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MatUratiON OF ciDer BY MalOlactic FerMeNtatiON - Scandbrewrev.dk

MatUratiON OF ciDer BY MalOlactic FerMeNtatiON - Scandbrewrev.dk

MatUratiON OF ciDer BY MalOlactic FerMeNtatiON - Scandbrewrev.dk

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MATURATION <strong>OF</strong> CIDER <strong>BY</strong> MALOLACTIC FERMENTATIONLike in wine, traditional cider often undergoes a secondarymalolactic fermentation, whereby lactic acid bacteria convertmalic acid into lactic acid. The sharp acidity of malic acidfrom the apples is substituted by the more soft acidity oflactic acid. The dicarboxylic acid malic acid is decarboxylatedinto the monocarboxylic acid lactic acid and carbon dioxide.The reaction is catalysed by the enzyme MLE (malolacticenzyme). In Lactobacillus collinoides, the enzyme is foundto have a pH-optimum of 4.9 and was repressed by applesugars. Other organic acids play an important role duringmaturation. Quinic acid and shikimic acid are converted todihydroshikimic acid and acetic acid and succinic acid areproduced by the lactic acid bacteria. Even a decrease in lacticacid has been observed.The lactic acid bacteria responsible for the MLF are foundin the oak vats. The predominant lactic acid bacteria arefound to be Lactobacillus plantarum in English cider vatsand Oenococcus oeni (former Leuconostoc oenos) in Frenchcider. In Spanish cider, Oenococcus oeni (Leuconostoc oenos)The optimal storage temperature for English cider was foundto be 15 °C and to be 22 °C for Spanish cider. In England,the cider is normally matured at room temperature, whilein France, the temperature is lower at 10-15 °C. Dissolvedoxygen in the cider during storage was found to giveundesirable oxidation flavours. Re-constituted concentratewas found not to promote the desirable flavour changes asfresh apple juice did, due to the lack of MLF.Continuous culturing of lactic acid bacteria for malolacticconversion has been made with success. Differences ingrowth kinetics were found between Oenococcus oeni andLactobacillus brevis.In laboratory scale, successful trials have been performed withimmobilisation of yeast and lactic acid bacteria in order toobtain simultaneous alcoholic and malolactic fermentation.Saccharomyces cerevisiae and Lactobacillus plantarum havebeen co-immobilised on a sponge-like matrix, Oenococcusoeni (Leuconostoc oenos) has been immobilised in Ca-alginateoo hoh oThe process ofmalolactic fermentationoo ho ho h + c o 2and Lactobacillus species have been found responsible forMLF. Other lactic acid bacteria belonging to the generaLactobacillus, Leuconostoc and Pediococcus have also beenidentified. The MLF is reported to appear above 1 millioncells/ml of lactic acid bacteria. Application of a malolacticstarter culture of Oenococcus oeni on an industrial scale wasperformed with success in production of Spanish cider.and Saccharomyces bayanus and Oenococcus oeni (Leuconostocoenos) have been co-immobilised in a Ca-alginate matrix.However, a lower content of higher alcohols and a highercontent of diacetyl have been found. Immobilisation ofOenococcus oeni in alginate beads showed better flavourcharacteristics than free cells. Immobilisation in generalimproves separation.In English and French cider making, the MLF takes placeafter the alcoholic fermentation. In Spanish cider, it isreported to take place simultaneously with the alcoholicfermentation. Inoculation with pure yeast and bacterialcultures in Spanish cider shows that sequential fermentationsare preferred to simultaneous fermentations. Yeast extractand fermentation lees are reported to have a positive impacton MLF. The maturation normally takes from one to fourmonths, but up to two years is practised.In a previous paper, an overview of the entire process of cidermaking has been given.PURE LACTIC CULTURESIn trials at the author’s private premises, MLF was obtainedapplying pure cultures of Oenococcus oeni added after the mainfermentation. The conversion took 11 days without sulphitingthe juice before the main fermentation and up to 21 days if upto 60 ppm sulphite was added before the main fermentation.SCANDINAVIAN BREWERS’ REVIEW . VOL.67 NO.3 2010 19

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