Chemical constituents and biological activities of different solvent extracts of Prosopis farcta growing in Egypt

1 Medicinal Chemistry Department, Theodor Bilharz Research Institute, Kornaish El-Nile, 12411 Warrak El-Hadar, Imbaba, P. O. Box 30, Giza, Egypt. 2 Microbial Chemistry Department, Genetic Engineering and Biotechnology Division, National Research Center, El Behoos Street 33, Dokki-Giza 12622, Egypt. 3 Chemistry Department, Faculty of Science, Ain Shams University, El-Khalifa El-Mamoun, 11566 Abbassia, Cairo, Egypt. 4 Chemistry Department, Faculty of Science, Mansoura University, Mansoura-35516, Mansoura, Egypt.


INTRODUCTION
Due to, the rapid development of drug-resistant microorganisms, appearance of new patients of life-threatening infections and the constant return of diseases, the search for the discovery of new drugs got strong attention from researchers (Demain, 2000;Strobel et al., 2004).So, it is necessary to concentrate on the antimicrobial activity of plant derived substances that are being still used as global traditional medicine (Savoia, 2012).Plant secondary metabolites are responsible for the antimicrobial activity.Vancomycin-resistant enterococci (VRE), methicillin-resistant Staphylococcus aureus (MRSA), multi-drug resistant (MDR)-Mycobacterium tuberculosis and MDR Gram-negative bacteria are documented as the most complicated infections to overcome and heal (Dahiya and Purkayastha, 2012).Increased illness and death, especially in the third world countries, have been due to the development of broadspectrum β-lactamases (ESBLs) and carbapenemases that target Gram-negative bacteria (WHO, 2002).To overcome the resistance problem, there is a command need to do a renewed effort to screen various medicinal plants for their potential antimicrobial traits, which are due to compounds synthesized in the secondary metabolism of the plant.Alkaloids, flavonoids, tannins, phenolic compounds, steroids, resins, fatty acids and gums are the most important of these bioactive compounds of plants which are capable of producing specific physiological effect on body.Medicinal plants are used to treat about 80% of the world's population especially in India.The plant materials used in traditional medicine are considered more effective and relatively cheaper than manufactured medicine (Iwu et al., 1999;Mann et al., 2008).On the other hand, anticancers were isolated from different plant species.The first anticancer agents introduced in clinical use were vinca alkaloids, that is, vinblastine (VLB) and vincristine (VCR) isolated from Catharanthus roseus (Parakash et al., 2013).
The genus Prosopis L., is widely spread in different dry and semi-dry regions worldwide like; Africa, Australia, America and Asia (Perez-Garcia et al., 2012;Peña-Avelino et al., 2014;Abdelmoteleb et al., 2017).Approximately, this genus comprises from 44 to 50 species (William and Jafri, 2015).Prosopis farcta (Banks et Sol.) Eig.(Family Fabaceae) is a little prickly spiny shrub; it is native of United States, Kuwait, Turkey, Iraq, Iran, Northern Africa, and South Western Asia (Sharifi-Rad et al., 2014).Different phytochemicals were reported to be isolated and identified from the plant viz., volatile constituents (Harzallah-Skhiri et al., 2006), proteins and unsaturated fatty acids (Lajnef et al., 2015), and flavonoids (Direkvand-Moghadam et al., 2014).A literature survey revealed that P. farcta has been used in the treatment of neurological disorders (Mollashahi et al., 2013) and cholesterol level (Omidi et al., 2013).Moreover, different parts of the plant (seeds, pods and leaves) were reported to show a wide range of biological activities including; antioxidant (Poudineh et al., 2015), antibacterial (Sharifi-Rad et al., 2014), hepatoprotective (Alharbi et al., 2017), anti-diabetic (Jafari et al., 2013), to reduce cardiac pain (Asadollahi et al., 2010), and antiparasitic (Gulalp and Karcioglu, 2008).To the best of our knowledge, there is little information in the literature about the chemical and biological investigations were carried out on the aerial part of P. farcta growing in Egypt.Therefore, the present study is aimed at the isolation and identification of the chemical constituents from different solvent extracts of P. farcta aerial part, and evaluation of their antimicrobial, anticancer and antioxidant activities.

