Introduction

Over the last few years, climate change and rising temperatures have had an undeniably significant effect on the grape and wine industry. Harvest dates have considerably advanced in the last decades. Data from Johannisberg (Rheingau, Germany) have shown that, on average, harvest now takes place two to three weeks earlier than the harvest from the late 18th and the early 20th centuries (Stock et al., 2005); this is negatively affecting wine quality.

Because of rising temperatures, berries are maturing much more quickly, with higher sugar levels and lower organic acid concentrations. The trend of higher pH values leads to an increasing risk of microbial infection and generally unstable wines. pH directly impacts the efficiency of sulphur dioxide (SO₂), which is mainly found in wine in two forms: free SO₂ and bound SO₂. Free SO₂ exists in three forms: molecular SO₂, bisulphite (HSO₃^-) and sulphite (SO₃^2-); the ratio of these three forms depends on the wine pH. Bisulphite is the main form of free SO₂ (94 to 99 %) found in wine. Bisulphite binds with acetaldehyde, which is a by-product of the oxidation of ethanol and is desirable in sherry wines, but considered a default in table wines. Sulphites, on the other hand, are present in very small quantities (0.01 to 0.12 %) and help prevent direct oxidation by removing free oxygen and reactive oxygen forms. Sulphites also deactivate the polyphenoloxidase enzyme, which is responsible for enzymatic browning. Molecular SO₂ comprises 0.5 to 6 % of total free SO₂ and has the effect of an anti-septic. The typical levels of molecular SO₂ needed to achieve microbial stability are between 0.6 and 0.8 mg/L (Ribéreau-Gayon et al., 2012). Higher pH leads to the lower antibacterial activity of SO₂, meaning that higher amounts are needed to successfully protect wines from early spoilage and organoleptic alterations (Lafon-Lafourcade and Peynaud, 1970). Today, to attain the same microbial stability levels in wine (pH 4, 15 % alcohol per volume stored at 15 °C), free SO₂ levels would need to be between 95 and 126 mg/L. These values imply that total SO₂ in wine can exceed legal limits set by the International Organization of Vine and Wine (OIV Resolution OENO 09/1998).

These characteristics (i.e., high pH and SO₂₎, make it very challenging to control bacterial growth. High pH (> 3.5) and low molecular SO₂ encourage the formation of undesirable volatile compounds, such as mousey off-flavours, via lactic acid bacteria (Costello et al., 1993; Grbin et al., 1996). Mousey off flavours are associated with the smell of poorly-maintained rodent cages. However, some of the descriptors can vary; for example, popcorn and wet cloth. Bacteria, such as Lactobacillus sp. and Pediococcus sp., are known to grow in these conditions and are responsible for the production of undesirable volatile compounds; they are thus considered to induce spoilage in wine.

An optimal pH level is not only necessary for wine stability and microbiological equilibrium, but is also directly linked to wine colour and sensory properties. Climate change has been proved to affect anthocyanins, which has an impact on wine colour. Higher temperatures in vineyards (30 °C and higher) lead to lower levels of anthocyanins (Buttrose et al., 1971; Spayd et al., 2002; Tarara et al., 2008). Wine pH is known to play an important role in the colour of wine, because it affects the equilibrium between different forms of anthocyanins (Brouillard and Delaporte, 1977). It can also condition certain polymerisation reactions or the condensation of red wine pigments (Gil et al., 2012).

Furthermore, wine pH greatly impacts wine sensory perception. Total acidity and pH are often associated with the freshness of wine. Wine acidity, and more importantly wine pH, play an important role in the preservation of wine aroma and flavour. Wine pH can also play a major role in the sensation of sourness and astringency (Sowalsky and Noble, 1998).

Dealing with Wine acidity is thus a very important challenge, especially in the face of climate change. Different methods have been applied (Table 1), the main one being the acidification of must and wine, which consists of increasing total acidity and thus decreasing pH (OIV, 2017). All acidification practices are performed so that the initial acidity is not increased by more than 54 meq/L, equivalent to 4 g/L of tartaric acid (OIV, 2017). In Europe, the maximum acidity permitted for must is 1.5 g/L and 2.5 g/L for wine in tartaric acid equivalents (Regulation EU 1308, 2013).

This review thus focuses on the chemical, physical and microbiological acidification of must and wine.

Chemical acidification

Chemical acidification is a process used to adjust acidity levels in wine and is the most popular method for pH reduction in winemaking. The most commonly used acid in this process is tartaric acid, which is naturally found in grapes and plays a significant role in the taste and structure of the wine. However, in addition to tartaric acid, we will be discussing other possible and important acidifying agents, such as malic, citric, lactic and fumaric acid, which are used by winemakers to ensure the highest quality of their product.

Figure 1. Organic acids.

Save View full size Expand inline Collapse inline

1. Tartaric acid

Dihydroxybutanedioic acid (Figure 1), commonly known as tartaric acid (TA) is a diprotic acid that has two carboxylic groups whose pKas (at 25 °C) are 2.98 and 4.34 (Figure 2) (Lide et al., 2005). It is commonly used as an acidulant for when small acidity corrections are needed. TA has a sour taste and gives food a sharp, tart flavour. It is often added as an antioxidant (E334) to products like carbonated beverages, fruit jellies and effervescent tablets. Out of all the organic acids known to have an effect on microorganisms, TA is the least antimicrobial and inhibits less microbial growth (Gurtler and Mai, 2014).

Figure 2. Dissociation curve of tartaric acid.

Save View full size Expand inline Collapse inline

TA is the strongest acid and naturally present in grapes in amounts of between 5 and 10 g/L. The isomer found in grapes is the L-(+)-TA form and is synthesised from glucose (Saito and Kasai, 1978). TA was the first acid to be permitted by the OIV for acidification purposes. TA is mainly used in wine post-fermentation, but can also be used in must when the pH is higher than 3.5. When added to wine or must, tartaric acid dissociates, forming hydronium ions, which increase total acidity and bitartrate. At a pH of 3.5, 23.4 % of TA is present in its undisassociated form (H₂T), 67.5 % in its bitartrate form (HT^-) and 9.1 % in its totally disassociated form (T^2-). The bitartrate (HT^-) often reacts with potassium to form potassium bitartrate, also known as potassium hydrogen tartrate (KHT). KHT has a very low solubility in water and can crystallise, a phenomenon often referred to as tartaric precipitation. TA precipitation is a well-known problem and can occur unpredictably. KHT crystals are harmless, but are considered unappealing by the consumer. To help prevent this phenomenon, winemakers remove the excess salt by cooling the wine at -4 °C over several days to induce KHT precipitation prior to bottling. A limitation of this method, known as cold stabilization (Maujean, 1994),is that it is not possible to have full control over the remaining KHT concentration. This problem has led to the development of other KHT removal techniques, like ion exchange resins (Mourgues, 1993) and electrodialysis (Escudier et al., 1993) described hereafter.

