Abstract
Zygosaccharomyces bailii and two closely related species, Z. parabailii and Z. pseudobailii (“Z. bailii species complex”, “Z. bailii sensu lato” or simply “Z. bailii (s.l.)”), are frequently implicated in the spoilage of acidified preserved foods and beverages due to their tolerance to very high concentrations of weak acids used as food preservatives. The recent sequencing and annotation of these species’ genomes have clarified their genomic organization and phylogenetic relationship, which includes events of interspecies hybridization. Mechanistic insights into their adaptation and tolerance to weak acids (e.g., acetic and lactic acids) are also being revealed. Moreover, the potential of Z. bailii (s.l.) to be used in industrial biotechnological processes as interesting cell factories for the production of organic acids, reduction of the ethanol content, increase of alcoholic beverages aroma complexity, as well as of genetic source for increasing weak acid resistance in yeast, is currently being considered. This chapter includes taxonomical, ecological, physiological, and biochemical aspects of Z. bailii (s.l.). The focus is on the exploitation of physiological genomics approaches that are providing the indispensable holistic knowledge to guide the effective design of strategies to overcome food spoilage or the rational exploitation of these yeasts as promising cell factories.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Abbott DA, Knijnenburg TA, de Poorter LMI, Reinders MJT, Pronk JT, van Maris AJA (2007) Generic and specific transcriptional responses to different weak organic acids in anaerobic chemostat cultures of Saccharomyces cerevisiae. FEMS Yeast Res 7:819–833
Antunes M, Palma M, Sá-Correia I (2018) Transcriptional profiling of Zygosaccharomyces bailii early response to acetic acid or copper stress mediated by ZbHaa1. Sci Rep 8:14122
Arez BF, Alves L, Paixão SM (2014) Production and characterization of a novel yeast extracellular invertase activity towards improved Dibenzothiophene Biodesulfurization. Appl Biochem Biotechnol 174:2048–2057
Arneborg N, Jespersen L, Jakobsen M (2000) Individual cells of Saccharomyces cerevisiae and Zygosaccharomyces bailii exhibit different short-term intracellular pH responses to acetic acid. Arch Microbiol 174:125–128
Branduardi P (2002) Molecular cloning and sequence analysis of the Zygosaccharomyces bailii HIS3 gene encoding the imidazole glycerolphosphate dehydratase. Yeast 19:1165–1170
Branduardi P, Sauer M, De Gioia L, Zampella G, Valli M, Mattanovich D, Porro D (2006) Lactate production yield from engineered yeasts is dependent from the host background, the lactate dehydrogenase source and the lactate export. Microb Cell Fact 5:4
Braun-Galleani S, Ortiz-Merino RA, Wu Q, Xu Y, Wolfe KH (2018) Zygosaccharomyces pseudobailii, another yeast interspecies hybrid that regained fertility by damaging one of its MAT loci. FEMS Yeast Res 18:foy079
Cabral S, Prista C, Loureiro-Dias MC, Leandro MJ (2015) Occurrence of FFZ genes in yeasts and correlation with fructophilic behaviour. Microbiology 161:2008–2018
Čadež N, Fülöp L, Dlauchy D, Péter G (2015) Zygosaccharomyces favi sp. nov., an obligate osmophilic yeast species from bee bread and honey. Antonie Van Leeuwenhoek 107:645–654
Canonico L, Comitini F, Oro L, Ciani M (2016) Sequential fermentation with selected immobilized Non-Saccharomyces yeast for reduction of ethanol content in wine. Front Microbiol 7:278
Carmelo V, Santos H, Sá-Correia I (1997) Effect of extracellular acidification on the activity of plasma membrane ATPase and on the cytosolic and vacuolar pH of Saccharomyces cerevisiae. Biochim Biophys Acta 1325:63–70
