Genome-wide identification of Saccharomyces cerevisiae genes required for tolerance to acetic acid

被引:190
作者
Mira, Nuno P. [1 ]
Palma, Margarida [1 ]
Guerreiro, Joana F. [1 ]
Sa-Correia, Isabel [1 ]
机构
[1] Univ Tecn Lisboa, Inst Biotechnol & Bioengn, Ctr Biol & Chem Engn, Inst Super Tecn, P-1049001 Lisbon, Portugal
关键词
MAJOR FACILITATOR SUPERFAMILY; PLASMA-MEMBRANE TRANSPORTER; SNF1; PROTEIN-KINASE; VACUOLAR H+-ATPASE; POTASSIUM-TRANSPORT; ADAPTIVE RESPONSE; INTRACELLULAR PH; SALT TOLERANCE; IRON REGULON; WEAK ACIDS;
D O I
10.1186/1475-2859-9-79
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Acetic acid is a byproduct of Saccharomyces cerevisiae alcoholic fermentation. Together with high concentrations of ethanol and other toxic metabolites, acetic acid may contribute to fermentation arrest and reduced ethanol productivity. This weak acid is also a present in lignocellulosic hydrolysates, a highly interesting non-feedstock substrate in industrial biotechnology. Therefore, the better understanding of the molecular mechanisms underlying S. cerevisiae tolerance to acetic acid is essential for the rational selection of optimal fermentation conditions and the engineering of more robust industrial strains to be used in processes in which yeast is explored as cell factory. Results: The yeast genes conferring protection against acetic acid were identified in this study at a genome-wide scale, based on the screening of the EUROSCARF haploid mutant collection for susceptibility phenotypes to this weak acid (concentrations in the range 70-110 mM, at pH 4.5). Approximately 650 determinants of tolerance to acetic acid were identified. Clustering of these acetic acid-resistance genes based on their biological function indicated an enrichment of genes involved in transcription, internal pH homeostasis, carbohydrate metabolism, cell wall assembly, biogenesis of mitochondria, ribosome and vacuole, and in the sensing, signalling and uptake of various nutrients in particular iron, potassium, glucose and amino acids. A correlation between increased resistance to acetic acid and the level of potassium in the growth medium was found. The activation of the Snf1p signalling pathway, involved in yeast response to glucose starvation, is demonstrated to occur in response to acetic acid stress but no evidence was obtained supporting the acetic acid-induced inhibition of glucose uptake. Conclusions: Approximately 490 of the 650 determinants of tolerance to acetic acid identified in this work are implicated, for the first time, in tolerance to this weak acid. These are novel candidate genes for genetic engineering to obtain more robust yeast strains against acetic acid toxicity. Among these genes there are number of transcription factors that are documented regulators of a large percentage of the genes found to exert protection against acetic acid thus being considered interesting targets for subsequent genetic engineering. The increase of potassium concentration in the growth medium was found to improve the expression of maximal tolerance to acetic acid, consistent with the idea that the adequate manipulation of nutrient concentration of industrial growth medium can be an interesting strategy to surpass the deleterious effects of this weak acid in yeast cells.
引用
收藏
页数:13
相关论文
共 60 条
  • [1] AIKING H, 1976, ARCH MICROBIOL, V108, P117, DOI 10.1007/BF00425101
  • [2] The histone deacetylase Rpd3p is required for transient changes in genomic expression in response to stress
    Alejandro-Osorio, Adriana L.
    Huebert, Dana J.
    Porcaro, Dominic T.
    Sonntag, Megan E.
    Nillasithanukroh, Songdet
    Lwill, Jessica
    Gasch, Audrey P.
    [J]. GENOME BIOLOGY, 2009, 10 (05):
  • [3] Yeast protein expression profile during acetic acid-induced apoptosis indicates causal involvement of the TOR pathway
    Almeida, Bruno
    Ohlmeier, Steffen
    Almeida, Agostinho J.
    Madeo, Frank
    Leao, Cecilia
    Rodrigues, Fernando
    Ludovico, Paula
    [J]. PROTEOMICS, 2009, 9 (03) : 720 - 732
  • [4] Increased tolerance and conversion of inhibitors in lignocellulosic hydrolysates by Saccharomyces cerevisiae
    Almeida, Jodo R. M.
    Modig, Tobias
    Petersson, Anneli
    Hahn-Hagerdal, Barbel
    Liden, Gunnar
    Gorwa-Grauslund, Marie F.
    [J]. JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2007, 82 (04) : 340 - 349
  • [5] Engineering yeast transcription machinery for improved ethanol tolerance and production
    Alper, Hal
    Moxley, Joel
    Nevoigt, Elke
    Fink, Gerald R.
    Stephanopoulos, Gregory
    [J]. SCIENCE, 2006, 314 (5805) : 1565 - 1568
  • [6] POTASSIUM REQUIREMENTS OF SACCHAROMYCES-CEREVISIAE
    CAMACHO, M
    RAMOS, J
    RODRIGUEZNAVARRO, A
    [J]. CURRENT MICROBIOLOGY, 1981, 6 (05) : 295 - 299
  • [7] A novel approach for the improvement of stress resistance in wine yeasts
    Cardona, Fernando
    Carrasco, Purificacion
    Perez-Ortin, Jose Enrique
    del Olmo, Marcel li
    Aranda, Agustin
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2007, 114 (01) : 83 - 91
  • [8] Effect of extracellular acidification on the activity of plasma membrane ATPase and on the cytosolic and vacuolar pH of Saccharomyces cerevisiae
    Carmelo, V
    Santos, H
    SaCorreia, I
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1997, 1325 (01): : 63 - 70
  • [9] Effect of acetic acid and pH on the cofermentation of glucose and xylose to ethanol by a genetically engineered strain of Saccharomyces cerevisiae
    Casey, Elizabeth
    Sedlak, Miroslav
    Ho, Nancy W. Y.
    Mosier, Nathan S.
    [J]. FEMS YEAST RESEARCH, 2010, 10 (04) : 385 - 393
  • [10] Transcription of the yeast iron regulon does not respond directly to iron but rather to iron-sulfur cluster biosynthesis
    Chen, OS
    Crisp, RJ
    Valachovic, M
    Bard, M
    Winge, DR
    Kaplan, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (28) : 29513 - 29518