The instability of calcium tartrate (CaT) in wine is another issue linked to TA. Similar to potassium bitartrate (KHT), calcium can react with the bitartrate ion (HT-) to form calcium tartrate. The chances of precipitation occuring increase when calcium levels reach 60 mg/L in red wine and 80 mg/L in white wine (Ribéreau-Gayon et al., 2012). While less common than potassium bitartrate instability, calcium tartrate instability is more problematic, as it is not as easily prevented by traditional stabilisation methods, such as cold treatment stabilisation (Maujean et al., 1984). One approach to preventing the precipitation of CaT crystals is the use of electrodialysis in the same way it is used for KHT removal.

Thus, while tartaric acid plays a critical role in shaping the taste and quality of wine, its interaction with other compounds in wine, particularly calcium and potassium, presents challenges that require careful management in order to maintain the stability and aesthetic appeal of the final product. Moreover, when added in high amounts, TA may induce a bitter taste and increase the wine’s astringency, and it is responsible for the tart taste.

2. Malic acid

Malic acid (MA) (Figure 1), or 2-hydroxybutanedioic acid, is a diprotic acid, whose pKas at 25 °C are 3.40 and 5.11 (Figure 3) (Lide et al., 2005). At a pH of 3.5, 47 % of the total concentration of MA is present in its undisassociated form (H₂M), 51.7 % in the disassociated form (HM^-) and only 1.2 % in the totally disassociated form (M^2-) (Usseglio-Tomasset, 1985).

Figure 3. Dissociation curve of malic acid.

Save View full size Expand inline Collapse inline

MA is the most widespread fruit acid. It has a flavour reminiscent of apple and sourness and contributes to the sour taste in unripe apples. It is mainly used as an acidulant (E296) in apple-containing products, such as cider, because of its taste. MA has a direct impact on the organoleptic properties of wines; it increases the sourness and freshness of wines while reducing the pH (Amerine and Ough, 1970; Carvalho et al., 2001). Before veraison, MA concentration can be found in quantities as high as 25 g/L. By harvest, the malic acid concentration in berries decreases sharply to between 1 and 6.5 g/L (Ribéreau-Gayon et al., 2012; Ruffner et al., 1982). This reduction in MA concentration is due to the respiration process during which malic acid is metabolised. In warmer climates, the loss of malic acid through respiration is more pronounced. Malic acid concentration levels are directly linked to maturity and temperature (Buttrose et al., 1971; Kliewer, 1971).

During winemaking, L-malic acid undergoes malolactic fermentation (MLF) and is transformed to lactic acid by the action of lactic acid bacteria (LAB). MLF occurs often in red wines and seldomly in white wines. The removal of malic acid via MLF usually induces an average increase in pH of 0.1 to 0.3 (Margalit, 1997). When added prior to fermentation, a racemic mixture of malic acid is used, of which most of the L-malic acid will be removed by MLF and, because of its resistance to microbial attack, D-malic acid will remain, maintaining the wine at a low pH.

Adding malic acid to finished wine could be useful for red wines from warmer regions, where hot temperatures lead to lower concentrations of malic acid. This acid, however, makes a favourable substrate for the growth of LAB. Due tothis characteristic, the use of MA for acidification should not be contemplated for adjusting pH or total acidity; rather, this substance can be considered for enabling LAB to carry out their own metabolic pathways, boosting the aromatic and gustatory complexity of the final product. However, because MA addition can initiate a second MLF, it can lead to the wine becoming cloudy and slightly sparkling.

3. Lactic acid

Lactic acid (LA) (Figure 1), 2-hydroxypropanoic acid, is a monoprotic acid, whose pKa at 25 °C is 3.86 (Figure 4) (Lide et al., 2005), meaning that it is a weaker acid than TA and MA. In the food industry, LA is used as a preservative, a curing agent and a flavouring agent (E270).

Figure 4. Dissociation curve of lactic acid.

Save View full size Expand inline Collapse inline

LAB synthesises LA from malic acid via MLF. Because LA is less acidic than MA, MLF decreases the total acidity and, as mentioned earlier, induces an average increase in pH of 0.1 to 0.3 (Margalit, 1997). MLF can be avoided in order to maintain the higher acidity of wines from warm areas, for example. However, allowing wines to undergo MLF before bottling increases stability. LA helps increase the acidity of wine by prolonging the sensory perception of sourness (Carvalho et al., 2001).

There are three advantages to adding lactic acid to wine: it can be added just before bottling without risk of precipitation; it produces a rounder and smoother mouthfeel than malic acid; and it gives the wine a sweet taste.

Being the weakest acid permitted by the OIV for wine acidification purposes, LA must be added in higher quantities to achieve the same pH decrease as malic or tartaric acids.

4. Citric acid

The 2-hydroxypropane-1,2,3-tricarboxylic acid, also known as citric acid (CA) (Figure 1), is a triprotic acid, whose pKa at 25 °C are 3.13, 4.76 and 6.40 (Figure 5) (Lide et al., 2005). CA is a naturally occurring acid in many fruits and vegetables, especially citrus-like fruits. It is a weak acid often used as a natural preservative in many foods (E330), or to add a sour taste to drinks or food. CA is a very important metabolite in the Krebs cycle (Ribéreau-Gayon et al., 2012).

Figure 5. Dissociation curve of citric acid.

Save View full size Expand inline Collapse inline

In wine, CA is commonly found in quantities within the range of 0.1 to 0.7 g/L. Wine bacteria use CA for metabolism. It is first degraded into acetic acid and pyruvic acid (Shimazu et al., 1985), and the pyruvic acid is then metabolised forming lactic acid and a fraction of diacetyl, acetoin and 2,3-butanediol. An increase in CA concentration is correlated with an increase in diacetyl concentration. CA can help antioxidants by chelating metal ions and thus helping prevent browning (Jiang and Fu, 1998).

CA addition in must is only permitted by the OIV to prevent iron hazes; the remaining residue should not exceed 1 g/L (Zoecklein, 2012). When added to wine, CA enhances the taste of many white wines, while contributing to a citric character. The main disadvantage of this acid is its microbial instability, as it increases the growth of unwanted microorganisms in the wine. LAB can metabolise citric acid to form acetic acid and diacetyl (Capozzi et al., 2021; Sumby et al., 2019).

