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Series GSE269873 Query DataSets for GSE269873
Status Public on Jun 17, 2024
Title Expression Patterns of Mal genes and Association with Differential Maltose and Maltotriose Transport rate of Two Saccharomyces pastorianus Yeasts
Organism Saccharomyces pastorianus
Experiment type Expression profiling by high throughput sequencing
Summary Beer brewing is a well-known process that still faces great challenges, such as the total consumption of sugars present in the fermentation media. Lager-style beer, major worldwide beer type, is elaborated by Saccharomyces pastorianus (Sp) yeast which must ferment high maltotriose content worts, but its consumption represents a notable problem, especially among Sp strains belonging to group I. Factors like fermentation conditions, presence of maltotriose transporters, transporter copy number variation, and genetic regulation variations contribute to this issue. We assess the factors affecting fermentation in two Sp yeast strains: SpIB1, with limited maltotriose uptake, and SpIB2, known for efficient maltotriose transport. Here, SpIB2 transported significantly more maltose (28%) and maltotriose (32%) compared to SpIB1. Furthermore, SpIB2 expressed all MAL transporters (ScMALx1, SeMALx1, ScAGT1, SeAGT1, MTT1, and MPHx) on the first day of fermentation, while SpIB1 only exhibited ScMalx1, ScAGT1, and MPH2/3 genes. Some SpIB2 transporters had polymorphic transmembrane domains (TMD) resembling MTT1, accompanied by higher expression of these transporters and its positive regulator genes like MAL63. These findings suggest that, in addition of the factors mentioned above, positive regulators of Mal transporters contribute significatively to phenotypic diversity in maltose and maltotriose consumption among the studied lager yeast strains.
 
Overall design The goal is to assess the underling genes involved in the phenotypic diversity of maltose and maltotriose consumption of two lager yeast strains (SpIB1 and SpIB2). Both yeasts were subjected to lager fermentation in a standard wort for 5 days and samples were collected during day 2 and 5.
We then performed a gene expression analysis using the RNA-seq data from both yeasts on days 2 and 5 of fermentation.
Web link https://journals.asm.org/doi/10.1128/aem.00397-24
 
Contributor(s) Pereyra Alférez B, García JH, Hernández Vásquez CI, del Rocio Pérez Ortega E, Damas Buenrostro LC, Martzinez Segundo AG
Citation(s) 38975758
Submission date Jun 14, 2024
Last update date Nov 06, 2024
Contact name Benito Pereyra Alférez
E-mail(s) benito.pereyraal@uanl.edu.mx, cesar.hernandezvsqz@uanl.edu.mx
Organization name Universidad Autónoma de Nuevo León
Department Instituto de Biotecnología
Lab Laboratorio 4
Street address Av. Pedro de Alba S/N
City San Nicolás de los Garza
State/province Nuevo León
ZIP/Postal code 66455
Country Mexico
 
Platforms (1)
GPL34596 Illumina HiSeq 2500 (Saccharomyces pastorianus)
Samples (12)
GSM8329256 SpIB1 lager yeast, day 2, rep1
GSM8329257 SpIB1 lager yeast, day 2, rep2
GSM8329258 SpIB1 lager yeast, day 2, rep3
Relations
BioProject PRJNA1124045

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Supplementary file Size Download File type/resource
GSE269873_RAW.tar 590.0 Kb (http)(custom) TAR (of TXT)
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Raw data are available in SRA

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