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International Journal of Dairy Science

Year: 2016 | Volume: 11 | Issue: 2 | Page No.: 41-51
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ABSTRACT

A new approach to prevent the proliferation of microorganisms or protect food from oxidation is using of essential oils or plant extracts. Among the antimicrobial agents, Commiphora myrrha is considered as natural and safe materials. The antimicrobial activity of Commiphora myrrha-essential oil against different species of pathogenic gram-positive as well as gram-negative bacteria were investigated. Data revealed that all tested microorganisms were susceptible to the action of Commiphora myrrha. Their Minimum Inhibitory Concentration (MIC) ranged from 2-5 μL mL–1 for all microorganisms. Processed Cheese Spreads (PCSs) samples were prepared by using five ratios of Commiphora myrrha-Essential Oil (EO) to evaluate their properties and their acceptability. Their properties were estimated through one year of storage at 5±2°C. Obtained results showed that using 2% (w/w) Commiphora myrrha-EO for preparing PCS gave satisfactorily sensory properties. The appearance was well shiny; gumminess and oil separation were absent. The penetration of satisfied treatment of myrrh (2%) was (33.5, 32.0, 31.2, 30.00 and 29.20 mm) compared to control samples (33.0, 30.5, 26.5, 25.1 and 24.5 mm) when fresh and after 1, 3, 6 and 12 months, respectively. On the other hand, meltability took the same trend; the treated-samples gained 85.4, 81.6, 80.0, 79.1 and 78.2 mm comparing with control samples 81.6, 80.5, 78.7, 77.1 and 76.6 mm, respectively. Therefore, it could be concluded that using of 2% w/w Commiphora myrrha-essential oil produced acceptable and satisfied processed cheese spreads and it could be used as a natural preservation in dairy products.
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Received: October 28, 2015;   Accepted: December 17, 2015;   Published: February 15, 2016

INTRODUCTION

Commiphora myrrha (Myrrh) family (Burseraceae) is native to Northeastern Africa, especially Somalia. Myrrh is one of the oldest known medicines and was widely used by the ancient egyptians. It is commonly known in Arabic as bitter gum. Myrrh has been traditionally used from northern Africa east through India to treat a huge range of ailments, as an anti-inflammatory, analgesic, emmenagogue, antibacterial and for oral maladies (Groom, 1981; Lewis and Elvin-Lewis, 2003). For instance, myrrh is an important product used in pharmaceutical industries, cosmetics and perfumery as well as in traditional medicines (Massoud et al., 2001; Salah, 2014). It is an excellent remedy for mouth and throat problems with a drying, slightly bitter taste and it useful for skin problems, atherosclerosis, hemorrhoid, heptoses, high cholesterol, stomatosis, immune depression and hyperglycemia (Helal et al., 2005). The myrrh’s Gum-resin-volatile oil is the main used part, where it contains (30-60%) gum including acidic polysaccharides, resin (25-40%), volatile oil (3-8%), herabolene, eugenol and many furansesquiterpenes (Chevallier, 1996; Duke, 2002; Helal et al., 2005). In another report, the plant produces an oleogum resin that is 2-8% essential oil (El-Shahat et al., 2012) 23-40% resin, 40-60% gum and 10-25% bitter principles (Su et al., 2011). Some active constituents of myrrh include the sesquiterpenes furanodiene-6-one and methoxyfuranoguaia-9-ene-8-one, which have antibacterial, antifungal and local anesthetic activities (Dolara et al., 2000) and furanoeudesma-1,3-diene and curzarene, which have potent analgesic effects (Dolara et al., 1996). The furanoses-quiter-penoidslind-estrene and its analogues make up 19% of the essential oil and are responsible for the famous scent associated with myrrh (Jensen). Other important constituents are terpenoids, steroids, flavonoids, lignans, carbohydrates and long chain aliphatic alcohol derivatives; these various metabolites give myrrh its manifold biological activities (Su et al., 2011).

