Phenylalanine ammonia‐lyase and phenolic compounds in leaves and fruits of Olea europaea L. cv. Picual during ripening

BACKGROUND: The kinetic and molecular properties of phenylalanine ammonia‐lyase (PAL) in leaves and fruit of the olive tree (Picual variety) have been studied during the seasonal process of fruit maturation. The concentrations of total phenolic compounds, oleuropein, hydroxytyrosol and tyrosol, have also been determined. This study has been made in rainfed 30‐year‐old olive trees in Jaén, Spain, cultivated by the traditional method. RESULTS: PAL specific activity was assayed and hyperbolic kinetics were observed in both organs. The K_m value for L ‐Phe was 0.22 mmol L^?1 in leaf and 0.26 mmol L^?1 in fruit. In leaf, the highest PAL specific activity was found in the stage prior to veraison. By immunoblot, a PAL‐immunoreactive 75 kDa polypeptide was detected in leaf and fruit. In leaf, the level of this protein progressively rose until the last stages of ripening at the same time that total phenols increased. In fruit, PAL activity and protein change as in two series coinciding with different fruit‐maturation period. By immunohistochemistry under light microscopy, PAL was located in the epidermis and parenchyma cells of leaf and fruit. CONCLUSION: These results demonstrate the involvement and regulation of PAL during fruit ripening of olive, cv. Picual. Copyright © 2008 Society of Chemical Industry     

Effect of nitric oxide on reactive oxygen species and antioxidant enzymes in kiwifruit during storage

BACKGROUND: The accumulation of reactive oxygen species (ROS) in kiwifruit can cause oxidative damage during storage. Little research has been carried out on the effects of nitric oxide (NO) on oxidative damage to kiwifruit. Therefore the aim of the present study was to evaluate the ability of 0.5, 1 and 2 µmol L^?1 NO aqueous solutions to alleviate oxidative damage to kiwifruit during storage. RESULTS: The most marked effect was obtained with 1 µmol L^?1 NO solution, which significantly reduced the accumulation of malondialdehyde, superoxide and hydrogen peroxide, delayed the decrease in vitamins C and E, maintained the content of soluble solids, inhibited the activity of lipoxygenase and peroxidase and increased the activity of superoxide dismutase and catalase in kiwifruit during storage. The 0.5 µmol L^?1 NO solution was too weak to significantly affect the content of ROS and the activity of enzymes. However, treatment with 2 µmol L^?1 NO solution promoted the accumulation of ROS, decreased the activity of antioxidant enzymes and accelerated peroxidation in kiwifruit during storage. CONCLUSION By increasing the activity of antioxidant enzymes and maintaining the content of vitamins C and E, treatment with 1 µmol L^?1 NO aqueous solution could protect kiwifruit against oxidative damage caused by ROS during storage. Copyright © 2008 Society of Chemical Industry     

Effects of exogenous nitric oxide on contents of soluble sugars and related enzyme activities in 'Feicheng' peach fruit

BACKGROUND: Sugar content is one of the main characteristics related to the quality of fruit. Research confirms that nitric oxide (NO) involves a physiological process and prolongs the storage life of fruit. However, little attention has been paid to the effects of NO on sugar metabolism in fruit during storage. In this study, the effect of different concentrations (0, 10, 30 µmol L^?1) of exogenous NO treatment on sugar content and related enzyme activities in ‘Feicheng’ peach fruit was investigated during storage (0–12 days after harvest) at room temperature (25 °C). RESULTS: Results showed that the decrease of firmness and accumulation of sugar and acid:sugar ratio in peach fruit during storage were significantly inhibited by treatment with 10 µmol L^?1 NO. Treatment with 10 µmol L^?1 NO could promote fructose and glucose metabolism during the first 4 days of storage, and increase the content of sucrose and the activities of sorbitol dehydrogenase, sorbitol oxidase and sucrose phosphate synthase in peach fruit during storage. However, acid invertase activity from 8 to 12 days of storage and neutral invertase activity during the first 4 days of storage were inhibited by treatment with 10 µmol L^?1 NO. At the same time, treatment with 10 µmol L^?1 NO inhibited sucrose synthase (SS) activity in decomposition during storage and SS activity in synthesis from 8 to 12 days of storage. CONCLUSION: Treatment with 10 µmol L^?1 NO had a significant impact on content of soluble sugars and related enzyme activities in ‘Feicheng’ peach fruit during storage (0–12 days) at room temperature (25 °C). Copyright © 2011 Society of Chemical Industry     

