Phenolic acids and abscisic acid in Australian Eucalyptus honeys and their potential for floral authentication

Seven phenolic acids related to the botanical origins of nine monofloral Eucalyptus honeys from Australia, along with two abscisic isomers, have been analyzed. The mean content of total phenolic acids ranges from 2.14 mg/100 g honey of black box (Eucalyptus largiflorens) honey to 10.3 mg/100 g honey of bloodwood (Eucalyptus intermedia) honey, confirming an early finding that species-specific differences of phytochemical compositions occur quantitatively among these Eucalyptus honeys. A common profile of phenolic acids, comprising gallic, chlorogenic, coumaric and caffeic acids, can be found in all the Eucalyptus honeys, which could be floral markers for Australian Eucalyptus honeys. Thus, the analysis of phenolic acids could also be used as an objective method for the authentication of botanical origin of Eucalyptus honeys. Moreover, all the honey samples analyzed in this study contain gallic acid as the main phenolic acid, except for stringybox (Eucalyptus globoidia) honey which has ellagic acid as the main phenolic acid. This result indicates that the species-specific differences can also be found in the honey profiles of phenolic acids. Furthermore, the analysis of abscisic acid in honey shows that the content of abscisic acid varies from 0.55 mg/100 g honey of black box honey to 4.68 mg/100 g honey of bloodwood honey, corresponding to the contents of phenolic acids measured in these honeys. These results have further revealed that the HPLC analysis of honey phytochemical constituents could be used individually and/or jointly for the authentication of the botanical origins of Australian Eucalyptus honeys.     

Flavonoids,phenolic acids and abscisic acid in Australian and New Zealand Leptospermum honeys

Flavonoids, phenolic acids and abscisic acid of Australian and New Zealand Leptospermum honeys were analyzed by HPLC. Fifteen flavonoids were isolated in Australian jelly bush honey (Leptospermum polygalifolium), with an average content of 2.22 mg/100 g honey. Myricetin (3,5,7,3′,4′,5′-hexahydroxyflavone), luteolin (5,7,3′,4′-tetrahydroxyflavone) and tricetin (5,7,3′,4′,5′-pentahydroxyflavone) were the main flavonoids identified. The mean content of total phenolic acids in jelly bush honey was 5.14 mg/100 g honey, with gallic and coumaric acids as the potential phenolic acids. Abscisic acid was quantified as twice the amount (11.6 mg/100 g honey) of the phenolic acids in this honey. The flavonoid profile mainly consisted of quercetin (3,5,7,3′,4′-pentahydroxyflavone), isorhamnetin (3,5,7,4′-tetrahydroxyflavone 3′-methyl ethyl), chrysin (5,7-dihydroxyflavone), luteolin and an unknown flavanone in New Zealand manuka (Leptospermum scoparium) honey with an average content of total flavonoids of 3.06 mg/100 g honey. The content of total phenolic acids was up to 14.0 mg/100 g honey, with gallic acid as the main component. A substantial quantity (32.8 mg/100 g honey) of abscisic acid was present in manuka honey. These results showed that flavonoids and phenolic acids could be used for authenticating honey floral origins, and abscisic acid may aid in this authentication.     

Phenolic profile and antioxidant properties of Polish honeys

The phenolic components of honeys have great participation in their nutritional value and antioxidant activity. Moreover, phenolic components are promising markers for the determination of botanical and geographical origin of honey. The purpose of the present work was to study the antioxidant activity and profiles of phenolic acids and flavonoids of honeys of various origins. The total phenolic content of honeys varied from 4.46 to 15.04 mg of gallic acid equivalents per 100 g of product and the total phenolic acid content determined chromatographically varied from 201.05 to 2089.08 μg per 100 g of product. Buckwheat honey exhibited the highest antioxidant activity and contained the highest total phenolic amount, whereas rape honey exhibited the lowest values in this respect. Moreover, the buckwheat honey contained the highest amount of phenolic acids. There were significant linear correlations between total phenolic content and antioxidant activity of honey extracts in the reaction with DPPH^? (1,1‐diphenyl‐2‐picrylhydrazyl) and ABTS^{? +} (2,2′‐azinobis‐(3‐ethylbenzothiazoline‐6‐sulfonic acid)) free radicals. In most samples, p‐coumaric acid was the dominant phenolic acid (39.1–677.2 μg per 100 g). The honeys also contained considerable amount of gallic acid (6.0–913.8 μg per 100 g). Among flavonoids naringenin was predominant in the most studied honey samples.     

