Research Article

Acacia Decurrens (Wild) an Invasive South Africa Tree: Chemical Profile, Antibacterial and Antioxidant Activities

Okoli Bamidele*, Molefe Nnana, Ledwaba Imelda and Modise Sekomeng

Institute of Chemical and Biotechnology, Vaal University of Technology, South Africa

Submission: August 29, 2017; Published: September 07, 2017

*Corresponding author: Joseph Bamidele Okoli, Institute of Chemical and Biotechnology Vaal University of Technology, South Africa, Tel: +27767619418; Email: okolib@binghamuni.edu.ng

How to cite this article: Okoli B, Molefe N, Ledwaba I, Modise S. Acacia Decurrens (Wild) an Invasive South Africa Tree: Chemical Profile, Antibacterial and Antioxidant Activities. Organic & Medicinal Chem IJ. 2017; 3(3): 555611. DOI: 10.19080/OMCIJ.2017.03.555611.

Abstract

The present study describes the profile, antimicrobial and antioxidant potential of the stem bark of Acacia decurrens. The methanol and hexane fractions had 20% and 0.2% extract yield respectively. The GC-MS result of the hexane, chloroform, and ethyl acetate fractions confirm the presence of 52 compounds and the ICP analysis of the stem bark was found to contain high levels of Co, Zn, Mn, Ca, Ni, Mg, Cr, K and Fe; which is an indication of hyper accumulation capacity. The UV-Visible spectra of showed various peaks which are indication of important radical scavenging Chromophores. Phytochemical screening indicated that the alkaloid (0.6-3.3%) and saponins (5.1-8.6%) contents of the various fractions were significantly lower than the tannin (30.9-55.8 mg TAE/g), steroid (13.92-41.2%), phenol (40.6-65.5 mg GAE/g) and flavonoids (210.2-284.9 mg RUE/g) contents. The disk and well diffusion methods were used to determine the sensitivity and MIC of the fractions. The ethyl acetate and methanol were the most potent antibacterial fractions with 75% and 65% inhibition respectively with MIC of 12.5 μg/ml compared with ampicillin. The antioxidant activity of the fractions was analysed by different methods and revealed good antioxidant potential with different IC₅₀ values of 42.2-49.6 mg/mL for ABTS and 37.8-75.0 μg/ml for DPPH respectively, compared to standard antioxidants.

Keywords: A. decurrens; antioxidant; antibacterial; DPPH; ABTS; ICP-OES; GC-MS, UV/visible

Abbreviations: TC: Tannin Content; TFC: The Total Flavonoids; ZI: Zones Of Inhibition; MHB: Muller-Hinton Broth Medium

Introduction

Acacia decurrens (Willd), commonly known as black wattle or early green wattle is a perennial tree or shrub, in the subfamily Mimosoideae of the pea family Fabaceae. They are present in all terrestrial habitats, including alpine settings, rainforests, woodlands, grasslands, coastal dunes and deserts [1] and due to their prolific nature; they are being classified as invasive in some countries. The Acacia is repeatedly mentioned in the Book of Exodus, perhaps referring to Acacia raddiana, in regards to the construction of the Tabernacle [2]. The edible flowers and seed pods are used to produce dyes, while the trees are grown for firewood, fast-growing windbreak or shelter tree [3] and the edible gum from the trunk of the is used as a low-quality Arabic gum. In South Africa, Acacia decurrens is classified as an invasive species [4], threatening native wildlife [5]. Native wildlife may not have evolved defenses against the invader or they cannot compete with a species that has no predators and these can be exploited for its pharmacological potentials (such as antiproliferative, antimicrobial and antioxidant activities) against native infections.

