Background
Foodborne diseases are taking thousands of lives every year. Forty-five million people become food poisoned, 128,000 people are hospitalized, and it takes 3000 lives in the USA annually [1]. Therefore, food safety is an important issue for consumers and the food industry. The food industry is now following the consumer opinions for safer additives, especially natural preservatives [2, 3]. Discovering plants and their active ingredients to prevent or cure infections, including foodborne diseases, could be a great achievement [3]. There are at least two important reasons for clinical scientists to get interested in the potential antimicrobial effects of plants. The first reason is the increasing resistance of bacteria to common antimicrobial agents and the second is the unpleasant side effects of synthetic antimicrobial agents. More than that, the antibacterial effects of various medicinal plants are being investigated due to the toxicological concerns associated with the synthetic antioxidants and preservatives [4, 5].
P. granatum L. (Punicaceae) is widely cultivated in Iran and has an extensive geographical distribution from Iran to Himalayas in northern India [6]. Punica granatum var. pleniflora is endemic to Iran and grows as a bush or shrub 2–5 m in height. The flowers are odorless but colorful red or reddish, 3.5 to 7 cm in length, campanulate or cylindrical. Flowers are two types. One of them is the fertilized with large and long- styled, long-stamened, and colorful flowers. The other is the unfertilized with smaller, barren and short- styled, short-stamened flowers, in which the stigma is far below the anthers [7, 8]. The unfertilized flowers are commonly known as “Golnar” in Iranian traditional and complementary medicine [9‐11].
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Golnar has been extensively used in Iranian traditional medicine as an astringent, haemostatic, and antimicrobial agent. It has also been used as a treatment for bronchitis, diarrhea, digestive problems, infected wounds, and diabetes [9‐11]. P. granatum fruit (pomegranate) and its pericarp are known to have high molecular weight phenolic compounds including condensed tannins and hydrolysable tannins [12‐14]. Several studies indicate that P. granatum peels can slow bacterial growth and inhibit toxins produced by bacteria [15‐17]. To the best of our knowledge there is no study on antimicrobial activity of Golnar.
In this study, we investigated the antibacterial activity of Golnar against bacteria causing foodborne diseases, based on the traditional use of Golnar as an antibacterial agent. In addition, the total phenolic and flavonoid contents of ethanol extract and its fractions were determined.
Methods
Plant material
Shade dried Golnar were obtained from Darab, Fars Province, Iran in November 2012 and were identified by Dr. Asgarpanah in Department of Pharmacognosy, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran. A sample was deposited in the herbarium of the university with voucher specimen No.733. Flowers were then ground down to fine powder by a mechanical miller.
Preparation of ethanol extract
750 g of the grounded Golnar was exhaustively extracted by maceration with EtOH (3 × 1.5 lit). The extract was evaporated to yield the residue (195 g). The dried ethanol extract (EE) was kept in the refrigerator at 4 °C.
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Preparation of fractions
According to the pre-evaluation of the antibacterial effect of EE, the extract was fractioned by chloroform (C), ethyl acetate (EA), methanol (M) and water (W), successively. The obtained fractions were filtered through paper filter Whatman No. 1 to remove the solid particles and then concentrated on rotary evaporator. The samples were then stored at 4 °C.
Bacterial strains
Six different microorganisms including Staphylococcus aureus ATCC 25923, Bacillus cereus PTCC 1247, Listeria monocytogenes ATCC 7644, Escherichia coli ATCC 25922, Shigella dysantriae PTCC 1188, and Salmonella typhi ATCC 19430 were used for evaluation of antibacterial effects of the extract and the fractions. The microorganisms were obtained from Iranian Research Organization for Science and Technology, Persian Type Culture Collection (PTCC), Tehran, Iran. The microorganisms were cultured on Mueller Hinton Agar (MHA) medium (Merck, Germany) and incubated at 37 °C for 24 h.
Antibacterial susceptibility test
The agar well-diffusion method was conducted for primary evaluation of the inhibitory effects of EE and its fractions against test microorganisms [18, 19]. The Muller Hinton agar (MHA) medium was purchased from Merck Company, Germany. The wells (6 mm diameter) were made in the medium which was streaked with a suspension of the microorganism in saline with a turbidity equivalent to a 0.5 McFarland standard.
