CRISPRi screen highlights chromatin regulation to be involved in formic acid tolerance in Saccharomyces cerevisiaeShow others and affiliations
2023 (English)In: Engineering Microbiology, ISSN 2667-3703, Vol. 3, no 2, article id 100076Article in journal (Refereed) Published
Abstract [en]
Formic acid is one of the main weak acids in lignocellulosic hydrolysates that is known to be inhibitory to yeast growth even at low concentrations. In this study, we employed a CRISPR interference (CRISPRi) strain library comprising >9000 strains encompassing >98% of all essential and respiratory growth-essential genes, to study formic acid tolerance in Saccharomyces cerevisiae. To provide quantitative growth estimates on formic acid tolerance, the strains were screened individually on solid medium supplemented with 140 mM formic acid using the Scan-o-Matic platform. Selected resistant and sensitive strains were characterized in liquid medium supplemented with formic acid and in synthetic hydrolysate medium containing a combination of inhibitors. Strains with gRNAs targeting genes associated with chromatin remodeling were significantly enriched for strains showing formic acid tolerance. In line with earlier findings on acetic acid tolerance, we found genes encoding proteins involved in intracellular vesicle transport enriched among formic acid sensitive strains. The growth of the strains in synthetic hydrolysate medium followed the same trend as when screened in medium supplemented with formic acid. Strains sensitive to formic acid had decreased growth in the synthetic hydrolysate and all strains that had improved growth in the presence of formic acid also grew better in the hydrolysate medium. Systematic analysis of CRISPRi strains allowed identification of genes involved in tolerance mechanisms and provided novel engineering targets for bioengineering strains with increased resistance to inhibitors in lignocellulosic hydrolysates. © 2023 The Author(s)
Place, publisher, year, edition, pages
Elsevier Inc. , 2023. Vol. 3, no 2, article id 100076
Keywords [en]
Chromatin, CRISPRi library, Formic acid, Lignocellulosic hydrolysates, Screening, Tolerance, Yeast, acetic acid, glucose, guide RNA, xylose, acid tolerance, Article, carbon source, cell transport, cell vacuole, chromatin assembly and disassembly, clustered regularly interspaced short palindromic repeat, concentration (parameter), controlled study, gene identification, gene repression, nonhuman, phenomics, RNA sequence, Saccharomyces cerevisiae
National Category
Microbiology
Identifiers
URN: urn:nbn:se:ri:diva-64311DOI: 10.1016/j.engmic.2023.100076Scopus ID: 2-s2.0-85151595257OAI: oai:DiVA.org:ri-64311DiVA, id: diva2:1755095
Note
We acknowledge the Novo Nordisk Foundation (NF19OC0057685), The Swedish Research Council (Dnr 2018–04713) and the Hasselblad Foundation for financial support.
2023-05-052023-05-052023-05-05Bibliographically approved