Summary
Hemicell® is a patented enzyme-based feed ingredient produced by
ChemGen Corp. The product's primary enzymatic activity, endo-B-D-Mannanase
degrades galactomannan polymers.
In this analysis, historical evidence for the anti-nutritive effect of
galactomannan in chicken feed is reviewed and compared to the occurrence of
galactomannan in common feed components. It is demonstrated that, based on the
historical evidence, a broiler diet composed of 30% soybean meal and 60% corn
contains an amount of galactomannan expected to deteriorate broiler performance
by about 7.5 points in adjusted feed conversion.
Analysis of Literature Examples
Available literature (1-8) was reviewed for the effect of galactomannan
inclusion in feed on growth performance using one consistent calculation
method. The studies included in this analysis were done at different times
(between 1964-1983) by different research groups with widely varying diet
ingredients and control feed efficiencies. Also, the period of the growth cycle
analyzed varied. For example the data could be from day 1 to 14, 1 to 21, or
from day 28 to 56, or could include a complete growth cycle.
The data in the publications were reported in different ways. In this
re-analysis, performance data is reported as "points" calculated as weight
points and feed/gain points in the following way. For data provided up to 14 or
21 days, a weight point was calculated by the following formula:
(lb.test - lb.control) / (0.4 lb/point) = weight points
For older birds, the value of 0.06 lb/point was used in the calculation.
The feed/gain (F/G) points were calculated as:
(F/G control - F/G test) / (0.01/point) = F/G points
The sum of the F/G points and weight points (usually a negative number) are
plotted in figure 1a as negative points. In all cases when significant amounts
of galactomannan were included in the feeds, the major contribution to the
deterioration in performance was from the worsening of the Feed/Grain
calculation. A linear curve was fit to the data (setting zero F/G points at
zero percent added guar gum) after removing a few data points at the extremes
(positive points or negative points less than negative 200).
Sufficient information to clearly calculate exactly how much galactomannan was
added to the various feed formulations was generally not available in the
publications. For example, guar meal was typically the source of galactomannan,
but the galactomannan content of the guar meal was not always measured.
However, in two cases (1,8), both the protein content and the galactomannan
content of the guar meal used was reported. A plot of this correlation is shown
in Figure 2. In the cases where only the protein content of the meal was given,
the percent of gun was predicted from Figure 2. Since the percent of gum in the
beans from which the meal was prepared is likely to vary with the exact variety
and growth conditions, these estimates likely contribute to the scatter seen in
the data. When purified guar gum was used, this analysis assumes it is 100%
galactomannan although there could be some impurity such as protein. It also
assumes that "guar splits", the raw material used to make guar gum after
removal from guar meal, is composed mostly of guar gum.
Despite the diverse nature of the data and the difficulty in exactly matching
the nutritional content of control and test diets, there is a clear overall
trend showing an increase in negative points proportional to the dose of
galactomannan gum in the diet. In 75 of 81 tests there was a negative effect of
galactomannan inclusion in the diet (Figure 1a). The anti-nutritional effect of
guar meal and other galactomannan containing materials such as copra (9,10) has
prevented the effective commercial use of these materials despite a favorable
protein content (11,5).
Galactomannan Content of Commonly Used Feed Ingredients
Legume seed (including soybean, and alfalfa) are known to contain
galactomannans. Of 163 types of legume seeds tested, 75% contained
"mucilage-yielding" endosperms (12). Mucilage is a classical term for viscous
polysaccharide polymers that include galactomannan. On a weight basis,
galactomannan is five times as viscous as starch, and is one of the most
viscous polysaccharides known (16). Mannose and galactose are also present as
significant proportions of the non-starch polysaccharides of many commonly used
feedstuffs (Table 1) such as wheat, maize, sorghum, barley, oats and rye (13)
and canola meal (14). This type of composition data does not establish the
exact content of galactomannan since other types of polymers could contain
mannose and galactose. It does indicate the upper limit of galactomannan
content. Soybean meal, one of the most widely used feed components has the
largest mannose and galactose percentages of the feed components listed in
Table 1. The galactomannan from soybeans has been purified and soybean hulls
have a high content of galactomannan (15).
We believe the effectiveness of Hemicell® in improving the
feed/grain performance of poultry and swine feeds is primarily due to the
degradation of galactomannans that are present in currently used feed
formulations by the endo-B-D-Mannanase enzyme activity present in
Hemicell®. Figure 1b is the expanded view of the curve in figure
1a, showing expected effects of low amounts of galactomannan on broiler
performance.
In a diet with 30% soybean meal and 60% corn and assuming all the mannose is
derived from the galactomannan, a galactomannan content of 0.424% is predicted.
From figure 1b, a performance deterioration of 7.5 points would be expected
from such a galactomannan content.
In controlled broiler pen trials using diets containing 30% soybean meal and
60% corn, the addition of Hemicell® improved the adjusted feed
conversion on average by 7.7 points. Thus, Hemicell®'s digestion
of galactomannan polymer improved broiler performance by an amount consistent
with the prediction from historical data.
Table 1: Mannose and Galactose Content of Non-Starch Polysaccharides of Some Common Feed Ingredients
| Feed Component |
% of Dry Weight Total Non-Starch Polysaccharides |
Monosaccharides as % of Non-Starch Polysaccharides Mannose |
Monosaccharides as % of Non-Starch Polysaccharides Galactose |
| From Chesson (13) |
| wheat |
11.9 |
0.9 |
2.7 |
| wheat bran |
33.7 |
0.2 |
1.8 |
| maize (No. 3) |
11.7 |
0.8 |
3.6 |
| sorghum grain |
12.2 |
0.8 |
1.6 |
| soybean meal (48) |
22.7 |
5.4 |
20.7 |
| rapseed meal |
19.6 |
2.5 |
7.7 |
| oats |
16.0 |
1.9 |
2.5 |
| rye |
12.2 |
5.7 |
3.0 |
| From Slominski (14) |
| canola meal (rapeseed) |
13.7* |
4.8 |
19.3 |
*non-starch and non-cellulose polysaccharides (cellulose was reported as 4.89%)
References
1. Anderson, J.O. and R.E. Warnick (1964) Value of enzyme supplements in
rations containing certain legume seed meals or gums. Poultry Science 43:
1091-1097.
