Patent Application
20250057194
The present invention relates to a beverage composition comprising fermented acerola or fermented acerola extract. A further aspect of the invention is a method of preparing a beverage composition.
Acerola is a rich natural source of ascorbic acid and contains a plethora of phytonutrients like carotenoids phenolics, anthocyanins and flavonoids. The flavour profile is usually sour and astringent, and taste may vary due to the seasonal fluctuation. Acerola usually needs to be blended with sweet fruit juices and purees such as pineapple and mango, or sweetened with sugar to increase its desirability.
Many people desire new flavours in their beverages and sweet tastes, but would prefer not to consume beverages with added flavouring, especially synthetic flavourings or sugary fruit juices. The provision of acerola beverages with added flavour complexity and less astringency and sourness would therefore be of commercial value.
Any reference to prior art documents in this specification is not to be considered an admission that such prior art is widely known or forms part of the common general knowledge in the field. As used in this specification, the words “comprises”, “comprising”, and similar words, are not to be interpreted in an exclusive or exhaustive sense. In other words, they are intended to mean “including, but not limited to”.
An object of the present invention is to improve the state of the art and to provide a new product to overcome at least some of the inconveniences described above, or at least to provide a useful alternative. The object of the present invention is achieved by the subject matter of the independent claims. The dependent claims further develop the idea of the present invention.
Accordingly, the present invention provides in a first aspect a beverage composition comprising fermented acerola or fermented acerola extract wherein the weight ratio of the sum of 3-methylbutyl acetate, 2-methylbutyl acetate, isobutyl acetate, 2-phenylethyl acetate and 2-phenylethanol to 2,3-butanedione is greater than 150.
A second aspect of the invention provides a container for use in a beverage preparation device, the container containing the beverage composition of the invention.
In a third aspect, the invention provides a method of preparing a beverage composition comprising fermenting an aqueous acerola extract wherein the fermentation is performed by yeast comprising Pichia yeast.
A further aspect of the invention provides use of acerola fermented with Pichia kluyveri NYSC 5485 (CNCM I-5525) to produce a beverage.
Acerola can be made into a beverage by extracting the juice from acerola berries or pureeing the berries to form a “smoothy”. These beverages are sour and astringent. The inventors were surprised to find that, through fermentation with Pichia yeast, the acerola beverage remained low in ethanol, but the fermentation enhanced the aromatic perception and complexity, with less prominent sourness and astringency. The fermented beverage did not have the buttery and fatty notes that can be perceived as off flavour in a fermentation.
Consequently the present invention relates in part to a beverage composition comprising (for example consisting of) fermented acerola or fermented acerola extract wherein the weight ratio of the sum of 3-methylbutyl acetate, 2-methylbutyl acetate, isobutyl acetate, 2-phenylethyl acetate and 2-phenylethanol to 2,3-butanedione is greater than 150, for example greater than 200, for example greater than 250, for example greater than 500, for example greater than 750, for example greater than 1000, for example greater than 1250, for further example greater than 1400. This ratio can be calculated from the weight concentrations in parts per million as follows:
The compound 2,3-butanedione is also known as diacetyl. It provides a buttery or fatty note. A high ratio of the sum of 3-methylbutyl acetate, 2-methylbutyl acetate, isobutyl acetate, 2-phenylethyl acetate and 2-phenylethanol to 2,3-butanedione corresponds to enhanced fruity and floral notes without the buttery and fatty notes that can be perceived as off flavour in a fermentation. The enhanced fruity notes act to mask the bitterness, sourness and astringency.
Acerola plants (Malpighia emarginata) are a tropical fruit-bearing shrubs or small trees in the family Malpighiaceae. Common names include acerola cherry, Guarani cherry, Barbados cherry, West Indian cherry and wild crepe myrtle. Acerola berries are rich in vitamin C and also contain vitamins A, B1, B2, and B3, as well as carotenoids and bioflavonoids.
In the present invention the term “acerola” refers to the berries or processed forms of berries from acerola plants unless otherwise stated.
In the context of the present invention the term “fermentation” refers to a process in which the activity of microorganisms brings about a change (typically a desirable change) to a foodstuff or beverage. The fermentation may be with yeasts and/or bacteria. The fermentation may be anaerobic or aerobic. Fermentation is one of the oldest means of preserving and enhancing foods.
