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.
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.
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:
MM: 60g cassava bran + 30g maize meal + 10g Aspergillus-niger
RB: 60g cassava bran + 30g rice bran + 10g Aspergillus-niger
CR: 60g cassava bran + 30g cassava root meal + 10g Aspergillus-niger
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.
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.
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:
Control: Traditional diet based on rice bran
ECB: Enriched cassava bran replacing 30% of rice bran in the traditional diet
CB: Non-enriched cassava bran replacing 30% of rice bran in the traditional diet.
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.
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.
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 was performed using the general linear model procedure of the ANOVA option in the Minitab software. Sources of variation were treatments and error.
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 |
Rice |
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 |
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.
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 |
14 |
7 |
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./SE |
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 |
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./SE |
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 |
Incubating cassava bran with Aspergillus-niger in the presence of 1% ammonium sulphate increased the true protein from 2 to 6% in DM
Pigs grew faster with better feed conversion using the enriched cassava bran compared with the non-enriched product.
This research was partially financed by the bilateral SAREC project 2000-2002.
.
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ith the un-enriched product