Chen Y, Nielsen J (2016) Biobased organic acids production by metabolically engineered microorganisms. Curr Opin Biotechnol 37:165–172
Ciani M, Comitini F, Mannazzu I, Domizio P (2010) Controlled mixed culture fermentation: a new perspective on the use of non- Saccharomyces yeasts in winemaking. FEMS Yeast Res 10:123–133
Contreras A, Hidalgo C, Henschke PA, Chambers PJ, Curtin C, Varela C (2014) Evaluation of non-Saccharomyces yeasts for the reduction of alcohol content in wine. Appl Environ Microbiol 80:1670–1678
Contreras A, Hidalgo C, Schmidt S, Henschke PA, Curtin C, Varela C (2015) The application of non-Saccharomyces yeast in fermentations with limited aeration as a strategy for the production of wine with reduced alcohol content. Int J Food Microbiol 205:7–15
Dang TDT, De Maeseneire SL, Zhang BY, De Vos WH, Rajkovic A, Vermeulen A, Van Impe JF, Devlieghere F (2012) Monitoring the intracellular pH of Zygosaccharomyces bailii by green fluorescent protein. Int J Food Microbiol 156:290–295
Dato L, Branduardi P, Passolunghi S, Cattaneo D, Riboldi L, Frascotti G, Valli M, Porro D (2010) Advances in molecular tools for the use of Zygosaccharomyces bailii as host for biotechnological productions and construction of the first auxotrophic mutant. FEMS Yeast Res 10:894–908
Desmoucelles C, Pinson B, Saint-Marc C, Daignan-Fornier B (2002) Screening the yeast “disruptome” for mutants affecting resistance to the immunosuppressive drug, mycophenolic acid. J Biol Chem 277:27036–27044
Destruelle M, Holzer H, Klionsky DJ (1994) Identification and characterization of a novel yeast gene: the YGP1 gene product is a highly glycosylated secreted protein that is synthesized in response to nutrient limitation. Mol Cell Biol 14:2740–2754
Diezemann A, Boles E (2003) Functional characterization of the Frt1 sugar transporter and of fructose uptake in Kluyveromyces lactis. Curr Genet 43:281–288
Domizio P, Romani C, Lencioni L, Comitini F, Gobbi M, Mannazzu I, Ciani M (2011a) Outlining a future for non-Saccharomyces yeasts: Selection of putative spoilage wine strains to be used in association with Saccharomyces cerevisiae for grape juice fermentation. Int J Food Microbiol 147:170–180
Domizio P, Romani C, Comitini F, Gobbi M, Lencioni L, Mannazzu I, Ciani M (2011b) Potential spoilage non-Saccharomyces yeasts in mixed cultures with Saccharomyces cerevisiae. Ann Microbiol 61:137–144
dos Santos SC, Sá-Correia I (2015) Yeast toxicogenomics: lessons from a eukaryotic cell model and cell factory. Curr Opin Biotechnol 33:183–191
Englezos V, Rantsiou K, Cravero F, Torchio F, Ortiz-Julien A, Gerbi V, Rolle L, Cocolin L (2016) Starmerella bacillaris and Saccharomyces cerevisiae mixed fermentations to reduce ethanol content in wine. Appl Microbiol Biotechnol 100:5515–5526
Escribano R, González-Arenzana L, Garijo P, Berlanas C, López-Alfaro I, López R, Gutiérrez AR, Santamaría P (2017) Screening of enzymatic activities within different enological non-Saccharomyces yeasts. J Food Sci Technol 54:1555–1564
European Commission (2011) COMMISSION REGULATION (EU) No 1129/2011 of 11 November 2011, amending Annex II to Regulation (EC) No 1333/2008 of the European Parliament and of the Council by establishing a Union list of food additives
Fernandes AR, Mira NP, Vargas RC, Canelhas I, Sá-Correia I (2005) Saccharomyces cerevisiae adaptation to weak acids involves the transcription factor Haa1p and Haa1p-regulated genes. Biochem Biophys Res Commun 337:95–103
