CC BY
29DOI: https://doi.org/10.21323/2414-438X-2021-6-4-375-380
/p\creative ^commons
Available online at https://www.meatjournal.ru/jour Original scientific article Open Access
NEW APPLICATION OF MICROBIAL L-GLUTAMINASE A t d iReceived 10102021
Accepted in revised 15.11.2021
AS A FLAVOR ENHANCING AGENT IN BEEF BURGERS Accepted or publication 24.11.2021
Reda M. Mohamed, Wael A. Bazaraa*, Ahmed M. Alian, Nagwa M. EL-Shimi
Cairo University, Faculty of Agriculture, Giza, Egypt
Keywords: microbial L-glutaminase, beefburger, sensory evaluation, monosodium glutamate, flavor enhancer Abstract
L-glutaminase (L-glutamine amidohydrolase EC3.5.1.2) is the key enzyme in enhancing the taste and aroma of oriental fermented foods by increasing their glutamic acid content and as a result imparting a palatable taste. Beefburgers were prepared using different levels of the partially purified L- glutaminase (2.0 to10.0 U/100 g) prepared from Aspergillus oryzae NRRL 32567. Beefburgers treated with 6.0 U/100g and the others treated with monosodium glutamate (5000ppm) were chemically, sensory and microbio-logically evaluated and compared to untreated control during frozen storage at -18 °C for 3 months. Treatment with L-glutaminase (6 U/100g) resulted in an increase of443% in glutamic acid and a reduction of 63% in glutamine contents resulting in an enhanced preferable taste and odor of the prepared beef burgers. Burgers treated with 6.0 U/100g exhibited the best odor, texture, taste and overall quality scores when compared to the untreated control and samples treated with monosodium glutamate (5000 ppm). During the frozen storage of all samples, an expected slight, but significant (p<0.05), increase in the total mesophilic bacterial count was evident and such increase was quite acceptable since numbers did not exceed the limit of 5.7x10s cfu/g. Similarly, the total psychrotrophs did not exceed 3.7x10 cfu/g.
For citation: Mohamed, R.M., Bazaraa, W.A., Alian, A.M., El-Shimi, N.M. (2021). New application of microbial l-glutaminase as a flavor enhancing agent in beef burgers. Theory and practice of meat processing, 6(4), 375-380. https://doi.org/10.21323/2414-438X-2021-6-4-375-380
Introduction
L-Glutaminase (L-glutamine amidohydrolase EC3.5.1.2) catalyzes the hydrolysis of L-glutamine to L-glutamic acid and ammonia [1,2]. L-glutaminase is generally regarded as a key enzyme in enhancing the taste and aroma of oriental fermented foods such as soy sauce by increasing their glu-tamic acid content and thereby imparting a palatable taste [3,4,5]. Amino acids that are produced by the enzymatic degradation of the proteins contained in the raw materials are well known as basic flavor components of fermented condiments. L-glutamic acid is one such flavor enhancing amino acid produced by the hydrolytic action of L-gluta-minase on L-glutamine [6,7].
Monosodium glutamate (MSG) gives the taste "umami", which has been widely recognized as the fifth basic taste besides sweet, acid, salty and bitter. It has been widely used as a flavor enhancer in the food industry. However, there is some questions about its safety, since it may cause some side effects for some people such as wheezing, changes in the heart rate and difficulty in breathing [8,9]. Therefore, the need to develop a safer natural flavor enhancer as an alternative to MSG has been increased.
Glutamic and aspartic acids are well known amino acids contributing not only fine taste, "umami" and sharp sour taste but also nutritional effects to food [10,11]. Therefore, in the present study, microbial L-glutaminase has replaced the use of monosodium glutamate to enhance flavor in beef burgers. Besides, the effect of such replacement on
the chemical, sensory and microbiological quality of the produced burger were evaluated.
Materials and methods
Enzyme
Partially purified Aspergillus oryzae NRRL 32567 L-glutaminase was utilized in this study [12,13].
Raw materials
Frozen lean beef and fat were purchased from the local market in Giza, Egypt. Soy flour was obtained from Food Technology Research Institute, Agricultural Research Center, Giza, Egypt.