5. Fumaric acid

Fumaric acid (Figure 1), (2E)-but-2-enedioic acid, is a diprotic acid whose pKas at 25 °C are 3.02 and 4.38 (Figure 6) (Lide et al., 2005). Fumaric acid (FA) originally derived its name from the plant, Fumaria officinalis, from which this organic acid was isolated for the first time (Roa Engel et al., 2008). FA is an intermediary metabolite in the citric acid cycle, being converted into L-malic acid through the action of the fumarase enzyme (Akiba et al., 1984; Pines et al., 1996). Due to its low molecular weight, 116.073 g/mol, FA has a greater buffering capacity than other food grade acids at a pH of around 3.0.

Figure 6. Dissociation curve of fumaric acid.

Save View full size Expand inline Collapse inline

FA is the cheapest of the food-grade acids and is non-toxic; it has been used as an antibacterial agent and acidulant in the food and juice industry since 1946 (Das et al., 2016; Straathof and van Gulik, 2012). It is classified as a food additive other than sweeteners and colouring with the E number E297 under the European Union Commission Regulations N° 1129/2011. It has a fruit-like flavour.

Because of its dicarboxylic group, FA has a high acidifying power. It is naturally present in in small quantities in both the red and white berries of grapes (from 5.11 to 10.69 mg/L) (Eyduran et al., 2015; García Romero et al., 1993). In addition to pH reduction, FA can be used for its antibacterial properties, which has been demonstrated in different food and drink, such as non-heat processed vegetables, apple cider inoculated with E.Coli and vacuum-packaged ground beef (Comes and Beelman, 2002; Lu et al., 2011; Podolak et al., 1996). FA also has antifungal properties (Akao and Kuroda, 1991).

Due to its action of lowering pH, FA also limits bacterial development and growth (Gurtler and Mai, 2014). When added before MLF, it not only decreases pH but also inhibits LAB activities by affecting the biosynthesis of pyrimidines (Cofran and Meyer, 1970; Pilone et al., 1974; Silver and Leighton, 1982); this was observed when FA was added in amounts of between 0.4 and 1.5 g/L after alcoholic fermentation (Bauer and Dicks, 2004). More recently, FA has been shown to completely inhibit the growth of O. Oeni when in amounts of 0.3 to 0.6 g/L at a pH of 3.3 (Morata et al., 2019). A study of the addition of FA to different varieties has shown that it has a long-lasting effect on O. Oeni and could thus be a more permanent solution than classical SO₂ addition (Morata et al., 2023).

The FA threshold in white wine has been described by Ough (1963) as being 1 g/L, which is the lowest threshold compared to tartaric and citric acid. The sensory threshold of FA in red wine is around 1387 mg/L (Gancel et al., 2022). FA is perceived as being more sour than citric acid and malic acid (Buechsenstein and Ough, 1979). A recent study has shown that in concentrations of 0.6 g/L FA improves the perception of acidity and body in wine (Morata et al., 2019).

However, FA can be challenging to work with since it is very difficult to dissolve it in water, as it has a solubility of less than 10 g/L (Yang et al., 2011). FA solubility in wine is around 15 g/L at 25 °C, making it one of the least soluble organic acids in wine in comparison with tartaric, malic and citric acid (respectively 1049.3 g/L, 1047.0 g/L, 1079.7 g/L) (Gancel et al., 2022).

FA in concentrations of up to 3 g/L is already permitted for wine acidification purposes in countries like the USA, Canada and Chile (Smith and Hong-Shum, 2008). The OIV has adopted a new resolution for the authorisation of FA addition in wine (300 to 600 mg/L) in order to prevent MLF (OIV-OENO 581A-2021). It is yet to be permitted for acidification purposes in OIV member countries.

Table 2. Summary of organic acids and their potential for wine acidification use.

View popup Expand inline Collapse inline

	Mw g/mol	pKa at 25°C	Solubility in SB - CS wine at 25°C g/L	Concentration required for lowering pH by 0.1 in SB - CS wine* g/L	Thresholds in SB wine g/L	Thresholds in CS wine g/L
Tartaric acid	150.087	2.98 – 4.341	1049.3 – 922.32	0.34 – 0.312	1.62	1.12
Malic acid	134.087	3.40 – 5.111	1047.0 – 932.32	0.51 – 0.3912	1.32	0.82
Lactic acid	90.080	3.861	–	0.44 – 0.452	1.62	1.92
Citric acid	192.124	3.13 – 4.76 – 6.401	1079.7 –1056.72	0.47 – 0.532	2.32	1.32
Fumaric acid	116.073	3.02 – 4.381	14.9 – 9.32	0.22 – 0.202	1.92	1.32

SB = Sauvignon blanc, CS = Cabernet-Sauvignon
* Intitial wine pH: SB = 3.34, CS = 3.61

¹ Lide et al., 2005. ² Gancel et al., 2022

Physical acidification

As seen in the previous section, the addition of organic acids to wine to reduce its pH is now a common practice. However, it can be challenging to control this pH reduction, as well as to overcome the adverse effects and difficulties of working with organic acids, such as tartaric acid precipitation, the risk of a second MLF if malic acid is used, or the difficulty in dissolving fumaric acid. Many physical acidification methods have been developed that can be used as alternatives to some traditional oenological practices.

1. Ion exchange resins

The use of cation exchange resins is one available option for concurrently lowering pH, decrease cation concentration and restrict the formation of tartrate salts (Esau and Amerine, 1966; Mira et al., 2006).

Acidification using ion exchange resins is a process consisting of treating wine through a polymerised insoluble granular medium in order to exchange positive or negative ions. This medium is composed of a polymeric matrix of styrene and divinylbenzene, which is attached to different ionised functional groups (carboxylic acid or sulfonic acid for acidic resins and various types of amino groups for basic exchangers). Three different techniques involving ion exchange resins exist: i) the use of a cation exchange resin from which the protons (H⁺) replace the potassium ions in the wine, ii) the use of an anion exchange resin from which the tartrate ion is exchanged for hydroxyl (OH^-), and iii) the use of a mixture of both resins, with both potassium and tartrate ions being exchanged for H⁺ and OH^-, such that the potassium bitartrate is swapped for water. As per the 442/2012 and 443/2012 resolution of the OIV and the 144/2013 EU regulation, only the first method using the cation exchange resin is authorised as an alternative method for acidifying wines.

In the cation exhange method, a powerful acid solution, such as sulfuric or hydrochloric acid, is used to activate the resin beads during standard wine treatment. The beads are then rinsed with soft water and loaded with the wine. As the wine passes through the column, the hydrogen ions (H⁺) on the resins are exchanged for the wine cations, such as potassium K⁺. This exchange leads to a reduction in cation concentration and wine pH, and also reduces the risk of tartaric acid precipitation via the formation of tartrate salts (KTH) (Benı́tez et al., 2002; Ibeas et al., 2015; Lasanta et al., 2013; Mira et al., 2006; Palacios et al., 2001; Walker et al., 2004).

