Omani propolis: chemical profiling, antibacterial activity and new propolis plant sources
© Popova et al.; licensee Chemistry Central Ltd. 2013
Received: 2 August 2013
Accepted: 11 September 2013
Published: 22 September 2013
Propolis (bee glue) is a resinous honeybee product having a long history of application in many countries as a traditional remedy for treating wounds, burns, soar throat, stomach disorders, etc. It has been proved to possess beneficial biological effects, including antimicrobial, antioxidant, anti-inflammatory, cytotoxic, antiulcer, and many others. Bees gather propolis from diverse resinous plant parts and in different phytogeographic regions its chemical composition might vary significantly. In this article we report the results of the first study on the chemical profiles of propolis from Oman, its plant origin and antibacterial activity.
The chemical profiles of Omani propolis extracts were obtained by GC-MS analysis after silylation. Over 50 individual compounds were identified in the samples, belonging to different compound types: sugars, polyols, hydroxy acids, fatty acids, cardanols and cardols, anacardic acids, flavan derivatives, triterpenes, prenylated flavanones and chalcones. The profiles were dissimilar from other known propolis types. They demonstrate that although Oman is not a large country, the plant sources of propolis vary significantly, even in the same apiary and the same season. Based on chemical profiles, and isolation and identification of major marker compounds (new propolis constituents), new plant sources of propolis were found: Azadiracta indica (neem tree) and Acacia spp. (most probably A. nilotica). The ethanol extracts of the studied propolis samples demonstrated activity against S. aureus (MIC < 100 μg. mL-1) and E. coli (MIC < 380 μg. mL-1).
Omani propolis is different form the known propolis types and demonstrates significant chemical diversity. Its most important plant source is the resin of Azadirachta indica, and as a result its typical components are С5-prenyl flavanones. Other plant sources have been identified, too, playing some role in resin collection by bees in Oman: Acacia spp. (most probably A. nilotica) and Mangifera indica. The results demonstrate also the potential of Omani propolis as antimicrobial.
KeywordsPropolis Chemical profiling Propolis plant sources Azadiracta indica Acacia Antibacterial activity
Propolis (bee glue) is a resinous honeybee product collected by bees from plants and used as a building material and as a defensive antimicrobial substance in their hives . It has a long history of application in many countries as a traditional remedy for treating wounds, burns, soar throat, stomach disorders, etc . In the last decades, the medicinal properties of propolis attracted the attention of scientists and nowadays a lot of data exist concerning its chemical composition and diverse biological effects, including antimicrobial, antioxidant, immunomodulating, anti-inflammatory, cytotoxic, antiulcer, and many other activities [2–5]. It is a popular ingredient of food supplements, health foods and beverages, cosmetics .
Bees gather propolis from diverse resinous parts of living plants and in different phytogeographic regions its chemical composition might vary significantly due to the specificity of the local flora and the choices it offers to bees. At present, several propolis types are known, according to their chemical profiles and source plants: poplar type (European) propolis, Brazilian green propolis (Baccharis type), red South American propolis (Dalbergia type), Mediterranean propolis (rich in diterpenes from Cupressus spp.) , etc. Numerous studies have revealed that in different environments honeybees are capable of finding appropriate propolis floral sources with significant antimicrobial activities . Because of this, new propolis types from unexplored regions of the world have the potential to provide valuable leads to secondary metabolites with important bioactivities. In this article we report the results of the first study on the chemical profiles of propolis from Oman, its plant origin and antibacterial activity.
Results and discussion
Concerning the presence of chalcones, it is important to note that flavanones can easily turn to chalcones under the conditions of silylation for GC-MS analysis . In order to check whether the chalcones are native constituents of Omani propolis, we examined the 1H-NMR spectra of the extracts from the latter samples, looking for the typical doublets (J ~ 16 Hz) of the α- and β-protons of the chalcone skeleton in the range δ 6.7 – 7.4 and δ 7.3 – 8.0 . We were unable to detect any such signals in the 1H-NMR spectra, which lead to the conclusion that chalcones registered in GC-MS are artifacts produced from the corresponding flavanones and are not present in the native propolis.
