Chemical Composition and Antimicrobial Activities of Essential Oils of Some Coniferous Plants Cultivated in Egypt

Taghreed A. Ibrahim; Atef A. El-Hela; Hala M. El-Hefnawy; Areej M. Al-Taweel; Shagufta Perveen

doi:10.22037/ijpr.2017.1949

Chemical Composition and Antimicrobial Activities of Essential Oils of Some Coniferous Plants Cultivated in Egypt

authors:

Taghreed A. Ibrahim ^{a
, b
, *} , Atef A. El-Hela ^c , Hala M. El-Hefnawy ^b , Areej M. Al-Taweel ^a , Shagufta Perveen ^a

a Department of Pharmacognosy, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.

b Departmaent of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, Egypt.

c Department of Pharmacognosy, Faculty of Pharmacy, Al – Azhar University, Nasr City, Cairo, Egypt.

Iranian Journal of Pharmaceutical Research : IJPR: Vol.16, issue 1; 328-337

article type: Original Article

received: May , 2015

accepted: June , 2015

DOI: https://doi.org/10.22037/ijpr.2017.1949

how to cite: Ibrahim T A, El-Hela A A, El-Hefnawy H M, Al-Taweel A M, Perveen S. Chemical Composition and Antimicrobial Activities of Essential Oils of Some Coniferous Plants Cultivated in Egypt. Iran J Pharm Res. 2017;16(1):e124900. https://doi.org/10.22037/ijpr.2017.1949.

Abstract

Family Cupressaceae is the largest coniferous plant family. Essential oils of many species belonging to family Cupressaceae are known to have several biological activities specially antimicrobial activity. The essential oils from aerial parts of Calocedrus decurrens Torr., Cupressus sempervirens stricta L. and Tetraclinis articulata (Vahl) Mast. were prepared by hydrodistillation. The chemical composition of the essential oils has been elucidated by gas chromatography-mass spectroscopy analysis. The prepared essential oils were examined against selected species of Gram-positive, Gram-negative bacteria and Candida species. Broth dilution methods were used to detect minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and minimum fungicidal concentration (MFC). Sixteen compounds were identified in the essential oils of both Calocedrus decurrens and Cupressus sempervirens L. and fifteen compounds were identified in the essential oil of Tetraclinis articulata. δ-3-Carene (43.10%), (+)-Cedrol (74.03%) and Camphor (21.23%) were the major constituents in the essential oils of Calocedrus decurrens, Cupressus sempervirens L. and Tetraclinis articulata, respectively. The essential oils showed strong antimicrobial activities against the selected microorganisms in concentration range 0.02 3- 3.03 µL/mL. This study could contribute to the chemotaxonomic characterization of family Cupressaceae. In addition, it proved that the essential oils under investigation possess potential antimicrobial properties.

Keywords

Calocedrus Cupressaceae Cupressus monoterpene sesquiterpene Tetraclinis

Introduction

The use of essential oils to control many diseases and their effective usage as antimicrobial agents (1-5) in addition to their use as functional ingredients in foods, drinks, toiletries and cosmetics is gaining momentum, both for the growing interest of consumers in ingredients from natural sources and also because of increasing concern about potentially harmful synthetic additives (6). Essential oils are complex mixture of natural compounds, mostly of plant origin, extremely volatile and with an intense odour. Even if they represent only a small fraction of the plant from which they are derived, they give the whole plant the characteristic of aromatic smell for which these plants are employed by drug, food and perfume industries (7). The species that show the largest content of essential oils belong to many families as Asteraceae, Lamiaceae, Apiaceae, Rutaceae, Lauraceae, Myrtaceae, Magnoliaceae, Pinaceae and Cupressaceae (8-10).

Family Cupressaceae is a common ornamental plants, cultivated around the world, and particularly in South America, Mediterranean basin and North Africa, It is the most widely distributed of all gymnosperm families, occurring in diverse habitats on all continents. Cupressaceae is also the most important conifer family in modern horticulture, members of this family are important for their timber, resin, fruit and as ornamentals (11-13).

Several species belonging to family Cupressaceae have been used in folk medicine as astringent, antiseptic, pulmonary antiseptic, antispasmodic, lymphatic tonic, antibacterial, antihemorrhagic, capillary protector, antipyretic and pelvic decongestant (14). Many biologically active compounds have been reported from Cupressaceae species such as essential oils, diterpenes, flavonoids, and sterols (14, 15).

