The levels of S-alk(en)yl-L-cysteine sulphoxides during the growth of the onion (Allium cepa l.)

Flavour precursors, the S-alk(en)yl-L -cysteine sulphoxides, change considerably in both concentration and total amount during the growth of onions. For the brown onion cv. Pukekohe Long Keeper (PLK) and for the white onion cv. Dehyso, (±)-S-1-propyl-L -cysteine sulphoxide (±PCSO) is the predominant flavour precursor, with (±)-trans-S-1-propenyl-L -cysteine sulphoxide (±PECSO) and (±)-S-1-methyl-L -cysteine sulphoxide (±MCSO) in a minor role. For PLK the greatest concentration of all three precursors is just prior to bulbing (3.6±1.1 mg g^?1 fresh weight); for Dehyso the greatest concentration is at bulbing (4.6±0.6 mg g^?1 fresh weight); Both varieties show a mid-season reduction in flavour precursor concentration (of about 45%), followed by a small but significant increase in ±PCSO concentration during the end of season leaf die-down. The total amount of the three flavour precursors per bulb in both varieties shows a maximum in late January (360±107 mg for PLK, 602±144 mg for Dehyso). In the subsequent months there is a dramatic reduction in the total amount of ±PECSO and ±MCSO, and a slight reduction in ±PCSO. Both varieties show an increase in the amount of ±PCSO at leaf die-down. The relative proportions of these flavour precursors change with bulb age and cultivar. These results suggest that white onions used for drying and processing could be harvested from bulbing onwards. Furthermore, when onion cultivars and onion plant selections are assessed for flavour, care needs to be given to the stage of maturity of the onion.     

Quantitative analysis of the major γ glutamyl peptides in onion bulbs (Allium cepa)

Quantitative analysis of the major γ glutamyl peptides present in cultivars of onion (Allium cepa L) bulbs representing brown, white and red varieties was achieved by ion exchange and electrophoretic separations and by quantitation involving integration of ninhydrin-developed spots on thin layer chromatography. γ Glutamyl trans-prop(I)enyl cysteine sulphoxide was found to be the major γ glutamyl peptide in each of the three cultivars at levels between 1.24 and 2.18 mg g^?1 fresh weight, followed by S-2-carboxypropyl glutathione (0.45-0.60 mg g^?1 fresh weight) and γ glutamyl phenylalanine (0.09-0.16 mg g^?1 fresh weight). Conclusive identification of each of the compounds was achieved by NMR spectroscopy and by GC-MS of the n-butyl, trifluoroacetyl derivatives of the hydrolysis products.     

Investigations on the conversion of onion aroma precursors S‐alk(en)yl‐L‐cysteine sulphoxides in onion juice production

Onion flavour develops when the cells are disrupted, allowing the enzyme alliinase (EC 4.4.1.4) to act upon the aroma precursors S‐alk(en)yl‐L ‐cysteine sulphoxides (ACSOs). For maximum flavour release, optimal cell disintegration and complete enzymatic conversion of ACSOs are desired. To assess an industrial scale onion juice extraction in regard to the extent of cell disintegration and the rate of enzymatic ACSO conversion, samples from all mass flows (ie onion, macerate, juice and pomace) were subjected to ACSO analysis. Applying a modified HPLC method, which allows baseline separation of the aroma precursors, three ACSOs, namely methyl‐, propyl‐ and 1‐propenyl‐L ‐cysteine sulphoxides (MCSO, PCSO and 1‐PeCSO), were determined. Initial ACSO ratios changed in the course of increasing degree of comminution from 17:83 to 100:0 (MCSO/1‐PeCSO). Only negligible amounts of PCSO were detected (<9.2 nmol g^?1 fresh weight (fw)), contributing less than 0.2% to the total ACSO content. For evaluation of the disintegration efficiency a chart was established consisting of an abscissa representing a percentage scale of ruptured cells and ordinates for the development of the marker parameters ACSOs and reaction product pyruvate relative to their initial contents. From this correlation a cell disintegration percentage after grinding of about 70% was deduced according to the determined ACSO contents. On a molar basis, macerate, juice and pomace showed 15, 0.6–2.4 and 0.7–1.0% of initial ACSO contents respectively. Only trace amounts of 1‐PeCSO were found in the juice (<16 nmol g^?1 fw). MCSO was converted to almost 90%, indicating that enzymatic transformation, in a practical sense, goes to completion. Copyright © 2004 Society of Chemical Industry     