Figure 7. Diagram of cation exchanger resin conditions for wine acidification.

Save View full size Expand inline Collapse inline

The use of cation exchange resins in red winemaking is a useful tool for decreasing pH, as well as for improving tartaric stability. However, its use can be problematic due to the strong affinity of the styrene-divinylbenzene matrix for anthocyanins and polyphenols (Ibeas et al., 2015; Lasanta et al., 2013; Mira et al., 2006). The cation exchange treatment of red wine has been found to result in a slight decrease in anthocyanins and tannins, as well as a decrease in colour hue and an increase in colour intensity, likely due to the decrease in wine pH. However, the treatment was found to have little impact on volatile compounds, and the wines processed using cation exchangers were perceived to have a higher overall quality in the sensory evaluation (Lasanta et al., 2013).

Cation exchange resins have been studied for their potential to acidify white wines. In the study of Just-Borràs et al. (2022), the base wine used for sparkling white wine was treated with cation exchange resin, resulting in a significant decrease in pH and an increase in titratable acidity. Cisilotto et al. (2019) focused on Chardonnay must, which was treated with cation exchange resin and fermented to produce wines with a lower pH of 3.15 (control) to 2.97. The results showed an improvement in oxidative stability of the treated wines and significant changes in the concentration of several volatile compounds, which could affect the wines' sensory properties.

After the treatment, cation exchange resins can be regenerated using concentrated solutions of sulfuric acid and sodium chloride (Ribéreau-Gayon et al., 2012). However, this process requires a significant amount of water, and the resulting effluents must be treated and recycled as special waste, meaning the technology is quite costly to the environment and unsustainable.

2. Electrodialysis

Electrodialysis is an electrochemical process that moves dissolved ions from one solution to another with the help of an electrical potential. The difference between electrodialysis and a classical exchange process is that electrodialysis uses ion-selective semi-permeable membranes to segregate ions based on their charge. There are three types of ion-exchanged membranes used in electrodialysis: anion-exchange membranes, cation-exchange membranes and bipolar membranes. Ion-exchange membranes are thin and dense, and they have insoluble walls composed of polymeric material permeable to ions, whereas cationic and anionic membranes are only permeable to cations and anions respectively (El Rayess and Mietton-Peuchot, 2016). Cationic membranes are composed of styrene-divinylbenzene copolymers with sulfonic functional groups (SO₃^2-), while anionic membranes are made of styrene-divinylbenzene copolymers that are functionalised with quaternary ammonium (NR₄⁺) (International Organization of Vine and Wine, 2017). Bipolar membranes comprise a cation exchange membrane laminated with an anion exchange membrane, through which cations or anions cannot permeate.

Electrodialysis was first used in oenology for wine tartaric stabilisation (Escudier et al., 1993). The principle of electrodialysis for tartrate stabilisation is based on the migration of anions (such as TH^- and T^-) towards the positive electrodes (anode), while cations (K⁺) are attracted to the negative electrode (cathode) under the influence of an electric field.

Electrodialysis with bipolar membranes (EBM) can precisely adjust the pH of must or wine with a precision of 0.05 units, irrespective of the initial pH, without altering the tartaric and malic acid contents and matrix wine compounds (such as alcohol, aromas and polyphenols). EBM can be used for both acidification and deacidification; when used for acidification, the bipolar membranes are coupled with cationic membranes (Figure 7). The process of wine acidification via EDM involves the circulation of wine within a membrane pack, allowing it to flow between cationic membranes and the cationic side of bipolar membranes. Water flows in an adjacent compartment. Upon application of an electric field, the potassium ions move towards the cathode, cross the cationic membranes and are extracted from the wine, becoming concentrated in the water, which is transformed into brine. Within the wine compartment, potassium is replaced by protons (H⁺) formed at the bipolar membrane junction. Similarly, bitartrate ions tend to move towards the anode, but are prevented from crossing the cationic layer of the bipolar membrane and hence remain in the wine. As a result, the wine preserves bitartrate (and the conjugate bases of other organic acids) and is enriched with H⁺ ions, leading to a decrease in pH and an increase in total acidity.

Figure 8. Diagram of membrane assembly and operating conditions for wine acidification by electromembrane techniques.

Save View full size Expand inline Collapse inline

EBM treatments have been reported to have positive effects on wine composition, such as improving the balance of the acidic fraction, particularly in relation to tartaric acid addition. Wines treated with EBM are perceived to be fresher and lighter on the palate compared to untreated products. In addition, treated wines do not exhibit the harsh mouthfeel that is commonly associated with the addition of tartaric acid (Moutounet et al., 2005). Other classical parameters, such as must sugars, alcohol content and polyphenolic compounds, are not impacted by EBM treatment (Granès et al., 2008). However, this technique is associated with significant water consumption (Halama et al., 2015).

Microbiological acidification

Microbiological approaches can be used to deal with low acidity in wine. The use of S. cerevisiae strains is one such option, as they can produce small quantities of malic, lactic or succinic acid. Another approach is the use of L. thermotolerans, which can increase lactic acid levels by several grams per liter and lower the pH by several decimal units. S. bacillaris, on the other hand, can generate α-ketoglutaric acid and pyruvic acid, while C. stellata is known for producing significant amounts of succinic acid.

Conclusion

The most commonly used acidification technique, chemical acidification is well known and multiple options are available. Tartaric acid is widely used by winemakers to reduce pH and increase total acidity. However, the use of tartaric acid can lead to the precipitation of tartrate salt and, if added in too high concentrations, its use can result in imbalanced and harsh wine. When added to wine, malic acid increases the sourness and freshness of young wines; however, as malic acid is a good substrate for LAB, it should not be considered for pH adjustment. Lactic acid, on the other hand, produces rounder and smoother wines. Being the weakest acid permitted by the OIV for wine acidification, it needs to be added in higher quantities to obtain the same pH decrease as malic or tartaric acids. While citric acid enhances the taste of white wines, it is not microbiologically stable and its use entails the high risk of producing unwanted compounds such as acetic acid. Fumaric acid is a promising acidifying agent, as it has the greatest acidifying power of all the aforementioned organic acids. Its use is already permitted by the OIV for preventing MLF.

While the addition of organic acids is a common practice for reducing wine pH, physical acidification methods such as ion exchange resins and electrodialysis with bipolar membranes have been developed as alternatives to traditional oenological practices. Cation exchange resins are used to treat wine by exchanging ions to lower the pH, decrease cation concentration and restrict the formation of tartrate salts. However, the use of cation exchange resins can lead to some problems, such as reduced colour and tannins in red wines. Electrodialysis with a bipolar membrane, on the other hand, uses ion-selective semi-permeable membranes to segregate ions based on their charge. Electrodialysis has been shown to be efficient in reducing the pH of wine without impacting classical oenological parameters and in improving its organoleptic properties, making it fresher and lighter on the palate. However, both of these techniques have environmental impacts resulting from the regeneration of resins and high water consumption.

