CAR1 as a new selective marker for genetic engineering of wine yeasts.
Arginine
CAR1 gene
CRISPR-Cas9
Ethyl carbamate
Genetic engineering
Nitrogen source
Selective marker
Wine yeast
Journal
Journal of microbiological methods
ISSN: 1872-8359
Titre abrégé: J Microbiol Methods
Pays: Netherlands
ID NLM: 8306883
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
received:
17
08
2023
revised:
06
10
2023
accepted:
07
10
2023
medline:
10
11
2023
pubmed:
12
10
2023
entrez:
11
10
2023
Statut:
ppublish
Résumé
A common problem in engineering industrial yeasts, and wine yeasts in particular, is the lack or scarcity of selective markers for introducing desired genetic changes. Almost all such markers, which are usually auxotrophic mutations, would reduce the growth characteristics of yeast strains. However, a potentially useful marker could be the CAR1 gene encoding arginase, the deletion of which reduces the accumulation of the carcinogen ethyl carbamate in wine, making such a deletion beneficial for wine production and maintainable in wine yeast strains. Here we demonstrate the use of the CAR1 gene as a selective marker. First, we observe that complete deletion of CAR1 in a triploid wine strain of Saccharomyces cerevisiae causes strong growth inhibition on a medium containing arginine as the only nitrogen source. Then, we show that strains with CAR1 deletion can be reliably transformed using CAR1 as a plasmid marker. Thus, the CAR1 gene can be used as a convenient selective marker in genetic engineering of wine yeasts, in particular using CRISPR/Cas9 technology.
Identifiants
pubmed: 37820871
pii: S0167-7012(23)00174-4
doi: 10.1016/j.mimet.2023.106840
pii:
doi:
Substances chimiques
Saccharomyces cerevisiae Proteins
0
Urethane
3IN71E75Z5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
106840Informations de copyright
Copyright © 2023. Published by Elsevier B.V.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.