Favorgen, Austria). The purified PCR product was sent for DNA sequencing at First BASE Laboratories, Malaysia. The sequences were assembled and aligned with the BioEdit version 7.0.5.3 program [35]. Then, the sequences were compared with the GenBank database (
3. Results
3.1. Yeast Isolation and Communities of Yeast in Grease Traps
Fourteen grease samples were collected from grease traps in eight canteens in Kasetsart University, and 175 yeast isolates were obtained. The D1/D2 domain sequence analysis revealed that 150 isolates (85.71% of total) were identified as 36 described yeast species, whereas 25 isolates (14.29% of total) showed a difference of nucleotide substitution greater than 1% in the D1/D2 domain of the LSU rRNA gene when compared with their closest species. These isolates required more analysis to indicate whether they were undescribed or described yeasts. Surprisingly, Rhodotorula mucilaginosa was the only basidiomycetous yeast found in this study, and 149 isolates (85.14% of total) were identified to be 35 species of 15 genera including Allodekkera, Aureobasidium, Candida (in Debaryomyces, Saccharomyces, Pichia, Phaffomyces, Trichomonas, Metschnikowia and insertae sedis clade), Cyberlindnera, Exophiala, Kazachstania, Kodamaea, Lodderomyces, Magnusiomyces, Meyerozyma, Pichai, Saccharomyces, Schwanniomyces, Wickerhamiella and Zygoascus of the phylum Ascomycota. (Table 1). The results suggest that the majority of yeast species found in the grease traps belong to the phylum Ascomycota, and the yeast population was mainly represented as the genus Candida (69.33% of described yeast species), with Candida tropicalis being the most abundant yeast species from the entire yeast population (31 isolates and equivalent to 20.67% of described yeast species). The proportion of yeast genera in grease trap samples is shown in Figure 1.
The phylogenetic relationships among the obtained yeast in the phyla Ascomycota and Basidiomycota and their closely related species are shown in Figure 2. It is obviously shown that 25 isolates of total yeasts from grease samples appeared to be undescribed yeast species. However, they were also subjected to screening for lipase-producing ability.
3.2. Lipase Production and Lipid Accumulation
A rapid method used for investigating of lipase production was done on a Tween 80 medium by measuring the occurrence of the turbid zone, which is the calcium salt of the fatty acids released as a product of lipid hydrolysis. A total of 175 yeast isolates were subjected to screening for lipase production on Tween 80 agar after five days of cultivation. Table S1 shows that 61 isolates produced lipase with a range of 1.1–5.6 on the lipase activity index (LI), although some isolates showed lipase activity irrespective of the incubation period. Among the 61 isolates determined, the strain DMKU-JMGT1-45 showed the highest lipase activity with 5.6 LI value. The strain was then subjected to quantitative analysis for lipase activity. The result revealed that the strain DMKU-JMGT1-45 possessed lipase activity of 38.89 ± 9.62 and 155.56 ± 14.70 U/mL in the YM medium and the YM plus 1% olive oil medium, respectively, when cultivated at 30 °C and 170 rpm for five days. This result suggests that the strain DMKU-JMGT1-45 has potential for lipase production in a medium with oil supplementation; however, the strain was able to produce lipase even with oil omission. It is therefore of interest to investigate the lipase production and enzyme characteristics of this yeast strain in order to obtain information that hints at broader applications of the enzyme. Moreover, yeast with lipase production ability may be related, as previously mentioned, to the ability to accumulate lipids. A study of lipid accumulation and lipid profile was also reported in the strain DMKU-JMGT1-45.
The qualitative analysis of yeast cellular lipid content that used Nile red staining revealed that the strain DMKU-JMGT1-45 contained lipid granules inside the cell (Figure 3). The fatty acid profile of the strain DMKU-JMGT1-45 cellular lipid was determined. The fatty acid contents in the strain DMKU-JMGT1-45 are shown in Table 2, while the three main fatty acid contents were found to be summed feature 8 (C18:1 Cis 9 (ω 9)/ C18:1 (ω 8), C16:1 Cis 9 (ω 7), and C16:0 with 39.90 %, 27.61% and 14.97% of the total fatty acids, respectively. Oleic acid (C18:1) is one of the main fatty acid components of biodiesel. Thus, oleaginous yeast is considered as an alternative oil source for biodiesel production. However, fatty acid composition or even the type of fatty acid—such as saturated fatty acids (SFA) or unsaturated fatty acids (UFA)—affect the physical properties of biodiesel. For example, those fatty acids that contain little or no unsaturation were found to be more suitable for biodiesel production than polyunsaturated fatty acids. Unsaturated fatty acids with four double bonds or more become limiting to biodiesel production due to their susceptibility to oxidation [38]. Therefore, an optimum ratio of SFA to UFA is necessary for biodiesel use. However, the technical specifications for biodiesel depend on the country or region.