Ammonium nitrate fertility levels influence flavour development in hydroponically grown ‘Granex 33’ onion

High levels of nitrogen (N) fertility have been shown to influence bulb flavour characteristics in onion (Allium cepa L). To test the effects of lower levels of N fertility on onion bulb flavour, ‘Granex 33’ onions were grown hydroponically in a greenhouse with varying solution N levels. Eleven levels were tested by increasing the concentration of NH₄NO₃ in solutions from 20 to 140 mg l^?1 N. Mature plants were harvested and evaluated for plant leaf and bulb fresh weights (FWs), bulb soluble solids content (SSC), bulb total pyruvic acid, bulb total sulphur (S), and bulb sulphate (SO₄^2?). To determine the effect of N on the flavour biosynthetic pathway of onion, total and individual S‐alk(en)yl cysteine sulphoxides and related peptide intermediates were also tested. Leaf and bulb FWs responded quadratically to N concentration, as did total bulb S. Bulb SO₄^2? and SSC, though significantly influenced by N concentration, did not respond with a meaningful trend. Bulb pyruvic acid increased linearly with N level increases, as did (+)‐S‐propyl‐L ‐cysteine sulphoxide. Total precursors, (+)‐S‐methyl‐L ‐cysteine sulphoxide, and trans‐(+)‐S‐1‐propenyl‐L ‐cysteine sulphoxide responded quadratically to N levels. At lower N levels, trans‐(+)‐S‐1‐propenyl‐L ‐cysteine sulphoxide content was highest relative to the other precursors. However, at elevated N levels, (+)‐S‐methyl‐L ‐cysteine sulphoxide accumulated in the highest concentrations. Peptide intermediates 2‐carboxypropyl glutathione and γ‐glutamyl propenyl cysteine sulphoxide responded linearly and quadratically respectively to increasing N fertility levels. Nitrogen fertility levels can influence flavour intensity and quality and should be considered when growing onions for flavour attributes. Copyright © 2003 Society of Chemical Industry     

Composition and bioavailability of oxalates in baked taro (Colocasia esculenta var. Schott) leaves eaten with cows milk and cows milk and coconut milk

Taro leaves are an important food in the Pacific Islands but the overall oxalate composition and its nutritional effect has not been investigated. The oxalate contents of taro leaves were determined using chemical and in vitro extraction methods. Maori‐type taro leaves contained 524.2 ± 21.3 mg total oxalates 100 g^?1 fresh weight (FW) and 241.1 ± 20.9 mg soluble oxalates 100 g^?1 FW while the Japanese‐type leaves contained 525.6 ± 19.9 mg total oxalates 100 g^?1 FW and 330.4 ± 28.3 mg soluble oxalates 100 g^?1 FW. Maori‐type taro leaves contained 416.4 ± 1.5 mg gastric soluble oxalates 100 g^?1 FW and 212.4 ± 34.8 mg intestinal soluble oxalates 100 g^?1 FW while the Japanese‐type leaves contained 433.3 ± 9.7 mg gastric soluble oxalates 100 g^?1 FW and 224.2 ± 38.7 mg intestinal soluble oxalates 100 g^?1 FW). Human feeding experiments were conducted to determine the availability of the oxalates in the baked leaves following additions of cows milk and coconut milk. The consumption of a test meal of baked taro leaves resulted in a significant increase (P < 0.001) in the output of urinary oxalate in the following 6 h when compared to the output of oxalate during a reference collection. When the leaves were baked with cows milk or cows milk and coconut milk combined and consumed there was a small non‐significant reduction in urinary oxalate output which suggests that less soluble oxalate was absorbed from these mixtures.     

