Isolation and Characterization of Yeasts Able to Assimilate Sugarcane Bagasse Hemicellulosic Hydrolysate and Produce Xylitol Associated with Veturius transversus (Passalidae, Coleoptera, and Insecta).
Yeasts are microorganisms of the Fungi kingdom, distributed in the phyla Ascomycota, Basidiomycota, and Deuteromycota . On the other hand, beetles are the most abundant order of insects (Coleoptera, Insecta, Arthropoda, and Metazoa), with more than 400,000 species currently described .
The association of yeasts with beetles was decisive in the evolutionary success of these insects, the microbiota being indispensable to them, playing fundamental roles such as in the synthesis of amino acids, lipids, pheromones, and digestive enzymes and in biodetoxification [3, 4]. According to Suh et al. , the microbial content of a xylophagous beetle's gut is a hyperdiverse source of undescribed species.
Xylitol is a promising polyol of five carbons, with medical applications in middle ear otitis  and obesity prevention . It is obtained from D-xylose reduction, performed by microbial fermentation or a chemical process . As this latter releases a high number of by-products, demanding several steps for purification, sampling efforts aiming to isolate microbes with ability to produce xylitol keep being necessary.
Recent yeast and yeast-like fungi sampling efforts have increased the number of known species and strains able to produce vitamins, enzymes, and other products from fermentation of sugars such as ethanol and xylitol . In this way, isolation and characterization of wild-type yeasts and yeast-like fungi remains an important approach.
The aim of this work was to isolate and characterize yeasts associated with the xylophagous beetle Veturius transversus (Passalidae, Coleoptera, and Insecta) able to assimilate sugarcane bagasse hemicellulosic hydrolysate (SBHH) as sole carbon source and produce xylitol by D-xylose fermentation.
2. Material and Methods
Under authorization (protocol number 34652-1) of the Instituto Chico Mendes de Conservafao da Biodiversidade (Brazilian authority for biodiversity access), 15 beetles were collected from the Central Amazon Rainforest (3[degrees]06'05.20" S, 59[degrees]58'23.14 W). They were identified as V. transversus, a highly representative passalid beetle in this region. Three samples were deposited in the Entomological collection Paulo Burnheim (UFAM, Brazil).
The beetles were washed in 70% ethanol for 1min, the elytra were removed, and the gut was dissected. Fragments of intestine of about 1 cm were incubated for 48 h (120 rpm, 28[degrees]C) in tubes with 10 mL of SBHH, prepared as previously described [10, 11]. After this time, 100 [micro]L of this suspension was spread on SBHH added to agar. Yeasts and yeast-like colonies were isolated in Petri dishes containing Sabouraud agar (yeast extract, 10 g/L; glucose, 40 g/L; agar, 20 g/L).
To evaluate their ability to ferment D-xylose, a loopful of each isolate was cultured in tubes containing 10 mL of YNBX medium (yeast nitrogen base without amino acids, 6.7 g/L; D-xylose, 40 g/L). After 7 days of incubation at 28[degrees]C and 120 rpm, the medium content was centrifuged and the supernatant was analysed by an HPLC system using a Rezex RPM monosaccharide column (300 x 7.8 mm, Pb2+ 8%, Phenomenex). The D-xylose consumption rate (%) was calculated according to the final and initial D-xylose concentrations. Xylitol yield (g x [g.sup.-1]) was calculated by the ratio xylitol produced:D-xylose consumed.
For taxonomic identification, biochemical characterization was performed using kit ID32C (BioMerieux[R]), according to the manufacturer's instructions. The results were plotted in the online application ApiWeb[R] (https://apiweb.biomerieux.com) for physiological similarity identification.
Furthermore, the isolates were evaluated by genomic internal transcribed spacer (ITS) and ribosomal gene nucleotide sequences. The DNA was extracted according to Harju et al.  and amplified by PCR using primers ITS1 (5' TCC GTA GGT GAA CCT GCC 3') and ITS4 (5' TCC TCC GCT TAT TGA TAT GC 3'). The PCR products were used to perform a sequencing reaction using a BigDye[R] kit (Applied Biosystems), and nucleotide sequences were obtained in an Applied Biosystems 3130 Genetic Analyzer[R] automatic sequencer.
