Effects of a novel variant of the yeast γ-glutamyl kinase Pro1 on its enzymatic activity and sake brewing.
Proline
Saccharomyces cerevisiae
Sake yeast
Succinate
γ-Glutamyl kinase Pro1
Journal
Journal of industrial microbiology & biotechnology
ISSN: 1476-5535
Titre abrégé: J Ind Microbiol Biotechnol
Pays: Germany
ID NLM: 9705544
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
27
04
2020
accepted:
23
07
2020
pubmed:
5
8
2020
medline:
2
4
2021
entrez:
5
8
2020
Statut:
ppublish
Résumé
Sake is a traditional Japanese alcoholic beverage brewed with the yeast Saccharomyces cerevisiae. Sake taste is affected by sugars, organic acids, and amino acids. We previously isolated mutants resistant to the proline analogue azetidine-2-carboxylate derived from a diploid sake yeast strain. Some of the mutants produced a greater amount of proline in the brewed sake. One of them (strain K-9-AZC) carried a novel mutation in the PRO1 gene encoding the Gln79His variant of the γ-glutamyl kinase Pro1, a key enzyme in proline biosynthesis in S. cerevisiae. This mutation resulted in extreme desensitization to feedback inhibition by proline, leading to proline overproduction. Interestingly, sake brewed with K-9-AZC contained 3.7-fold more proline, but only 25% less succinate than sake brewed with the parent strain. Metabolome analysis suggests that the decrease in succinate was attributable to a lower level of 2-oxoglutarate, which is converted into glutamate. The approach here could be a practical method for breeding of yeast strains involved in the diversity of sake taste.
Identifiants
pubmed: 32748014
doi: 10.1007/s10295-020-02297-1
pii: 10.1007/s10295-020-02297-1
pmc: PMC7658068
doi:
Substances chimiques
Saccharomyces cerevisiae Proteins
0
Proline
9DLQ4CIU6V
Phosphotransferases (Carboxyl Group Acceptor)
EC 2.7.2.-
glutamate 5-kinase
EC 2.7.2.11
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
715-723Subventions
Organisme : The NARO Bio-oriented Technology Research Advancement Institution
ID : 30017B
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