Assessment of the flavour of fresh uncooked onions by taste‐panels and analysis of flavour precursors,pyruvate and sugars

Flavour in fresh onions is dominated by volatile sulphenic and thiosulphenic acids that are liberated once alk(en)yl cysteine sulphoxide (ACSO) flavour precursors are cleaved by the enzyme alliinase after tissue disruption. The levels of pyruvate and ACSOs in over 100 samples of onions marketed in the UK were measured, and compared with assessment by taste‐panels. There was a linear relationship between the content of ACSOs and pyruvate. Measurements of pyruvate indicated that the marketing classification of some types of onion did not correspond to their pyruvate levels. A significant linear relationship was found between a sensory measure of strength and pyruvate over the range 1.2–9.3 µmol pyruvate g^?1 fresh weight. In most cases, when a flavour classification of sweet, mild or strong was applied to a sample of onions based on pyruvate content, the taste‐panels agreed with the categorization. The taste‐panels were unable to identify a sweet flavour in onions, except at low levels of pyruvate. Taste‐panels were able to define a likeability character (attractiveness of flavour) for onions, which correlated with the level of pyruvate. However, for some varieties, the flavour classification or likeability did not correspond to predictions based on pyruvate levels alone. Pyruvate measurements were seen as a suitable method for routine quality control once the characteristics of a variety of onion had been established, but initial evaluations should include well‐designed taste‐panel assessments. Copyright © 2004 Society of Chemical Industry     

Total phenol,flavonoid, proanthocyanidin and vitamin C levels and antioxidant activities of Mauritian vegetables

Ten Mauritian vegetables, broccoli, cauliflower, white cabbage, lettuce, Chinese cabbage, mugwort, carrot, onion, tomato and chilli pepper, were analysed for their total phenol, flavonoid, proanthocyanidin and vitamin C contents and antioxidant capacity. Antioxidant activities of the vegetables ranged from 0.43 to 3.68 µmol g^?1 fresh weight Trolox equivalent antioxidant capacity (TEAC) and from 0.60 to 8.47 µmol g^?1 fresh weight ferric reducing antioxidant power (FRAP). Levels of total phenols in the vegetables varied between 132 and 1189 µg g^?1 fresh weight and those of total flavonoids between 45 and 944 µg g^?1 fresh weight, while proanthocyanidins were detected at very low levels in only a few vegetables. Vitamin C contents varied between 25 and 748 µg g^?1 fresh weight. Quercetin was the dominant flavonoid aglycone in the hydrolysed vegetable extracts, with values in the range of 15–390 µg g^?1 fresh weight. There were strong correlations between antioxidant capacity and total phenols (TEAC, r = 0.91; FRAP, r = 0.83) and total flavonoids (TEAC, r = 0.89; FRAP, r = 0.82). Vitamin C contents showed poor correlation with TEAC values (r = 0.33), while no correlation was observed with FRAP values. Highest antioxidant capacities were observed in Chinese cabbage (Brassica chinensis L), onion (Allium cepa L), mugwort (Artemisia vulgaris Cantley) and broccoli (Brassica oleracea L var botrytis L subvar cymosa). Mauritian vegetables therefore represent a significant source of phenolic antioxidants, with quercetin derivatives being most abundant, and this may contribute to their potential health benefits. Copyright © 2004 Society of Chemical Industry     

The effect of storage on the oxalate content of New Zealand grown oca

Four lines of oca, No. 38 and 41, Inca Gold and Market were grown in four replicated plots and the soluble oxalate content was determined on the freshly harvested tubers and tubers that had been stored for 6 weeks at 16.4 ± 0.5 °C. The mean dry matter content of freshly harvested tubers was 14.3 ± 0.5 g 100 g^?1 fresh weight (FW), and after storage was 14.6 ± 0.5 g 100 g^?1 FW. The mean soluble oxalate content of freshly harvested tubers was 162.1 ± 8.8 mg 100 g^?1 FW, and, after 6 weeks storage, 173.5 ± 0.9 mg 100 g^?1 FW. The different cultivars behaved differently during storage, the soluble oxalate content of Inca Gold tubers fell 7.2% while the soluble oxalate content of the other three cultivars increased (mean 13%).     

