White cabbage fermentation improves ascorbigen content,antioxidant and nitric oxide production inhibitory activity in LPS-induced macrophages

Consumption of foods rich in dietary antioxidants and anti-inflammatory compounds is becoming a key strategy to lower oxidative stress and inflammation. The objective of this work was to study the effect of fermentation and starter culture on ascorbigen (ABG) and vitamin C content, as well as antioxidant and anti-inflammatory properties of white cabbage (Brassica oleracea var. capitata cv. Megaton). Lactobacillus plantarum CECT 748 (LP), Leuconostoc mesenteroides CECT 219 (LM) or a mixed culture of both strains at 1:1 ratio (LPM) were used as starter cultures in sauerkraut manufacture. Microbiological and sensorial quality of sauerkraut was also examined. White cabbage fermentation increased (P < 0.05) ABG content (up to 12-fold), oxygen radical absorbance capacity (ORAC) values (up to 2-fold) and NO production inhibitory potency (up to 2.6-fold). Vitamin C content slightly decreased (P < 0.05) up to 1.4-fold during fermentation. LM sauerkraut showed the highest (P < 0.05) ABG concentration (204.8 μmol/100 g d.w.), ORAC values (164.0 μmol Trolox/g d.w.) and NO inhibitory potency (IC₅₀ = 60.8 μg extract/mL). The microbiological quality of LM, LP and LPM sauerkrauts was satisfactory. Experimental sauerkrauts showed higher overall acceptability (P < 0.05) compared to commercial products. Consequently, selection of starter culture is of great importance in the manufacture of sauerkraut with improved content of bioactive compounds and health-promoting potential.     

Sterol and vitamin D2 concentrations in cultivated and wild grown mushrooms: Effects of UV irradiation

Raw and processed mushroom samples including wild grown (chanterelles and king bolete) and cultivated samples (white and brown button, portabella, shiitake, oyster) were bought from the food market and analysed for sterols and vitamin D₂ contents. The different commercial mushrooms selected are abundant in almost every Swedish and European supermarket or outdoor market. Ergosterol was the most abundant sterol found in mushrooms present in somewhat higher concentrations in cultivated mushrooms (4.0-5.0 mg/g dry matter (d.m.)) than those found in wild mushrooms (1.7-3.5 mg/g d.m.). In addition, three closely related minor sterols, including ergosta-7,22-dienol, ergosta-5,7-dienol, and ergosta-7-enol were identified. Chanterelles and king bolete were found to be good sources of vitamin D₂ (0.7-2.2 μg/g d.m.) compared with cultivated mushrooms that had a low content (< 0.1 μg/g d.m.). Canned samples of Agaricus bisporus/white were slightly lower in ergosterol and vitamin D₂ compared to fresh samples. Irradiation with UV light in the A region (366 nm) only slightly affected ergosterol and vitamin D₂ content. In contrast, irradiation with UV light conducted in the C region (254 nm, 0-2 h, 20 cm distance) for fresh white button mushrooms and freeze-dried chanterelles resulted in nonsignificant decrease in ergosterol content, whereas vitamin D₂ increased up to 9-fold (Cantharellus tubaeformis) and 14-fold (A. bisporus/white), respectively.     

Phenolic content, antioxidant, anti-inflammatory and anticancer activities of the edible halophyte Suaeda fruticosa Forssk

Suaeda fruticosa is an edible and medicinal halophyte known for its hypoglycaemic and hypolipidaemic activities. In this study, novel biological activities of the shoot extracts related to their phenolics were investigated. Results showed an appreciable total phenolic (31.8 mg GAE/g DW) in shoot extracts. The estimation of antioxidant capacities using oxygen radical absorbance capacity (ORAC method) and a cell based-assay (WS1) of four extracts (hexane, dichloromethane, methanol and water) showed that shoot methanol extract exhibit the highest antioxidant activities. The same extract displayed the utmost anti-inflammatory activity, inhibiting nitric oxide (NO) release, by 66.4% at 160 μg/ml in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. Besides, the dichloromethane extract showed the highest anticancer activity against human lung carcinoma (A-549) and colon adenocarcinoma cell lines (DLD-1, Caco-2 and HT-29) with specificity against DLD-1 (IC₅₀ = 10 ± 1 μg/ml). These findings demonstrate the remarkable potentiality of this edible halophyte as valuable source of antioxidants which exhibit original and interesting anti-inflammatory and anticancer capacities.     

