alexa Phytochemical and Biological Studies of Some Myrtus (Myrtus communis L.) Populations of South West Region of Zagros (Iran)

ISSN: 2329-6836

Natural Products Chemistry & Research

  • Research Article   
  • Nat Prod Chem Res 2017, Vol 5(7): 290
  • DOI: 10.4172/2329-6836.1000290

Phytochemical and Biological Studies of Some Myrtus (Myrtus communis L.) Populations of South West Region of Zagros (Iran)

Alireza Salimi Beni1*, Mehrzad Kocheki Shahmokhtar1, Asad Masoumiasl2 and Habibollah Khajehsharifi1
1Department of Chemistry, Yasouj University, Yasuj, Iran
2Agricultural Department, Yasouj University, Yasuj, Iran
*Corresponding Author: Alireza Salimi Beni, Department of Chemistry, Yasouj University, Yasuj, Iran, Tel: +987431004000, Email: [email protected]

Received Date: Aug 12, 2017 / Accepted Date: Aug 21, 2017 / Published Date: Aug 30, 2017

Abstract

Myrtus communis L. is one member of the Myrtaceae family. It is one of the important medicinal plants in the Zagros region of Iran. The Essential oils include a large percentage of compounds called terpenes. In this study, the chemical composition of essential oils of Myrtus (Myrtus communis L.) was identified by the GC-MS method. Results showed that essential oils of populations from different regions have a series of similar compounds, but different in quality and quantity. In fact, they have several organic compounds such as hydrocarbons, alcohols, ketones, aldehydes, ethers, esters, oxides and other volatile oil and so on. Percentage of essential oils in different populations were variable. Essential oil of “Basht” population has 35 compounds such as 1,8-cineole, linalool, α- pinene and lynalyl acetate. Essential oils of “Dehno-Rostam” population has 30 compounds include 1, 8 cineole, linalool, α terpineol, α-pinene. Essential oils of “Sarab-Bahram” population has 19 compounds include α-pinene, 1,8- cineole, linalool, and α terpineol. Essential oils of “Keveshk” population has 29 compounds such as 1,8-cineole, α- pinene, linalool, and α-terpineol and Essential oils of “Tang-Tamoradi” population has 25 compounds include Eugenol, δ-3-carene, 1,8-cineole, and α-terpineol. Aqueous extracts of those populations were evaluated, and the results showed that they have antibacterial properties against Escherichia coli, Bacillus subtilis and Pseudomonas aeruginosa, but have not any antifungal activity (Aspergillus oryzae).