The term “fermented acerola” refers to acerola which has been subjected to a process in which the activity of microorganisms such as yeasts brings about a chemical change in the organic components of the acerola, typically a desirable change. The fermented acerola may have been fermented in an aqueous medium, for example with yeast. The fermented acerola may be a dried acerola which had been added to an aqueous fermentation medium and fermented before being separated from the aqueous fermentation medium and dried. The fermented acerola may have been fermented in a “solid-state” fermentation, for example adding a starter culture of yeast to acerola, for example to fresh acerola berries, or a pulp comprising the flesh of acerola berries.
The term “acerola extract” refers to material extracted from acerola, for example an aqueous extract of acerola, such as acerola juice, or acerola powder reconstituted with water. The term “fermented acerola extract” refers to an extract of acerola where the acerola extract has been fermented, for example an aqueous acerola extract where the aqueous extract has been fermented, such as by yeast. The fermented acerola extract may be a dried fermented acerola extract.
In an embodiment the beverage composition (for example the beverage) has a weight ratio of the sum of 2-phenylethyl acetate and 2-phenylethanol to 2-phenylacetaldehyde of greater than 3000, for example greater than 4000, for example greater than 6000, for example greater than 8000, for further example greater than 8500.
The ratio can be calculated from the weight concentrations in parts per million as follows:
Higher esters such as 2-phenylethyl acetate are initially produced during the fermentation of sugars with Pichia, but as the fermentation proceeds, higher alcohols such as 2-phenylethanol are produced. A high ratio of the sum of 2-phenylethyl acetate and 2-phenylethanol to 2-phenylacetaldehyde corresponds to a pleasant aroma balance in the fermented beverage.
In an embodiment, the beverage composition comprises less than 10 g/kg acetic acid on a dry basis, for example less than 1 g/kg acetic acid on a dry basis, for further example less than 0.5 g/kg acetic acid on a dry basis. The acid acid “bite” in the flavour profile of beverages such as kombucha or kefir is not always desired by consumers who seek a gentler flavour profile.
Many consumers seek beverages with a complex, refreshing taste as a replacement to alcoholic drinks. In an embodiment, the beverage composition has an ethanol content below 1.2wt %, for example below 0.5wt %, for example below 0.2wt %, for further example below 0.05wt %.
The beverage composition may be selected from the group consisting of a ready to drink beverage, a beverage liquid concentrate, a soluble beverage powder, dried aromatic plant material and combinations of these.
The ready to drink beverage may be a fermented acerola infusion or a water flavoured with fermented acerola. The ready to drink beverage may additionally comprise other components such as flavourings or stabilizers. The ready to drink beverage may be carbonated. The ready to drink beverage may additionally comprise fruit or fruit juice, such as strawberry, orange, lemon, lime, peach, pomegranate, watermelon, blackberry or cranberry. The ready to drink beverage may additionally comprise herbs such as mint or basil. The ready to drink beverage may additionally comprise flower extracts such as hibiscus or rose. The ready to drink beverage may comprise added vitamins and minerals. The ready to drink beverage may comprise beneficial microorganisms, replicating or non-replicating. The beneficial microorganisms may for example be probiotics.
Beverage preparation devices (for example beverage preparation machines) which accommodate extractable portioned ingredients provide a convenient method of preparing beverages. Such portioned ingredients are generally packed in a container, configured for example as a pod, pad, sachet, pouch, capsule or the like. An aspect of the invention provides a container for use in a beverage preparation device, the container containing the beverage composition of the invention. The container being for the preparation of a beverage when inserted into a beverage preparation device. The container may for example be a beverage capsule, among other configurations. In an embodiment, the container contains the beverage composition of the invention. For example the container may contain dried fermented acerola or dried fermented acerola extract. The container may contain dried fermented acerola and/or dried fermented acerola extract, these may be combined with other dry ingredients such as tea, herbal tea, dried fruit, soluble coffee or roast and ground coffee.
An aspect of the invention provides a method of preparing a beverage composition comprising fermenting an aqueous acerola extract wherein the fermentation is performed by yeast comprising Pichia yeast.
