Yeast flocculation

Last updated

Yeast flocculation typically refers to the clumping together (flocculation) of brewing yeast once the sugar in a wort has been fermented into beer. In the case of "top-fermenting" ale yeast ( Saccharomyces cerevisiae ), the yeast creates a krausen, or barm on the top of the liquid, unlike "bottom-fermenting" lager yeast ( Saccharomyces pastorianus ) where the yeast falls to the bottom of the brewing vessel.[ citation needed ]

Contents

Process

Cell aggregation occurs throughout microbiology, in bacteria, filamentous algae, fungi and yeast. [1] Yeast are capable of forming three aggregates; mating aggregates, for DNA exchange; chain formation; and flocs as a survival strategy in adverse conditions. [2] Industrial brewing strains rarely mate. Therefore, only chain formation and flocculation are of relevance to the brewing industry.

Yeast flocculation is distinct from agglomeration (‘grit’ formation), which is irreversible and occurs most commonly in baker's yeast when strains fail to separate when resuspended. [3] Agglomeration only occurs following the pressing and rehydration of yeast cakes and both flocculent and non-flocculent yeast strains have been shown to demonstrate agglomeration. [4] It is also distinct from the formation of biofilms, which occur on a solid substrate.

Louis Pasteur is erroneously credited with first describing flocculation of brewer’s yeast. Brewer's yeast flocculation has been the subject of many reviews. [5] Flocculation has been defined as the reversible, non-sexual aggregation of yeast cells that may be dispersed by specific sugars [6] or EDTA. [7] The addition of nutrients other than sugars has been demonstrated not to reverse flocculation. [8] This is as opposed to mating aggregates formed as a prelude to sexual fusion between complementary yeast cells. [9]

For flocculation to occur the yeast must be flocculent and certain environmental conditions [10] must be present. Several factors are important in cell-to-cell binding such as surface charge, hydrophobic effects and zymolectin interactions. [11] The importance of these forces in brewing yeast flocculation was unrecognized in the past but work by Speers et al. (2006) [12] have indicated the importance of zymolectin and hydrophobic interactions. As the cells are too large to be moved by Brownian motion, for binding of two or more cells to occur the cells must be subjected to low level of agitation.

Zymolectin interaction theory

The accepted mechanism of flocculation involves a protein-carbohydrate model. [13] Fully flocculent yeast cells exhibit carbohydrate α-mannan receptors and protein zymolectins. [14] Zymolectins are so termed as they may not be true bivalent lectins. [15] [16] It has been suggested that zymolectin interactions between the protein and mannan moities results in the flocculation phenotype [17] with Ca2+ ions required for the correct conformation of the zymolectins. Co-flocculation between Kluyveromyces and Schizosaccharomyces has been shown to be by a “lectinic” mechanism. [18]

Flocculation zymolectins and phenotypes

Three flocculation phenotypes have been elucidated based on the zymolectins they produce: Flo1 (Stratford and Assinder, 1991) NewFlo (Stratford and Assinder, 1991) and Mannose Insensitive (MI). [19] These flocculation phenotypes differ in the time of the onset of flocculation and the sugar inhibition of flocculation. The genetic control of yeast flocculation has not been extensively studied. Recent reports suggest genes encoding lectin-like proteins exhibit close sequence homology. [20] Furthermore, it seems that FLO genes have interchangeable functions that can compensate for one another. [21]

Flocculation phenotypes

The Flo1 phenotype is inhibited by mannose [22] occurs in both ale and lager strains. [23]

The NewFlo phenotype differs from that of Flo1 in several ways. Firstly NewFlo flocculation is inhibited by mannose, glucose and maltose. [24] Secondly the NewFlo lectin is putatively encoded by the FLO10 gene. [25] Studies by the Speers group have indicated little change in zymolectin levels through a fermentation. It is argued that lectin maturation occurs some fourteen hours after the cessation of cell division [26] and is therefore not concomitant with entry into stationary phase, although this is strain dependent. [27] However the molecular proof of this maturation is near non-existent. The picture is complicated by changes in cell surface hydrophobicity and CO2 driven shear which confounds flocculation measurements often erroneously solely attributed to zymolectin interactions. While flocculation (clumping and settling) occurs at this time, this flocculation occurs as a result of changes in hydrophobicity and a decline in shear due to which is in turn to low CO2 evolution.

Related Research Articles

<span class="mw-page-title-main">Mannose</span> Chemical compound

Mannose is a sugar monomer of the aldohexose series of carbohydrates. It is a C-2 epimer of glucose. Mannose is important in human metabolism, especially in the glycosylation of certain proteins. Several congenital disorders of glycosylation are associated with mutations in enzymes involved in mannose metabolism.

