Evidence map›Paper›PMID 41484924›Full record

ArticleJournal of biological engineering2026

Thiol release improvement in Saccharomyces cerevisiae oenological strains by CRISPR/Cas9-based IRC7 molecular cisgenesis.

Sara Granuzzo, Matteo Bosaro, Paolo Antoniali, Raffaele Lopreiato

Abstract read
In one paragraph

Article in Journal of biological engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Sara GranuzzoDepartment of Biomedical Sciences, University of Padova, via U.Bassi 58, 35131, Padova, Italy.
Matteo BosaroItaliana Biotecnologie Srl, via San Cassiano 99, 28069, Trecate - Novara, Italy.
Paolo AntonialiItaliana Biotecnologie Srl, via San Cassiano 99, 28069, Trecate - Novara, Italy.
Raffaele LopreiatoDepartment of Biomedical Sciences, University of Padova, via U.Bassi 58, 35131, Padova, Italy. raffaele.lopreiato@unipd.it.

Funding

Università degli Studi di Padova DOR2395544/23
6 · The paper itself

Abstract

backgroundPolyfunctional thiols are essential contributors to the aromatic profile of varietal white wines like Sauvignon Blanc. These compounds are released during fermentation by Saccharomyces cerevisiae cells from grape-derived precursors, with the carbon-sulfur β-lyase encoded by the IRC7 gene playing a crucial role. However, most oenological yeast strains lack the fully functional IRC7 allele, limiting their thiol-releasing ability.

resultsIn this study, we used CRISPR/Cas9-based cisgenesis to replace the native allele with the fully active IRC7

conclusionsThis work demonstrates that targeted IRC7 gene editing via CRISPR/Cas9 is a precise and efficient strategy to enhance thiol production in oenological yeasts, without compromising fermentative behavior or aromatic identity. Importantly, although the strains are formally GMOs, the modification mimics natural allelic variation. Our findings provide a foundation for developing next-generation wine yeasts optimized for high-aroma varietal wines and support the broader application of genome editing in fermentation biotechnology.

Indexed as

CisgenesisSaccharomyces cerevisiaeThiolic compoundsYeast fermentation

Identifiers

PMID41484924
PMCPMC12866068

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.