Over the past few decades, many aspects of the manufacture of processed cheese have been reviewed by many authors (Shimp, 1985; Abd El-Salam et al., 2005; Dimitreli and Thomareis, 2007; Kapoor and Metzger, 2008). The production of processed cheese started in Europe and could date to the mid-1890s. Natural cheeses have limited shelf life and depending on many factors (i.e., level of moisture content, sanitary conditions during the manufacturing stages and storage conditions of the product). Their storage can range from a few weeks to a couple of years. It is possible to suggest that the idea of processed cheese originated from a desire to extend the shelf life of natural cheese or to develop a new type of cheese that was milder in taste or more stable (Berger et al., 1989). On the other hand, spreadable processed cheese has higher moisture content than other processed cheese. The standard American FDA set was moisture content 44-60% and natural cheese content no less than 51%. Thanks to the heating, emulsifying and sterilization processing, this considered as preservative factors (Guo, 2004; Attalla et al., 2014). In this regard, the content of sorbic acid/sorbate as preservative in cheeses with high moisture has been studied (Rinaldoni et al., 2014).

The goal of this study is using E.O. of Commiphora myrrha as antimicrobial agent to produce extended shelf life spreadable processed cheese and evaluate their acceptability by evaluating their chemical, rheological, microbiological and sensory parameters.

MATERIALS AND METHODS

Materials:

• Ras cheese (one month old) was obtained from Arabic Food Industrial Co. (Dometty), 6th October City, Egypt
• Matured Cheddar cheese (8 months old) and Kasomelas emulsifying salt (K-2394-Rhone-Poulenc Chimie, France) were obtained from International Dairy and Food Co. (Green Land), 10th Ramadan City, Egypt
• Low heat Skim Milk Powder (SMP) and butter were obtained from local market (purchased from Irish Dairy Board, Grattow Hawse, Ireland)
• Myrrha plant (Commiphora myrrha) belonging to family (Burseraceae) was purchased from Thailand as a white fine crystals
• Bacterial strains: Five pathogenic bacterial strains were obtained from Microbiological Resources Center (Cairo MIRCEN): Listeria monocytogenes (EMCC 1875);, Staphylococcus aureus (ATCC13565) Bacillus cereus (EMCC1080), used as gram-positive bacteria. Escherichia coli O157:H7 (ATCC51659) and Salmonella typhimurium (ATCC 25566) used as gram- negative

The chemical composition of the ingredients, which used in the manufacturing of processed cheese spreads, is presented in Table 1.

Five concentrations of myrrh’s-Essential-Oil (EO) were used in manufactured of spread-processed cheese to serve five treatments (T1, T2, T3, T4 and T5) as well as control. Table 2 illustrated the components of different blends used in spread-processed cheese.

Table 1:Chemical composition of ingredients used in manufacture of processed cheese spreads
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Table 2: Components (kg/100 kg) of different blends with different ratios of EO used in manufacture of processed cheese spreads
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Methods
Essential oil extraction and (GC/MS) analysis: Hydro distillation in clevenger apparatus had been used for essential oil extraction. The GC/MS analysis was performed with a Hewlett Packard model 5890. Gas chromatography equipped with 5 series. Mass selective detector 9144 (HP) was also conducted as reported by Mohamed et al. (2013). Table 3 illustrated the main active compounds of Commiphora myrrha-essential oil.

Growth conditions of pathogenic bacteria: Stock cultures of Listeria monocytogenes, Staphylococcus aureus, Bacillus cereus, Escherichia coli O157:H7 and Salmonella typhimurium were sub-cultured twice onto Tryptone Soya Agar (TSA) followed by incubation at 37°C. Cultures were prepared from subcultures and grown overnight in Tryptone Soya Broth medium (TSB, Oxoid, Basingstoke, UK) under optimal conditions for each microorganism as reported by Mohamed et al. (2013).

Antimicrobial assay using the disc diffusion method: Essential oil was evaluated for its antimicrobial activity on (TSA) at 37°C. Antimicrobial EO was tested undiluted as well as diluted in Tween 20 at concentrations of 25, 50 and 75 mL/100 mL, the amount of undiluted EO added to filter paper disc was 10 μL while 20 and 60 μL were added from diluted EO. The concentration of bacteria inoculated in TSA was 2×10 CFU mL–1 with inoculated volume (0.1 mL). Sterilized filter paper discs (Whatman No. 1, 6 mm in diameter) were placed on the surface of TSA.

