Use of Nonconventional Yeasts for Modulating Wine Acidity: Comparison
Please note this is a comparison between Version 3 by Peter Tang and Version 2 by Alice Vilela.

In line with consumer preferences and due to the effects of global climate change, new trends have emerged in wine fermentation and technology. Consumers are looking for wines with less ethanol and fruitier aromas but also with a good balance in terms of acidity and mouthfeel. Nonconventional yeasts contain a wide range of different genera of non-Saccharomyces. If they were considered spoilage yeasts in the past, they are used to enhance the aroma profile of wine or modulate wine composition.

  • wine acidity
  • Lactobacillus plantarum
  • Lachancea thermotolerans
  • Schizosaccharomyces pombe
  • Candida stellate
  • Torulaspora delbrueckii
  • Zygotorulaspora florentina
  • Pichia kudriavzevii
  • Stermerella bacillaris

1. Acids Present in Grapes and Wines and Their Perceived Taste

Organic acids, next to sugars, are the most abundant solids in grape juice. They are a significant constituent of juice and wine. Responsible for the sour/acid taste, they influence wine stability, color, and pH. The quality and quantity of organic acids in conjunction with the sugars significantly affect the mouthfeel quality of wines [1].
Many factors, such as grape variety, soil composition, and climatic conditions influence acid composition and concentration within the grape-must or wine. Accumulation of grape acids, namely tartaric acid, usually occurs at the beginning of grape berry development and is largely completed at the beginning of ripening [2].
Amerine [3] reported that in berries, tartaric, malic, citric, ascorbic, phosphoric, and tannic acids were present, and soon after, Stafford [4] confirmed the occurrence of all but ascorbic and tannic acids in grapevine leaves and included oxalic acid, in the form of idioblast crystals of calcium oxalate. Kliewer [5] identified 23 acids in berries, although most were found only in trace amounts. Nowadays, we know that, by far, the predominant acids are tartaric and malic, which together may account for over 90% of the total acidity in the berry, existing at crudely a 1:1 to 1:3 ratio of tartaric to malic acid [6], both contributing to the pH of the juice, must, and wine during vinification and subsequent aging (Figure 1) [7].
Figure 1.
Grape-berry flavor zones and distribution of tartaric and malic acids.
Tartaric and malic acids are diprotic, with two dissociable protons per molecule. It is the first proton dissociation, with pKa values of around 2.98 (tartaric) and 3.46 (malic), which are meaningful properties in a winemaking context. At a typical wine pH (3.4), tartaric acid will be three times as acidic as malic acid [7].
The bitartrate and bimalate monoanions have important sensory roles in wine taste. Malic acid presents a harsh metallic taste (Table 1), sometimes correlated with the taste of green apples. In contrast, the taste attributed to tartaric acid is frequently called ‘mineral’ or citrus-like. To compensate for malic acid ‘lost’ in the late stages of berry ripening, adding tartaric acid at crush, or after that, can be performed, providing, in this way, control of must/wine pH. However, unlike malic acid, tartaric acid is not a metabolic substrate for lactic acid bacteria or even yeasts.
Table 1.
Organic acids present in grapes and wines and primary acids’ sensory descriptors [8].
(1) Present in wine made with grapes infected with Botrytis cinerea.
Citric acid, which presents a pleasant citrus-like taste (Table 1), has many uses in wine production. Citric acid is a weak organic acid with antimicrobial activity against molds and bacteria. It can create a relationship with antioxidants by chelating metal ions, thus helping in browning prevention. Citric acid occurs in the metabolism of almost every organism because it is an essential intermediate in the tricarboxylic acid cycle (TCA cycle) [9], Figure 2.
Figure 2.
Schematic representation of the main steps, intermediated compounds, and enzymes of the TCA cycle [10].
During the winemaking process, it is advisable to monitor the concentration of organic acids to ensure the quality of the wine. A distinction is made between acids directly produced in grapes (tartaric, malic, and citric) and those originating during the fermentation—alcoholic and malolactic—succinic, lactic, and acetic acids, among others [11], Table 1.