Genus Cupressus comprising about 20 species; Cupressus sempervirens L. commonly known as Cypress and known in Arabic as Sarȗ, Sarw, Serwal, Sharbin and Shagaret el Hayat (16), is native to eastern North America (17) and grown in Egypt as ornamental tree. The essential oil of the leaves of the plant cultivated in Alexandria, Egypt was studied; the main oil constituents were cedrol (21.29%), δ-3-carene (17.85%) and α-pinene (6.90%) and proved to have antimicrobial activities (18). Essential oil of the aerial parts of Cupressus sempervirens cultivated in Safx, Tunisia was studied, 24 compounds were identified, where α-pinene (37.14%), δ-3-careen (19.67%) and R (+)-limonene (5.43%) were the main oil constituents, the oil exhibited a significant antimicrobial activities (19).

Calocedrus decurrens (Incense Ceder) is a tree native to Oregon and California, known for its aromatic wood and manufacturing of pencils (20)]. Heartwood essential oil of C. decurrens was studied, it was found that p-cymene and p-menthane derivatives were the main components (20). Von Rudloff (21) reported that leaf oil of C. decurrens from the pacific northwest, USA, was dominated by limonene (31.31%), δ-3-carene (21%) and α-pinene (9.2%) while Robert & Sanko (22) proved that the oils of C. decurrens from two populations in Oregon and one disjunct population in southern California were high in δ-3 carene (15.20%- 20.00%), limonene (18.21-23.62%), α-pinene (8.7-15.8%), terpinolene (5.72- 8.01%), α-fenchyl acetate (3,5- 9.71%) and cedrol (0.8- 1.2%) (21,22).

Tetraclinis articulata (Cartagena Cypress, known in Arabic as Ahrar, Berbouch and Megloub (23) is an endemic species of North Africa, Malt and Spain (24). Various parts of this tree are used in folk medicine for its multiple therapeutic effects, it is mainly used against childhood respiratory and intestinal infections (24)], gastric pains, diabetes, hypertension and used as antidiarrheal, antipyretic, diuretic, antirheumatic and oral hypoglycemic (24-26). Twenty-seven compounds were detected in Algerian T. articulata leaves, bornyl acetate (52.11%), caryophyllene (7.51%), germacrene D (5.61%) and caryophyllene oxide (5.01%) were the major components, the oil exhibited antifungal (27), antibacterial (28), antioxidant and anti-inflammatory activities (29).

Fifty-Six compounds were detected in Tunisian T. articulata plant, where α-pinene (31.32%), linalool acetate (18.18%), alloaromadendrene (7.55%) and γ-caryophyllene (4.16%) were the major constituents in the oil prepared by hydrodistillation method, the oil exhibited antioxidant activities (30, 31).

The main objective of this study was to identify the chemical composition of the essential oils from the aerial parts of C. decurrens, C. sempervirens and T. articulata cultivated in Egypt, and to determine their antimicrobial activities, in an attempt to contribute to the use of these essential oils as alternative products.

Experimental

Plant materials

The aerial parts of Calocedrus decurrens Torr. (California Incense-Cedar), Cupressus sempervirens L. (Mediterranean or Italian Cypress) and Tetraclinis articulata (Vahl) Mast. (Cartagena Cypress) were collected from El-Orman Garden, Giza, Egypt on April 2012, at the flowering period. The identity of the plants was kindly verified by Terase Labib, General Manager and Specialist of Plant Taxonomy in El-Orman Botanical Garden, Giza, Egypt. Voucher specimens were deposited in the Department of Pharmacognosy, Faculty of Pharmacy, Al -Azhar University, Cairo, Egypt.

Preparation of the essential oil

The essential oils were prepared from the fresh aerial parts of C. decurrens, C. sempervirens and T. articulata (500 g) by hydro distillation using Clevenger-type apparatus. The oils were dried over anhydrous sodium sulphate and stored in sealed glass vials at 4-6 ^oC prior to analysis. Percentage yields were determined according to Egyptian Pharmacopoeia 1984 (32). Percentage yields and physical properties of the essential oils are illustrated in Table 1.

GC/ MS analysis of the essential oil

The prepared essential oils were subjected to GC/MS analysis using Shimadzu GC//MS – QP 5050 A, fitted with a DB-1 fused silica capillary column (30 m, 0.53 mm ID, 1.51 µM film thickness). Software Class 5000. searched library: Wiley 229 LIB. Carrier gas: Helium (flow rate 1 mL/min.). Ionization mode: EL (70 ev). Temperature program: 40 ⁰C (static for 2 min) then gradually increasing at a rate of 2 ⁰C/min up to 250 ⁰C (static for 7.50 min). Detector temperature 250 ⁰C. Injector temperature 250 ⁰C.