Keywords: Myrtus communis L.; Zagros; Essential oil; Antimicrobial; Antifungal

Introduction

Myrtus communis L. (Myrtaceae) is an evergreen shrub, typical of the Mediterranean regions, which grows spontaneously in many countries, the scientific name for this Myrtus communis L. is taken from its Persian name. It is traditionally used as an antiseptic, antimicrobial, disinfectant drug and hypoglycaemic agent [1]. Different parts of this plant find various widely uses in the food industry, such as for flavouring meat and sauces, and in the cosmetic industry and so on [2]. Common myrtle belongs to the Myrtaceae family, which include approximately 145 genera and over 5500 species [3]. The genus Myrtus includes the flowering plant with near 16 species reported in areas of the Middle East and Asia [4]. M. communis L. known in fact myrtle is one of the main aromatic and medicinal species of this family. It is an evergreen sclerophyll shrub or small tree, 1.8-2.5 m height, with a small bush and deeply fissured grove [5]. True Myrtle is characterized by its branches, which form a close full head, gross covered with ovate or lanceolate evergreen leaves. Their leaves are 3-5 cm long and include tannins, flavonoids and volatile oils [6]. This part is a so aromatic plant since of the high essential oil content in its leaf, flower and fruit glands. It has solitary auxiliaries white or rosy flowers followed by black a several-seeded berry, which is globular in shape with dark red to violet in color [7]. There are two major fruits according to whether the color dark or white. The dark color is more current, but there are as well cultivated white-colored types, which they have yielded much bigger fruit than their wild counterparts [8]. Myrtle grows abundantly from the northwestern to the eastern Mediterranean, including bordering countries and western Asia, also Aegean regions [9]. Myrtles native to Southern Europe, North Africa and western Asia. It is also distributed in Southern America, Northwestern Himalaya and Australia. Myrtle is cultivated in gardens, especially in the Northwest Indian region, because of its odor flowers [10]. Myrtle has been used since ancient times as a spice, also for medicinal, antiseptic, food preparation and spice purposes. Myrtle as a condiment finds no wide application because of its bitterness, despite the pleasant odor. The taste is very intense, quite nasty and strongly bitter, so its culinary application is limited to the region of origin, such as Italy [11,12]. Its berries and leaves are usually used for the industrial formulation of sweet liquors with advertising digestive properties [13,14]. Its leaves are very fragrant and have been extensively employed in the perfume and cosmetic industries, particularly in Portugal [15] and Turkey [6]. It is traditionally used as an antiseptic, disinfectant and hypoglycemic agent [1]. Generally, in folk medicine, a decoction of leaves and fruits is used orally for the treatment of stomach aches, hypoglycaemia, disbiosis, cough, constipation, poor appetite, as well as also externally for wound healing [16]. Essential oils are aromatic and volatile compounds found only in 11% of the plant kingdom [17]. Essential oils and their components can be very hopeful biological agents, to their relative safety, wide acceptation by consumers and exploitation of potential multi-purpose use [18]. They are stored in plants in special fragile secretory structures, such as glands, secretory hairs, secretory ducts, secretory pit or resin ducts [19-22]. The total essential oil content of plants is generally so low and scarcely more than 1% of biomass [23]. For example, the essential oil yields in leaf stalk and flower of M. communis var. Italical were respectively 0.61%, 0.08% and 0.30% (w/w) [24]. Essential oils are hydrophobic and thus only slightly solvable in water. They are soluble in alcohol, non-polar or weakly polar solvents, beeswax, and oils. Most essential oils are colorless or light yellow, liquid and have a lower density than water [25]. Essential oils are complex mixtures containing many diverse compounds. Chemically they are derived from terpenes and their oxygenated compounds [26]. The chemical composition of the myrtle essential oil has been explained by many authors [2,27-29]. Compounds that have been found in myrtle oils include E-2-hexenal, Z-3-hexenol, hexanol, tricyclene, α-thujene, α-pinene, sabinene, β- pinene, myrcene, δ-3-carene, α-terpinene, p-cymene, limonene, 1,8- cineole, E-β-ocimene, E-oxide, terpinolene, linalool, terpinene-4-ol, borneol, p-cymene-8-ol, α-terpineol, myrtenol, nerol, cis-carveol, geraniol, linalylacetate, bornyl acetate, eugenol, myrtenyl acetate, α- terpinyl acetate, geranyl acetate, neryl acetate, methyl eugenol, β- caryophyllene, α-humulene, allo-aromadendrene, germacrene-D, caryophyllene oxide and camphene.

Materials and Methods

Plant material and essential oil

In June with the use of plant distribution maps for Myrtus communis L. five regions for sampling was selected. The different geographical characteristics of these regions were measured. Latitude, longitude and altitude to the global coordinate system (GPS) were measured (Table 1). Then samples (leaf and twigs) were dried away from the sun for ten days. Dried leaves transferred to the Phyto chemistry Laboratory and extraction essential oils by Clevenger for 3 hours. Finally, essential oils after dehydration kept in the dark glass bottle in the refrigerator (in 4ºC). Percentage of essential oils in this studied population were shown in Table 2.

Row Name of Location Altitude (m) Latitude Longitude
1 Basht 930 302029 511142
2 Dehno Rostam 810 301854 512158
3 Sar Ab Bahram 1037 300229 513330
4 Keveshk 1712 302650 512916
5 Tang Tamoradi 1623 303048 512509

Table 1: Geographical characteristics of studied regions.

Name of Location Percentage of essential oils
Basht 2.2
Dehno-Rostam 2.1
Sarab-Bahram 1.6
Keveshk 2.0
Tang-Tamoradi 0.8

Table 2: Percentage of essential oils in studied populations.

Preparation of the extracts

The aqueous extract was obtained as follows: 80 ml of water added in 10 g of plant material in a round-bottomed flask, then put it on the electric mixer for 24 h. Then it was a smooth operation and filtered by Whatman paper No. 42.

Preparation of the culture medium

Based on the directions on the container culture media, culture media powder is dissolved in distilled water and heater stirred until the boil, Then the flask door closed with cotton for 20 min at 121°C inside the autoclave to be sterilized. After leaving autoclave poured about 15 ml of culture medium in each plate after cooling to keep in the refrigerator. Broth as the liquid culture medium is not necessary to pour plates can be directly stored in the fridge after sterilization and cooling.