Acetic acid, in quantities higher than 0.8–0.90 gL−1 [11], is immediately recognizable due to the vinegar smell and acrid taste, causing the wine to be considered spoiled. The maximum acceptable limit for volatile acidity in most wines is 1.2 gL−1 of acetic acid [12]. Acetic acid can appear on the grapes or the grape must due to the presence of yeasts like Hansenula spp. and Brettanomyces spp., filamentous fungi (Aspergillus niger, Aspergillus tenuis, Cladosporium herbarum, Penicillium spp., and Rhizopus arrhizus), and bacteria (LAB-like indigenous Lactobacilli, and acetic acid bacteria). During alcoholic fermentation, acetic acid usually is formed in small quantities (0.2–0.5 gL−1 acetic acid) as a byproduct of S. cerevisiae metabolism. If the amounts are higher, some contamination spoilage yeasts and bacteria can be present: Candida krusei, Candida stellate, Hansaniaspora uvarum/Kloeckera apiculate, Pichia anomala, Saccharomycodes ludwigii, Acetobacter pasteurianus, and Acetobacter liquefaciens; after malolactic fermentation, heterofermentative species of Oenococcus and Lactobacillus also have the potential to produce acetic acid through the metabolism of residual sugar [13].
Succinic acid, with a sour, salty, and bitter taste, is the primary acid yeast produces during fermentation. This acid is resistant to microbial metabolism under fermentative conditions. From 1991 to 2003, Coulter and coworkers [14] studied 93 red and 45 white Australian wines. They found that the concentration of succinic acid in red wines reached from “none” (detection limit of 0.1 gL−1) to 2.6 gL−1, with a mean value of 1.2 gL−1, while the concentration in white wines was between 0.1 gL−1 to 1.6 gL−1, with a mean value of 0.6 gL−1. Thus, succinic acid is vital to wine acidity [14].
Lactic acid, usually perceived as sour and spicy, is mainly produced by lactic acid bacteria during malolactic fermentation. However, small amounts can also be synthesized by yeast.
Today, the range of wines on the market is enormous. On the other hand, wine companies tend to develop a style. Last year, I managed to attribute “medals” to balanced flavor profile wines with bordering notes of vegetal-green, chemical, earthy, or sulfur characters, aromas of fruit and oak, hot/full mouthfeel (generally related to the alcohol content), low bitterness, and high sweetness [15]. Consumers and winemakers, giving more importance to flavors and sweetness, tend to “despise” acidity, even if it is one of the most essential components of the wine. So, the wine industry must be able to modulate wine acidity, considering the concept of “healthy” and “biological,” without adding enological products.

2. Wine Biological Acidity Modulation by Bacteria via Malolactic Fermentation

Physicochemical deacidifying wines is time-consuming, requires labor capital input, and may reduce wine quality [16]. Biological deacidification of wine with malolactic bacteria (MLB), most often strains of Oenococcus oeni, previously known as Leuconostoc oenos [17], is the traditional method for removing excess wine acidity. However, one crucial thing must be considered: of wine’s total acidity, biological deacidification only affects the malic acid portion; it does not reduce tartaric acid. While during alcoholic fermentation, wine yeast strains convert the grape sugars into ethanol and other flavors/mouthfeel compounds, after sugar depletion and the decline of the yeast population, LAB proliferates by utilizing the remaining sugars and performs malolactic fermentation (MLF). Despite its name, “malolactic fermentation,” this biological process is not a fermentation, but an enzymatic reaction in which malic acid (l (−) malic acid) is decarboxylated to lactic acid (l (+) lactic acid) and CO2, Figure 3, [18,19][18][19]. This process also reduces the potential carbon source for spoilage microorganisms and leads to wine microbial stabilization [20].
Figure 3.
Schematic representation of malolactic enzyme action. Malolactic bacteria convert sharp green-apple-like malic acid into softer, much less tart lactic acid, releasing CO
2
.
During MLF, the metabolism of O. oeni can improve the wine’s sensory characteristics by producing a myriad of secondary metabolites [21]. However, the success of MLF is influenced by oenological parameters, such as temperature, pH, alcohol content, SO2 concentration [22], and yeast inhibitory metabolites, such as medium chain fatty acids [23] or peptic fractions [24]. Several working groups are focused on alternative LAB, such as Lactobacillus plantarum, to perform MLF in wine [25,26][25][26]. Lactobacillus plantarum can survive under winemaking stress conditions. During the fermentation process, they are also able to produce a vast number of secondary metabolites important for the wine’s aroma and flavor, including β-glucosidases, esterases, phenolic acid decarboxylases, and citrate lyases [27,28,29] once they contain genes encoding essential enzymes that are active under winemaking conditions [30,31]. They can even improve red wine’s color and solve problems associated with wine filtration due to tannase activities [29][27]. More specific studies have found that depending on the stress conditions in the wine, the gene coding for the malolactic enzyme works differently for O. oeni [32][28] and L. plantarum [33][29]. Miller et al. [33][29] found that the expression of the mle (malolactic enzyme) L. plantarum gene presented an increased expression in the middle of MLF and was inducible by the presence of malic acid and low pH wine values, decreasing, nevertheless, in the fact of ethanol. Later, Iorizzo and coworkers [34][30] reported that some strains of L. plantarum could grow at pH values ranging from 3.2 to 3.5 and in the presence of 13% (v/v) ethanol. Several strains of L. plantarum were also found to tolerate the presence of sulfite in the concentrations used in winemaking [35][31]. Moreover, L. plantarum strains produce high lactic acid concentrations, which may contribute to “biological acidification” in low-acidity wines, thus improving wine mouthfeel [36][32].