Isolation of eriocitrin (eriodictyol 7‐O‐rutinoside) as an arachidonate lipoxygenase inhibitor from Lumie fruit (Citrus lumia) and its distribution in Citrus species

An inhibitory compound acting against rat platelet 12‐lipoxygenase was isolated from the peel of Lumie fruit (Citrus lumia) by activity‐guided separation. It was identified as eriocitrin (eriodictyol 7‐O‐rutinoside) by spectroscopic analyses. Eriocitrin inhibited 5‐lipoxygenase (IC₅₀29.1 µmol L^?1) from rat peritoneal polymorphonuclear leukocytes in addition to 12‐lipoxygenase (IC₅₀22.3 µmol L^?1). Its aglycone, eriodictyol (5,7,3′, 4′‐tetrahydroxyflavanone), was a much more potent inhibitor of both 12‐lipoxygenase (IC₅₀0.07 µmol L^?1) and 5‐lipoxygenase (IC₅₀0.20 µmol L^?1). It also inhibited the production of leukotriene B₄ in intact peritoneal polymorphonuclear leukocytes stimulated with calcium ionophore A23187 (IC₅₀12.7 µmol L^?1). The distribution of eriocitrin in 39 citrus fruits was investigated by high‐performance liquid chromatography analysis. Lumie, eureka lemon (Citrus limon), Sambokan (Citrus sulcata), Sudachi (Citrus sudachi) and Koji (Citrus leiocarpa) fruits were found to contain high levels of eriocitrin in both peel and juice vesicles. Copyright © 2006 Society of Chemical Industry     

APPLICATION OF A NEW CONTINUOUS FLOW SPECTROPHOTOMETRIC METHOD FOR THE CHARACTERIZATION OF POLYPHENOL OXIDASE NATURALLY IMMOBILIZED ON COCONUT FIBER

The association of continuous flow injection and spectrophotometry affords a simple, novel and rapid way of monitoring continuously the activity of naturally immobilized enzymes in their natural environment, thus eliminating cumbersome purification. The method was applied to determine the activity of polyphenol oxidase (PPO) enzymes naturally immobilized on coconut (Cocus nucifera, L.) fiber tissues. Maximum enzyme activity occurred at a temperature of 25C and at pH 6.0 using catechol as substrate. Thermal stability was assayed in a temperature range of 20 to 75C. The PPO exhibited excellent thermal stability, with only 50% loss in its activity at 75C after 4.3 min exposure. For catechol apparent Michaelis‐Menten constant (apparent Km), apparent Vmax and the apparent activation energy were 9.1 × 10^?3 mol L^?1, 0.20 abs min^?1 and 10.5 kcal mol^?1, respectively. The immobilized PPO showed high activity for o‐diphenols. The reactivity order was caffeic acid > pyrogallol > catechol. Complete inhibition of the enzyme was observed with 1 × 10^?3 mol L^?1 concentration of cyanide, thiourea, L‐cysteine, ascorbic acid, sodium sulfite, nitrates of cadmium, zinc and mercury, individually. Benzoic acid, 3‐hydroxy‐benzoic acid, 4‐acetamidephenol, sodium azide, resorcinol, L‐cystine and EDTA at equal concentrations inhibited PPO partially.     