The aqueous acerola extract may for example be acerola juice, acerola pulp or acerola powder reconstituted with water.
The yeast may be predominantly Pichia yeast, for example, more than 50% of the microorganism colony forming units present during fermentation may be Pichia. For example more than 50% of the yeast colony forming units may be Pichia, for example more than 60, 70, 80, 90% of the yeast colony forming units may be Pichia. For example, essentially all the yeast colony forming units present during fermentation may be Pichia, for further example, essentially all the microorganism colony forming units present during fermentation may be Pichia.
The beverage composition prepared by the method of the invention may be a acerola beverage, for example a beverage comprising fermented acerola or fermented acerola extract. The beverage composition prepared by the method of the invention may have an ethanol content below 1.2 wt %, for example below 0.5 wt %, for example below 0.2 wt %, for further example below 0.05 wt %. In an embodiment, the beverage composition prepared by the method of the invention is the beverage composition of the invention.
The aqueous acerola extract may be obtained by steeping acerola berries, for example acerola pulp, in water. The acerola may be dried and/or ground before steeping. The term steeping refers to immersing and soaking a material in liquid. The acerola may be steeped in water for at least 2 minutes, for example at least 3 minutes, for example at least 4 minutes, for example at least 5 minutes, for example at least 10 minutes, for example at least 15 minutes, for example at least 20 minutes, for example at least 30 minutes, for example at least 60 minutes, for further example at least 120 minutes. During the steeping process, components of the acerola are extracted into the water. The steeping may be performed at a temperature between 4° C. and 98° C., for example between 20° C. and 95° C., for example between 60° C. and 95° C.
Although acerola contains some fermentable sugar, further fermentable sugar may be added to the aqueous acerola extract, for example sucrose or glucose. The fermentable sugar may be fructose or glucose. The fermentable sugar may be in the form of honey. For example fermentable sugar may be added to the aqueous acerola extract at a level of between 2 and 10 wt. %, for example between 3 and 7 wt. %.
The ratio of acerola on a dry basis to water during fermentation may be between 1:1 and 1:100 by weight, for example between 1:2 and 1:95 by weight, for example between 1:10 and 1:90 by weight, for example between 1:30 and 1:70 by weight, for further example between 1.3 and 1:6.
The temperature of the aqueous acerola extract is adjusted to a temperature suitable for yeast growth before fermentation, for example between 20° C. and 37° C., for example between 25° C. and 35° C., for example between 28° C. and 32° C. The temperature may for example be adjusted using a laminar flow heat exchanger. Yeast is added to the aqueous acerola extract to commence fermentation. Fermenting the aqueous acerola extract maybe performed at a temperature between 25° C. and 35° C., for example between 28° C. and 32° C. Fermenting the aqueous acerola extract may be performed for at least 2 hours, for example at least 6 hours, for example at least 12 hours, for example at least 24 hours, for further example at least 48 hours.
The fermentation may be performed at a pH between 3 and 8, for example between 4 and 6.
The fermentation may be performed in the presence of a nitrogen source such as yeast extract or yeast peptone. The fermentation may be performed in the presence of added amino acids such as valine, leucine, isoleucine and/or phenylalanine, for example at a level of between 0.05 wt. % and 0.1 wt. % of the aqueous acerola extract.
The fermentation may be performed in anaerobic, microaerobic or aerobic conditions. For example, the partial oxygen pressure in the fermenter may be from 0 to 30%, for example from 1 to 20%, for further example from 2 to 10%.
The fermentation may be performed in the presence or absence of non-water-soluble components of acerola, for example the acerola skin and/or seeds.
Preferably the acerola has not been subjected to chemical processing such as hydrolysis before fermentation.
The fermentation may be performed by adding one or more yeasts (for example Pichia yeasts) at an initial combined yeast level of at least 103 CFU/g, for example at least 104 CFU/g, for example at least 105 CFU/g, for example at least 106 CFU/g, for further example at least 107 CFU/g.
The fermentation may be performed in the absence of acetic acid bacteria to avoid generating an acid “bite” in the flavour profile, such as may be obtained with kefir or kombucha fermentations. In an embodiment the fermentation is performed in the absence of lactic acid bacteria.
