Sida-SAREC 1988-2003

Citation of this paper

 

Protein enrichment of cassava by-products using Aspergillus-niger
 and feeding the product to pigs

 

Nguyen Van Phong, Nguyen The Hoa Ly, Nguyen Van Nhac and Du Thanh Hang

 Hue University of Agriculture and Forestry

 

Abstract
 

A fermentation procedure to increase the protein content of cassava bran with Aspergillus niger is described. The organism was grown in a cassava bran medium with different inorganic nitrogen (ammonium sulphate) levels (0,  0.5,  1.0 and 1.5% N in DM). The fermentation time was 144hr.

 

The true protein contents were 3.3, 5.2,  6.4 and 5.1% in DM, for the four levels of ammonium sulphate, respectively. The enriched cassava bran supported higher growth rates and better feed conversion  than the non-enriched product when included in a fattening diet for pigs, both on-station and on-farm.

 

The results indicate that the fungal-enriched cassava bran can be safely used in diets for fattening pigs.

 

Key words: Aspergillus niger, cassava bran, protein, pigs, growth, conversion

 

Introduction

About 200 tonnes per month of cassava roots are processed into starch by artisan methods in the Hue city area. Two by-products from this process are bran ("Afrecho") and fines ("Mancha") with about 100 tonnes  produced monthly. Most of the by-products are utilized for feeding live stock. However, they are low in protein content (about 0.50% in DM),  so that  large quantities of protein-rich oilseed and fish meals have to be added to raise the concentration and the quality of the protein. 

The protein-enrichment  of cassava bran using microbial techniques was therefore investigated. The aims were to  determine  whether Aspergillus niger, in the presence of added inorganic nitrogen,  could be used to increase  the protein content of cassava bran and thus improve it's feeding value for pigs.
 

Materials and methods

 

Propagation of the fungus

 

The strain of Aspergillus niger used in the investigation was obtained from the Department of Microbiology, University of  Danang. It had been isolated originally from cassava bran.

 

The cassava bran used as the fermentation medium was taken  from a small starch-processing mill in the Hue area and had been dried. Three different carbohydrate sources were compared in the following fermentation media (g/100g) in  order to propagate the culture:

 

The cassava bran, rice bran, maize meal, and cassava root meal were steamed for 25 minutes and then cooled to ambient temperature (30ºC) before incubating with Aspergillus-niger spores,  keeping the moisture content of the mixture at 60%. The media were spread in a thin layer (2-3 cm) on a tray and were fermented aerobically. Test samples were also fermented in petri dishes to observe the development of the fungal cultures.

 

Samples were taken after 6 days of incubation and analysed for dry matter (DM), crude protein (CP), crude fibre (CF), and ash. On the basis of the analysis the medium containing rice bran was selected  for  propagating the culture for the production experiment.

 

Production experiment

 

The following experiment was designed to determine the optimum level of addition of ammonium sulphate. The selected levels were: 0, 0.5, 1.0 and 1.5 g (NH4)2SO4 added to 90g of cassava by-product and with 10 g of Aspergillus-niger as inoculum.

 

Cassava bran was adjusted to a moisture content of 50 to 55%.  The inoculum of Aspergillus-niger was one week old and was added to the cassava bran in the ratio 1: 9,  mixed well, and placed in an aerated area.  Samples were taken for chemical analysis at 0, 3, 6 and 9 days after incubation.

 

Feeding trial on-station

 

The experiment was carried out from September to November, 2001 on the University farm. Three treatments were compared using 12 pigs (Large White x Mong Cai) with average weight of  26.5kg. The treatments were:

The composition of the control diet was (%): rice bran 40, maize meal 4, groundnut cake 10, fish meal 10. The pigs were weighed on the initial and final day of the experiment. Refusals were collected the following morning before the first meal for calculating feed intake and feed conversion.

