SciELO - Scientific Electronic Library Online

 
vol.34 número2 índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Articulo

Indicadores

Links relacionados

  • En proceso de indezaciónCitado por Google
  • En proceso de indezaciónSimilares en Google

Compartir


South African Journal of Animal Science

versión On-line ISSN 2221-4062
versión impresa ISSN 0375-1589

S. Afr. j. anim. sci. vol.34 no.2 Pretoria  2004

 

Chemical composition, true metabolisable energy content and amino acid availability of grain legumes for poultry

 

 

T.S. BrandI, II, III, #; D.A. BrandtI, II, IV; C.W. CruywagenII

IEisenburg Agricultural Research Centre, Private Bag X1, Elsenburg 7607, South Africa
IIDepartment of Animal Science, University of Stellenbosch, Stellenbosch 7600, South Africa
IIIDept. of Anatomy and Physiology, Faculty of Veterinary Science, University of Pretoria, Pretoria 0002, South Africa
IVAFGRI Feeds, P.O. Box 135, Isando 1600, South Africa

 

 


ABSTRACT

Samples of sweet yellow lupins (Lupinus luteus; n = 4), broad leaf lupins (Lupinus albus; n = 12), narrow leaf lupins (Lupinus angustifolius; n = 8), faba beans (Vicia faba; n = 2), field peas (Pisum sativum; n = 4) and narbon beans (Vicia narbonensis; n = 2) were collected over a two-year period. The physical characteristics (thousand seed and hectolitre mass), chemical composition (dry matter, ash, crude protein (CP), ether extract, acid detergent fibre, neutral detergent fibre and mineral content), energy values (nitrogen corrected true metabolisable energy content (TMEn for roosters)) as well as the lysine and methionine availability (with roosters) of the samples were determined. Lupinus albus had the highest TMEn (12.49 MJ/kg), followed by field peas (11.35 MJ/kg) and narbon beans (11.25 MJ/kg), faba beans (10.90 MJ/kg), L. angustifolius (10.46 MJ/kg) and L. luteus (10.20 MJ/kg). Lupinus luteus had the highest CP concentration (393.6 g/kg) followed by L. albus (381.9 g/kg), L. angustifolius (338.9 g/kg), faba beans (260.0 g/kg), field peas (247.4 g/kg) and narbon beans (237.6 g/kg) (values on a dry matter basis). Lupinus luteus had the highest lysine concentration (22.2 g/kg), followed by L. albus (19.6 g/kg), field peas (19.3 g/kg), L. angustifolius (18.6 g/kg), narbon beans (17.5 g/kg) and faba beans (17.0 g/kg).

Keywords: Lupins, faba beans, field peas, narbon beans, energy content, amino acid availability, poultry


 

 

Introduction

The need for protein in human and animal diets is increasing all over the world. Protein, especially for use in animal feed, is becoming scarcer and more expensive. This is particularly relevant as far as traditional protein sources, such as fish meal and meat and bone meal are concerned. Throughout the world today there is also a growing resistance against the use of animal protein sources in animal feeding (Brand, 2002). It is desirable, therefore, that the nutritional potential of alternative plant protein feeds, such as grain legumes is fully exploited.

Grain legumes contain moderately high levels of protein and amino acids and are promising alternatives (Wiseman, 1987; Brand et al., 1995). Grain legumes that are cultivated in the Mediterranean rainfall area of South Africa include lupins (Lupinus spp), faba beans (Vicia faba), field peas (Pisum sativum) and narbon beans (Vicia narbonensis). Among these lupins normally contain the highest concentration of protein (299-357 g/kg; May et al., 1993), followed by faba beans (234-388 g/kg; Garrido et al., 1991), peas (145-285 g/kg; Reichert & MacKenzie, 1982) and narbon beans (210-228 g/kg; Eason et al., 1990). However, comparative studies on the composition and nutritive value of the different types of lupins (L. luteus, L. albus and L. angustifolius), faba beans and narbon beans for monogastric animals are limited.

This study was conducted to determine and compare the physical characteristics, chemical composition and energy values for poultry of these locally produced legume grains.

 

Materials and Methods

Samples of L. luteus (2 cultivars), L. albus (6 cultivars), L. angustifolius (4 cultivars), faba beans (1 cultivar), peas (1 cultivar) and narbon beans (1 cultivar) cultivated in the Western Cape area of South Africa were collected over a two-year period.