Finally, there are several microbiological approaches to dealing with low acidity in wine. Saccharomyces strains, such as S. Cerevisiae, can produce low quantities of organic acids, including malic, lactic and succinic acid, while Lachancea thermotolerans is a non-Saccharomyces yeast that can increase lactic acid levels and lower pH by several decimal units. Other non-Saccharomyces strains, such as Candida zemplinina, can also produce organic acids that can impact the total acidity of wine. The choice of yeast strains for wine fermentation depends on various factors, including grape variety, climate, and desired wine style. Nonetheless, these microbiological approaches can provide winemakers with useful tools for controlling wine acidity and improving wine quality.

References

• Akao, M., & Kuroda, K. (1991). Antifungal Activity of Fumaric Acid in Mice Infected with Candida albicans. Chemical & Pharmaceutical Bulletin, 39(11), 3077–3078. https://doi.org/10.1248/cpb.39.3077
• Akiba, T., Hiraga, K., & Tuboi, S. (1984). Intracellular Distribution of Fumarase in Various Animals 1. Journal of Biochemistry, 96, 189–195. https://doi.org/10.1093/oxfordjournals.jbchem.a134812
• Amerine, M. A., & Ough, C. S. (1970). Effect of Pre- and Post-Fermentation Addition of Acids on the Composition and Quality of the Wines Produced. American Journal of Enology and Viticulture, 21(3), 131–135.
• Bauer, R., & Dicks, L. M. T. (2004). Control of Malolactic Fermentation in Wine. A Review. South African Journal of Enology and Viticulture, 25(2), Article 2. https://doi.org/10.21548/25-2-2141
• Benito, S. (2018a). The impact of Torulaspora delbrueckii yeast in winemaking. Applied Microbiology and Biotechnology, 102(7), 3081–3094. https://doi.org/10.1007/s00253-018-8849-0
• Benito, S. (2018b). The impacts of Lachancea thermotolerans yeast strains on winemaking. Applied Microbiology and Biotechnology, 102(16), 6775–6790. https://doi.org/10.1007/s00253-018-9117-z
• Benito, S. (2019). The Management of Compounds that Influence Human Health in Modern Winemaking from an HACCP Point of View. Fermentation, 5(2), Article 2. https://doi.org/10.3390/fermentation5020033
• Benito, S. (2020). Combined Use of Lachancea thermotolerans and Schizosaccharomyces pombe in Winemaking: A Review. Microorganisms, 8(5), Article 5. https://doi.org/10.3390/microorganisms8050655
• Benı́tez, P., Castro, R., & Barroso, C. G. (2002). Removal of iron, copper and manganese from white wines through ion exchange techniques: Effects on their organoleptic characteristics and susceptibility to browning. Analytica Chimica Acta, 458(1), 197–202. https://doi.org/10.1016/S0003-2670(01)01499-4
• Brouillard, R., & Delaporte, B. (1977). Chemistry of anthocyanin pigments. 2. Kinetic and thermodynamic study of proton transfer, hydration, and tautomeric reactions of malvidin 3-glucoside. Journal of the American Chemical Society, 99(26), 8461–8468. https://doi.org/10.1021/ja00468a015
• Buechsenstein, J., & Ough, C. (1979). Comparison of citric, dl-malic, and fumaric acids as wine acidulants. American Journal of Enology and Viticulture, 30(2), 93–97.
• Buttrose, M. S., Hale, C. A., & Kliewer, W. M. (1971). Effect of temperature on the composition of « Cabernet-Sauvignon » berries. American Journal of Enology and Viticulture, 22(2), 71 75. https://doi.org/10.5344/ajev.1971.22.2.71
• Capozzi, V., Tufariello, M., De Simone, N., Fragasso, M., & Grieco, F. (2021). Biodiversity of Oenological Lactic Acid Bacteria: Species- and Strain-Dependent Plus/Minus Effects on Wine Quality and Safety. Fermentation, 7(1), Article 1. https://doi.org/10.3390/fermentation7010024
• Carvalho, E. C. P., Costa, S., Franco, C., & Curvelo-Garcia, A. S. (2001). Acidification of musts and wines. Application of L-tartaric, L-lactic and DL-malic acids. Bulletin de l’OIV (France).
• Castrillo, D., Rabuñal, E., Neira, N., & Blanco, P. (2019). Oenological potential of non-Saccharomyces yeasts to mitigate effects of climate change in winemaking: Impact on aroma and sensory profiles of Treixadura wines. FEMS Yeast Research, 19(7), foz065. https://doi.org/10.1093/femsyr/foz065
• Chidi, B. S., Rossouw, D., Buica, A. S., & Bauer, F. F. (2015). Determining the Impact of Industrial Wine Yeast Strains on Organic Acid Production Under White and Red Wine-like Fermentation Conditions. South African Journal of Enology and Viticulture, 36(3), Article 3. https://doi.org/10.21548/36-3-965
• Ciani, M., Morales, P., Comitini, F., Tronchoni, J., Canonico, L., Curiel, J. A., Oro, L., Rodrigues, A. J., & Gonzalez, R. (2016). Non-conventional Yeast Species for Lowering Ethanol Content of Wines. Frontiers in Microbiology, 7. https://doi.org/10.3389/fmicb.2016.00642
• Cisilotto, B., Rossato, S., Ficagna, E., Wetzstein, L., Gava, A., Gugel, G., Delamare, A. P., & Echeverrigaray, S. (2019). The effect of cation exchange resin treatment of grape must on the chemical and sensory characteristics of base wines for sparkling wine. Ciência e Técnica Vitivinícola, 34, 91–101. https://doi.org/10.1051/ctv/20193402091
• Cofran, D. R., & Meyer, B. J. (1970). The Effect of Fumaric Acid on Malo-Lactic Fermentation. American Journal of Enology and Viticulture, 21(4), 189–192.
• Comes, J. E., & Beelman, R. B. (2002). Addition of Fumaric Acid and Sodium Benzoate as an Alternative Method To Achieve a 5-log Reduction of Escherichia coli O157:H7 Populations in Apple Cider. Journal of Food Protection, 65(3), 476–483. https://doi.org/10.4315/0362-028X-65.3.476