 

Feeding trial on-farm

The experiment was carried out from February to May, 2002 in Phu Thuorng village. There were  two treatments applied to 12 pigs (Large White x Mong Cai), six castrated males and six females, of average initial weight of 28 kg. One group was  fed a diet of 30% enriched cassava bran + 70% basal  diet; the other group was fed a diet of 30% non-enriched cassava + 70% of basal diet. The diet was divided equally into 3 meals per day at 7.00, 12.00 and 17.00. The pigs were weighed at the beginning and at the end of the experiment which lasted 70 days.

Chemical analysis

Samples were analysed for DM, N and ash according to AOAC (1990) procedures.  True protein was determined by the Stutzer method. The samples were  boiled with water to dissolve the amides. True protein was then precipitated with copper hydroxide and the aqueous mixture was filtered to separate the amides from the protein. The true protein which remained in the residue on the filter paper was analysed for N by the standard Kjeldahl procedure.

Statistical analysis

 

Statistical analysis was performed using the general linear model procedure of the ANOVA option in the Minitab software. Sources of variation were treatments and error.

 

Results and discussion

 

Incubation experiments

The rice bran appeared to be the best medium for propagating the Apergillus niger, as measured by the increase in protein after 6 days of incubation (Table 1).

Table 1: Effect of incubation with Aspergillus niger on the changes in protein in the fermentation media which was a mixture of  cassava bran and one of the following carbohydrate sources

 

Maize
 meal

Rice
 bran

Cassava root meal

Crude protein, % in DM

Before incubation

3.67

4.67

1.05

After 6 d incubation

7.7

14.3

3.5

Increase in % units

4.03

9.63

2.25

 

Production experiments

The true protein of the media increased rapidly during the first 6 days of incubation  with no further increase up to 9 days (Table 2; Figure 1).

Table 2: Mean values for concentrations of crude and true protein after incubation for 0, 3, 6 and 9 days with increasing levels of ammonium sulphate

 

Level of ammonium sulphate, %

 

Prob./SEM

0

0.5

1.0

1.5

0 days        

 

Crude protein

1.7

2.0

2.4

2.6

 

3 days

 

 

 

 

 

True protein

3.1

3.4

5.4

4.1

0.001/0.09

Crude protein

4.2

5.8

7.0

6.8

 

6 days

 

 

 

 

 

True protein

3.3

5.2

6.4

5.1

0.001/0.09

Crude protein

4.5

7.1

9.8

8.9

 

9 days

 

 

 

 

 

True protein

3.2

5.3

6.4

5.5

0.001/0.07

Crude protein

4.6

7.3

8.1

9.5

 

Figure 1: True protein production in cassava by-product incubated with Aspergillus niger in presence of ammonium sulphate
at levels of 0 to 1.5% in the DM of the medium

The greatest increase in true protein content was with the addition of 1% of ammonium sulphate; however the relative conversion of crude to true protein appeared to be best with 0.5%  ammonium sulphate (Figure 2).

 

Figure 2: Fermenting cassava by-product with Aspergillus niger in presence of ammonium sulphate
at levels of 0 to 1.5% in the DM of the medium (data after 6 days of incubation)

 

Similar findings were reported by by  Balagopalan and Padmaja (1988) who developed a solid state fermentation process  for  the protein enrichment of cassava flour and cassava starch factory wastes using the  fungus Trichoderma pseudokonigii rifai. The results showed that using this process it was possible to convert the substrate to a protein-enriched animal feed, using the minimum of nutrients [0.15% (NH4)2SO4].

 

There appeared to be a small increase in the lipid concentration of the media after incubation with Aspergillus, but this was not affected by addition of ammonium sulphate (Table 3).