The hectolitre mass (HLM) of the samples was determined by using the upper level of a two level funnel (South African Wheat Board 1986), while the thousand seed mass (TSM) of the samples was determined with an automatic seed counter. Samples were analysed for dry matter (DM), ash, crude protein (CP), ether extract (EE) and minerals by standard AOAC methods (AOAC 1984). Acid detergent fibre (ADF) and neutral detergent fibre (NDF) fractions were determined according to procedures described by Van Soest (1963) and Van Soest & Wine (1967). The non-structural carbohydrate (NSC) content of the samples was calculated according to Smith (1995) as: NSC = 100 - (NDF + CP + EE + Ash). Amino acid analysis, after acid hydrolysis in a sealed tube, was done on a Beckmann Model 6300 amino acid analyser. The nitrogen corrected true metabolisable energy (TMEn) content of the samples was determined with poultry as described by McNab & Blair (1988). Six replicates per sample were used in a metabolism trial with adult roosters. The amino acid availability (lysine and methionine) in the samples, corrected for endogenous amino acid losses was also determined in vivo. Samples collected during the different years from the different cultivars were pooled for each grain legume type for statistical comparison by analysis of variance (Snedecor & Cochran, 1980).

 

Results

The chemical composition, physical characteristics and mineral composition of the different grain legumes are presented in Table 1. No significant differences in CP concentration were observed between L. luteus and L. albus, while L. angustifolius had a lower (P < 0.05) CP level than the other lupin types. Faba beans, field peas and narbon beans did not differ in CP level, but values were lower (P < 0.05) than those of the lupin samples. The EE level of L. albus was 74% higher (P < 0.05) than that of L. luteus and 106% higher (P < 0.05) than L. angustifolius. Faba beans, narbon beans and field peas did not differ in EE content, but observed values were lower (P < 0.05) than those of lupins. Field peas had the lowest ADF concentration followed by faba beans with a 60% higher (P < 0.05) value. No significant differences were observed between narbon beans and faba beans and narbon beans and L. albus, while L. albus had a higher (P < 0.05) ADF content than faba beans. Lupinus luteus had a 17% higher (P < 0.05) ADF concentration than L. albus, while L. angustifolius had a 20% (P < 0.05) higher ADF content than L. luteus. Peas had a lower (P < 0.05) NDF value than the rest of the grain legumes. No significant differences in NDF were observed between faba beans, L. albus and narbon beans. Lupinus luteus and L. angustifolius did not differ significantly from each other, but had higher (P < 0.05) NDF values than the other legume grains. The NSC content was the highest in narbon beans, with the lowest value for faba beans.

The calcium concentration of the samples varied between 1.0 g/kg (faba beans) and 1.9 g/kg (L. angustifolius). Phosphorus concentration varied between 4.2 g/kg (L. angustifolius) and 7.6 g/kg (L. luteus). No extreme differences in trace mineral concentrations occurred except for the manganese concentration of L. albus, which contained approximately 10 times more manganese than the other legume grains.

Peas, faba beans and narbon beans had the highest HLM and did not differ from each other. Lupinus luteus had a lower (P < 0.05) HLM than faba beans and L. angustifolius than narbon beans, while no differences were found between L. luteus and L angustifolius. Lupinus albus had a lower (P < 0.05) HLM than the rest of the grain legume species. Faba beans, L. albus and peas had the highest TSM and differed significantly (P < 0.05) from each other, while no difference occurred between field peas and narbon beans. Lupinus angustifolius and L. luteus did not differ from each other but had a lower (P < 0.05) TSM than narbon beans.

The dry matter digestibility, energy content as well as the lysine and methionine availability of the grain legumes are presented in Table 2. Peas had the highest dry matter digestibility (corrected for endogenous losses) (DMD), but did not differ from values obtained for narbon beans and faba beans. Lupinus albus had a lower (P < 0.05) DMD than narbon beans while no differences were observed between L. albus and faba beans. Lupinus angustifolius and L. luteus did not differ from each other but had a lower (P < 0.05) DMD than L. albus. Lupinus albus had the highest TMEn value, although not significantly higher than that of peas and narbon beans. No significant differences in TMEn were observed between peas, narbon beans, faba beans, L. angustifolius and L. luteus. However, Faba beans, L. angustifolius and L. luteus had a lower (P < 0.05) TMEn than L. albus.