The adaptation of A. indica to hot and dry climates has made it one of the most commonly planted species in arid and semi-arid areas , and it is widespread in Oman . The material collected by bees seems to be the resin, produced by resin glands on the leafy shoots of neem trees . The chemical composition of this resin is largely unknown; only one prenylated flavanone derivative, 8-prenyl-5,7-dihydroxy-3’-(3-hydroxy-3-methylbutyl)-4’-methoxyflavanone 3 has been identified in it so far. This flavanone has been isolated from neem resin glands as a new natural product  and no other source of 3 has yet been reported, thus it is a good taxonomic marker for A. indica resin. Compound 3 was detected in samples OM-2, OM-6 and OM-7. It was tentatively identified in the GC-MS profiles of the samples on the basis of its characteristic mass spectral fragmentation. The spectrum of the silylated compound is characterized by a low intensity molecular ion peak at m/z 656, corresponding to a molecular formula C26H32O6 and base peak at m/z 641 [M-15]+, This molecular formula corresponds to a flavanone with one prenyl group, one hydroxylated pentyl group, two OH and one OCH3 groups. The mass spectrum displays the typical fragments of a flavanone bearing 5 and 7 hydroxyl groups and one prenyl group in ring A: ions at m/z 349 [A1 – CH3]+, 321 [A1 – CH3 - CO]+, 309 (98%) [A1 – C4H7]+. On the other hand, the presence of a non-aromatic silyloxy group is indicated by the ion m/z 552 [M-CH3-OTMS]+. The position of the methyl group and the hydroxylated pentyl group in ring B are supported by the presence of the fragment ions at m/z 293 [B2]+ and 291 [B3]+. The peak at m/z 497, resulting from the loss of the hydroxylated side chain, supports the structure 8-prenyl-5,7-dihydroxy-3’-(3-hydroxy-3-methylbutyl)-4’-methoxyflavanone 3 (analogous peak was detected in the spectrum of the unsilylated compound ). The occurrence of compound 3 in Omani propolis thus provides an evidence for the contribution of A. indica as propolis source.
This finding adds a new species to the list of propolis source plants. It is important to note that A. indica is one of the most widely used medicinal plants in India since ancient times ; it possesses diverse biological activities, including antibacterial, antiviral and antifungal properties. Antifungal activity has been demonstrated for some individual neem constituents, including compound 3. Considering this fact, the choice of bees for resin source is not surprising.
The prenylated flavanones were detected in all Omani samples studied excluding OM-1. In the latter sample, the only secondary metabolites found were triterpenic compounds (individual compounds could not be identified), their source remaining unclear.
Another feature of this sample is the high concentration of the cyclitol derivative pinitol 8, also new for propolis. Indeed, pinitol has been found in several honey types but always as a minor constituent , so it is highly improbable that it has come into propolis from honey, unlike glucose and other carbohydrates. Pinitol together with the flavan derivatives form a combination of phytochemicals that can point to the plant source of this particular propolis sample: it is a combination typical for many Acacia species [33, 34]. Taking into consideration the distribution of Acacia nilotica in Oman , it is the most probable major source of OM-4. The presence of some amounts of prenylated flavanones/chalcones proves the importance of the neem tree as a secondary source for this sample.
It is noteworthy that all samples contain triterpenes but different samples contain different triterpenes and many of them could not be identified by GC-MS. The one common for all samples was cycloartenol. The exact plant origin of the triterpene compounds is yet unknown, but triterpenes are widely distributed in plant kingdom and the potential sources are numerous.
