The Metabolism of Respiring Carbon Sources by Dekkera bruxellensis and Its Relation with the Production of Acetate.

Acetate production Disulfiram Oxidative metabolism Pdh bypass Respiration

Journal

Applied biochemistry and biotechnology
ISSN: 1559-0291
Titre abrégé: Appl Biochem Biotechnol
Pays: United States
ID NLM: 8208561

Informations de publication

Date de publication:
Oct 2023
Historique:
accepted: 17 02 2023
medline: 21 9 2023
pubmed: 4 3 2023
entrez: 3 3 2023
Statut: ppublish

Résumé

Dekkera bruxellensis has been studied for several aspects of its metabolism over the past years, which has expanded our comprehension on its importance to industrial fermentation processes and uncovered its industrial relevance. Acetate is a metabolite often found in D. bruxellensis aerobic cultivations, whereas its production is linked to decreased ethanol yields. In a previous work, we aimed to understand how acetate metabolism affected the fermentation capacity of D. bruxellensis. In the present work, we evaluated the role of acetate metabolism in respiring cells using ammonium or nitrate as nitrogen sources. Our results showed that galactose is a strictly respiratory sugar and that a relevant part of its carbon is lost, while the remaining is metabolised through the Pdh bypass pathway before being assimilated into biomass. When this pathway was blocked, yeast growth was reduced while more carbon was assimilated to the biomass. In nitrate, more acetate was produced as expected, which increased carbon assimilation, although less galactose was uptaken from the medium. This scenario was not affected by the Pdh bypass inhibition. The confirmation that acetate production was crucial for carbon assimilation was brought by cultivations in pyruvate. All physiological data were connected to the expression patterns of PFK1, PDC1, ADH1, ALD3, ALD5 and ATP1 genes. Other respiring carbon sources could only be properly used by the cells when some external acetate was supplied. Therefore, the results reported herein helped in providing valuable contributions to the understanding of the oxidative metabolism in this potential industrial yeast.

Identifiants

pubmed: 36867386
doi: 10.1007/s12010-023-04398-w
pii: 10.1007/s12010-023-04398-w
doi:

Substances chimiques

Nitrates 0
Carbon 7440-44-0
Galactose X2RN3Q8DNE
Acetates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6369-6391

Subventions

Organisme : FACEPE
ID : APQ-1452-2.01/10
Organisme : CNPq
ID : 472533/2013-4
Organisme : CNPq
ID : 474847/2013-6
Organisme : CNPq
ID : 446927/2014-7

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Gilberto Henrique Teles (GH)

Laboratory of Microbial Genetics, Department of Genetics, Federal University of Pernambuco, Av. Moraes Rego, 1235. Cidade Universitária, Recife, PE, 50.670-901, Brazil.

Mariana Rodrigues Xavier (MR)

Laboratory of Microbial Genetics, Department of Genetics, Federal University of Pernambuco, Av. Moraes Rego, 1235. Cidade Universitária, Recife, PE, 50.670-901, Brazil.

Jackeline Maria Da Silva (JM)

Department of Antibiotics, Federal University of Pernambuco, Recife, Brazil.

Rafael Barros De Souza (RB)

Laboratory of Microbial Metabolism, Institute of Biological Sciences, University of Pernambuco, Recife, Brazil.

Will de Barros Pita (W)

Department of Antibiotics, Federal University of Pernambuco, Recife, Brazil.

Marcos Antonio de Morais (MA)

Laboratory of Microbial Genetics, Department of Genetics, Federal University of Pernambuco, Av. Moraes Rego, 1235. Cidade Universitária, Recife, PE, 50.670-901, Brazil. marcos.moraisjr@ufpe.br.

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