A Study On Possible Use of Calcium Propionate and Ascorbic Acid in The Production of Cassava Bread
A Study On Possible Use of Calcium Propionate and Ascorbic Acid in The Production of Cassava Bread
A Study On Possible Use of Calcium Propionate and Ascorbic Acid in The Production of Cassava Bread
Abstract: There is little or no information on the use of legal additives in the production of cassava bread, a baked
product made with cassava flour and most often in combination with wheat flour. In this study, calcium
propionate (anti moulding agent) and ascorbic acid (a food antioxidant) were assessed as food additives in cassava
bread samples made with cassava flour from two cassava varieties (TME419 and TMS30572) with 60%, 80% and
90% wheat flour inclusion. The molds associated with the spoilage of bread were studied. Results showed that
0.6% calcium propionate inclusion in the bread samples could make the bread to have safe level of molds even at
four days post processing storage at ambient temperature (26-29ºC). The studies on colony count in breads at
different storage intervals showed that treatment containing 0.6% calcium propionate 0.3% ascorbic acid proved
to be most effective against control of count. Most molds isolated belonged to the genera Rhizopus, Aspergillus, and
Pencillium. After analyzing the samples, Rhizopus was found to be the most occurring fungi in bread.
The fresh bread samples with the additives were also generally acceptable by the consumers (sensory panelists) in
an organoleptic evaluation with the ratings of the samples having 80-90% wheat flour inclusion not being
significantly different (P=0.05) with that of 100% wheaten bread.
Keywords: Cassava flour, cassava bread, food additives, calcium propionate, ascorbic acid, mould.
spoilage, there are concerns regarding potential hazards of mycotoxin contamination, which could affect human health
(Legan, 1993).Moldiness caused by molds and ropiness due to bacterial contaminations are the major factors responsible
for microbial spoilage of bread (Pyler and Gorton, 1988). However the dominant spoilage flora varies with the type of
1 . INTRODUCTION
In recent years, scientists in Nigeria have developed a baked product known as cassava bread that is largely made with
cassava (Manihot esculenta) flour alone or as composite with common wheat (Triticum aestivum) flour (Shittu et al,
2007; Oti and Ukpabi, 2007). Generally, common wheat flour inclusion in cassava bread production enhances consumers’
acceptability of the baked product. This is based on the fact that cassava flour has no gluten and the presence of gluten in
wheat flour makes it most suitable for production of yeast leavened products such as wheaten bread (Tarar et al., 2010).
Considerate efforts have been made to promote the use of composite flours (from locally grown crops in Nigeria to
replace a portion of wheat flour in bread production) so as to reduce the demand for imported wheat and stimulate the use
of locally grown non-wheat agricultural produce as floury food materials. High Quality Cassava Flour (HQCF) has gained
popularity in the West African sub region over the past few years as a raw material in the production of baked products
such as bread (Eddy et al., 2007; Komlaga et al, 2012).
Oti and Ukpabi (2007) reported the possibility of 20% substitution of cassava flour to wheat flour in large scale bread
production in Nigeria. Similarly Komlaga et al. (2012) reported high level of consumer acceptability of bread baked with
10% and 20% cassava flour substitution in Ghana. However, they observed that bread baked with ≥30% substitution was
not highly acceptable to consumers when compared to those baked with 100% wheat flour. Although bread is regarded as
the second most highly consumed non-indigenous food product after rice in Nigeria, it has limited shelf life. Bread
spoilage mainly results from mold contamination, (moldiness) especially Penicillium and Aspergillus (Smith et al., 2004;
Pateras, 2007). Bread is prone to rapid microbial spoilage, particularly mold growth, due to post-baking contamination
during cooling, slicing and wrapping, which greatly limits its shelf life. Thus methods of mold control are of great
importance to the bakery industry (Smith et al., 2004). In addition to substantial economic losses associated with fungal
Page | 132
Research Publish Journals
ISSN 2348-313X (Print)
International Journal of Life Sciences Research ISSN 2348-3148 (online)
Vol. 5, Issue 2, pp: (132-137), Month: April - June 2017, Available at: www.researchpublish.com
bread, the storage temperature and the season. At present, wheaten breads often spoil within 48 hours of production. The
use of techniques such as attention to hygiene within the bakery and use of preservatives and other additives are currently
being employed to improve consumer acceptability and the shelf life of baked bread made with wheat flour (Alais and
Linden, 1999).
