Volume 3 - Issue 5

Research Article Biomedical Science and Research Biomedical Science and Research CC by Creative Commons, CC-BY

Inhibition of Escherichia coli, Pseudomonas Aeruginosa, Staphylococcus Aureus and Enterococcus Feacalis through Malus Domestica Extracts to Eliminate Food Borne Illness

*Corresponding author: Umar Farooq, Department of Food Science and Technology, MNS University of Agriculture, Multan, Pakistan.

Received: June 17, 2019; Published: June 28, 2019

DOI: 10.34297/AJBSR.2019.03.000701


The present study was designed to evaluate the antibacterial activity of aqueous extracts of Malus domestica (peel and pomace) against foodborne pathogens (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Enterococcus feacalis). Extraction conditions (temperature and time) were optimized to obtain maximum yield by using response surface methodology. Antibacterial potentials of the extracts were examined through disc inhibition zone technique and the results were compared with commercial antibiotic. Results indicated that maximum antibacterial activity was shown by peel extract against Staphylococcus aureus with average zone of inhibition 19.25±0.89 mm while pomace 12.75±0.71 mm. The antibacterial activities of peel extract were comparable with commercial antibiotic (20.13±0.83 mm). Escherichia coli were appeared to be the most resistant with inhibition induced by the extracts of peel 15.00±1.07 mm and pomace11.50±0.53mm.

Keywords:Food borne pathogens; Food safety; Food borne illness; Malus domestica; Extract; Antibacterial activity


Pathogenic microbial agents such as bacteria, fungi and viruses are major threats to food safety as well as community health [1]. These microorganisms cause number of diseases, such as Gastrointestinal tract infection, diarrhoea, nausea, intestinal disorders, abdominal bloating, allergies and inflammatory disorders. Use of antibiotics have shown the cure and suppression of diseases but it also lead to increase resistance as well as expansion of strains [2]. This situation has necessitated a search for natural antimicrobial agent against pathogenic microbes to control such disorders and to ensure food safety. Fruits phytochemicals and their extracts with identified antimicrobial activities have great importance in the treatment of many infectious diseases [3]. Recent study has exposed that peel and seed of many fruits like apple peel, grape peels and seeds [4], pomegranate peel [5], mango seed kernel [6] and wampee peel [7] may possibly have antimicrobial property. All components of plants separately or in combination show antimicrobial activity and antimicrobial agents can be found in any part of plant as in stalks, bark, leaves, roots, fruits, flowers, seeds, pods, latex, stems, fruit rind and hull [8]. Apple fruit and its extract have been used as medicine for prevention and treatment of different diseases [9].

Malus domistica (Apple) is the pomaceous produce of apple tree, in family rose (Rosaceae) and species Malus domestica [10]. Biological assays showed that apple polyphenols have a wide range of pharmacological effects, such as anti-bacterial [11], antiviral [12], antioxidant activity [13], and the inhibition of colon carcinogenesis [14]. There is huge amount of apple by-products (peel and pomace) are generated as a result of processing, which is an abundant source of phytochemicals and these kinds of bio resources could be used for extraction of fruit phenolics [15]. These compounds offer very strong facts of antimicrobials uniqueness. Thus, the recovery of apple polyphenols from pomace as an excellent healthcare product is another important biotechnological application [16].

Various studies have revealed that apple extracts exhibit antimicrobial activity [17]. Malaviya and Mishra [18] evaluated the alcoholic and aqueous extracts of apple to check the antimicrobial activity against fungi and bacteria. Comparison of both extracts showed that the aqueous extracts of apple fruit demonstrated greater antimicrobial activity against Gram positive bacteria (B. subtilis and S. aureus) as compared to Gram negative bacteria (P. aeruginosa and E. coli). Muthusamy and Ranasinghe [19] have studied the antimicrobial activity of selected apple phenolics (chlorogenic acid, catechin and phloridzin). These three tested phenolic compounds suppressed the growth of E. coli (Gram negative bacteria) and Listeria innocua (Gram positive bacteria), the two pathogenic bacteria. Jelodarian [20] also evaluated the antimicrobial activity of apple fruit. But there is no comprehensive research about the antibacterial activity of apple by-products (peel ad pomace).