As described above, the strain DMKU-JMGT1-45 obviously possesses both a lipase-producing ability and lipid accumulation. It was therefore of interest to describe the strain DMKU-JMGT1-45 as well as its companion strain, DMKU-JMGT4-14, due to the 53 and 87 nucleotide substitutions in the D1/D2 domains of the LSU rRNA gene and ITS region, respectively, when compared to the closest species.
3.3. Molecular Genetic Characterization
According to the criterion proposed by [39], the yeast strain showed greater than 1% nucleotide substitutions of the D1/D2 domain of the LSU rRNA gene, compared with the type strains of species representing a distinguished species (the multiple alignment of the D1/D2 domain of the large subunit (LSU) rRNA gene, SSU, RPB I, RPB II and EF-1α, and genes of the strains DMKU-JMGT1-45T, DMKU-JMGT4-14, C. incommunis and Deakozyma indianesis are shown in Figures S1–S5, respectively). Meanwhile, according to the guidelines proposed by [40], the discrimination of current yeast genera possessing similarity thresholds of lower than 96.31% for ITS and 97.11% for LSU are taken to be different taxa. Based on the analysis of sequence similarity of the D1/D2 domain of the LSU rRNA gene and the ITS region, the strains DMKU-JMGT1-45T and DMKU-JMGT4-14 differ from their closest species, Candida incommunis CBS 5604T, by 10.41% nucleotide substitutions (53 nucleotide substitutions and 25 gaps of 509 nucleotides) and 20.96% nucleotide substitutions (87 nucleotide substitutions and 46 gaps of 415 nucleotides) of the ITS region. This result revealed that the strains DMKU-JMGT1-45T and DMKU-JMGT4-14 are clearly distinguished from their closest species. In order to study the phylogenetic placement of these strains, a phylogenetic tree was constructed. Since the sequences of these yeast were quite different from other yeasts, the information on the D1/D2 domain of the LSU rRNA gene alone may not be enough to clearly classify the position of the strains. Therefore, phylogenetic tree analysis was constructed by using SSU, the D1/D2 domain of the LSU rRNA gene, EF-1α, and the RNA polymerase subunits 1 (RPB1) and 2 (RPB2) genes of type species from their related species. The accession numbers of the proposing strain and reference strains are shown in Table S2. A phylogenetic analysis based on five genes revealed that the two strains formed a distinguished cluster that was separated from C. incommunis CBS 5604T and D. indianensis CBS 12903T with high bootstrap support (Figure 4).
3.4. Phenotypic Characterization
The phenotype characteristics of L. siamensis DMKU-JMGT1-45T and L. siamensis DMKU-JMGT4-14 were identical, while the main difference between L. siamensis DMKU-JMGT1-45T and C. incommunis and D. indianensis was its ability to assimilate melibiose, raffinose, inulin, starch, L-arabinose, D-ribose and methanol as a carbon source, as well as in its carbohydrate fermentation, acid production, and its ability to grow in a medium supplemented with cycloheximide. The strains DMKU-JMGT1-45T and DMKU-JMGT4-14 showed positive results in glucose, maltose and trehalose fermentation, positive results in acid production, and negative results in their ability to grow in a medium supplemented with cycloheximide, whereas C. incommunis CBS 5604T showed negative, negative, and positive results, respectively (Table 3). The spore formation of these three species is unknown. According to the results of DNA sequence analysis and phenotypic data, the strains DMKU-JMGT1-45T and DMKU-JMGT4-14 were identical and could not be assigned to any currently recognized genera. Consistent with this, we propose the genus Limtongella gen. nov. to accommodate members of the clade.
3.5. Description of gen. nov.
Limtongella (Lim.tong.el’la. L. nom. f. n. Limtongella is named in honor of Professor Savitree Limtong for her outstanding studies of yeast systematics in Thailand).
Cells are ovoid and cell division is by multilateral budding. Pseudohyphae are produced. Ascospore formation has not been observed in individual or mixed cultures. Carbohydrate may or may not be fermented. Diazonium blue B (DBB) and urease are negative. Starch-like compounds are not produced.
Phylogenetic placement: Saccharomycetales, Saccharomycotina, Ascomycota.
The type species of the genus is Limtongella siamensis.
MycoBank accession number is MB832635.
