Cargando…
Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5
Metabolic pathways play an indispensable role in supplying cellular systems with energy and molecular building blocks for growth, maintenance and repair and are tightly linked with lifespan and systems stability of cells. For optimal growth and survival cells rapidly adopt to environmental changes....
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448058/ https://www.ncbi.nlm.nih.gov/pubmed/23050242 http://dx.doi.org/10.3389/fonc.2012.00118 |
_version_ | 1782244214380167168 |
---|---|
author | Kitanovic, Ana Bonowski, Felix Heigwer, Florian Ruoff, Peter Kitanovic, Igor Ungewiss, Christin Wölfl, Stefan |
author_facet | Kitanovic, Ana Bonowski, Felix Heigwer, Florian Ruoff, Peter Kitanovic, Igor Ungewiss, Christin Wölfl, Stefan |
author_sort | Kitanovic, Ana |
collection | PubMed |
description | Metabolic pathways play an indispensable role in supplying cellular systems with energy and molecular building blocks for growth, maintenance and repair and are tightly linked with lifespan and systems stability of cells. For optimal growth and survival cells rapidly adopt to environmental changes. Accumulation of acetic acid in stationary phase budding yeast cultures is considered to be a primary mechanism of chronological aging and induction of apoptosis in yeast, which has prompted us to investigate the dependence of acetic acid toxicity on extracellular conditions in a systematic manner. Using an automated computer controlled assay system, we investigated and model the dynamic interconnection of biomass yield- and growth rate-dependence on extracellular glucose concentration, pH conditions and acetic acid concentration. Our results show that toxic concentrations of acetic acid inhibit glucose consumption and reduce ethanol production. In absence of carbohydrates uptake, cells initiate synthesis of storage carbohydrates, trehalose and glycogen, and upregulate gluconeogenesis. Accumulation of trehalose and glycogen, and induction of gluconeogenesis depends on mitochondrial activity, investigated by depletion of the Hap2-3-4-5 complex. Analyzing the activity of glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), pyruvate kinase (PYK), and glucose-6-phosphate dehydrogenase (G6PDH) we found that while high acetic acid concentration increased their activity, lower acetic acids concentrations significantly inhibited these enzymes. With this study we determined growth and functional adjustment of metabolism to acetic acid accumulation in a complex range of extracellular conditions. Our results show that substantial acidification of the intracellular environment, resulting from accumulation of dissociated acetic acid in the cytosol, is required for acetic acid toxicity, which creates a state of energy deficiency and nutrient starvation. |
format | Online Article Text |
id | pubmed-3448058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34480582012-10-04 Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 Kitanovic, Ana Bonowski, Felix Heigwer, Florian Ruoff, Peter Kitanovic, Igor Ungewiss, Christin Wölfl, Stefan Front Oncol Oncology Metabolic pathways play an indispensable role in supplying cellular systems with energy and molecular building blocks for growth, maintenance and repair and are tightly linked with lifespan and systems stability of cells. For optimal growth and survival cells rapidly adopt to environmental changes. Accumulation of acetic acid in stationary phase budding yeast cultures is considered to be a primary mechanism of chronological aging and induction of apoptosis in yeast, which has prompted us to investigate the dependence of acetic acid toxicity on extracellular conditions in a systematic manner. Using an automated computer controlled assay system, we investigated and model the dynamic interconnection of biomass yield- and growth rate-dependence on extracellular glucose concentration, pH conditions and acetic acid concentration. Our results show that toxic concentrations of acetic acid inhibit glucose consumption and reduce ethanol production. In absence of carbohydrates uptake, cells initiate synthesis of storage carbohydrates, trehalose and glycogen, and upregulate gluconeogenesis. Accumulation of trehalose and glycogen, and induction of gluconeogenesis depends on mitochondrial activity, investigated by depletion of the Hap2-3-4-5 complex. Analyzing the activity of glycolytic enzymes, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), pyruvate kinase (PYK), and glucose-6-phosphate dehydrogenase (G6PDH) we found that while high acetic acid concentration increased their activity, lower acetic acids concentrations significantly inhibited these enzymes. With this study we determined growth and functional adjustment of metabolism to acetic acid accumulation in a complex range of extracellular conditions. Our results show that substantial acidification of the intracellular environment, resulting from accumulation of dissociated acetic acid in the cytosol, is required for acetic acid toxicity, which creates a state of energy deficiency and nutrient starvation. Frontiers Media S.A. 2012-09-21 /pmc/articles/PMC3448058/ /pubmed/23050242 http://dx.doi.org/10.3389/fonc.2012.00118 Text en Copyright © 2012 Kitanovic, Bonowski, Heigwer, Ruoff, Kitanovic, Ungewiss and Wölfl. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Oncology Kitanovic, Ana Bonowski, Felix Heigwer, Florian Ruoff, Peter Kitanovic, Igor Ungewiss, Christin Wölfl, Stefan Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 |
title | Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 |
title_full | Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 |
title_fullStr | Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 |
title_full_unstemmed | Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 |
title_short | Acetic acid treatment in S. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex Hap2-3-4-5 |
title_sort | acetic acid treatment in s. cerevisiae creates significant energy deficiency and nutrient starvation that is dependent on the activity of the mitochondrial transcriptional complex hap2-3-4-5 |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448058/ https://www.ncbi.nlm.nih.gov/pubmed/23050242 http://dx.doi.org/10.3389/fonc.2012.00118 |
work_keys_str_mv | AT kitanovicana aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 AT bonowskifelix aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 AT heigwerflorian aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 AT ruoffpeter aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 AT kitanovicigor aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 AT ungewisschristin aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 AT wolflstefan aceticacidtreatmentinscerevisiaecreatessignificantenergydeficiencyandnutrientstarvationthatisdependentontheactivityofthemitochondrialtranscriptionalcomplexhap2345 |