In an embodiment the fermentation is performed in the absence of Saccharomyces subspecies. For example the fermentation may be performed in the absence of Saccharomyces cerevisiae. S. cerevisiae is used for winemaking and beer brewing. In addition to generating alcohol which may not be desired, S. cerevisiae generates a “fermented”, winey, yeasty flavour note rather than a fresh fruity note.
In an embodiment the fermentation is performed in the absence of a yeast selected from the group consisting of Zygosaccharomyces bailii, Schizosaccharomyces pombe, Torulaspora delbreuckii, Rhodotorula mucilaginosa, Brettanomyces bruxellensis and Candida stellate. These yeasts are commonly found in kombucha “tea-fungus” cultures.
The inventors found that fermentation of acerola with Pichia kluyveri gave particularly good results. A beverage composition comprising acerola or acerola extract fermented with Pichia kluyveri had an enhanced aromatic perception and complexity, with less prominent sourness and astringency.
Pichia kluyveri occurs naturally around the world, for example on olives, grapes and coffee. In an embodiment the Pichia yeast is predominantly Pichia kluyveri, for example, more than 50% of the microorganism colony forming units present during fermentation may be Pichia kluyveri. For example more than 50% of the yeast colony forming units may be Pichia kluyveri, for example more than 60, 70, 80, 90% of the yeast colony forming units may be Pichia kluyveri. For example, essentially all the yeast colony forming units present during fermentation may be Pichia kluyveri, for further example, essentially all the microorganism colony forming units present during fermentation may be Pichia kluyveri.
Pichia kluyveri NCYC 246 (alternatively designated CBS 188) is the type-strain of Pichia kluyveri. It is publicly available, for example from the National Collection of Yeast Cultures, Quadram Institute Bioscience, Norwich, UK.
In an embodiment the Pichia yeast is Pichia kluyveri NCYC 246. For example more than 50% of the yeast colony forming units present during fermentation may be Pichia kluyveri NCYC 246. For example, more than 50% of the microorganism colony forming units present during fermentation may be Pichia kluyveri NCYC 246. For example, essentially all the yeast colony forming units present during fermentation may be Pichia kluyveri NCYC 246. For further example, essentially all the microorganism colony forming units present during fermentation may be Pichia kluyveri NCYC 246.
Pichia kluyveri NCYC 2781 (alternatively designated Maize Silage Isolate 86) is publicly available, for example from the National Collection of Yeast Cultures, Quadram Institute Bioscience, Norwich, UK.
In an embodiment the Pichi yeast is Pichia kluyveri NCYC 2781. For example more than 50% of the yeast colony forming units present during fermentation may be Pichia kluyveri NCYC 2781. For example, more than 50% of the microorganism colony forming units present during fermentation may be Pichia kluyveri NCYC 2781. For example, essentially all the yeast colony forming units present during fermentation may be Pichia kluyveri NCYC 2781. For further example, essentially all the microorganism colony forming units present during fermentation may be Pichia kluyveri NCYC 2781.
Pichia kluyveri is widely distributed in nature, for example being found on fruits such as coffee cherries and olives. Pichia kluyveri NYSC 5485, collected and isolated from a coffee fermentation in Nicaragua, was deposited with the Collection Nationale de Cultures de Microorganismes (CNCM), Institut Pasteur, 25 rue du Docteur Roux, F-75724 PARIS Cedex 15, France, on 23rd June 2020 and given the deposit number CNCM 1-5525.
In an embodiment, the yeast is Pichia kluyveri NYSC 5485 (CNCM I-5525). For example more than 50% of the yeast colony forming units present during fermentation may be Pichia kluyveri NYSC 5485 (CNCM I-5525). For example, more than 50% of the microorganism colony forming units present during fermentation may be Pichia kluyveri NYSC 5485 (CNCM 1-5525). For example, essentially all the yeast colony forming units present during fermentation may be Pichia kluyveri NYSC 5485 (CNCM I-5525), For further example, essentially all the microorganism colony forming units present during fermentation may be Pichia kluyveri NYSC 5485 (CNCM I-5525).