No significant differences were observed in the lysine content of the different grain legumes. The lysine concentration of the different types of legumes varied between 22.2 g/kg for L. luteus to 17.0 g/kg for faba beans. However, lysine content of the sources, expressed as a percentage of protein, differed significantly (P < 0.05). Peas, for example, had a 52% higher value than L. albus. Lupinus luteus and peas were superior in methionine content and did not differ from each other. Lupinus albus had a lower (P < 0.05) methionine content than L. luteus. Lupinus angustifolius, faba beans and narbon beans did not differ from each other but had a lower (P < 0.05) methionine content than L. albus. Methionine content, expressed as percentage of protein was, for example, 80% higher in field peas than in L. angustifolius. No significant differences were observed in lysine or methionine availability coefficients of different grain legumes. The lysine availability coefficients varied from 82.3% for faba beans to 89.8% for narbon beans. Methionine availability coefficients varied from 75.4% for faba beans to 84.5% for narbon beans.

 

Discussion

King (1990) found CP levels for L. albus and L. angustifolius of respectively 387 g/kg DM and 322.5 g/kg DM. These values correspond well to values found in the present study. According to Gous (1998) the lysine availability of L. albus varied between 80.0 - 89.0%, while the methionine availability varied between 81.1 - 90.7%. The lysine availability values were similar to values found in the present study, while Gous (1998) reported higher methionine availabilities. The lysine and methionine availability for L. angustifolius (84.1 and 83.6%) cv Merrit and (82.8 and 77.3%) (Gous 1998) were in the same range as the present values. The TMEn values for L. albus cultivars, Esta, Kiev and Astra (15.18 MJ/kg, 14.82 MJ/kg and 12.82 MJ/kg, respectively) recorded by Gous (1998) were higher than the values obtained in the present study. Similarly, the TMEn values for L. angustifolius obtained in the present study were lower than literature values (Helderberg, 11.41 MJ/kg; Eureka, 10.66 MJ/kg; Merit, 11.31 MJ/kg) (Gous 1998). Bourdon et al. (1987) reported that the EE level in L. albus is 110.3 g/kg, which is higher than the values found in the present study. According to Brand (1996) the ADF and NDF values of South African lupins were 166 g/kg and 198 g/kg (L. albus cv Hamburg), and 234 g/kg and 268 g/kg (L. luteus cv Eureka), respectively. The ADF values obtained in the present study were similar to those values, but the NDF values were lower.

Reichert & MacKenzie (1982) found the CP level of field peas to vary between 145 g/kg and 289 g/kg. Gatel (1984) found the average CP and lysine concentrations of field peas to be 255 g/kg and 18.6 g/kg, respectively. These values were slightly lower than the values found in the present study. The methionine concentration of peas was 2.1 g/kg (Jacyno et al., 1992), which is slightly higher than the value found in this study. The average EE content of the pea cultivars studied was similar to the value (11 g EE/kg) presented by Gatel (1984). According to Bourdon et al. (1987) the ADF and NDF values of peas are 87.0 g/kg and 120.0 g/kg, respectively. The ADF value corresponds with the values in the present study, while their NDF value is higher. According to Savage & Deo (1989) the TMEn value of peas vary from 12.32 to 15.63 MJ/kg, which is higher than values obtained in the present study.

Faba beans normally contain between 280.0 g/kg (Jacyno et al., 1992) and 300.0 g/kg (Bourdon et al., 1987) protein, while the lysine and methionine concentrations are 19.0 g/kg and 2.4 g/kg (Bourdon et al., 1987). Bourdon et al. (1987) found the ME value for faba beans to be 12.75 MJ/kg. This value is considerably higher than the value found in the present study. The ADF and NDF values of faba beans collected in the present study were considerably higher than literature values (95.4 g/kg and 126.4 g/kg respectively; Bourdon et al., 1987), which probably explains the lower observed TMEn value.

The CP content of narbon beans may vary between 260.0 g/kg and 320.0 g/kg (Abd El Moneim 1992). This value is higher than the value found in the present study. Eason et al. (1990) indicated that the methionine and lysine concentration of narbon beans were 2.1 g/kg and 15.6 g/kg, respectively. These values are higher for methionine and lower for lysine than values found in the present study. The apparent nitrogen corrected ME (AMEn) value for narbon beans was 11.93 MJ/kg, with ADF, NDF and EE values of respectively 129.0, 211.0 and 12.0 g/kg (Eason et al., 1990). Ether extract and ADF values are similar to values found in this study, while the NDF was found to be considerably lower in the present study.

The Ca, P and trace element concentrations for lupins, faba beans and peas recorded in the present study compared well with those reported by Thacker & Bowland (1985) and Wiseman (1987).