Composition,antimicrobial, antiradical and spasmolytic activity of Ferula heuffelii Griseb. ex Heuffel (Apiaceae) essential oil

The essential oil from underground parts of Ferula heuffelii from N.E. Serbia, was analysed using GC and GC–MS. The main compounds of the essential oil were elemicin (35.4%) and myristicin (20.6%). The essential oil exhibited the best antimicrobial activity against two strains of Candida albicans (MIC = 7.0 and 13.7 μg/ml), as well as against Micrococcus luteus (MIC = 13.7 μg/ml), Staphylococcus epidermidis (MIC = 17.6 μg/ml), Bacillus subtilis (MIC = 21.1 μg/ml) and Micrococcus flavus (MIC = 28.2 μg/ml). In the DPPH radical scavenging assay, essential oil showed substantial activity with SC₅₀ = 22.43 μl/ml. The essential oil was also tested for antispasmodic activity. It inhibited spontaneous contraction of isolated rat ileum dose-dependently, and at the concentration of 86.64 μg/ml exhibited 50% of the maximum effect of atropine. After incubation with 75.00 μg/ml of essential oil, acetylcholine did not induce contractions of ileum, and at 250.00 μg/ml, the essential oil almost completely abolished the spasmodic effect of potassium chloride (80 mM).     

Ultrasonic assisted enzymatic digestion (USAED) coupled with high performance liquid chromatography and electrothermal atomic absorption spectrometry as a powerful tool for total selenium and selenium species control in Se-enriched food supplements

The suitability of hyphenated USAED with HPLC separation and ET-AAS determination as a new rapid methodology for Se control in Se-enriched food supplements is demonstrated. Total Se determination and Se speciation are accomplished in a single sample treatment using low sample amounts (ca. 10 mg), and low extracting volume (1 mL). The total Se content in seven of the 10 Se-enriched supplements studied was in agreement with the values obtained after microwave pressurized acid digestion, MW, (test t, p = 0.05). The Se species studied were Se(IV), Se(VI), SeMet, SeMeSeCys, and SeCys₂, being some of the most common found in the 10 supplements studied. Although SeMet was the Se species expected to be present at the highest concentration in most Se-enriched food supplements, we detected it in only three of the 10 samples studied. In the other seven samples, two of them had Se(IV) as the main Se species. The other five supplements had Se species that did not match with any of the five standards selected by us. We have also systematically demonstrated that ultrasonication does not alter the following Se species: Se(IV), Se(VI), SeMet, SeMeSeCys, and SeCys₂. The new procedure can be easily adapted to more Se species and can be routinely used for Se control in Se-enriched food supplements. Concerning the supplements studied, our results suggest that stricter control on the Se content in enriched food supplements in terms of Se species will need to become mandatory.     

Daily selenium intake in a moderate selenium deficiency area of Suzhou,China

In this study the daily dietary Selenium (Se) intake in Suzhou was investigated to determine whether residents in such a developed region were susceptible to moderate Se deficiency. Concentrations of Se in typically consumed foods in Suzhou were determined. Based on food Se content and the daily per capita consumption, the estimated Se intake in Suzhou was 43.9 ± 3.8 μg day⁻¹. The results revealed that pork and cereals were the major sources of Se daily intake and contributed 24.7% and 22.6% to the daily Se intake, respectively. The Se content in hair of local residents was 389.9 ± 103.6 μg kg⁻¹ for male and 322.9 ± 101.8 μg kg⁻¹ for female. A significant linear correlation between the daily Se intake and the hair Se concentration was established. The hair Se concentration could be used to bioindicate the level of Se intake for longer period.     

The influence of latitude on the concentration of vitamin D3 and 25-hydroxy-vitamin D3 in Australian red meat

There is little information on the vitamin D content of Australian red meat or on the possible influence of latitude on this content. To determine the content of vitamin D₃ and 25-hydroxy-vitamin D₃ (25OHD₃), lamb and beef were analysed from 34° S with LC–IT-MS. To investigate the possible influence of latitude on vitamin D in meat, the lean meat and fat from five cuts of beef were analysed from 17° S and 41° S. Lamb contained 0.10 μg vitamin D₃/100 g and 0.20 μg 25OHD₃/100 g lean meat, while beef contained 0.12 μg vitamin D₃ and 0.27 μg 25OHD₃/100 g (lean meat). Latitude had no effect on the vitamin D₃ (P = 0.21) or 25OHD₃ (P = 0.29) content of lean beef, but fat from cattle in the 17° S latitude group contained significantly higher (P < 0.01) concentrations of vitamin D₃ than fat from the 41° S group of cattle.     