3.6. Description of sp. nov.
Limtongellasiamensis (si.a.men’sis.N.L. fem.adj. siamensis of or belonging to Siam, the old name of Thailand, where the type strain was isolated).
Yeast cells, after three days of cultivation on YM agar, are ovoidal and divided by multilateral budding. After three days incubation on YM agar at 25 °C, colonies are white, smooth, butyrous and glistening to dull surface. Ascospore are not formed in individual or mixed culture on any test medium. Pseudohyphae are observed on PDA at 25 °C after three days (Figure 5). Growth occurs at 15, 25, 30 and 35 °C on YM broth. Fermentation of sugars is absent. Glucose, galactose, sorbose, cellobiose, lactose (slow), maltose, melibiose (slow), sucrose, trehalose, melizitose, raffinose (slow), inulin (slow), starch (slow),
4. Conclusions
In the present study, we have described yeast communities in grease traps, which are high lipid-accumulating habitats. Our results showed that ascomycetous yeast was the dominant yeast and Candida tropicalis was the most common yeast found in the grease trap. In addition, 61 yeast isolates from the total showed lipase activity index (LI) values of between 1.1 and 5.6, and the highest LI value belonged to the strain DMKU-JMGT1-45T. After quantitative analysis in a liquid medium, the strain DMKU-JMGT1-45T showed the ability to produce lipase, even in a medium without oil supplementation. We also found lipid accumulation inside the cells of this strain. The main fatty acid found in strain DMKU-JMGT1-45T was a C18:1, which is one of the common biodiesel components. These data are preliminary information for lipase production and lipid accumulation studies of this strain for future work to investigate whether it can be applied in the industry. Surprisingly, the strain DMKU-JMGT1-45T showed a significant difference in the D1/D2 domain of the large subunit (LSU) rRNA gene to other described yeasts in GenBank. Hence, we propose the genus Limtongella gen. nov. to accommodate the novel species Limtongella siamensis. These results suggest that a grease trap is a good source to study yeast communities as well as to discover a potent lipase-producing yeast, which is an important enzyme in industrial applications.
Supplementary Materials
The following are available online at
Author Contributions
V.S. performed the data curation, formal analysis, investigation, methodology and writing—original draft. J.A. performed investigation and methodology. W.B. and P.K. performed formal analysis and validation. C.B. provided supervision, validation, and writing—review and editing. N.S. provided conceptualization, funding acquisition, project administration, resources, supervision, and writing—review and editing. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by the Thailand Research Fund through the TRF Research-Team Promotion Grant (RTA608004) and the Royal Golden Jubilee PhD program grant no. PHD/0070/2560 and International SciKU Branding program.
Conflicts of Interest
The authors declare no conflict of interest.
Figures and Tables
Enlarge this image.Figure 2. Phylogenetic relationships among the sequences of the D1/D2 domain of the large subunit (LSU) rRNA gene of representative yeast species from grease traps in the phylum Ascomycota, the phylum Basidiomycota, and their closely related yeast sequences retrieved from the GenBank database, as calculated using maximum likelihood method (GTR model). Undescribed species are presented in red color and the isolated yeast are presented in bold letters. Numbers on branches represent the bootstrap percentage (>50%) from 1000 random replications.
Enlarge this image.Figure 3. Photomicrographs of the Nile red-stained cells of Limtongella siamensis DMKU-JMGT1-45 diluted two folds from a cell density og 1.7 × 109 cell/mL when cultivated in a nitrogen-limited medium II broth at 150 rpm and 28 °C for 72 h. Bar, 20 μm: (a) bright-field image; (b) fluorescence image.
Enlarge this image.Figure 4. Phylogenetic tree based on maximum likelihood (GTR model) analysis of the small subunit rRNA (SSU), the D1/D2 domain of the large subunit (LSU) rRNA gene, elongation factor-1α (EF-1α), RNA polymerase subunits 1 (RPB1) and 2 (RPB2) sequences showing the taxonomic placement of Limtongella siamensis DMKU-JMGT1-45T and its sister species (both are shown in bold letters) within the family Trichomonasceae and related genera in the order Saccharomycetales. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) are shown next to the branches (50%). Schizosaccharomyces pombe CBS 356T served as the outgroup species. T, type strain.
Enlarge this image.Figure 5. Morphology of Limtongella siamensis nov. (DMKU-JMGT1-45T): (a) budding cells in a YM broth after three days at 25 °C; (b) pseudohyphae formed on PDA after three days at 25 °C. Bars, 10 µm.
