Spathaspora brunopereirae sp. nov. and Spathaspora domphillipsii sp. nov., two d-xylose-fermenting ascosporogenous yeasts from Amazonian Forest biomes

References

1. Nguyen NH, Suh SO, Marshall CJ, Blackwell M. Morphological and ecological similarities: wood-boring beetles associated with novel xylose-fermenting yeasts, Spathaspora passalidarum gen. sp. nov. and Candida jeffriesii sp. nov. Mycol Res 2006; 110:1232–1241 [View Article]
   [Google Scholar]
2. Cadete RM, Melo MA, Dussán KJ, Rodrigues RCLB, Silva SS et al. Diversity and physiological characterization of d-xylose-fermenting yeasts isolated from the Brazilian Amazonian forest. PLoS One 2012; 7:e43135 [View Article]
   [Google Scholar]
3. Gisele de F, Luana T, Samila RPN, Maxwel AA. Efficient production of second generation ethanol and xylitol by yeasts from Amazonian beetles (Coleoptera) and their galleries. Afr J Microbiol Res 2017; 11:814–824 [View Article]
   [Google Scholar]
4. Ren Y, Chen L, Niu Q, Hui F. Description of Scheffersomyces henanensis sp. nov., a new d-xylose-fermenting yeast species isolated from rotten wood. PLoS One 2014; 9:e92315 [View Article]
   [Google Scholar]
5. Cadete RM, Rosa CA. The yeasts of the genus Spathaspora: potential candidates for second-generation biofuel production. Yeast 2018; 35:191–199 [View Article] [PubMed]
   [Google Scholar]
6. Barbosa AC, Cadete RM, Gomes FCO, Lachance M-A, Rosa CA. Candida materiae sp. nov., a yeast species isolated from rotting wood in the Atlantic Rain Forest. Int J Syst Evol Microbiol 2009; 59:2104–2106 [View Article] [PubMed]
   [Google Scholar]
7. Cadete RM, Melo MA, Zilli JE, Vital MJS, Mouro A et al. Spathaspora brasiliensis sp. nov., Spathaspora suhii sp. nov., Spathaspora roraimanensis sp. nov. and Spathaspora xylofermentans sp. nov., four novel (d)-xylose-fermenting yeast species from Brazilian Amazonian forest. Antonie van Leeuwenhoek 2013; 103:421–431 [View Article]
   [Google Scholar]
8. Lopes MR, Morais CG, Kominek J, Cadete RM, Soares MA et al. Genomic analysis and d-xylose fermentation of three novel Spathaspora species: Spathaspora girioi sp. nov., Spathaspora hagerdaliae f. a., sp. nov. and Spathaspora gorwiae f. a., sp. nov. FEMS Yeast Res 2016; 16:fow044 [View Article]
   [Google Scholar]
9. Wang Y, Ren Y-C, Zhang Z-T, Ke T, Hui F-L. Spathaspora allomyrinae sp. nov., a d-xylose-fermenting yeast species isolated from a scarabeid beetle Allomyrina dichotoma. Int J Syst Evol Microbiol 2016; 66:2008–2012 [View Article] [PubMed]
   [Google Scholar]
10. Morais CG, Batista TM, Kominek J, Borelli BM, Furtado C et al. Spathaspora boniae sp. nov., a d-xylose-fermenting species in the Candida albicans/Lodderomyces clade. Int J Syst Evol Microbiol 2017; 67:3798–3805 [View Article]
    [Google Scholar]
11. Varize CS, Cadete RM, Lopes LD, Christofoleti-Furlan RM, Lachance M-A et al. Spathaspora piracicabensis f. a., sp. nov., a D-xylose-fermenting yeast species isolated from rotting wood in Brazil. Antonie Van Leeuwenhoek 2018; 111:525–531 [View Article] [PubMed]
    [Google Scholar]
12. Lv SL, Chai CY, Wang Y, Yan ZL, Hui FL. Five new additions to the genus Spathaspora (Saccharomycetales, Debaryomycetaceae) from southwest China. MycoKeys 2020; 75:31–49 [View Article] [PubMed]
    [Google Scholar]
13. Feng X, Merow C, Liu Z, Park DS, Roehrdanz PR et al. How deregulation, drought and increasing fire impact Amazonian biodiversity. Nature 2021; 597:516–521 [View Article] [PubMed]
    [Google Scholar]
14. Lopes MR, Lara CA, Moura MEF, Uetanabaro APT, Morais PB et al. Characterisation of the diversity and physiology of cellobiose-fermenting yeasts isolated from rotting wood in Brazilian ecosystems. Fungal Biol 2018; 122:668–676 [View Article] [PubMed]
    [Google Scholar]
15. Kurtzman CP, Fell JW, Boekhout T, Robert V. Methods for isolation, phenotypic characterization and maintenance of yeasts. In Kurtzman CP, Fell JW, Boekhout T. eds The Yeasts, a Taxonomic Study, 5th edn. Amsterdam: Elsevier; 2011 pp 87–110
    [Google Scholar]
16. White TJ, Bruns T, Lee S, Taylor JW. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In Innis MA, Gelfand DH, Sninsky JJ, White TJ. eds PCR Protocols: A Guide to Methods and Applications San Diego, CA: Academic Press; 1990 pp 315–322
    [Google Scholar]
17. O’Donnell K. Fusarium and its near relatives. In Reynolds DR, Taylor JW. eds The Fungal Holomorph: Mitotic, Meiotic and Pleomorphic Speciation in Fungal Systematic Oregon: CAB International; 1993 pp 225–233
    [Google Scholar]
18. Kurtzman CP, Robnett CJ. Identification and phylogeny of ascomycetous yeasts from analysis of nuclear large subunit (26S) ribosomal DNA partial sequences. Antonie van Leeuwenhoek 1998; 73:331–371 [View Article]
    [Google Scholar]
19. Lachance MA, Bowles JM, Starmer WT, Barker JS. Kodamaea kakaduensis and Candida tolerans, two new ascomycetous yeast species from Australian hibiscus flowers. Can J Microbiol 1999; 45:172–177 [View Article]
    [Google Scholar]
20. Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874 [View Article]
    [Google Scholar]
21. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic Local Alignment Search Tool. J Mol Biol 1990; 215:403–410 [View Article] [PubMed]
    [Google Scholar]
22. Lachance M-A. Phylogenies in yeast species descriptions: in defense of neighbor-joining. Yeast 2022; 39:513–520 [View Article]
    [Google Scholar]
23. Palladino F, Rodrigues R, Cadete RM, Barros KO, Rosa CA. Novel potential yeast strains for the biotechnological production of xylitol from sugarcane bagasse. Biofuels Bioprod Bioref 2021; 15:690–702 [View Article]
    [Google Scholar]