Analysis of the essential oils

To determine the composition of the essential oils of the leaves was used gas chromatography and gas chromatography (Agilent, Model N 6890) connected mass spectrometry (GC-MS). HPS column (30 meter), its diameter was 250 micrometers and thickness of stationary phase 0.25 m. Helium was used as the carrier gas at a flow rate of 1.0 ml/min. Diluted samples (1/100 in n-Hexan, v/v) of 1 μl were injected manually in split mode (split ratio 1/30). Oven temperature was programmed from 50 to 220ºC at a rate of 5ºC/min and from 220ºC to 280ºC at a rate 20ºC/min and held at for 2 min. Oil constituents were identified by MS data obtained from Wiley (http://eu.wiley. com/ wileycad/wileyTitle/productCd.htm) and NIST (http://www.nist.gov/srd/nist1a.htm) libraries.

Biological activity

In-vitro biological activity of the extracts against two Gram negative bacteria such as Escherichia coli (ATCC 25922) and Pseudomonas aeroginosa (ATCC 9027) and Gram-positive bacteria including S. Bacillus subtilis (ATCC: 6633) and also a fungal strain such as A. oryzae , were carried out using the disk diffusion method [30,31]. For this mean, the Petri dishes were prepared as follows: i) a layer of culture medium (Muller Hinton Agar (Merck, Germany) for bacterial strains and Sabouraud dextrose agar (SDA) for fungal strains was poured on the surface of plates, ii) 100 μl of spore suspension of bacteria and/or fungi including nearly 0.5 × 106 colony-forming units (CFU/ml) was inoculated on the surface of culture medium, iii) The prepared discs (that had been soaked in the various concentrations of Extracts; 12.5, 25 and 50 mg/ml in physiological saline) were placed at different positions on a surface of plates. Then, the plates were incubated at 37 ºC for 24 h for bacterial strains and 27 ºC for three days for Aspergillus oryzae [32,33]. Antimicrobial activities of extracts were evaluated based on the diameter of the zone of inhibition (mm) and listed in Table 8. Amoxicillin, Erythromycin, Fluoxamine and Cephalexin were used as reference bactericidal drugs (positive controls) Table 9.

Results And Discussion

The geographical characteristics of the study regions (latitude, longitude and altitude) were shown in Table 1. Essential oil extraction by Clevenger and dehydration by Na2SO4 then compounds in essential oils were identified by chromatography connected to mass spectrometry (GC-MS). Chemical compounds were identified in different populations was shown in Tables 3-7. In the essential oil of Basht population was identified 35 compounds and 1,8-cineole, linalool, α-pinene and lynalyl acetate have the highest percent (Table 3).

The dehno-Rostam population has 30 compounds and 1,8-cineole, linalool, α terpineol, α-pinene have the highest percent (Table 4). In Sarab-Bahram population was identified 19 compounds and α-pinene, 1,8-cineole, linalool, and α terpineol have the highest percent (Table 5). Keveshk population has 29 compounds and 1,8-cineole, α-pinene, linalool, and α-terpineol have the highest percent (Table 6). Tang- Tamoradi population has 25 compounds and Eugenol, δ-3-carene, 1,8-cineole, and α-terpineol have the highest percent (Table 7). The antibacterial activities of the extracts were listed in Table 8 as the diameter of inhibition zone from the growth (in mm). The results show that extracts have the good antibacterial activity against all studied bacteria strains. Antibacterial activities of Basht, Dehno-Rostam, Sarab-Bahram and Keveshk populations was similar and have most effect on Pseudomonas aeruginosa, Escherichia coli and Bacillus subtilis , respectively. Antibacterial activity Tangeh-tamoradi population has different and has the greatest effect on the Pseudomonas aeruginosa, Bacillus subtilis and Escherichia coli , respectively. Antibacterial activity of Amoxicillin, Erythromycin, Fluoxamine and Cephalexin were (positive controls) shown in Table 9. The Aqueous extracts of those populations have not any antifungal activity against Aspergillus oryzae .

Row Compounds name Retention time (min) Percent
1 Isobutyl isobutyrate 3.855 1.48
2 a–Pinene 4.288 7.98
3 Camphene 5.171 4.12
4 d-3-carene 5.347 2.73
5 P-cymene 5.586 3.56
6 Unknown 5.864 1.30
7 1,8–cineol 6.355 12.89
8 Ocimene 7.241 0.78
9 ?-terpinene 7.330 0.53
10 Linalool oxide 7.510 0.25
11 a–terpinolene 7.825 0.33
12 Linalool 8.214 12.10
13 Allo ocimene 8.933 0.30
14 Trans-pinocarveol 9.305 0.39
15 Cis-verbinol 9.378 0.45
16 Unknown 9.585 0.44
17 Borneol 9.962 0.11
18 4-terpineol 10.213 0.70
19 ?-terpineol 10.618 4.43
20 Unknown 10.699 1.52
21 Myrtenal 10.866 6.24
22 Trans-geraniol 11.568 0.68
23 Citronellol 11.745 0.75
24 Linalyl acetate 12.381 7.73
25 Bornyl acetate 13.088 0.24
26 Myrtenyl acetate 13.834 0.05
27 a-terpenyl acetate 14.909 6.15
28 Neryl acetate 15.073 0.95
29 Granyl acetate 15.218 0.17
30 Terpinyl propionate 15.743 4.50
31 Methyl eugenol 16.380 2.55
32 Trans-Caryophellene 16.864 2.08
33 a-Humulene 17.669 1.90
34 Caryo phellene oxide 20.952 2.15
35 Humulene oxide (II) 21.570 1.12

Table 3: Compounds in essential oils of Basht population.