Galeote V, Bigey F, Devillers H, Neuvéglise C, Dequin S (2013) Genome sequence of the food spoilage yeast Zygosaccharomyces bailii CLIB 213T. Genome Announc 1:e00606–e00613
Gancedo JM, Gancedo C (1986) Catabolite repression mutants of yeast. FEMS Microbiol Lett 32:179–187
Ganga MA, Martínez C (2004) Effect of wine yeast monoculture practice on the biodiversity of non-Saccharomyces yeasts. J Appl Microbiol 96:76–83
Garavaglia J, Habekost A, Bjerk TR, de Souza Schneider R de C, Welke JE, Zini CA, Valente P (2014) A new method for rapid screening of ester-producing yeasts using in situ HS-SPME. J Microbiol Methods 103:1–2
Garavaglia J, Schneider R de C de S, Camargo Mendes SD, Welke JE, Zini CA, Caramão EB, Valente P (2015) Evaluation of Zygosaccharomyces bailii BCV 08 as a co-starter in wine fermentation for the improvement of ethyl esters production. Microbiol Res 173:59–65
Garay-Arroyo A, Covarrubias AA, Clark I, Nino I, Gosset G, Martinez A (2004) Response to different environmental stress conditions of industrial and laboratory Saccharomyces cerevisiae strains. Appl Microbiol Biotechnol 63:734–741
Gasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown PO (2000) Genomic expression programs in the response of yeast cells to environmental changes. Mol Biol Cell 11:4241–4257
Gentzsch M, Tanner W (1996) The PMT gene family: protein O-glycosylation in Saccharomyces cerevisiae is vital. EMBO J 15:5752–5759
Gobbi M, De Vero L, Solieri L, Comitini F, Oro L, Giudici P, Ciani M (2014) Fermentative aptitude of non-Saccharomyces wine yeast for reduction in the ethanol content in wine. Eur Food Res Technol 239:41–48
Godinho CP, Prata CS, Pinto SN, Cardoso C, Bandarra NM, Fernandes F, Sá-Correia I (2018) Pdr18 is involved in yeast response to acetic acid stress counteracting the decrease of plasma membrane ergosterol content and order. Sci Rep 8:7860
Goffeau A, Barrell BG, Bussey H et al (1996) Life with 6000 genes. Science 274(546):563–567
Gonçalves P, Rodrigues de Sousa H, Spencer-Martins I (2000) FSY1, a novel gene encoding a specific fructose/H(+) symporter in the type strain of Saccharomyces carlsbergensis. J Bacteriol 182:5628–5630
Graves T, Narendranath NV, Dawson K, Power R (2006) Effect of pH and lactic or acetic acid on ethanol productivity by Saccharomyces cerevisiae in corn mash. J Ind Microbiol Biotechnol 33:469–474
Guerreiro JF, Mira NP, Sá-Correia I (2012) Adaptive response to acetic acid in the highly resistant yeast species Zygosaccharomyces bailii revealed by quantitative proteomics. Proteomics 12:2303–2318
Guerreiro JF, Sampaio-Marques B, Soares R, Varela Coelho A, Leão C, Ludovico P, Sá-Correia I (2016a) Mitochondrial proteomics of the acetic acid -induced programmed cell death response in a highly tolerant Zygosaccharomyces bailii -derived hybrid strain. Microb Cell 3:65–78
Guerreiro JF, Muir A, Ramachandran S, Thorner J, Sá-Correia I (2016b) Sphingolipid biosynthesis upregulation by TOR complex 2-Ypk1 signaling during yeast adaptive response to acetic acid stress. Biochem J 473:4311–4325
Holyoak CD, Stratford M, McMullin Z, Cole MB, Crimmins K, Brown AJ, Coote PJ (1996) Activity of the plasma membrane H(+)-ATPase and optimal glycolytic flux are required for rapid adaptation and growth of Saccharomyces cerevisiae in the presence of the weak-acid preservative sorbic acid. Appl Environ Microbiol 62:3158–3164
Holyoak CD, Bracey D, Piper PW, Kuchler K, Coote PJ (1999) The Saccharomyces cerevisiae weak-acid-inducible ABC transporter Pdr12 transports fluorescein and preservative anions from the cytosol by an energy-dependent mechanism. J Bacteriol 181:4644–4652