The extract and the fractions were serially diluted from 500 to 1.95 mg/ml by sterile Tween 20 (20 % v/v). 100 μl of different concentrations of C, EA, M, W fractions, EE extract, and solvent (as negative control) were added to each well on MHA medium. The plates were then incubated overnight at 37 °C and the zones of inhibition were measured. The test was repeated three times and the means of the results were reported.
Minimum inhibitory concentration (MIC)
The MIC of the extract and its fractions were determined by macro broth dilution method according to CLSI (Clinical Laboratory Standardization Institute) [19, 20]. The inoculums with a turbidity equivalent to 0.5 McFarland standard (1.5× 108 cfu/ml) were prepared by making a direct broth suspension of isolated colonies selected from 24 h cultured bacteria on MHA plate.
Serial dilutions of ethanol extract and its fractions were prepared volumetrically in sterile tubes using Muller Hinton Broth (MHB) medium (Merck, Germany). The 0.5 McFarland suspensions were diluted by MHB (1:150). One ml of these adjusted inoculums were added to each of the tubes containing 1 ml of dilutions of the ethanol extract or its fractions. Therefore, the final inoculums were 5 × 105 CFU/ml. The tubes were incubated for 24 h at 37 °C, and then evaluated for bacterial growth. The lowest concentration with no visible growth was considered as minimum inhibitory concentrations (MICs) of the extract and the fractions [20].
Minimum bactericidal concentration (MBC)
To confirm MICs and to establish MBC, 50 μl of each tube with no visible growth was removed and inoculated in MHA plates. After 48 h of aerobic incubation at 37 °C, the numbers of surviving microorganisms were determined. MBC was defined as the lowest concentration at which no growth of bacteria was seen [20]. Each experiment was repeated at least three times.
Total phenolic content
Folin Ciocalteu reagent was used for the analysis of total phenolic content of the extract and the fractions [3]. Stock solutions of the ethanol extract and the fractions in methanol (10 mg/ml) were prepared and 0.02 ml of each stock solution was added to 1.58 ml of distilled water in a test tube. Then, 0.1 ml of diluted Folin Ciocalteau reagent was added to the test tube. The mixture was kept at room temperature for 3 min and then, 0.3 ml Na2CO3 7.5 % solution was added. After 30 min, absorbance of the mixture was measured at 765 nm by UV-spectrophotometer (Multispec-1501 Shimadzu). A standard curve was prepared using gallic acid (Merck, Germany). The determinations were carried out in triplicate and the total phenolic content was expressed as gallic acid equivalents (mg of GAE/g of sample) [3].
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Total flavonoid content
The total flavonoid contents were measured by a colorimetric assay [21, 22]. The dried extract was dissolved in 80 % methanol to obtain a final concentration of 1 mg/ml. The calibration curve was prepared using 0.1–1 ml aliquots of Rutin solution, 500 μL of the acetic acid solution, 2 ml of the pyridine solution and 1 ml of the aluminum chloride solution. The final volume was adjusted to 10 ml with 80 % methanol and the final Rutin concentration was 1–10 μg/ml. To quantify the flavonoids, 0.5 ml of the ethanol extract or the fractions was transferred to a test tube and 0.5 ml of the acetic acid solution, 2 ml of the pyridine solution, 1 ml of the reagent aluminium chloride solution and 6 ml of 80 % methanol were added. The samples were kept at room temperature for 30 min and the absorbances of the mixtures were measured in 420 nm. The test was performed three times and the flavonoid content was expressed as milligrams of Rutin equivalents (RE) per gram of sample of extracts (mg RE/g) [21, 22].
Statistical analysis
Data were presented as mean ± SD in all tables. One-way ANOVA and Tukey’s post test were used to compare the total phenolic or flavonoid content of the ethanol extract and the fractions. Graphpad Prism 5.0 (GraphPad Software, Inc., CA, USA) was used for statistical analysis. In all experiments a value of P < 0.05 was considered significant.
Results
Yield of the fractionation
The fractionation yields are shown in Table 1.