By considering the significant functionality of apple peel and pomace, present study was designed to optimize the extraction conditions by using response surface methodology and then to inhibit the food-borne pathogens (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Enterococcus feacalis) by the use of aqueous extracts of apple peel and pomace in comparison with commercially available antibiotics.

Materials and Methods

Sample preparation

Fresh apples were purchased from a local market of Sargodha of golden verity and were brought to the Food Microbiology Laboratory, Institute of Food science and Nutrition, University of Sargodha in plastic bags. The fruits were washed, dried and then peel was manually separated. The peels and pomace (after juice extraction) were dried in an oven (BINDER) at 55°C for 3 days. Then dried peels and pomace were powdered in a grinder (MOULINEX) and stored in plastic bags for next step of extraction.

Extraction procedure

Five gram of each dried and ground samples (pomace or peels) were weighed on a sensitive balance (SHIMADZU) and then transferred to two fifty millilitre conical flask. One hundred millilitre distilled water was added into flask and placed on hot plates (VELP SCIENTIFICA). Each conical flask mouth was covered with aluminium foil to avoid the excessive evaporation. The liquid extract was separated from solids by using muslin cloth. Then again it was filtered through Whatman No. 1 filter paper by using vacuum suction filtration assembly. The supernatant was then transferred to a rotary evaporator (HB DIGITAL, HEIDOLPH) at 60°C to evaporate the water under vacuum. Then the extract was dried in hot air oven at 60°C until constant weight. All samples were extracted in duplicates.

Experimental design

Firstly, screening experiments were conducted through a single factor experimental design. Independent factors, such as temperature and time were investigated to find most important independent factors and their respective ranges to maximize percentage extraction yield (response variable). Orthogonal experimental design was used employing significant independent factors for the optimization through response surface methodology (RSM).

Single factor experiments

Before using RSM, the initial experiments were carried out to select the significant variables in extract recovery as well as the experimental range for independent factors. In single factor analysis, extraction temperature and extraction time were found to be the most important factors to obtain maximum recovery. Each sample was extracted with water at 30, 50, 70, and 90oC for 45 min and at 60°C for 15, 30, 45 and 60 minutes. The liquid solid ratio (5g/100ml) and particle size (40 mesh) was kept constant.

Response surface modelling

Orthogonal test design (Table 1) was employed for optimization of extraction conditions. Two factors (coded and uncoded value) and three levels were examined for the optimum combination of extraction variables based on the highest extraction yield of samples in initial experiment. Extraction yield was taken as response Y with standard deviation (Table 2). The variables Xi were implicit as xi based on Equation (1):

Where xi was the coded value (-1, 0, +1,) of an independent variable, was the real value of an independent variable at the centre point, and ΔXi was the step change value.

Statistical analysis

All data was replicated thrice, and results were averaged. Design expert SAS 9.2 was used for optimization. Single factor experiments were presented on Excel sheet (Microsoft office Enterprise 2007). Multiple linear regression analysis was conducted by the statistical software (SAS 9.2). Experimental data were fitted into a secondorder polynomial model as shown in equation (2):

where Xi and Xj were the independent variables effecting the responses Y; β0, βi, βii, βij were the regression coefficients of variables for intercept, linear, quadratic and interaction terms, respectively; k was the number of variables (k = 2). The quality of fit of the polynomial model was articulated by the coefficient of determination R2, and the statistical significances were probed by determining the F-value at a probability (p) at 0.001, 0.01, or 0.05.

Microorganisms and culture media

The food-borne pathogens Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Enterococcus feacalis were obtained from Food Microbiology Laboratory, Institute of Food Science and Nutrition, University of Sargodha, Sargodha. These cultures were maintained on nutrient agar plate by continuous subculturing after 10 - 15 days.

Assessment of antimicrobial activity

The antimicrobial effects of the apple extracts were evaluated against isolated strains of pathogens by “disc diffusion method” as suggested by Sadeghian et al. [21] with some modifications.

Results and discussion


The preliminary extraction of these compounds was performed at various temperatures and times to observe significant variable and range for maximum recovery of the extracts.