3. Wines Biological Acidity Modulation by Nonconventional Yeasts

The malolactic fermentation process is not free from collateral effects (production of off-flavors, wine quality loss, and human health issues due to the production of biogenic amines). Benito et al. [37][33] developed a new red winemaking methodology by combining two non-Saccharomyces yeast strains as an alternative to the traditional MLF. According to the authors, malic acid is consumed by Schizosaccharomyces pombe, while Lachancea thermotolerans produces lactic acid to increase the acidity of wines made from low acidity musts. The main fermentative properties of interesting non-Saccharomyces yeasts reported as advantageous for fermented beverages and that can modulate wine acidity are described in Table 2.
Table 2.
Percentage of ethanol formed during fermentation, sugars fermented, main volatile compounds formed, and effect on wine acidity of seven non-
Saccharomyces
yeasts.
(i) The musts were obtained from botrytized Semillon grapes with initial sugar concentrations of 360 gL−1 [43][39]. (ii) Variable according to strain. (iii) Some Zygosaccharomyces are fructophilic. Z. rouxii and Z. bailii possess genes (FFZ) that encode specific fructose facilitators and proteins [49][45]. (iv) In white grape juice, not added with SO2, with 231 gL−1 sugar content [48][44]. (v) Z. bailii is known to consume acetic acid [50][46]. (vi) In microvinifications with chemically defined grape juice with similar nitrogen and acidic fraction composition to Patagonian Pinot noir juice (gL−1: glucose 100 gL−1, fructose 100 gL−1, potassium tartrate five gL−1, l-malic acid 3 gL−1, citric acid 0.2 gL−1, quickly assimilable nitrogen 0.208 gL−1 and pH 3.5) [51][47]. (vii) Pichia kudriavzevii presents the ability to produce ethanol from xylose. Xylose is a sugar found in wood, which can be used as an alternative for ethanol production, particularly useful in the biofuel industry [52][48]. (viii) A decrease of up to 0.7% (v/v) of ethanol when S. cerevisiae was inoculated with a delay of 48 h concerning the inoculation of Starmerella bacillaris [53][49]. (xix) S. bacillaris shows fructophilic, cryotollerant, and osmophylic characters of interest for the winemakers [55][51]. (x) Sauvignon Blanc wines fermented by mixed cultures (S. bacillaris and S. cerevisiae) contained significantly higher levels of thiols [57][53]. Schizosaccharomyces pombe, Lachancea thermotolerans and Torulaspora delbrueckii are presently produced at the industrial level by biotechnological companies [38][34]. Torulaspora delbrueckii is commercialized in the form of a pure culture, selected for its properties to increase aromatic complexity, mouthfeel, low production of volatile acidity, and high resistance to initial osmotic shock, and it is highly recommended for the fermentation of late harvest wines in sequential culture with S. cerevisiae.

References

  1. Liu, H.F.; Wu, B.H.; Fan, P.G.; Xu, H.Y.; Li, S.H. Inheritance of sugars and acids in berries of grape (Vitis vinifera L.). Euphytica 2007, 153, 99–107.
  2. Cosme, F.; Gonçalves, B.; Inês, A.; Jordão, A.M.; Vilela, A. Grape and wine metabolites: Biotechnological approaches to improve wine quality. In Grape and Wine Biotechnology; Morata, A., Loira, I., Eds.; InTechOpen: London, UK, 2016; pp. 187–214.