In this study, a preliminary investigation into the chemical composition, antimicrobial and antioxidant potential of A. decurrens will be conducted, for the first time. Major chronic and degenerative diseases such as atherosclerosis, ischemic heart disease, ageing, diabetes mellitus, cancer, immunosuppression, neurodegenerative diseases are caused by oxidative stress [6] and are one of the most important routes for producing free radicals in foods, drugs and even in living systems [7]. Antioxidative defense mechanisms have proven over time to be the most effective method of combating oxidative stress caused by free radicals. Recently, there has been an upsurge of interest in the pharmacological potentials of plants as antioxidants in reducing oxidative stress-induced tissue injury [8-9]. This research is focused on the generic protocol using a bioassay- guided approach based on straight forward testing of the plant fractions followed by in vitro biological activity testing.

Material and Methods

Chemicals

Ethanol, methanol, hexane, ethyl acetate, chloroform, DMSO, ampicillin, nutrient broth sodium hydrogen carbonate, gallic acid, rutin hydrate, 2,2-dyphenyl-1-picrylhydrazyl (DPPH), 2,2'-azinobis(3-ethylbenzothia-zoline-6-sulfonic acid) (ABTS), potassi⌝um persulfate (di-potassium peroxdisulfate), potassium persul⌝fate, Folin-Ciocalteu's phenol reagent, ascorbic acid, aluminium chloride were obtained from Sigma-Aldrich Chemicals Co., St Louis, MO, USA. All reagents used in this study are of analytical grade.

Equipment

The fresh stem bark of A. decurrens was harvested around October 2016 near Vaal Dam Road, Heidelberg (26.5033°S, 28.4397°E), and South Africa, diced, and dried at an ambient temperature at a relatively low humidity. Authentication of the of A. decurrens stem bark was carried out by the South Africa National Biodiversity Institute, Pretoria, and voucher specimen number: 1200-1, and was deposited at Pretoria National Botanical Garden. The extraction was performed by serial maceration using 4 L of each solvent: hexane, chloroform, ethyl acetate, and methanol with slight agitation at 111 revs/min for seven days. The solvents were removed.

Plant Materials

The fresh stem bark of A. decurrens was harvested around October 2016 near Vaal Dam Road, Heidelberg (26.5033°S, 28.4397°E), and South Africa, diced, and dried at an ambient temperature at a relatively low humidity. Authentication of the of A. decurrens stem bark was carried out by the South Africa National Biodiversity Institute, Pretoria, and voucher specimen number: 1200-1, and was deposited at Pretoria National Botanical Garden. The extraction was performed by serial maceration using 4 L of each solvent: hexane, chloroform, ethyl acetate, and methanol with slight agitation at 111 revs/min for seven days. The solvents were removed.

Extraction and Determination of plant yield

The A. decurrens was diced to facilitate drying at a relative humidity of 55% at ambient temperature and the dried stem barks were pulverized using a hammer mill. The powder was stored in polyethene bags to prevent moisture absorption and contamination. Exactly 2 kg of the powdered stem bark were macerated at ambient temperature in 4 L of hexane, chloroform, ethyl acetate and methanol sequentially for seven days each with slight agitation at 111 revs/min. Afterwards, the extracts were filtered through Whatman filter paper No. 42 (125 mm) then through cotton wool and dried to constant weight in open air.

Qualitative Phytochemical Screening

The Phytochemical screening of the fractions was carried out using standard qualitative procedures [10].

Quantitative Phytochemical Screening

The Total Phenolic Content (TPC) was determined as described by Vuong, Hirun, Roach, Bowyer, Phillips, Scarlett [11], the results were expressed as mg of gallic acid equivalents per g of sample (mg GAE/g). The Total Flavonoids (TFC) was measured as described by Zhishen, Mengcheng, Jianming [12], the results were expressed as mg of rutin equivalents per g of sample (mg RUE/g). The Tannin Content (TC) was determined as described by Rajeev, Pawan, Gagandeep [13], and the results were expressed as mg of tannin equivalents per g of sample (mg TAE/g). The alkaloid content was determined as described by Fazel, Hamidreza, Rouhollah, Mohammadreza [14], saponins content determined by the method of Makkar, Siddhuraju, Becker [15] and the terpenoids content Ferguson [16] and expressed as percentage respectively