Identification of the essential oil

Compounds were identified by comparison of their retention indices (RI), obtained on a non-polar DB-1 column relative to C5- C24 n-alkanes, with those provided in the literature, in addition to Library searched data base Willey 229LIB and by comparing mass fragmentation patterns with those of the available references and with published data (33-35). The percentage composition of the essential oils was determined by computerized peak area measurements. Results were calculated as mean values after two injections for each essential oil. Results are presented in Tables 2,3.

Test organisms

Pure strains of bacteria (Staphylococcus aureus ATCC 13709, Staphylococcus epidermidis ATCC 35984, Streptococcus pyogenes ATCC 19615,Eschrechia coli ATCC 9637, Klebsiella pneumoniae ATCC 1705, Proteus vulgaris ATCC 8427, Pseudomonas aeruginosa ATCC 27853 and Shigella boydii ATCC 9905) as well as pure strains of Candida albicans ATCC 10231, Candida glabrata ATCC 90030, Candida krusei ATCC 14243 and Candida parapsilosis ATCC 22019 were used. All micro-organisms were kindly supplied from the Microbiology Department, Faculty of Pharmacy, Al-Azhar University, Nasr City, Cairo, Egypt.

Testing for antimicrobial activities

Minimum Inhibitory Concentrations (MICs) were determined using the broth microdilution method (36, 37). Determination of antimicrobial activities against yeast was achieved by microdilution method using serial dilutions of the essential oils (0.008–64.00 μL/mL), which were prepared in 96-well microtiter plates by microdilution method using RPMI-1640 media (Sigma, St. Louis, MO, USA) buffered with MOPS (Sigma). The antibacterial activities were determined by serial dilutions of the essential oils (0.03–128.00 μL/mL, DMSO) in Mueller–Hinton broth (Merck, Darmstadt, Germany). Test yeasts or bacteria strains were suspended in media and the cell densities were adjusted to 0.5 McFarland standards at 530 nm wavelength using a spectrophotometeric method. Inoculums (0.1 mL) were added to the microtiter plates, which were incubated in a humid atmosphere at 30 °C for 24–48 h (yeast) or at 37 °C for 24 h (bacteria). In addition, positive (medium with inoculums but without essential oil) and negative (Uninoculated medium, 200 μL) growth controls were prepared. The growth in each well was compared with the growth in the control well. MICs were visually determined and defined as the lowest concentration of the essential oil produced ≥ 50% growth inhibition for fungi and ≥95% growth reduction for bacteria compared with the growth in the control well. Each experiment was performed in triplicate. Gentamycin (Sigma-Aldrich, Steinheim, Germany) and nystatin (Merck, Darmstadt, Germany) in concentration range (0.001- 64.00 µg/mL, sterile distilled water) were used as standard antibacterial and antifungal drugs, respectively.

In addition, media from wells with fungi showing no visible growth were further cultured on Sabouraud dextrose agar (Merck, Darmstadt, Germany) and from wells with bacteria showing no visible growth on Mueller-Hinton agar (Merck, Darmstadt, Germany) to determine the minimum fungicidal concentrations (MFC) and minimum bactericidal concentrations (MBC).

Statistical Analysis

Results were expressed as the mean ± standard deviation; statistical analysis of experimental results were based on the analysis of variance method. Differences were considered statistically significant at the level of P < 0.001.

Results and Discussion

A noticeable variation was observed in the percentage yield of hydrodistilled essential oil prepared from the aerial parts of calocedrus incense cedar, C. sempervirens, and T. articulata, cultivated in Egypt yielding (1.41%, 0.32% and 1.71%), respectively. Results of GC/MS analysis of essential oils of plants under investigation showed qualitative and quantitative variations. Sixteen compounds were determined in essential oils of C.decurrens and C. sempervirens, while fifteen compounds were identified in essential oil of T. articulata.

