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    Lactic fermentation

    Directed fermentations.

    THE PROCESS IN MOTION

    What does a lactic fermentation change?

    Start the scene or choose a stage. The animation simplifies the mechanism; what follows gives the details and the available references.

    Closing starves the acetic ones

    Every coffee fermentation is already lactic in part; the process changes the relative share of the lactic acid bacteria. They draw their energy from fermentation alone. Acetic bacteria, those of vinegar, need oxygen to oxidize alcohol. Closing the tank therefore does not feed the lactic ones: it starves the acetic ones. Nobody purges the tank, the oxygen is consumed.

    Read the stages without animation
    1. Closing starves the acetic onesEvery coffee fermentation is already lactic in part; the process changes the relative share of the lactic acid bacteria. They draw their energy from fermentation alone. Acetic bacteria, those of vinegar, need oxygen to oxidize alcohol. Closing the tank therefore does not feed the lactic ones: it starves the acetic ones. Nobody purges the tank, the oxygen is consumed.
    2. Submerge, or notIn the trial on the Arara cultivar, bioreactors of 200 liters each receive about 124 kg of cherries; the submerged variant adds 60 liters of water, 30% of the volume. Submerged, Lactobacillus reaches 80.9% of the bacteria; with no added water, 67.4%, with Weissella occupying 21.9%.
    3. Hold 27 °C, sometimes inoculateA chamber held at 27 °C raised the relative abundance of Lactobacillus by 10.8%. The closed tank warms little by itself, by 0.5 to 3.7 °C, whereas the open tank gains 5.1 to 17.6 °C. When one inoculates, it is to impose a dominant population from the start.
    4. The pH drops and keeps orderThe pH goes from 5.8 to 4.4 in a closed Brazilian tank: the enterobacteria at the start cannot bear this acidity and recede. The heterofermentative lactics yield lactic acid, carbon dioxide and ethanol or acetic acid. Cenicafé places the tipping point at 72 hours: beyond it, the viability of the embryo and the physical quality of the bean decline.
    5. Wash, dry, restThe lot is washed then dried to 11 or 12% moisture; in the Arara trial, hulling takes place only after 30 days of rest at room temperature.

    To remember: Lactic is an orientation, not a category: closing the tank removes an advantage from the acetic bacteria, without guaranteeing a lactic flora.

    Read the full article and its sources ↓
    FamilyDirected fermentations
    Also calledlactic process, lactic acid fermentation, directed lactic fermentation, lactic natural, lactic washed, LAB fermentation

    Where it is practiced

    Two things that bear the same name must be told apart. Lactic fermentation as a phenomenon is universal. Lactic acid bacteria appear in almost every published microbiological survey of coffee. The process called lactic, for its part, is a deliberate, recent practice, confined to specialty microlots.

    The published work is concentrated on a few sites.

    • Colombia, with Cenicafé, the national coffee research center, on arabica var. Castillo harvested at the Naranjal experimental station, in Caldas, at 1,381 meters.
    • Brazil, in two distinct places: the Federal University of Lavras, on canephora Conilon, and the Federal University of Uberlândia, on arabica cv. Arara, at the Chuá farm in Minas Gerais, at 1,050 meters.
    • Ecuador, where De Bruyn and colleagues sampled a plantation near Nanegal, at 1,329 meters, from May to July 2014.
    • Yunnan in China, where Zhang and colleagues followed concrete tanks near Jinghong, at 1,300 meters, from December 2015 to January 2016.

    The dating is checked on the laboratory side, not the trade side. The first scientific article on coffee to use the term self-induced anaerobic fermentation appeared online in December 2021, in Food Microbiology. Published trials of lactic acid bacteria inoculation on coffee then follow without interruption: Cassimiro in 2023, Rabelo in 2024, Shen in 2025. The word lactic circulated on bags before that, without it being possible to fix its first occurrence.

    A portable pH meter with a probe shows a reading of 5.89 after measuring a liquid sample collected in a cup
    Portable pH meter showing a field readingTommy Gustaviano Yeza · CC BY-SA 3.0

    The principle

    Every coffee fermentation is already lactic in part. What the process changes is not the presence of lactic acid bacteria, it is their relative share. There is therefore no threshold that would tip a lot into the category: there is a slider.