Multi-element determination in some foods and beverages using silica gel modified with 1-phenylthiosemicarbazide

ABSTRACT

1-Phenylthiosemicarbazide bonded modified silica gel (PTC-SG) was synthesised and characterised by FTIR, SEM and elemental analysis for a novel separation/preconcentration of multiple elements based on solid phase extraction. The analytical parameters including pH of solutions, amounts of PTC-SG, flow rates of sample, eluent type and sample volume were optimised. The adsorption capacities of PTC-SG were found to be 7.9, 6.4, 6.3, 8.3, 7.2, 8.9 and 6.6 mg/g for Cu(II), Cd(II), Pb(II), Co(II), Cr(III), Ni(II) and Mn(II), respectively. The limit of detection (LOD) was calculated as 3x the standard deviation(s) of the reagent blank (k = 3, N = 21) and the LOD values were obtained to be 0.98 µg L^?1 (Cu), 0.65 µg L^?1 (Cd), 0.57 µg L^?1 (Pb), 1.12 µg L^?1 (Co), 1.82 µL^?1 (Cr), 1.67 µg L^?1 (Ni) and 0.55 µg L^?1 (Mn). Certified reference materials were used to test the validation of the present method. The new solid phase extraction method was successfully applied to determination of the amount of multiple elements in food and beverage samples.     

Oil content,phenolic profiling and antioxidant potential of Tunisian olive drupes

BACKGROUND: The aim of this work was to investigate the effect of the maturation process of the olive fruit on oil content, phenolic profile and antioxidant activity of four Tunisian cultivars (Zelmati, Chemchali, Chemlali and Chétoui). RESULTS: The average oil content of the studied varieties ranged between 17.50% and 20.25% at the first stage of maturation and from 30.20% to 35% in the last harvest. Qualitative and quantitative analysis of phenolic compounds were carried out using HPLC and LC‐MS/MS. Twenty‐six biophenolic compounds were identified. In all samples, hydroxytyrosol and oleuropein were the major compounds identified while rutin and luteolin 7‐O‐glucoside were the two main flavonoids. The total phenolic content varied from 3.46 to 4.30 g kg^?1 at the first stage of maturation and from 8.71 to 11.52 g kg^?1 of fruit fresh weight at the last maturation phase. Total flavonoid content reached 432.80 mg kg^?1. The antioxidant activity of the extract was evaluated by DPPH and ABTS assays. The IC₅₀ values of the olive extracts ranged from 2.69 to 10.96 µg L^?1 and from 2.15 to 3.03 mmol L^?1 trolox equivalent at the last stage of maturation. CONCLUSION: A relationship between the changes in phenolic content and the physicochemical changes in Tunisian olive fruit during maturation was established. These findings could be used for controlling the production processes and correlating the oil sensorial characteristics to the polyphenolic pattern. Copyright © 2010 Society of Chemical Industry     

Voltammetric analysis of DL‐α‐tocopherol with a paste electrode

BACKGROUND: A voltammetric study of vitamin E (DL‐ α‐tocopherol) detection using square wave stripping and cyclic voltammetry is discussed in this paper. The working sensor was made by mixing carbon nanotube powder with DNA (double‐stranded calf thymus DNA) and mineral oil. In this electrode, the anodic peak was obtained for ? 0.6 V in a 0.1 mol L^?1 phosphate electrolyte solution. RESULTS: Under optimized stripping conditions, analytical linear working ranges of 0.5–4.0 µg L^?1 and 40.0–160.0 µg L^?1 were obtained. The RSD precision was pegged at 0.105% with seven points using an 80 µg L^?1 spike. The detection limit (S/N) was found to be 0.056 µg L^?1 (1.30 × 10^?10 mol L^?1). CONCLUSION: The developed method was found to be applicable to quality control analysis in the food, pharmaceutical and other manufacturing sectors. Copyright © 2008 Society of Chemical Industry     

Scirpusin A,a hydroxystilbene dimer from Xinjiang wine grape,acts as an effective singlet oxygen quencher and DNA damage protector