  3. Amerine, M.A. The Maturation of Wine Grapes. Wines Vines 1956, 37, 53–55.
  4. Stafford, H. Distribution of Tartaric Acid in the Leaves of Certain Angiosperms. Am. J. Bot. 1959, 46, 347–352.
  5. Kliewer, W. Sugars and Organic Acids of Vitis vinifera. Plant Physiol. 1966, 41, 923–931.
  6. Lamikanra, O.; Inyang, I.; Leong, S. Distribution and effect of grape maturity on organic acid content of red Muscadine grapes. J. Agric. Food Chem. 1995, 43, 3026–3028.
  7. Ford, C.M. The Biochemistry of Organic Acids in the Grape. In The Biochemistry of the Grape Berry; e-Book, Gerós, H., Chaves, M., Delrot, S., Eds.; Bentham Science Publishers: Sharjah, UAE, 2012; pp. 67–88. ISBN 978-1-60805-360-5.
  8. Boulton, R.B.; Singleton, V.L.; Bisson, L.F.; Kunkee, R.E. Principles and Practices of Winemaking; Chapman and Hall: New York, NY, USA, 1996; pp. 102–181.
  9. Sharma, R.K. Citric Acid. In Natural Food Antimicrobial Systems; Naidu, A.S., Ed.; CRC Press LLC: New York, NY, USA, 2000.
  10. Citric Acid Cycle. Available online: https://commons.wikimedia.org/wiki/File:Citric_acid_cycle_with_aconitate_2.svg#/media/File:Citric_acid_cycle_with_aconitate_2.svg (accessed on 30 January 2019).
  11. Ribéreau-Gayon, P.; Glories, Y.; Maujean, A.; Dubourdieu, D. Alcohols, and other volatile compounds. The chemistry of wine stabilization and treatments. In Handbook of Enology, 2nd ed.; John Wiley & Sons Ltd.: Chichester, UK, 2006; Volume 2, pp. 51–64.
  12. Office Internationale de la Vigne et du Vin. International Code of Oenological Practices; OIV: Paris, France, 2010.
  13. Vilela-Moura, A.; Schuller, D.; Mendes-Faia, A.; Silva, R.F.; Chaves, S.R.; Sousa, M.J.; Côrte-Real, M. The impact of acetate metabolism on yeast fermentative performance and wine quality: Reduction of volatile acidity of grape musts and wines—Minireview. Appl. Microbiol. Biotechnol. 2011, 89, 271–280.
  14. Coulter, A.D.; Godden, P.W.; Pretorius, I.S. Succinic acid-how is it formed, what is its effect on titratable acidity, and what factors influence its concentration in wine? Wine Ind. J. 2004, 19, 16–24.
  15. Hopfer, H.; Heymann, H. Judging wine quality: Do we need experts, consumers or trained panelists? Food Qual. Prefer. 2014, 32, 221–233.
  16. Pretorius, I.S. Tailoring wine yeast for the new millennium: Novel approaches to the ancient art of winemaking. Yeast 2000, 16, 675–729.
  17. Dicks, L.M.T.; Dellaglio, F.; Collins, M.D. Proposal to reclassify Leuconostoc oenos as Oenococcus oeni gen. nov., comb. nov. Int. J. Syst. Bacteriol. 1995, 45, 395–397.
  18. Henick-Kling, T. Malolactic fermentation. In Wine Microbiology and Biotechnology; Fleet, G.H., Ed.; Harwood Academic Publishers: Reading, UK, 1993; pp. 289–327.
  19. Volschenk, H.; Van Vuuren, H.J.J.; Viljoen-Bloom, M. Malic acid in wine: Origin, function and metabolism during vinification. S. Afr. J. Enol. Vitic. 2006, 27, 123–136.
  20. Lasik-Kurdyś, M.; Majcher, M.; Nowak, J. Effects of Different Techniques of Malolactic Fermentation Induction on Diacetyl Metabolism and Biosynthesis of Selected Aromatic Esters in Cool-Climate Grape Wines. Molecules 2018, 23, 2549.
  21. Bartowsky, E.; Borneman, A. Genomic variations of Oenococcus oeni strains and the potential to impact on malolactic fermentation and aroma compounds in wine. Appl. Microbiol. Biotechnol. 2011, 92, 441–447.
  22. Lerm, E.; Engelbrecht, L.; du Toit, M. Malolactic fermentation: The ABC’s of MLF. S. Afr. J. Enol. Vitic. 2010, 31, 186–212.
  23. Alexandre, H.; Costello, P.J.; Remize, F.; Guzzo, J.; Guilloux-Benatier, M. Saccharomyces cerevisiae-Oenococcus oeni interactions in wine: Current knowledge and perspectives. Int. J. Food Microbiol. 2004, 93, 141–154.