Plant material
The aerial parts of P. farcta (Banks et Sol.) Eig.(Fabaceae) were collected from Alkharga Oasis, Alwady Algaded, Egypt on March, 2015.The plant was identified by Prof. Dr. Ibrahim A. Mashaly, Professor of Plant Ecology and Flora, Botany Department, Faculty of Science, Mansoura University, Egypt.

Extraction and fractionation
The aerial parts were dried in an oven at 45°C for 24 h and been grinded to give 1.5 kg of dried powder.Then, powdered materials were soaked in MeOH for 72 h, at room temperature.After filtration, the solvent was evaporated using rotatory evaporator, resulting crude extract that was undergo further solvent extraction using different organic solvents that is, n-hexane, methylene chloride, ethyl acetate and n-butanol.

Antimicrobial activity
The antimicrobial activity was evaluated by filter paper disc method (Murray et al., 1998;Sardari et al., 1998).Briefly, filter paper discs, 5 mm diameter, were saturated with 200 µg of tested extract.Stock cultures of the test organisms were obtained from the Microbiological Laboratory, Faculty of Medicine, Mansoura University.Bacteria test microbes used were S. aureus, Streptococcus pyogenes, Klebsiella pneumonia, Escherichia coli, Bacillus subtilis, Erwenia carotovora, Shigella sp., Erwinia sp., Enterobacter aerogenes, Pseudomonas aeruginosa, Proteus vulgaris and Staphylococcus epidermis.Whereas the fungus used was Candida albicans.The bacterial test microbes (10 6 cells/ml) were swapped on plates containing nutrient agar medium (DSMZ1) whereas, the fungus test microbe (10 8 cell/ml) was swapped on plates containing Czapek-Dox medium (DSMZ130).The filter paper discs-containing the tested extracts were put on the surfaces of the inoculated plates.The plates were then incubated at 37 and 30°C, for bacteria and fungus test microbes respectively.The appearance of clear zones (mm diameter) was detected after 24 h of incubation.The activity index (%) is also measured as a correlation of the clear zone of tested extract compared to standard antibiotics (Ampicillin, Streptomycin, Kanamycin, Tobarmycin and Clotrimazole).The activity index was measured according to the following equation:

Anticancer activity (MTT assay)
The anticancer activity was evaluated according to the reported procedure (Mauceri et al., 1998), using four human tumor cell lines namely; hepatocellular carcinoma (HePG-2), mammary gland breast cancer (MCF-7), human prostate cancer (PC3), and Epitheliod carcinoma (Hela).The cell lines were obtained from ATCC via Holding company for biological products and vaccines (VACSERA), Cairo, Egypt.5-fluorouracil was used as a standard anticancer drug for comparison.Briefly, the different cell lines mentioned above were used to determine the inhibitory effects of extracts/compounds on cell growth using the MTT assay.This colorimetric assay is based on the conversion of the yellow tetrazolium bromide (MTT) to a purple formazan derivative by mitochondrial succinate dehydrogenase in viable cells.The cells were cultured in RPMI-1640 medium with 10% fetal bovine serum.Antibiotics added were 100 units/ml penicillin and 100 µg/ml streptomycin at 37°C in a 5% CO2 incubator.The cells were seeds in a 96-well plate at a density of 1.0x104 cells/well at 37°C for 48 h under 5% CO2.After incubation the cells were treated with different concentration of compounds and incubated for 24 h.After 24 h of drug treatment, 20 µl of MTT solution at 5 mg/ml was added and incubated for 4 h.Dimethyl sulfoxide (DMSO) in volume of 100 µl is added into each well to dissolve the purple formazan formed.The colorimetric assay is measured and recorded at absorbance of 570 nm using a plate reader (EXL 800, USA).The relative cell viability in percentage was calculated as (A570 of treated samples/A570 of untreated sample) X 100.