Formulation of beef burgers
Beef burgers were prepared, in accordance with the Egyptian standard specification for beef burgers (ES: 1688-2005) [14], as follows: 60% frozen lean beef, 20% fat, 10% soy flour, 1.3% spices mixture, 1.7% salt, 1% corn starch, 1% casein and 5% onion. All ingredients were well mixed and then the mixture was divided into two batches. The first batch was divided into six treatments (a control and five treatments with partially purified L-glutaminase at different concentrations, from 2.0 to 10.0 U/100 g). Each treatment was separately mixed for 5 min at medium speed to obtain homogeneous mixture. This mixture was shaped using a commercial burger maker to obtain burgers of approximately 9 cm diameter, 50 g in weight and 0.5 cm thick. Burgers were then cooked by frying in
Copyright © 2021, Mohamed et al.This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.
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sunflower oil and evaluated by sensory analysis. The second batch was divided into three portions; the first was used as control, the second (treatment A) was mixed with 5000 ppm of monosodium glutamate, while, the third batch (treatment B) was mixed with 6.0 U/100g of the partially purified glutaminase (as the best enzyme concentration). Each treatment was processed as described before to obtain beef burgers that were packed in foam plates and stored at -18 °C for 3 months. After storing, samples from the three treatments were chemically and microbiologically evaluated (after thawing) every month. Sensory evaluation was performed on the cooked burgers only at the end of storage.
Enzyme assay
The glutaminase activity was assayed according to Imada et al. [15]. One unit of glutaminase was defined as the amount of enzyme that liberates 1 ^mol of ammonia under optimal assay conditions.
Chemical analyses
Moisture, protein, fat, crude fibers, total ash and total carbohydrates of beef burger samples were determined according to the official methods [16]. Free amino acids (FAA) were analyzed by HPLC [17]. The pH value of beef burger samples was measured by homogenizing 10 g of sample with 100 ml distilled water for 30 sec. The pH of the prepared sample was measured using a pH meter (Orion 301, USA) at 20 °C [18].
Microbiological quality
Samples (30 g) were aseptically taken from each beef burger and homogenized with peptone water (0.1%) in a Lab-Blender for 3 min to have a final dilution of 1:10. Serial decimal dilutions were made using the same diluent and then plated in duplicate for bacterial counts. Aerobic mesophilic bacteria were determined on plate count agar (Merck, Darmstadt, Germany) after 48 h incubation at 30 °C. Mold and yeast were counted on acidified potato dextrose agar (Merck, Darmstadt, Germany) after 48 h incubation period at 28 °C. Coliform group was determined on MacConkey agar (Merck, Darmstadt, Germany) after 48 h incubation at 37 °C. Psychrotrophs were determined on plate count agar (Merck, Darmstadt, Germany) after ten-day incubation at 7 °C [19].
Sensory evaluation
Burgers were assessed for a number of sensory characteristics by ten members from the Food Science Department, Faculty of Agriculture, Cairo University, Egypt. They were selected on the basis of interest and experience in sensory evaluation and availability. Panelists were instructed to evaluate color, texture, taste, odor and overall quality using 10-point hedonic scale for grading the quality of samples where, 10 points indicated the highest acceptability and 5 was the acceptance boundary. On the other hand, 4 points indicated unacceptable samples [20].
Statistical analysis
Results were subjected to one way analysis of variance, ANOVA [21], and data were presented as the mean of three experiments.
Results and discussion
Chemical composition of frozen beef
The chemical composition of the frozen beef meat was as follows (g/100 g fresh weight): 75.0, moisture; 18.5, protein; 5.56, fat; 1.0, ash and zero total carbohydrates. These results were in accordance with those of Gehan and Emara [22] and Kassem et al. [23].
