NEW TOOLS TO HELP OVERCOME STUCK FERMENTATIONS IN WINE

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NEW TOOLS TO HELP OVERCOME STUCK FERMENTATIONS IN WINE Anne-Ortiz Julien1, Anthony Silvano1, Didier Théodore1, Françoise Raginel1, Ann Dumont2 1Lallemand SAS, 19, rue des Briquetiers, 3172 Blagnac, France 2 Lallemand, 162, rue Préfontaine, Montréal, Canada Stuck fermentation is where fermentation has ceased prematurely or the rate of fermentation is considered too low for practical purposes, leaving a higher residual sugar content than desired in the wines at the end of the fermentation (Figure 1) (Bisson 1999, Henschke and Jiranek 1993). Not only does it delay the completion of AF, but it can also lead to the formation of off-aromas. For winemakers, a residual sugar concentration of less than 2 g/l is considered dry or completed (Bisson 1999). 3 Brix 25 2 15 Normal Long Lag Becoming Sluggish Sluggish Throughout Stuck Fermentation 1 5-5 5 1 15 2 25 3 35 Time (Hours) Figure 1. Types of fermentation problems (adapted from UC Davis Wine Fermentation). What are the factors leading to stuck fermentation? Twenty years ago, it was thought that stuck fermentations were mainly due to 2 things: nitrogen deficiency and the glucose/fructose ratio of the must. Recently, researchers have learned more about the topic, and we now know that other factors come into play. Glucose/fructose ratio: Saccharomyces cerevisiae is a glucophilic yeast, preferring glucose over fructose. During fermentation, glucose is consumed at a higher rate than fructose, and the proportion of fructose increases as fermentation progresses. This can lead to imbalances in the wines and, under the stressful conditions found at the end of fermentation, make it more difficult for wine yeast to utilize this non-preferred sugar. The preference for glucose over fructose is yeast dependent, and the discrepancy between glucose and fructose consumption is not a fixed parameter, but rather is dependent on the yeast s genetic background and on external conditions (Berthels et al. 24). 1

Nitrogen deficiency: Nitrogen is the most important yeast nutrient and has a significant impact on wine fermentation. It influences both fermentation kinetics and wine profile (Agenbach 1977, Bezenger and Navarro 1987). Grape musts contain nitrogen under different forms: proteins, peptides, ammonium ions (NH4 +) and alpha amino acids. The yeast assimilable nitrogen (YAN) is composed of ammonium and -amino acids, except proline which is not assimilable by yeast. The minimum quantity of YAN in must is 15 to 2 mg/l, and lower levels are considered nitrogen deficient. When the must is deficient in nitrogen, it will limit yeast growth and fermentation speed (Bely et al. 199, Julien et al. 2). YAN content has the most influence on fermentation speed; it impacts yeast biomass at the beginning of fermentation, as well as sugar transport kinetics during fermentation (Figure 2). As soon as a must is nitrogen depleted at the end of the growth phase, there is a decrease in protein synthesis and sugar transport activity (Bely et al. 1994). If nitrogen deficiency is the only issue, and no other factors are lacking, the consequence is a slow or sluggish fermentation, but the yeast viability is maintained and AF can eventually be completed. dco2/dt(g.l-1.h-1) x(*1-1cell.-1) 2.5 2. 