Table 3: Concentration of main active compounds of hydro-distillates of Commiphora myrrha
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The inhibition zone diameter was measured (the filter paper disc) using vernier calipers and expressed in millimeter (Mohamed et al., 2013). All experiments were performed in duplicate.

Minimum Inhibitory Concentration (MIC) assay: Minimum Inhibitor Concentrations (MIC) was determined by using agar dilution methods (Prudent et al., 1995). Series dilutions of oil, ranging from 0.001-0.007 mL mL–1 were prepared in Nutrient Agar. Plates were dried at room temperature for 30 min prior to spot inoculation with 0.1 mL of culture containing approximately 105 CFU mL–1 of each organism. Inoculated plates were incubated at 37°C for 18 h and the MIC was determined. Inhibition of bacterial growth in plates containing the tested oil was judged by comparison with growth in blank control plates. The MIC were calculated as the lowest concentration of oil which inhibited visible growth of each organism on agar plate (Delaquis et al., 2002). Experiments were carried out in duplicate.

Processed cheese spreads preparation: Processed Cheese Spreads (PCSs) were prepared as described by Abdel-Hamid et al. (2000). Five concentrations of EO (Table 2) were added at the blends before cooking (85°C/15 min) to serve 5 treatments (T1, T2, T3, T4 and T5), respectively. Three replicates of each treatment were prepared. All samples were stored at 5±2°C for 12 months.

Methods of analysis: Chemical composition of processed cheese: The resultants PCSs were freshly analyzed for their Total Solids (TS), Total Protein (TP), Soluble Nitrogen (SN) contents and fat according to AOAC. (2007), salt and ash as mentioned by IDF (1964). The pH value was determined during storage period using a digital laboratory pH meter (HI 93 1400, Hanna instruments) with glass electrode. Total Volatile Fatty Acids (TVFAs) contents (0.1 N NaOH/100 g) were also determined according to Kosikowski (1986).

Physicochemical properties: Melting quality was determined by the method of Savello et al. (1989). Oil separation index of processed cheese was estimated according to Thomas et al. (1980). Penetration was also calculated, using penetrometer Cochler Co. INC. USA.

Color parameters: Color was measured using Hunter Colorimeter model D2s A-2 (Hunter, 1975). Tri-stimulus values of the color namely L, a and b were measured

Where:

L : Value represents darkness from black (0) to white (100)
a : Value represents color ranging from red (+) to green (-)
b : Value represents color ranging from yellow (+) to blue (-)

Sensory properties: Sensory properties of the processed cheese spreads were evaluated by panel test by the staff members at the Dairy Dept., National Research Centre, Cairo, Egypt; using the graphical descriptor scale limits scheme.

Statistical analysis: Statistical analysis was performed according to the User’s Guide given by SAS (2004) using Least Significant Differences (LSD).

RESULTS AND DISCUSSION

Growth inhibition of some pathogens by myrrh-EO: The tested oil showed highly inhibition activity against the five bacterial strains using the disc diffusion method as mentioned in Table 4. The results revealed that gram-positive bacteria were more susceptible than gram-negative one. Commiphora myrrha essential oil had a highly enhanced inhibitory effect; the most susceptible was Listeria monocytogenes and the most resistant was E. coli O157:H7. Brieskorn and Nobel (1980, 1982, 1983) had mentioned that the essential oils of Commiphora species are rich in furanosesquiterpenoids, which have been found to possess anesthetic, antibacterial, antifungal, anti-hyperglycemic properties. Five furanosesquiterpenoids; 3-methoxy-4-furanogermacra-10 (15)-dien-6-one,2-methoxy-4-furanogermacra-1(10)-en-6-one, furanogermacra-1(10)-4-dien-6-one and curzerenone (6,7-dihydro-5-isopropenyl-3, 6- dimethyl-6-vinyl benzofuran-4-one were isolated from myrrh gum. Moreover, Hili et al. (1997) tested fifty-one essential oils extracted from Commiphora myrrha for their antimicrobial activity against three bacteria, Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli and four yeasts, Torulopsis utilis, Schizosaccharomyces pombe, Candida albicans and Saccharomyces cerevisiae using the drop diffusion method. All showed antimicrobial activity against at least one of the micro-organisms. Also, the essential oil extract of Commiphora myrrha showed significant antimicrobial activity against Escherichia coli, Proteus vulgaris, Shigella flexneri, Salmonella paratyphi B and Klebsiella pneumoniae (Abdalla, 2005).