Chemical composition of frozen beef burgers
The moisture content of prepared beef burgers at zero time was 62.51, 62.49 and 63% for control, treatment A and treatment B samples, respectively. A slight reduction in the moisture content during burger frozen storage was expected and it was due to the evaporation of moisture through the polyethylene bags [24,25]. The protein content was 15.2, 15.18 and 15.5% for the control, treatment A and treatment B samples, respectively at zero time. A very slight decrease in the protein content during frozen storage at -18 °C was noted and might be a result of slight protein degradation by meat enzymes [26]. Also, at zero time, the fat content was 16.72, 16.70 and 16.3%, ash content was 1.73, 1.75 and 1.77%, crude fibers content was 1.26, 1.33 and 1.00% and carbohydrate content was 2.58, 2.55 and 2.45% for the control, treatment A and treatment B samples, respectively. On the other hand, during storage at -18 °C, storage such values were slightly increased for all samples due to a decrease in the moisture content [25,27,28]. The hydrolysis of meat proteins generates polypeptides that can be further degraded to smaller peptides and free amino acids. This degradation can be produced by endogenous and microbial enzymes as reported by different authors [29,30,31]. The results for free amino acids generated during beef burger processing of both the control and treatment B are presented in Table 1. Mainly, results clearly show an increase in the amount of glutamic acid from 23 to 125 mg/100 g and a decrease in glu-tamine content from 119 to 75 mg/100 g in the control and treatment B samples, respectively. These results were the direct effect of the added L-glutaminase. Such findings were confirmed when both odor and taste scores increased by the addition of L-glutaminase up to 6.0 U/100 g (Table 2). It was reported that the large amounts of hydrophobic amino acids (such as methionine, valine, leucine and tryptophan, which are usually associated with bitter taste) were generated during processing [32,33]. Some of these amino acids, especially the branched-chain amino acids, have been proved to be metabolized by Debaryomyces sp. generating volatile compounds in dry fermented sausage [34]. Meanwhile, high quantities of alanine and glutamic acid caused a sweet taste and umami sensation, respectively, the final sausages [35]. Therefore, the balance of these free amino acids will affect the sensory characteristics of the product [36,37].
Table 1. Free amino acid (FAA, mg per 100 g dry matter) concentration in beef burgers at zero time
FAA Control Treatment B
Asparagine 3.4 3.9
Glutamic acid 23.0 125.0
Serine 8.3 9.2
Glycine 20.6 25.0
Glutamine 119.0 72.0
Alanine 58.0 61.0
Arginine 7.1 7.4
Proline 8.2 9.4
Tyrosine 5.3 10.0
Histidine 4.2 6.1
Threonine 6.7 8.2
Valine 8.5 10.0
Methionine 3.4 9.2
Tryptophan 2.1 4.1
Leucine 9.0 13.0
Sensory evaluation of beef burgers as affected by different levels of partially purified glutaminase Beef burgers were prepared using different levels of partially purified glutaminase (2.0 to 10.0 U/100 g) and data are presented in Table 2. Results indicate that, odor scores ranged from 6.5 to 9.0 and the best odor was observed for the sample with enzyme treatment of 6.0 U/100g. Meanwhile, increasing the enzyme concentration above 6.0 units caused a gradual decrease in the odor attribute. Increasing the enzyme concentration, up to 8.0 U/100 g, in burger treatments caused an increase in texture scores. This increase in texture scores may be due to the increase in the proteases content contaminating the partially purified glutaminase. These proteases improved tenderness of beef burgers as compared with the control sample. Regarding taste, it was noticed that by increasing the glutaminase level, the taste scores increased reaching the highest level of 9.0 for samples treated with 6.0 U/100 g followed by a gradual decrease where scores of 7.5 and 6.0 were obtained for samples treated with 8.0 and 10.0 U/100 g, respectively. Such decrease in scores was due to the appearance of bitter taste (as distinguished by panelists) which was probably due to the degradation of protein and an increase in the bitter amino acids such as: methionine, valine, leucine and tryptophan [32]. The highest color score (8.8) was recorded for the control sample. By increasing the enzyme level, the color attribute decreased due to the increase in Table 2. Sensory evaluation of beef burgers as affected by different
the undesirable dark color, which was probably due to the formation of the Maillard reaction between reducing sugars and the formed amino acids and the lowest score (6.0) obtained at 10.0 U/100 g. Also, the highest overall quality score of 8.6 was given by the panelists for the sample treated with 6.0 U/100 g followed by the score of 8.0 for the sample treated with 4.0 U/100 g. Therefore, the concentration of 6.0 U/100 g was selected as the best enzyme concentration and was used for the further experiments.
Data in Table 3 indicate that the pH values of different beef burgers (control, treatment A and treatment B) at zero time ranged from 6.15 to 6.60 with significant differences (5% level) between them. Similarly, the pH values of all samples during storage showed significant differences (p < 0.05). A slight but significant decrease in pH values for all samples was noted after one month of storage. This might be due to the breakdown of glycogen to lactic acid [24]. Then, pH values were stable until the end of storage.