Antioxidant activity (ABTS assay)
The antioxidant activity was evaluated via 2,2-azino-di-[3ethylbenzo-thiazolin-sulphonate] (ABTS) method.Briefly, for each of the investigated sample 2 mL of ABTS solution (60 mM) was added to 3 M MnO2 solution (25 mg/ml) all prepared in phosphate buffer (pH 7, 0.1 M).The mixture was shaken, centrifuged, filtered, and the absorbance (Acontrol) of the resulting green-blue solution (ABTS radical solution) was adjusted at ca. 0.5 at 734 nm.Then, 50 ml of (2 mM) solution of the test compound in spectroscopic grade MeOH/ phosphate buffer (1:1) was added.The absorbance (Atest) was measured and the reduction in color intensity was expressed as % inhibition.The % inhibition for each compound is calculated from the following equation: % Inhibition = Acontrol-Atest/Acontrol x 100 Ascorbic acid (vitamin C) was used as standard antioxidant (positive control).Blank sample was run without ABTS and using MeOH/phosphate buffer (1:1) instead of sample.Negative control sample was run with MeOH/phosphate buffer (1:1) instead of Saad et al. 69 tested sample (El-Gazzar et al., 2009).

GC/MS analysis
GC/MS analysis was performed at the Central Laboratory of the Ministry of Agriculture, Al-Bhooth Str., Cairo, on Agilent 6890 gas chromatograph equipped with an Agilent mass spectrometric column PAS-5ms (30 m x 0.32 mm x0.25 um film thickness).The plant extracts were injected under the following conditions.Helium was used as carrier gas at approximately 1.0 ml /min, pulsed splitless mode.The solvent delay was 3 min, and the injection size was 1.0 µl.The mass spectrophotometric detector was operated in electron impact ionization mode an ionizing energy of 70 eV scanning from m/z 50 to 500.The ion source temperature was 230°C and the quadrupole temperature was 150°C.The electron multiplier voltage (EM voltage) was maintained at 1250 V above auto tune.The instrument was manually tuned using perfluorotributyl amine (PFTBA).The GC temperature program was started at 60°C then elevated to 280°C at rate of 8°C/min and 10 min hold at 280°C the detector and injector temperature were set at 280 and 250°C, respectively.Wiley and Nist 05 mass spectral data base was used in the identification of the separated peaks.

RESULTS AND DISCUSSION
Identification and characterization of the isolated compounds (1-4)

Antimicrobial activity
The antimicrobial activity of the different solvent extracts, that is, n-hexane, methylene chloride, ethyl acetate and n-butanol of P. farcta was evaluated using disk agar assay against twelve pathogenic microbial strains.The results revealed that the n-hexane extract showed moderate antimicrobial activity (relative to the used standard antibiotic) against only three tested strains that is, Shigella spp., E. coli and P. vulgaris with inhibition zones of 4.7, 8.3 and 6.3 mm, respectively; compared to Streptomycin, Ampicillin as standard antibiotics with inhibition zones of 14, 24 and 18 mm respectively.Also, the methylene chloride extract showed moderate antimicrobial activity against three tested strains namely; Erwinia spp., E. coli and S. epidermis with inhibition zones of 6.2, 7.2 and 8.4 mm respectively; compared to Streptomycin and Ampicillin as standard antibiotics with inhibition zones of 35, 24 mm respectively (Table 3).On the other hand, the ethyl acetate extract exhibited strong antimicrobial effect against four tested strains namely; Shigella spp., E. coli, P. vulgaris and C. albicans with inhibition zones of 7.3, 11, 6 and 7.3 mm, respectively; compared to Streptomycin, Ampicillin and Clotrimazole with inhibition zones of 14, 24, 18 and 20 mm, respectively.Moreover, the n-butanol extract exhibited strong antimicrobial effect against six tested strains namely; Shigella spp., Erwinia spp., E. coli, P. vulgaris, S. epidermis and C. albicans with inhibition zones of 11, 9, 17, 12.4, 9.7 and 11 mm, respectively; compared to Streptomycin, Ampicillin and Clotrimazole with inhibition zones 14, 35, 24, 18, 24 and 20 mm respectively (Table 4).The antibacterial activity of the 85% methanol extract of different parts of P. farcta growing in Iran against methicillin-resistant S. aureus (MRSA) was evaluated with inhibition zones of 5, 6, 8 and 12 mm, respectively for roots, leaf, pods and seeds extracts (Sharifi-Rad et al., 2014).Also, Miri et al. (2015) reported on the antibacterial activity of silver nanoparticles (Ag-NPs) from the crude extract of P. farcta growing in Iran against four human pathogenic bacteria namely; S. aureus, B. subtilis, E. coli and P. aeruginosa with inhibition zone of 9.5, 9, 9.5 and 9.5 mm respectively (Miri et al., 2015).In, conclusion these extracts may be used as a source of naturally occurring antimicrobial agents and alternative to the synthetic antibiotics to overcome the microbial infections.