The inventors have found that especially good results were obtained by fermenting acerola with Pichia kluyveri NYSC 5485. Fermenting acerola with Pichia kluyveri NYSC 5485 resulted in a higher weight ratio of the sum of 3-methylbutyl acetate, 2-methylbutyl acetate, isobutyl acetate, 2-phenylethyl acetate and 2-phenylethanol to 2,3-butanedione, corresponding to enhanced fruity and floral notes without the buttery and fatty notes that can be perceived as off flavour in a fermentation.
The fermentation may be performed by adding Pichia kluyveri, for example Pichia kluyveri NYSC 5485 (CNCM I-5525), at an initial yeast level of at least 103 CFU/g, for example at least 104 CFU/g, for example at least 105 CFU/g, for example at least 106 CFU/g, for further example at least 107 CFU/g.
The genetic sequence of Pichia kluyveri NYSC 5485 (CNCM I-5525) was analysed using PacBio sequencing technology. DNA purification was performed using a Qiagen Gentra Puregene Yeast kit. Twelve DNA fragments were identified. These may be individual chromosomes; 11 chromosomes and 1 mitochondrion DNA (SEQ ID NO:4). The genetic sequences are filed in electronic form as SEQ ID NO:1-SEQ ID NO:12.
In an embodiment of the method of the invention, the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99% identity) to SEQ ID NO:1, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:2, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:3, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:5, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:6, a genetic sequence having at least 99% identity to SEQ ID NO:7, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:8, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:9, a genetic sequence having at least 99% identity to SEQ ID NO: 10, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:11, or a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:12.
In an embodiment of the method of the invention, the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99% identity) to SEQ ID NO:1, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:2, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:3, a genetic sequence having at least 99.5% identity to SEQ ID NO: 4, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:5, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:6, a genetic sequence having at least 99% identity to SEQ ID NO:7, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:8, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:9, a genetic sequence having at least 99% identity to SEQ ID NO:10, a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:11 and a genetic sequence having at least 98% identity (for example at least 99% identity) to SEQ ID NO:12.
In an embodiment of the method of the invention, the Pichia yeast comprises a genetic sequence having a global nucleotide identity at least 98% (for example at least 99%) to the combination of SEQ ID NOs: 1-12. By the term “combination of SEQ ID NOs: 1-12” it is meant that the sequence identity comparison is performed against all the individual DNA fragments as if concatenated into a single sequence.
In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:1. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:2. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:3. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:5. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:6. In an embodiment the Pichia yeast comprises a genetic sequence having at least 99% identity to SEQ ID NO:7. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:8. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:9. In an embodiment the Pichia yeast comprises a genetic sequence having at least 99% identity to SEQ ID NO:10. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:11. In an embodiment the Pichia yeast comprises a genetic sequence having at least 98% (for example at least 99%) identity to SEQ ID NO:12.
The names by which yeasts are referred to may change with time. It should be understood that the yeast according to the method of the invention may comprise the genetic sequence identities described in the preceding paragraphs for the Pichia yeast of the invention regardless of the name applied to the yeast.
An aspect of the invention provides a method of preparing a beverage composition comprising fermenting an aqueous acerola extract wherein the fermentation is performed by yeast comprising a genetic sequence having a global nucleotide identity at least 98% (for example at least 99%) to the combination of SEQ ID NOs: 1-12.
In an embodiment, the fermentation is performed in the presence of non-water-soluble components of acerola and the aqueous acerola extract is separated from the non-water-soluble components after fermentation. For example the non-water-soluble components of acerola may be separated from the aqueous acerola extract using a filter system. After fermentation, the aqueous acerola extract becomes fermented acerola extract.
The fermented acerola extract may be packaged as a ready-to-drink beverage, for example packaged in a bottle or a can. The fermented acerola extract may have a concentration of between 2 and 60 wt. % total dissolved solids, for example a concentration of 2 to 25 wt. % total dissolved solids. Additional ingredients such as flavours and preservatives may be added to the fermented acerola extract before it is packaged as a ready-to-drink beverage. The fermented acerola extract may be heat-treated to de-activate or kill the yeast and any spoilage organisms before being packaged. The fermented acerola extract may be passed through a filter to remove the yeast and any spoilage organisms before being packaged.