James SA, Stratford M (2003) Spoilage yeasts with emphasis on the genus Zygosaccharomyces. In: Boekhout T, Robert V (eds) Yeasts in food: beneficial and detrimental aspects. Elsevier, Hamburg, pp 171–196
James SA, Stratford M (2011) Zygosaccharomyces. In: Kurtzman CP, Fell JW, Boekhout T (eds) The yeasts: a taxonomic study, 5th edn. Elsevier, London, pp 937–947
James S, Bond C, Stratford M, Roberts I (2005) Molecular evidence for the existence of natural hybrids in the genus. FEMS Yeast Res 5:747–755
Jönsson LJ, Alriksson B, Nilvebrant N-O (2013) Bioconversion of lignocellulose: inhibitors and detoxification. Biotechnol Biofuels 6:16
Kawahata M, Masaki K, Fujii T, Iefuji H (2006) Yeast genes involved in response to lactic acid and acetic acid: acidic conditions caused by the organic acids in Saccharomyces cerevisiae cultures induce expression of intracellular metal metabolism genes regulated by Aft1p. FEMS Yeast Res 6:924–936
Kuanyshev N, Ami D, Signori L, Porro D, Morrissey JP, Branduardi P (2016) Assessing physio-macromolecular effects of lactic acid on Zygosaccharomyces bailii cells during microaerobic fermentation. FEMS Yeast Res 16:fow058
Kumar S, Stecher G, Li M, Knyaz C, Tamura K (2018) MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 35:1547–1549
Kurtzman CP, Fell JW, Boekhout T (2011) The yeasts: a taxonomic study, 5th edn. Elsevier
Leandro MJ, Sychrova H, Prista C, Loureiro-Dias MC (2011) The osmotolerant fructophilic yeast Zygosaccharomyces rouxii employs two plasma-membrane fructose uptake systems belonging to a new family of yeast sugar transporters. Microbiology 157:601–608
Lindahl L, Genheden S, Eriksson LA, Olsson L, Bettiga M (2016) Sphingolipids contribute to acetic acid resistance in Zygosaccharomyces bailii. Biotechnol Bioeng 113:744–753
Lindberg L, Santos AX, Riezman H, Olsson L, Bettiga M (2013) Lipidomic profiling of Saccharomyces cerevisiae and Zygosaccharomyces bailii reveals critical changes in lipid composition in response to acetic acid stress. PLoS ONE 8:e73936
Liu C-L, Lievense JC (2005) Lactic acid producing yeast
Loureiro V, Malfeito-Ferreira M (2003) Spoilage yeasts in the wine industry. Int J Food Microbiol 86:23–50
Lussier M, Sdicu AM, Bussereau F, Jacquet M, Bussey H (1997) The Ktr1p, Ktr3p, and Kre2p/Mnt1p mannosyltransferases participate in the elaboration of yeast O- and N-linked carbohydrate chains. J Biol Chem 272:15527–15531
Macpherson N, Shabala L, Rooney H, Jarman MG, Davies JM (2005) Plasma membrane H+ and K+ transporters are involved in the weak-acid preservative response of disparate food spoilage yeasts. Microbiology 151:1995–2003
Martorell P, Stratford M, Steels H, Fernandez-Espinar MT, Querol A (2007) Physiological characterization of spoilage strains of Zygosaccharomyces bailii and Zygosaccharomyces rouxii isolated from high sugar environments. Int J Food Microbiol 114:234–242
Merín MG, Morata de Ambrosini VI (2015) Highly cold-active pectinases under wine-like conditions from non- Saccharomyces yeasts for enzymatic production during winemaking. Lett Appl Microbiol 60:467–474
Mira NP, Teixeira MC, Sá-Correia I (2010a) Adaptive response and tolerance to weak acids in Saccharomyces cerevisiae: a genome-wide view. OMICS 14:525–540
Mira NP, Palma M, Guerreiro JF, Sá-Correia I (2010b) Genome-wide identification of Saccharomyces cerevisiae genes required for tolerance to acetic acid. Microb Cell Fact 9:79
Mira NP, Becker JD, Sá-Correia I (2010c) Genomic expression program involving the Haa1p-regulon in Saccharomyces cerevisiae response to acetic acid. OMICS 14:587–601