2. Vohra, P. and F.H. Kratzer (1964) The use of guar meal in chicken rations.
Poultry Science 43: 502-503.
3. Vohra, P. and F.H. Kratzer (1965) Improvement of guar meal by enzymes.
Poultry Science 44: 1201-1205.
4. Couch, J.R., Y.K. Bakshi, T.M. Ferguson, E.B. Smith and C.R. Creger (1967)
The effect of processing on the nutritional value of guar meal for broiler
chicks. British Poultry Science 8: 243-250.
5. Verma, S.V.S. and J.M. McNab (1982) Guar meal in diets for broiler
chickens. British Poultry Science 23: 95-105.
6. Ray, S., M.H. Pubolos and J. McGinnis (1982) The effect of a purified guar
degrading enzyme on chicken growth. Poultry Science 61: 488-494.
7. Patel, M.B. and J. McGinnis (1985) The effect of autoclaving and enzyme
supplementation of guar meal on the performance of chicks and laying hens.
Poultry Science 64: 1148-1156.
8. Nagpal, M.L., O.P. Agrawal and I.S.Bhatia (1971) Chemical and biological
examination of guar-meal (Cyamopsis tetragonoloba L.) Indian J. Anim. Sci. 41:
283-293.
9. A.F. Zamora, M.R. Calapardo and E.S. Luis (1988) Nutritional value of copra
meal treated with bacterial mannanase in broiler diets. Proceedings of the
Eighth International Conference on Global Impacts of Applied Microbiology and
International Conference on Applied Biology and Biotechnology. August 1-5, 1988
(Hong Kong), Chinese University Press, pp 497-507.
10. Rao, G.R., T.R. Doraiswamy, K. Indira, B. Mahadeviah and M.R.
Chandrasekhara (1965) Effect of fiber on the utilization of protein in coconut
cake: metabolism studies on children. J. Exptl. Biol. 3: 163-165.
11. Molina, M.R. and P.A. LaChance (1973) Studies on the utilization of
coconut meal: a new enzymatic - chemical method for fiber free protein
extraction of defatted coconut flour. J. Food Sci. 38: 607-610.
12. Anderson, E. (1949) Ind. Eng. Chem. 41: 2887.
13. Chesson, A. (1987) Supplementary enzymes to improve the utilization of
pig and poultry diets. In Recent Advances in Animal Nutrition -1987, Haresign,
W. and D.J.A. Cole (eds), pp71-89, Butterworths, Boston, MA.
14. Slominski, B.A. and L.D. Campbell (1990) Non-starch polysaccharides of
canola meal: quantification, digestibility in poultry and potential benefit of
dietary enzyme supplementation. J. Sci. Food Agric. 53: 175-184.
15. Whistler, R.L. and J. Saarnio (1957) Galactomannan from soybean hulls.
J. Am. Chem. Soc. 79: 6055-6057.
16. Whistler, R.L. and C.L. Smart (1953) Galactomannans, Chapter XI (In)
"Polysaccharide Chemistry", Academic Press, New York.
Further References
- Maisonnier, S., Gomez, J., Carre, B. 2001. Nutrient digestibility and intestinal viscosities in broiler chickens
fed on wheat diets, as compared to maize diets with added guar gum. British Poultry Science (2001), 42: (102-110)
- Bosscher, D., Van caillie-Bertrand, M., Deelstra, H., 2003. Do thickening properties of locust bean gum affect
the amount of calcium, iron and zinc available for absorption from infant formula? In vitro studies.
International Journal of Food sciences and Nutrition,2003, Volume 54, Number 4, 261-268.
- Gulliford, M.C., Bicknell, E.J., Scarpello, J.H.B., 1988. Effect of Guar on amino acid absorption and the
blood glucose, insulin, C-peptide and glucagons responses to jejunal amino acid and glucose perfusion in man.
European Journal of Clinical Nutrition, 1988, 42, 871-876.
- Torsdottir, I., Alpsten, M., Andersson, H., Einarsson, S., 1989. Dietary guar gum effects on postprandial
blood glucose, insulin and hydroxyproline in humans. American Institute of Nutrition, 1989, 0022-3166/89.
- Mariotti, F., Pueyo, M.E., Tome, D., Benamouzig, R., Mahe, S., 2001. Guar gum does not impair the absorption
and utilization of dietary nitrogen but effects early endogenous urea kinetics in humans. Am J Clin Nutr 2001, 74:487-93.
- Nieuwenhoven, M. A., Kovacs, E., Brummer, R., Westerterp-Plantenga, M.S., Brouns, F., 2001. The effect
of different dosages of guar gum on gastric emptying and small intestinal transit of a consumed semisolid meal.
Journal of the American College of Nutrition, 20s01, Vol. 20, No. 1, 87-91.
- Williams, J.A., Lai, C., Corwin, H., Ma, Y., Maki, K., Garleb, K.A., Wolf, B.W., 2004. Inclusion of Guar
Gum ans Alginate into a Crispy Bar improves Postprandial Glycemia in Humans. American Society for
Nutritional Sciences, 2004, 022-3166/04.