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Genome assembly and variant analysis of two Saccharomyces cerevisiae strains isolated from stingless bee pollen.
de Almeida, Eduardo Luís Menezes; da Silveira, Wendel Batista; Fietto, Luciano Gomes; Silva, Mayara Salgado; Santana, Weyder Cristiano; Eller, Monique Renon.
Affiliation
  • de Almeida ELM; Laboratory of Microbial Physiology, Department of Microbiology, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
  • da Silveira WB; Laboratory of Microbial Physiology, Department of Microbiology, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
  • Fietto LG; Department of Biochemistry and Molecular Biology, Universidade Federal de Viçosa, Viçosa, Brazil.
  • Silva MS; Department of Food Technology, Federal Institute of Education, Science and Technology of Ceará, Limoeiro Do Norte, Brazil.
  • Santana WC; Department of Entomology - Universidade Federal de Viçosa, Viçosa, Brazil.
  • Eller MR; Department of Food Technology - Universidade Federal de Viçosa, Viçosa, Brazil. Electronic address: monique.eller@ufv.br.
Gene ; 927: 148722, 2024 Nov 15.
Article in En | MEDLINE | ID: mdl-38914244
ABSTRACT
Products from stingless bees are rich reservoirs of microbial diversity, including yeasts with fermentative potential. Previously, two Saccharomyces cerevisiae strains, JP14 and IP9, were isolated from Jataí (Tetragonisca angustula) and Iraí (Nannotrigona testaceicornis) bees, respectively, aiming at mead production. Both strains presented great osmotic and sulfite tolerance, and ethanol production, although they have a high free amino nitrogen demand. Herein, their genomes were sequenced, assembled, and annotated, and the variants were compared to the S. cerevisiae S288c reference strain. The final assembly of IP9 and JP14 presented high N50 and BUSCO scores, and more than 6430 protein-coding genes. Additionally, nQuire predicted the ploidy of IP9 as diploid, but the results were not enough to determine the ploidy of JP14. The mitochondrial genomes of IP9 and JP14 presented the same gene content as S288c but the genes were rearranged and fragmented in different patterns. Meanwhile, the genes with mutations of high impact (e.g., indels, gain of stop codon) for both yeasts were enriched for transmembrane transport, electron transfer, oxidoreductase, heme binding, fructose, mannose, and glucose transport, activities related to the respiratory chain and sugar metabolism. The IP9 strain presented copy number gains in genes related to sugar transport and cell morphogenesis; in JP14, genes were enriched for disaccharide metabolism and transport, response to reactive oxygen species, and polyamine transport. On the other hand, IP9 presented copy number losses related to disaccharide, thiamine, and aldehyde metabolism, while JP14 presented depletions related to disaccharide, oligosaccharide, asparagine, and aspartate metabolism. Notably, both strains presented a killer toxin gene, annotated from the assembling of unmapped reads, representing a potential mechanism for the control of other microorganisms population in the environment. Therefore, the annotated genomes of JP14 and IP9 presented a high selective pressure for sugar and nitrogen metabolism and stress response, consistent with their isolation source and fermentative properties.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pollen / Saccharomyces cerevisiae / Genome, Fungal Limits: Animals Language: En Journal: Gene Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pollen / Saccharomyces cerevisiae / Genome, Fungal Limits: Animals Language: En Journal: Gene Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: Netherlands