Bioactivities of essential oil and extract of Thymus argaeus,Turkish endemic wild thyme

BACKGROUND: Thymus argaeus Boiss. & Bal. (Lamiaceae), an endemic plant species of Turkey known as wild thyme, is traditionally used as a spice and a wild tea in the Inner Anatolia region of Turkey. In this study the composition of the essential oil and the antimicrobial and antioxidant effects of the methanolic extract and essential oil of T. argaeus were determined. RESULTS: The main components of the essential oil were linalool (499 g kg^?1), α‐terpineol (150 g kg^?1), linalyl acetate (97 g kg^?1) and thymol (94 g kg^?1). The total phenolic, flavanol and flavonol contents of the extract were 83.31 ± 0.59 mg gallic acid equivalent g^?1, 6.26 ± 0.00 mg catechin equivalent g^?1 and 28.81 ± 0.21 mg rutin equivalent g^?1 respectively. The antioxidant activities of the extract and essential oil determined by the 2,2‐diphenyl‐1‐picrylhydrazyl radical‐scavenging method were 830.18 ± 0.42 and 20.47 ± 2.3 mg g^?1 respectively. The antimicrobial activities of the extract and essential oil against 13 bacteria and two yeasts were studied by the agar diffusion method. The micro‐organisms most sensitive to the essential oil were Aeromonas hydrophila and Pseudomonas aeruginosa, while the micro‐organism most sensitive to the extract was P. aeruginosa. CONCLUSION: Only the extract of T. argaeus could be used as a natural antioxidant, while both the extract and the essential oil could be useful as natural antimicrobial agents in food preservation. Copyright © 2009 Society of Chemical Industry     

Increase in low molecular size uronic acid in ripening banana fruit

Uronic acid soluble in ethanol/water (4:1 v/v) increased from 9 ± 1 mg kg^?1 fresh weight in pulp of unripe banana fruit. Musa (AAA Group, Cavendish subgroup) ‘Williams’, to 53 ± 13 mg kg^?1 fresh weight in fruit ripened for 13 days. This increase began within the first 2 days of ripening. Uronic acid soluble in phenol/acetic acid/water (2:1:1 w/v/v) increased from 15 ± 5 to 86 ± 17 mg kg^?1 fresh weight during the first 8 days of ripening, accompanied by a decrease in cell wall uronic acid from 10·2 ± 0·8 to 4·4 ± 0·4 g kg^?1 fresh weight. Most or all of the uronic acid in extracts of ripe pulp cochromatographed with monogalacturonic acid. The results were consistent with hydrolysis of cell wall polyuronides by exopolygalacturonase (EC 3.2.1.67).     

Betalain and Phenolic Compositions,Antioxidant Activity of Tunisian Red Beet (Beta vulgaris L. conditiva) Roots and Stems Extracts

In the present study, betalains content, phenolic composition, and antioxidant activity of different parts of red beet (Beta vulgaris L. conditiva) (i.e., roots and stems) were compared. Crude extract of root showed the highest betalain content with a maximum of 53 ± 4 mg betanin eq and 46 ± 3 mg vulgaxantin I eq g^?1 of extract stems showed higher total phenolic concentration than roots, ranging between 2.0 ± 0.4 and 14.6 ± 0.5 mg gallic acid eq^?1 of extract. Chemical composition was analyzed using LC-MS. Betalains (vulgaxanthin I, betanin, and isobetanin) and phenolics (gallic acid, ferulic acid, chlorogenic acid, caffeic acid, vanillic acid, syringic acid, ellagic acid myricetin, quercetin, rutin, kampferol) were identified in roots and stems. Betalain extract obtained from roots showed higher antioxidant activity than extract obtained from stems.     

Implications of spatial and temporal changes in concentration of pyruvate and glucose in onion (Allium cepa L.) bulbs during controlled atmosphere storage

BACKGROUND: Pungency and perceived sweetness are important quality assurance parameters for onion producers; however, there is still a paucity of information describing the spatial changes within the bulb of some taste‐related compounds during storage. Accordingly, onion bulbs of cultivars (cvs.), SS1 (low pungency, low dry matter) and Renate (pungent, high dry matter) bulbs, were divided into 12 sections and both spatial and temporal variations of pyruvate and glucose were recorded during standard controlled atmosphere storage. RESULTS: Pyruvate within cv. SS1 bulbs reached 8.3 µmol g^?1 fresh weight (FW) from pre‐storage levels of less than 3.4 µmol g^?1 FW, whilst pyruvate changes in cv. Renate remained in the ‘pungent’ category, between 12 µmol g^?1 FW and 15 µmol g^?1 FW; thus having fewer implications for marketing and quality assurance. Glucose concentrations were significantly higher for both cvs. in the neck region as compared to basal tissue. Higher glucose levels were recorded in the core of the bulb than in outer scales of cv. Renate. The opposite was found for cv. SS1. There was an inverse correlation of ? 0.69 and ? 0.87 between glucose and pyruvate for cvs. SS1 and Renate, respectively. CONCLUSION: In order to measure overall bulb flavour, it is recommended that sampling procedures, particularly for routine pungency determination, be carried out on bulb quarters or wedges rather than equatorial sections. Copyright © 2009 Society of Chemical Industry     