Elemental Analysis

Aqua regia digestion (HCl-HNO₃): A mixture of concentrated HCl and HNO₃, in the ratio of 3:1 is used as the aqua regia mixture. According to Muinde, Nguu, Ogoyi, Shiundu [17], 1.0 g of diced stem bark was digested in 10 ml of aqua regia mixture in digestion tubes for 3 hrs at 60 °C. After cooling the entire digest were filtered and transferred into 50 ml standard volumetric flask with deionized water Reagent blanks were prepared similarly to the samples. All sample solution was clear and diluted 10 times before analysis.

ICP-OES measurement: The measurement was calibrated by the method of external standards with Rh, Re as the internal standard. The reagent blank solution contained 1% of concentrated HNO₃. Mixed standard solutions containing 7 elements, Cr, Ni, Zn, Fe, Co, K and Ca were prepared in reagent blank solutions [18].

Spectroscopic Analysis

UV-Visible Spectroscopic Analysis Of The Fractions

The fractions of A. decurrens were analysed in the UV- Visible range between 200-900 nm using PerkinElmer Spectrophotometer and the characteristic peaks were recorded.

GC - MS analysisof the fractions

The analysis was carried out on Clarus 500 PerkinElmer Gas Chromatograph with an Elite -5 (100% Dimethylpolysiloxane) column coupled to a mass spectrometer detector The GC-MS method used in the study involves setting the column at an initial temperature of 110 oC and held for 2 min. After 2 mins the oven temperature has raised the rate of 5 oC/min, to 280 oC, and held for 9 min. The carrier gas (He) flow rate was maintained 1 ml/ min while the injection port temperature was kept at 250 oC. The solutions of the fractions were injected in split mode as 10:1. Mass spectral scan range was set at 45-450 (m/z).

Antimicrobial Assay

Preparation of Inoculum

The test organism Micrococcus luteus (ATCC 26883) Staphylococcus aureus (ATCC 25923), Escherichia coli (NCTC 11954), Salmonella typhi (ATCC 29692), Klebsiella pneumonia (BAA 1706), Shigella sonnei (ATCC 25931), Staphylococcus epidermis (ATCC 12228), Listeria monocytogenes (ATCC(R) BAA- 751TM) and Enterococcus faecalis (ATCC 22735) were obtained from the Department of Biotechnology, Vaal University of Technology, South Africa. Stock culture was maintained at 4°C on slants of nutrient agar. The active stock culture was inoculated in fresh tubes of Muller-Hinton Broth Medium (MHB) and the bacteria were incubated for 24 h at 37°C.

Screening for the Antimicrobial Potential of the fractions

The bacteria cultures were grown in nutrient broth liquid medium at 37 °C. After 24 h of growth, each microorganism, at a concentration of 10⁶ cells/mL, was inoculated on the surface of nutrient broth plates. A 6 mm in diameter disk impregnated with 1000|ig/ml of the fractions was placed on the surface of the inoculated Petrie dish and incubated at 37 °C for 24 h. The Zones Of Inhibition (ZI) were measured after 24 hrs and fractions with ZI more than 7 mm were reported as being sensitive [19]. In this study, the 2% DMSO and Tween 80 were used to dissolve the fractions in the culture media and were used as the negative control. And they showed no inhibitions in this study. These tests were performed in triplicate.

Determination of the Minimum Inhibitory Concentration (MIC)

The fractions with ZI more than 7 mm were subjected to further antimicrobial assay to determine theMinimal Inhibitory Concentration. Serial dilution of the active fractions of concentrations about 12.5-50 μg/ml were prepared and was used to impregnate the disk overnight. The impregnated disk was placed on the inoculated plates and incubated overnight at 37°C. After 24 hrs, the MIC of each fraction and ampicillin sodium salt (positive control) was determined [20]. These tests were performed in triplicate.

Antioxidant Assay

DPPH assay

The antioxidant activity of the fractions was examined on the basis of the scavenging effect on the stable 2,2-diphenyl-1- picrylhydrazyl (DPPH) free radical [21]. Freshly prepared 300 μl of 0.05 mM ethanolic solution of DPPH was added to 40 |il of each fraction with concentrations of 0.02 - 2 mg/ml. To the mixture, 2.7 ml of 96% ethanol was added and vortexed vigorously. The mixture was left incubate for 5mins at ambient temperature and absorbance measured spectrophotometrically at 517 nm. A blank sample was prepared and all determinations were performed in triplicate. The radical scavenging activities of the tested fractions expressed as a percentage of inhibition were calculated according to the following equation [21].

Present (%) Inhibition of DPPH Activity = [(AB-AA) / AB] x 1 00

Where A_A and A_B are the absorbance values of the test and of the blank, respectively. A percent inhibition versus concentration curve was plotted and the concentration of fractions required for 50 % inhibition was determined and represented as LD₅₀ (μM) for each of the test solutions. All determinations were carried out in triplicate.

ABTS assay

Experiments were performed according to Re, Pellegrini, Proteggente, Pannala, Yang, Rice-⌝Evans [22], with small modifications. ABTS of 7 mM and potassium persul⌝fate of 2.45 mM were prepared in distilled water and these two solutions mixed. The mixture was allowed to stand in the dark at ambient temperature for 16 hrs to generate the ABTS radical (ABTS•+). The ABTS radical solution was diluted with distilled H2O to an absorbance of 1.00 at 734 nm and the fractions of concentrations 0.02 - 2 mg/mL were added to diluted ABTS•+ solution and the absorbance reading was taken after 6 min of incubation at 734 nm. Results are presented as the ability of extract to scavenge 50 % of free radical ABTS•+ (1C50). All determinations were carried out in triplicate. Ascorbic acid was used as a positive control.

Results And Discussion

Influence Of Solvent On The Recovery Yield Of Secondary Metabolite

The fractions obtained from the four solvent extractions were different in colours and nature (Table 1). The methanol fraction gave the greatest yield (20 %), whereas the hexane fraction had the lowest yield (0.2 %) (Figure 1) and there was a significant difference in extraction yield between the methanol and the other fractions. This implies that most of the secondary metabolite is highly polar. These results are consistent with the previous studies of materials, which reported that extraction solvents significantly affect the recovery yields of a secondary metabolite from the plant (Table 1).

According to some researchers, aqueous, methanol and ethanol have been proven as effective solvents to extract phytochemical compounds from different plants [23]. The differences in the dielectric constants and polarities of the solvents used, result in different extraction yields of the secondary metabolite. These findings further confirm that extraction solvent plays an important role in extractability of secondary metabolite from the materials and each material has a more suitable solvent for extraction of secondary metabolite [24] (Figure 1).

Preliminary Phytochemical Screening

The results provide evidence of the presence of terpenoids, phenols, tannins, flavonoids, saponins, alkaloids in various fractions of A. decurrens stem bark. The major outcome of the present investigation revealed that the samples tested contained high concentrations of health-enhancing phytochemical constituents which are an indication that the plant has a medicinal value other than the tree being grown for firewood, or as a fast-growing windbreak or shelter tree [25] (Table 2).

NA, absent; +, low in abundance; ++, moderate in abundance; +++, high in abundance

The compounds identified in the fractions include steroids and tannins, which are known to mediate cardiotonic (Table 2) and possesses insecticidal, antioxidant, antimicrobial activities [26], phenols and flavonoids which may possess antioxidative, antidiabetic, anticarcinogenic, antimicrobial, antiallergic, antiinflammatory and antimutagenic activities [26-27] Ghani A [28] reported that ethnomedicinally the stem bark is being used for the treatment of diarrhoea and as an astringent.

Quantitative Phytochemical Screening

The alkaloids were present in the hexane and chloroform (0.6 - 3.3) %, steroids in hexane, chloroform, ethyl acetate and methanol (13.92 - 41.2) % and saponins in ethyl acetate and methanol (5.1 - 8.6) % (Figure 2). Alkaloids, saponins, and steroids have not been implicated as potent antioxidantcompounds because of their mechanism of action while phytochemical compounds like phenols, flavonoids, and tannins have been greatly implicated as potent antioxidant compounds [29] (Figure 2).

The total phenolic content of the chloroform, ethyl acetate, and methanol, calculated from the calibration curve (R2 = 0.9903), ranges from 406 ± 1.70 - 655 ± 0.35 mg GAE/g (Figure 3) , total flavonoid content of the ethyl acetate and methanol (R2 = 0.9986) were 210.24 ± 2.20 - 284.92 ± 1.02 mg RUE/g (Figure 4) and total tannin content of the hexane, chloroform, ethyl acetate and methanol of A. decurrens stem bark fractions (R2 = 0.9921) were 30.87 ± 1.73-55.80 ± 2.00 mg TAE/g (Figure 5). Phenolic compounds have redox properties, which allow them to act as antioxidants [30]. There is a significant rise in the amount of tannin and flavonoids extracted as the polarity of the solvent changes from hexane, chloroform, ethyl acetate to methanol because tannins are water soluble polyphenol compounds [31] and flavonoids are composed of a simple skeleton containing two phenol rings connected by a propionic chain [32]. The hypertolerance for heavy metals by the plant is justified by a lot of secondary metabolites with chelating potentials which the lone pairs of an electron can be deposited in the empty d-orbitals, keep the metals in an inactive state (Figures 3-5).

UV-visible absorption of the A. decurrens fractions

The fractions have similar absorption maxima with the hexane and ethyl acetate fractions having an additional absorption maximum in the visible region at 410(0.116) and in the UV region 390(0.648) and 345(0.663) nm respectively. There is a remarkable difference in the absorption pattern of the methanol fraction compared to the other fractions indicating a different structural feature of its compositional compounds, as confirmed in the report of Masayoshi [33], that there is a close relationship between the absorption of the organic compound and its structure. The three absorption maxima of the methanol fraction are all in the UV region, which is an indication of the absence of extensively conjugated compounds. The UV-visible absorption results are in conformity with the qualitative phytochemical screening (Table 2) result, with similar secondary metabolites present.

Elemental composition of A. decurrens stems bark

The concentration of nine metals were analysed using PerkinElmer Elan DRC II inductively coupled plasma mass Altec Mercury Analyzer AMA 254 and the elemental concentrations are presented in Figure 6. The stem bark was found to have high concentrations of heavy metals such as Co, Zn, Mn, Fe, Ni and Cr due to bioaccumulation. This is an indication that the plant has a high phyto- tolerance capacity and can be employed for green remediation [34] (Figure 6). The hyper-accumulation capacity for heavy metals due to A. decurrenshyper-tolerance, or phytol tolerance potential; explains the adaptive evolution of A. decurrens to hostile environments through many generations which have earned its invasive classification in South Africa [4]. The sorption potential is high and will have an adverse effect on native wildlife and vegetation but can be exploited as a source of controlled green-herbicide.

GC-MS analysis of the A. decurrens fractions

The GC-MS analysis of the stem bark clearly stems bark shows the presence of fifty-two major compounds in the hexane, chloroform, and ethyl acetate fractions in which most of the other compounds are presence in less than 20% composition of the fractions. The hexane, chloroform and ethyl acetate fractions contain eight, fourteen thirteen majort compounds respectively with retention time and m/z values presented in Table 3. The hexane and ethyl acetate fractions showed similar absorption maxima in the visible region at 410(0.116) and in the UV region 390(0.648) and 345(0.663) nm respectively due to the presence of possible chromophores on the major compounds in the hexane and f ethyl acetate fractions. There is also a remarkable similarity in the free radical scavenging activities of the hexane, similarity of the secondary metabolites but with different IC50 chloroform, and ethyl acetate fractions due to the structural because of some distinct compounds present (Table 3).

Evaluation of the antimicrobial potential of plant fractions

The data pertaining to the antimicrobial potential of the plant fractions are presented in Table 4 and Table 5. All the fractions from A. decurrens presented antimicrobial activity to at least one of the tested microorganisms with the fractions from ethyl acetate and methanol presenting the highest activities,tested and ampicillin was active against all the organisms expect for E coli and K pneumonia. Such results were not totally unexpected since these bacteria form resistance to penicillin is mediated by penicillinase, rendering the antibiotic ineffective (Table 4).

Among the fractions, the ethyl acetate fraction showed the highest antimicrobial activity comparable to the control. However,no activity against resistant bacteria likes E coli and K pneumonia due to the absence of potent compounds against or due to the presence of resistance genes in plasmids of the organism [35].On the other hand, E faecalis, S aureus, S sonnei, S epidermis and L monocytogenes which are also resistant to different antibiotics,had their growth inhibited by the ethyl acetate and methanol fractions. M luteus was observed to have shown susceptibility all the fractions despite the fact that M luteus survive in oligotrophic environments for extended periods of time [36] (Figure 7), the sensitivity is an indication that the extracts contain potent compound for the treatment of opportunistic infection caused by M luteus such as recurrent bacteremia, septic shock, septic arthritis, endocarditis, meningitis, intracranial suppuration, and cavitating pneumonia in immunosuppresed patients.

The data obtained, through the determination of MIC, shows that the polar fractions of the extract contain potent antibacterial compounds (Table 5). The ethyl acetate and methanol fractions showed anti-bacteria activity towards the same set of tested organism (Table 4) with MIC of 12.5 μg/ml. This observed MIC for the polar fractions is comparable with the MIC of ampicillin, this is an indication that the polar extracts act as an irreversible inhibitor of the enzyme transpeptidase, which is needed by bacteria to make the cell wall just like ampicillin [37] (Figure 7). The two critical stages of bacterial cell wall production in binary fission is usually breached by Ampicillin ultimately leading to cell lysis; therefore, ampicillin, ethyl acetate, and methanol fractions can be referred to as being bacteriolytic [37]. The hexane and chloroform fractions show very low and similar activity MIC with the hexane fraction being more potent against E coli, S typhi and M luteus with MIC of 25 -50 5 μg/ml. The similarity in activity can be justified by the presence of closely related compounds as indicated in the GC-MS result.

Antioxidant Assay

The fractions exhibited moderate radical scavenging activity. The hexane fraction and chloroform fractions showed comparative antioxidant activities and are more potent when compared with the radical scavenging activities of the ethyl acetate and methanol fractions. The radical scavenging potential in the form of their IC₅₀ values revealed that ascorbic acid (IC50 = 31.7 mg/mL) >chloroform fraction (IC₅₀ = 37.8 mg/mL) >ethyl acetate fraction (IC₅₀ = 46 mg/mL) >methanol fraction> (IC₅₀ = 48.6 mg/mL) >hexane fraction (IC₅₀ = 75 mg/mL). Similar results were observed using ABTS analysis, the radical scavenging decreases in the order chloroform fraction (IC₅₀ = 42.2 mg/mL) >methanol fraction (IC₅₀ = 44.6 mg/mL) >ethyl acetate fraction (IC₅₀ = 49.6 mg/mL) > ascorbic acid (IC₅₀ = 54.7 mg/mL) >hexane fraction (IC₅₀ = 54.7 mg/mL (Figure 8).

Ascorbic acid standard acts as a chain breaking the free radical chains [38-39]. The scavenging activity observed for the different fractions is a function of the secondary metabolites present and their hydrogen-donating ability which reduces the blue-green ABTS* and purple DPPH *coloured solutions. The phytochemical screening showed that the chloroform fraction with IC₅₀ 3 7 mg/mL against the DPPH* and IC₅₀ 42.2 mg/mL against the ABST* is the most potent due to the relatively high phenolic (65.5 mg GAE/g) and tannin (47.5 mg TAE/g) contents, which is in agreement with the work of RE Beyer [38], which reported direct correlation between the phenolic and tannin contents to the antioxidant activity.

The ethyl acetate and methanol fractions were potent antioxidant compounds with relative good IC₅₀ due to the presence of flavonoids, phenols and tannins, while the antioxidants activity of the hexane fraction with IC₅₀ 75 mg/mL against the DPPH* and IC₅₀ 57.8 mg/mL against the ABST* is the least potent due to the absence principle antioxidant metabolites (Figure 8) [39]. The A. decurrens stem bark extracts showed higher antioxidant activity with DPPH when compared to ABTS, with more potent activity than the positive control (ascorbic acid) in the ABTS assay, Brand-Williams, et al. [40] reported similar slow reaction of most antioxidants which were tested with the ABTS. The phytochemical screening of the chloroform fraction indicates the presence of phenols and GC-MS spectrum with fourteen distinct compounds from the hexane fraction which are most likely phenols. This distinct set of compounds has greatly impacted on the antioxidant activity of the chloroform fraction, as the free radical scavenging ability is facilitated by their hydroxyl groups.

Flavonoids, including flavones, flavonols, and condensed tannins, are plant secondary metabolites present in the ethyl acetate and methanol fractions owe their antioxidant activities to the presence of free OH groups, especially 3-OH hence, the trend of scavenging activity observed in the extracts. Flavonoids have antioxidant activity in vitro and also act as antioxidants in vivo depending onto the presence of free OH groups, especially 3-OH [41,42]. A lot of phenols and flavonoids justify the comparative scavenging potential of the extracts and not necessarily a number of flavonoids alone.

Conclusion

The findings from this study confirm chloroform as the most effective solvent for extracting potent antioxidant compounds while the ethyl acetate and methanol as the most effective solvent for extracting potent anti-bacteria compounds. The phytochemical constituent presence in the chloroform fraction were sterols, flavonoids, alkaloids, tannins and phenols which are known to exhibit antioxidant activity while the ethyl acetate and methanol were discovered to contain terpenoids, phenols, tannins, flavonoids, saponins, glycosides. The GC-MS of the hexane, chloroform, and ethyl acetate extracts confirms the presence of fifty-two compounds with the methanol fraction excluded due to the poor peak resolution as a result of the large quantity of polar biologically active phytochemical substances.

Plant ethyl acetate and methanol fractions have great potential as antimicrobial compounds against the tested microorganisms with MIC of 12.5 μg/ml. Thus, they can be used in the treatment of infectious diseases caused by resistant microbes. The efficiency of antioxidants in chloroform, ethyl acetate, and methanol fractions, studied using ABTS and DPPH radical scavenging assay, indicated that the IC₅₀ for chloroform and the other fractions is dependent on the quantity of phenolic, tannins and the presence of free OH groups, especially 3-OH compounds present in the flavonoids. The free radical scavenging activity in the chloroform fraction is comparatively stronger than other fractions. This is the first report on the antioxidant activity and the hyperaccumulator capacity for heavy metals by A. decurrens.

Acknowledgement

We are thankful to Directorate of research, Vaal University of Technology, Vanderbijlpark, Gauteng, South Africa, for providing all necessary facilities to conduct the experiment.

Conflict of Interest Statement

We declare that we have no conflict of interest.

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