<i>Saccharomyces cerevisiae</i> Species of yeast

Saccharomyces cerevisiae is a species of yeast. The species has been instrumental in winemaking, baking, and brewing since ancient times. It is believed to have been originally isolated from the skin of grapes. It is one of the most intensively studied eukaryotic model organisms in molecular and cell biology, much like Escherichia coli as the model bacterium. It is the microorganism behind the most common type of fermentation. S. cerevisiae cells are round to ovoid, 5–10 μm in diameter. It reproduces by budding.

<i>Candida albicans</i> Species of fungus

Candida albicans is an opportunistic pathogenic yeast that is a common member of the human gut flora. It can also survive outside the human body. It is detected in the gastrointestinal tract and mouth in 40–60% of healthy adults. It is usually a commensal organism, but it can become pathogenic in immunocompromised individuals under a variety of conditions. It is one of the few species of the genus Candida that cause the human infection candidiasis, which results from an overgrowth of the fungus. Candidiasis is, for example, often observed in HIV-infected patients. C. albicans is the most common fungal species isolated from biofilms either formed on (permanent) implanted medical devices or on human tissue. C. albicans, C. tropicalis, C. parapsilosis, and C. glabrata are together responsible for 50–90% of all cases of candidiasis in humans. A mortality rate of 40% has been reported for patients with systemic candidiasis due to C. albicans. By one estimate, invasive candidiasis contracted in a hospital causes 2,800 to 11,200 deaths yearly in the US. Nevertheless, these numbers may not truly reflect the true extent of damage this organism causes, given new studies indicating that C. albicans can cross the blood–brain barrier in mice.

<span class="mw-page-title-main">Lectin</span> Carbohydrate-binding protein

Lectins are carbohydrate-binding proteins that are highly specific for sugar groups that are part of other molecules, so cause agglutination of particular cells or precipitation of glycoconjugates and polysaccharides. Lectins have a role in recognition at the cellular and molecular level and play numerous roles in biological recognition phenomena involving cells, carbohydrates, and proteins. Lectins also mediate attachment and binding of bacteria, viruses, and fungi to their intended targets.

In evolutionary biology, inclusive fitness is one of two metrics of evolutionary success as defined by W. D. Hamilton in 1964:

<span class="mw-page-title-main">Flocculation</span> Process by which colloidal particles come out of suspension to precipitate as floc or flake

In colloidal chemistry, flocculation is a process by which colloidal particles come out of suspension to sediment in the form of floc or flake, either spontaneously or due to the addition of a clarifying agent. The action differs from precipitation in that, prior to flocculation, colloids are merely suspended, under the form of a stable dispersion and are not truly dissolved in solution.

<span class="mw-page-title-main">Concanavalin A</span> Lectin (carbohydrate-binding protein) originally extracted from the jack-bean

Concanavalin A (ConA) is a lectin originally extracted from the jack-bean. It is a member of the legume lectin family. It binds specifically to certain structures found in various sugars, glycoproteins, and glycolipids, mainly internal and nonreducing terminal α-D-mannosyl and α-D-glucosyl groups. Its physiological function in plants, however, is still unknown. ConA is a plant mitogen, and is known for its ability to stimulate mouse T-cell subsets giving rise to four functionally distinct T cell populations, including precursors to regulatory T cells; a subset of human suppressor T-cells is also sensitive to ConA. ConA was the first lectin to be available on a commercial basis, and is widely used in biology and biochemistry to characterize glycoproteins and other sugar-containing entities on the surface of various cells. It is also used to purify glycosylated macromolecules in lectin affinity chromatography, as well as to study immune regulation by various immune cells.

<i>Saccharomyces</i> Genus of fungi

Saccharomyces is a genus of fungi that includes many species of yeasts. Saccharomyces is from Greek σάκχαρον (sugar) and μύκης (fungus) and means sugar fungus. Many members of this genus are considered very important in food production where they are known as brewer's yeast, baker's yeast and sourdough starter among others. They are unicellular and saprotrophic fungi. One example is Saccharomyces cerevisiae, which is used in making bread, wine, and beer, and for human and animal health. Other members of this genus include the wild yeast Saccharomyces paradoxus that is the closest relative to S. cerevisiae, Saccharomyces bayanus, used in making wine, and Saccharomyces cerevisiaevar. boulardii, used in medicine.

