Production of a saccharide composition comprising glucans and mannans by alkaline and acid hydrolysis of yeast cells
The present invention is directed to a method of production of an immunostimulatory composition having a saccharide fraction, the method including the steps of hydrolyzes of yeast cells and recovering the soluble fraction. The saccharide fraction having composition thus obtained may be incorporated as a food or beverage component or be used as a pharmaceutical for treatment of specific conditions.
1. A soluble immunostimulatory composition comprising an effective amount of soluble fraction produced by a method comprising the steps of:
(i) providing yeast cell wall material;
(ii) subjecting the yeast cell wall material to hydrolysis with alkali at a pH of 9 to 14, followed by hydrolysis with acid at pH 1.5 to 4, and then optionally neutralizing the hydrolyzed material; and
(iii) separating a soluble fraction from the hydrolyzed material obtained in step (ii);
wherein the soluble fraction obtained in step iii) comprises starch, water-soluble mannan in an amount from 5-25% w/w dry weight of the total soluble fraction, and water-soluble beta-1-6 glucan in an amount from 0.001-10% w/w dry weight of a total soluble fraction,
wherein the water-soluble mannan comprises mannose epitopes and at least 5% of the mannose epitopes are Manα3Manα2-containing saccharides, and
wherein the soluble fraction has a mannan/starch ratio of at least about 0.95.
2. The composition of claim 1 , wherein the amount of Manα3Manα2-containing saccharides is at least 5%.
3. The composition of claim 1 , wherein
step ii) comprises subjecting said yeast cell wall material to hydrolysis with alkali at a pH 9 to 14 and a temperature of 10° to 100° C. for 10 min to 18 hours and hydrolysis with acid at a pH 1.5 to 4 and a temperature of 30° to 100° C. for 1 to 48 hours, and then neutralising the hydrolyzed material.
4. The composition of claim 1 , wherein the soluble fraction obtained in step iii) is subjected to further fractionation.
5. The composition of claim 4 , wherein said fractionation is performed by chromatography, phase separation, precipitation, or ultrafiltration.
6. The composition of claim 5 , wherein said fractionation is performed by ultrafiltration.
7. The composition of claim 6 , wherein the ultrafiltration is performed with a membrane cut-off of at least 500 Da to obtain an ultrafiltrated soluble saccharide fraction.
8. The composition of claim 1 , wherein the soluble fraction comprises water-soluble beta 1-6 glucan in an amount from 0.005-5% w/w dry weight of the total soluble fraction.
9. The composition of claim 1 , wherein the soluble fraction comprises water-soluble beta1-6 glucan in an amount from 0.01-3% w/w dry weight of the total soluble fraction.
10. The composition according to claim 1 , wherein the composition is selected from the group consisting of: food supplement, pharmaceutical, nutraceutical, and animal feed.
11. A method of treating a subject in need of immunostimulation, comprising administering to the subject an effective amount of the composition according to claim 1 .
12. A method for producing a soluble immunostimulatory composition that contains a soluble saccharide fraction, comprising the steps of:
(i) providing yeast cell wall material;
(ii) subjecting the yeast cell wall material to hydrolysis with alkali at a pH of 9 to 14, followed by hydrolysis with acid at pH 1.5 to 4, and then optionally neutralizing the hydrolyzed material; and
(iii) separating a soluble fraction from the hydrolyzed material obtained in step (ii);
wherein the soluble fraction obtained in step iii) comprises starch, water-soluble mannan in an amount from 5-25% w/w dry weight of the total soluble fraction, and water-soluble beta-1-6 glucan in an amount from 0.001-10% w/w dry weight of a total soluble fraction,
wherein the water-soluble mannan comprises mannose epitopes and at least 5% of the mannose epitopes are Manα3Manα2-containing saccharides, and
wherein the soluble fraction has a mannan/starch ratio of at least about 0.95.
13. The method of claim 12 , further comprising step iv) subjecting the soluble fraction of step iii) to fractionation.
14. The method of claim 12 , wherein water solubility of the composition is at least 95%.
15. The method of claim 12 , wherein material is not fractionated between acid and alkaline hydrolysis in step ii), or wherein material is fractionated between hydrolysis with acid and alkaline in step ii) and both soluble and non-soluble fractions are subjected to a second hydrolysis.
16. The method of claim 12 , wherein step (ii) comprises subjecting the yeast cell wall material to hydrolysis with alkali at a pH of 9 to 14 at a temperature of 10° C. to 100° C. for 10 minutes to 18 hours, followed by hydrolysis with acid at pH 1.5 to 4 at a temperature of 30° C. to 100° C. for 1 to 48 hours, and then neutralizing the hydrolyzed material.
17. The method of claim 13 , wherein said fractionation is performed by ultrafiltration with a membrane cut-off of at least 500 Da to obtain an ultrafiltrated soluble saccharide fraction.
18. A composition produced by the method of claim 12 , wherein the saccharide fraction comprises 1,6-linked glucose monomers and mannans, and wherein the ratio of 1,6-linked glucose monomers and mannans is 1 to 40 and optionally wherein the saccharide fraction comprises β1-6 glucan 0.001-10% of the dry weight and mannan 1.0-50% of the dry weight.