Characterization of Valuable Compounds from Winter Melon (<Emphasis Type="Italic">Benincasa hispida</Emphasis> (Thunb.) Cogn.) Seeds Using Supercritical Carbon Dioxide Extraction Combined with Pressure Swing Technique

In this study, we describe the extraction of different valuable compounds from winter melon seeds using supercritical carbon dioxide extraction combined with pressure swing technique (SCE-PST). The effects of the extraction variables, namely pressure, holding time (HT), and continuous extraction time (CT), were optimized by response surface methodology (RSM) to maximize the crude extraction yield (CEY). The optimal conditions were at pressure of 181.35 bar, HT of 9.93 min, and CT of 50.14 min. Under these conditions, the experimental CEY was 235.70?±?0.11 mg g^?1 with a relatively strong antioxidant activity (64.42?±?0.21 % inhibition of DPPH^· radicals, 67.36?±?0.34 % inhibition of ABTS^·+ radicals) and considerable amount of phenolic compounds (42.77?±?0.40 mg gallic acid equivalent/g extract). The high-performance liquid chromatography (HPLC) analysis revealed that the bioactive phenolic compounds increased significantly using PST (p?<?0.05), where gallic acid had the highest concentration (0.688?±?0.34 mg g^?1). The extract obtained using optimal SCE-PST conditions contained more than 83.65 % total unsaturated fatty acids (UFAs) and linoleic acid accounted for 67.33?±?0.22 % in the total extract. From the results, the SCE efficiency in terms of extract quantity and quality has been enhanced significantly applying PST. Finally, the results were compared with previous published findings using supercritical carbon dioxide, ultrasound-assisted, and Soxhlet extraction. It was found that higher CEY could be achieved using Soxhlet extraction even through the quality of SCE-PST extracts in terms of antioxidant activity and phenolic compounds was better.     

Antimicrobial and antioxidant activity of crude onion (Allium cepa,L.) extracts

Antioxidant and antimicrobial activity of the ethyl acetate and water subfractions of methanolic extracts of three Spanish onion varieties were assayed. Flavonoids were mainly present in ethyl acetate subfraction being 34.92 ± 0.75, 7.95 ± 0.16, 0.38 ± 0.01 μmol of rutin eq. g^?1 D.W. and its antioxidant capacity was 74.86 ± 1.77, 24.59 ± 0.67, 4.55 ± 0.44 μmol Trolox g^?1 D.W. of Grano de Oro, Fuentes de Ebro and Calçot de Valls varieties, respectively. The antimicrobial activity of flavonol standards and onion extracts was evaluated against some food spoiler microorganisms. Quercetin and kaempferol were inhibitory against gram positive bacteria such as Bacillus cereus, Staphylococcus aureus, Microcroccus luteus and Listeria monocytogenes. Gram negative bacteria Escherichia coli and Pseudomonas aeruginosa were less sensible to the antimicrobial effect of both flavonol standards and Candida albicans was totally resistant. Among the onion extracts tested only ethyl acetate subfraction showed antimicrobial inhibition.     

Effect of drying kinetics on main bioactive compounds and antioxidant activity of acerola (Malpighia emarginata D.C.) residue

This study investigates the drying kinetics of residue of acerola, in a fixed‐bed dryer, analysing the effect of the process variables on the antioxidant properties of the residue. A complete factorial design 3² has been performed, where the independent variables studied were as follows: air velocity (0.5, 1.0 and 1.5 m s^?1) and air‐drying temperature (40, 50 and 60 °C). The bioactive compounds studied were L‐ascorbic acid, total phenolic, total flavonoids and antioxidant activity (expressed as IC₅₀) was determined using free radical DPPH^?. Both independent variables studied have shown to be statistically significant. The content of ascorbic acid was the highest at 60 °C and 1.0 m s^?1 (126.2 ± 0.004 mg 100 g^?1) while for the fresh residue 16.12 ± 0.003 mg 100 g^?1, whereas the total phenolic showed the highest content at 50 °C and 1.5 m s^?1 (46.2 ± 0.003 mg gallic acid.100 g^?1) while for the fresh residue 12.59 ± 0.001 mg gallic acid.100 g^?1. The drying conditions play an important role in determining the final quality of the product mainly in terms of antioxidant activity.     