Table 1
The yield of fractions from Golnar ethanol extract
Type of fractions | Yield % |
|---|---|
Methanol | 25 |
Water | 25 |
Ethyl acetate | 10 |
Chloroform | 10 |
Evaluation of antibacterial effect by the Agar Diffusion Method
The diameter of inhibition zones made by the ethanol extract (EE) and its fractions (C, EA, M, W) are shown in Table 2. Tween 20 (20 % V/V), as negative control, showed no inhibitory effect against the tested strains. As shown in Table 2, the ethanol extract and its fractions showed antibacterial activity against all of the tested microorganisms (diameters of zone of inhibition ranging between 10 and 34 mm). The largest inhibition zone made by TE extract and its fractions was against S. aureus. The methanol and water fractions reflected larger inhibition zones while ethyl acetate and chloroform fractions showed smaller zones.
Table 2
Mean of Growth inhibition zone diameter (mm) of ethanol extract of Golnar and its fractions (n = 3)
Extract concentration | 500 mg/ml | 250 mg/ml | 125 mg/ml | 62.5 mg/ml | 31.25 mg/ml | 15.62 mg/ml | 7.8 mg/ml | 3.9 mg/ml | 1.95 mg/ml | |
|---|---|---|---|---|---|---|---|---|---|---|
Microorganism | ||||||||||
Staphylococcus aureus ATCC 25923 | M | 32 ± 0 | 30 ± 0.6 | 29 ± 1 | 28 ± 1 | 27 ± 0 | 26 ± 0.6 | 25 ± 0.6 | 24 ± 1 | 23 ± 0 |
W | 34 ± 0.6 | 32 ± 1 | 31 ± 1 | 30 ± 0.6 | 28 ± 1 | 27 ± 0.6 | 26 ± 1 | 25 ± 0.6 | 24 ± 0.6 | |
EA | 31 ± 1 | 28 ± 1 | 27 ± 1 | 26 ± 0.6 | 24 ± 1 | 22 ± 0 | 18 ± 0 | 15 ± 1 | 13 ± 0 | |
C | 19 ± 1 | 16 ± 0 | 14 ± 0.6 | 13 ± 0.6 | - | - | - | - | - | |
EE | 32 ± 0 | 30 ± 0 | 28 ± 0.6 | 27 ± 1 | 25 ± 1 | 24 ± 1 | 23 ± 1 | 22 ± 0 | 21 ± 0.6 | |
Bacillus cereus PTCC 1247 | M | 29 ± 0 | 21 ± 0 | 19 ± 1 | 17 ± 1 | 16 ± 1 | 15 ± 0.6 | 14 ± 0.6 | 13 ± 0.6 | 12 ± 0.6 |
W | 28 ± 1 | 23 ± 1 | 22 ± 0 | 19 ± 0 | 18 ± 0 | 16 ± 0 | 14 ± 0.6 | 13 ± 0.6 | 12 ± 0.6 | |
EA | 29 ± 0.6 | 23 ± 0.6 | 20 ± 0.6 | 14 ± 1 | 13 ± 1 | 12 ± 0 | 11 ± 0 | 10 ± 0 | - | |
C | 17 ± 0 | 13 ± 1 | 12 ± 1 | 11 ± 1 | 10 ± 0.6 | - | - | - | - | |
EE | 28 ± 0.6 | 25 ± 0.6 | 23 ± 0 | 19 ± 0 | 18 ± 1 | 16 ± 1 | 15 ± 1 | 12 ± 0 | 11 ± 0 | |
Listeria monocytogenes ATCC 7644 | M | 30 ± 0 | 26 ± 1 | 22 ± 0.6 | 19 ± 0.6 | 17 ± 0.6 | 15 ± 0 | 14 ± 0 | 11 ± 0 | 10 ± 0.6 |
W | 30 ± 0.6 | 25 ± 1 | 23 ± 1 | 20 ± 0 | 17 ± 0 | 15 ± 0 | 14 ± 0.6 | 12 ± 0.6 | 11 ± 0.6 | |
EA | 28 ± 0 | 22 ± 0 | 20 ± 1 | 17 ± 0.6 | 13 ± 1 | - | - | - | - | |
C | 18 ± 1 | 14 ± 1 | 11 ± 0.6 | - | - | - | - | - | - | |
EE | 32 ± 1 | 28 ± 1 | 26 ± 1 | 26 ± 0 | 22 ± 0 | 18 ± 0 | 14 ± 0.6 | 13 ± 0.6 | 11 ± 0.6 | |
Shigella dysantriae PTCC 1188 | M | 32 ± 0.6 | 29 ± 0.6 | 28 ± 0.6 | 28 ± 0 | 27 ± 0 | 26 ± 1 | 25 ± 1 | 24 ± 0 | 23 ± 0.6 |
W | 30 ± 1 | 28 ± 0.6 | 27 ± 0.6 | 26 ± 0 | 25 ± 0 | 24 ± 0 | 22 ± 0.6 | 20 ± 1 | 19 ± 1 | |
EA | 30 ± 0 | 27 ± 0 | 24 ± 0.6 | 21 ± 0.6 | 20 ± 0.6 | 19 ± 0 | 17 ± 0 | 15 ± 0.6 | 12 ± 0.6 | |
