Clove (Eugenia caryophylata = Syzygium aromaticum) is one of the most important herbs in traditional medicine. It is locally known as cengkeh and grows naturally in Moluccas Islands, People in Moluccas usually use cloves in cooking, either the whole part or in ground form. This spice is also used for cigarettes known as kreteks  in Indonesia, Asia, and Europe. Beside cloves, people also use its essential oils for medical purpose, since it active against oral associated bacteria and fungi  . Previous studies have reported the antifungal    , antioxidant    , antibacterial    and anti-inflammatory   properties of clove oil. The main component of clove oil, eugenol, has been used as an anti-cancer   and as a starting material for synthesis analog L-α-metil DOPA  . Studies of clove essential oil from different parts of the world showed that the major components of the clove oil usually include eugenol, β-caryophyllene, α-humulene, caryophyllene oxide and eugenyl acetate respectively, and vary in concentration    The studies reveal a great variability in chemical compositions of the clove essential oils. Eighteen components were identified in essential oil from Turkey clove bud, where major components are eugenol (87%), eugenyl acetate (8.01%) and β-caryophyllene (3.56%)  . There are ten components in clove essential oil, with the main components are eugenol (77.81%), eugenyl acetate (21.30%) and β-caryophyllene (8.44%)  . Thirty-eight components were identified in the clove leaf oil from Bangladesh, and the main components are eugenol (74.30%), eucalyptol (5.80%), α-cadinol (2.43%). Thirty one components in bud oil were identified and the main components are eugenol (47.70%), β-caryophyllene (18.90%), benzdene-1-ethyl-3-nitro (11.10%) and benzoic acid 3-(1-methylethyl) (8.90%)  . Studies on the bud and leaf essential oil of clove from India and Madagascar were found 28 and 35 components respectively from the bud oils and the leaf oil from Madagascar is 22 components. Major components in the bud oil from India are eugenol (70%) followed by β-caryophyllene (19.5%) and eugenyl acetate (2.1%). A comparison of components of bud and leaf oils from Madagascar is 82.6%: 82.0% for eugenol, 7.2%: 13.0% for β-caryophyllene, and 6.0%: 0.4% for eugenyl acetate  . It has been shown that there are 10 components of bud, leaf and stem essential oils of cloves from Madagascar, Indonesia and Zanzibar. Major components in the bud essential oil from Madagascar and Indonesia are eugenol (72.08% - 80.31% and 77.32% - 82.36%), β-caryophyllene (2.36% - 6.38% and 5.34% - 8.64%) and eugenyl acetate (11.68% -21.32% and 8.61% - 10.55%). Major components in the leaf essential oil from Madagascar and Indonesia are eugenol (80.87% - 83.35% vs 75.04% - 77.54%), β-caryophyllene (11.65% - 15.02% vs 17.04% - 19.53%) and eugenyl acetate (0.29% - 1.45% vs 0% - 0.06%). Major component oil of Madagascar, Indonesia and Zanzibar stem essential oils are eugenol (91.81% - 96.65%, 88.76% - 89.28% and 87.52% - 89.47%), β-caryophyllene (1.66% - 4.48%, 7.40% - 7.75% and 7.19% - 9.70%),  . The essential oils of clove from Amboina Island have been reported  . As far as we know, this is the first report of the anti-bacterial activity of this clove oil from Amboina Island.
Buds, leaves and stems of clove plant were collected from Ureng Village, Amboina Island, Moluccas and treated as the raw materials. The raw materials were dried under the sun for six until seven days.
2.2. Essential Oil Isolation from Buds, Leaves and Stems
The dried plant materials (1.0 kg) of buds, leaves (1.0 kg) and stems (600 g) were treated by steam-distillation method by conventional steam distiller, for 6 hours. The essential oil samples were dried by anhydrous sodium sulfate (Na2SO4) and stored in cool until further analysis conducted.