Influence of temperature on recovery of water-soluble compounds

Conventional extraction and concentration of apple extract (peel and pomace) was done at temperature ranging from 30ºC to 90ºC for 45 minutes (fixed). (Figure 1a) indicated that the recovery of soluble compounds was increased with the increment in temperature up to 70ºC and then decline in percent recovery of the extract was observed. Maximum recovery from peel was obtained at 70ºC followed by 90ºC and 50ºC, which was 16.33, 14.67 and 12.67%, respectively. The results were in accordance with the findings of Wisaam et al. (2012) who observed 18.00% yield of water-soluble extracts of dried fruit peel at 50ºC.

Similarly, the maximum recovery of extract from apple pomace was observed at 70°C with mean percent recovery of 16.67% (Figure 1a). Least recovery was obtained at temperature 30ºC with mean percent recovery of 3.67% (Figure 1b). Some researchers had also observed similar results while working on various fruit extracts and reported that the extraction yield was increased with temperature and was maximum at 60°C [22-24] and 50°C [25].

Biomedical Science & Research

Figure 1: Influence of temperature (◦C) on the extraction of water-soluble compounds from apple peel (a) and pomace (b).

Influence of time on recovery of water-soluble compounds

The results depicted in (Figure 2a) revealed that the extraction of water-soluble compounds from apple peel and pomace was gradually increased with increment in time up to 30 minutes and after this there was a decline in percent recovery of the extracts at 60˚C temperature (fixed). The maximum recovery of 18.67% and 22.17% was obtained for peel and pomace. The extraction rate was highly dependent on time of treatment and it was observed that by increasing the time, the extraction yield was also increased but after 30 minutes there was a decline in percent recovery of the extract. The results were similar to the findings of Wissam et al. [26], who also reported reduced extraction rate of aqueous fruit peel extracts after 30 min of treatment. This decline in recovery might be due to degradation of polyphenols and proanthocyanins (components of extract) (Figure 2b).

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Figure 2:Influence of time (min) on the extraction of water-soluble compounds from apple peel (a) and pomace (b).

Optimization of extraction conditions

To assess the effects of two independent variables including extraction time (X1) and temperature (X2), response surface methodology was employed for extraction of water-soluble compounds from apple peel and pomace. For this purpose, on the basis of single factor results, the temperature conditions being selected were 70˚C as central point and the upper and lower levels being chosen were 90˚C and 50˚C, respectively. Similarly, depending upon the central point for time period (30 minutes), 45 minutes and 15 minutes were taken as upper and lower level of time factor for the preparation of various combinations of time and temperature through RSM. Similar temperature and time combinations were also used by some previous scientists for extraction of watersoluble compounds from fruits or parts of the fruits. Dent et al. [23] performed extraction for a period of 30, 60 and 90 minutes at 60˚C and 90˚C.

(Table 1) present the running variables and mean percent recovery with standard deviation (Y). By applying multiple regression analysis on the experimental data, the model for the response variable could be expressed by the following quadratic polynomial equation in the form of coded values.

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Table 1:

The result of statistical analysis (ANOVA) regarding effect of time and temperature on mean percent recovery of water-soluble compounds showed that the combine effect of time and temperature on extraction from peel and pomace was non-significant. While the combination of temperature and temperature and time and time showed significant results.

Analysis of response surfaces

Three-dimensional response surface and two-dimensional contour plots are the graphical representations of regression equation and are very useful to judge the relationship between independent and dependent variables. Different shapes of the contour plots indicate whether the mutual interactions between the variables are significant or not. Circular contour plot means the interactions between the corresponding variables are negligible, while elliptical contour suggests the interactions between the corresponding variables are significant [27] . The effect of extraction time and temperature on recovery of water-soluble compounds from peel and pomace was illustrated in the three-dimensional response surfaces and 2-dimensional contour plots (Figure 3a-3d). Response surface revealed that the optimum extraction yield of apple extracts was observed at 70˚C for 30 minutes of treatment with mean recovery of 27.9 % of peel and 25.3 % of pomace.

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Figure 3:Response surface and Contour plot showing the effect of temperature (X1, °C) and time (X2, min) on recovery of water-soluble compounds from apple peel (a and c) and pomace (b and d).