Presently, there is dearth of information on the use of relevant additives in the production of cassava bread. The aim of
this study was therefore to evaluate the possible use of calcium propionate (anti roping and molding agent) and ascorbic
acid (a food antioxidant and bread improver) in producing cassava bread samples with varying levels of wheat flour
inclusion. The antimicrobial activities of propionates in wheaten bread are known to inhibit the growth of molds and
bacteria without having any damaging effects on the leavening yeasts (Alais and Linden, 1999).
Fig. 1: Flow chart for the production of cassava flour for baked products.
Shelf life determination:
The bread produced was packed in the conventional transparent polyethylene bags and stored at room temperature
Page | 133
Research Publish Journals
ISSN 2348-313X (Print)
International Journal of Life Sciences Research ISSN 2348-3148 (online)
Vol. 5, Issue 2, pp: (132-137), Month: April - June 2017, Available at: www.researchpublish.com
(27±2°C). The bread was observed daily through the transparent polythene bags to determine when spoilage would occur.
The total mould load was determined at the beginning of spoilage on the 1 st, 4th, and 8th, day by carefully and
aseptically taking 10g of the moldy outer layer of the bread using sterile scalpel and homogenizing in 90ml of 0.1%(w/v)
sterile peptone water for 3 min in a stomacher (A.J. Seward and Co.London). Ten fold serial dilutions were subsequently
prepared by transferring 1ml of the homogenate into 0.1% (w/v) peptone water as diluents. Further serial dilutions were
carried out and 1ml of appropriate dilution was aseptically plated using the pour plate technique on Potato dextrose agar
supplemented with chloramphenicol. At the end of the incubation period (3-5 days) the colonies were enumerated and
expressed as colony forming units per gram (cfu/g) (Vanderzannt and Splittstoesser, 1992). The different colonies on each
plate were isolated, purified, and stored on PDA slants for further characterization and identification. The fungi were
identified under the light microscope (x40) and recorded using the scheme of Barnet and Hunter.
Sensory evaluation:
A 9- point Hedonic scale (1-9) was used for a sensory evaluation of the freshly prepared bread samples using 20
semi-trained sensory panelists and following the procedure as outlined by Iwe (2007) . The panelists were pre-trained
to score for appearance, color, taste, aroma, texture and general acceptability independently and objectively with a
pre-trial scoring test. Scoring was done on 9-point Hedonic scale where 9 represents like extremely, 5 neither like nor
dislike and 1 = dislike extremely.
Statistical analysis:
Statistical Package SAS version 8e software (SAS Institute Inc., Cary, NC, USA) was used for statistical analysis.
Differences between samples in each item were tested using analysis of variance (ANOVA) and Duncan’s Multiple Range
as a post-hoc test when the analysis of variance indicated significant differences in the means.
TMS 30572 TME 419 TMS 30572 TME 419 TMS 30572 TME 419
10% cassava flour inclusion NG NG NG 6.0x103 9.0x107 9.0x107
20% cassava flour inclusion NG NG 1x103 3.5x103 9.0x107 9.0x107
40% cassava flour inclusion NG NG NG 3.5x103 13.5x107 17.25x107
3 3
100% wheat flour NG NG 7x10 7x10 NG NG
NG=no growth
Different preservatives effectively controlled fungal growth to a count between 0 to 10x 10 3 in bread samples prepared
from the two cassava varieties respectively. The results at day 4 are in line with findings of Masood et al. (2001) who
observed the maximum number of colonies range of 6-8 x 10 3 cfu with the use of additives like Calcium propionate
(0.15%), Lactic acid (0.10%) and Acetic acid (0.10%).The microbial population at day4 in all the bread samples were
within the recommended limits (105 Cfu/g) for microbial contamination in ready-to-eat food as stipulated by the
International Commission on Microbiological Specification for Foods (ICMSF, 2012). Preservatives help to reduce or
prevent wastage of food through spoilage caused by microorganisms. Longer shelf life enables a greater variety of
Page | 134
Research Publish Journals
ISSN 2348-313X (Print)
International Journal of Life Sciences Research ISSN 2348-3148 (online)
Vol. 5, Issue 2, pp: (132-137), Month: April - June 2017, Available at: www.researchpublish.com
products to be kept in store and in the home saranraj and geetha(2010) The majority of moulds isolated from this study
belong to Rhizopus stolonifer, Apergillus niger and Penicillium sp as shown in (Table 3).