2.3. Gas Chromatographs (GC)
GC analysis of clove essential oil was performed on a Shimadzu QP-2010, equipped with a FID and Rtx-5MS using a fused silica capillary column (30 m × 0.25 mm ID, film thickness 1.0 μm). Oven temperature was from 80˚C for 5 minutes and programmed heating from 80˚C to 280˚C at a rate of 16˚C for 6 minutes, and injector temperature 270˚C; detector temperature 280˚C; pressure of carrier nitrogen gas at inlet 7 psi, split ratio 40 and volume was 0.5 μL.
2.4. Gas Chromatography-Mass Spectrometry (GC-MS)
GC-MS analyses of clove essential oil were performed using Shimadzu QP-2010 Plus at 70 eV and 320˚C with auto sampler, system equipped with Rtx-5MS fused silica capillary column (30 m × 0.25 mm ID, film thickness 1.0 μm). Oven temperature was from 70˚C for 5 minutes, than programmed heating from 70˚C to 220˚C at a rate of 10˚C for 6 minutes, and from 280˚C for 5 min, injector temperature 270˚C. 100% pure helium gas was used as a carrier gas at the constant flow rate 2.30 mL/min, split ratio 40, ion source temperature 210˚C  . The spectrum of the unknown component was compared with the spectrum of known components stored in the Wiley 7 library. Name, molecular weight and structure of the component of the test materials were ascertained.
2.5. Antibacterial Assay
1) Bacterial strains and media
Four strains of bacteria use to assess the antibacterial properties is two Gram positive (Bacillus subtilis FNCC0060 and Staphylococcus aureus ATCC6538) and two Gram negative bacteria (Escherichia coli FNCC0091 and Salmonella typhimurium FNCC0157). All bacteria were grown on nutrient agar (Oxoid).
2) Disc diffusion test
Diameter of zone of inhibition was determined using the disc diffusion method as previously described by Lai et al., 2010  with minor modification. It was performed using a 24 h culture at 37˚C in 10 ml of nutrient broth (Oxoid). The cultures were adjusted to approximately 108 CFU/ml with sterile saline solution based on a McFarland turbidity standard of 0.5. Three hundred microliters of the suspensions were spread over the plates containing Mueller-Hinton agar (Merck) using a sterile cotton swab in order to get a uniform microbial growth on both control and test plates. The essential oils were dissolved in aqueous dimethylsulfoxide (Merck) with Tween 80 (0.5% v/v for easy diffusion). Under aseptic conditions, empty sterilized discs (Whatman, 6 mm diameter) were impregnated with 20 μL of different concentrations (1:1, 1:5, 1:10, 1:20) of the respective essential oils on the agar surface. Paper disc moistened with aqueous DMSO was placed on the seeded petri plate as a negative control. A standard disc containing ampicilin (50 μg/mL) was used as positive control. All petridishes were sealed with sterile laboratory parafilm to avoid eventual evaporation of the test samples. The plates were left for 30 min at room temperature to allow the diffusion of oil, and then they were incubated at 37˚C for 24 h. Antimicrobial activity was indicated by the presence of clear inhibition zones around the discs. Studies were performed in triplicate, and mean value was calculated.
3) Determination of minimum inhibitory and bactericidal concentrations
The essential oils, which exhibited the best antimicrobial activity in the paper disk diffusion assay, and some individual constituents, were selected for determining the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) using broth dilution method (Mith et al. 2014),  with minor modification. One colony of each bacterial strain was sampled with a loop, then inoculated in 20 mL Nutrient broth (NB, Oxoid) and incubated for 18 - 24 h at 37˚C. The bacterial concentration in the inoculum was standardized at 0.5 on the McFarland turbidity scale, equivalent to 108cfu/mL. An aliquot (1 mL) of this suspension was transferred to a sterile tube and the volume was adjusted to 10 mL with sodium chloride solution (0.8%, w/v) to obtain a concentration of 107 cfu/mL. Working inoculums were prepared by transferring 200 µL aliquots of this suspension to three test tubes and adjusting the volumes to 10 mL with NB medium to give final concentrations of 2 × 105 cfu/mL. Each essential oil (500 µL) was dissolved in dimethyl sulfoxide (100 µL) and the volume was made to 5 mL with sterile NB containing 1% Tween 80 to provide a stock solution containing 100 µL/mL of oil. Serial dilutions of each essential oil stock were made with NB to yield final concentrations ranging from 100; 50; 25; 10; 5; 2.5; 1 and 0.5 µL/mL and mixed with bacterial suspensions with a final concentration of bacteria approximately 5 × 104 cfu/mL. Final solutions were incubated for 24 h at 37˚C in microplate well sterile. The MIC was considered as the lowest concentration that prevented the visible growth and spectrophotometer set at 595 nm. The MBC was determined by subculturing 100 µL from each negative test tube onto plate count agar (PCA) plates. MBC was defined as the lowest concentration resulting in a negative subculture or giving presence of only one colony after incubation. The experiments were carried out in three replicates.