BACKGROUND: Grapes and red wines are rich sources of phenolic compounds such as anthocyanins, catechins, flavonols and stilbenes, most of which are potent antioxidants showing cardioprotective properties. We first isolated scirpusin A, a hydroxystilbene dimer, from a wine grape of Xinjiang, and studied its antioxidant activity. RESULTS: Reactive oxygen species scavenging effects and the protection against reactive singlet oxygen‐induced DNA damage of scirpusin A have been investigated in our experiments. The concentration of scirpusin A required to inhibit 50% of ¹O₂ generation was 17 µmol L^?1, while addition of scirpusin A at 140 µmol L^?1 caused complete inhibition. Further kinetic study revealed that the reaction of Scirpusin A with singlet oxygen has an extremely high rate constant (k_a = 4.68 × 10⁹ L mol^?1 s^?1). Scirpusin A (140 µmol L^?1) exhibited significant inhibition effects on pBR322 DNA breakage. However, scavenging effects of scirpusin A on superoxide anion O₂^?? and hydroxyl radical ·OH were not potent as the inhibitor rates at a concentration of 1400 µmol L^?1 were 28.83% and 19.5%, respectively. CONCLUSION: The present study shows that scirpusin A is a selective quencher of singlet oxygen and a protector against reactive singlet oxygen‐induced pBR322 DNA damage at very low concentrations. Copyright © 2010 Society of Chemical Industry     

Antioxidant activity of hydrolysates derived from porcine plasma

BACKGROUND: In China alone, more than 400 million pigs are slaughtered each year to provide meat. Porcine blood is rich in proteins but is usually discarded, which can cause environmental contamination. Recovering porcine blood and converting it to high‐value products is therefore economically and environmentally desirable. However, very little information on antioxidant peptides from porcine blood by‐products is currently available. In this study the antioxidant properties of porcine plasma hydrolysates PPE and PPA prepared with pepsin and papain respectively were investigated. RESULTS: Both PPE and PPA showed excellent antioxidant activity in a linoleic acid system (AL) compared with α‐tocopherol (VE) at the same concentration (P < 0.01). Their activities were respectively 3.33 and 1.83 times stronger than that of VE at a concentration of 10 µg mL^?1 and 5.4 and 5.6 times stronger at 100 µg mL^?1. The 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) radical‐scavenging activity (DRSA) reached 48.4 and 43.1% for PPE and PPA respectively at 500 µg mL^?1. The ferrous ion‐chelating power (FICP) of PPE at 100 µg mL^?1 was about 1.5 times stronger than that of 10 µmol L^?1 ethylene diamine tetraacetic acid (EDTA) in a 50 µmol L^?1 Fe²⁺ system, whereas the FICP of PPA at 100 µg mL^?1 was 61% that of 10 µmol L^?1 EDTA. Furthermore, PPE was separated on Resource 15RPC and Superdex peptide 10/300GL columns, and the antioxidant activity of the peptides and its relationship to their polarity and molecular weight (MW) were analysed. The hydrolysate was divided into four groups (R1–R4) with hydrophobicities ranging from weak to strong by Resource 15RPC, while it was divided into three groups (S1, MW 7–12 kDa; S2, MW 3–7 kDa; S3, MW 1–3 kDa) by Superdex peptide 10/300GL. CONCLUSION: The results showed that AL was significantly and positively correlated with the relative amounts of R1, S2 and S3 and that DRSA was dependent on R3 and S1. The fractions of PPE were not responsible for FICP. Copyright © 2009 Society of Chemical Industry     

Infusions of Portuguese medicinal plants: Dependence of final antioxidant capacity and phenol content on extraction features