C | 18 ± 0.6 | 15 ± 1 | 13 ± 1 | 12 ± 1 | - | - | - | - | - | |
EE | 30 ± 1 | 27 ± 0 | 25 ± 0 | 24 ± 0.6 | 23 ± 1 | 21 ± 1 | 20 ± 1 | 19 ± 0 | 18 ± 0 | |
Salmonella typhi ATCC 19430 | M | 31 ± 0.6 | 24 ± 0 | 21 ± 0 | 18 ± 0.6 | 14 ± 0.6 | 13 ± 0.6 | 12 ± 0.6 | 11 ± 0.6 | 10 ± 0 |
W | 30 ± 0 | 25 ± 0 | 22 ± 0 | 16 ± 0.6 | 13 ± 0.6 | 12 ± 0.6 | 10 ± 0.6 | - | - | |
EA | 23 ± 0.6 | 19 ± 1 | 15 ± 1 | 12 ± 1 | 11 ± 1 | - | - | - | - | |
C | 14 ± 1 | 10 ± 1 | - | - | - | - | - | - | - | |
EE | 27 ± 0.6 | 24 ± 0 | 22 ± 0 | 21 ± 0 | 17 ± 0 | 14 ± 0 | 11 ± 0.6 | - | - | |
Escherichia coli ATCC 25922 | M | 28 ± 1 | 19 ± 1 | 15 ± 0.6 | 11 ± 0 | 10 ± 0 | - | - | - | - |
W | 25 ± 0.6 | 15 ± 0.6 | 12 ± 0 | 10 ± 0 | - | - | - | - | - | |
EA | 23 ± 1 | 18 ± 1 | 15 ± 1 | 12 ± 0.6 | - | - | - | - | - | |
C | 12 ± 0 | - | - | - | - | - | - | - | - | |
EE | 22 ± 1 | 15 ± 0.6 | 13 ± 0.6 | 10 ± 0 | - | - | - | - | - | |
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Determination of MIC
Table 3 shows MIC values of the extract and the fractions against all tested microorganism. The MIC values obtained in this study ranged from 0.19 to 12.5 mg/ml. The ethanol extracts and the methanol and water fractions showed the lowest MIC (0.19 mg/ml) against S. aureus. This indicates the highest sensitivity of S. aureus among the six microorganisms tested in this study. E. coli was the most resistant microorganism against all of the fractions (MIC equal to 12.5 mg/ml for the chloroform fraction and 3.12 mg/ml for the water and the methanol fractions).
Table 3
Minimum inhibitory concentration (mg/ml) of ethanol extract of Golnar and its fractions (n = 3)
Extract and fractions | M mg/ml | W mg/ml | EA mg/ml | C mg/ml | EE mg/ml |
|---|---|---|---|---|---|
Microorganism | |||||
Staphylococcus aureus ATCC 25923 | 0.19 | 0.19 | 0.39 | 3.12 | 0.19 |
Bacillus cereus PTCC 1247 | 0.19 | 0.19 | 0.39 | 3.12 | 0.39 |
Listeria monocytogenes ATCC 7644 | 1.56 | 3.12 | 3.12 | 6.25 | 6.25 |
Escherichia coli ATCC 25922 | 3.12 | 3.12 | 6.25 | 12.5 | 6.25 |
Shigella dysantriae PTCC 1188 | 0.39 | 0.39 | 0.39 | 6.25 | 0.39 |
Salmonella typhi ATCC 19430 | 1.56 | 3.12 | 3.12 | 6.25 | 6.25 |
Determination of MBC
MBC of the ethanol extract and the fractions are shown in Table 4. The MBC values obtained in this study ranged from 0.78 to 50 mg/ml. The lowest MBC value of 0.78 mg/ml was observed from EE extract against S. aureus which reflects the highest sensitivity of S. aureus among the six microorganisms tested in this study. Similar to results of MIC determination, E. coli was the most resistant microorganism against all the fractions and the extract (MBC equal to 50 mg/ml for chloroform fraction). It may be because of the differences in their cell wall composition and presence of second membrane in Gram negative bacteria cellwall.