2.6. Statistical Analysis
The means were analysed by one way analysis of variance (ANOVA) followed by Tukey’s post hoc multiple comparison test using SPSS software package version 17.0 for windows. The results were expressed as mean ± SD. P values <0.05 were considered as significant.
3. Results and Discussion
3.1. Performance of Bud, Leaf and Stem Essential Oil of Clove
The clove essential oils of buds, leaves and stems were distilled from dried plant material on equipment of the steam distillation. Average yields essential oils isolate in different part of clove were calculated toward the dried materials. The results of clove oil from buds, leaves, and stems were 6.85% (w/w), 3.21%, (w/w) and 2.58% (w/w), respectively.
3.2. Chemical Composition of Bud, Leaf and Stem Clove Essential Oils
GC and GC-MS were use to analyze the clove essential oils from buds, leaves and stems. Five components were identified and quantified, as shown in Table 1, according to their elution order on the Rtx-5 column. The major components of bud are eugenol (75.30%) and eugenyl acetate (20.93%). The major component of leaf are eugenol (82.97%), β-caryophylene (12.84%). The major component of stem oil is eugenol (97.75%). Three major components were observed by GC-MS analysis for ion chromatogram in bud, leaf and stem clove oils. In comparison to standard library data, the peak at m/z 164 (M+), C10H12O2, was identified as eugenol, the peak at m/z 204 (M+), C15H24, was identified as β-caryophylene and the peak at m/z 206 (M+), C12H14O3, was identified as eugenyl acetate. The are two minor components in the mass spectrum, the peak at m/z 204 (M+), C15H24, was identified as humulene and the peak at m/z 220 (M+) C15H24O, was identified as caryophylene oxide. The spectral data matched that given in previous report  .
Based on this result, it can be inferred that oil from stem contain higher eugenol content than bud and leaf oil, but lower β-caryophylene and eugenyl acetate content than on bud and leaf oil. Moreover oil from leaf contains higher β-caryophylene content than bud and stem, and oil from bud contain higher in eugenyl acetate content than oil from leaf and stem.
The function of secondary metabolite in plant as protectant, attractant and repellent. The repelent in flower dependsvariable factor like phytochemical  .
Table 1. Chemical composition of bud, leaf and stem clove essential oils.
Figure 1. A typical gas chromatogram of the bud essential oil.
Figure 2. A typical gas chromatogram of leaf the essential oil.
Figure 3. A typical gas chromatogram of the stem essential oil.
Figure 4. MS Specturm of clove essential oil, (a) Eugenol, (b) β-caryophylene, (c) Humulene, (d) Eugenyl acetate, (e) Caryophylene oxide.
In the recent study bud contain compounds more than leaf and stem so that more production of compounds.
3.3. Antibacterial Activity of the Oils
The antibacterial activity of oil from stem, leaf and bud clove against four strain pathogen bacterial is summarized in Tables 2-4. The stem and leaf clove oils with inhibition zone of 15.05 ± 0.200 and 13.5 ± 0.322 mm, respectively, were found to be more active against Escherichia coli, than the bud clove oil with inhibition zone of 11.10 ± 0.153 mm. Similar results were found against Staphylococcus aureus and Bacillus subtilis. For Staphylococcus aureus, inhibiton of leaf and stem oils are 14.57 ± 0.513 mm and 13.47 ± 0.451 mm, respectively, while the inhibition zone of bud oils is 8.57 ± 0.404 mm. For Bacillus subtilis, inhibiton
Table 2. Antibacterial activity of clove oil against Escherichia coli FNCC0091 and Salmonella typhimurium FNCC0157.
