Yeast (
Saccharomyces cerevisiae) Glucan Polysaccharides –
Occurrence, Separation and Application in Food, Feed and Health Industries 57
Only some of these effects can be promoted by regular yeast cell wall preparations.
However separating the bioactivities caused by the selenomethionine-containing yeast
proteins from the activity caused by the polysaccharide parts of selenized yeast cell walls is
difficult. Comparison of genomic activity in tissues taken from animals fed with SelPlex® to
those fed with Bio-Mos® spiked with selenomethionine indicates very large differences in
the regulation of multiple groups of genes for both treatments (Kwiatkowski et al., 2011),
which may indicate that the bioactivity of Sel-Plex® involves cooperation between the
selenoprotein and the polysaccharide components of selenized yeast cell walls.
Indeed, selected extracts from selenized yeast/yeast cell walls (Kwiatkowski et al., 2011)
show potential as future, possible treatments of diseases such as type 2 diabetes, cancer and
Alzheimer’s.
5. β-(1→3)(1→6)-D-glucan as valuable by product from yeast
fermentation
The commercial source from which the bulk yeast cell wall polysaccharides (including β-
glucan) are produced uses the same strains of yeast as are used in fuel alcohol production.
Le Saffre/ADM, Lallemand, Enzyme Development (New York) and DSM Life Sciences
(Delft) are the largest suppliers of yeast for fuel ethanol producers in the United States and
the European Union. Major factors that affect yeast cell wall composition include yeast
strain (Hahn-Hagerdal et al., 2005), growth conditions (growth medium, temperature,
osmotic pressure, toxic metabolites) and the time of harvesting (Aguilar-Uscanaga &
Francois, 2003; Klis et al., 2002; Klis et al., 2006). Fuel alcohol fermentation is a high stress
process (Devantier et al., 2005) and the cell walls of the yeast collected as its byproduct
contain a high amount of β-glucans (Basso et al., 2008; Knauf & Kraus, 2006; Jones &
Ingledew, 1994). In general, yeast strains of Saccharomyces cerevisiae that are used in baking
(baker’s yeast) have a higher β-glucan-to-α-mannan ratio than those that are used for
alcohol fermentation (brewer’s yeast), therefore it is advantageous to use pure baker’s yeast
for producing high quality (1→3)(1→6)-β-D-glucan for medicinal applications (Kim et al.,
2007). The process of separating various yeast components has been heavily patented.
However, the differences in the technologies are minor and in principle do not differ from
the methodology described by Manners and Fleet (1976). The process starts from autolysing
yeast cells at a temperature between 45
o
C and 65
o
C at slightly acidic pH, to release yeast cell
walls that are insoluble and denser than the cytoplasmic contents and can be separated by
centrifugation (Wheatcroft et al., 2002). These steps can be followed by incubating the yeast
cell walls with alkaline protease at a pH of 9 to 10 to solubilize mannans and leave behind
insoluble β-glucan (Zapata et al, 2008), which can then be physically separated from the
liquid fraction by centrifugation and subsequent washing (Sedmak, 2006). Additional
enzymes, like glucoamylase and lipase, can be used to hydrolyze α-glucan from α β-glucan,
which is still present in the cell wall material and to solubilize the residue lipids from cell
membranes. The final step of β-glucan production is a spray-drying that produces a white-
to-maroon colored powder that does not carry any taste or aroma and is useful for feed and
food applications. Further alkaline and acidic treatments of the food-grade β-glucan (Kelly,
The Complex World of Polysaccharides
58
2001) yields high purity (98.5% β-glucan, <0.1% mannan, 0.4% α-glucan, 0.3% protein, 0.2%
chitin) microparticulate β-glucan with reduced molecular weight (from ~1-3 MDa to ~150
kDa) that is much more easily absorbed by the digestive tract and shows improved activity
compared with food-grade products containing only ~65% β-glucan. Even further
hydrolysis produces soluble yeast β-glucan (Jamas et al., 1998; Lee et al., 2001) that still
retains most of the particular β-glucan bioactivities (Janusz et al., 1986; Wakshull et al.,
1999).
Yeast
Saccharomyces cerevisiae, its cell wall and products of its fractionation are generally
recognized as safe (GRAS) by the US Food and Drug Administration (FDA, 1997), and they
can be legally used as food ingredients but not as food additives. The European Food Safety
Authority (EFSA) issued an opinion that yeast β-glucans are a “safe food ingredient” (EFSA,
2011) that can be used as a “food supplement” up to 375 mg/day and in foods for “particular
nutritional uses” at dose levels up to 600 mg/day. (The uses of yeast cell wall as an animal
feed ingredient were discussed in section 4 of this chapter).
Food-grade yeast β-glucans such as BetaRight® and WGP® (Biothera, Inc.) are used as
ingredients in baked foods, beverages, ceral, yogurt, fruit juices, chocolate and as food
thickeners in salad dressings, ice cream, mayonnaise, sauces and cheese. The majority of
these applications have been patented (Zechner-Krpan et al., 2009; Thammakiti et al., 2004)
and a critical review of 300 patented applications is available (Laroche & Michaud, 2007).
Yeast β-glucans improve food rheological properties, gelling, water and oil-holding
properties, without impacting its taste or odor (Petravic-Tominac et al., 2011). Beta-glucans
also add health benefits (Laroche & Michaud, 2007) like antioxidative, bacteriostatic and
immunostimmulating activities. Cosmetic products used in skin treatment contain yeast β-
glucans as moisturizing and moisture-retaining components that also provide a proper
moistening feeling. Because of its emulsion-stabilizing effects, pleasant texture and
antioxidant activity yeast β-glucans can prevent skin injuries caused by solar radiation and
therefore are used in sun-screens, oils and gels (Michiko & Yutaka, 2007). Deodorants
containing yeast β-glucans have proved to be useful in oral preparations, mouthwashes and
diapers (Michiko et al., 2005). Acid-treated cell walls (AYC) can be used as new binders in
pharmaceutical formulations and, when mixed with traditional fillers like
hydroxypropylcellulose or polyvinylpyrrolidone, yield harder pills with very short (~2 min)
dissolution times (Yusa et al., 2002). Its adhesive and biological properties can be also
utilized in producing coating for surgical instruments (Klein, 2003) and in the manufacture
of packaging for the food industry (Cope, 1987). Its antibacterial and antiviral properties
have found application in the control of plant pests (Kitagawa, 2007) and viral invasions
(Slovakova et al., 1997).
6. Medicinal application of native and chemically modified forms of
β-(1→ 6)(1→3)-D-glucan
Approximately 2000 research and review papers covering β-(1→6)(1→3)-D-glucan
bioactivity and its medicinal applications have been published since the 1960’s, and the