Table 1

Yield and physical properties of essential oils prepared from C.decurrens, C. sempervirens and T. articulata fresh aerial parts

Plant	*C. decurrens*	*C. semervirens*	*T .articulata*
Specific gravity	0.8884	0. 8879	0.8921
Essential oils (g % of fresh weight)	1.42	0.30	1.71
Refractive index at 25 ⁰C	1.343	1.463	1.399

Table 2

Chemical composition of essential oils of C.decurrens, C. sempervirens and T. articulata aerial parts

No.	R_t(min.)	KI*	Compound	Percentage (%)
No.	R_t(min.)	KI*	Compound	C.decurrens	*C. sempervirens*	*T. articulat*a
1	11.5	834	Isovaleric acid	-	0.73	-
2	12.3	934	α-pinene	2.59	4.60	5.92
3	12.8	1000	Decyne	-	0.57	-
4	13.5	1011	δ-3-Carene	43.10	3.80	-
5	13.7	1026	p-Cymene	2.56	-	1.65
6	14.3	1047	(R)-(+)-Limonene	0.74	-	3.00
7	14.9	1062	γ-terpinene	2.67	-	-
8	15.6	1075	Fenchone	-	-	9.48
9	16.2	1088	Terpinolene	3.74	0.31	-
10	17.2	1098	Linalool	3.91	-	-
11	17.8	1102	(-)-α-Thujone	1.84	0.30	-
12	18.7	1120	α-Fenchol	13.07	-	-
13	19.2	1123	(+)-Fenchol	-	-	13.85
14	20.6	1143	Camphor	-	-	21.23
15	21.5	1165	(-)-Borneol	-	2.33	-
16	23. 7	1185	(+)-α-Terpineol	-	0.50	3.12
17	24.4	1221	α-Fenchyl acetate	14.16	-	4.83
18	25.6	1262	Chrysanthenyl acetate	-	-	3.30
19	26.6	1285	Bornyl acetate	-	-	15.03
20	26.8	1287	Isobornyl acetate	-	-	8.39
21	27.5	1290	Thymol	0.79	4.25	-
22	28.2	1352	α-Terpenyl acetate	-		3.47
23	28.4	1370	(+)-Curcuphenol	-	0.45	-
24	29.8	1418	β-Caryophyllene	1.72	-	3.51
25	30.2	1461	(−)-allo-aromadendrene	0.65	-	1.75
26	31.8	1495	Zingiberene	-	0.93	-
27	35.8	1576	Spathulenol	-	0.92	1.47
28	36.9	1581	(-)-Caryophyllene oxide	-	3.31	-
29	37.5	1596	(+)-Cedrol	4.51	74.03	-
30	38.9	1653	α-Cadinol	2.25	2.19	-
31	43.01	1984	Palmitic acid	1.70	-	-
32	47.75	2200	Stearic acid	-	0.78	-

Kovats Index on DB-1 column in reference to n-alkanes

Table 3

Classification of essential oils constituents of C. decurrens, C. sempervirens and T. articulata aerial parts and their percentages

Class	Percentage of constituents (%)
Class	*C. decurrens*	*C. sempervirens*	*T. articulata*
1-Monoterpenes
Oxygenated	33.77	7.38	82.70
Non Oxygenated	55.40	9.28	10.57
2-Sesquiterpenes
Oxygenated	6.76	80.90	1.47
Non Oxygenated	2.37	0.93	5.26
3-Fatty acids	1.70	0.78	-
4-Misceleneous group	-	0.73	-

Table 4

Antibacterial activities (MIC and MBC) of C. decurrens, C. sempervirens and T. articulata essential oils

Microorganism	Mean (µL/mL) ± Standard Deviation						Gentamycin Mean (µg/mL) ± Standard Deviation
	C. *decurrens*		C. sempervirens		*T. articulata*		Gentamycin Mean (µg/mL) ± Standard Deviation
	MIC90	MBC	MIC90	MBC	MIC90	MBC	MIC90	MBC
Gram-positive
Staphylococcus aureus	< 64	-	1.148 ± 0.067	3.031± 0.093	1.319 ± 0.074	3.031 ± 0.18	0.02 ± 0.004	1 ± 0.023
Staphylococcus epidermidis	0.442 ± 0.027	2.244 ± 0.092	0.047 ± 0.002	0.391± 0.073	0.023 ± 0.009	0.155 ± 0.062	0.02 ± 0.003	1 ± 0.046
Streptococcus pyogenes	< 64	-	0.84 ± 0.064	2.378± 0.13	< 64	-	0.02 ± 0.003	1 ± 0.028
Gram-negative
E. coli	< 64	-	0.037 ± 0.006	0.155 ± 0.052	0.659 ± 0.063	1.515 ± 0.052	0.04 ± 0.002	2 ± 0.027
Klebsiella pneumonia	0.500 ± 0.031	1.023± 0.11	1.319 ± 0.056	1.64 ± 0.080	2.828 ± 0.076	4.49 ± 0.24	0.02 ± 0.003	1 ± 0.027
Proteus vulgaris	1.414 ± 0.072	5.04 ± 0.094	1.414 ± 0.051	2.828 ± 0.160	3.031 ± 0.058	4.59 ± 0.095	0.02 ± 0.003	1 ± 0.050
Pseudomonas aeruginosa	1.515± 0.042	2.297 ± 0.056	0.42 ± 0.035	1.00 ± 0.062	2.378 ± 0.052	6.72 ± 0.27	0.037 ± 0.004	2 ± 0.032
Shigella boydii‎	0.435± 0.054	1.148 ± 0.072	0.84 ± 0.035	2.378 ± 0.120	0.757 ± 0.036	1.00 ± 0.064	0.02 ± 0.001	1 ± 0.032