Table 4
Minimum bactericidal concentration (mg/ml) of ethanol extract of Golnar and its fractions (n = 3)
Extract and fractions | M mg/ml | W mg/ml | EA mg/ml | C mg/ml | EE mg/ml |
|---|---|---|---|---|---|
Microorganism | |||||
Staphylococcus aureus ATCC 25923 | 1.56 | 1.56 | 3.12 | 12.50 | 0.78 |
Bacillus cereus PTCC 1247 | 1.56 | 1.56 | 3.12 | 12.50 | 1.56 |
Listeria monocytogenes ATCC 7644 | 6.25 | 6.25 | 12.50 | 12.50 | 25.00 |
Escherichia coli ATCC 25922 | 12.50 | 12.50 | 25.00 | 50.00 | 25.00 |
Shigella dysantriae PTCC 1188 | 3.12 | 3.12 | 3.12 | 25.00 | 1.56 |
Salmonella typhi ATCC 19430 | 6.25 | 12.50 | 12.50 | 25.00 | 25.00 |
Total phenolic content
After making a standard calibration curve by gallic acid (y = 1.48× –0.05, r2 = 0.99), the total phenolic content of the extract and the fractions were measured. The total phenolic content was ranged from 3.8 to 18.1 mg GAE/g of dry powder. As shown in Table 5, the chloroform fraction (C) had the lowest and the methanol fraction (M) had the highest total phenolic contents.
Table 5
Total phenolic and flavonoid of the ethanol extract of Golnar and its fractions (n = 3)
Extract and fractions | Phenolic content (mg GAE/g) | Flavonoid content (mg Rutin/g) |
|---|---|---|
Water | 17.8 ± 1.3ac | 2.6 ± 0.35hig |
Methanol | 18.1 ± 1.5a | 3.3 ± 0.14bk |
Ethanol extract | 17.6 ± 2.3c | 1.9 ± 0.3f |
Ethyl acetate | 8.2 ± 2.14bdj | 1.3 ± 0.14ad |
Chloroform | 3.8 ± 0.9bdej | 1.1 ± 0.12hdf |
Total flavonoid content
Standard calibration curve of Rutin was used to evaluate the content of flavonoid in the extract and the fractions (y = 0.02× –0.05, r
2
= 0.97). Results are shown in Table 5. The lowest flavonoid content was seen in the chloroform fraction (1.1 mg RE/g of dry powder) and the highest was seen in the methanol fraction (3.3 mg RE/g of dry powder).
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Discussion
Golnar has been used in traditional Iranian medicine for healing wounds, treating large intestine ulcers, strengthening gums, and the treatment of diarrhea and oral infections [9‐11]. In this study, we evaluated the antibacterial effects of the ethanol extract of Golnar and its fractions against bacterial strains that cause food poisoning. Among the bacteria used in this study, E. coli is the most common cause of diarrhea in developing countries [23]. The second most common cause of bacterial foodborne diseases in the United States is Salmonella. Shigella dysantriae is the third important microorganism involved in food and water contamination [24]. Other bacteria such as S. aureus and B. cereus are also involved in food poisoning [25, 26]. L. monocytogenes is a Gram-positive bacterium responsible for the severe foodborne illness, listeriosis. This disease is primarily transmitted through various foods such as fish, dairy products, cured or processed meat, egg, poultry, seafood, salad, fruits and vegetables [27]. Listeriosis is a severe infection and has been associated with a mortality rate as high as 30–40 % [28]. Using synthetic preservatives for prevention and antibiotics for treatment of foodborne diseases may result to several unpleasant effects including hypersensitivity, immune-suppression and allergic reactions [29]. Therefore, there is an increasing need to develop new alternative natural agents as preservative or antibacterial agents [30].
In this study, the antibacterial activity of the ethanol extract and its fractions were primarily evaluated by the agar well diffusion method. The results indicated a broad spectrum activity against both gram positive and gram negative bacteria. The largest inhibition zone (34 mm) was seen with the water fraction for S. aureus at the concentration of 500 mg/ml. The smallest inhibition zone at this concentration was seen for E. coli with the diameter of 12 mm related to the chloroform fraction. The results showed that S. aureus (Gram positive bacteria) and Shigella dysantriae (Gram negative bacteria) could be more sensitive based on their larger inhibition zones.