1.5 1..5 5 1 15 Time (h).6.5.4.3.2.1 Ndt(g.L -1.) Fermentation with NO nitrogen deciciency (high YAN) Fermentation rate (g/l of CO 2 released/hr (dco 2 /dt) Yeast population (X) Kinetic of nitrogen consumption (N) Fermentation with nitrogen deciciency (low YAN) Fermentation rate (g/l of CO 2 released/hr (dco 2 /dt) Yeast population (X) Kinetic of nitrogen consumption (N) Figure 2. Nitrogen depletion during the yeast growth phase. Sablayrolles J.M. Sitevi conference 215 Nutritional imbalances: Recently, a study by Bruno Blondin s research team (Duc et al. 216) demonstrated that nitrogen starvation in alcoholic fermentation does not trigger yeast mortality and thus also does not trigger stuck fermentation. Indeed, in such conditions, yeast reacts with a system of stress responses to maintain its viability during all alcoholic fermentation. On the contrary, lipid limitation does not induce any appropriate stress response by the yeast, leading to yeast cell death, and thus stuck fermentation. This yeast cell death is modulated by nitrogen level. In cases where there is a low lipid content and high nitrogen level, yeast mortality during alcoholic fermentation is increased and can occur in the first stage of the fermentation. (Tesnières et al. 213). Studies have been conducted to identify other nutrient limitations that provoke yeast cell death. In cases where there are nutritional imbalances (e.g., high nitrogen and starvation in oleic acid, panthotenate and nicotinic acid) high mortality have been observed (Figure 3). This very new data demonstrate the importance of a good nutritional balance (minerals, vitamins, sterols, organic nitrogen) not only to maintain yeast viability and avoid stuck fermentation, but also to limit the risk of off-flavours and deviations such as H 2 S production. An imbalance between high YAN and low pantothenic acid levels in must significantly drives H 2 S production. (Wang 23, Blondin 216). When choosing a nutrient, quality is as important as quantity since only organic nutrients will provide those optimal growth factors as well as organic nitrogen while providing a better nutritional balance than with chemical DAP alone. 2

Viable cells (%) 1 9 8 7 6 5 4 3 2 1 2 4 6 8 1 CO 2 produced (g/l) Low nitrogen High nitrogen/low oleic acid High nitrogen/low ergosterol High nitrogen/low panthothenic acid High nitrogen/low nicotinic acid Figure 3. Impact of various vitamins and sterols (in high YAN conditions) on yeast populations during AF Vitamins & minerals: Minerals such as magnesium, zinc and potassium are absolutely essential to the growth and metabolism of yeast (Walker, 1994). Minerals: Are cofactors of several glycolytic enzymes Increase ATPase activity and help pump the compounds across the yeast membrane Increase yeast tolerance to ethanol and temperature Have an antagonistic effect on the toxicity of heavy metals Regulate cellular growth Regulate the formation of alcohol and esters Vitamins are organic compounds essential to the optimum growth of yeasts cells and their capacity to survive under stressful conditions. Vitamin deficiencies can induce sudden changes in fermentation kinetics. The majority act as enzymatic cofactors. They can also intervene in energy transfers or in supporting membrane integrity. Biotin, for example, favours the production of esters and better cellular viability (Bohlscheid et al. 27). When biotin is deficient, cellular growth is affected significantly (Figure 4). Pantothenic acid (Vitamin B5) helps prevent H 2 S production volatile acidity. Thiamine function of thiamine has been the subject of numerous studies, and thiamine deficiency can cause stuck fermentation. The concentration of thiamine has a large influence on fermentation kinetics; its presence increases the production of yeast biomass and fermentation speed (Bataillon et al. 1996). 3

25 2 2 levels of YAN: 6 mg/l 3 concentrations of biotine: µg/l 25 mg/l 1 µg/l 1 µg/l 15 1 } µg/l of biotine, with 6 or 25 mg/l of YAN Stuck fermentations with high mortality in biotine deficiency even with high nitrogen level 5 Figure 4. Glucose/Fructose concentration during AF with Lalvin EC-1118 in synthetic must (from Bohlscheid et al. 27) Lack of oxygen and the role of sterols: Oxygen plays an essential role in alcoholic fermentation, fostering the development of an adequate yeast population and maintaining their vitality (Sablayrolles and Barre 1986). Oxygen is required for the synthesis of survival factors such as sterols and