In an embodiment the aqueous acerola extract is concentrated after being fermented, for example to be packaged as a liquid concentrate suitable to be diluted by the consumer before consumption. The aqueous acerola extract may be concentrated as an intermediate product for the manufacture of ready-to-drink products, for example in a different location. The fermented acerola extract may have a concentration of 25 to 60 wt. % total dissolved solids, for further example a concentration of 50 to 60 wt. % total dissolved solids. The dissolved solids may for example be measured by passing the extract through a fine filter to remove non-dissolved solids, weighing the filtrate to establish the total weight, evaporating the filtrate and then weighing the residue to obtain the weight of the dissolved solids.
The aqueous acerola extract after fermentation (for example the fermented acerola extract) may be concentrated to form a powder, such as a soluble beverage powder. For example, the aqueous acerola extract after fermentation (the fermented acerola extract) may be dried by spray drying or freeze drying to form a soluble beverage powder. For example, the aqueous acerola extract after fermentation may be spray dried together with a carrier such as maltodextrin to form a soluble beverage powder. The soluble beverage powder may be packaged and sold as such, or it may be used as an intermediate product for the manufacture of ready-to-drink products, for example in a different location. The soluble beverage powder may be filled into a container for use in a beverage preparation device. The soluble beverage powder may be combined with other ingredients, for example dry ingredients such as tea, herbal tea, dried fruit, soluble coffee or roast and ground coffee. For example, the soluble beverage powder may be combined with other ingredients and filled into a container for use in a beverage preparation device. The soluble beverage powder may be combined with milk powder or beverage creamer powder and optionally sugar to form a beverage mix. After fermenting the aqueous acerola extract in the presence of the of non-water-soluble components of acerola, the non-water-soluble components of acerola become fermented acerola. In an embodiment, the of non-water-soluble components of acerola, present during the fermentation of the aqueous acerola extract, is separated from the aqueous acerola extract after fermentation and then dried, for example using a rotary drier. The dried non-water-soluble components of acerola may be filled into a container for use in a beverage preparation device, or filled into a permeable bag such as a “tea-bag”. The dried of non-water-soluble components of acerola may be combined with other dry ingredients such as tea, herbal tea, dried fruit, soluble coffee or roast and ground coffee. In the context of the present invention, the term tea refers to the dried leaves, leaf-buds, twigs or stems of the plant Camellia sinensis. The tea may for example be C. sinensis var. sinensis, or C. sinensis var. assamica. The term “herbal tea” refers to infusions made from the dried flowers, fruit, leaves, seeds or roots of plants other than Camellia sinensis.
In an embodiment, the non-water-soluble components of acerola, present during the fermentation of the aqueous acerola extract, are dried together with the aqueous acerola extract after fermentation, for example by freeze drying or spray drying. The dried non-water-soluble components of acerola (e.g. dried fermented acerola) together with dried aqueous acerola extract after fermentation (e.g. dried fermented acerola extract) may be filled into a container for use in a beverage preparation device, or filled into a permeable bag such as a “tea-bag”. The dried non-water-soluble components of acerola, and dried aqueous acerola extract after fermentation may be combined with other dry ingredients such as tea, herbal tea, dried fruit, soluble coffee or roast and ground coffee.
An aspect of the invention provides for the use of acerola fermented with Pichia kluyveri NYSC 5485 (CNCM I-5525) to produce a beverage.
Fermented acerola according to the invention may be obtained in a “solid-state” fermentation, for example adding a starter culture of Pichia yeast to acerola, for example fresh acerola berries or berries that have been squashed to a pulp. The term “solid-state” fermentation refers to fermentation taking place on solid materials. There is liquid water present in a solid-state fermentation, but the term is used in contrast to a liquid fermentation such as may occur in aqueous solution in a fermentation vessel.
An aspect of the invention provides a method of preparing a beverage composition comprising;
The starter culture of yeast may be added as a liquid or a powder to the acerola. The acerola (for example acerola pulp) may have a moisture content of between 45 and 55 wt. % when the starter culture of yeast is added. The acerola (for example acerola pulp) may be treated with steam before fermentation to reduce the quantity of environmental microorganisms before adding yeast. The fermentation may occur at a solids content greater than 40 wt. %, for example greater than 45 wt. %, for further example greater than 50 wt. %.