  24. Nehme, N.; Mathieu, F.; Taillandier, P. Impact of the co-culture of Saccharomyces cerevisiae-Oenococcus oeni on malolactic fermentation and partial characterization of a yeast-derived inhibitory peptidic fraction. Food Microbiol. 2010, 27, 150–157.
  25. Berbegal, C.; Peña, N.; Russo, P.; Grieco, F.; Pardo, I.; Ferrer, S.; Spano, G.; Capozzi, V. Technological properties of Lactobacillus plantarum strains isolated from grape must fermentation. Food Microbiol. 2016, 57, 187–194.
  26. Lucio, O.; Pardo, I.; Krieger-Weber, S.; Heras, J.M.; Ferrer, S. Selection of Lactobacillus strains to induce biological acidification in low acidity wines. LWT Food Sci. Technol. 2016, 73, 334–341.
  27. Brizuela, N.; Tymczyszyn, E.E.; Semorile, L.C.; La Hens, D.V.; Delfederico, L.; Hollmann, A.; Bravo-Ferrada, B. Lactobacillus plantarum as a malolactic starter culture in winemaking: A new (old) player? Electron. J. Biotechnol. 2019, 38, 10–18.
  28. Olguín, N.; Bordons, A.; Reguant, C. Multigenic expression analysis as an approach to understanding the behavior of Oenococcus oeni in wine-like conditions. Int. J. Food Microbiol. 2010, 144, 88–95.
  29. Miller, B.J.; Franz, C.M.; Cho, G.S.; du Toit, M. Expression of the malolactic enzyme gene (mle) from Lactobacillus plantarum under winemaking conditions. Curr. Microbiol. 2011, 62, 1682–1688.
  30. Iorizzo, M.; Testa, B.; Lombardi, S.J.; García-Ruiz, A.; Muñoz-González, C.; Bartolomé, B.; Moreno-Arribas, M.V. Selection and technological potential of Lactobacillus plantarum bacteria suitable for wine malolactic fermentation and grape aroma release. LWT Food Sci. Technol. 2016, 73, 557–566.
  31. Bravo-Ferrada, B.M.; Hollmann, A.; Delfederico, L.; La Hens, D.V.; Caballero, A.; Semorile, L. Patagonian red wines: Selection of Lactobacillus plantarum isolates as potential starter cultures for malolactic fermentation. World J. Microbiol. Biotechnol. 2013, 29, 1537–1549.
  32. Berbegal, C.; Spano, G.; Tristezza, M.; Grieco, F.; Capozzi, V. Microbial Resources and Innovation in the Wine Production Sector. S. Afr. J. Enol. Vitic. 2017, 38, 156–166.
  33. Benito, A.; Calderón, F.; Palomero, F.; Benito, S. Combined use of selected Schizosaccharomyces pombe and Lachancea thermotolerans yeast strains as an alternative to the traditional malolactic fermentation in red wine production. Molecules 2015, 20, 9510–9523.
  34. Morata, A.; Suárez-Lepe, J.A. New biotechnologies for wine fermentation and ageing. In Advances in Food Biotechnology, 1st ed.; Ravishankar Rai, V., Ed.; John Wiley & Sons, Ltd.: West Sussex, UK, 2016; pp. 287–301.
  35. Vilela, A. Targeting Demalication and Deacetification Methods: The Role of Carboxylic Acids Transporters. Biochem. Physiol. 2017, 6, 224.
  36. Vilela, A. Lachancea thermotolerans, the Non-Saccharomyces Yeast that Reduces the Volatile Acidity of Wines. Fermentation 2018, 4, 56.
  37. Suárez-Lepe, J.A.; Morata, A. New trends in yeast selection for winemaking. Trends Food Sci. Technol. 2012, 23, 39–50.
  38. Ferraro, L.; Fatichenti, F.; Ciani, M. Pilot scale vinification process using immobilized Candida stellata cells and Saccharomyces cerevisiae. Process. Biochem. 2000, 35, 1125–1129.
  39. Bely, M.; Stoeckle, P.; Masneuf Pomarède, I.; Dubourdieu, D. Impact of mixed Torulaspora delbrueckii Saccharomyces cerevisiae culture on high sugar fermentation. Int. J. Food Microbiol. 2008, 122, 312–320.