All fractions and the ethanol extract showed inhibitory effects against S. aureus at a concentration equal to 1.95 mg/ml and higher. However, the chloroform fraction showed inhibitory effect at 62.5 mg/ml and higher concentrations. This profile of the antibacterial effect of the ethanol extract and the fractions were confirmed by determining the MICs and MBCs. In fact, the polar fractions generally showed better antibacterial activity, which can be related to the total phenolic content of the fractions. Polyphenols are hydrophilic phytochemicals and hydrophilic solvents are more effective agents for the extraction [31, 32]. The total phenolic content of the extract and its fractions were expressed in term of gallic acid equivalent. According to the results, EE contains 17.6 mg GAE/g of phenolic content, while methanol and water fractions contain 18.1 mg GAE/g and 17.8 mg GAE/g, respectively. The ethyl acetate and chloroform fractions contain only 8.2 mg GAE/g and 3.8 mg GAE/g of phenolic contents, respectively. Moreover, one-way ANOVA followed by Tukey’s test revealed a significant decrease in phenolic content in the ethyl acetate and chloroform fractions compared to the water fraction (P < 0.001), methanol fraction (P < 0.001), and ethanol extract (P < 0.001). The antimicrobial activities of phenolic compounds have been demonstrated in previous studies [31, 33]. Our results are in agreement with the previous studies on pomegranate (P. granatum fruit) [17]. Although chemical components of Golnar were not analyzed in this study, however, it could be suggested that the phenolic compounds are involved in the antibacterial effects we reported.
Quantitative evaluations of antimicrobial activity were done against test microorganisms using the broth dilution method. Considering the MICs, the best results were related to EE extract, as well as M and W fractions (0.19 mg/ml) against S. aureus. Gram negative bacteria were more resistant to the extract. Presence of an outer membrane in Gram negative bacteria can explain the resistance. E. coli was found to be the most resistant bacteria with the MIC of 12.5 mg/ml for the most effective fraction and 50 mg/ml for the least effective fraction. Al-zoreky has reported that the 80 % methanol extract of pomegranate fruit peels has similar effects on Gram positive and Gram negative bacteria [2].
The highest flavonoid content was measured in the methanol fraction (P < 0.001 and P < 0.05 compared with the ethanol extract and the water fraction, respectively), in which the most antibacterial action was also observed. It has been shown that the antimicrobial efficacy of the herbal extracts correlates with their flavonoid contents [34]. In addition, many flavonoids have also shown anti-infective effects through making complexes with different proteins inside the bacterial cell walls or extracellular proteins [34, 35] Such a relation between antibacterial effects and flavonoid content was suggested from the results of this study.
It has been shown that pomegranate pericarp extract enhances the antibacterial activity of ciprofloxacin against extended-spectrum beta-lactamase and metallo-beta-lactamase producing Gram-negative bacilli [3]. Considering the antibacterial effects of Golnar, there is a potential benefit in using the extract in combination with classic antibacterial agents to improve the antibacterial effects and consequently reduce the side effects of the agents.
Conclusion
From the results of the present study, it could be concluded that the methanol and the water fractions have similar effects on Gram positive bacteria. Antibacterial effects of the methanol and water fractions on Gram negative bacteria are also relatively similar except for the methanol extract which revealed to be more effective on Salmonella typhi. The ethyl acetate and chloroform fractions have less effect on microorganisms, suggesting that the active antibacterial agents are most concentrated in polar fractions. The results of this study complies the traditional use of Golnar as an antibacterial agent against foodborne diseases. Moreover, there is potential for its use in the food industry and in medicine as a preservative. Clearly, further studies are necessary to evaluate the efficacy of the extract in different indications.
Acknowledgements
The authors would like to thank Miss Mehrab for her support.
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Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
PNS operated the phenolic and flavonoid content determination tests and data collection. JA experiment design, literature search, providing plant material and extract and fractions preparation. MF performed the statistical analysis and drafted the manuscript. AM designed the research, carried out the antibacterial tests, and coordinated the study and corresponding author of the manuscript. All authors read and approved the final manuscript.
Authors' information
Not applicable.