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Adaptive mutations in sugar metabolism restore growth on glucose in a pyruvate decarboxylase negative yeast strain
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2015 (Engelska)Ingår i: Microbial Cell Factories, ISSN 1475-2859, E-ISSN 1475-2859, Vol. 14, artikel-id 116Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background: A Saccharomyces cerevisiae strain carrying deletions in all three pyruvate decarboxylase (PDC) genes (also called Pdc negative yeast) represents a non-ethanol producing platform strain for the production of pyruvate derived biochemicals. However, it cannot grow on glucose as the sole carbon source, and requires supplementation of C2 compounds to the medium in order to meet the requirement for cytosolic acetyl-CoA for biosynthesis of fatty acids and ergosterol. Results: In this study, a Pdc negative strain was adaptively evolved for improved growth in glucose medium via serial transfer, resulting in three independently evolved strains, which were able to grow in minimal medium containing glucose as the sole carbon source at the maximum specific rates of 0.138, 0.148, 0.141 h(-1), respectively. Several genetic changes were identified in the evolved Pdc negative strains by genomic DNA sequencing. Among these genetic changes, 4 genes were found to carry point mutations in at least two of the evolved strains: MTH1 encoding a negative regulator of the glucose-sensing signal transduction pathway, HXT2 encoding a hexose transporter, CIT1 encoding a mitochondrial citrate synthase, and RPD3 encoding a histone deacetylase. Reverse engineering of the non-evolved Pdc negative strain through introduction of the MTH1(81D) allele restored its growth on glucose at a maximum specific rate of 0.053 h(-1) in minimal medium with 2% glucose, and the CIT1 deletion in the reverse engineered strain further increased the maximum specific growth rate to 0.069 h(-1). Conclusions: In this study, possible evolving mechanisms of Pdc negative strains on glucose were investigated by genome sequencing and reverse engineering. The non-synonymous mutations in MTH1 alleviated the glucose repression by repressing expression of several hexose transporter genes. The non-synonymous mutations in HXT2 and CIT1 may function in the presence of mutated MTH1 alleles and could be related to an altered central carbon metabolism in order to ensure production of cytosolic acetyl-CoA in the Pdc negative strain.

Ort, förlag, år, upplaga, sidor
2015. Vol. 14, artikel-id 116
Nyckelord [en]
Pyruvate decarboxylase, Genomic DNA sequencing, Yeast, Reverse engineering, MTH1, Hexose transporter, Citrate synthase, Histone deacetylase
Nationell ämneskategori
Biologiska vetenskaper
Identifikatorer
URN: urn:nbn:se:kth:diva-172674DOI: 10.1186/s12934-015-0305-6ISI: 000359105100001PubMedID: 26253003Scopus ID: 2-s2.0-84938561675OAI: oai:DiVA.org:kth-172674DiVA, id: diva2:850319
Forskningsfinansiär
Science for Life Laboratory - a national resource center for high-throughput molecular bioscienceVetenskapsrådetNovo NordiskEU, Europeiska forskningsrådet, 247013
Anmärkning

QC 20150901

Tillgänglig från: 2015-09-01 Skapad: 2015-08-27 Senast uppdaterad: 2017-12-04Bibliografiskt granskad

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Av författaren/redaktören
Hallström, Björn M.
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Proteomik och nanobioteknologiScience for Life Laboratory, SciLifeLab
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Microbial Cell Factories
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