Row Compounds name Retention time (min) Percent
1 Isobutyl isobutyrate 3.770 2.4
2 Unknown 4.031 1.00
3 a-Pinene 4.233 10.32
4 b-Pinene 4.861 3.72
5 d-3-careen 4.984 4.20
6 Unknown 5.206 2.70
7 T-b-Ocimene 5.315 2.82
8 P-cymene 5.561 6.80
9 1,8-cineol 6.315 16.02
10 cis-ß-Ocimene 6.962 2.40
11 g-terpinene 7.114 2.32
12 a-terpinolene 7.710 1.25
13 Linalool 8.161 14.54
14 Allo ocimene 8.826 0.62
15 Trans-pinocarveol 9.174 0.60
16 Undecane,5-methyl 9.305 0.72
17 Iso Borneol 9.768 0.56
18 4-terpineol 10.068 0.73
19 a-terpineol 10.744 11.10
20 trans-(+)-carveol 11.160 0.40
21 Trans-geraniol 11.470 1.11
22 Linalyl acetate 12.160 7.60
23 a-citral 12.496 0.16
24 Myrtenalacetate 13.824 1.11
25 Methyl granate 13.948 0.48
26 Neryl acetate 14.970 1.70
27 Methyl eugenol 16.294 0.08
28 Trans-Caryophellene 16.634 0.80
29 a-Humulene 17.481 0.91
30 Caryo phellene oxide 20.782 0.83

Table 4: Compounds in essential oils of Dehno-Rostam population.

Row Compounds name Retention time (min) Percent
1 a-Pinene 4.515 33.9
2 P-cymene 5.581 9.22
3 1,8-cineol 6.415 22.1
4 a-terpinolene 7.623 1.3
5 Linalool 7.966 11.92
6 Undecane,5-methyl 8.559 1.23
7 Iso Borneol 9.630 1.21
8 4-terpineol 9.927 1.2
9 a-terpineol 10.324 3.92
10 Nerol 11.184 1.05
11 Linalyl acetate 11.930 2.82
12 Trans anethole 12.779 1.03
13 Methyl granat 13.707 0.92
14 Myrtenel acetate 13.835 1.05
15 Methyl eugenol 15.879 1.9
16 Trans-Caryophellene 16.497 1.2
17 a-Humulene 17.375 1.12
18 Caryo phellene oxide 20.726 1.46
19 Humulene oxide (II) 21.30 1.45

Table 5: Compounds in essential oils Sarab-Bahram population.

Row Compounds name Retention time (min) Percent
1 Iso butyl iso butyrate 3.912 2.34
2 a-Pinene 4.365 13.2
3 b-Pinene 4.869 6.32
4 pseudo limonene 5.079 6.28
5 d-3-careen 5.279 2.6
6 Unknown 6.019 2.61
7 1,8–cineol 6.393 15.21
8 b-Ocimene 6.748 3.12
9 g-terpinene 6.986 2.72
10 a-terpinolene 7.647 1.2
11 Linalool 8.088 1.8
12 Allo ocimene 8.645 1.42
13 Unknown 8.919 1.02
14 Trans-pinocarveol 9.025 1.14
15 Undecane,5-methyl 9.203 1.31
16 4-terpineol 9.950 0.7
17 a-terpineol 10.404 12.23
18 Linalyl acetate 12.079 9.94
19 Trans anethole 12.811 1.0
20 Myrtenal acetate 13.850 1.23
21 Neryl acetate 14.818 1.31
22 Unknown 14.934 0.88
23 Granyl acetate 15.407 2.9
24 Unknown 15.830 2.8
25 Methyl eugenol 15.953 0.91
26 Trans-Caryophellene 16.550 0.42
27 a-Humulene 17.413 1.4
28 Caryo phellene oxide 20.701 1.04
29 Humulene oxide (II) 21.343 0.95

Table 6: Compounds in essential oils of Keveshk population.