One of the most common fungi involved in spoilage of bread is Rhizopus stolonifer, often referred to as the ‘bread
mould’. Most common source of microbial spoilage is due to mold growth. According to the previous studies (Banwart,
2004) bread molds like Mucor and Rhizopus are found to grow first during bread spoilage. This is followed by some other
fungi like Aspergillus, Penicillium and Fusarium sp. Molds are the primary spoilage organisms reported in baked foods,
with Aspergillus, Penicillium, and Eurotium being the most commonly isolated genera. These organisms synthesize toxic
secondary metabolites called mycotoxins that have serious health implications The presences of Aspergillus niger,
Rhizopus stolonifer and pencillium spp have been reported as an indication of contamination as they are common
spoilage organisms of carbohydrate containing food Ezeama and Amajor,(2015).
Table 2 Frequency of occurrence of fungi
Fungal Isolates Frequency (%)
Rhizopus sp 60
Aspergillus sp 40
Pencillium sp 20
Table 3 Cultural morphological characteristics and identification
Fungal Isolate Cultural Characteristics Morphological Characteristics
Rhizopus sp White cottony mycelia, Sporangiospores are produced inside a
with black dots and covers spherical sporangium.
the entire plate Columella is present on the top of the
sporagiophore. Root-like rhizoids are found
Aspergillus sp Yellow or yellowish green Conidiophores arise from a footcell.
colonies with distinct Club shaped vesicles at top of the
margin conidiophores. Conidia are found in chains.
Penicillium sp Fast-growing colonies in Conidiophores arise from a footcell.
green colour with dense Club shaped vesicles at top of the
conidia conidiophores. Conidia are found in chains.
The Preference Test data show that the level pf substitution affected the degree of acceptance/preference of cassava bread.
Bread prepared by using 10% and 20% HQCF substitution had a higher rating compared to samples prepared using 40%
substitution. However, inclusion of ascorbic acid improved the texture and taste of bread baked using 40% substitution
with cassava flour from TME 419 variety. Ascorbic acid is generally used in the food industry as an enhancer to improve
the sensory attributes such as texture, colour and taste.
Table 4: Preference Test of TME419 Cassava Flour Bread Samples with Ascorbic Acid
Bread sample Appearance Taste Aroma Texture Color General Acceptance
10% cassava flour inclusion 7.30a 6.20ba 6.35a 6.20b,a 7.20a 6.90a
20% cassava flour inclusion 6.05a 6.00b 5.95a 6.35b,a 6.30a 6.15a
40% cassava flour inclusion 6.00a 6.00b 6.10a 6.35b 6.35a 6.65b
100% wheat flour 7.14a 6.95b 6.55a 6.60a 7.15a 6.80a
Values in a column with the same letter are not significantly different (P=0.05)
Table 5: Preference Test of TMS30572 Cassava Flour Bread Samples with Ascorbic Acid
Bread sample Appearance Taste Aroma Texture Color General Acceptance
10% cassava flour inclusion 7.30a 6.00a 6.40a 6.30a 7.3a 6.95b,a
Page | 135
Research Publish Journals
ISSN 2348-313X (Print)
International Journal of Life Sciences Research ISSN 2348-3148 (online)
Vol. 5, Issue 2, pp: (132-137), Month: April - June 2017, Available at: www.researchpublish.com
20% cassava flour inclusion 7.20a 6.90a 6.75a 6.75a 6.75a 7.20a
40% cassava flour inclusion 6.70a 6.15a 6.00a 6.00a 6.00a 6.15b
100% wheat flour inclusion 7.14a 6.95b 6.55a 6.60a 7.15a 6.80a
Values in a column with the same letter are not significantly different (P=0.05)
Though the fresh bread samples were generally liked by the test panelists, there is a need to undertake a sensory
evaluation of stored cassava bread samples in a future experimentation. This will assist in having a full quality assurance
package for cassava bread producers, consumers and marketers.
4. CONCLUSION
The results from this study shows the use of calcium propionate and ascorbic acid as legal food additives in the recipe for
preparation of bread from 10%, 20% and 40% inclusions of HQCF can assist in shelf-stability of the product for a
maximum of 4days at room temperature. However, as the 40% HQCF bread was not acceptable to the consumers, there is
therefore the need to modify the recipe for preparation of bread at this level of substitution in order to increase its
acceptability by consumers.
REFERENCES
[1] Alais, C and Linden, G. (1999). Food Biochemistry. Aspen Publishers, Gaithersburg, Maryland.