The superior TMEn value of L. albus is a result of the significantly higher EE content as well as the lower husk to kernel ratio. The husk of L. albus constitutes 180.0 g/kg of the seed, while the husk of L. angustifolius constitutes 260.0 g/kg of the seed. Most of the fibre is situated in the husk of the seed (Brand, 1996). The relatively high TMEn value found with field peas is probably a result of a low fibre content. The higher TMEn value found with narbon beans compared to faba beans may be related to the anti-nutritional factors present in faba beans (Jacyno et al., 1992). The low digestibility and TMEn of L. albus and L. angustifolius were partly a result of the high fraction of ADF, as well as the presence of the pentosans, arabinose and xylose in the fibre which is indigestible in poultry (Jacyno et al., 1992). According to Evans & Cheung (1993) the arabinose and xylose concentrations of L. angustifolius are 47.0 g/kg and 36.0 g/kg, respectively. The pentosan concentrations of soybean, peas and faba beans were 57.0, 48.0 and 32.0 g/kg, respectively. Regression analysis on the data gathered on the chemical composition of lupins revealed that the EE content accounted for 66% of the variation in TMEn, while ash and EE accounted for 74% of the variation in TMEn. Gross energy and CP accounted for 81% of the variation in TMEn.

 

Conclusion

It is evident from this study that large variations occurred in the composition and energy content of grain legumes. Values obtained in this study may be useful in future diet formulations. It is evident that most of the grain legumes contain high levels of fibre, which may limit high inclusion levels of these sources, especially in diets for broilers. Anti-nutritional factors may also be a detrimental factor in the utilization of legume grains (Van der Poel et al., 1993). These include alkaloids (Erikson, 1985), alpha-glycosides (Bourden et al., 1987) and high levels of manganese (Batterham, 1979) in lupins, trypsin inhibitors (Marquart et al., 1976), tannins (Jansman et al., 1993) and haemaglutonin (Marquart et al., 1976) in faba beans as well as high levels of non-starch polysaccharides (Jansman et al., 1993) in all grain legumes. Future studies may be necessary to collect more information on the presence of anti-nutrition factors in grain legumes as well as optimum inclusion levels in poultry diets.

 

Acknowledgements

The authors wish to acknowledge the Elsenburg Agricultural Research Centre and the Protein Research Foundation of South Africa who funded this study.

 

References

Abd El Moneim, A.M., 1992. Narbon vetch (Vicia narbonesis L): A potential feed legume crop for dry areas in western Asia. J. Agron. Crop. Sci. 169, 347-355.         [ Links ]

AOAC, 1984. Official methods of analysis (13th ed.). Association of Official Analytical Chemists, Inc., Washington, DC, 1094 pp.         [ Links ]

Batterham, E.S., 1979. Lupinus albus cv Ultra and Lupinus angustifolius cv Unicrop as protein concentrates for growing pigs. Aust. J. Agric. Res. 30, 369-375.         [ Links ]

Brand, T.S., 2002. A review on research performed in the Mediterranean rainfall area of South Africa on alternative plant protein sources in pig diets. Pig News and Inf. 23, 9N-15N.         [ Links ]

Brand, T.S., 1996. Chemiese samestelling en voedingswaarde van ontdopte lupienesaad. Elsenburg J. 1, 23-25.         [ Links ]

Brand, T.S., Olckers, R.C. & Van der Merwe, J.P., 1995. Evaluation of faba beans (Vicia faba cv Fiord) and sweet lupins (Lupinus albus cv Kiev) as protein source for growing pigs. S. Afr. J. Anim. Sci. 25, 31-35.         [ Links ]

Bourdon, D., Fevreir, C., Perez, J.M., Lebas, F., Leclercq, B., Lessire, M. & Sauveur, B., 1987. Tables of raw materials. In: Feeding non-ruminant livestock. Ed. Wiseman, J., Butterworths, London. pp. 134-205.         [ Links ]

Eason, P.J., Johnson, R.J. & Castleman, G.H., 1990. Effects of dietary inclusion of narbon beans (Vicia narbonensis) on the growth of broiler chickens. Aust. J. Agric. Res. 41, 565-571.         [ Links ]

Erickson, J.P., 1985. Lupins show potential as protein source for livestock. Feedstuffs 57, 22-23.         [ Links ]

Evans, A.J. & Cheung, P.C.K., 1993. The carbohydrate composition of cotyledons and hulls of cultivars of Lupinus angustifolius from Western Australia. J. Sci. Food Agric. 61, 189-194.         [ Links ]