Drying the fermented acerola may commence while some fermentation continues. For example, the acerola (for example acerola pulp) may be placed in a container such as a tank, the starter culture added and then fermentation allowed to proceed for 1-4 days before the fermented acerola is removed from the container and dried. For further example, the starter culture may be added to the acerola (for example acerola pulp) before the acerola (for example acerola pulp) is slowly dried, for example on a rack or suspended tray. Once fermentation has started, the acerola may be slowly dried whilst fermentation continues. For example the fermented acerola may be dried to a moisture content of below 20 wt. % (for example below 15 wt. %) over a period of between 1 and 30 days, for example between 4 and 20 days. The drying temperature may be less than about 40° C., for example between about 25° C. and 35° C. A fan can be used to blow dry air over the material until the acerola (for example acerola pulp) are dry. The fermented acerola (for example acerola pulp) may be dried in the sun. The acerola pulp may contain acerola skins and seeds.
The yeast may be Pichia, for example Pichia kluyveri, for further example Pichia kluyveri NYSC 5485. The yeast may comprise a genetic sequence having a global nucleotide identity at least 98% (for example at least 99%) to the combination of SEQ ID NOs: 1-12.
The container for the preparation of a beverage when inserted into a beverage preparation device may be in the form of a pod, pad, sachet, pouch, capsule or the like.
The ready-to-drink beverage may be filled into a bottle or can. The fermented acerola may be combined with other extractable materials such as tea, herbal tea, dried fruit, soluble coffee or roast and ground coffee before being extracted with water to form a ready-to-drink beverage.
The fermented acerola may be combined with tea, herbal tea, dried fruit, soluble coffee or roast and ground coffee in a container for the preparation of a beverage when inserted into a beverage preparation device.
Those skilled in the art will understand that they can freely combine all features of the present invention disclosed herein. In particular, features described for the product of the present invention may be combined with the method of the present invention and vice versa. Further, features described for different embodiments of the present invention may be combined. Where known equivalents exist to specific features, such equivalents are incorporated as if specifically referred to in this specification.
Further advantages and features of the present invention are apparent from the figures and non-limiting examples.
An infusion was prepared using organic acerola soluble powder (Raab Vitalfood, Germany) as starting material. A hot infusion was firstly made by adding 20 g of dry starting material in 1000 ml of water at 100°° C., and steeping for 10 min. Afterwards, the infusion was placed in an ice bath until the temperature fell below 30° C. The infusion was then filtered through sieves to remove any additional pieces. The filtrate (aqueous acerola extract) was distributed equally as control (Ref) or for different fermentation variants.
Fermented acerola was made by fermenting the infusion with glucose (2% m/m) and different starter cultures, including Pichia kluyveri NYSC 5485 (CNCM I-5525), P. kluyveri NCYC 246 (the type strain of Pichia kluyveri), P. kluyveri NCYC 2781, commercial brewer's yeast Saccharomyces cerevisiae (SafAle S-33, LeSaffre, France) and a symbiotic culture of bacteria and yeasts (SCOBY) pellicle from Kombucha tea fermentation. All strains (except for SCOBY) were grown from glycerol vial in a food-grade yeast-peptone liquid medium, and inoculated in the reference acerola brew with optical density (OD at 600 nm) of 0.5. All the inoculated infusions were stored at microaerobic condition at 30° C. for 24 h. After the incubation, each fermented infusion underwent filter sterilization (0.2 μm).
The sensory profiles of different variations of acerola infusions were tasted. The control tasted astringent and bitter. The acerola infusion fermented with Saccharomyces cerevisiae had a fruity beer-like character. The acerola fermented with SCOBY had a very sharp acidity. The acerola infusions fermented with the two different Pichia yeasts were very fruity with less perceived bitterness, sourness and astringency compared to the control. No buttery and fatty off notes were identified in the acerola fermented with Pichia yeasts. Acerola fermented with Pichia kluyveri NYSC 5485 was found to have a cleaner aroma profile when compared to that fermented with Pichia kluyveri NCYC 246.