unsaturated fatty acids (David and Kirsop 19973, Aries and Kirsop 1978, Alexandre et al. 1994, Fornairon-Bonnefond et al., 22), which are components of the yeast cell membrane. They play a key role in the membrane structure, helping maintain membrane fluidity, cell integrity and viability (Figure 5). During the yeast growth phase, each multiplication cycle dilutes the lipid content of the yeast cell. When lipids become insufficient, the yeast cell membrane does not function properly under limiting oxygen conditions. Sterols, located around the membrane proteins responsible for flux selectivity between the interior and the exterior of the cell, are no longer synthesized. During fermentation, as the ethanol level increases, yeast mortality increases. Without an adequate yeast sterol concentration, yeast cell wall permease activity suffers. When these proteins do not function adequately under increased ethanol concentration, there is an accumulation of H+ ions in the intracellular medium, and the yeast requires more energy to expel them outside the cell. This will rapidly lead to the acidification of the cell (drop of intracellular ph), resulting in cell death and stuck fermentation. So the more sterols are synthesized in the membrane, the better the resistance to ethanol. It is important to rehydrate the yeast cells with a yeast protector (such as the Natstep range of products) that will supply sterols to the yeast membrane (Soubeyrand et al. 25). 4

Figure 5. Yeast cell membrane and some of its constituents during AF. The sterols maintain membrane fluidity, resulting in a clean AF. Improper yeast rehydration and handling: Proper yeast rehydration is key to successful alcoholic fermentation (AF) as it is a crucial phase for the survival and efficiency of the wine yeast. If the yeast is not properly rehydrated, more than half of the yeast population can die. It is very important to follow manufacturer s instructions, particularly with respect to both the rehydration medium and temperature. During yeast rehydration, the active dry yeast will absorb water and recover its original form. The organs inside the cell continue rehydrating and a part of them disperses in the rehydration water. This loss can represent between 2-3% of the yeast s dry weight and can result in a micronutrient deficit. Rehydrating in wine must, at the wrong temperature and the recommended dosage, will all influence wine yeast performance. In order to initiate fermentation, there must be a minimum of 16 cells/ml. When using a 25 g/hl inoculum of active dry yeast, there will be approximately 5x16 cells/ml, which is usually sufficient for a regular AF, a good implantation in the must, and ultimately, no sluggish or stuck fermentation is rehydrated properly. For example, in Figure 6, the length of AF is shortened considerably when the dosage is at 2 g/hl (internal results). 19 Spontaneous Density 14 5 g/hl 1 g/hl 2 g/hl 99 3 5 7 1 15 AF (days) Figure 6. Impact of inoculation rate on AF Lack of temperature management: Fermentation temperature is important based not only on the type of wine to be fermented (red, white, rosé) but also the yeast used. Different yeasts, under different conditions, will be more sensitive to cooler or warmer tem- 5

peratures during AF. Each selected yeast is characterized with a range of optimal AF performance, which must be carefully respected to avoid stuck fermentation. AF will be affected by extreme temperatures (either too low or too high), since it has been shown that ethanol toxicity increases at extreme temperatures. The yeast cell membrane is weakened, which eventually leads to cell death. Inhibitory metabolites: Grape must composition may have inhibiting toxic compounds that affect yeast viability and fermentative activity and that are responsible for sluggish or stuck alcoholic fermentation. Inhibiting toxic compounds, such as short and medium chain fatty acids (SMCFA), have been widely noted for their inhibition of alcoholic fermentation. Pesticide residues (fungicide, herbicide, insecticide) can also seriously affect yeast viability and compromise the end of fermentation. Recent studies have also shown that they can negatively impact the production of aromas (namely esters) and fruit character of wine (Noguerol-Pato et al. 214). HOW TO CURE A SLUGGISH OR STUCK FERMENTATION? Yeast cells have the extraordinary capacity to adapt to different stress factors in a difficult environment of the grape must (high sugar, low ph, gradual ethanol increase, nutrient depletion, competition with other microorganisms, etc.). However, difficult conditions can prevail, resulting in a fermentation that won t finish, and actions must be taken to cure stuck fermentation where the density is not decreasing anymore, or very slowly, and some offaromas might be creeping up. Quick actions are necessary to avoid microbial spoilage and the appearance of wine faults (H 2 S, Brett odours, VA, etc.) and to get fermentation going again. A reliable protocol that can be applied quickly and efficiently can help tackle the different causes of AF problems. Cleaning the must: Grape must may contain toxic compounds that inhibit fermentation, such as short and medium chain fatty acids (SMCFA) and pesticides. A new generation of yeast hull products with good absorption capacity and an affinity for these types of compounds is now available. Trials have shown that yeast hulls such as RESKUE favour complete and steady fermentations thanks to the removal of SMCFA and pesticide residues (Figures 7 & 8). Isobutyric acid Isovaleric acid Hexanoic acid Octanoic acid Decanoic acid Reskue.5 1 1.5 2 2.5 3 3.5 4 Control mg/l Figure 7. Lab-scale trial, Chardonnay, France, 212. Level of SMCFA at the end of alcoholic fermentation after addition of different cell-walls (4 g/hl) at the 3/4 of the alcoholic fermentation. 6

1 A. White wine 1 B. Rosé wine 8 8 % 6 4 2 Dimetomorph Metalaxyl-M Metiocarb Primetanil % 6 4 2 Dimetomorph Metalaxyl-M Metiocarb Primetanil Figure 8. Lab-scale trials, White (A) and Rosé (B) wines contaminated with several pesticide residues, Spain, 213. Pesticide removal (%) after addition of Reskue at 4 g/hl. Using the right yeast Many factors influence the course of AF, and choosing the right yeast is crucial, especially when the conditions are difficult. When fermentation stops mid-stream, the must generally contains much more fructose than glucose, the type of sugar that yeasts prefer. To overcome this glucose/fructose imbalance, it is important to choose a yeast that has a strong affinity for fructose, the predominant sugar in stuck fermentation, but also a yeast that is alcohol tolerant and responds well to nutrient supplementation. In trials carried out over the years, one yeast stood out (Figure 9) among all selected yeasts available: Uvaferm 43, which is more capable of fermenting fructose and has a very high fermentation capacity and a high alcohol tolerance. 5. MS3 26 Glc/Fru; 24 C; 25 g/hl 4.5 4. 3.5 FI: Fructophilic index 3. 2.5 2. 1.5 1..5 43 YSEO BC Yeast A QA23 YSEO Yeast B Yeast C Yeast D EC 1118 IOC 18 27 Cross Evolution K1M L46 BM4X4 BM45 V1116 D21 VN L2323 D254 YSEO 71B YSEO Figure 9. Fructose affinity of different wine yeast in synthetic medium MS3 26Glc/Fru; 24ºC; 25 g/hl Even with these properties, at Lallemand R&D we drew on our premium knowledge of yeast growth and metabolism to develop a production process that makes yeast cells more resistant to stress conditions caused by high alcohol content. Uvaferm 43 was then optimized and pre-acclimated during multiplication with specific micronutrients and survival factor protection. Survival factors include specific sterols and polyunsaturated fatty acids that strengthen the yeast membrane. As a result, yeast cells are then more robust, with a lower mortality rate after inoculation, and require less time to acclimate to the must. This simplifies the process of restarting your fermentation with only a few steps using the new Uvaferm 43 Restart. 7