Mira NP, Munsterkotter M, Dias-Valada F et al (2014) The genome sequence of the highly acetic acid-tolerant Zygosaccharomyces bailii-Derived interspecies hybrid strain ISA1307, isolated from a sparkling wine plant. DNA Res 21:299–313
Mollapour M, Piper P (2001a) Targeted gene deletion in Zygosaccharomyces bailii. Yeast 18:173–186
Mollapour M, Piper PW (2001b) The ZbYME2 gene from the food spoilage yeast Zygosaccharomyces bailii confers not only YME2 functions in Saccharomyces cerevisiae, but also the capacity for catabolism of sorbate and benzoate, two major weak organic acid preservatives. Mol Microbiol 42:919–930
Mollapour M, Shepherd A, Piper PW (2009) Presence of the Fps1p aquaglyceroporin channel is essential for Hog1p activation, but suppresses Slt2(Mpk1)p activation, with acetic acid stress of yeast. Microbiology 155:3304–3311
Morales P, Rojas V, Quirós M, Gonzalez R (2015) The impact of oxygen on the final alcohol content of wine fermented by a mixed starter culture. Appl Microbiol Biotechnol 99:3993–4003
Ortiz-Merino RA, Kuanyshev N, Braun-Galleani S, Byrne KP, Porro D, Branduardi P, Wolfe KH (2017) Evolutionary restoration of fertility in an interspecies hybrid yeast, by whole-genome duplication after a failed mating-type switch. PLoS Biol 15:e2002128
Ortiz-Merino RA, Kuanyshev N, Byrne KP, Varela JA, Morrissey JP, Porro D, Wolfe KH, Branduardi P (2018) Transcriptional response to lactic acid stress in the hybrid yeast Zygosaccharomyces parabailii. Appl Environ Microbiol 84:AEM.02294–17
Padilla B, Gil JV, Manzanares P (2016) Past and future of Non-Saccharomyces yeasts: from spoilage microorganisms to biotechnological tools for improving wine aroma complexity. Front Microbiol 7:411
Palma M, Goffeau A, Spencer-Martins I, Baret PV (2007) A phylogenetic analysis of the sugar porters in hemiascomycetous yeasts. J Mol Microbiol Biotechnol 12:241–248
Palma M, de Roque FC, Guerreiro JF, Mira NP, Queiroz L, Sá-Correia I (2015) Search for genes responsible for the remarkably high acetic acid tolerance of a Zygosaccharomyces bailii-derived interspecies hybrid strain. BMC Genomics 16:1070
Palma M, Dias PJ, Roque FC, Luzia L, Guerreiro JF, Sá-Correia I (2017a) The Zygosaccharomyces bailii transcription factor Haa1 is required for acetic acid and copper stress responses suggesting subfunctionalization of the ancestral bifunctional protein Haa1/Cup2. BMC Genomics 18:75
Palma M, Münsterkötter M, Peça J, Güldener U, Sá-Correia I (2017) Genome sequence of the highly weak-acid-tolerant Zygosaccharomyces bailii IST302, amenable to genetic manipulations and physiological studies. FEMS Yeast Res 17:fox025
Palma M, Guerreiro JF, Sá-Correia I (2018) Adaptive response and tolerance to acetic acid in Saccharomyces cerevisiae and Zygosaccharomyces bailii: a physiological genomics perspective. Front Microbiol 9:274
Pilkington BJ, Rose AH (1989) Accumulation of Sulphite by Saccharomyces cerevisiae and Zygosaccharomyces bailii as Affected by Phospholipid Fatty-acyl Unsaturation and Chain Length. Microbiology 135:2423–2428
Pina C, Gonçalves P, Prista C, Loureiro-Dias MC (2004) Ffz1, a new transporter specific for fructose from Zygosaccharomyces bailii. Microbiology 150:2429–2433
Piper P, Mahé Y, Thompson S, Pandjaitan R, Holyoak C, Egner R, Mühlbauer M, Coote P, Kuchler K (1998) The Pdr12 ABC transporter is required for the development of weak organic acid resistance in yeast. EMBO J 17:4257–4265
Piper P, Calderon CO, Hatzixanthis K, Mollapour M (2001) Weak acid adaptation: the stress response that confers yeasts with resistance to organic acid food preservatives. Microbiology 147:2635–2642
Querol A, Pérez-Torrado R, Alonso-del-Real J, Minebois R, Stribny J, Oliveira BM, Barrio E (2018) New trends in the uses of yeasts in oenology. Adv Food Nutr Res 177–210