    These bacteria eat the sugars of the mucilage, the layer of sugary flesh stuck to the parchment. Two metabolic pathways exist, and they do not yield the same thing.

    The homofermentative ones follow ordinary glycolysis, called the Embden-Meyerhof-Parnas pathway. They yield almost only lactic acid, about two molecules per molecule of glucose. The heterofermentative ones take the phosphoketolase pathway, named after the enzyme that cleaves the sugar into two fragments. This pathway yields, per molecule of glucose, one molecule of lactic acid, one of carbon dioxide, and one of ethanol or acetic acid. It therefore explains why a so-called lactic tank gives off gas and smells of alcohol. The heterofermentative genera most often recorded in coffee are Leuconostoc, Weissella and Lactiplantibacillus. At Cenicafé, it is Weissella that dominates, followed by Leuconostoc and Lactiplantibacillus. When fructose is available, these bacteria reduce it to mannitol, a sugar alcohol. They use it as an electron acceptor, to balance their redox budget.

    Acidification is the second effect, and it is what protects the lot. In a closed Brazilian tank followed layer by layer, the pH went from 5.8 to 4.4. The enterobacteria that dominate the starting flora cannot bear this acidity and recede. Acidification is thus both the product of fermentation and its enforcer.

    What remains is the lever of management, and it does not act on the lactic bacteria. It acts on their competitors. Lactic acid bacteria draw their energy from fermentation alone and do without oxygen. Acetic bacteria need it: they oxidize alcohol into acetic acid, that of vinegar, and this oxidation consumes oxygen. Closing the tank therefore does not feed the lactic bacteria, it starves the acetic ones.

    This lever is not reliable for all that, and it must be said. In the closed Brazilian tank cited above, it was the enterobacteria that dominated, and the lactic bacteria remained a minority. Closing a tank does not guarantee a lactic flora, it merely removes an advantage from the acetic bacteria.

    The sequence

    • Harvest of ripe cherries and sorting. Ripeness sets the available sugar and the starting pH, and therefore the speed at which acidification will set in.
    • Choice of material: whole cherry or pulped coffee. Cenicafé compared the two over 192 hours. Whole cherry gives more glucose and less lactic acid than pulped coffee. The authors attribute the surplus of glucose to the complex carbohydrates of the pulp, which add a source of carbon. They attribute the deficit of lactic acid to a better balance between acetic and lactic bacteria in an open tank.
    • Loading into a closed tank fitted with an airlock. The Uberlândia trial on cv. Arara used high-density polyethylene bioreactors of 200 liters, loaded with about 124 kilos of cherries. The lids carried a one-way valve, which lets carbon dioxide out without letting air in.
    • Submerged variant: addition of 60 liters of water, or 30 percent by volume. The water evens out the temperature and slows gas exchange. In this trial, the submerged route brought the genus Lactobacillus to 80.9 percent of the bacterial community. In a solid medium, that is, with no added water, it did not exceed 67.4 percent, with Weissella then occupying 21.9 percent.
    • Setting anoxia. Nobody purges the tank: the oxygen present is consumed by the microorganisms themselves, and the headspace of the tank saturates with carbon dioxide. The medium becomes anoxic by exhaustion, not by driving the air out. The term anaerobic is therefore improper in the strict sense, and the literature speaks of self-induced anaerobic fermentation.
    • Thermal management. In the Arara trial, a chamber regulated at 27 degrees raised the relative abundance of Lactobacillus by 10.8 percent, compared with tanks left in the shade without regulation. The closed tank warms little by itself. At Cenicafé, with an ambient temperature held at 20.1 degrees, it gained only 0.5 to 3.7 degrees. The open tank, for its part, gained from 5.1 to 17.6 degrees.
    • Inoculation, when it takes place. In Cassimiro's work, Leuconostoc mesenteroides was already present in the cherries at 8.54 log10 cells per milliliter, and stayed there to the end. The aim of inoculation is to short-circuit competition by imposing a dominant population from the start.
    • Duration. Published trials on closed tanks run around 24 to 72 hours. Cenicafé went as far as 192 hours and places the tipping point at 72 hours. Beyond it, the physical quality of the bean and the viability of the embryo decline, whatever the management.
    • Monitoring. The pH is measured continuously. Cenicafé measures the glucose and lactic acid of the mucilage with Reflectoquant reflectometric strips, other teams by liquid chromatography. The point of monitoring is to see early whether acidification is setting in, because a tank that does not acidify has drifted toward another flora.
    • Washing, then drying to 11 or 12 percent moisture. In the Arara trial, hulling took place only after 30 days of rest at room temperature.