Anticancer activity
The in vitro anticancer activity of different solvent extracts of P. farcta was evaluated against four human tumor cell lines viz., hepatocellular carcinoma (HePG-2), mammary gland breast cancer (MCF-7), human prostate cancer (PC3) and Epitheliod carcinoma (Hela).According to National Cancer Institute (NCI) criteria, the plant extract with IC 50 (µg/ml): 1-10 was considered very strong; 11-20 (strong); 21-50 (moderate); 51-100 (weak) and above 100 (non-cytotoxic).Therefore, the ethyl acetate extract showed very strong anticancer activity against Hela and MCF-7 cell lines with IC 50 of 6.9 and 8.8 µg/ml compared to 5-fluorouracil as standard with IC 50 of 4.8 and 5.4 µg/ml respectively.On the other hand the n-butanol extract showed very strong anticancer activity against MCF-7, HePG-2 and PC3 cell lines with IC 50 of 5.6, 8.4 and 9.6 µg/ml respectively (Table 5).To the best of our  Clotrimazole/ 20 0 0 0 0 knowledge, there is very little information about the anticancer activity reported about the plant.The anticancer activity of the hydroalcoholic extract of P. farcta was evaluated against MKN45 (human gastric cancer) cell line (Dejamfekr and Khaleghian, 2016).The above mentioned results suggest that P. farcta plant may be used as a source of naturally occurring anticancer agents.

Free radical scavenging antioxidant activity (ABTS assay)
The free radical antioxidant activity of different solvent extracts of P. farcta was evaluated via ABTS assay which based on their abilities to reduce the radical cation ABTS +°.The results in (Table 6) revealed that the % inhibition of ABTS radical was 83.1, 82.0, 87.2 and 87.0% ).The IC 50 value of the ABTS free radical activity of the methanol extract of P. farcta fruits growing in Tunisia was 270 μg/ml (Lajnef et al., 2015).To the best of our knowledge, there are limited reports about the antioxidant activity of P. farcta using the ABTS assay, but there are available data about other assays that is, the antioxidant activity of four solvent extracts from pod and seed of P. farcta was evaluated using DPPH assay, and the IC 50 of the tested extracts from pod part were 1.0, 6.15, 3.55 and 7.75 µg/ml respectively for ethanol, methanol, octanol and n-heptane extracts, while and the IC 50 of the tested extracts from seed part were 2.0, 1.51, 0.95 and 4.45 µg/ml respectively for ethanol, methanol, octanol and n-heptane extracts (Poudineh et al., 2015).
The antioxidant activity of plant extracts as a complex mixture may be attributed to the presence of polyphenolic compounds due to therir abilities to act as free radicals scavengers either in individual mode or via synergetic mode (co-activity) (Ivanova et al., 2005;Djeridane et al., 2006).

Figure 1 .
Figure 1.Chemical structures of pure compounds were isolated from the EtOAc and n-BuOH extracts of P. farcta.

Figure 2 .
Figure 2. Gas ion chromatogram of the n-hexane extract of P. farcta aerial part.

Figure 3 .
Figure 3. Gas ion chromatogram of the methylene chloride extract of P. farcta aerial part.

Table 1 .
The compounds identified in the n-hexane extract of P. farcta by GC/MS analyses.

Table 2 .
The compounds identified in the methylene chloride extract of P. farcta by GC/MS analyses.

Table 3 .
The inhibition zones in mm and activity index% of the n-hexane and methylene chloride extracts of P. farcta compared to standard antibiotics.Microorganism Standard

Table 4 .
The inhibition zones in mm and activity index% of the ethyl acetate and n-butanol extracts of P. farcta compared to standard antibiotics.

Table 5 .
In vitro anticancer activity of different solvent extracts of P. farcta against four human tumor cell lines compared to 5-fluorouracil as standard.

Table 6 .
In vitro ABTS free radical antioxidant activity of different solvent extracts of P. farcta compared to ascorbic acid.