Evaluation of antimicrobial activity of various extracts of apple

The extracts obtained can potentially be used in the treatment of infectious diseases caused by microorganisms that are showing emergence of resistance to currently available antibiotics. The antimicrobial effects of the apple peel and pomace extracts were evaluated by disc diffusion method. In the present study, the antibacterial potential of aqueous extracts of apple peel and pomace were evaluated against different pathogens (E. coli, P. aeruginosa, S. aureus and E. feacalis) and also compared with a commercially available antibiotic (Figure 4). The results obtained so far are explained one by one as follow:

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Figure 4: Antibiogram of antimicrobial activity of peel and pomace extracts and antibiotics.

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Table 3:Average antibacterial activity of extracts and antibiotic.

Average values of zones of inhibition were presented in (Table 3).

The results revealed that the antimicrobial potential of apple extracts was more prominent against Gram’s +ve bacteria. Kalmenson et al. [28] and Parikh et al. [29], who recommended that the Gram +ve bacteria are less resistant than that of Gram – ve bacteria. The greater resistance of Gram’s negative bacteria against plant extracts than Gram positive bacteria might be due to the differences in chemical composition and structure of cell wall of both types of microorganisms as described by Holley and Patel [30].

Escherichia coli (E. coli) and Pseudomonas aeruginosa (P. aeruginosa) both are Gram negative food-borne pathogens with respect to their cell structure. The extracts showed reasonable/ significant antibacterial activity against E. coli as compared with antibiotic (ciprofloxacin). The results for antibacterial activity of apple extracts and antibiotic against E. coli are given in (Figure 5a). The zone of inhibitions for antibiotic, peel extract and pomace extract were 22.50 mm, 15.00 mm and 11.50mm, respectively. Similarly, antibacterial activity of apple extracts and antibiotic against P. aeruginosa is given in (Figure 5b). The maximum inhibition zone against P. aeruginosa was observed in case of antibiotic followed by peel extract with mean inhibition zone of 19.00 mm and 13.50mm, respectively and the minimum inhibition was observed in case of pomace extract with mean inhibition zone of 9.05 mm. The results were closely related to the findings of Fratianni et al. [31] who observed 6 mm to 13mm inhibitory zone of apple extracts against E. coli. Some other researchers also reported that the apple extract have 11 mm and 6 mm (0.6 cm) inhibition zones against P. aeruginosa [18, 20].

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Figure 5: Antibacterial activity of apple extracts against Escherichia coli (a), Pseudomonas aeruginosa (b), Staphylococcus aureus (c) and Enterococcus faecalis (d)

The Gram’s +ve bacteria selected for the experiment were Staphylococcus aureus (S. aurous) and Enterococcus feacalis (E. feacalis). The results of disc diffusion method against S. aurous and E. feacalis are given in (Figure 5c & 5d). Inhibition zones of apple extracts and antibiotic against S. aurous are given in Fig. 5c. The zone of inhibitions for antibiotic, peel extract and pomace extract were 20.13 mm, 19.25 mm and 12.75 mm, respectively. The maximum inhibition zone against E. feacalis was observed in case of antibiotic followed by peel extract with mean inhibition zone of 19.50 mm and 17.63mm, respectively and the minimum inhibition was observed in case of pomace extract with mean inhibition zone of 14.00 mm as shown in (Figure 5d). The similar results were also observed by Malaviya and Mishra [18] and Alberto et al. [17], who reported that water extract of apple showed higher activity against Gram’s positive bacteria (S. aureus and E. feacalis). The antimicrobial potential of the apple extracts could be related to the presence of various functional/bioactive compounds like phenolics [32]. The apple also contains various phytochemicals, which give precious properties to the apple with special reference to antimicrobial potential against different infectious diseases [33].


The results directed that extracts of apple peel and pomace possessed noteworthy antibacterial activity of clinical significance against the bacterial strains. All the extracts showed inhibition against these pathogens (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Enterococcus feacalis). Apple peel has maximum inhibition (19.25 mm) against S. aureous. So, it could be concluded that the antimicrobial (antibacterial) activity was found to be higher in apple peel than that of apple pomace. Moreover, the Gram’s positive bacteria were found to be more susceptible to antibacterial potentials of apple peel and pomace, while Gram’s negative bacteria showed relative resistance against extracts. From these results it was concluded that the food-borne pathogens and diseases can be controlled by the use of apple peel and pomace water-soluble extracts, which might be a cheaper and safe (natural) way of the treatment.


I am highly thankful to my research committee for their intellectual and technical guidance.

Conflict of interest

Authors has no conflict of interest.


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