ISSN 2074-9414 (Print),
ISSN 2313-1748 (Online)

Resistance to Sulfur Dioxide as a Criterion for Selecting Saccharomyces cerevisiae for Organic Winemaking

Abstract
Sulfur dioxide is a popular conserving agent and antioxidant in winemaking. Unfortunately, it is bad for human health. Some yeast strains can reduce the dose of sulfur dioxide. Such yeasts should have good fermentation activity and dominate when inoculated into grape must. In addition, it should not synthesize sulfur dioxide and SO2-binding substances. The synthesis of sulfur dioxide and carbonyl compounds by yeast is related to the mechanisms of sulfur dioxide detoxification. The research objective was to study the relationship between the resistance of yeast to sulfur dioxide and its ability to synthesize sulfur dioxide and acetaldehyde during growth.
The study featured 17 yeast strains of the genus Saccharomyces. The yeasts were cultivated on grape must in a CGQ device until the stationary growth phase. The concentration of free and bound forms of sulfur dioxide was determined by titration, while that of aldehydes was determined by bisulfite method. The sulfite resistance of strains was measured by the growth response of yeast cells to sulfur dioxide using CGQ technology.
Yeast strains differed in the degree of sulfur dioxide resistance. The samples were divided according to the increase in the lag phase time: by ≥ 8 h (sensitive), by 2–6 h, without changes (resistant). At Wilks L = 0.228 and α = 0.05, the sensitive cultures in a SO2-free medium had the highest value of minimal generation time in the exponential growth phase (5.3 ± 2.1 h). The resistant samples demonstrated the highest synthesis of acetaldehyde (54.7 ± 11.1 mg/L) and sulfur dioxide (21.0 ± 10.3 mg/L). The second group cultures had the lowest content of SO2-bound forms in the medium (10.9 ± 4.2 mg/L) and were in an interposition in terms of other indicators.
The time it takes a yeast strain to adapt to sulfur dioxide can be used as a parameter for the primary culture selection in eco-winemaking. According to the physiological and biochemical profile, the resistant strains can be recommended for the production of SO2-low wines, while the samples from the second test group proved optimal for organic wines. Further research will expand the range of yeast strains and their indicators.
Keywords
Yeasts, CGQ technology, lag phase, generation, synthesis, acetaldehyde, sulfur dioxide, eco-winemaking
Contribution
E.V. Ostroukhova supervised the project. I.V. Peskova analyzed and processed experimental data. T.N. Tanashchuk performed the microbiological research and processed the results. N.Yu. Lutkova and M.A. Vyugina were responsible for the experiments.
CONFLICTS OF INTEREST
The authors declare that there is no conflict of interest regarding the publication of this article.
ACKNOWLEDGEMENTS
The authors express their gratitude to the staff of the Laboratory of Microbiology of the All-Russian National Research Institute of Viticulture and Winemaking “Magarach” of the RAS for providing yeast cultures from their Collection of Winemaking Microorganisms, as well as to all colleagues involved in the publication preparation.
FUNDING
The research was performed on the premises of the All-Russian National Research Institute of Viticulture and Winemaking “Magarach” of the RAS (“Magarach”), public assignment No. 0833-2019-022.
REFERENCES
  1. Guerrero RF, Cantos-Villar E. Demonstrating the efficiency of sulphur dioxide replacements in wine: A parameter review. Trends in Food Science and Technology. 2015;42(1):27–43. https://doi.org/10.1016/j.tifs.2014.11.004
  2. Romano P, Ciani M, Fleet GH. Yeasts in the production of wine. New York: Springer; 2019. 515 p. https://doi.org/10.1007/978-1-4939-9782-4
  3. Costanigro M, Appleby C, Menke SD. The wine headache: Consumer perceptions of sulfites and willingness to pay for non-sulfited wines. Food Quality and Preference. 2014;31:81–89. https://doi.org/10.1016/j.foodqual.2013.08.002
  4. Zara G, Nardi T. Yeast metabolism and its exploitation in emerging winemaking trends: From sulfite tolerance to sulfite reduction. Fermentation. 2021;7(2). https://doi.org/10.3390/fermentation7020057
  5. Walker ME, Zhang J, Sumby KM, Lee A, Houlès A, Li S, et al. Sulfate transport mutants affect hydrogen sulfide and sulfite production during alcoholic fermentation. Yeast. 2021;38(6):367–381. https://doi.org/10.1002/yea.3553
  6. Divol B, du Toit M, Duckitt E. Surviving in the presence of sulphur dioxide: Strategies developed by wine yeasts. Applied Microbiology and Biotechnology. 2012;95:601–613. https://doi.org/10.1007/s00253-012-4186-x
  7. Garcıa-Rıos E, Nuevalos M, Barrio E, Puig S, Guil- lamon JM. A new chromosomal rearrangement improves the adaptation of wine yeasts to sulfite. Environmental Microbiology. 2019;21(5):1771–1781. https://doi.org/10.1111/1462-2920.14586
  8. Valero E, Tronchoni J, Morales P, Gonzalez R. Autophagy is required for sulfur dioxide tolerance in Saccharomyces cerevisiae. Microbial Biotechnology. 2019;13(2):599–604. https://doi.org/10.1111/1751-7915.13495
  9. Zimmer A, Durand C, Loira N, Durrens P, Sherman DJ, Marullo P. QTL dissection of lag phase in wine fermentation reveals a new translocation responsible for Saccharomyces cerevisiae adaptation to sulfite. PLoS ONE. 2014;9(1). https://doi.org/10.1371/journal.pone.0086298
  10. Casalone E, Colella CM, Daly S, Gallori E, Moriani L, Polsinelli M. Mechanism of resistance to sulphite in Saccharomyces cerevisiae. Current Genetics. 1992;22(6):435–440. https://doi.org/10.1007/BF00326407
  11. Magarach Common Use Center: Collection of Winemaking Microorganisms [Internet]. [cited 2022 Jun 10]. Available from: http://magarach-institut.ru/kollekcija-mikroorganizmov-vinodelija-magarach
  12. Kishkovskaya SA, Tanashchouk TN, Ivanova EV, Skorikova TK. Collection of microorganisms of winemaking of institute “Magarach” and role in microbiological supply industry. Viticulture and Winemaking. 2016;46:46–51. (In Russ.).