    What it gives in the cup

    What is measured, first, and the picture is not unambiguous.

    Cassimiro and colleagues inoculated Leuconostoc mesenteroides on canephora Conilon in a closed tank. This lot is classed fine, that is, between 80.0 and 89.0 points, while the other treatments stay in premium, between 70.0 and 79.0. The descriptors recorded are caramel, fruit and spices. It is the clearest positive result available on lactic inoculation. It concerns canephora, however, not arabica.

    Cenicafé provides the counterweight, and it is severe. On arabica, comparing open and closed tanks over 192 hours, sensory quality did not move. It varies neither with the raw material, nor with the fermentation condition, nor with the duration. The p values are 0.6669, 0.5740 and 0.3338 respectively. The mean stands at 83.14 SCA points, with a standard deviation of 0.39, and all the samples fall between 80.75 and 85.00. In other words, the study that measured lactic acid production most finely found no corresponding difference in the cup.

    The trial on cv. Arara built a decision tree linking microbial composition and sensory score, with 96.43 percent accuracy. The discriminating genus is not the one you would expect: it is Leuconostoc, above 2.6 percent relative abundance. Only when Leuconostoc is rare does the dominance of Lactobacillus become decisive, from 88.73 percent. The rule remains soft on that side: above the threshold, the association with a good cup is only 67 percent. This is moreover a correlation from a statistical model, not a causal demonstration.

    A Colombian trial on var. Castillo shows a clear sensory improvement after inoculation, but it does not allow it to be attributed to the microorganisms. The starter poured into the tank also contained wheat flour, brown sugar and 30 kilos of crushed pineapple. The authors moreover note that the inoculum did not colonize the tank, and attribute the difference to the nutrients supplied.

    What is claimed, next. The commercial vocabulary of lactic is stable from one seller to another: yogurt, cream, butter, enveloping texture, sweetness. No published blind trial attributes these descriptors to lactic acid itself. The same gesture shifts dozens of other compounds, and nothing makes it possible to apportion them.

    We must be clear about the missing link. De Bruyn and colleagues measured the metabolites by liquid chromatography coupled with mass spectrometry. The lactic acid, acetic acid and mannitol produced in the mucilage are found in the endosperm, that is, in the bean itself. In the dry process, the outer layers contain 1.0 to 2.1 percent lactic acid in dry matter. The migration is therefore established. On the other hand, no published study links a measured lactic acid content in the green bean to a cupping score. The chain stops before the cup.

    What goes wrong

    The central risk is duration, not the closing of the tank. At Cenicafé, embryo viability and the proportion of sound beans fall significantly with time, in all conditions. The starting lot showed 84.3 percent sound beans and 83.3 percent embryo viability. The authors' conclusion places the tipping point beyond 72 hours.

    A widespread idea must be corrected here. One often reads that the lactic acid being sought would itself be what damages the seed. Cenicafé does report this link, but by citing earlier work, not as a result of its own. Its own data go the other way. The closed tank produced more lactic acid and better embryo viability than the open tank. It is in the open tank that the loss is greatest, and whole cherry in a closed tank is what is damaged least, up to 120 hours.

    A green coffee bean remains a living seed, and this is what the tetrazolium test measures. In an open tank, the degradation of the embryo starts after 48 hours and falls to 25 percent at 192 hours. The resulting defect bears the usual names of the trade: fermented, over-fermented, stinker for an isolated bean that has turned putrid.

    Whole cherry in an open tank is the most explicitly discouraged case. It is sometimes sold under the names double fermentation, pre-coffee cherry or fruit reserve. Cenicafé judges it inadvisable beyond 24 hours. The reason is twofold: physical quality degrades and embryo viability collapses.