Table 3. pH values of beef burgers during frozen storage at -18 °C for 3 months.
Storage time (month)
Treatments
Zero 1 2 3
*C **6.15c a 6.05c b 6.02c b 6.01c„ b
A 6.25b a 6.15b b 6.12b b 6.11b b
B 6.60a a 6.47a b 6.46a b 6.45a b
* C = Control, A = treatment with monosodium glutamate at 5000 ppm, B = treatment with partially purified glutaminase (6.0 U/100 g) ** Means followed by different superscripts (within each column) and different subscripts (within row) are significantly different (p < 0.05).
Microbiological quality of beef burger
The total bacterial count has been used to assess sanitary quality and safety of various meat products. High microbi-al load leads to certain undesirable changes in color, flavor and accumulation of their toxins in meat [38]. The results (Table 4) indicate that at zero time all samples including control were acceptable in terms of microbiological quality since the microbial load range was 3.1-3.3 x 103 cfu/g, which was much lower than the limit (105 cfu/g) of the Egyptian Standard Specification (ES: 1688-2005) of frozen beef burgers [14]. It is essential to start with clean raw materials to get high quality products even over a period of long-term storage. During storage, an expected slight, but significant (p < 0.05), increase in the microbial count was evident and such increase was quite acceptable since numbers did not exceed the limit of 103. This could be due els (2.0 to 10.0 U/100 g) of partially purified glutaminase ± SD
Characteristic Treatments
*C 2U 4U 6U 8U 10U
Odor **7.0d ± 0.00 7.5c ± 0.01 8.2b ± 0.03 9.0a ± 0.00 7.2d ± 0.01 6.5e ± 0.01
Color 8.8a ± 0.02 8.5b ± 0.00 8.2c ± 0.01 7.5d ± 0.02 7.0e ± 0.01 6.0f ± 0.00
Texture 7.5d ± 0.00 8.0c ± 0.01 8.5b ± 0.02 8.9a ± 0.00 9.0a ± 0.00 8.0c ± 0.02
Taste 6.5d ± 0.01 7.5c ± 0.01 8.0b ± 0.00 9.0a ± 0.01 7.5c ± 0.02 6.0e ± 0.01
Overall quality 7.0d ± 0.03 7.7c ± 0.02 8.2b ± 0.01 8.6a ± 0.02 7.7c ± 0.03 6.1e ± 0.00
* C = Control ** Means followed by different superscripts within each row are significantly different (p < 0.05).
to an increase in the amounts of free nitrogen compounds as well as fatty acids due to the slow activity of proteases and lipases during storage, which allow for better micro-bial growth.
Microorganisms that can grow at refrigerated conditions have usually been called psychrotrophic microorganisms. They are a subgroup of mesophilic microorganisms and when presented in large numbers can cause a variety of off-flavors as well as physical damage to refrigerated food [39]. Psychrotrophic bacterial counts (cfu/g) in beef burgers (treatment A and B as well as control) were monitored during storage at — 18 °C for three months (Table 5).
Table 4. Total bacterial count (cfu/g) in beef burgers during frozen storage at -18 °C for 3 months.
Treatments Storage time (month)
Zero 1 2 3
* C = Control, A = treatment with monosodium glutamate at 5000 ppm, B = treatment with partially purified glutaminase (6.0 U/100 g).
** Means followed by different superscripts (within each column) and different subscripts (within each row are significantly different (p < 0.05).
Table 5. Psychrotrophic count (cfu/g) in beef burgers during frozen storage at -18 °C for 3 months.
Treatments Storage time (month)
Zero 1 2 3
* C = Control, A = treatment with monosodium glutamate at 5000 ppm, B = treatment with partially purified glutaminase (6.0 U/100 g).
** Means followed by different superscripts (within each column) and different subscripts (within row) are significantly different (p < 0.05).
*** Estimated Standard Plate Count (ESPC/g).
Counts in the control and treatment B show a similar trend, where a slight increase in the psychrotrophic count was noted during storage and did not exceed 102 cfu/g. On the other hand, samples A showed no growth at all and this was probably due to the inhibiting effect of monosodium glutamate [40]. Similarly, a slight but significant increase, in the mold and yeast count was observed during storage with no significant differences between control and sample B. Sample A showed lower counts and this was probably due to the inhibitory effect of monosodium
glutamate [40,41] and in all cases numbers did not exceed 3.6 x 103 cfu/g, which is very acceptable. The Egyptian Standard (ES: 1688-2005) [14] for frozen beef burgers indicates that the coliform group count should not exceed 102 cfu/g. However, there was no evidence of the presence of the co-liform group in any treatment as well as the control.