Table 5

Antifungal activities (MIC and MFC) of C. decurrens, C. sempervirens and T. articulata essential oils

Microorganism	Mean (µL/mL) ± Standard Deviation						Nystatin Mean (µg/mL) ± Standard Deviation
	C. *decurrens*		C. sempervirens		*T. articulata*		Nystatin Mean (µg/mL) ± Standard Deviation
	MIC90	MFC	MIC90	MFC	MIC90	MFC	MIC90	MFC
Candida albicans	< 64	-	0.42 ± 0.027	1.319 ± 0.066	0.659 ± 0.053	1.515 ± 0.085	0.84 ± 0.062	1 ± 0.062
Candida glabrata	< 64	-	< 64	-	< 64	-	0.84 ± 0.032	1 ± 0.045
Candida krusei	< 64	-	< 64	-	< 64	-	1.148 ± 0.065	2 ± 0.034
Candida parapsilosis	0.824 ± 0.052	2.828 ± 0.182	0.757 ± 0.067	1.64 ± 0.058	0.659 ± 0.042	1.148 ± 0.087	0.84 ± 0.076	1 ± 0.041

Table 2. showed that δ-3-carene (43.10%), (+)-cedrol (74.03%) and camphor (21.23%) were the major constituents of the essential oils of C. decurrens, C. sempervirens and T. articulata, respectively. In addition alpha- fenchyl acetate (14.16%) and α- fenchol (13.07%) were predominant in essential oil of C. decurrens; α-pinene (4.60%) and δ-3-carene (3.80%) were dominated in essential oil of C. sempervirens and T. articulata essential oil showed the presence of bornyl acetate and and (+)-fenchol in a percentage of 15.03% and 13.85%, respectively.

Tables 2,3. showed that the highest percentage of oxygenated monoterpenes was observed in the essential oil of T. articulata (82.70%) followed by C. decurrens (33.77%) and C. sempervirens (7.38%). Camphor (21.23%) was the major oxygenated monoterpene in essential oil of T. articulata followed by bornyl acetate (15.03%), while α-fenchyl acetate (14.16%) and α-fenchol (13.07%) were the major oxygenated monoterpenes in the essential oil of C. decurrens. Whereas, thymol (4.25%) and borneol (2.33%) were the major oxygenated monoterpenes detected in the essential oil of C. sempervirens.

Essential oil of C. decurrens showed the highest percentage of non-oxygenated monoterpenes (55.40%) followed by T. articulata (10.57%) and C. sempervirens (9.28%). δ-3-carene (43.10%) represented the major non-oxygenated monoterpene in the essential oil of C. decurrens followed by terpinolene (3.74%). α-pinene (5.92%) was the major non-oxygenated monoterpene in the essential oil of T. articulata followed by limonene (3.00%). While the main non-oxygenated monoterpene in the essential oil of C. sempervirens was α -pinene (4.60%) followed by δ-3-carene (3.80%). Essential oil of C. sempervirens showed the highest percentage of oxygenated sesquiterpenes (80.90%) followed by C. decurrens (6.76%) and T. articulata (1.47%). (+)-Cedrol (74.03%) was the main constituent of the oxygenated sesquiterpenes of the essential oil of C. sempervirens followed by caryophyllene oxide (3.31%), also (+)-cedrol (4.51%) constituted the main oxygenated sesquiterpenes of the essential oil of C. decurrens followed by α-cadinol (2.25%), while spathulenol (1.47%) was the only oxygenated sesquiterpene detected in the essential oil of T. articulata. Essential oil of T. articulata showed the highest percentage of non-oxygenated sesquiterpenes (5.26%) followed by C. decurrens (2.37%) and C. sempervirens (0.93%). Zingibrene (0.93%) was the only detected sesquiterpene hydrocarbon in the essential oil of C. sempervirens while, β-caryophyllene (1.72% and 3.51%) and allo-aromadanderene (0.65% and 1.75%) were the only detected non-oxygenated sesquiterpenes in the essential oils of C. decurrens and T. articulata, respectively.