Effect of modifiers for As,Cu and Pb determinations in sugar-cane spirits by GF AAS

Palladium plus magnesium nitrates with and without Ir, Ru and W were evaluated for the simultaneous determination of As, Cu and Pb in cachaça by graphite furnace atomic absorption spectrometry. For 20 μL of sample, 5 μL Pd(NO₃)₂ and 3 μL Mg(NO₃)₂ dispensed together onto the Ir-coated platform of the THGA, analytical curves in the 0–30.0 μg L⁻¹ As, 0–1.50 mg L⁻¹ Cu and 0–60.0 μg L⁻¹ Pb were built up and typical linear correlation coefficients were always better than 0.999. The limit of detection was 1.30 μg L⁻¹ As, 140 μg L⁻¹ Cu and 0.90 μg L⁻¹ Pb. As, Cu and Pb contents in 10 cachaça samples agreed with those obtained by ICP-MS. Recoveries of spiked samples varied from 96% to 106% (As), 97% to 112% (Cu) and 92% to 108% (Pb). The relative standard deviation (n = 12) was typically 2.7%, 3.3% and 1.9%.     

Identification and quantitative determination of glucosinolates in seeds and edible parts of Korean Chinese cabbage

Glucosinolates (GSLs) have attracted major interest due to the chemopreventive properties of some of their transformation products. GSLs in the seeds and edible parts of Korean Chinese cabbage (Brassicacampestris L. ssp. pekinensis) were identified and quantified by LC–ESI–MS and LC–UV. As a result, nine GSLs were identified: progoitrin, glucoraphanin, glucoalyssin, gluconapin, 4-hydroxy-3-indolylmethyl, glucobrassicanapin, glucoerucin, glucobrassicin, and 4-methoxyglucobrassicin. The total GSL levels were 268–198 and 23.0–15.8 μmol/g dry weight (DW) for seeds and edible parts, respectively. Gluconapin (197 μmol/g DW) was the highest individual GSL in seeds, whereas 4-methoxyglucobrassicin (6.08–4.94 μmol/g DW) and glucobrassicanapin (8.18–3.09 μmol/g DW) were found in the edible parts. In addition, LC–MS profiles of the nine GSLs identified from Korean Chinese cabbage were subjected to principal components analysis (PCA) to evaluate differences among samples. The metabolome among the four cultivar seed or edible parts was clearly separated by PCA.     

Effect of processing and storage of Jameed on conjugated linoleic acid content and fat and cholesterol oxidation

The influence of Jameed processing and storage on fat and cholesterol oxidation, hydrolytic rancidity, and conjugated linoleic acid (CLA) was evaluated by determining peroxide value (PV), 7-ketocholesterol, free fatty acids content (FFAs) and total CLA. Three different sizes of Jameed pieces (ca. 50, 200 and 400 g balls) were used to investigate the influence of storage for 0, 1, 3, 5 and 7 months on the above lipid oxidation parameters. No significant (P>0.05) effect of the Jameed processing steps on lipid changes was found with the exception of the sun drying steps, that caused an increase of PV, 7-ketocholesterol and FFA contents and a decrease in CLA content. This trend was also observed during storage of Jameed at room temperature and kept exposed to light and atmospheric air. The PV values of the 50, 200 and 400 g balls after 7 months of storage were 35.3, 19.4 and 20.4 meq O₂ kg⁻¹ of fat, that were 17, 11 and 12 times higher compared with the corresponding values of the fresh samples (1.9 meq O₂ kg⁻¹ of fat ). The 7-ketocholesterol of the tested samples increased from about 5.7 μg g⁻¹ to 210, 120 and 125 μg g⁻¹ for the 50, 200 and 400 g balls, respectively. FFA content increased remarkably during storage, from about 1.3 g kg⁻¹ at the beginning of storage to 8.6 g kg⁻¹ of fat after 7 months with no significant (P>0.05) effect for the size of Jameed pieces on FFAs content. On the contrary, a decrease of about 43%, 26% and 26% of the original value (5.7 mg kg⁻¹ of fat) in CLA content was found for the stored Jameed pieces of 50, 200 and 400 g, respectively.     