1Values are mean diameter of inhibitory zone (mm) ± SD of three replicates, followed by different letters in column are signiﬁcantly different (P < 0.05). The diameter of paperdisk (6 mm) is included. 2Ampicillin (100 µg/mL) used as positive control and DMSO used as negative control. 3-: no antibacterial activity.
Table 3. Antibacterial activity of clove oil against Bacillus subtilis FNCC0060 and Staphylococcus aureus ATCC6538.
1Values are mean diameter of inhibitory zone (mm) ± SD of three replicates, followed by different letters in column are signiﬁcantly different (P < 0.05). The diameter of paper disk (6 mm) is included. 2Ampicillin (50 µg/mL) used as positive control and DMSO used as negative control. 3-: no antibacterial activity.
Table 4. Minimum inhibitory concentration (MIC) and minimal bactericide concentration (MBC) of clove oil1.
1Ampicilin was employed as positive control. The MBC to ampicilin was 100 µg/mL in all experiments.
of leaf and stem oils are 12.23 ± 0.252 mm and 12.80 ± 0.265 mm, respectively, while the inhibition zone of bud oils 10.5 ± 0.500 mm. Different results were found against Salmonella typhimurium, where stem oil with inhibition zone of 13.67 ± 0.764 mm is more active than bud oil with inhibition zone of 11.70 ± 0.577 mm, but is the same active as leaf oil with inhibition zone of 12.67 ± 0.577 mm.
Minimum inhibitory concentration (MIC) and minimum bactericide concentration (MBC) for selected three oils ranged from ≥2.5 to ≥10.0 μL/mL and ≥10 to ≥50 μL/mL (Table 4). This study revealed MIC and MBC values for leaf oil range from 2.5 to 5.0 μL/mL and 10 to 25 μL/mL, respectively. In addition, for stem oil, MIC and MBC values range from 2.5 to 10.0 μL/mL and 10 to 50 μL/mL, respectively. Finally, for bud oils MIC and MBC values range from 5 to 10.0 μL/mL and 25 to 50 μL/mL, respectively.
The essential oil from the stem of E. caryophylata showed high antibacterial activity against E. coli and S. aureus (MIC = 2.5 μL/mL and MBC = 10 μL/mL), and the leaf oil showed high antibacterial activity against E. coli (MIC = 2.5 μL/mL and MBC = 10 μL/mL).
In vitro studies in this work showed that the clove oils inhibited bacterial growth but their effectiveness varied and oil from stem of clove exhibited strong activity against the selected bacterial strains. This shows that antibacterial activity related to the components of eugenol contained in the cloves where the stem contains the highest compared to the leaf and bud. It has been previously reported  that oils induce antimicrobial activity because of the high concentration of eugenol and eucalyptol components. This result showed eugenol compound have aromatic ring and hydroxyl group as determining of antibacterial activity. Previous research showed that the antimicrobial activity of eugenol caused by the disruption of the bacterial cell membrane  .
The chemical composition of essential oils from clove (Eugenia caryophylata) was investigated. Essential oil from bud, leaf and stem clove oil, was obtained from steam distillation method, and its chemical composition was determined by GC and GC-MS. Main components in the bud oil are eugenol (75.30%), eugenyl acetate (20.93%) and β-caryophyllene (3.00%); in leaf oil, eugenol (82.97%), β-caryophyllene (12.84%), while in stem oil, eugenol (97.75%). The Oils were tested for their in vitro antibacterial activities against Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and the Gram-negative bacteria (Escherichia coli and Salmonella typhimurium). The essential oil of buds, leaves and stems displayed marked broad spectrum antibacterial activity against Gram-positive and Gram-negative bacteria.
The authors are grateful to the Director General of Research and Community Service, Ministry of Research, Technology and Higher Education Indonesia for its financial support.