In trials done with Uvaferm 43 Restart, it was shown that an average of one week was gained when restarting a stuck ferment, as illustrated in Figure 1 in a Primitivo from Puglia, Italy. 12 1 Uvaferm 43 Uvaferm 43 RESTART Sugar (g/l) 8 6 4 At the end of fermentation 43 Restart Alcool 14.7 Residual 1.1 sugars 43 Yseo 14.75 1.9 2 Volatile Acidity.75.78 Sept. 3 Oct. 19 Oct. 21 Oct. 24 Oct. 26 Oct. 28 Oct. 3 Nov. 2 Nov. 4 Nov. 6 Time (Days) Figure 1. Sugar consumption with 2 different yeasts to complete fermentation after restarting a stuck Primitivo wine from Italy. In terms of fructose consumption, we can see that in both white and red wines, Uvaferm 43 Restart is very efficient for overcoming stuck fermentations. Fructose (g/l) 1 9 8 7 6 5 4 3 2 1 Nov. 15 Nov. 2 Nov. 25 Nov. 3 Dec. 5 Dec. 1 Dec. 15 Time (Days) White Wine 1 / Uvaferm 43 White Wine 2 / 43 Restart Red Wine 2 / Uvaferm 43 Red Wine 2 / 43 Restart Figure 11. Fructose consumption in white and red wines with two different yeast (ISVEA, Toscane, Italy) The right nutrition Right at the beginning of fermentation, vitamins, minerals and available nitrogen are consumed very quickly. This can cause sluggish and stuck fermentation as indicated above. It is then key to add nutrients naturally rich in these elements, such as Fermaid O, to feed the yeasts when restarting a stuck fermentation. Fermaid O or Nutrient Vit Nature (when added at 1/3 sugar depletion) supply critical nutrients to help the yeast avoid stressed conditions. It is one of the best nutrients available for wine yeast as it only contains organic nitrogen and all the essential elements for the yeast to complete AF. 8

AN IMPROVED PROTOCOL We now understand that when restarting a stuck fermentation, even with a clean must/wine, the proper yeast and the best nutrients, using an efficient protocol will secure the process. With the help of the experts at Inter-Rhône (France), a protocol was developed to make the process simple, fast and efficient. NEW PROTOCOL Simply RESTART a stuck wine: Volume of wine = 1 hl Wine < 2 C Volume 1 hl Stuck wine preparation Adjust SO 2 Level depending on analysis Specific cell wall addition (Reskue ) 4 kg Rack-off after 24-48 h 2 Pied-de-cuve 2-25 C constant Volume 5 hl Add to the rehydrated yeast 1.3 hl water 2 kg sugar 3.3 hl stuck wine detoxified Fermaid O :.2 kg 24 > 48 hours After rack-off, T of the wine will be increased to 2 C. When density reaches 1 (48 h - 72 h) 1 Yeast rehydration: Uvaferm 43 RESTART : 4 kg Gentle stirring (2-3 minutes) 3 minutes 2-25 C constant Volume 1 hl Incorporation of the Pied-de-cuve (5 hl) to the stuck wine detoxified Add 4 kg of Fermaid O Water 37 C with ADY Water = 4 L CONCLUSION Proper fermentation management begins when choosing the yeast to ferment the wine and how it will be prepared for AF. A yeast adapted to must conditions and wine style development or to showcase the terroir is crucial. It must be rehydrated properly with a protector such as Go-Ferm Protect or Go-Ferm Protect Evolution to ensure its membrane is in optimal shape in the difficult wine environment. It must be properly fed with the right nutrients such as Fermaid O. Sometimes, carrying out all the right preparations still may not be enough to overcome extreme or unmanageable conditions. When an AF is sluggish or stuck, there are now efficient and reliable ways to solve this issue. Proper must detoxification with Reskue yeast hulls and use of the robust Uvaferm 43 Restart as part of an easy-to-use protocol are sure ways to ensure wine quality. References Agenbach W. A. A study of must nitrogen content in relation to incomplete fermentations, yeast production and fermentation activity. Proc. South African Soc. Enol. Vitic., Cape town, South Africa. Stellenbosch SA, 66-87. (1977) Alexandre H., T.N. Long, M. Feuillat, and C. Charpentier. Contribution à l étude des bourbes : influence sur la fermentiscibilité des moûts. Revue française d oenologie, 146, 11-19. (1994) Aries V and B.H. Kirsop. Sterols biosynthesis by strains of Saccharomyces cerevisiae in presence and absence of dissolved oxygen. J. Inst. Brew. 84: 118-122. (1978) Bataillon M., A. Rico, J.M. Sablayrolles, J.M. Salmon and P. Barre. Early thiamine assimilation by yeasts under enological conditions: impact on alcoholic fermentation kinetics. J Ferm. Bioeng. 82: 145-15. (1996) 9