The obtained sequences were compared to the NCBI database (https://www.ncbi.nlm.nih.gov/) using BLAST (Basic Local Alignment Search Tool) and deposited in GenBank. For phylogenetic relationship analysis, nucleotide sequences were aligned using Clustal-W and analysed by neighbour-joining (bootstrap, 2000 replicas), provided by MEGA 6.0 . Nucleotide sequences from the genomic ITS region of Meyerozyma guilliermondii (GenBank JN974905), Trichosporon mycotoxinivorans (GenBank JX891097), and Scheffersomyces stipitis (GenBank GU256745) were included in the phylogenetic tree as reference groups, this last being the external group.
A total of 20 colonies were isolated and evaluated, correspondent to 10 species of four genera, Candida (12 isolates), Cryptococcus (five isolates), Debaryomyces (one isolate), and Geotrichum (two isolates); their biochemical profiles are described in Table 1.
Nucleotide sequence BLAST results identified three different groups, one close to Candida tropicalis, another composed of members of the species Williopsis saturnus, and the third composed of the genus Geotrichum sp. The fragment length was about 550 bp for C. tropicalis and W saturnus, containing 18S rDNA (partial), ITS1 (complete), 5.8S rDNA (complete), ITS2 (complete), and 28S rDNA (partial). For Geotrichum sp., fragment length was on average 250 bp, containing ITS1 (partial), 5.8S rDNA (complete), and ITS2 (partial).
For isolates 07,16, and 18, identity greater than or equal to 99% allows us to conclude that these are members of the species W saturnus. Isolates 03,08,09,10,11, and 20 presented identity varying from 97% to 99% with C. tropicalis, making it admissible that they are closely related to this species, here named clade C. tropicalis. The other isolates presented identity varying from 92% to 96% with Geotrichum sp. or Galactomyces spp.
Considering the short length of the fragment, which allows classification only at genus level and the synonymy between Geotrichum and Galactomyces, they were classified as clade Geotrichum sp. The complete BLAST results and GenBank accession number of sequences are presented in Table 2.
Neighbour-joining phylogenetic analysis endorsed the conclusion about the three groups that clade W. saturnus is close to Meyerozyma guilliermondii and Scheffersomyces stipitis, whereas C. tropicalis and Geotrichum sp. are closely related to Trichosporon mycotoxinivorans. The phylogenetic tree is presented in Figure 1.
Fermentation tests indicated that none of the isolates produces ethanol using xylose as carbon source. This result was expected because xylose fermentation to ethanol is an uncommon feature, being presented by less than 1% of known yeast species . However, most of them were able to produce xylitol, onlyisolates 12 and 13 (Geotrichum sp.) being unable to do this. The highest yield was observed in isolate 01 (Geotrichum sp.), reaching 0.502 g x [g.sup.-1] and consuming 92.6% of the D-xylose. The complete results are presented in Table 3.
All isolates were able to assimilate D-xylose, a common feature in yeasts able to metabolize SBHH because this is the most abundant monosaccharide in hemicellulose . Candida is the most representative, but that occurs because there are a great number of asexual phase (anamorph) species classified in this genus, which is a polyphyletic group [5,16].
The other genera, Cryptococcus and Debaryomyces, have remarkable biotechnological potential in incorporation of lipids in their biomass, being reported as oleaginous yeasts [17,18]. Suh and Blackwell  describe the genus Geotrichum as dimorphic fungi, being anamorphs of the genera Dipodascus and Galactomyces and growing being yeast-like according to environmental conditions.
All biochemical profile results presented similarity with species able to perform pentose fermentation and/or another process with biotechnological potential. However, according to Barnett , biochemical profiles maybe used as complementary information but cannot be conclusive for taxonomic identification because they can present high variation, with it being recommended to evaluate genomics data. According to Hou-Rui et al. , up to 1% of nucleotide substitution in a ribosomal domain is permitted for strains of a single biological species, rDNA sequence analysis being a simple and reliable tool for taxonomic identification.
The phylogenetic analysis endorses that predicted by Barnett , noticeable because clade W. saturnus is composed of isolates with three different biochemical profiles, whereas clade C. tropicalis is composed of five different biochemical profiles (one of those C. tropicalis) and clade Geotrichum has eight different biochemical profiles. Furthermore, there were some isolates with the same biochemical profile distributed in all clades, strengthening that hypothesis.