Related results were obtained by Friedman et al. (2002), Elaissi et al. (2011) and Mohamed et al. (2013).

Minimum Inhibitory Concentrations (MIC) assay: The application of Myrrh essential oil in manufacture of processed cheese spreads requires determination of the less concentration of the oil which gave the highly inhibition effect with highly acceptable sensory properties of the final product and low defects. Table 5 reflected that the concentration was ranged from 2-5 μL mL–1 to achieve the complete inhibition effect.

Chemical composition of processed cheese spreads: Table 6 showed the gross chemical compositions of different blends of processed cheese spreads with different concentrations of myrrh’s EO at fresh and during 1, 3, 6 and 12 months of storage periods compared to control.

Table 4: Inhibition growth zone of some pathogenic bacterial strains by Commiphora EO
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Three replicates were done

Table 5: Minimum inhibitory concentration of myrrh essential oil against some pathogenic bacteria
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Table 6: Chemical composition of processed cheese spreads fortified with Myrrh-EO when fresh and during storage periods at 5EC for 3 months
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*Filter paper disc diameter was 6 mm

The similarity in chemical composition of all studied samples could be explained with the uniformity of the ingredients used. The results indicated that there were slightly significant differences between fresh samples and during storage compared to control in TS, Fat/DM, TP, salt/ moisture and ash contents. The TS in all samples were slightly increased and this would possibly be as a result from the loss of moisture during storage. The results were in accordance with Krumov et al. (2010), Mansour et al. (2011) and Suleiman et al. (2011). In addition, the data demonstrated that both Fat/DM and salt/moisture slightly increased during storage while there were slightly differences between control and treatment samples in TP. Total protein was slightly higher in control samples either fresh or during storage periods compared to treated samples. Increasing concentrations of myrrh’s essential oil causing significantly increase (p>0.05) in soluble nitrogen at fresh and during storage periods compared to control samples as shown in Fig. 1. The changes in SN during storage could be the result of enzymatic activity of resistant proteinases present in the product. It could be also due to the hydrolysis of polyphosphate in emulsifying salts which caused more solubilization of proteins. These results are in agreement with Awad et al. (2014).

On the other hand, data which presented in Fig. 2 showed the difference in pH values between control compared to different samples when fresh and during 12 months of storage period. It could be noticed that pH values increased with increasing of essential oil concentrations. This increase may be due to the action of EO in inhibition of acidity forming and the alkaline effect of EO itself. During storage, pH values slightly decreased in all treatments. The decrease in pH during storage could be related to the hydrolysis occurred in emulsifying salts and their interaction with proteins. These data were agreed with Mansour et al. (2011) and Awad et al. (2014).

In Fig. 3, the data illustrated the TVFAs values in control and treated samples. There were clear differences between control and treatments when fresh and during storage period. TVFAs took an increasing trend during storage in all samples. This increase was mainly attributed to the residual activity of heat resistant lipases in cheese formula. Consequently, hydrolysis of purified polysaccharides of gum myrrh gave high yields of a mixture of neutral sugars and acidic oligosaccharides. Moreover, Foda et al. (2010) indicated that increasing of spearmint essential oil concentration, more than 1.0 mL kg–1 retentate, significantly increased these values.

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Fig. 1:
Changes of SN (%) of processed cheese spreads fortified with different concentration of myrrh’s EO when fresh and during storage period for 12 months at 5±2°C

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Fig. 2:
Changes of pH values of processed cheese spreads fortified with different concentration of myrrh’s EO when fresh and during storage period for 12 months at 5±2°C

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Fig. 3:
Changes of TVFAs values of processed cheese spreads fortified with different concentration of myrrh’s EO when fresh and during storage period for 12 months at 5±2°C

Presented data also indicated that prolonging the cold storage for 12 months significantly (p>0.05) increased (TVFAs) values compared with fresh processed cheese spreads. These results in agreement with those obtained by Abd El-Salam et al. (1993), who reported that the changes in TVFAs occur during the first 15-30 days of storage which related with maximum bacterial growth and high concentration of total volatile free fatty acids in cheese.