Bely M., J.M. Sablayrolles, and P. Barre. Description of alcoholic fermentation kinetics: its variability and significance. American Journal of Enology and Viticulture. 41 (4), 319-324. (199) Bely M., J.M. Salmon, and P. Barre. Assimilable nitrogen additions and hexose transport activity during enological fermentations. J. Inst. Brew. 1:279-282 (1994) Berthels NJ, R.R. R.R. Cordero Otero, F.F. Bauer, J.M. Thevelein, I.S. Pretorius (24) Discrepancy in glucose and fructose utilisation during fermentation by Saccharomyces cerevisiae wine yeast strains. FEMS Yeast Res 4(7):683-9 Bisson, L. 1999. Stuck and Sluggish Fermentations. Am J Enol Vitic. 5: 17-119 Bezenger M., J.M. Navarro. Influence de l azote sur la fermentation alcoolique en milieu modèle simulant les conditions de l oenologie. Sciences des aliments, 7, 41-6. (1987) Bohlscheid J.C. 1, J.K. Fellman2, X.D. Wang3, D. Ansen4, C.G. Edwards Bohlscheid J.C. 1, J.K. Fellman2, X.D. Wang3, D. Ansen4, C.G. Edwards The influence of nitrogen and biotin interactions on the performance of Saccharomyces in alcoholic fermentations David, M. and B. Kirsop. 19973. A Correlation between Oxygen Requirements and the Products of Sterol Synthesis in Strains of Saccharomyces cerevisiae. Journal of General Microbiology, 77, 529-53 I Duc, C., I. Sanchez, M. Pradal, J. Noble2, A. Ortiz-Julien,C. Tesnière and B. Blondin. Yeast Cell Death Triggered By Nutrient Starvation in Wine Alcoholic Fermentation. Oral conference, PYFF6: 6th Conference on Physiology of Yeasts and Filamentous Fungi. Abstract Book, 11-14, July 216, Lisbon, Portugal Fornairon-Bonnefond C., V. Desmaretz, E. Rosenfeld, J.M. Salmon. Oxygen addition and sterol synthesis in Saccharomyces cerevisiae during enological fermentation. J. Biosci. Bioeng., 93, 176-182. (22) Henschke P and V Jiranek. Yeast metabolism of nitrogen compounds. Wine Microbiology and Biotechnology. Fleet G.H. (Eds) 77-165. (1993) Julien A, J.L. Roustan, L. Dulau, J.M. Sablayrolles. Comparison of nitrogen and oxygen demands of enological yeasts: Technological consequences. Am. J. Enol. Vitic. 51 (3). (2) Noguerol-Pato Raquel, Thais Sieiro-Sampredro, Carmen González-Barreiro, Beatriz Cancho-Grande and Jesús Simal-Gándara. Effect on the Aroma Profile of Graciano and Tempranillo Red Wines of the Application of Two Antifungal Treatments Onto Vines Molecules 19 (8), 12173-12193. 214 Sablayrolles J.M. and P. Barre. Evaluation des besoins en oxygène de fermentations alcooliques en conditions oenologiques stimulées. Sci. Alim. 6 : 373-383. (1986) Soubeyrand V., V. Luparia, P. Williams, T. Doco, A. Vernhet, A. Ortiz-Julien, J.M. Salmon. Improvement of the Fermenting Capacity of Active Dry Yeast (ADY) by Solubilized Sterols during Rehydration. J. Agric. Food Chem. 25 Tesnière C.1, P. Delobel, M. Pradal, B. Blondin. 213. Impact of Nutrient Imbalance on Wine Alcoholic Fermentations: Nitrogen Excess Enhances Yeast Cell Death in Lipid-Limited Must. PLoS One 8 (4), e61645 Walker GM. The role of magnesium in Biotechnology. Critic. Rev. Biotechnol. 14: 311-354. (1994) (Walker et al. 216). Wang X.D., J.C. Bohlscheid and C.G. Edwards. 23 Fermentative activity and production of volatile compounds by Saccharomyces grown in synthetic grape juice media deficient in assimilable nitrogen and/or pantothenic acid Journal of Applied Microbiology, 94, 349-359 1