Quantitative volatile profiling of the acerola infusions was conducted by headspace/solid phase microextraction coupled with gas chromatogram and mass spectrometry (HS/SPME-GC-MS). The apparatus used was a gas chromatograph (Agilent Technology 8890 GC System) coupled with a mass spectrometer (Agilent
Technology 7010B TQ).
Initially, 1.0 ml of the acerola infusion samples were incubated in a 10-mL screw-top headspace vial at 30° C. for 10 min, followed by extraction using a SPME fiber (PDMS/DVB, Supelco) at 30° C. for 10 min. All vials were placed in a tray cooled at 6°° C. before analysis. The volatiles were thermally desorbed from the SPME fiber at 250° C. in splitless mode and resolved with a capillary column (DB-WAX, Agilent). The gas chromatograph oven temperature was programed initially at 35° C. for 5 min, then raised to 230°° C. at 4° C./min, then at 230° C. for 10 min. Helium was used as the carrier gas at a flow rate of 1 ml/min. The targeted compounds were identified by pure standards and quantified in MSD ChemStation software (Agilent). All samples were measured in duplicate.
Levels of 3-methylbutyl acetate, 2-methylbutyl acetate, isobutyl acetate, 2-phenylethyl acetate, 2-phenylethanol, 2,3-butanedione, 2-phenylacetaldehyde, ethanol and acetic acid in parts per million after 24 hours are listed in the table below.
P. kluyveri
P. kluyveri
P. kluyveri
S. cerevisiae
The sample fermented with SCOBY had a high level of acetic acid, corresponding to 222 g/kg on a dry basis.
The weight ratios A and B of the aroma components are in the following table.
P. kluyveri
P. kluyveri
P. kluyveri
S. cerevisiae
The samples fermented with a Pichia yeasts (NYSC5485, NCYC2781 and NCYC246) show higher ratios A and B than the control and the samples fermented with S. cerevisiae or SCOBY. P. kluyveri NYSC 5485 delivers a higher value for ratios A and B than the type strain P. kluyveri NCYC 246 or P. kluyveri NCYC 2781.
The genetic sequence of Pichia kluyveri NYSC 5485 (CNCM I-5525) and P. kluyveri NCYC 246 were analysed using PacBio sequencing technology. DNA purification was performed using a Qiagen Gentra Puregene Yeast kit. Twelve DNA fragments were identified for P. kluyveri NYSC 5485 and 15 for the type strain P. kluyveri NCYC 246. The genetic sequences for P. kluyveri NYSC 5485 are filed in electronic form as SEQ ID NO:1-SEQ ID NO:12 and the genetic sequences for P. kluyveri NCYC 246 filed as SEQ ID
NO: 13-SEQ ID NO:27. The mitochondrion DNA was SEQ ID NO:4 for P. kluyveri NYSC 5485 and SEQ ID NO:20 for P. kluyveri NCYC 246.
The genetic sequence of Pichia kluyveri NYSC 5485 (CNCM I-5525) was compared with that of P. kluyveri NCYC 246 using the software OrthoANlu. The global average nucleotide identity was found to be 97.91%.
Correspondences between the different sequences are given in the table below. Some sequences for Pichia kluyveri NYSC 5485 correspond most closely with a combination of sequences for P. kluyveri NCYC 246 and vice versa.
Pichia kluyveri
P. kluyveri
The type strain P. kluyveri NCYC 246 comprised a genetic sequence with a maximum identity to each SEQ ID NO:1-12 taken individually as follows: SEQ ID NO:1, 97.85%; SEQ ID NO: 2, 97.40%; SEQ ID NO:3, 97.86%; SEQ ID NO:4, 99.02%; SEQ ID NO:5, 98.05%; SEQ ID NO:6, 97.93%; SEQ ID NO:7, 98.12%; SEQ ID NO:8, 97.07%; SEQ ID NO:9, 97.20%;
5 SEQ ID NO:10, 98.33%; SEQ ID NO:11, 97.526%; SEQ ID NO:12, 97.77%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 21216398.4 | Dec 2021 | EP | regional |
| 22151536.4 | Jan 2022 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2022/085344 | 12/12/2022 | WO |