Simultaneous multi-channel hydride generation atomic fluorescence spectrometry determination of arsenic,bismuth, tellurium and selenium in tea leaves

A novel, rapid and sensitive method for the simultaneous multi-channel hydride generation atomic fluorescence spectrometry (HG-AFS) determination of total arsenic (As), total bismuth (Bi), total tellurium (Te) and total selenium (Se) in tea leaves was proposed. The operating parameters of self-made multi-channel HG-AFS were optimised, including negative high voltage of photo multiplier tube (PMT), the flow rates of carrier and shield gas, observation height and lamp currents. The conditions of hydride generation for As, Bi, Te and Se were studied in details. Under optimal conditions, the method detection limits (MDL) for As, Bi, Te and Se in tea leaves were 0.0152 μg g⁻¹, 0.0080 μg g⁻¹, 0.0022 μg g⁻¹ and 0.0068 μg g⁻¹, respectively. The proposed method was successfully applied to the simultaneous determination of As, Bi, Te and Se in various tea leaves and the spike recoveries were in the range of 90–103%. The accuracy of method was validated by analysing a tea certified reference material. The obtained values were consistent with the certified ones.     

Determination of lead and cadmium in food samples by the coprecipitation method

In this study, the coprecipitation method developed using a combination of 2-mercaptobenzothiazole (MBT) as a chelating reagent and copper as coprecipitate carrier was used for the determination of trace lead and cadmium in various food samples by graphite furnace atomic absorption spectrometry (GFAAS). The method was applied for the determination of Pb(II) and Cd(II) in salami, sausage, chicken, anchovy, spinach, cabbage, onion, dill, parsley, lettuce, tea and rice samples. The matrix modifiers were added as 50 μg NH₄H₂PO₄ + 3 μg Mg(NO₃)₂ for both Pb(II) and Cd(II). The signals were measured as peak area. The concentrations of Pb(II) and Cd(II) in the food samples were found to be in the range of 6.63 ng g⁻¹ (anchovy) −3.30 μg g⁻¹ (spinach) and 2.67 ng g⁻¹ (salami) −0.51 μg g⁻¹ (lettuce), respectively.     

Chemical characterisation and speciation of organic selenium in cultivated selenium-enriched Agaricus bisporus

The selenium concentration in Agaricus bisporus cultivated in growth compost irrigated with sodium selenite solution increased by 28- and 43-fold compared to the control mushroom irrigated solely with water. Selenium contents of mushroom proteins increased from 13.8 to 60.1 and 14.1 to 137 μg Se/g in caps and stalks from control and selenised mushrooms, respectively. Selenocystine (SeCys; detected as [SeCys]₂ dimer), selenomethionine (SeMet), and methyl-selenocysteine (MeSeCys) were separated, identified and quantified by liquid chromatography–electrospray ionisation-mass spectrometry from water solubilised and acetone precipitated proteins, and significant increases were observed for the selenised mushrooms. The maximum selenoamino acids concentration in caps and stalks of control/selenised mushrooms was 4.16/9.65 μg/g dried weight (DW) for SeCys, 0.08/0.58 μg/g DW for SeMet, and 0.031/0.10 μg/g DW for MeSeCys, respectively. The most notable result was the much higher levels of SeCys accumulated by A. bisporus compared to SeMet and MeSeCys, for both control and selenised A. bisporus.     

Chemiluminescence microflow injection analysis system on a chip for the determination of nitrite in food

A new microflow injection analysis (μFIA) system on a chip for the determination of nitrite is described. The chip is produced by using two transparent poly(methylmethacrylate) (PMMA) slices measured 50 × 40 × 5 mm, and the microchannels etched by CO₂ laser are 200 μm wide and 100 μm deep with the volume of reaction area about 1.8 μL. Nitrite is sensed by the chemiluminescence (CL) reaction of luminol with ferricyanide that is the product of the reaction of ferrocyanide with nitrite in acidic medium. The syringe pump with an accurate timer controls all reagents, including the sample. The linear range of the nitrite concentration is 8–100 μg L⁻¹ and the detection limit is 4 μg L⁻¹ (S/N = 3). The proposed method has good reproducibility with the relative standard deviation 4.1% for 50 μg L⁻¹ of nitrite (n = 9) and is very sensitive and simple. It has been successfully applied to the determination of nitrite in food.     