BACKGROUND: Aqueous extracts of most medicinal plants traditionally employed in Portugal (at the ratio of 1 g plant: 110 mL water) have been assayed for total antioxidant capacity and phenol content, in order to elucidate their claimed medicinal features. RESULTS: The antioxidant activity was assessed by the ABTS^?+ method; the ascorbic acid equivalent values ranged from 1.4280 ± 0.1261 g L^?1 for avocado (Persea americana (Lauraceae)) obtained by infusion of powder, down to 0.0027 ± 0.0012 g L^?1 for olive (Olea europaea (Oleaceae)) obtained by infusion of leaves. Total phenol content was determined by the Folin–Ciocalteu procedure; the gallic acid equivalent values ranged from 0.5541 ± 0.0289 g L^?1 for avocado obtained by infusion of powder, down to 0.0053 ± 0.0014 g L^?1 for olive obtained by boiling leaves. A good correlation between total antioxidant capacity and total phenol content was found. CONCLUSION: The method of powder infusion should be chosen if high concentration of antioxidants are sought. On the other hand, a high antioxidant capacity and a high phenol content correlate well with the empirically established (and widely publicised) capacity to treat respiratory infections. Copyright © 2007 Society of Chemical Industry     

Antioxidant activity and phenolic content of wine vinegars produced by two different techniques

BACKGROUND: The presence of phenolics in fruit, red wine and vinegar has positive health effects due to their significant antioxidant activity. The aim of the study was to determine the effects of two different vinegar production methods on antioxidant activity and phenolic level of vinegars derived from Ulugbey Karasi grapes. Traditional surface and industrial submerge methods were used to make vinegar. Samples were taken from fresh red grape juice, maceration, wine, traditional vinegar and industrial vinegar. RESULTS: Total phenolic content of traditional and industrial vinegar samples were 2690 mg L^?1 and 2461 mg L^?1 GAE, respectively. ORAC values of traditional and industrial vinegar samples were 10.50 µmol mL^?1and 8.84 µmol mL^?1 TE, respectively. Antioxidant activity values of traditional and industrial vinegars were 13.50 mmol L^?1 and 10.37 mmol L^?1 TEAC, respectively. Gallic acid, catechin, epicatechin, chlorogenic acid, caffeic acid, syringic acid, p‐coumaric acid and ferulic acid were detected in grape juice, wine and vinegar samples. The content of catechin in industrial vinegar (27.50 mg L^?1) was significantly higher than that of in traditional vinegar (13.76 mg L^?1) (P < 0.05). Traditional vinegar had higher amounts of chlorogenic and syringic acids than the industrial vinegar (P > 0.05). CONCLUSION: Results of this study showed that different production methods affected the functional constituents of wine vinegars. Copyright © 2010 Society of Chemical Industry     

α-Glucosidase- and α-amylase-inhibitory activities of phlorotannins from Eisenia bicyclis

BACKGROUND: In an effort to develop alternative therapeutic agents, strong inhibitory activity against α‐glucosidase and α‐amylase was detected in Eisenia bicyclis methanolic extract. RESULTS: In this study, two phlorotannins were isolated from E. bicyclis and characterised by chromatography and nuclear magnetic resonance. The active substances were identified as fucofuroeckol A (FF) and dioxinodehydroeckol (DD). To the authors' knowledge, this is the first report of the identification of these substances in E. bicyclis. However, to date, no antidiabetic activity of FF and DD has been reported. Both phlorotannins demonstrated significant inhibitory activity against α‐glucosidase and α‐amylase. FF showed potent antidiabetic activity, with IC₅₀ values of 131.34 nmol L^?1 against α‐glucosidase and 42.91 µmol L^?1 against α‐amylase. The corresponding IC₅₀ values of DD were 93.33 nmol L^?1 and 472.7 µmol L^?1. Furthermore, kinetic analysis revealed that FF and DD exhibited non‐competitive inhibitory activity against α‐glucosidase. CONCLUSION: These results suggest that FF and DD may be candidates for the development of an antidiabetic pharmaceutical agent or food additive. Copyright © 2012 Society of Chemical Industry     

Effect of garlic consumption on total antioxidant status and some biochemical and haematological parameters in blood of rats