The antibacterial activities of C. decurrens, C. sempervirens and T. articulata essential oils against the tested Gram-positive and Gram- negative baeteria are shown in Table 4. The essential oils under investigation inhibited the growth of S. epidermidis at concentrations 0.023- 0.442 µL/mL. Essential oil of C. sempervirens showed inhibition of the growth of S. pyogenes at concentration 0.84 µL/mL, while essential oils of C. decurrens and T. articulata at concentrations up to 64 µL/mL showed no inhibition of the growth of S. pyogenes. E. coli showed no susceptibility to essential oil of C. decurrens, while all the tested Gram-negative microorganisms showed growth inhibition by the effect of essential oils of C. sempervirens and T. articulata at concentrations range 0.037- 3.031 µL/mL. In addition, all the tested essential oils excreted bactericidal activities against all the susceptible Gram-positive and gram-negative microorganisms at concentration range 0.155- 6.72 µL/mL. C. sempervirens showed the highest antibacterial activities against most of the tested bacterial strains.

The antifungal activities of the essential oils of C. decurrens, C. sempervirens and T. articulata against tested yeast strains are shown in Table 5. Essential oil of C. decurrens showed no activities against all the tested yeast strains except C. parapsilosis which showed growth inhibition at concentration 0.824 µL/mL. C. glabrata and C. krusei showed no susceptibility to any of the studied essential oils, while essential oils of C. sempervirens and T. articulata inhibited the growth of C. albicans and C. parapsilosis at concentration range 0.42- 0.757 µL/mL. The tested essential oils showed MFC against the susceptible Candida species ranging from 1.148 µL/mL to 2.828 µL/mL. C. sempervirens essential oil showed the highest fungicidal activities followed by T. articulata and C. decurrens.

From this study it could be concluded that the essential oils under investigation possess antimicrobial activities. C. sempervirens essential oil has the most potential antimicrobial properties followed by T. articulata essential oil. The results of the study are inaccordance with the previous investigations of essential oil of T. articulata, which proved the presence of α-pinene, camphor, linalool acetate, caryophyllene, alloaromadendrene, bornyl acetate and limonene as the major constituents in several studies of essential oil of different organs of T. articulata in different countries (27-31, 38, 39). Previous investigations on essential oil of C. decurrens from USA and Taiwan proved the presence of α-pinene, δ-3-carene, terpinene, terpinolene, linalool, α-fenchyl acetate, β-caryophyllene and cedrol (21, 22)] which were detected in this study. While, a previous study on essential oil of leaves of C. sempervirens cultivated in Egypt proved that cedrol constituted the major constituent of the oil followed by δ-3-carene and α-pinene (18) whilst the essential oil of the leaves of the plant cultivated in Tunisia showed the presence of α-pinene as a major component followed by δ-3-carene and limonene (19). As the composition of the essential oils revealed intraspecific chemical variability among the same species growing in different localities and different environmental conditions, this study could contribute to the chemotaxonomic characterization of family Cupressaceae.

From this study, it was concluded that the essential oils of plants of family Cupressaceae which were under investigation in this study showed low presence of non-oxygenated sesquiterpenes ranging from 0.93% to 5.26%. In addition to the occurrence of variable percentages of non-oxygenated monoterpenes (9.28%-55.4%), oxygenated monoterpenes (7.38%- 83.70%) and oxygenated sesquiterpenes (1.47%-80.90%). Meanwhile, α-pinene is the only common compound that was detected in all the tested essential oils.

The significant antimicrobial effect could be attributed to the presence of high percentage of oxygenated compounds specially cedrol (40). The results of antimicrobial activities proved in this study are in agreement with previous studies on the antimicrobial activities of essential oils of the plants under investigation (19, 27). Essential oil of the leaves of Tetraclinis articulata from Algeria showed antifungal activities against Fusarium species (27). Moreover, the essential oil of Cupressus sempervirens from Tunisia inhibited the growth of bacteria, fungi and yeast (19).

Conclusion

We believe that the present investigation together with previous studies provide support to the antimicrobial properties of the tested essential oils. They could be used as antimicrobial supplement in the developing countries towards the development of new therapeutic agents. Additional in-vivo studies and clinical trials would be needed to justify and further evaluate the potential of these oils as antimicrobial agents.