    The phenolic defect, that taste of medicine or plastic, did not appear just anywhere. At Cenicafé, a single sample in the whole trial shows it: whole cherry, open tank, 72 hours. In the Colombian trial on var. Castillo, it was perceived by the three certified tasters on the spontaneous fermentation. The authors associate it with high contents of phenol and aminophenol, specifying that this is the first published report linking these compounds to this defect.

    Acetic drift lurks as soon as air gets in, since acetic bacteria work only in the presence of oxygen. A badly set airlock, a tank opened to take a sample or an incomplete filling are enough to hand them back control.

    Tank heterogeneity is the least visible risk, because it produces not a defect but a blend. A Brazilian tank was loaded with 175 kilos of pulped coffee and 30 liters of water. Lactic acid was measured there at 5.06 grams per liter at the bottom, 4.70 in the middle and 2.18 at the top. The microbial composition did not vary from one layer to another: it is the metabolism that differs, not the flora. A lot managed this way is not one fermentation, it is the average of three.

    Temperature adds its own drift in an open tank. At Cenicafé, whole cherry in an open tank exceeds 30 degrees from 48 hours and never comes back down. It reached 37 degrees at 48 hours. Everything then speeds up, with no way of regaining control.

    Benchmarks

    • Tank pH, measured in Brazil layer by layerfrom 5.8 at the start to 4.4 at the end
    • Tipping point in duration72 hours, beyond it embryo viability and physical quality decline
    • Whole cherry in an open tankdiscouraged beyond 24 hours, above 30 °C from 48 hours
    • Sensory score at Cenicafé83.14 SCA points, standard deviation 0.39, no difference between treatments
    • Regulation at 27 °C+10.8 percent relative abundance of Lactobacillus against unregulated ambient
    • Gradient in a tank of 175 kg of pulped coffee5.06 g/L of lactic acid at the bottom, 2.18 g/L at the top
    • Lactic acid in the outer layers in the dry process1.0 to 2.1% of dry matter
    Gray areaThe missing link is the most troublesome. The migration of lactic acid into the bean is established. But no published study links a measured lactic acid content in the green bean to a cupping score. The common reasoning, more lactic acid therefore a lactic profile in the cup, has no direct experimental support. Nor was a measurement found establishing what becomes of this lactic acid at roasting. The process is standardized nowhere. No body defines a duration, a temperature, a content or a microbial population that would make one lot lactic and another not. Two producers who sell a lactic process do not describe the same thing, exactly as with the colors of honeys. Mannitol is often presented as the signature of heterofermentative lactic acid bacteria. The wording is too strong. Yeasts produce it too, and in the Colombian trial on var. Castillo it is the yeast-inoculated lot that contains the most. No source consulted establishes, moreover, its absence from the intact cherry. No reference pH range is published for this process. The only complete monitoring found gives 5.8 at the start and 4.4 at the end, on a Brazilian tank. Nothing allows it to be turned into a general range, since the starting pH depends on the ripeness of the cherries. The rise of Lactobacillus obtained at 27 degrees in the Arara trial is given as “an increase of 10.8 percent.” The publication does not say whether this is 10.8 points of relative abundance or a relative rise of 10.8 percent. The two readings do not cover the same effect. The data on temperature contradict one another. Cenicafé attributes the strongest lactic activity to lower tank temperatures. The Arara trial obtains more Lactobacillus by regulating at 27 degrees than by leaving it at ambient. The two trials differ in country, material and reference ambient, and nothing in the publications makes it possible to reconcile them. The clearest positive sensory result, that of Cassimiro, concerns canephora Conilon. Its transposition to arabica is not verified. And the finest study on arabica, that of Cenicafé, finds no sensory difference between treatments. The total duration of the fermentation could not be verified in Cassimiro's work: the abstract mentions only one measurement point at 36 hours. The Arara trial is often cited as a lactic trial, but half of its treatments carried a starter of Saccharomyces cerevisiae RX60. What is read there about lactic acid bacteria is therefore mixed with the effect of an added yeast. Commercial starter cultures remain opaque. In the Colombian trial on var. Castillo, the starter was a mixture of two commercial strains of Saccharomyces cerevisiae, undisclosed under a verbal confidentiality clause. This trial therefore inoculated a yeast, not a lactic acid bacterium, although it observes shifts in the lactic flora. The Lactobacillus assignment in this work comes from 16S ribosomal RNA sequencing at genus rank. The taxonomy of this group was redrawn in 2020, into 23 new genera, including Lactiplantibacillus and Paucilactobacillus. Cenicafé already uses the revised names, the Arara trial keeps Lactobacillus. The counts of the two studies are therefore not comparable at the same rank. The first commercial occurrence of the term lactic process could not be fixed, nor the first inoculation of lactic acid bacteria on coffee. The published trials that were verified begin in 2023, which does not prove that there were none before. Finally, two practical parameters are published nowhere: the actual pressure that prevails in these closed tanks, in bar, and the setting of the valves used.
    Peñuela-Martínez, Osorio-Giraldo, Buitrago-Zuluaga and Medina-Rivera (Cenicafé), “Development of Fermentation Strategies for Quality Mild Coffee Production (Coffea arabica L.) Based on Oxygen Availability and Processing Time,” Foods 14(17):3001, 2025, doi 10.3390/foods14173001, sections 3.1 to 3.4, tables 1 and 2 and conclusion. De Bruyn, Zhang, Pothakos et al., “Exploring the Impacts of Postharvest Processing on the Microbiota and Metabolite Profiles during Green Coffee Bean Production,” Applied and Environmental Microbiology 83(1):e02398-16, 2017, doi 10.1128/AEM.02398-16, materials and methods and metabolomic results on endosperm and outer layers. Cassimiro, Batista, Fonseca et al., “Wet fermentation of Coffea canephora by lactic acid bacteria and yeasts using the self-induced anaerobic fermentation (SIAF) method enhances the coffee quality,” Food Microbiology 110:104161, 2023, doi 10.1016/j.fm.2022.104161. Silva, Costa et al., “Microbial community dynamics during Coffea arabica cv. Arara fermentation and their relationship with specialty coffee quality,” Scientific Reports 16:21933, 2026, doi 10.1038/s41598-026-44864-z, fermentation methods and decision trees. Madrid-Restrepo, León-Inga, Peñuela-Martínez, Cala and Reyes, “Metagenomic, metabolomic, and sensorial characteristics of fermented Coffea arabica L. var. Castillo beans inoculated with microbial starter cultures,” mSystems 11(1):e01364-25, 2026, doi 10.1128/msystems.01364-25, starter composition and sensory analysis. da Silva Vale, Balla, Rodrigues et al., “Understanding the Effects of Self-Induced Anaerobic Fermentation on Coffee Beans Quality: Microbiological, Metabolic, and Sensory Studies,” Foods 12(1):37, 2023, doi 10.3390/foods12010037, vertical gradient in a tank of 175 kilos and pH monitoring. Zhang, De Bruyn, Pothakos et al., “Influence of Various Processing Parameters on the Microbial Community Dynamics, Metabolomic Profiles, and Cup Quality During Wet Coffee Processing,” Frontiers in Microbiology 10:2621, 2019, doi 10.3389/fmicb.2019.02621, Yunnan trials. de Melo Pereira, da Silva Vale et al., “Self-induced anaerobiosis coffee fermentation: Impact on microbial communities, chemical composition and sensory quality of coffee,” Food Microbiology 103:103962, 2022, doi 10.1016/j.fm.2021.103962, first publication on coffee using this term. Zheng, Wittouck, Salvetti et al., “A taxonomic note on the genus Lactobacillus: Description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacillaceae and Leuconostocaceae,” International Journal of Systematic and Evolutionary Microbiology 70:2782-2858, 2020, doi 10.1099/ijsem.0.004107. Elhalis, Cox and Zhao, “Yeasts are essential for mucilage degradation of coffee beans during wet fermentation,” Yeast 40(9):425-436, 2023, doi 10.1002/yea.3888, on the respective share of yeasts and bacteria in the degradation of mucilage.
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