• Comitini, F., Gobbi, M., Domizio, P., Romani, C., Lencioni, L., Mannazzu, I., & Ciani, M. (2011). Selected non-Saccharomyces wine yeasts in controlled multistarter fermentations with Saccharomyces cerevisiae. Food Microbiology, 28(5), 873–882. https://doi.org/10.1016/j.fm.2010.12.001
• Costello, P., Stockley, C. S., Lee, T., & Henschke, P. A. (1993). Current selection criteria of lactic acid bacteria for malolactic fermentation. 142–147.
• Das, R. K., Brar, S. K., & Verma, M. (2016). Fumaric Acid. In Platform Chemical Biorefinery (pp. 133–157). Elsevier. https://doi.org/10.1016/B978-0-12-802980-0.00008-0
• Dequin, S., Baptista, E., & Barre, P. (1999). Acidification of Grape Musts by Saccharomyces cerevisiae Wine Yeast Strains Genetically Engineered to Produce Lactic Acid. American Journal of Enology and Viticulture, 50(1), 45–50. https://doi.org/10.5344/ajev.1999.50.1.45
• El Rayess, Y., & Mietton-Peuchot, M. (2016). Membrane Technologies in Wine Industry: An Overview. Critical Reviews in Food Science and Nutrition, 56(12), 2005–2020. https://doi.org/10.1080/10408398.2013.809566
• Englezos, V., Rantsiou, K., Cravero, F., Torchio, F., Pollon, M., Fracassetti, D., Ortiz-Julien, A., Gerbi, V., Rolle, L., & Cocolin, L. (2018). Volatile profile of white wines fermented with sequential inoculation of Starmerella bacillaris and Saccharomyces cerevisiae. Food Chemistry, 257, 350–360. https://doi.org/10.1016/j.foodchem.2018.03.018
• Esau, P., & Amerine, M. A. (1966). Synthetic ion-exchange resins in wine research. American Journal of Enology and Viticulture, 17(4), 268–276.
• Escudier, J., Saint-Pierre, B., Batlle, J., & Moutounet, M. (1993). Procedé et dispositif automatique de stabilisation tartrique de vins. French Patent FR, 2709308-A1.
• Eyduran, S. P., Ercisli, S., Akin, M., Beyhan, O., Gecer, M. K., Eyduran, E., & Erturk, Y. E. (2015). Organic acids, sugars, vitamin C, antioxidant capacity and phenolic compounds in fruits of white (Morus alba L.) and black (Morus nigra L.) mulberry genotypes. Journal of Applied Botany and Food Quality, 88. https://doi.org/10.5073/JABFQ.2015.088.019
• Gancel, A.-L., Payan, C., Koltunova, T., Jourdes, M., Christmann, M., & Teissedre, P.-L. (2022). Solubility, acidifying power and sensory properties of fumaric acid in water, hydro-alcoholic solutions, musts and wines compared to tartaric, malic, lactic and citric acids. OENO One, 56(3), Article 3. https://doi.org/10.20870/oeno-one.2022.56.3.5455
• García Romero, E., Sánchez Muñoz, G., Martín Alvarez, P. J., & Cabezudo Ibáñez, M. D. (1993). Determination of organic acids in grape musts, wines and vinegars by high-performance liquid chromatography. Journal of Chromatography A, 655(1), 111–117. https://doi.org/10.1016/0021-9673(93)87018-H
• Gil, M., Kontoudakis, N., González, E., Esteruelas, M., Fort, F., Canals, J. M., & Zamora, F. (2012). Influence of Grape Maturity and Maceration Length on Color, Polyphenolic Composition, and Polysaccharide Content of Cabernet-Sauvignon and Tempranillo Wines. Journal of Agricultural and Food Chemistry, 60(32), 7988–8001. https://doi.org/10.1021/jf302064n
• Gobbi, M., Comitini, F., Domizio, P., Romani, C., Lencioni, L., Mannazzu, I., & Ciani, M. (2013). Lachancea thermotolerans and Saccharomyces cerevisiae in simultaneous and sequential co-fermentation: A strategy to enhance acidity and improve the overall quality of wine. Food Microbiology, 33(2), 271–281. https://doi.org/10.1016/j.fm.2012.10.004
• Goold, H. D., Kroukamp, H., Williams, T. C., Paulsen, I. T., Varela, C., & Pretorius, I. S. (2017). Yeast’s balancing act between ethanol and glycerol production in low-alcohol wines. Microbial Biotechnology, 10(2), 264–278. https://doi.org/10.1111/1751-7915.12488
• Granès, D., Bouissou, D., Lutin, F., Moutounet, M., & Rousseau, J. (2008). "L’élévation du pH des vins: Causes, risques œnologiques, impacts de la mise en œuvre de moyens d’acidification.
• Grbin, P., Costello, P., Herderich, M., Markides, A., Henschke, P., & Lee, T. (1996). Developments in the sensory, chemical and microbiological basis of mousy taint in wine. https://digital.library.adelaide.edu.au/dspace/handle/2440/40834
• Gurtler, J. B., & Mai, T. L. (2014). Preservatives | Traditional Preservatives – Organic Acids. In Encyclopedia of Food Microbiology (pp. 119–130). Elsevier. https://doi.org/10.1016/B978-0-12-384730-0.00260-3
• Halama, R., Kotala, T., & Vrána, J. (2015). Modification of the organoleptic properties of beverages. Desalination and Water Treatment, 56(12), 3181–3190. https://doi.org/10.1080/19443994.2014.981929
• Hranilovic, A., Bely, M., Masneuf-Pomarede, I., Jiranek, V., & Albertin, W. (2017). The evolution of Lachancea thermotolerans is driven by geographical determination, anthropisation and flux between different ecosystems. PLOS ONE, 12(9), e0184652. https://doi.org/10.1371/journal.pone.0184652
• Ibeas, V., Correia, A. C., & Jordão, A. M. (2015). Wine tartrate stabilization by different levels of cation exchange resin treatments: Impact on chemical composition, phenolic profile and organoleptic properties of red wines. Food Research International, 69, 364–372. https://doi.org/10.1016/j.foodres.2015.01.003
• Jiang, Y., & Fu, J. (1998). Inhibition of polyphenol oxidase and the browning control of litchi fruit by glutathione and citric acid. Food Chemistry, 62(1), 49–52. https://doi.org/10.1016/S0308-8146(97)00144-1
• Just-Borràs, A., Pons-Mercadé, P., Gombau, J., Giménez, P., Vilomara, G., Conde, M., Cantos, A., Canals, J. M., & Zamora, F. (2022). Effects of using cationic exchange for reducing pH on the composition and quality of sparkling wine (Cava). OENO One, 56(2), 179–192. https://doi.org/10.20870/oeno-one.2022.56.2.5399