Summary of described yeast discovered in grease traps.
| Yeast Taxa | GenBank Accession Number (D1/D2 Domain) | No. of Yeast Isolates |
|---|---|---|
| Ascomycota | ||
| Saccharomycotina | ||
| Debaryomycetaceae | ||
| Candida aaseri | NG_054858 | 16 |
| Candida metapsilosis | NG_054815 | 2 |
| Candida natalensis | NG_055225 | 4 |
| Candida neustonensis | NG_054803 | 1 |
| Candida orthopsilosis | NG_054816 | 6 |
| Candida parapsilosis | U45754 | 2 |
| Candida tropicalis | NG_054834 | 31 |
| Lodderomyces elongisporus | U45763 | 1 |
| Meyerozyma guilliermondii | U45709 | 1 |
| Schwanniomyces etchellsii | U45809 | 2 |
| Dipodascaceae | ||
| Magnusiomyces ingens | U40127 | 3 |
| insertae sedis | ||
| Candida rugosa | FJ768915 | 3 |
| Metschnikowiaceae | ||
| Candida pseudointermedia | NG_055407 | 1 |
| Kodamaea ohmeri | NG_042527 | 1 |
| Phaffomycetaceae | ||
| Candida mengyuniae | EU043158 | 12 |
| Cyberlindnera jadinii | EF550309 | 2 |
| Pichiaceae | ||
| Allodekkera sacchari | AB698502 | 1 |
| Candida boidinii | U70242 | 1 |
| Candida ethanolica | U71073 | 5 |
| Candida cylindracea | NG_055155 | 7 |
| Candida pseudolambica | U71063 | 7 |
| Candida sorboxylosa | U62314 | 1 |
| Pichia kudriavzevii | NG_055104 | 4 |
| Pichia manshurica | NG_055078 | 4 |
| Pichia occidentalis | NG_055110 | 2 |
| Saccharomycetaceae | ||
| Candida glabrata | AY198398 | 1 |
| Kazachstania humilis | KY106507 | 5 |
| Saccharomyces cerevisiae | NG_042623 | 2 |
| Trichomonasaceae | ||
| Candida suthepensis | AB565751 | 2 |
| Wickerhamiella pararugosa | NG_055327 | 2 |
| Wickerhamiella infanticola | KY106515 | 11 |
| Zygoascus bituminiphila | NG_055308 | 1 |
| Zygoascus polysorbophila | DQ438188 | 3 |
| Pezizomycotina | ||
| Saccotheciaceae | ||
| Aureobasidium melanogenum | FJ150926 | 1 |
| Herpotrichiellaceae | ||
| Exophiala dermatitidis | KF928508 | 1 |
| Basidiomycota | ||
| Sporidiobolaceae | ||
| Rhodotorula mucilaginosa | NG_055716 | 1 |
The fatty acid contents in Limtongella siamensis DMKU-JMGT1-45 and other oleaginous yeasts.
| Yeast Species | Fatty Acid (% of Total Fatty Acid) | |||||
|---|---|---|---|---|---|---|
| C16:0 | C16:1 | C18:0 | C18:1 | C18:2 | C18:3 | |
| Limtongella siamensis DMKU-JMGT1-45 | 15 | 28 | 1.1 | 40 | 2 | nd |
| Cryptococcus albidus | 12 | 1 | 3 | 73 | 12 | nd |
| Rhodotorula glutinis | 37 | 1 | 3 | 47 | 8 | nd |
| Rhodotorula graminis | 30 | 2 | 12 | 36 | 15 | 4 |
| Yarrowia lipolytica | 11 | 6 | 1 | 28 | 51 | 1 |
nd, not detectable; C16:0, palmitic acid; C16:1, palmitoleic acid; C18:0, stearic acid; C18:1, oleic acid; C18:2, linoleic acid; and C18:3, linolenic acid.
Table 3Differential characteristic between Limtongella siamensis DMKU-JMGT1-45T, Candida incommunis CBS 5604T and Deakozyma indianensis CBS 12903T. Species: 1, Limtongella siamensis DMKU-JMGT1-45T gen. nov., sp. nov.; 2, Candida incommunis CBS 5604T data from [32]; and 3, Deakozyma indianensis CBS 12903T data from [18].
| Characteristics | 1 | 2 | 3 |
|---|---|---|---|
| Assimilation of carbon compounds | |||
| Melibiose | + | − | − |
| Raffinose | + | − | − |
| Inulin | + | − | − |
| Starch | + | − | − |
| L-arabinose | + | − | − |
| D-ribose | + | − | − |
| Methanol | + | − | − |
Abbreviations: +, positive; w, weakly positive; s, slowly positive; v, variable; −, negative.
© 2019 by the authors.