[2] Eddy, N. O., Udofia, P. G. and Eyo, D. ( 2007) Sensory evaluation of wheat/cassava composite bread and effect of
label information on acceptance and preference. African Journal of Biotechnology, 6 (20): 2415-2418
[3] International Commission on Microbiological Specification for Foods.USDA information office. Accessed online
at http://fsrio.nal.usda.gov/sanitation-and-quality-standards/microbiological-standards-and-guidelines.Accessed 21/
11/2012. (ICMSF)(1998??). Microbial ecology of food commodities. Academic Press, New York, London,
pp522532
[4] Iwe, M. O. (2007). Current Trends in Sensory Evaluation of Foods. Rojoint Communcation Services, Enugu
(Nigeria):
[5] Komlaga G. A., Glover-Amengor, M. Dziedzoave, N. T. and Hagan, L. L. (2012). Consumer acceptability of
wheat/cassava composite bread. World Rural Observations ;4 (2):78-81
[6] Tarar, O.M., Rehman, S., Mueen-ud-din, G. and Murtaza, M.A. (2010). Studies on the shelf life of bread using
acidulants and their salts. Turk J Biol 34: 133-138.
[7] Obasi, S. C., Ukpabi, U. J., Okporie, P. J., Etim, C. and Mba, P. (2016). Effects of Raw Material and Product
Storage on Some Quality Characteristics of Cassava Flour Produced With Selected Yellow Cassava Varieties.
Journal of Raw Materials Research, 10 (2): 45 – 62.
[8] Oti, E. and Ukpabi, U. J. (2007). Cassava for Bread Making in Nigeria. National Root Crops Research Institute,
Umudike/ Nigerian Institute of Food Science and Technology, Lagos.
[9] Pyler, E. J. and Gorton, L.A. (1988). Baking Science and Technology. Sosland Publishing Co. Kansas. :p219
[10] Shittu, T. A., Raji. A. O., Sanni, L. O. (2007). Bread from composite cassava-wheat flour: 1. Effect of baking time
and temperature on some physical properties of bread loaf. Food Research International, 40: 280-290
[11] Ukpabi, U. J. (2009). Roots and Tubers in Nigeria as Sources of Industrial Raw-Materials. In: Nigerian Agro Raw
Materials Development; Vol. 1: Some Industrial Crops and Salient Issues (P. A. Onwualu, S. C. Obasi and U. J.
Ukpabi Eds), RMDRC Publications, Raw Materials Research and Development Council, Abuja. pp 1-19.
[12] Ukpabi, U. J. (2010). Farmstead bread making potential of lesser yam (Dioscorea esculenta) flour in Nigeria.
Australian Journal of Crop Science, 4(2), 68 – 73.
Page | 136
Research Publish Journals
ISSN 2348-313X (Print)
International Journal of Life Sciences Research ISSN 2348-3148 (online)
Vol. 5, Issue 2, pp: (132-137), Month: April - June 2017, Available at: www.researchpublish.com
[13] Smith, J.P., Daifas, D.P., El-Khoury, W., Koukoutsis, J., El-Khoury, A.( 2004.) Shelf life and safety concerns of
bakery products – a review. Critical Reviews in Food Science and Nutrition 44 (1), 19–55.
[14] Pateras, I.M.C., (2007). Bread spoilage and staling. In: Cauvain, S.P., Young, L.S.(Eds.),Technology of Bread
making. Blackie Academic and Professional, London, pp.275–298.
[15] Legan, J. D, (1993). Mould spoilage of bread: the problem and some solution. Int. Biodeterior. Biodegrad. 32: 33-53.
[16] Vanderzannt, C., Splittstoesser, D.F,( 1992). Compendium of methods for the Microbiological examination of food,
3rd ed. American public health association, Washington DC.
[17] Barnett HL, Hunter BB. 1987. Illustrated general of imperfect fungi. 4th ed. Macmillan, New York, NY, USA. p
240.
[18] Banwart, G.J. (2004). Basic Food Microbiology. A Westport Publication. Pp. 505-544.
[19] Saranraj, p., Geetha, M. (2012). Microbial Spoilage of Bakery Products and Its Control by Preservatives.
International Journal of Pharmaceutical & Biological Archives 2012; 3(1):38-48.
[20] Ezeama C.F., Amajor, J.U(2015) Microbiological Profile, Shelf stability and some Physicochemical properties of
Fermented flour from different sweet potato cultivars Journal of Food Technology Research, 2015,2(2): 33-45.
Page | 137
Research Publish Journals