  13. Ivanova E. Study of acid-reducing ability of collection strains of wine yeast fungi-saccharomycetes. Norwegian Journal of Development of the International Science. 2021;(54–1):3–5. (In Russ.). https://doi.org/10.24412/3453-9875-2021-54-1-3-5
  14. Morgan SC, Haggerty JJ, Johnston B, Jiranek V, Durall DM. Response to sulfur dioxide addition by two commercial Saccharomyces cerevisiae strains. Fermentation. 2019;5(3). https://doi.org/10.3390/fermentation5030069
  15. Bruder S, Reifenrath M, Thomik T, Boles E, Herzod K. Parallelized online biomass monitoring in shake flasks enables efficient strain and carbon source dependent growth characterization of Saccharomyces cerevisiae. Microbial Cell Factories. 2016;15. https://doi.org/10.1186/s12934-016-0526-3
  16. Kuzmina SS, Kozubaeva LA, Egorova EYu, Kulushtayeva BM, Smolnikova FKh. Effect of berry extracts on Saccharomyces cerevisiae yeast. Food Processing: Techniques and Technology. 2021;51(4):819–831. (In Russ.). https://doi.org/10.21603/2074-9414-2021-4-819-831
  17. Makarov AS, Lutkov IP. Yeast race effect on the quality of base and young sparkling wines. Foods and Raw Materials. 2021;9(2):290–301. https://doi.org/10.21603/2308-4057-2021-2-290-301
  18. García-Ríos E, Guillamón JM. Sulfur dioxide resistance in Saccharomyces cerevisiae: beyond SSU1. Microbial Cell. 2019;6(12):527–530. https://doi.org/10.15698/mic2019.12.699
  19. Noble J, Sanchez I, Blondin B. Identification of new Saccharomyces cerevisiae variants of the MET2 and SKP2 genes con-trolling the sulfur assimilation pathway and the production of undesirable sulfur compounds during alcoholic fermentation. Microbial Cell Factories. 2015;14. https://doi.org/10.1186/s12934-015-0245-1
  20. Li E, Mira de Orduña R. Acetaldehyde metabolism in industrial strains of Saccharomyces cerevisiae inhibited by SO2 and cooling during alcoholic fermentation. OENO One. 2020;54(2):351–358. https://doi.org/10.20870/oeno-one.2020.54.2.2391
  21. Kishkovskaia SA, Tanashchuk TN, Avdanina DA, Eldarov MA, Ivanova EV, Shalamitskiy My, et al. Screening for promising yeast strains for sherry wine production using genetic and enological markers. Agricultural Biology. 2021;56(3):537–548. (In Russ.). https://doi.org/10.15389/agrobiology.2021.3.537eng
  22. Li E, Mira de Orduña R. Acetaldehyde kinetics of enological yeast during alcoholic fermentation in grape must. Journal of Industrial Microbiology and Biotechnology. 2017;44(2):229–236. https://doi.org/10.1007/s10295-016-1879-7
  23. Peskova IV, Ostroukhova EV, Zaitseva OV, Lutkova NYu, Vyugina MA. The role of technological factors in the formation of SO2-binding complex of base wines. Magarach. Viticulture and Vinemaking. 2021;23(1):83–90. https://doi.org/10.35547/IM.2021.96.76.014
How to quote?
Peskova IV, Tanashchuk TN, Ostroukhova EV, Lutkova NYu, Vyugina MA. Resistance to Sulfur Dioxide as a Criterion for Selecting Saccharomyces cerevisiae for Organic Winemaking. Food Processing: Techniques and Technology. 2023;53(1):60–68. (In Russ.). https://doi.org/10.21603/2074-9414-2023-1-2415
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