Acknowledgements

References

1.
Chang C, Chang W, Chang S. Antibacterial activities of plant essential oils against Legionella pneumophila. Water Res. 2008;42:278-86. [PubMed ID: 17659763].
2.
Dordevic S, Petrovic S, Dobric S, Milenkovic M, Vucicevic D, Zizic S, Kukić J. Antimicrobial, anti-inflammatory, anti-ulcer and antioxidant activities of Carlina acanthifolia root essential oil. J. Ethnopharmacol. 2007;109:458-63. [PubMed ID: 17011148].
3.
Ibrahim H, Aziz H, Syamisr D, Mohammad N, Mother M, Ali R, Awang K. Essential oils of Alpinia conchigera Griff and their antimicrobial activities. Food Chem. 2009;113:575-77.
4.
Sacchetti G, Maietti S, Muzzoli M, Scaglianti M, Manfredini S, Radice M, Bruni R. Comparative evaluation of 11 essential oils of different origin as functional antioxidants, antiradicals and antimicrobials in foods. Food Chem. 2005;91:621-32.
5.
Tatsadijeu N, Jazet D, Nagassoum M, Etoa F, Mbofung M. Investigations on the essential oil of Lippia rugosa from Cameroon for its potential use as antifungal agent against Aspergillus flavus Link ex. Fries. Food Control. 2009;20:161-6.
6.
Reische D, Lillard D, Eitenmiller R. Antioxidants in food lipids. In: Ahoh CC, Min DB, editors. Chemistry, nutrition and biotechnology. New York: Marcel Dekker; 1998. p. 423-48.
7.
Van M, Svendsen AA. Simple method for detection of glycosidic bound monoterpenes and other volatile compounds occurring in fresh plant material. Flavour Frag. J. 1989;4:59-61.
8.
El-Hamouly M, Ibrahiem M. GC/ MS Analysis and antimicrobial evaluation of volatile constituents of Conyza dioscoridis L growing in Egypt. Alex. J. Pharm. Sci. 2003;17:75-80.
9.
James D, Mary B, Judi D, Paggy A. Handbook of Medicinal Herbs. 2nd ed. Boca Raton. Florida, USA: CRC Press; 2002.
10.
Miller J, Knowles F. Introduced forest trees in New Zealand: recognition, role and seed source 9. The cypresses: Cupressus spp. and Chamaecyparis spp. FRI Bulletin 124/9. Christchurch. New Zealand. New Zealand: Forest Service; 1990.
11.
Cronquist A, Holmgren A, Holmgren N, Reveal J, Holmgren P. Intermountain flora vascular plants of the intermountain west. Vol. four. 4th ed. The New York Botanical Garden, New York: Elsevier, New York, Columbia; 1984. p. 459-60.
12.
Hyam R, Pankhurst R. Plants and their Names: A Concise Dictionary. 1st ed. New York: Oxford University Press Inc; 1995.
13.
Silba J. An international census of the Coniferae. Phytologia memoirs. London: Corvallis, OR: H.N. Moldenke and A.L. Moldenke. Company ltd; 1986. p. 1-79.
14.
List P, Horhammer L. Handbuch der Pharmazeutischen Praxis. Berlin: Springer- Verlage; 1979.
15.
Morte M, Honrubia M. Tetraclinis articulata (Cartagena Cypress). In: Bajaj Y, editor. Biotechnology in Agriculture and forestry. vol. 35. Heidelberg: Berlin: Springer- Verlag; 1996. p. 407-23.
16.
James AD. Dake›handbook of medicinal plants of the bible. CRC press, Tylor & Francis group. NY, USA; 2008. 161 p.
17.
Amouroux P, Jean D, Lamaison J. Antiviral activities in-vitro of Cupressus sempervirens on two human retroviruses HIV and HTLV. Phytother. Res. 1998;12:367-68.
18.
Elansary H, Salem M, Ashmawy N, Yacout M. Chemical composition, antibacterial and antioxidant activities of leaves essential oils from Syzygium cumini L, Cupressussempervirens L and Lantana camara L from Egypt. J. Agric. Sci. 2012;4:144-52.
19.
Boukhris M, Regane G, Yangui T, Sayadi S, Bouaziz M. Chemical composition and biological potential of essential oil from Tunisian Cupressus sempervirens L. Journal of Arid Land Studies. 2012;22:329-32.
20.
Sheeba V, Rick G, Gonzalez-Herrandez M, Nicholas P, Marc D, Joe K. Composition of the heartwood essential oil of incense cedar (Calocedrus decurrens Torr). Holzforschung. 2011;65:333-36.