Table 3: Concentrations of ether extract after incubation for 0, 3, 6 and 9 days with increasing levels of ammonium sulphate

Incubation, days

Level of ammonium sulphate, %

 

Prob./SEM

0

0.5

1.0

1.5

0

3.0

3.0

3.0

3.1

0.646/0.35

3

3.9

4.3

4.5

4.1

0.429/0.39

6

4.5

4.3

4.4

4.5

0.720/0.23

9

4.5

4.3

4.5

5.0

0.610/0.29

 

The procedure for the commercial production of protein-enriched cassava bran is shown in Figure 3. 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 Figure 3: Outline of the process for protein-enrichment of cassava bran

 

The overall changes in the cassava bran after incubation with Aspergillus  are shown in Table 4.

Table 4: Composition of cassava bran before and after protein-enrichment

 

Cassava bran

Enriched cassava bran

DM, % fresh basis

52.2

64.8

As % of DM

 

 

Crude protein

2.4

9.8

True protein

1.1

6.4

Crude fibre

7.2

6.8

Ether extract

3.0

4.4

Ash

2.5

2.4

HCN, mg/kg DM

14

7.0

 

On-station feeding trial


The pigs fed the diet with enriched cassava bran grew faster, and had better feed conversion, than those fed the non-enriched product (Table 5), the overall performance being similar to that on the traditional diet. The implication is that the nutritive value (mainly the protein content) of the enriched cassava bran diet had been improved to a level comparable with the rice bran. 

Table 5: Growth performance, feed intake and conversion of pigs fed with and without the protein- enriched cassava bran replacing rice bran in the traditional diet

 

Traditional

Enriched cassava bran

Non-enriched cassava bran

Prob./SEM

Initial LW (kg)

27.5

26.5

26.8

0.64/0.34

Final LW (kg)

57.8

55.3

50.8

0.041/0.27

Daily gain (g)

423

410

343

0.001/11

Daily intake (kg DM)

1.78

1.73

1.51

0.01/0.021

Feed conversion (kg DM./kg gain)

4.12

4.20

4.35

0.001/0.027

 

On-farm trial

 

The results in the on-farm trial (Table 6) were similar to those on-station. Growth rates and feed conversion were improved on the enriched cassava bran diet compared to the non-enriched product.

Table 6: Effect of the enriched cassava bran diet on the growth performance and feed conversion of pigs in the on-farm trial

 

Enriched cassava bran

Non-enriched cassava bran

Prob./SEM

Initial weight (kg)

28.2

28.0

0.635/0.348

Final weight (kg)

61.1

56.7

0.032/0.292

Daily gain (g)

439

382

0.038/0.020

Feed conversion (kg DM/kg gain)

4.05

4.65

0.035/0.082

 

Conclusions

 

 

Acknowledgements

This research was partially financed by the bilateral SAREC project 2000-2002.

.

References

 

AOAC 1990 Official Methods of Analysis 13th Edition. Association of Official Analytical Chemists, Washington DC

Pancaras.J.Muidi and Jon F.Hanssen.Nutritive value of cassava root meal enriched by trichoderma harziamun for chickens. Sci.food Agric.1981,32, 647-654.

Muidi.P.J Thomke.S and Hanssen. 1981.Protein quality studies on rates fed on cassava root meal enriched with cephalo sporium 152 anim.Feed sci.Technol 6(197-108)

Manilal et .al ( 1987) Amylo glucosidase and cellulasa activity of Aspergillus niger in cassava starch factory wastes.tropical tuber crops production and utilisation .

Faoanimal production and health paper 95.Roots ,Tuber,Plantains and Bananas in animal feeding (135)

Le Hong Mai and Nguyen Dinh Quen.Studies on Aspergillus- niger.VS1.Agric. Biol.Chemi 1982 .46(1667-1669)

Dang Van Loi andNguyen Dinh Quyen . Studies oncellulase of Aspegillus niger.Bio.engineering .7/1998.

Paraska.S. and Saeow.N 1987. Use of cassava enriched with protein(Aspergillus nige and yeast) in the growing fattening pig diets.Kasetsart jurnal natual sciences 21

(1) Thai Land .sum.

 

 

ith the un-enriched product

 Go to top