Chemical composition,antimicrobial, cytotoxic and antioxidant activities of the essential oil of Artemisia indica Willd

Essential oil from the aerial parts of Artemisia indica was analysed by GC-FID and GC–MS. A total of 43 compounds representing 96.8% of the oil were identified and the major components were found to be artemisia ketone (42.1%), germacrene B (8.6%), borneol (6.1%) and cis-chrysanthenyl acetate (4.8%). Antimicrobial activity of the oil was evaluated against seven clinically significant bacterial and two fungal strains. The essential oil and its major constituents exhibited moderate to potent, broad-spectrum antibacterial and antifungal activities targeting both Gram-positive and Gram-negative bacteria. In vitro cytotoxicity evaluation against four human cancer cell lines THP-1 (leukemia), A-549 (lung), HEP-2 (liver) and Caco-2 (colon) showed that the essential oil exhibited concentration dependant growth inhibition in the 10–100 μg/ml dilution range, with IC₅₀ values of 10 μg/ml (THP-1), 25 μg/ml (A-549), 15.5 μg/ml (HEP-2) and 19.5 μg/ml (Caco-2). It was interesting to note that the essential oil also exhibited potent antioxidant activity.     

The protective ability of Mediterranean dietary plants against the oxidative damage: The role of radical oxygen species in inflammation and the polyphenol,flavonoid and sterol contents

Ten hydroalcoholic extracts of edible plants from the Calabria region (Italy) were evaluated for their in vitro antioxidant and antiradical properties and in vivo topical anti-inflammatory activity. All the extracts had radical-scavenging and/or antioxidant properties, the most active plants being hawkweed oxtongue and viper’s bugloss. The best free radical (DPPH·)-scavenging activity was found in hawkweed oxtongue and chicory leaves extracts (IC₅₀ = 25 and 26 μg/ml, respectively). Hawkweed oxtongue, poppy and viper’s bugloss extracts showed the greatest inhibition of linoleic acid oxidation (IC₅₀ = 3 μg/ml). Viper’s bugloss and hawkweed oxtongue extracts had the greatest antioxidant effect on bovine brain peroxidation (IC₅₀ = 11 and 22 μg/ml). All the extracts also showed an anti-inflammatory effect: 300 μg/cm² provoked oedema reductions ranging from 18% to 43%. Cress was the most active plant. Chicory leaves contained the highest amount of phenolics (190 mg/g) whilst Rush crimps contained the highest amount of flavonoids (32.9 mg/g), followed by hawkweed oxtongue (15.8 mg/g). Cress contained the highest number of sterols. Among them, γ-sitosterol (12.2%) and ergost-5-en-3-ol (3β) (4.5%) were found to be the major constituents. Moreover, three of the identified molecules (stigmasta-5,23-dien-3β-ol, stigmasta-5,24(28)-dien-3-ol (3β,22E) and 9,19-cyclolanost-24-en-3-ol (3β)) were found in this plant only.     

Fast determination of arsenic,selenium, nickel and vanadium in fish and shellfish by electrothermal atomic absorption spectrometry following ultrasound-assisted extraction

Ultrasound-assisted extraction of As, Se, Ni and V from fish and shellfish has been applied as a fast and reliable sample pre-treatment method for accurate determination of the four elements by electrothermal atomic absorption spectrometry with Zeeman (As, Se) or Deuterium (Ni, V) background correction. A multivariate optimization approach has been employed for establishing the effect of variables influencing the extraction process. Under suitable conditions, quantitative extractions occurred from a 10 mass sample (particle size <100 μm) suspended in 1.5 mL of acidic extractant (0.5 or 3% v/v HNO₃) and subjected to high intensity ultrasound (50% amplitude; 3 min). The method was successfully validated against the following certified reference materials: NRCC-DORM-2 dogfish muscle, NRCC-DOLT-2 dogfish liver, NRCC-TORT-2 lobster hepatopancreas, NIST-SRM 1566b oyster tissue and BCR 627 tuna fish. The following seafood samples were analyzed: hake (Merluccius merluccius), sole (Solea solea), clam (Venerupis rhomboides), prawn (Panaeus kerathurus), cuttlefish (Sepia officinalis), shrimp (Palaemon elegans), razor shell (Ensis ensis), cockle (Cardium edule), Mussel (Mytilus galloprovincialis), edible crab (Cancer pagurus), meagrin (Lepidorhombus whiffiagonis). The concentration ranges (μg/g, dry weight) for the elements determined were as follows: As (12.6–190), Se (0.73–2.34), Ni (2.94–46) and V (0.82–5.14). The detection limits (LODs), defined as 3s/m (s being the standard deviation of 10 blank and m the slope of the calibration graph), in dry tissue were 0.6, 0.3, 0.2 and 0.4 μg/g for As, Se, Ni and V, respectively. Between-batch precision was expressed as relative standard deviation from three separate extractions was in the range 3–10%.     