21.
Von Rudloff E. The leaf terpene composition of incense cedar and coast redwood. Can. J. Chem. 1981;59:285-98.
22.
Robert P, Sanko N. The leaf essential oils of the genus Calocedrus. J. Essent. Oil Res. 2006;18:654-58.
23.
Bajaj YPS. Biotechnology in agriculture and forestry. Vol. 35. Berlin, Heidelberg: Springer; 2010. 407 p.
24.
Bourkhiss B, Ouhssine M, Hnach M, Bourkhiss M, Satrani B, Ouhssine M, Satrani B. Chemical composition and bioactivities of branches essential oil of Tetraclinis articulata. Bull. Soc. Pharm. Bord. 2007;146:75-84.
25.
Bellakhdar J, Honda G, Miki W. Herb-Drugs and herbalists in the Maghrib. Tokyo: Institute of the study of Languages and Cultures of Asia and Africa, International Geology Review; 1982.
26.
Bourkhiss M, Hnach M, Lakhlifi T, Bourkhiss B, Ouhssine M, Satrani B. Production and characterization of the sawdust of wood essential oil of Tetraclinis articulata (Vahl) Masters. Bull. Soc. Roy. Sci. Liege. 2010;79:4-11.
27.
Fatima Z, Meryem A, Hammadi A, Sid A. Evaluation of Tetraclinis articulata essential oil from Algeria flora as a potential source of antifungal activities and study of its chemical composition. J. Indian Acad. Wood Sci. 2013;10:9-15.
28.
Abi-Ayad F, Abi-Ayad M, Lazzouni H, Rebiahi S, Bessiere A. Antibacterial activities of essential oil extracted from leaves of Tetraclinis articulata (Vahl) Masters from Algeria flora. J. Microbiol. Biotechnol. Res. 2011;1:1-6.
29.
Djouahri A, Boudarene L, Meklati BY. Effect of extraction method on chemical composition, antioxidant and anti-inflammatory activities of essential oil from the leaves of Algerian Tetraclinis articulata (Vahl) Masters. Industrial Crops and Products . 2013;44:32-6.
30.
Nejia H, Jalloul B, Severine C, Mehrez R, Jean-stephane C. Comparison of different methods for extraction from Tetraclinis articulata: yield, chemical composition and antioxidant activities. Food Chem. 2013a;141:3537-45. [PubMed ID: 23993518].
31.
Nejia H, Severine C, Jalloul B, Philippe D, Mehrez R, Jean-stephane C. Supercritical CO2 extraction of Tetraclinis articulata: chemical composition, antioxidant activities and mathematical modeling. J. Supercritical Fluids. 2013b;82:72-82.
32.
Egyptian Pharmacopoeia. Vol. 1. 3rd ed. Cairo: Ministry of Health, General Organization for Government Printing Office, Cairo; 1984.
33.
Adams R. Identification of Essential oils by Ion Trap Mass Spectrometry. New York: Academic Press; 1989.
34.
Eight Peak Index of Mass spectra. vol., 1& 2. 2ed Ed. Mass Spectrometry Data Center in Collaboration with ICI, LTD., Organic division; 1974.
35.
Islam T, Salama M. Chemical composition and bioactivities of volatile oils from Ocimum basilicum L cultivated in Egypt. Egypt. J. Biomed. Sci. 2007;24:218-31.
36.
Wayne PA. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically; Approved Standard. 7th ed. Clinical and Laboratory Standards Institute, CLSI M7-A7; 2006a.
37.
Wayne PA. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; approved standard. 2nd ed. Clinical and Laboratory Standards Institute, CLSI M7-A7; 2006b.
38.
Chikhoune A, Hazzit M, Kerbouche L, Baaliouamer A, Aissat K. Tetraclinisarticulata (Vahl) Masters essential oil: chemical composition and biological activities. J. Essent. Oil Res. 2013;25:300-7.
39.
Jemia M, Chaabane S, Senatore F, Bruno M, Kchouk M. Studies on the antioxidant activities of the essential oil and extract of Tunisian Tetraclinisarticulata (Vahl) Mast (Cupressaceae). Nat. Prod. Res. 2013;27:1419-30. [PubMed ID: 23082942].
40.
Zhou Y, Wenxiong L, Wei C, Xintuo Y. Chemical components and antimicrobial activities of essential oils in Cunninghamia lanceolata heartwood. Chin. J. Appl. Ecol. 2005;16:2394-98.

comments