Row Compounds name Retention time (min) Percent
1 a-Pinene 4.240 3.92
2 b-Pinene 4.370 4.54
3 d-3-careen 4.856 10.96
4 t-b-ocimene 5.459 2.37
5 Unknown 5.606 5.53
6 Unknown 6.228 2.15
7 1,8-cineol 6.441 10.32
8 a-terpinolene 7.506 1.22
9 Linalool 8.039 5.56
10 Allo ocimene 8.804 0.95
11 Camphor 9.353 3.54
12 Iso Borneol 9.960 4.51
13 a-terpineol 10.724 8.25
14 Unknown 11.152 4.43
15 Linalyl acetate 12.224 7.47
16 Bornyl acetate 12.883 0.76
17 Myrtenyl acetate 13.989 0.62
18 Eugenol 15.610 11.5
19 Granyl acetate 16.28 2.04
20 Methyl eugenol 16.430 2.93
21 Trans-Caryophellene 16.866 2.82
22 a-Humulene 17.626 0.48
23 Caryo phellene oxide 20.094 1.05
24 Unknown 20.899 2
25 Unknown 24.437 0.08

Table 7: Compounds in essential oils of Tang-Tamoradi population.

Name of Location Gram negative Gram positive
  Escherichia coli Pseudomons aeruginosa Bacillus subtilis
50 (mg/mL) 25 (mg/mL) 12.5 (mg/mL) 50 (mg/mL) 25 (mg/mL) 12.5 (mg/mL) 50 (mg/mL) 25 (mg/mL) 12.5 (mg/mL)
Basht 13.72 10.10 7.66 18.76 17.53 14.53 11.48 9.77 8.46
Dehno-Rostam 15.14 12.48 9.80 17.88 14.64 11.88 12.85 12.41 9.30
Sarab-Bahram 12.99 9.65 6.88 14.06 11.53 8.38 12.45 11.51 9.00
Keveshk 13.21 9.57 6.00 15.20 11.20 9.66 13.04 9.03 6.83
Tang-Tamoradi 10.80 9.73 6.00 15.49 13.07 9.28 12.21 10.66 9.03

Table 8: Diameter of zone of inhibition (mm) of extracts in studied populations.

Antibiotics Escherichia coli Pseudomonas aeruginosa Bacillus subtilis
Amoxicillin (30 µg) 24.00 22.63 18.15
Erythromycin (15 µg) 20.33 21.27 27.44
Fluoxamine (15 µg) 33.33 23.11 38.37
Cephalexin (25 µg) 19.1 15.00 35.67

Table 9: Diameter of the zone of inhibition (mm) of Antibiotics.

Conclusion

This paper deals with the Environmental variation of the essential oil M. communis L. grown in South West region of Zagros. It should be noted that plants from this location are examined for the first time. The monoterpene fraction is the main chemical group of the essential oil in all populations. Essential oils of different populations have a series of compounds are similar and different in terms of quality and quantity. The essential oils are made of a complex mix of chemical compounds that those are different in terms of chemical compounds. In fact, there are a variety of organic compounds such as hydrocarbons, alcohols, ketones, aldehydes, ethers, esters, oxides and other volatile oil and so on. Percentage of essential oil in different regions is different. The results show that extracts have the good antibacterial activity against all studied bacteria strains. Antibacterial activities of Basht, Dehno-Rostam, Sarab-Bahram and Keveshk populations were similar and have the most effect on Pseudomonas aeruginosa, Escherichia coli and Bacillus subtilis , respectively. The antibacterial activity of the Tangeh- Tamoradi population was different and has the greatest effect on the Pseudomonas aeruginosa, Bacillus subtilis and Escherichia coli , respectively. The Aqueous extracts of those populations have not any antifungal activity against Aspergillus oryzae . This study shows that the combination of some Myrtus (Myrtus communis ) populations in a different area can vary in terms of quality and quantity that these differences could be due to genetic or non-genetic factors. The result shows the aqueous extracts of Myrtus communis L. populations weren’t a good alternative for antibiotics. The present results exhort additional and more in-depth studies on the phenolic, fat acid, glucoside and terpenoids composition of the plant extracts and assessment of the antibacterial activity of each compound separately also other biological properties.

Acknowledgment

This work was carried out with the financial support of Yasouj University (YU).

References

Citation: Salimi Beni A, Kocheki Shahmokhtar MK, Masoumias A, Khajehsharifi H (2017) Phytochemical and Biological Studies of Some Myrtus (Myrtus communis L.) Populations of South West Region of Zagros (Iran) . Nat Prod Chem Res 5: 290. Doi: 10.4172/2329-6836.1000290

Copyright: © 2017 Salimi Beni A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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