BACKGROUND: The effect of diet garlic supplementation on total antioxidant status (TAS), nitric oxide (NO) and routine biochemical and haematological parameters was investigated in blood of rats. A total of 30 male rats were divided equally into two groups. Each of 15 rats of treatment group was fed 600 mg kg^?1 garlic solution in distilled water by gavage and controls only received distilled water. After garlic consumption for 1 month, blood serum total antioxidant, nitrate and some biochemical and haematological tests including serum lipids parameters, blood sugar, complete blood count (CBC), and haemoglobin were measured. RESULTS: The garlic treatment group showed significantly increase in the mean level of TAS from 0.77 ± 0.10 mol L^?1 to 1.18 ± 0.11 mol L^?1 (P < 0.01) and nitrate (a NO metabolite) from 0.78 ± 0.06 µmol L^?1 to 1.44 ± 0.27 µmol L^?1 (P < 0.05) in the blood sera of rats compared with the controls. There were no significant differences between the routine biochemical and haematological parameters. CONCLUSION: Garlic consumption should have antioxidant properties and may not affect the lipids profile and total blood cell counts. Copyright © 2009 Society of Chemical Industry     

Sulfate determines the glucosinolate concentration of horseradish in vitro plants (Armoracia rusticana Gaertn., Mey. & Scherb.)

BACKGROUND: Horseradish plants (Armoracia rusticana) contain high concentrations of glucosinolates. Former studies have revealed that Armoracia plants cultivated in vitro have markedly lower glucosinolate concentrations than those grown in soils. Yet, these studies neglected that the sulfate concentration in the growth medium may have had a strong impact on glucosinolate metabolism. Accordingly, in this study horseradish in vitro plants were cultivated with differing sulfate concentrations and the glucosinolate concentrations were quantified by ion pair HPLC. RESULTS: Cultivation in 1.7 mmol L^?1 sulfate (as used in the prior studies) resulted in the accumulation of 16.2 µmol g^?1 DW glucosinolates, while the glucosinolate concentration increased to more than 23 µmol g^?1 DW when 23.5 mmol L^?1 sulfate was used in the medium. Correspondingly, the glucosinolate concentration decreased to 1.6 µmol g^?1 DW when sulfate concentration was lowered to 0.2 mmol L^?1. CONCLUSION: Since the glucosinolate accumulation in relation to the sulfate concentration follows a typical saturation curve, we deduce that the availability of sulfate determines the glucosinolate concentration in horseradish in vitro plants. © 2012 Society of Chemical Industry     

Fate of aflatoxin B(1) in contaminated corn gluten during acid hydrolysis

BACKGROUND: Aflatoxins are a group of mycotoxins that cause serious chronic disease outbreaks and contaminate several food products such as corn and its by‐product, corn gluten. The aim of the current study was to evaluate the effect of hydrochloric acid (HCl) on aflatoxin B₁ (AFB₁) degradation in contaminated corn gluten under different HCl concentrations, hydrolysis temperatures and hydrolysis times. RESULTS: During the wet milling process the highest AFB₁ level (45.68 µg kg^?1) (37.86%) was found in corn gluten fraction. Treatment with 1 mol L^?1 HCL at 110 °C resulted in degradation of AFB₁ by 27.6% (33.07 µg kg^?1) after 4 h and reached 42.5% (26.26 µg kg^?1) after 8 h. Increasing HCl concentration from 1 to 3 mol L^?1 HCl resulted in increased degradation of AFB₁, while complete degradation occurred in the presence of 5 mol L^?1 HCl after 4 h at 110 °C. Meanwhile, half‐life time of AFB₁ was recorded after 2 h at 100 °C and was < 2 h at 110 °C in the presence of 3 mol L^?1 HCl. CONCLUSION: It could be demonstrated that the manufacture of hydrolyzed vegetable protein is a suitable method for decontamination of aflatoxin in highly contaminated grains, especially gluten fractions. The hydrolysis reaction could be considered in terms of first‐order reaction kinetics of AFB₁ degradation. Copyright © 2010 Society of Chemical Industry     

Heat Inactivation Kinetics of Apple Polyphenoloxidase and Activation of its Latent Form