Rasmussen JE, Schultz E, Snyder RE, Jones RS, Smith CR (1995) Acetic Acid as a Causative Agent in Producing Stuck Fermentations. Am J Enol Vitic 46:278–280
Rodrigues F, Zeeman AM, Alves C, Sousa MJ, Steensma HY, Corte-Real M, Leão C (2001) Construction of a genomic library of the food spoilage yeast Zygosaccharomyces bailii and isolation of the beta-isopropylmalate dehydrogenase gene (ZbLEU2). FEMS Yeast Res 1:67–71
Rodrigues F, Zeeman AM, Cardoso H, Sousa MJ, Steensma HY, Corte-Real M, Leão C (2004) Isolation of an acetyl-CoA synthetase gene (ZbACS2) from Zygosaccharomyces bailii. Yeast 21:325–331
Rodrigues F, Sousa MJ, Ludovico P, Santos H, Côrte-Real M, Leão C (2012) The fate of acetic acid during glucose co-metabolism by the spoilage yeast Zygosaccharomyces bailii. PLoS ONE 7:e52402
Rojas V, Gil JV, Piñaga F, Manzanares P (2001) Studies on acetate ester production by non-Saccharomyces wine yeasts. Int J Food Microbiol 70:283–289
Rosa CA, Lachance M-A (2005) Zygosaccharomyces machadoi sp. n., a yeast species isolated from a nest of the stingless bee Tetragonisca angustula. Lundiana 6 (supplement):27–29
Sá-Correia I, Guerreiro JF, Loureiro-Dias MC, Leão C, Côrte-Real M (2014) Zygosaccharomyces. In: Batt CA, Tortorello ML (eds) Encyclopedia of food microbiology, 2nd edn. Elsevier Ltd, Academic Press, Cambridge, Massachusetts, pp 849–855
Saksinchai S, Suzuki M, Chantawannakul P, Ohkuma M, Lumyong S (2012) A novel ascosporogenous yeast species, Zygosaccharomyces siamensis, and the sugar tolerant yeasts associated with raw honey collected in Thailand. Fungal Divers 52:123–139
Sauer M, Branduardi P, Valli M, Porro D (2004) Production of L-Ascorbic acid by metabolically engineered Saccharomyces cerevisiae and Zygosaccharomyces bailii. Appl Environ Microbiol 70:6086–6091
Schüller C, Mamnun YM, Mollapour M, Krapf G, Schuster M, Bauer BE, Piper PW, Kuchler K (2004) Global phenotypic analysis and transcriptional profiling defines the weak acid stress response regulon in Saccharomyces cerevisiae. Mol Biol Cell 15:706–720
Simões T, Teixeira MC, Fernandes AR, Sá-Correia I (2003) Adaptation of Saccharomyces cerevisiae to the herbicide 2,4-dichlorophenoxyacetic acid, mediated by Msn2p- and Msn4p-regulated genes: important role of SPI1. Appl Environ Microbiol 69:4019–4028
Simões T, Mira NP, Fernandes AR, Sá-Correia I (2006) The SPI1 gene, encoding a glycosylphosphatidylinositol-anchored cell wall protein, plays a prominent role in the development of yeast resistance to lipophilic weak-acid food preservatives. Appl Env Microbiol 72:7168–7175
Solieri L, Chand Dakal T, Giudici P (2013) Zygosaccharomyces sapae sp. nov., isolated from Italian traditional balsamic vinegar. Int J Syst Evol Microbiol 63:364–371
Sousa MJ, Miranda L, Corte-Real M, Leão C (1996) Transport of acetic acid in Zygosaccharomyces bailii: effects of ethanol and their implications on the resistance of the yeast to acidic environments. Appl Env Microbiol 62:3152–3157
Sousa MJ, Rodrigues F, Corte-Real M, Leão C (1998) Mechanisms underlying the transport and intracellular metabolism of acetic acid in the presence of glucose in the yeast Zygosaccharomyces bailii. Microbiology 144:665–670
Sousa-Dias S, Goncalves T, Leyva JS, Peinado JM, Loureiro-Dias MC (1996) Kinetics and regulation of fructose and glucose transport systems are responsible for fructophily in Zygosaccharomyces bailii. Microbiology 142:1733–1738
Steels H, James SA, Roberts IN, Stratford M (2000) Sorbic acid resistance: the inoculum effect. Yeast 16:1173–1183