In this study, eight propolis samples were studied. Six of them were collected at the same apiary (region of Rumai) in different months of 2011, and only two samples (OM-3 and OM-8) originated from another location, Saham. Surprisingly, samples collected at virtually the same time of year from the same apiary from neighboring hives demonstrated different chemical profiles, for example OM-4 (September 10th) and OM-5 (September 11th). On the other hand, samples from different seasons were similar: OM-2 (June) and OM-6 (September). This difference indicates that propolis collection could be directed by some random factors.
The two samples from Saham (OM-3 and OM-8) have in common the presence of cardols and anacardic acids which sets them apart from the other samples, but they also display considerable quantitative differences between them.
Antimicrobial activity of Omani propolis samples (extracts with 70% ethanol)
Minimum Inhibitory concentration (μg. mL-1)
Al samples demonstrated good antibacterial activity, taking into consideration that natural products which produce minimum inhibitory concentrations (MIC) in the range 100–1000 mg mL-1 in in vitro susceptibility tests can be classified as antimicrobials . The MIC for all tested samples against E. coli were higher (lower activity) than against S. aureus. Most Omani samples were more active than a typical poplar type propolis sample from Bulgaria, both against S. aureus and E. coli.
There was a statistically significant correlation (r = 0,9646; p < 0.01) between the MIC against S. aureus and E. coli. The most active samples against both microorganisms were OM-6 and OM-7, the samples richest in prenylated flavonoids. Prenylated flavonoids are known to possess antimicrobial activity [36, 37] and that may be the explanation of this observation.
The results obtained in the present study lead to the conclusion that Omani propolis is different form the known propolis types and demonstrates significant chemical diversity. Its most important plant source turns out to be the resin of Azadirachta indica, and as a result its typical components are С5-prenyl flavanones. Other plant sources have been identified, too, playing some role in resin collection by bees: Acacia spp. (most probably A. nilotica) and Mangifera indica. Further studies of propolis from the region of the Persian Gulf should clarify the importance of neem and Acacia species as propolis sources.
The results demonstrate also the potential of Omani propolis as antimicrobial. The presence of biologically active phenolic constituents (prenylflavanones, cardols, anacardic acids, etc.) is an indication for its potential for application in complementary and alternative medicine, cosmetics and health foods.
36.4 ± 0.4
49 ± 1
23.4 ± 0.7
34.8 ± 0.1
30 ± 1
35 ± 1
41 ± 2
Saham - propolis on textile fabric
Extraction and sample preparation
Propolis was cooled in a refrigerator, grinned and extracted twice with 70% ethanol (1:10, w:v) at room temperature for 24 h. A part of the ethanol extract (5 mL) was evaporated to dryness. The balsam yield was determined by two parallel measurements. (Balsam content could not be determind only in sample OM-9 because propolis couls not be separated quantitatively from the textile fabric). The dry extract (combined from the two parallel measurments) was further analyzed by GC-MS after silylation, as well as for its antimicrobial activity. About 5 mg of the extract were mixed with 50 μL of dry (water-free) pyridine and 75 μL of bis(trimethylsilyl)-trifluoroacetamide (BSTFA) and heated at 80°C for 20 min. The silylated extracts and reference compounds were analysed by GC– MS.
The GC–MS analysis was performed with a Hewlett–Packard gas chromatograph 5890 series II Plus linked to a Hewlett–Packard 5972 mass spectrometer system equipped with a 30 m long, 0.25 mm i.d., and 0.5 μm film thickness HP5-MS capillary column. The temperature was programmed from 60 to 300°C at a rate of 5°C/min, and a 10 min hold at 300°C. Helium was used as a carrier gas at a flow rate of 0.8 mL/min. The split ratio was 1:10, the injector temperature 280°C, the interface temperature 300°C, and the ionization voltage 70 eV. Every extract was analyzed in duplicate.