Physical properties of processed cheese spreads
Penetration: Figure 4a indicated that all treated samples had higher penetration values than control samples. The data revealed that increasing the concentration of myrrh’s essential oil ratios caused significant increasing (p>0.05) of penetration values, so the highest sample was (T5) which had the highest concentration compared to control. This increase could be due to the unique composition of myrrh. The main constituents of the myrrh oleo-gum resin are 2-8% volatile oil (El-Shahat et al., 2012) 23-40% resin and 40-60% gum (Su et al., 2011). The gum is water-soluble and contains polysaccharides, proteoglycans and proteins, as well as the compounds D-galactose, L-arabinose and 4-methyl D-glucoronic acid. The volatile oil is consists of steroids, sterols and terpenes (Hanus et al., 2005) including the furanosesquiterpenoids lindestrene (Table 3) and its analogues.

On the other hand, Fig. 4b also represented meltability values in processed cheese made with different concentrations of myrrh essential oil. It could be noticed that as increasing EO concentrations, the meltability was increased compared to control samples. It could be attributed to the specific composition of that EO that contains about 40-60% gum (Su et al., 2011). The cheese meltability showed a tendency to decrease along the storage period and the decrease was more noticeable in the control samples.

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Fig. 4(a-c):
Physical properties (a) Penetration, (b) Meltability and (c) Oil separation of processed cheese spreads fortified with different concentration of myrrh’s EO when fresh and during storage period for 12 months at 5±2°C

Table 7: Color parameters of different processed cheese spreads fortified with myrrh EO when fresh and during storage period for 12 months at 5±2°C
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*See Table 2, L: Value of darkness from black (0) to white (100), a: Color ranging from red (+) to green (-), b: Color ranging from yellow (+) to blue (-)

Oil separation took the same trend of meltability which had been showed in Fig. 4c. Increasing concentration of Myrrh’s essential oil caused increasing of oil separation when fresh and during storage compared to control samples. The highest oil separation values was in treatment 5 compared to control samples which had the lowest values. The oil separation value depends on the state of fat and protein in resultant processed cheese emulsion that can be affected by type and amount of raw materials in the base formula, pH value, cooking time and temperature. These results agree with Awad et al. (2014). The increase in oil separation value with prolonged storage time could be due to the drop in the pH value and changes that occurred in soluble nitrogen contents (Abdel-Hamid et al., 2000).

Color parameters: Table 7 reflected the color parameters of control and processed cheese spreads samples with different myrrh’s EO ratios when fresh and during cold storage for 12 months. Control samples had gained higher values of whiteness degree when fresh and during storage than the rest of treatments. Whiteness had been decreased with increasing of myrrh’s EO ratios in samples. As increasing ratios of myrrh’s EO in the samples the parameters (a and b) increasing. Parameter (b) which reflected, yellowish was higher pronounced than parameter (a) which reflected reddish, this may be due to the slightly yellow color of myrrh crystal.

Sensory evaluation of processed cheese spreads: Organoleptic properties were evaluated using graphical descriptor scale limits. Table 8 indicated that control samples had moderate shiny surface appearance, soft spreadable body and moderate strong flavor. Guminess and oil separation were absent in control sample and overall preference was like. Obtained data also revealed that no clear differences were observed between the four treatments (T2, T3, T4 and T5). The best result was obtained by 2% bitter gum (T1). This treatment had very much shiny appearance, very soft and spreadable body. The flavor was strong as well as guminess and oil separation was absent and overall preference was like very much.

Table 8: Sensory properties of processed cheese spreads fortified with Myrrh EO when fresh and during storage period for 12 months at 5±2°C
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Image for - Impact of Myrrh Essential Oil as a Highly Effective Antimicrobial Agent in Processed Cheese Spreads

CONCLUSION

It could be concluded that using 2 mL kg–1 Myrrah essential oil produced satisfied properties; highly antimicrobial activity with best acceptable organoleptic behavior in processed cheese spread.

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