The maximum theoretical yield for xylitol production from D-xylose fermentation is 1.0 g x [g.sup.-1]. Despite this, as microbes produce xylitol as a compatible solute, it is excreted in osmotic stress conditions and then consumed as the medium becomes less harsh ; common yields range from 40% to 70% . The highest yield value for microbial fermentation is reported by Granstrom et al.  for Candida sp., at 0.85 g x [g.sup.-1].
With Geotrichum sp. (isolate 01) being a wild-type strain with the capability to produce xylitol like some industrial strains, it can be considered a promising xylitol-producing yeast. This is the first work to report xylitol production by wild-type yeast strains associated with beetles from the Central Amazon Rainforest.
The yeast community associated with V transversus gut is rich in D-xylose-assimilating and xylitol-producing species, some of which present potential close to industrial strains. Geotrichum is a highly representative group in this community.
Geotrichum sp. (isolate 01) presents high xylitol yield, reaching about 50% of the maximum theoretical yield, and is a promising xylitol-producing strain.
Subsequent efforts must be concentrated on developing bioprocesses using these isolates.
Conflicts of Interest
The authors declare that there are no conflicts of interest.
Special thanks are due to Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), and Fundacao de Amparo a Pesquisa do Estado do Amazonas (FAPEAM). The authors are also grateful to Dra. Nair Otaviano Aguiar for beetle identification.
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Italo Thiago Silveira Rocha Matos, Enedina Nogueira Assuncao, Edson Junior do Carmo, Verena Makaren Soares, and Spartaco Astolfi-Filho
Departamento de Genetica, Universidade Federal do Amazonas, Av. Gal. Rodrigo Octavio, 3000 Manaus, AM, Brazil
Correspondence should be addressed to Italo Thiago Silveira Rocha Matos; firstname.lastname@example.org
Received 6 April 2017; Accepted 10 May 2017; Published 6 June 2017
Academic Editor: Giuseppe Comi
Caption: Figure 1: Neighbour-joining phylogenetic tree, endorsing the distribution of the isolates into three groups.
Table 1: Biochemical profiles of isolates from V. transversus, identified according to ApiWeb (BioMerieux). Isolate GAL ACT SAC NAG LAT ARA CEL RAF MAL TER 01 + + + + + + + + + + 02 + - + + + + + + + + 03 + - + + - - - - + + 04 + - + + + + + + + + 05 + - + + - - + - + + 06 + + + + - - - - + + 07 + - + + + + + + + + 08 + - + + + + + + + + 09 + - + + + + + + + + 10 + - + + + + + + + + 11 + + + + + + - - + + 12 - + - - - - - - - - 13 - + - - - - - - - - 14 + + + + + - - - + + 15 + + + + + - - + + + 16 + + + + + + - - + + 17 + + + + + - + - + + 18 + + + + - - - - + + 19 + + + + + - - - + + 20 + - + + - + + - + + Isolate 2KG MDG SOR XYL RIB GLY RHA PLE ERY MEL 01 + + + + + + + + + + 02 + + + + + + + + - - 03 + + + + - + - + - - 04 + + + + + + + + + + 05 + - + + + - + + - - 06 + + + + - + - + - - 07 + + + + + + + + + + 08 + + + + + + + + + + 09 + + + + + - - + - - 10 + + + + + + + + + + 11 + - + + - + - + + - 12 - - - + - + - - - - 13 - - - + - + - - - - 14 + + + + - + - + - - 15 + - + + - + - + - - 16 + + + + - + - + - - 17 + + + + + + - + - - 18 + + + + - + - + - - 19 + + + + - + - + - - 20 + - + + + - - + - - Isolate GRT MLZ GNT LVT MAN LAC INO GLU SBE GLN 01 + + + + + - - + - + 02 - - - - + + + + - - 03 - + - - + - - + - - 04 - - + - + - - + - - 05 + + + - - - - + - + 06 - + - + + + + + + + 07 + + + + + + + + + + 08 + + + + + + + + - + 09 - + + + + - - + - + 10 + + + + + + - + + + 11 - + - - + - - + - - 12 - - - - - - - + - - 13 - - - - - - - + - - 14 - + - - + - - + - - 15 - + - - - - - + + + 16 - + + - + - - + - - 17 - + - - + - + + - + 18 - + - + + + + + + + 19 - + - - + + - + - + 20 + + + - + - - + + + Isolate ESC Species Similarity (%) 01 + Cryptococcus humicola 98.4% 02 - Cryptococcus curvatus -- 03 - Debaryomyces etchellsii 79.1% Candida 04 - membranifa-ciens -- 05 - Candida intermedia -- 06 - Candida parapsilosis -- 07 + Cryptococcus humicola 99.2% 08 - Cryptococcus humicola 99.7% 09 - Candida tropicalis 53.6% 10 - Cryptococcus humicola 99.5% 11 + Candida famata -- 12 - Geotrichum capitatum 97.7% 13 + Geotrichum capitatum 97.7% 14 + Candida sake 99.5% 15 - Candida sake 99.0% 16 + Candida parapsilosis 83.1% 17 - Candida tropicalis -- 18 - Candida sake 95.4% 19 + Candida tropicalis 94.4% 20 + Candida intermedia 95.7% GAL: galactose, ACT: cycloheximide, SAC: sucrose, NAG: N-acetyl glucosamine, LAT: lactic acid, ARA: arabinose, CEL: cellobiose, RAF: raffinose, MAL: maltose, TRE: trehalose, 2KG: 2 keto-gluconate, MDG: a-methyl-glucopyranoside, SOR: sorbitol, XYL: xylose, RIB: ribose, GLY: glycerol, RHA: rhamnose, PLE: palatinose, ERY: erythritol, MEL: melibiose, GRT: sodium glucuronate, MLZ: melezitose, GNT: potassium gluconate, LVT: levulinic acid, MAN: mannitol, LAC: lactose, INO: inositol, GLU: glucose, SBE: sorbose, GLN: glucosamine, ESC: esculin iron citrate. Table 2: Identification of isolates according to BLAST result and nucleotide sequence GenBank accession number. Isolate Species Max identity (%) 01 Geotrichum sp. 93 02 Geotrichum sp. 95 03 Candida tropicalis 99 04 Geotrichum sp. 94 05 Galactomyces candidum 96 06 Geotrichum sp. 96 07 Williopsis saturnus 99 08 Candida tropicalis 98 09 Candida tropicalis 99 10 Candida tropicalis 98 11 Candida tropicalis 98 12 Galactomyces candidum 96 13 Galactomyces geotrichum 96 14 Geotrichum sp. 95 15 Geotrichum sp. 94 16 Williopsis saturnus 99 17 Geotrichum sp. 93 18 Williopsis saturnus 99 19 Geotrichum sp. 94 20 Candida tropicalis 97 Isolate Query coverage (%) e-value GenBank accession number 01 92 1e-119 KP276644 02 93 3e-131 KP276636 03 98 0.0 KP276645 04 100 1e-121 KP276637 05 97 1e-131 KP276638 06 99 1e-126 KP276639 07 100 0.0 KP257575 08 99 0.0 KP276646 09 99 0.0 KP276647 10 99 0.0 KP276648 11 99 0.0 KP276649 12 98 1e-136 KP276640 13 98 1e-136 KP276641 14 100 1e-125 KP276642 15 100 3e-102 KP288488 16 100 0.0 KP257574 17 99 7e-129 KP288487 18 100 0.0 KP257573 19 99 5e-134 KP276643 20 99 0.0 KP276650 Table 3: D-xylose consumption rate (%) and xylitol yield of each isolate. Isolate D-xylose Xylitol consumption yield rate (%) (g x [g.sup.-1]) 01 92.6 0.502 02 29.9 0.210 03 33.4 0.214 04 36.2 0.255 05 30.7 0.186 06 35.6 0.224 07 31.0 0.169 08 33.2 0.180 09 34.0 0.170 10 30.7 0.100 11 100.0 0.339 12 27.5 0.0 13 18.7 0.0 14 100.0 0.315 15 100.0 0.326 16 100.0 0.304 17 41.4 0.304 18 100.0 0.341 19 100.0 0.370 20 100.0 0.347
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|Title Annotation:||Research Article|
|Author:||Matos, Italo Thiago Silveira Rocha; Assuncao, Enedina Nogueira; do Carmo, Edson, Jr.; Soares, Verena|
|Publication:||International Journal of Microbiology|
|Date:||Jan 1, 2017|
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