  40. Velázquez, R.; Zamora, E.; Álvarez, M.L.; Hernández, L.M.; Ramírez, M. Effects of new Torulaspora delbrueckii killer yeasts on the must fermentation kinetics and aroma compounds of white table wine. Front. Microbiol. 2015, 6, 1222.
  41. Pacheco, A.; Santos, J.; Chaves, S.; Almeida, J.; Leão, C.; Sousa, M.J. The Emerging Role of the Yeast Torulaspora delbrueckii in Bread and Wine Production: Using Genetic Manipulation to Study Molecular Basis of Physiological Responses. In Structure and Function of Food Engineering; Eissa, A.A., Ed.; IntechOpen: London, UK, 2012; Chapter 13; pp. 339–370.
  42. Lencioni, L.; Romani, C.; Gobbi, M.; Comitini, F.; Ciani, M.; Domizio, P. Controlled mixed fermentation at winery scale using Zygotorulaspora florentina and Saccharomyces cerevisiae. Int. J. Food Microbiol. 2016, 234, 36–44.
  43. Lencioni, L.; Taccari, M.; Ciani, M.; Domizio, P. Zygotorulaspora florentina and Starmerella bacillaris in multistarter fermentation with Saccharomyces cerevisiae to reduce volatile acidity of high sugar musts. Aust. J. Grape Wine Res. 2018, 24, 368–372.
  44. Domizio, P.; Romani, C.; Lencioni, L.; Comitini, F.; Gobbi, M.; Mannazzu, I.; Ciani, M. 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. 2011, 147, 170–180.
  45. Pina, C.; Gonçalves, P.; Prista, C.; Loureiro-Dias, M.C. Ffz1, a New Transporter Specific for Fructose from Zygosaccharomyces bailii. Microbiology 2004, 150, 2429–2433.
  46. Vilela-Moura, A.; Schuller, D.; Mendes-Faia, A.; Côrte-Real, M. Reduction of volatile acidity of wines by selected yeast strains. Appl. Microbiol. Biotechnol. 2008, 80, 881–890.
  47. Mónaco, S.; Barda, N.; Rubio, N.; Caballero, A. Selection and characterization of a Patagonian Pichia kudriavzevii for wine deacidification. J. Appl. Microbiol. 2014, 117, 451–464.
  48. Hello, My Name is Pichia kudriavzevii; Eureka Brewing. Available online: https://eurekabrewing.wordpress.com/2014/02/16/hello-my-name-is-pichia-kudriavzevii (accessed on 16 February 2019).
  49. Englezos, V.; Rantsiou, K.; Cravero, F.; Torchio, F.; Ortiz-Julien, A.; Gerbi, V.; Rolle, L.; Cocolin, L. Starmerella bacillaris and Saccharomyces cerevisiae mixed fermentations to reduce ethanol content in wine. Appl. Microbiol. Biotechnol. 2016, 100, 5515–5526.
  50. Masneuf-Pomarede, I.; Juquin, E.; Miot-Sertier, C.; Renault, P.; Laizet, Y.; Salin, F.; Alexandre, H.; Capozzi, V.; Cocolin, L.; Colonna-Ceccaldi, B.; et al. The yeast Starmerella bacillaris (synonym Candida zemplinina) shows high genetic diversity in winemaking environments. FEMS Yeast Res. 2015, 5, fov045.
  51. Englezos, V.; Giacosa, S.; Rantsiou, K.; Rolle, L.; Cocolin, L. Starmerella bacillaris in winemaking: Opportunities and risks. Curr. Opin. Food Sci. 2017, 17, 30–35.
  52. Sadoudi, M.; Tourdot-Maréchal, R.; Rousseaux, S.; Steyer, D.; Gallardo-Chacón, J.-J.; Ballester, J.; Vichi, S.; Guérin-Schneider, R.; Caixach, J.; Alexandre, H. Yeast–yeast interactions revealed by aromatic profile analysis of Sauvignon Blanc wine fermented by single or co-culture of non-Saccharomyces and Saccharomyces yeasts. Food Microbiol. 2012, 2, 243–253.
  53. Englezos, V.; Rantsiou, K.; Cravero, F.; Torchio, F.; Pollon, M.; Fracassetti, D.; Ortiz-Julien, S.; Gerbi, V.; Rolle, L.; Cocolin, L. Volatile profile of white wines fermented with sequential inoculation of Starmerella bacillaris and Saccharomyces cerevisiae. Food Chem. 2018, 257, 350–360.
More
Video Production Service