Pattern recognition receptors (PRRs) play a crucial role in the proper function of the innate immune system. PRRs are germline-encoded host sensors, which detect molecules typical for the pathogens. They are proteins expressed mainly by cells of the innate immune system, such as dendritic cells, macrophages, monocytes, neutrophils, as well as by epithelial cells, to identify two classes of molecules: pathogen-associated molecular patterns (PAMPs), which are associated with microbial pathogens, and damage-associated molecular patterns (DAMPs), which are associated with components of host's cells that are released during cell damage or death. They are also called primitive pattern recognition receptors because they evolved before other parts of the immune system, particularly before adaptive immunity. PRRs also mediate the initiation of antigen-specific adaptive immune response and release of inflammatory cytokines.

Rhamnose is a naturally occurring deoxy sugar. It can be classified as either a methyl-pentose or a 6-deoxy-hexose. Rhamnose predominantly occurs in nature in its L-form as L-rhamnose (6-deoxy-L-mannose). This is unusual, since most of the naturally occurring sugars are in D-form. Exceptions are the methyl pentoses L-fucose and L-rhamnose and the pentose L-arabinose. However, examples of naturally-occurring D-rhamnose include some species of bacteria, such as Pseudomonas aeruginosa and Helicobacter pylori.

The terms glycans and polysaccharides are defined by IUPAC as synonyms meaning "compounds consisting of a large number of monosaccharides linked glycosidically". However, in practice the term glycan may also be used to refer to the carbohydrate portion of a glycoconjugate, such as a glycoprotein, glycolipid, or a proteoglycan, even if the carbohydrate is only an oligosaccharide. Glycans usually consist solely of O-glycosidic linkages of monosaccharides. For example, cellulose is a glycan composed of β-1,4-linked D-glucose, and chitin is a glycan composed of β-1,4-linked N-acetyl-D-glucosamine. Glycans can be homo- or heteropolymers of monosaccharide residues, and can be linear or branched.

The green-beard effect is a thought experiment used in evolutionary biology to explain selective altruism among individuals of a species.

<span class="mw-page-title-main">Langerin</span> Protein found in Homo sapiens

Langerin (CD207) is a type II transmembrane protein which is encoded by the CD207 gene in humans. It was discovered by scientists Sem Saeland and Jenny Valladeau as a main part of Birbeck granules. Langerin is C-type lectin receptor on Langerhans cells (LCs) and in mice also on dermal interstitial CD103+ dendritic cells (DC) and on resident CD8+ DC in lymph nodes.

The mannose receptor is a C-type lectin primarily present on the surface of macrophages, immature dendritic cells and liver sinusoidal endothelial cells, but is also expressed on the surface of skin cells such as human dermal fibroblasts and keratinocytes. It is the first member of a family of endocytic receptors that includes Endo180 (CD280), M-type PLA2R, and DEC-205 (CD205).

Anti-Saccharomyces cerevisiae antibodies (ASCAs) are antibodies against antigens presented by the cell wall of the yeast Saccharomyces cerevisiae. These antibodies are directed against oligomannose sequences α-1,3 Man n. ASCAs and perinuclear antineutrophil cytoplasmic antibodies (pANCAs) are the two most useful and often discriminating biomarkers for colitis. ASCA tends to recognize Crohn's disease more frequently, whereas pANCA tend to recognize ulcerative colitis.

<span class="mw-page-title-main">LMAN1</span> Protein-coding gene in the species Homo sapiens

Protein ERGIC-53 also known as ER-Golgi intermediate compartment 53 kDa protein or lectin mannose-binding 1 is a protein that in humans is encoded by the LMAN1 gene.

<i>N</i>-linked glycosylation Attachment of an oligosaccharide to a nitrogen atom

N-linked glycosylation, is the attachment of an oligosaccharide, a carbohydrate consisting of several sugar molecules, sometimes also referred to as glycan, to a nitrogen atom, in a process called N-glycosylation, studied in biochemistry. The resulting protein is called an N-linked glycan, or simply an N-glycan.

Epistasis refers to genetic interactions in which the mutation of one gene masks the phenotypic effects of a mutation at another locus. Systematic analysis of these epistatic interactions can provide insight into the structure and function of genetic pathways. Examining the phenotypes resulting from pairs of mutations helps in understanding how the function of these genes intersects. Genetic interactions are generally classified as either Positive/Alleviating or Negative/Aggravating. Fitness epistasis is positive when a loss of function mutation of two given genes results in exceeding the fitness predicted from individual effects of deleterious mutations, and it is negative when it decreases fitness. Ryszard Korona and Lukas Jasnos showed that the epistatic effect is usually positive in Saccharomyces cerevisiae. Usually, even in case of positive interactions double mutant has smaller fitness than single mutants. The positive interactions occur often when both genes lie within the same pathway Conversely, negative interactions are characterized by an even stronger defect than would be expected in the case of two single mutations, and in the most extreme cases the double mutation is lethal. This aggravated phenotype arises when genes in compensatory pathways are both knocked out.