Stratford M, Steels H, Nebe-von-Caron G, Novodvorska M, Hayer K, Archer DB (2013) Extreme resistance to weak-acid preservatives in the spoilage yeast Zygosaccharomyces bailii. Int J Food Microbiol 166:126–134
Suh S-O, Gujjari P, Beres C, Beck B, Zhou J (2013) Proposal of Zygosaccharomyces parabailii sp. nov. and Zygosaccharomyces pseudobailii sp. nov., novel species closely related to Zygosaccharomyces bailii. Int J Syst Evol Microbiol 63:1922–1929
Teixeira MC, Mira NP, Sá-Correia I (2011) A genome-wide perspective on the response and tolerance to food-relevant stresses in Saccharomyces cerevisiae. Curr Opin Biotechnol 22:150–156
Tenreiro S, Nunes PA, Viegas CA, Neves MS, Teixeira MC, Cabral MG, Sá-Correia I (2002) AQR1 gene (ORF YNL065w) encodes a plasma membrane transporter of the major facilitator superfamily that confers resistance to short-chain monocarboxylic acids and quinidine in Saccharomyces cerevisiae. Biochem Biophys Res Commun 292:741–748
Thomas DS, Davenport RR (1985) Zygosaccharomyces bailii— a profile of characteristics and spoilage activities. Food Microbiol 2:157–169
Torriani S, Lorenzini M, Salvetti E, Felis GE (2011) Zygosaccharomyces gambellarensis sp. nov., an ascosporogenous yeast isolated from an Italian “passito” style wine. Int J Syst Evol Microbiol 61:3084–3088
Vaidya AN, Pandey RA, Mudliar S, Kumar MS, Chakrabarti T, Devotta S (2005) Production and recovery of lactic acid for polylactide—an overview. Crit Rev Environ Sci Technol 35:429–467
Varela C, Dry PR, Kutyna DR, Francis IL, Henschke PA, Curtin CD, Chambers PJ (2015) Strategies for reducing alcohol concentration in wine. Aust J Grape Wine Res 21:670–679
Viegas CA, Sá-Correia I (1991) Activation of plasma membrane ATPase of Saccharomyces cerevisiae by octanoic acid. J Gen Microbiol 137:645–651
Wieczorke R, Krampe S, Weierstall T, Freidel K, Hollenberg CP, Boles E (1999) Concurrent knock-out of at least 20 transporter genes is required to block uptake of hexoses in Saccharomyces cerevisiae. FEBS Lett 464:123–128
Wu Q, Chen L, Xu Y (2013) Yeast community associated with the solid state fermentation of traditional Chinese Maotai-flavor liquor. Int J Food Microbiol 166:323–330
Xu Y, Zhi Y, Wu Q, Du R, Xu Y (2017) Zygosaccharomyces bailii is a potential producer of various flavor compounds in chinese maotai-flavor liquor fermentation. Front Microbiol 8:2609
Acknowledgements
Isabel Sá-Correia acknowledges all those who have, over the years, contributed to the fields of Yeast Physiological Genomics and Response and Adaptation to Weak Acids in her Laboratory. We are also grateful to K. Wolfe for the kind review of the genomics and taxonomy part of this chapter. Funding from “Fundação para a Ciência e a Tecnologia” (FCT) (current project contracts: PTDC/BBB-BEP/0385/2014, YEASTPEC ERA-IB-2/003/2015 and Ph.D. and postdoctoral fellowships), as well as funding received by the Institute for Bioengineering and Biosciences (iBB) from POR Lisboa 2020 (Project N. 007317) and FCT (UID/BIO/04565/2013) are also acknowledged.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Palma, M., Sá-Correia, I. (2019). Physiological Genomics of the Highly Weak-Acid-Tolerant Food Spoilage Yeasts of Zygosaccharomyces bailii sensu lato. In: Sá-Correia, I. (eds) Yeasts in Biotechnology and Human Health. Progress in Molecular and Subcellular Biology, vol 58. Springer, Cham. https://doi.org/10.1007/978-3-030-13035-0_4
Download citation
DOI: https://doi.org/10.1007/978-3-030-13035-0_4
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-13034-3
Online ISBN: 978-3-030-13035-0
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)