Garrido, A., Gomez-Cabrera, A., Guerrero, J.E. & Marquardt, R.R., 1991. Chemical composition and digestibility in vitro of Vicia faba L cultivars varying in tannin content. Anim. Feed Sci. Technol. 53, 205-211.         [ Links ]

Gatel, F., 1984. Signification de la qualité du fourrage et des stimuli asociés à la prise de nourriture. Ann. Zootech. 33, 111-118.         [ Links ]

Gous, R.M., 1998. Interim report to the Protein Research Trust on the evaluation of canola and lupins for pig and poultry feeding. Department of Animal Science & Poultry Science, University of Natal, Private Bag X1, Scottsville 3209, South Africa. 17 pp.         [ Links ]

Jacyno, E., Czarnecki, R., Owsianny, J., Wejksza, D. & Palusinski, J., 1992a. The effect of seeds of yellow lupin and pea as a source of protein in feeding pigs on their growth rate. Wld Rev. Anim. Prod. 27, 12-14.         [ Links ]

Jacyno, E., Czarnecki, R., Lubowicki, R. & Delecka, A., 1992b. Nutritive value of seeds of yellow lupin (Lupinus luteus), pea (Pisum sativum) and horse beans (Vicia faba) in feeding growing sows. Wld Rev. Anim. Prod. 27, 86-88.         [ Links ]

Jansman, A.J.M., Huisman, J. & Van der Poel, A.F.B., 1993. Ileal and faecal digestibility in piglets fed faba beans (Vicia faba L) varying in tannin content. Anim. Feed Sci. Technol. 43, 83-96.         [ Links ]

King, R.H., 1990. Lupins. In: Non-traditional feed sources for use in swine production. Eds. Thacker, P.A. & Kirkwood, R.N., Butterworths, London. pp. 237-246.         [ Links ]

Marquart, R.R., Campbell, L.D. & Ward, T., 1976. Studies with chicks on the growth depressing factor (s) in faba beans (Vicia faba L var. minor). J. Nutr. 106, 275-284.         [ Links ]

May, M.G., Otterby, D.E., Linn, J.G., Hansen, W.P., Johnson, D.G. & Putnam, D.H., 1993. Lupins (Lupinus albus) as a protein supplement for lactating dairy cows. J. Dairy Sci. 76, 2682-2691.         [ Links ]

McNab, J.M. & Blair, J.C., 1988. Modified assay for true and apparent metabolisable energy based on tube feeding. Br. Poult. Sci. 29, 697-707.         [ Links ]

Reichert, R.D. & MacKenzie, S.L., 1982. Composition of peas (Pisum sativum) varying widely in protein content. J. Agric. Food Chem. 30, 312-317.         [ Links ]

Savage, G.P. & Deo, S., 1989. The nutritional value of peas (Pisum sativum). A literature review. Nutr. Abstr. Rev. (Series A) 59, 67.         [ Links ]

Smith, W.A., 1995. Recent advances in dairy nutrition. Department of Animal Sciences, University of Stellenbosch, Stellenbosch 7600, South Africa.         [ Links ]

Snedecor, G.W. & Cochran, W.G., 1980. Statistical methods (7th ed.). Iowa State University Press. Ames, Iowa, USA. 593 pp.         [ Links ]

South African Wheat Board, 1992. Rules relating to the classification, grading and packing of wheat, barley, oats and rye. South African Wheat Board, P.O. Box 908, Pretoria, 0001, South Africa. 76 pp.         [ Links ]

Thacker, P.A. & Bowland, J.P., 1985. Faba beans: An alternative protein supplement for use in pig diets. Pig News and Inform. 6, 25-30.         [ Links ]

Van der Poel, A.F.B., Huisman, J. & Saini, H.S., 1993. Recent advances in research in anti nutritional factors in legume seeds. Wageningen Press, Wageningen. 550 pp.         [ Links ]

Van Soest, P.J., 1963. Use of detergents in the analysis of fibrous feeds. I. Preparation of fiber residues of low nitrogen content. J.A.O.C. 46, 825-835.         [ Links ]

Van Soest, P.J. & Wine, R.H., 1967. Use of detergents in analysis of fibrous feeds. II. Determination of plant cell wall constituents. J.A.O.C. 50, 50-55.         [ Links ]

Wiseman, J., 1987. Feeding of non-ruminant livestock. Butterworth, London. 208 pp.         [ Links ]

 

 

# Corresponding author. E-mail: tersb@elsenburg.com

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons