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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913

Braz. arch. biol. technol. vol.56 no.2 Curitiba Mar./Apr. 2013

http://dx.doi.org/10.1590/S1516-89132013000200014 

BIOLOGICAL AND APPLIED SCIENCES

 

Chemical composition and antibacterial activity of Aloysia triphylla (L'Hérit) Britton extracts obtained by pressurized CO2 extraction

 

 

Thaylise Vey ParodiI; Agueda Palmira de Castagna VargasII; Carina KrewerII; Érico Marlon de Moraes FloresIII; Bernardo BaldisserottoI; Berta Maria HeinzmannIV,*; José Vladimir de OliveiraV; Ariana Secco PopiolskiV; Mariane MinozzoV

IDepartamento de Fisiologia e Farmacologia
IIDepartamento Medicina Veterinária Preventiva
IIIDepartamento de Química
IVDepartamento de Farmácia Industrial; Universidade Federal de Santa Maria; 97105-900; Santa Maria – RS – Brasil
VDepartamento de Engenharia de Alimentos; URI; Av. Sete de Setembro, 1621; 97700-000; Erechim – RS – Brasil

 

 


ABSTRACT

This study investigated the chemical composition of five different extracts of Aloysia triphylla and their activity against Aeromonas sp. The extracts were obtained from the dried leaves by pressurized CO2 extraction at 30, 50 and 70ºC, and 100, 150, and 200 bar, and analyzed by GC/FID and GC-MS. The antibacterial activity was assayed by the microdilution method. The tested microorganisms comprised seven Aeromonas isolates obtained from the kidney of infected silver catfish, Rhamdia quelen. The yield, chemical composition and antibacterial activity of the extracts were dependent on the extraction conditions. Mono and sesquiterpenoids were the major constituents of all the extracts and the highest extraction yield was obtained at 70oC and 200 bar. A. triphylla presented moderate antibacterial activity against Aeromonas sp.

Key words: Aloysia triphylla, pressurized carbon dioxide extraction, Aeromonas sp.


 

 

INTRODUCTION

Aloysia triphylla (L'Herit.) Britton [syn. Aloysia citriodora Palau, Lippia citriodora (Ort.) HBK, Verbenaceae] is cultivated mainly due to the lemon-like scent emitted from its leaves and is utilized for the preparation of herbal tea (Argyropoulou et al. 2007) which is known to have antispasmodic, antipyretic, sedative, and digestive activity (Carnat et al. 1999; Valentão et al. 1999; Pascual et al. 2001; Gomes et al. 2005), antimicrobial activity (Oskay et al. 2005) and antioxidant properties (Pereira et al. 2007). This plant has a long history of folk use to treat asthma, spasms, cold, fever, flatulence, colic, diarrhea, indigestion, insomnia, and anxiety (Carnat et al. 1999; Pascual et al. 2001; Gomes et al. 2005). The supply of Aloysia triphylla is from the Mediterranean countries such as Morocco, Portugal, Italy, and France, as well as Southeastern Asian countries. Some Latin American countries such as Chile, Columbia, Uruguay and Brazil also produce and supply the leaves of A. triphylla (Bandoni et al. 2008).

The conventional processes for extracting the terpenoids such as hydrodistillation and solvent extraction are usually inferior to supercritical fluid extraction (SFE), mainly regarding selectivity. It is well known that the SFE process makes use of mild temperatures, which avoids the degradation of thermo-sensitive compounds, and the low water content limits hydrolytic processes (Crabas et al. 2003; Wenqiang et al. 2007). This extraction method offers many important advantages over the hydrodistillation such as low energy cost and the possibility of extraction optimization by changing the processing parameters such as temperature, content of modifier (co-solvent), dynamic extraction time and fine tuning the extraction pressure (Khajeh et al. 2004). Moreover, the use of carbon dioxide brings the additional advantages of being non-flammable, fairly non-toxic, cost-effective, easily removed from the extract following decompression (Scalia et al. 1999) and, to a certain extent, solubilizes the lipophilic substances (Sahena et al. 2009).

The genus Aeromonas comprises a group of Gram-negative, facultative anaerobic bacteria that are pathogenic to aquatic and terrestrial animals and have also been associated with a wide spectrum of infectious diseases in humans and animals (Paniagua et al. 1999; Krzyminska et al. 2009). The widespread distribution of Aeromonas species in the aquatic environment combined with the stress induced by intensive culture practices predisposes fish to infections (Saavedra et al. 2004). Aeromonas infection is a significant concern in aquaculture as it is often associated with high mortality and morbidity rates (Clermont et al. 2008).

In this context, the aim of this work was to investigate the influence of temperature and pressure on the extraction yield and chemical composition of the extracts obtained by the pressurized fluid extraction of A. triphylla leaves. In order to determine the best parameters for plant material extraction in terms of activity optimization, the antibacterial activity of the extracts against Aeromonas sp was also evaluated.

 

MATERIALS AND METHODS

The leaves of Aloysia triphylla were purchased from the local market of Santa Maria (RS, Brazil) and identified by Dr. Gilberto Dolejal Zanetti (Department of Industrial Pharmacy, UFSM). A voucher specimen (SMDB No. 11169) was deposited in the herbarium of the Department of Biology, UFSM. Leaves were dried at 40ºC in a ventilated drying oven and subsequently powdered in a knife mill, homogenized and the particles classified in a sieve (Taylor series), excluding the particles smaller than 200 mesh, then stored in light-protected plastic bags at - 4oC in a domestic freezer.

The experiments were performed in a laboratory scale unit (Mazutti et al. 2006). Basically, it consisted of of a CO2 (99.9% purity, purchased from White Martins) reservoir, two thermostatic baths, a syringe pump (ISCO 260D), a 0.1dm3 jacketed extraction vessel, an absolute pressure transducer (Smar, LD301) equipped with a portable programmer (Smar, HT 201) with a precision of + 0.12 bar, a collector vessel with a glass tube and a cold trap. About 25 g of dried and powdered leaves of A. triphylla were loaded into the extraction vessel. The CO2 was pumped into the bed at a constant flow rate of 2 g min-1, which was supported by two 300 mesh wire disks at both ends, and was kept in contact with the herbaceous matrix for at least one hour to allow the system to stabilize. Afterwards, the extract was collected by opening the micrometering valve and the CO2 mass flow was recorded by the pump recordings. Then the extract was weighed, the glass tube was re-connected to the equipment, and this procedure was repeated until no significant mass was extracted. The extraction was completed within approximately 120 min, isothermally at desired pressure and temperature. An experimental factorial design using three temperatures (30, 50 and 70ºC) and three pressure levels (100, 150 and 200 bar) was established so as to assess the influence of process variables on the extraction yield, extract composition and antimicrobial activity.

GC-FID and TIC analysis was performed on a Varian gas chromatograph (Model CP-3800) equipped with mass detector Saturno using a capillary column fused silica VF-5 MS (Varian) (30 m x 0.25 mm x 0.25 µm). The conditions of analysis included: injector 1177 (MS), 250ºC, split 1:20 (FID and MS); injetor 1093 (FID), 250ºC. The flow of the carrier gas (He) was 1 mL/min (both FID and MS). The column oven temperature was initially kept at 50ºC for 4 min and then heated up to 280°C (increasing rate 4ºC/min). Injection volume was 1 μL and the detector temperatures were 200ºC (MS) and 310ºC (FID). The GC-MS analysis was performed with eletronionization (70 eV).

The constituents of the extracts were identified based on the retention index (RI) determined by using a calibration curve of a homologous series of n-alkanes (C8-C32) injected under the same chromatographic conditions of the samples and fragmentation models of mass spectra. Both data were compared with the literature (Adams, 2001) and with the equipment's library (NIST, 1998). The quantitative data were obtained from the FID eletronic integration peak areas.

The tested microorganisms comprised seven Aeromonas sp. isolates obtained from the kidney of infected silver catfish, R. quelen. The isolates were phenotypically identified by the conventional methods to genus according to Quinn et al. (1994).

Inoculum suspensions were prepared as described in CLSI M7-A6 protocol (NCCLS, 2003) by diluting the scraped cell mass in 0.85% NaCl solution adjusted up to 0.5 in the McFarland scale and confirmed by spectrophotometrical reading at 580 nm. The cell suspensions were finally diluted to 5 x 104 UFC mL-1 to be used in the activity assays in microdilution plates, where each hole contained 200 μL Mueller-Hinton broth and different concentrations of the test extracts. Mueller-Hinton broth, methanol and bacterial inoculum were used as negative control. For positive control, Mueller-Hinton broth and bacterial inoculum were added. The plates were incubated at 37ºC for 24 h.

The different extracts were dissolved in methanol at the ratio of 1:2. The final extracts concentrations in the plates were: 25000; 12500; 6250; 3125; 1562.5; 781.25; 390.62; 195.31μg mL-1. The tests were performed in duplicate. After the incubation period, all the plates containing Mueller-Hinton broth were replicated and incubated at 37ºC for 24 h to evaluate the Minimum Bactericidal Concentration (MBC). Minimum Inhibitory Concentrations (MIC) were not determined due the difficulty of solubilizing the extract in the broth.

Data are reported as the mean values ± standard deviations (σ). The homogeneity of variances among the groups was tested with the Levene test. As the data did not present homogeneous variances, groups were compared by Kruskal-Wallis test, followed by Mann-Whitney post hoc tests. All the tests were performed with Statistica 5.1 (1997; StatSoft Inc., Tulsa, OK, USA). The minimum significance level was set at p < 0.05.

 

RESULTS AND DISCUSSION

The semisolid extracts obtained by the pressurized CO2 extraction were light or dark yellow in color, similar to the extracts of Ocimum basilicum L. obtained by the supercritical carbon dioxide extraction (Lachowicz et al. 1997). Figure 1 shows the extraction kinetics for all the experimental conditions. As commonly found for SFE of vegetable matrices, extraction kinetic curves were characterized by a linear portion followed by the decreasing and nearly zero extraction rates (Fig. 1). The cumulative yield of the extracts increased up to 100-120 min, except at 70oC and 100 bar. As seen from Table 1, the yield at this experimental condition was significantly lower than those obtained under the other experimental conditions. Here, the extraction yield is defined as the weight percentage of the extract in relation to the initial load of the raw material in the extractor (Table 1).

According to Table 1 and Figure 1, the highest extraction yield was obtained at 70°C and 200 bar, thus corroborating the positive influence of higher system pressures.

These cause an enhancement of solvent power, and system temperature, affecting the vapor pressure of the solute to be extracted (Khajeh et al. 2004). This result was in agreement with the best extraction yield obtained by the supercritical CO2 extraction of O. basilicum L., in which the highest yield was obtained at the highest temperature (50°C) and pressure (250 bar) (Mazutti et al. 2006). In the present study, at the highest temperature chosen, 70ºC, the pressure was really determinant for the extraction yield. Hence, the extract obtained at 100 bar showed the smallest yield, while the extract obtained at 200 bar presented the highest cumulative yield.

It is well known that supercritical fluid extraction recovery and selectivity depends greatly on the balance between the fluid density and solute vapor pressure. For instance, the extracts obtained at 30°C and 100 bar (Table 2), 30°C and 200 bar (Table 3), 50°C and 150 bar (Table 4), and 70°C and 200 bar (Table 5) contained mainly monoterpenoids (C10 compounds), which are lipophilic compounds with low molecular weight, followed by sesquiterpenoids (C15 compounds).

Both groups are the main constituents of the most essential oils and are easily extracted by hydrodistillation, as they are generally volatile. In the extracts obtained at 100 bar and 30ºC (Table 2), 150 bar and 50ºC (Table 4), and 200 bar and 70ºC (Table 5), the monoterpenoid citral were the major component, while in the extract obtained at 200 bar and 30ºC (Table 3), only one constituent, the monoterpenoid limonene was detected. Limonene has been extensively investigated due its application in the flavor and fragrance industries  (Erasto and Viljoen 2008) as well as its medicinal potential (Bakkali et al. 2008; Yoon et al. 2010). However, the extract obtained at 70°C and 100 bar (Table 6) showed the presence of high amount of caryophyllene oxide, a compound with sesquiterpenoid structure which has been considered to be an artifact produced during the distillation as a consequence of the relatively high temperatures involved (Silva et al. 2010). Sköld et al. (2006) also described the oxidation of caryophyllene when exposed to air, yielding the corresponding oxide. However, their findings did not explain the fact that only one extract contained large amounts of caryophyllene oxide, since the entire plant material was processed in the same way prior to extraction. There was no report in the literature about this compound as an artifact during the supercritical fluid extraction process. However, caryophyllene, which has been considered its precursor, was detected in three of the five extracts obtained (see Tables 2, 4, and 5).

As regards the number of constituents detected by GC, the extract obtained at 70°C and 200 bar was the richest one, with 29 different compounds (Table 5), followed by the extracts obtained at 50°C and 150 bar (27 compounds, Table 4), and at 30°C and 100 bar (23 compounds, Table 2). However, for the extracts obtained at 30°C and 200 bar and 70°C and 100 bar, only one constituent was detected, limonene and caryophyllene oxide, respectively (Tables 3 and 6).

The chemical composition varied according to the experimental conditions, but some similarities could be observed. A predominance of compounds with terpenoid structure was observed in all the extracts. Monoterpenoids were the major components in almost all the extracts and were absent only in the extract obtained at 70°C and 100 bar (Table 6). Only the extract obtained at 50°C and 150 bar contained squalene, a precursor of triterpenoids and steroids in the biosynthetic pathway of plants (Table 4).

It was also possible to obtain the compounds with a non-terpenoidic structure and a high molecular weight, which seemed to be influenced by the temperature and pressure since different structures were obtained at different extraction conditions (Tables 2, 4 and 5). The same method of extraction also presented variations in the extraction of compounds of high molecular weight from Tanacetum cinerariifolium when using different temperatures and pressures (Marongiu et al. 2009). In a general sense, this work showed that it was possible to select the most favorable conditions for the extraction of different terpene groups present in the leaves of A. triphylla. The qualitative and quantitative differences observed indicated that the main constituents of the extract could then be chosen by adjusting the operating parameters such as pressure and temperature.

Three of the extracts from the leaves of A. triphylla (those obtained at 100 bar and 30°C and at 200 bar and 30°C and 70°C) showed activity against Aeromonas sp (Table 1). Antibacterial activity against another genus of Gram-negative bacterium (Escherichia coli) was previously described for the ethanolic extract of A. triphylla (Oskay et al. 2005). The essential oil of this species also presented antibacterial activity against four Gram-negative clinical isolates from the urinary tract infections (Rojas et al. 2010).

The MBC values of the obtained extracts did not differ statistically among themselves, nevertheless differences appeared with regard to the extracts obtained at 50°C and 150 bar and also at 70°C and 100 bar (Table 1), which showed a weaker antibacterial activity. Probably this activity was due to the synergistic action of several components because most of them were present in small percentages. The present study did not analyze the antibacterial activity of the isolated substances from the extracts. However, considering the chemical class of the major components of each extract, it was observed that the extract with the weakest antibacterial activity was the only one, which did not have the monoterpenoids in its composition. This result, obtained for the extract produced at 70°C and 100 bar, indicated that the monoterpenoids were probably important for the antimicrobial activity of A. triphylla leaves extracts against Aeromonas sp. The caryophyllene oxide, which was identified as the major compound of this extract (Table 6), lacked the antimicrobial activity against yeasts, Gram-positive and Gram-negative bacteria at concentrations up to 1716 μg/mL (Silva et al. 2010). On the other hand, monoterpenoids are recognized as food preservatives due their antimicrobial activity (Singh et al. 2010).

The tolerance of Gram-negative bacteria such as Pseudomonas aeruginosa for monoterpene constituents in consequence of their outer membrane has been reported in the literature (Mann et al. 2000). This could be explained by the presence of a hydrophilic membrane in the outer portion of Gram-negative bacterial cell wall that blocks the penetration of hydrophobic substances (Ozturk and Ercisli 2006), such as terpene constituents that are part of the chemical composition of essential oils (Ceylan and Fung 2004) and were present in the extracts obtained by the supercritical fluid extraction as described in this work. This obstacle imposed by the Gram-negative bacteria could have reduced the antimicrobial activity of the substances reported for this purpose such as limonene (Ozturk and Ercisli 2006) and citral (Kim et al. 1995; Fisher and Phillips 2006). Although Gram-negative bacteria are usually more resistant to plant-origin antimicrobials, Aeromonas hydrophila has been described as the most sensitive one (Tajkarimi et al. 2010).

The essential oil of A. triphylla showed antibacterial activity against different strains (Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, Klebsiella pneumoniae) observing inhibition zones with diameters between 7 and 19 mm and MIC values between 10 and 60 mg/mL, without activity against Pseudomonas aeruginosa (Rojas et al. 2010). There was no activity of the oil of A. triphylla obtained by hydrodistillation of the aerial parts of the plant against P. aeruginosa. The antimicrobial activity against genito-urinary Gram-positive pathogens such as S. aureus (MIC ≥ 18.75 mm) and E. faecalis (MIC ≥ 17.75 mm) has also been observed for the essential oil of A. triphylla (Rojas et al. 2010).