Heat inactivation kinetics of crude polyphenoloxidase (PPO) from six apple cultivars (Golden Delicious, Starking Delicious, Granny Smith; Gloster, Starcrimson and Amasya) were studied at three temperatures (68°, 73° and 78°C). PPO activity initially increased and then decreased with heat, following a first order kinetic model. Increase in activity indicated presence of latent PPO. Regression coefficients for the linear portions of inactivation curves were computed to determine inactivation parameters. Reaction data at 78°C revealed that PPO in Amasya was the least and Starking Delicious the most heat-stable. Rate constants for heat inactivation at 78°C ranged from 15.99–28.27. 10^?2 min^?1. Activation energies varied between 54.7–77.2 kcal. mol^?1 with z values of 7.1–10.0C°.PPO in apples was generally more heat-stable than PPO in most fruits.     

Effect of integrated application of chitosan coating and modified atmosphere packaging on overall quality retention in litchi cultivars

BACKGROUND: The storage life of litchi is limited due to pericarp browning and decay. Modified atmosphere packaging (MAP) showed promising results for ensuring quality retention. However, to improve the efficiency of MAP the integrated treatment of a chitosan coating and MAP was investigated. RESULTS: The effect of chitosan (1.0 g L⁻¹) + MAP was compared with MAP (control), and was effective in preventing decay, browning and retaining the pericarp colour in the cultivar McLean's Red. Chitosan (1.0 g L⁻¹) + MAP significantly reduced polyphenol oxidase (PPO) and peroxidase (POD) activity, retained membrane integrity, anthocyanin content and prevented the decline of pericarp colour values during storage. The POD activity was greater than the PPO activity in the cultivars McLean's Red and Mauritius. The two cultivars differed in anthocyanin content and the activity of oxidation enzymes. The gas compositions within the packages were compared between chitosan at 1.0 g L⁻¹ and 20.0 g L⁻¹ concentration for both cultivars. Chitosan (20.0 g L⁻¹) + MAP lowered the respiration during storage in both cultivars compared to 1.0 g L⁻¹ + MAP. CONCLUSION: The McLean's Red cultivar is better suited for chitosan (1.0 g L⁻¹) + MAP integrated treatment than is Mauritius in retaining overall quality. Copyright © 2009 Society of Chemical Industry     

Migrated phthalate levels into edible oils

The determination of phthalates in edible oils (virgin olive oil, olive oil, canola oil, hazelnut oil, sunflower oil, corn oil) sold in Turkish markets was carried out using gas chromatography–mass spectrometry. Mean phthalate concentrations were between 0.102 and 3.863 mg L^?1 in virgin olive oil; 0.172 and 6.486 mg L^?1 in olive oil; 0.501 and 3.651 mg L^?1 in hazelnut oil; 0.457 and 3.415 mg L^?1 in canola oil; 2.227 and 6.673 mg L^?1 in sunflower oil; and 1.585 and 6.248 mg L^?1 in corn oil. Furthermore, the influence of the types of oil and container to the phthalate migration was investigated. The highest phthalate levels were measured in sunflower oil. The lowest phthalate levels were determined in virgin olive oil and hazelnut oil. The highest phthalate levels were determined in oil samples contained in polyethylene terephthalate.     

Prokaryotic expression and purification of Camellia sinensis polyphenol oxidase

BACKGROUND: Polyphenol oxidase (PPO) causes the postharvest loss of fruits and vegetables but is also a key factor in the quality development of tea. However, there are no reports on engineered active plant PPO purified from prokaryotic cells. RESULTS: In this study the ppo gene of about 1800 bp from Camellia sinensis cv. Yihongzao was successfully cloned and expressed in Escherichia coli. The PPOs purified from both the soluble fraction and the inclusion bodies showed activity. In addition, 1.0 × 10^?7 mol L^?1 Cu²⁺ and acidic conditions were found to be favourable for the engineered PPO catalysis of catechol oxidation. CONCLUSION: This paper represents the first report on C. sinensis ppo expression in E. coli and engineered active PPO purification. The results of the study provide a basis for the large‐scale preparation and application of PPO. Copyright © 2010 Society of Chemical Industry