98%
921
2 minutes
20
Xylanolytic enzyme systems in ascomycetous yeasts remain underexplored, despite the presence of yeasts in various xylan-rich ecological niches. In this study, we investigated the secreted xylanolytic machineries of three Blastobotrys species-B. mokoenaii, B. illinoisensis, and B. malaysiensis-by integrating genome annotation, bioinformatics, and secretome analyses of cultures grown on beechwood glucuronoxylan. Our findings demonstrate that these yeasts effectively hydrolyze xylan through the secretion of xylanases from the glycoside hydrolase (GH) family 11, which play a central role in cleaving the xylan backbone. Additionally, the yeasts produce a diverse array of other CAZymes, including members of GH families 3, 5, and 67, with putative roles in xylan degradation. We also report on the heterologous expression and functional characterization of the GH30_7 xylanase BmXyn30A from B. mokoenaii, which exhibits both glucuronoxylanase and xylobiohydrolase activities. We demonstrate additive effects between GH family 30 BmXyn30A and GH family 11 BmXyn11A during the hydrolysis of beechwood glucuronoxylan, where the enzymes exhibit complementary roles that enhance the deconstruction of this complex hemicellulose substrate. These findings broaden our understanding of the xylanolytic systems in yeasts and underscore the potential of Blastobotrys species as cell factories and natural xylanase producers. The enzymes they produce hold promise for biorefining applications, enabling efficient utilization of renewable xylan-rich plant biomass resources. KEY POINTS: • Extracellular GH11 xylanases dominate glucuronoxylan degradation in Blastobotrys yeasts. • Yeast GH30_7 enzyme shows multifaceted activity, supporting complex xylan breakdown. • Blastobotrys yeasts show promise as cell factories for industrial biotechnology applications.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316802 | PMC |
http://dx.doi.org/10.1007/s00253-025-13556-5 | DOI Listing |
Mycopathologia
August 2025
Département des Agents Infectieux, Service de Mycologie-Parasitologie, CHU de Poitiers, Poitiers, France.
Blastobotrys allociferrii is a yeast involved in human infection and colonization. Here, we present the first draft genome of B. allociferrii, which has been isolated from a human sample (CBS 18616).
View Article and Find Full Text PDFAppl Microbiol Biotechnol
August 2025
Department of Life Sciences, Division of Industrial Biotechnology, Chalmers University of Technology, 412 96, Gothenburg, Sweden.
Xylanolytic enzyme systems in ascomycetous yeasts remain underexplored, despite the presence of yeasts in various xylan-rich ecological niches. In this study, we investigated the secreted xylanolytic machineries of three Blastobotrys species-B. mokoenaii, B.
View Article and Find Full Text PDFMicrob Cell Fact
July 2025
Faculty of Engineering and Natural Sciences, Tampere University, Hervanta Campus, PO Box 527, Tampere, FI-33014, Finland.
Background: ,-muconic acid (ccMA), an important platform chemical, can be produced from lignin related molecules (LRM) via a specific two-branch catabolic route known as the β-ketoadipate pathway, which is present in certain soil bacteria. This pathway enables high production yields because ccMA is a native intermediate in one of its branches. However, commonly obtained LRM, such as -coumaric and ferulic acid, are typically metabolized through the branch that lacks the ccMA intermediate.
View Article and Find Full Text PDFBraz J Microbiol
September 2025
Laboratório de Microbiologia Polar e Conexões Tropicais, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, P. O. Box 486, Belo Horizonte, CEP 31270-901, MG, Brasil.
We evaluated the fungal diversity present in ornithogenically-influenced soils of the polyextreme Brazilian Archipelago of São Pedro and São Paulo, using a DNA metabarcoding approach. We detected 1,596,919 fungal DNA reads grouped into 232 amplicon sequence variants (ASVs). The phylum Ascomycota was the dominant phylum, followed by Basidiomycota, Blastocladiomycota, Mortierellomycota, Mucoromycota, Aphelidiomycota, Rozellomycota, Chytridiomycota and Zoopagomycota, in rank abundance order.
View Article and Find Full Text PDFBioresour Technol
June 2025
State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, 2005 Songhu Road, Shanghai 200438, PR China; Shanghai Engineering Research Center of Industrial Microorganisms, Fudan University, 2005 Songhu Road, Shanghai 200438, PR China. Electronic address:
To efficiently produce myo-inositol from glucose, the PGI1, ZWF1, ITR2, and MIOX5 genes in Kluyveromyces marxianus were knocked out to block glucose metabolism via the Embden-Meyerhof-Parnas (EMP) and pentose phosphate pathways (PPP), prevent myo-inositol oxidative degradation. The metabolically engineered KM-JC4 strain, introduced with myo-inositol synthesis genes, produced 80.7 g/L in a 5 L bioreactor using glucose and glycerol as carbon sources.
View Article and Find Full Text PDF