Sensory evaluation of beef burgers
The results for sensory evaluation of beef burgers after three months of storage are presented in Table 6. Most of beef burger characteristics have been affected by the enzymatic treatment (B). The highest odor, texture and taste scores (8.9, 8.9 and 8.5, respectively) were recorded for treatment B. Meanwhile, the lowest color score (7.0) was given by the panelists for treatment B; the color score decreased due to the increment in the undesirable dark color, which was probably due to the formation of the Maillard reaction between reducing sugars and the formed amino acids. Also, the highest overall quality score (8.6) was for treatment B. Therefore, it can be concluded that, the partially purified glutaminase improved the overall quality of frozen beef burgers especially, the enhancement in odor and taste.
Table 6. Sensory evaluation of beef burgers at the end of 3 month of frozen storage at -18 °C (±SD).
Characteristics Treatments
*G A B
Odor **7.0c ± 0.01 7.5Ь ± 0.00 8.9a ± 0.02
Golor 8.8a ± 0.00 8.7a ± 0.00 7.0Ь ± 0.01
Texture 7.9Ь ± 0.02 8.1Ь ± 0.01 8.9a ± 0.00
Taste 6.5c ± 0.00 7.7Ь ± 0.02 8.5a ± 0.01
Overall quality 7.3c ± 0.03 7.9b ± 0.02 8.6a ± 0.00
* C = Control, A = treatment with monosodium glutamate at 5000 ppm, B = treatment with partially purified glutaminase (6.0 U/100 g).
** Means followed by different superscripts within each row are significantly different (p < 0.05).
Conclusion
The extracellular L-glutaminase of Aspergillus oryzae NRRL 32567 was successfully utilized as a flavor enhancing agent in beef burgers. The produced burgers showed high sensory scores as well as high microbiological quality. As a result, L-glutamiase from this source could be considered as a potential flavor improver in food industries replacing monosodium glutamate. However more applications on other products should be also tested.
*G A B
**3.3 x 103
3.0 x 103a„
b
3.1 x 103a,
3.9 x 103a
c
3.2 x 103Ь„ b
3.7 x 103a
4.8 x 103a. 5.7 x 103a
ba
3.6 x 103c 4.2 x 103Ь
4.5 x 103Ь
a
. 5.7 x 103a
ba
d
*G A B
»1.6 x 102
***<10 <10
2.1 x 102i <10 1.8 x 102i
2.5 x 102ah 3.7 x 102a
ba
<10
<10
2.2 x 102ah 3.5 x 102a
ba
d
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AUTHOR INFORMATION
Reda M. Mohamed, PhD, Lecturer, Department of Food Science, Faculty of Agriculture, Cairo University. Gamaa Street, Giza, 12613, Egypt. Tel.: +2-115-659-47-47, E-mail: reda_karrim@yahoo.com ORCID: https://orcid.org/0000-0001-5817-9187
Wael A. Bazaraa, Professor, Department of Food Science, Faculty of Agriculture, Cairo University. Gamaa Street, Giza, 12613, Egypt. Tel.: +2-0100-415-49-49, E-mail: waelbazaraa@agr.cu.edu.eg ORCID: https://orcid.org/0000-0003-4696-9848 * corresponding author
Ahmed M. Alian, Emeritus Professor, Department of Food Science, Faculty of Agriculture, Cairo University. Gamaa Street, Giza, 12613, Egypt. Tel.: +2-122-362-31-40, E-mail: dr.alian@hotmail.com
Nagwa M. El-Shimi, Emeritus Professor, Department of Food Science, Faculty of Agriculture, Cairo University. Gamaa Street, Giza, 12613, Egypt. (Passed away)
All authors bear responsibility for the work and presented data. All authors made an equal contribution to the work.
The authors Mohamed R. M., Bazaraa W. A. and Alian A. M. were equally involved in writing the manuscript and bear the equal responsibility for plagiarism.
The authors declare no conflict of interest.