<span class="mw-page-title-main">Yeast in winemaking</span> Yeasts used for alcoholic fermentation of wine

The role of yeast in winemaking is the most important element that distinguishes wine from fruit juice. In the absence of oxygen, yeast converts the sugars of the fruit into alcohol and carbon dioxide through the process of fermentation. The more sugars in the grapes, the higher the potential alcohol level of the wine if the yeast are allowed to carry out fermentation to dryness. Sometimes winemakers will stop fermentation early in order to leave some residual sugars and sweetness in the wine such as with dessert wines. This can be achieved by dropping fermentation temperatures to the point where the yeast are inactive, sterile filtering the wine to remove the yeast or fortification with brandy or neutral spirits to kill off the yeast cells. If fermentation is unintentionally stopped, such as when the yeasts become exhausted of available nutrients and the wine has not yet reached dryness, this is considered a stuck fermentation.

<span class="mw-page-title-main">Grodziskie</span> Style of beer from Poland

Grodziskie is a historical beer style from Poland made from oak-smoked wheat malt with a clear, light golden color, high carbonation, low alcohol content, low to moderate levels of hop bitterness, and a strong smoke flavor and aroma. The taste is light and crisp, with primary flavors coming from the smoked malt, the high mineral content of the water, and the strain of yeast used to ferment it. It was nicknamed "Polish Champagne" because of its high carbonation levels and valued as a high-quality beer for special occasions.

References

  1. (Lewin, 1984; Stratford, 1992)
  2. (Calleja, 1987)
  3. (Guinard and Lewis, 1993)
  4. (Guinard and Lewis, 1993)
  5. (Stewart et al., 1975; Stewart and Russell, 1986; Calleja, 1987; Speers et al., 1992; Jin and Speers, 1999)
  6. (Burns, 1937; Lindquist, 1953, Eddy, 1955; Masy et al., 1992
  7. (Burns, 1937; Lindquist, 1953)
  8. (Soares et al., 2004)
  9. (Calleja, 1987)
  10. (such as agitation, absence of sugars, a microamount of Ca2+, ethanol, etc.; Jin and Speers 1999)
  11. (see following)
  12. Speers, R.A., Wan, Y-Q., Jin, Y-L., and R. J. Stewart, R.J. 2006. Effects of fermentation parameters and cell wall properties on yeast flocculation. J. Inst. Brew. 112:246-254.
  13. (Miki et al., 1982) (figure 1.3)
  14. (section 1.5.4)
  15. (Speers, Smart, Stewart and Jin,1998)
  16. Speers, R.A., Smart, K., Stewart, R., Jin, Y-L., 1998. Zymolectins in Saccharomyces cerevisiae. Letter J. Inst. Brew., 104:298.
  17. (section 4.1)
  18. (El-Behhari et al., 2000)
  19. (Masy et al., 1992; Dengis and Rouxhet, 1997)
  20. (Jin and Speers, 1991, 1999; Smart, 2001)
  21. (Guo et al., 2000)
  22. (Burns, 1937; Miki et al., 1982; Nishihara and Toraya, 1987; Kihn et al., 1988; Stratford, 1989; Stratford and Assinder, 1991)
  23. (Miki, 1982; Stratford and Assinder, 1991; Masy et al., 1992; Smit et al., 1982; Stratford, 1993; Stratford and Carter, 1993; Teunissen et al., 1993; Teunissen et al., 1995a, b; Bony et al., 1997; Braley and Chaffin, 1999; Fleming and Pennings, 2001; He et al., 2002; Verstrepen et al., 2003) and is associated with the FLO1 gene (Watari, 1991 Masy et al., 1992; Stratford, 1993; Stratford and Carter, 1993; Teunissen et al., 1993; Teunissen et al., 1995a, b; Bony et al., 1997; Braley and Chaffin, 1999)
  24. (Stratford and Assinder, 1991; Masy, 1992; Rhymes, 1999)
  25. (Guo et al., 2000; Smart, 2001)
  26. (Stratford, 1989; Stratford and Assinder, 1991; Masy 1992; D’Hautcourt and Smart, 1999)
  27. (D’Hautcourt and Smart, 1999; Verstrepen et al., 2003)