Antioxidant actions and phenolic and vitamin C contents of common Mauritian exotic fruits

Seventeen commonly consumed exotic fruits from Mauritius were analysed for their antioxidant capacity, total phenolics, proanthocyanidins, flavonoids and vitamin C content. Two independent methods were used to evaluate the antioxidant potential of total fruit extracts. The antioxidant activities of the fruits ranged from 1 to 47 µmol Trolox equivalent antioxidant capacity (TEAC) g^?1 fresh weight and from 0.3 to 34 micro/mol g fresh weight (FRAP) g^?1 fresh weight. Total phenolics in the fruits ranged from 118 to 5638 µg g^?1 fresh weight, proanthocyanidins from 7 to 2561 µg g^?1 fresh weight, flavonoids from 21 to 712 µg g^?1 fresh weight and vitamin C content from 8 to 1426 µg g^?1 fresh weight. There were strong correlations between antioxidant activity (assessed by both TEAC and FRAP) and total phenolics and proanthocyanidins. Flavonoids seemed to contribute less to the antioxidant potential of the fruits, while very poor correlations were observed between ascorbate content and antioxidant activity. The highest antioxidant capacities were observed in red and yellow Psidium cattleianum Sabine ‘Chinese guava’, sweet and acid Averrhoa carambola L ‘starfruit’, Syzygium cumini L Skeels ‘jamblon’ and white Psidium guajava L ‘guava’. These fruits were also characterised by high levels of total phenolics. Mauritian exotic fruits are thus a significant source of phenolic antioxidants, which may have potential beneficial effects on health. Copyright © 2003 Society of Chemical Industry     

Assessment of in vitro antioxidant, antibacterial and immune activation potentials of aqueous and ethanol extracts of Phyllanthus niruri

BACKGROUND: Recently much attention has been paid to biologically active plants because of their low production cost and fewer adverse effects compared with chemical drugs. In the present investigation the bioactivity of Phyllanthus niruri ethanol and aqueous extracts was evaluated in vitro. RESULTS: The ethanol extract of P. niruri showed a high level of flavonoid content (123.9 ± 0.002 mg g^?1), while the aqueous extract showed the highest 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH; IC₅₀6.85 ± 1.80 µmol L^?1) and 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid) (ABTS; 46.44 ± 0.53 µmol L^?1) free radical scavenging activities with high phenol content (376 ± 0.02 mg g^?1) and elevated levels of ferric reducing antioxidant power (FRAP; 23 883 ± 0.019 mmol g^?1) with excellent antibacterial activity against Staphylococcus aureus (20 mm inhibition zone) and Streptococcus agalactiae (12 mm inhibition zone), respectively, in addition to the best immune activation potential of human peripheral blood mononuclear cells (450.5%). CONCLUSIONS: It is clear from our results that both extracts of P. niruri has excellent bioactivity roles via elevated levels of antibacterial, antioxidant and percentage of peripheral blood mononuclear cell proliferation, which could lead to the development of medications for clinical use. Copyright © 2012 Society of Chemical Industry     

Carotenoids in yellow‐ and red‐fleshed papaya (Carica papaya L)