Although it was not possible to assign the activity against Aeromonas sp to a component in particular, oxygenated monoterpens such as citral which were present as a major component in three of the obtained extracts, showed inhibitory effect against Gram-negative and Gram-positive (Kim et al. 1997) microorganisms and antibacterial activity (Kim et al. 1995; Fisher and Philips 2006; Tajkarimi et al. 2010). Some monoterpenoids such as citral have been tested as preservatives in fish-based food products in order to reduce the contamination and to increase the useful life of these foods (Svodoba and Greenaway 2003; Burt 2004). Limonene also showed antimicrobial activity against the food-borne pathogens, fungi and resistant strains of Gram-positive and Gram-negative bacteria (Singh et al. 2010; Tajkarimi et al. 2010). Citral and limonene have been recognized by the regulatory agencies in the US and EU as safe for the use as food additive (Tajkarimi et al. 2010).

There are no reports regarding the antimicrobial activity of the non-terpene compounds found (Tables 2, 4 and 5). This is probably because the plants that present the terpenoids as secondary metabolites are generally superior in antimicrobial activity. However, the strength of this activity depends on external factors (Geiyd et al. 2005), including the agronomic practices and methodology of extraction, which would alter the chemical composition of the extracts and consequently influence their antimicrobial activity (Delaquis et al. 2002).

In general, the antimicrobial effect of essential oil is attributed to the C10 and C15 carbon terpenes with specific structural characteristics (Dorman and Deans 2000). Some of these terpene structures alone are bioactive and can interfere with the physical parameters of microorganisms such as absorption and bioavailability (Svodoba et al. 2006). The interaction between these terpenoid structures and microbes, which ultimately induces the antimicrobial activity is not well understood. The inhibitory effect of such molecules as citral and limonene (Svodoba and Greenway 2003) is generally explained by their interaction with the bacterial cell structural components (Belletti et al., 2004) like the phospholipid bilayer of the cell membrane, causing increase of permeability and leakage of intracellular constituents that are of vital importance for the bacteria (Singh et al. 2002). Some monoterpene alcohols can lead to inhibition of oxygen consumption, respiratory electron flow and oxidative phosphorylation of the microorganism (Reichling et al. 2009). Terpenes can also transpose the bacterial membrane, causing cell swelling, dissipation of pH gradients and electric potential (Sikkema et al. 1994).

However, when extracts are applied in a concentrated form as in the present study, the delivery of these hydrophobic compounds to bacterial cells may be reduced. An uneven distribution and accessibility of terpenes to bacterial cells may be one of the reasons for the relatively low bactericidal activity (Inouye et al. 2001), where the insolubility of the constituents in the culture medium may change the effectiveness of the extract besides chemical composition of plant material. Romeo et al. (2008) showed the antimicrobial efficacy of essential oil of A. triphylla in an experiment using a liquid medium. However, other essential oils in the same medium were less effective. Besides the differences in the chemical composition of these oils, the dependence of the bacterial metabolic activity from the growth medium, solid or liquid, might influence the microbial growth and survival (Skandamis et al. 2000).

Antimicrobial susceptibility tests with plant extracts using the microdilution plate may have drawbacks such as precipitation of some components in the extract and adherence of some microorganisms to the bottom of the hole making it difficult to analyze (Ostrosky et al. 2008). However, liquid medium was considered the best medium for the evaluation of antimicrobial activity using the natural compounds (Skandamis et al. 2000). Methanol was used to facilitate the dissolution of the extracts in a liquid culture medium and assess its minimum bactericidal activity (data not shown). In the present work, methanol showed no antimicrobial activity against Aeromonas. The lack of antimicrobial activity of methanol had also been found in Gram-negative bacteria (Pinto et al. 2001). Celiktas et al (2007) found low antimicrobial activity of methanol for the genus Staphylococcus and this activity was considered insignificant when compared to the essential oil tested.

 

CONCLUSION

The results obtained in the present work scientifically support the use of preparations of A. triphylla, traditionally used to treat the bacterial diseases. However, the antibacterial activity was influenced by the extraction conditions.

 

ACKNOWLEDGEMENTS

The authors thank Dr. Gilberto Dolejal Zanetti for the identification of the species. This work was supported by PRONEX/FAPERGS-CNPq and CAPES. B. Baldisserotto, A. P. C. Vargas, E. M. M. Flores and J. V. Oliveira were recipient of CNPq fellowships. T.V. Parodi, received PhD fellowships from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES).

 

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Received: December 01, 2011;
Revised: June 27, 2012;
Accepted: December 26, 2012.

 

 

* Author for correspondence: berta.heinzmann@gmail.com

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