• Kliewer, W. M. (1971). Effect of Day Temperature and Light Intensity on Concentration of Malic and Tartaric Acids in Vitis vinifera L. Grapes1. Journal of the American Society for Horticultural Science, 96(3), 372–377. https://doi.org/10.21273/JASHS.96.3.372
• Lafon-Lafourcade, S., & Peynaud, E. (1970). Sur l’action antibactérienne de l’anhydride sulfureux sous forme libre et sous forme combinée. OENO One, 8(2), 187–203. https://doi.org/10.20870/oeno-one.1974.8.2.2101
• Lasanta, C., Caro, I., & Pérez, L. (2013). The influence of cation exchange treatment on the final characteristics of red wines. Food Chemistry, 138(2), 1072–1078. https://doi.org/10.1016/j.foodchem.2012.10.095
• Lide, D. R., Baysinger, G., Chemistry, S., Berger, L. I., Goldberg, R. N., & Kehiaian, H. V. (2005). CRC Handbook of Chemistry and Physics. 2660.
• Lu, H. J., Breidt, F., JR., Péres-Díaz, I. M., & Osborne, J. A. (2011). Antimicrobial Effects of Weak Acids on the Survival of Escherichia coli O157:H7 under Anaerobic Conditions†‡. Journal of Food Protection, 74(6), 893–898. https://doi.org/10.4315/0362-028X.JFP-10-404
• Magyar, I., Nyitrai-Sárdy, D., Leskó, A., Pomázi, A., & Kállay, M. (2014). Anaerobic organic acid metabolism of Candida zemplinina in comparison with Saccharomyces wine yeasts. International Journal of Food Microbiology, 178, 1–6. https://doi.org/10.1016/j.ijfoodmicro.2014.03.002
• Maicas, S. (2021). Advances in Wine Fermentation. Fermentation, 7(3), Article 3. https://doi.org/10.3390/fermentation7030187
• Margalit, Y. (1997). Must and wine composition. Wine Chemistry., 40–44.
• Maujean, A., Malherbe, V., & Dupont, A. (1984). Traitement par le froid artificiel des vins de Champagne. I. Contrôle des traitements par le froid artificiel des vins de Champagne, efficacité des traitements selon la nature du collage des vins. OENO One, 18(1), 49–65. https://doi.org/10.20870/oeno-one.1984.18.1.1762
• Maujean, A. (1994). Traitement par le froid artificiel des vins en relation avec leur stabilisation vis-à-vis des troubles cristallins tartriques. Les Acquisitions Récents Dans Les Traitements Physiques Du Vin, 81–101.
• Mira, H., Leite, P., Ricardo-da-Silva, J. M., & Curvelo-Garcia, A. S. (2006). Use of ion exchange resins for tartrate wine stabilization. OENO One, 40(4), Article 4. https://doi.org/10.20870/oeno-one.2006.40.4.865
• Morata, A., Adell, E., López, C., Palomero, F., Suárez, E., Pedrero, S., Bañuelos, M. A., & González, C. (2023). Use of Fumaric Acid to Inhibit Malolactic Fermentation in Bottled Rioja Wines: Effect in pH and Volatile Acidity Control. Beverages, 9(1), Article 1. https://doi.org/10.3390/beverages9010016
• Morata, A., Bañuelos, M. A., López, C., Song, C., Vejarano, R., Loira, I., Palomero, F., & Suarez Lepe, J. A. (2019). Use of fumaric acid to control pH and inhibit malolactic fermentation in wines. Food Additives & Contaminants: Part A, 37(2), 228–238. https://doi.org/10.1080/19440049.2019.1684574
• Morata, A., Loira, I., Tesfaye, W., Bañuelos, M. A., González, C., & Suárez Lepe, J. A. (2018). Lachancea thermotolerans Applications in Wine Technology. Fermentation, 4(3), Article 3. https://doi.org/10.3390/fermentation4030053
• Mourgues, J. (1993). Utilisation des résines échangeuses d’ions.
• Moutounet, M., Saint-Pierre, B., & Batlle, J. (2005). Acidification des mouts et des vins par un Procédé Electromembranaire à Membranes Bipolaires. Meeting of Expert Group of OIV.
• Ough, C. S. (1963). Sensory Examination of Four Organic Acids Added to Wine. Journal of Food Science, 28(1), 101–106. https://doi.org/10.1111/j.1365-2621.1963.tb00166.x
• Palacios, V. M., Caro, I., & Pérez, L. (2001). Application of Ion Exchange Techniques to Industrial Process of Metal Ions Removal From Wine. Adsorption, 7(2), 131–138. https://doi.org/10.1023/A:1011600207978
• Pilone, G. J., Rankine, B. C., & Pilone, D. A. (1974). INHIBITING MALO-LACTIC FERMENTATION IN AUSTRALIAN DRY RED WINES BY ADDING FUMARIC ACID. 25(2), 9.
• Pines, O., Even-Ram, S., Elnathan, N., Battat, E., Aharonov, O., Gibson, D., & Goldberg, I. (1996). The cytosolic pathway of L-malic acid synthesis in Saccharomyces cerevisiae: The role of fumarase. Applied Microbiology and Biotechnology, 46, 393–399. https://doi.org/10.1007/s002530050835
• Podolak, R. K., Zayas, J. F., Kastner, C. L., & Fung, D. Y. C. (1996). Inhibition of Listeria monocytogenes and Escherichia coli O157:H7 on Beef by Application of Organic Acids†. Journal of Food Protection, 59(4), 370–373. https://doi.org/10.4315/0362-028X-59.4.370
• Porter, T. J., Divol, B., & Setati, M. E. (2019). Lachancea yeast species: Origin, biochemical characteristics and oenological significance. Food Research International, 119, 378–389. https://doi.org/10.1016/j.foodres.2019.02.003
• Rantsiou, K., Dolci, P., Giacosa, S., Torchio, F., Tofalo, R., Torriani, S., Suzzi, G., Rolle, L., & Cocolin, L. (2012). Candida zemplinina Can Reduce Acetic Acid Produced by Saccharomyces cerevisiae in Sweet Wine Fermentations. Applied and Environmental Microbiology, 78(6), 1987–1994. https://doi.org/10.1128/AEM.06768-11
• Redzepovic, S., Orlic, S., Majdak, A., Kozina, B., Volschenk, H., & Viljoen-Bloom, M. (2003). Differential malic acid degradation by selected strains of Saccharomyces during alcoholic fermentation. International Journal of Food Microbiology, 83(1), 49–61. https://doi.org/10.1016/S0168-1605(02)00320-3
• Ribéreau-Gayon, P., Glories, Y., Maujean, A., & Dubourdieu, D. (2012). Traité d’œnologie: Tome 2 - Chimie du vin. Stabilisation et traitements. https://hal.inrae.fr/hal-02809296