Vitamin A deficiency is a disorder of public health importance in Sri Lanka. A recent national survey revealed that 36% of preschool children in Sri Lanka have vitamin A deficiency (serum retinol <0.2 µg ml^?1). In view of its well‐established association with child morbidity and mortality, this is a reason for concern. One of the main fruits which has been recommended for prevention of vitamin A deficiency in Sri Lanka is papaya (Carica papaya L). In this study the carotenoid profiles of yellow‐ and red‐fleshed papaya were analysed by medium‐pressure liquid chromatography (MPLC) and UV‐vis spectrophotometry. A section of yellow‐fleshed papaya showed small carotenoid globules dispersed all over the cell, whereas in red‐fleshed papaya the carotenoids were accumulated in one large globule. The major carotenoids of yellow‐fleshed papaya were the provitamin A carotenoids β‐carotene (1.4 ± 0.4 µg g^?1 dry weight (DW)) and β‐cryptoxanthin (15.4 ± 3.3 µg g^?1 DW) and the non‐provitamin A carotenoid ζ‐carotene (15.1 ± 3.4 µg g^?1 DW), corresponding theoretically to 1516 ± 342 µg kg^?1 DW mean retinol equivalent (RE). Red‐fleshed papaya contained the provitamin A carotenoids β‐carotene (7.0 ± 0.7 µg g^?1 DW), β‐cryptoxanthin (16.9 ± 2.9 µg g^?1 DW) and β‐carotene‐5,6‐epoxide (2.9 ± 0.6 µg g^?1 DW), and the non‐provitamin A carotenoids lycopene (11.5 ± 1.8 µg g^?1 DW) and ζ‐carotene (9.9 ± 1.1 µg g^?1 DW), corresponding theoretically to 2815 ± 305 µg kg^?1 DW mean RE. Thus the carotenoid profile and organisation of carotenoids in the cell differ in the two varieties of papaya. This study demonstrates that carotenoids can be successfully separated, identified and quantified using the novel technique of MPLC. Copyright © 2003 Society of Chemical Industry     

Monitoring of free glutamic acid in Malaysian processed foods,dishes and condiments

A study to quantify the free glutamic acid content of six processed foods, 44 dishes and 26 condiments available in Malaysia was performed using high-performance liquid chromatography with a fluorescence detector (HPLC-FRD). Recovery tests were carried out with spiked samples at levels from 6 to 31 mg g^?1. High recovery in different matrices was achieved ranging from 88% ± 13% to 102% ± 5.12%, with an average of 97% ± 8.92%. Results from the study revealed that the average free glutamic acid content ranged from 0.34 ± 0.20 to 4.63 ± 0.41 mg g^?1 in processed foods, while in prepared dishes it was as low as 0.24 ± 0.15 mg g^?1 in roti canai (puffed bread served with curry or dhal) to 8.16 ± 1.99 mg g^?1 in dim sum (a small casing of dough, usually filled with minced meat, seafood, and vegetables, either steamed or fried). Relatively, the content of free glutamic acid was found to be higher in condiments at 0.28 ± 0 mg g^?1 in mayonnaise to 170.90 ± 6.40 mg g^?1 in chicken stock powder.     

Mineral contents of some aromatic plants,their growth soils and infusions

BACKGROUND: In this study, 18 kinds of medicinal plants were collected together with their soils from different regions of Turkey and their macro‐ and micro‐element and heavy metal contents were determined by inductively coupled plasma atomic emission spectrometry (ICP‐AES). In soils, pH, electrical conductivity, carbonate (lime), organic matter, texture, P, K, Ca, Mg, Fe, Cu, Mn, Zn and B were analysed. In plants and extracts, P, K, Ca, Mg, Fe, Cu, Mn, Zn, B, Na, Al, Li, Pb, Ni, Cd, Co and Cr contents were determined. Also, correlations between soil and plant and between plant and extract were established. RESULTS: Element concentrations ranged between 0.11 and 5160 µg g^?1 in soil samples, between 0.14 and 54400 µg g^?1 in plant samples and between 0.039 and 22033 µg g^?1 in extract samples. While sage was rich in Fe (981.3 µg g^?1), basil was abundant in P (9.8 mg g^?1), K (54.4 mg g^?1), Ca (22.6 mg g^?1), Mg (3.1 mg g^?1) and Zn (46.05 µg g^?1) and mint was rich in Li (23.50 µg g^?1). Moreover, while high levels of P (4100.9 µg g^?1), K (22033 µg g^?1) and Mg (529.15 µg g^?1) were found in basil extract, Ca (5979.3 µg g^?1) was present at high concentration in marjoram leaf extract. Also, Fe (4.25 µg g^?1) and Zn (17.51 µg g^?1) were detected at high levels in lime flower and mint extracts respectively. CONCLUSION: It was concluded that aromatic plants are important sources of nutrients and essential elements. Copyright © 2007 Society of Chemical Industry