Identification and quantification of compounds
The identification of individual compounds was performed using computer searches on commercial libraries, comparison with spectra of authentic samples and literature data. If no reference spectra were available, identification was performed based on the mass-spectral fragmentation, in such cases for some compounds only tentative structures were proposed. Some constituents remained unidentified because of the lack of relevant references and information (none of them major constituent). The quantification of individual constituents is based on internal normalization. The percentage figures in the tables refer to percent of the Total Ion Current, TIC, and are semi-quantitative.
Isolation of individual compounds
1H NMR (600 MHz) and 13C NMR (150 MHz), Bruker AV 600; spectra were taken in CDCl3 (deuterated chloroform) for compounds 1 and 2, in CD3OD (deuterated methanol) for compounds 6, 7a + 7b.
Individual compounds were isolated from the extract of sample OM-6 (7.1 g). The ethanol extract was concentrated in vacuo and extracted successively with petrol ether (3 x) and CHCl3 mg (3 x). The chloroform extract was evaporated to yield 2 g dry extract, which was subjected to column chromatography on a silica gel column (30 mm d. – 600 mm h; 150 g. silica gel) eluted with light petroleum — EtOAc (95:5 to 100% EtOAc) and 30 fractions were obtained. Fraction 4 yielded 2 mg of 7-O-methyl-8-prenylnaringenin 1, and fractions 9 – 11 yielded 67 mg of 3’,8-diprenylnaringenin 2.
Further individual compounds were isolated from the ethanol extract of sample OM-4 (3 g). The ethanol extract was concentrated in vacuo and extracted successively with petrol ether (3 x), CHCl3 mg (3 x) and EtOAc (3x). The petrol ether fraction contained mainly triterpenoids and was not further analyzed. The ethyl acetate extract was evaporated to dryness (200 mg) and subjected to preparative thin layer chromatography (PTLC) (silica gel 60 F254 glass plates Merck, 20×20 cm, 0.25 mm, mobile phaseCHCl3 – MeOH 8: 2; detection under UV light 254 and 366 nm), and two substances were isolated: 1.2 mg of fisetinidol 6 and 3 mg of a mixture of 2,3-trans-3,4-trans mollisacacidin 7a and 2,3-trans-3,4-cis mollisacacidin 7b.
1H NMR (600 MHz) and 13C NMR (150 MHz), Bruker AV 600; spectra were taken in CDCl3 (deuterated chloroform) for compounds 1 and 2, in CD3OD (deuterated methanol) for compounds 6, 7a + 7b.
The MIC of propolis extracts were determined using broth microdilution method with test strains Staphylococcus aureus 209, Escherichia coli WF + and Candida albicans 562 (obtained from the Bulgarian Type Culture Collection, institute for State Control of Drugs, Sofia). Stock solution of propolis extracts was prepared, as follows: 4–5 mg (exact weight) dry extract were dissolved in 1 mL 70% ethanol. This stock solution was used for serial dilution in a 96-wells microtiter microplate from 400 – 500 μg/mL to 200–250, 100–125, 50–62.5, 25–31.25, 12.25 -15.62, 6.12 - 7.81 μg/mL. For the broth microdilution test, 50 μL of bacterial suspension in exponential phase of the growth was added to the wells of a sterile 96-well microtiter plate already containing 50 μL of twofold serially diluted propolis extracts in growth medium. Control wells were prepared with culture medium and bacterial suspension only. Three wells of the microtitre plate were used for each concentration of tested propolis extracts as well as for control sample. Incubation of the microplate was done for 24 h in the cultivation conditions described above. The MIC is the concentration in the last well in the row where no development of the microorganism is detected.
Multivariate analysis of propolis chemical profiles was performed by principal component analysis (PCA), using the GC-MS data for the identified compounds expressed as a percentage of the Total Ion Current, respectively. Statistica Version 8.0 was used for the analyses.
Partial financial support from the Bulgarian National Science Fund -Project DRNF-02-13/2009 is acknowledged. The authors thank Ms. N. Kostova for NMR spectra.
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