• Roa Engel, C. A., Straathof, A. J., Zijlmans, T. W., van Gulik, W. M., & van der Wielen, L. A. (2008). Fumaric acid production by fermentation. Applied Microbiology and Biotechnology, 78(3), 379–389. https://doi.org/10.1007/s00253-007-1341-x
• Romboli, Y., Mangani, S., Buscioni, G., Granchi, L., & Vincenzini, M. (2015). Effect of Saccharomyces cerevisiae and Candida zemplinina on quercetin, vitisin A and hydroxytyrosol contents in Sangiovese wines. World Journal of Microbiology and Biotechnology, 31(7), 1137–1145. https://doi.org/10.1007/s11274-015-1863-9
• Ruffner, H., Brem, S., & Malipiero, U. (1982). The physiology of acid metabolism in grape berry ripening. Fruit Set and Development, XXI IHC 139, 123–128.
• Saito, K., & Kasai, Z. (1978). Conversion of Labeled Substrates to Sugars, Cell Wall Polysaccharides, and Tartaric Acid in Grape Berries. Plant Physiology, 62(2), 215–219. https://doi.org/10.1104/pp.62.2.215
• Shimazu, Y., Uehara, M., & Watanabe, M. (1985). Transformation of citric acid to acetic acid, acetoin and diacetyl by wine making lactic acid bacteria. Agricultural and biological chemistry, 49(7), 2147 2157. https://doi.org/10.1080/00021369.1985.10867041
• Silver, J., & Leighton, T. (1982). Control of malolactic fermentation in wine. Proceedings of the University of California, Davis Grape Wine Symposium (Webb, AD, Ed.), 170–175.
• Smith, J., & Hong-Shum, L. (2008). Food Additives Data Book. John Wiley & Sons.
• Snyder, E. C., Jiranek, V., & Hranilovic, A. (2021). Impact of Lachancea thermotolerans strain and lactic acid concentration on Oenococcus oeni and malolactic fermentation in wine. OENO One, 55(2), Article 2. https://doi.org/10.20870/oeno-one.2021.55.2.4657
• Sowalsky, R. A., & Noble, A. C. (1998). Comparison of the Effects of Concentration, pH and Anion Species on Astringency and Sourness of Organic Acids. Chemical Senses, 23(3), 343–349. https://doi.org/10.1093/chemse/23.3.343
• Spayd, S. E., Tarara, J. M., Mee, D. L., & Ferguson, J. C. (2002). Separation of Sunlight and Temperature Effects on the Composition of Vitis vinifera cv. Merlot Berries. American Journal of Enology and Viticulture, 53(3), 171–182. https://doi.org/10.5344/ajev.2002.53.3.171
• Stock, M., Gerstengarbe, F. W., Kartschall, T., & Werner, P. C. (2005). Reliability of climate change impact assessments for viticulture. Acta Horticulturae, 689, 29–40. https://doi.org/10.17660/ActaHortic.2005.689.1
• Straathof, A. J. J., & van Gulik, W. M. (2012). Production of Fumaric Acid by Fermentation. In X. Wang, J. Chen, & P. Quinn (Eds.), Reprogramming Microbial Metabolic Pathways (pp. 225–240). Springer Netherlands. https://doi.org/10.1007/978-94-007-5055-5_11
• Su, J., Wang, T., Wang, Y., Li, Y.-Y., & Li, H. (2014). The use of lactic acid-producing, malic acid-producing, or malic acid-degrading yeast strains for acidity adjustment in the wine industry. Applied Microbiology and Biotechnology, 98(6), 2395–2413. https://doi.org/10.1007/s00253-014-5508-y
• Sumby, K. M., Bartle, L., Grbin, P. R., & Jiranek, V. (2019). Measures to improve wine malolactic fermentation. Applied Microbiology and Biotechnology, 103(5), 2033–2051. https://doi.org/10.1007/s00253-018-09608-8
• Tarara, J. M., Lee, J., Spayd, S. E., & Scagel, C. F. (2008). Berry Temperature and Solar Radiation Alter Acylation, Proportion, and Concentration of Anthocyanin in Merlot Grapes. American Journal of Enology and Viticulture, 59(3), 235–247. https://doi.org/10.5344/ajev.2008.59.3.235
• Usseglio-Tomasset, L. (1985). [Vinification technologies which allow a reduction in doses of SO2 [sulphur anhydrid (free, combined, molecular), acetic anhydrid, ketonic acids, sulphur hydrogen, oxidases]]. Bulletin de l’OIV (France).
• Vaquero, C., Loira, I., Bañuelos, M. A., Heras, J. M., Cuerda, R., & Morata, A. (2020). Industrial Performance of Several Lachancea thermotolerans Strains for pH Control in White Wines from Warm Areas. Microorganisms, 8(6), 830. https://doi.org/10.3390/microorganisms8060830
• Vicente, J., Navascués, E., Calderón, F., Santos, A., Marquina, D., & Benito, S. (2021). An Integrative View of the Role of Lachancea thermotolerans in Wine Technology. Foods, 10(11), Article 11. https://doi.org/10.3390/foods10112878
• Vilela, A. (2018). Lachancea thermotolerans, the Non-Saccharomyces Yeast that Reduces the Volatile Acidity of Wines. Fermentation, 4(3), Article 3. https://doi.org/10.3390/fermentation4030056
• Vion, C., Muro, M., Bernard, M., Richard, B., Valentine, F., Yeramian, N., Masneuf-Pomarède, I., Tempère, S., & Marullo, P. (2023). New malic acid producer strains of Saccharomyces cerevisiae for preserving wine acidity during alcoholic fermentation. Food Microbiology, 112, 104209. https://doi.org/10.1016/j.fm.2022.104209
• Volschenk, H., van Vuuren, H. J. J., & Viljoen-Bloom, M. (2017). Malic Acid in Wine: Origin, Function and Metabolism during Vinification. South African Journal of Enology & Viticulture, 27(2). https://doi.org/10.21548/27-2-1613
• Walker, T., Morris, J., Threlfall, R., & Main, G. (2004). Quality, sensory and cost comparison for ph reduction of syrah wine using ion exchange or tartaric acid. Journal of Food Quality, 27(6), 483–496. https://doi.org/10.1111/j.1745-4557.2004.00675.x
• Yéramian, N., Chaya, C., & Suárez Lepe, J. A. (2007). l-(−)-Malic Acid Production by Saccharomyces spp. During the Alcoholic Fermentation of Wine (1). Journal of Agricultural and Food Chemistry, 55(3), 912–919. https://doi.org/10.1021/jf061990w
• Zoecklein, B. W. (2012). Production Wine Analysis. Springer Science & Business Media.