International Journal of Food Science and Nutrition Engineering
p-ISSN: 2166-5168 e-ISSN: 2166-5192
2018; 8(2): 45-51
doi:10.5923/j.food.20180802.04

Abdel Moneim E. Sulieman1, 2, Ohag M. Ohag2, Hassan M. Hassan3, Elnour Abdelmageed1, Vajid N. Veetil1
1Department of Biology, Faulty of Science, University of Hail, Kingdom of Saudi Arabia
2Food Science and Technology, Faculty of Engineering and Technology, University of Gezira, Wad-Medani, Sudan
3Kenana Freizlands Company, Kenana, Sudan
Correspondence to: Abdel Moneim E. Sulieman, Department of Biology, Faulty of Science, University of Hail, Kingdom of Saudi Arabia.
| Email: | ![]() |
This work is licensed under the Creative Commons Attribution International License (CC BY).
http://creativecommons.org/licenses/by/4.0/

The present study aimed to produce Gouda cheese at laboratory level and evaluation of the resultant cheese, in addition to its acceptance by panelists. Cow milk samples were collected and analyzed for chemical componentsduring three consecutive seasons. Slight differences were found in most of the chemical components during the three seasons, however all milk samples suited the production of Gouda cheese at laboratory level. The manufactured Gouda cheese was chemically evaluated and subjected to sensory analyses, and compared with standard Dutch Gouda cheese. The results show that the chemical components were 55% moisture, 41% fat, 24.5% protein. The contents of Na, potassium K and Ca of Laboratory-made Gouda cheese were non-significantly different from those of the standard Dutch Gouda cheese. Non-significant differences were noticed between the manufactured and Dutch Gouda cheese in chemical composition. The sensory evaluation revealed that Gouda cheese was generally acceptable by the panelists providing that the high contents of fat made its taste unacceptable to some of them. The study recommends encouraging the local dairy industry to introduce Gouda cheese so as to meet the local needs.
Keywords: Milk, Fat, Protein, Lactose, Sensory evaluation
Cite this paper: Abdel Moneim E. Sulieman, Ohag M. Ohag, Hassan M. Hassan, Elnour Abdelmageed, Vajid N. Veetil, Production and Quality Evaluation of Gouda Cheese Produced at Small Scale Level, International Journal of Food Science and Nutrition Engineering, Vol. 8 No. 2, 2018, pp. 45-51. doi: 10.5923/j.food.20180802.04.
Then, % protein = % N ×6.36Where: 14 = The molecular weight of nitrogen.T = Normality of acid, HCLN = Nitrogen contentFor the determination of fat content, Gerber tube was used to determine fat content of different samples according to the method described by DE Vleeschauwer et. al. [8]. The sample was homogenized by placing it in water bath at 40°C and cooled to 20°C. The butyrometer was filled with 10 ml H2SO4. 11 ml sample was pipetted in to the butyrometer. Then 2 ml amyl alcohols were added and the butyrometer was closed with a stopper. The contents were shaken vigorously until all protein particles were dissolved. The butyrometer was then placed in a water bath at 65°C for 5 minutes (fat column under the water surface). Moving the stopper regulated the fat column. The butyrometer was then placed in a centrifuge for 5 minutes, and then placed in a water bath at 65°C for 5 minutes. The fat content was read directly on the butyrometer scale in g/100 g sample.The procedure of AOAC [9] was used for the determination of lactose. Firstly: the invert sugar was determined by pipetting 5ml from each Fehling solutions A + B in a conical flask and then 10ml of distilled water were added. Then 3-5 drops of methylene blue were added as an indicator. Then the lactose standard was titrated until the final red precipitate occurred. Then Fehling factor was calculated from the following equation.Fehling factor: The titration × the concentration after the lactose was determined by preparing 10ml of milk (steamed or without treatment) in 100ml volumetric flask. Then the volume was completed to 100ml by adding distilled water. Then the mixture was filtered. Finally the sample was titrated against Fehling solution (A + B) as before. Then the concentration of lactose was calculated from the following equation:
The solids non-fat (SNF) contents in milk were calculated by using the following formula:
The total solids in milk samples was determined according to AOAC (2000) modified method. In that method 3 grams of samples were weighed into a dry clean crucible dish, then heated on water bath for 10-15min. the dish was then placed in an oven at 80°C overnight (16 hours) cooled down in a desiccators and weighed.The total solids (TS) content was calculated from the following equation:
Where:W1 = weight of the sample after drying.W2 = weight of the sample before drying.The density was determined according to Foley and Murphy [10]. In this method, 250 ml sample was mixed by rotating and inverting its container, vigorous shaking was avoided. Sufficient sample was added to a hydrometer to ensure some overflow when the hydrometer was inserted. The hydrometer was held by its stem, lowered into the sample until approximately reaching its equilibrium position. When the hydrometer came to rest, the reading on top of the meniscus was recorded and the temperature of the milk was recorded.
Where:W1 = weight of ash.W2 = weight of the sample.Dry matter content of cheese samples was determined according to AOAC [9] modified method. In that method 3 grams of samples were weighed into a dry clean crucible dish, then heated on water bath for 10-15min. the dish was then placed in an oven at 80°C overnight (16 hours) cooled down in a desiccator and weighed. The dry matter (DM) content was calculated from the following formula:
Where:W1 = weight of the sample after drying.W2 = weight of the sample.The pH of Gouda cheese samples were measured using digital pH meter (PN 9410. GL. Britain). The pH meter was calibrated with buffers of pH 4 and 7. The cheese samples were stirred using magnetic stirrer and the pH values was recorded according to AOAC [12].The titermetric determination of acidity of cheese samples was accomplished according to the AOAC (1980) method. The sample taken for determination of cheese acidity was 5m, which was pipetted into a 100ml conical flask. The pipette was washed with 5ml distilled water, and then six drops of phenolphthalein indicator were then added. The sample was then titrated with 0.1NNaOH until a stable pink color was formed. The titrable acidity was expressed as % lactic acid from the following formula.
Where 90 is the amount of lactic acid reacted with 1.0ml of 0.1N NaOH.

![]() | Figure 1. Milk Analyses in Sept |
![]() | Figure 2. Milk Analyses in Jan |
![]() | Figure 3. Milk Analyses in April |
![]() | Figure 4. Comparisons between three seasons |
|
|
|