Anti-oxidant,anti-proliferative and anti-inflammatory activities of the extracts from black raspberry fruits and wine

The purpose of the study was to determine polyphenols, anthocyanins and ascorbic acid in the extracts of black raspberry fruits and wine, along with their anti-oxidant, anti-proliferative and anti-inflammatory activities. Black raspberry fruits without or with seeds crushed were blended in 60% ethanol (FE and FES, respectively) or in water (FW and FWS, respectively). Black raspberry wine without or with seeds crushed (W and WS, respectively) were prepared. Polyphenol content was the highest in the FES (8.25 mg/g fruit). Generally the ethanol extracts with seeds crushed showed higher anti-oxidant activities with the lowest DPPH IC₅₀ (130 μg/ml (freeze-dried extract/reaction solution)) for the FES and the lowest ABTS IC₅₀ (198 μg/ml) for the WS. Cell viabilities were reduced by 13–70% when treated with 100 μg/ml (freeze-dried extract/medium) for HT-29 cells and 1000 μg/ml for LNCaP cells. The FES most actively suppressed nitric oxide production in LPS-stimulated RAW264.7 cells (p < 0.05). Superoxide dismutase and glutathione peroxidase activities treated with the extracts were higher than the control (p < 0.05).     

Ultraviolet irradiation: The generator of Vitamin D2 in edible mushrooms

Fresh Shiitake mushrooms (Lentinula edodes), Oyster mushrooms (Pleurotus ostreatus), Button mushrooms (Agaricus bisporus), and Abalone mushrooms (Pleurotus cystidus) were irradiated with Ultraviolet-A (UV-A; wavelength 315–400 nm), Ultraviolet-B (UV-B; wavelength 290–315 nm), and Ultraviolet-C (UV-C; wavelength 190–290 nm). Irradiation of each side of the mushrooms for 1 h, was found to be the optimum period of irradiation in this conversion. The conversions of ergosterol to vitamin D₂ under UV-A, UV-B, and UV-C were shown to be significantly different (p < 0.01). The highest vitamin D₂ content (184 ± 5.71 μg/g DM) was observed in Oyster mushrooms irradiated with UV-B at 35 °C and around 80% moisture. On the other hand, under the same conditions of irradiation, the lowest vitamin D₂ content (22.9 ± 2.68 μg/g DM) was observed in Button mushrooms.     

Identification of polyphenols in tobacco leaf and their antioxidant and antimicrobial activities

Crude polyphenols were extracted from tobacco leaf by 80% ethanol solution with ultrasonic treatment and then purified by a macroporous resin. The polyphenols from tobacco leaf (PTL) were subjected to analyses by reverse-phase high-performance liquid chromatography (RP-HPLC) and electrospray ionization mass spectrometry (ESI-MS). The dominant polyphenols in tobacco leaf were identified as chlorogenic acid and rutin. Furthermore, the antioxidant activities of PTL were investigated, including scavenging activities of 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals (5.02 μg/ml IC₅₀ value), hydroxyl radicals (49.6 μg/ml IC50 value) and superoxide anion radicals (44.0 μg/ml IC₅₀ value), inhibition activity of lipid peroxidation (132 μg/ml IC₅₀ value) and reducing power. The proliferation inhibition activities on Escherichia coli, Staphylococcus aureus and Bacillus subtilis were also measured for evaluating the antimicrobial activity of PTL. The diameters of inhibition zones were 20.23 ± 0.42, 17.66 ± 0.86 and 12.89 ± 0.29 mm, respectively. The results showed that PTL had great potential as antioxidant and antimicrobial agent.