Phenolic compounds and methylglyoxal in some New Zealand manuka and kanuka honeys

The principal phenolic compounds and methylglyoxal were analysed in New Zealand Leptospermum scoparium (manuka) and Kunzea ericoides (kanuka) honeys. These honeys shared six phenolic acids as primary components and differentiation was possible as relative proportions varied. Manuka honey contained an elevated concentration of a trimethoxybenzoic acid and methylglyoxal; and 2-methoxybenzoic acid and methylglyoxal concentrations were linearly correlated in fresh manuka honey. Kanuka honey contained an elevated concentration of methoxyphenyllactic acid. The concentration of the phenolic components increased with maturation in both honey types; and this profile development, along with a corresponding increase of methylglyoxal concentration, was linear in manuka honey. Nectar analysed from the plant species contained the same phenolic components as the honeys. These results demonstrated the phenolic profile could be used to differentiate the honey types, heat treatment of honey could be identified, and the presence of these components may contribute to the efficacy of these honeys in therapeutic uses.     

Phenolic composition,antioxidant and antimicrobial activities of free and bound phenolic extracts of Moringa oleifera seed flour

Phenolic compounds, antioxidant and antibacterial activities of defatted Moringa oleifera seed flour (DMF) were investigated. The total phenolic and flavonoid contents were measured using colorimetric methods. Free phenolic acid and flavonoid profiles were analyzed by high performance liquid chromatography, while antioxidant capacities were evaluated using scavenging assays of 1,1-diphenyl-2-picrylhydrazyl radical (DPPH), ferric reducing antioxidant power and total antioxidant capacity. The results showed that extractability of phenolic compounds was significantly higher (p < 0.05) in bound phenolic extract (4173.00 ± 32.22 mg gallic acid equivalents (GAE)/100 g) than in free phenolic extract (780.00 ± 14.2 mg GAE/100 g) and it showed higher antioxidant and antimicrobial activities. The IC₅₀ value for DPPH radical scavenging activity was 0.9 ± 0.05 and 14.9 ± 0.07 mg/mL for bound phenolic and free phenolic extracts, respectively. Bound phenolic extract was more effective (minimum inhibitory concentration (MIC), 0.06–0.157%) than free phenolic extract (MIC, 0.117–0.191%) against tested bacteria. Ten phenolic compounds (gallic acid, p-coumaric acid, ferulic acid, caffeic acid, protocatechuic acid, cinnamic acid, catechin, epicatechin, vanillin and quercetin) were identified and quantified in both extracts. These natural plant phenolics from Moringa seeds could be a good source of antioxidants and antibacterials for food and pharmaceutical industries.     

Phenolic profile and antioxidant activity of the Algerian ripe date palm fruit (Phoenix dactylifera)

The aim of this study was to determine the phenolic profile of seven different varieties of ripe date palm fruit (Phoenix dactylifera) from Algeria by LC–DAD–MS (ESI+), to investigate their respective antioxidant activities by the DPPH^· method and to estimate their phenolic content using the Folin–Ciocalteu method. The total phenolic content was in the range of 2.49 ± 0.01 to 8.36 ± 0.60 mg gallic acid equivalents (GAE) per 100 g fresh fruit. This fruit was shown to possess an antioxidant activity, giving values of antiradical efficient (AE) from 0.08 ± 0.00 to 0.22 ± 0.00. The phenolic contents and the antiradical efficiencies of the different varieties were highly correlated (R²=0.975). All the varieties were found to contain mainly p-coumaric, ferulic and sinapic acids and some cinnamic acid derivatives. Three different isomers of 5-o-caffeoylshikimic acid were detected. Different types of flavonoids were identified, mainly flavones, flavanones and flavonol glycosides.     

Physicochemical and melissopalynological characterization of Estonian summer honeys

The samples of 14 honeys, retained from Estonian beekeepers, were analyzed for parameters such as pH, moisture content, free acidity, electrical conductivity, diastase activity, hydroxymethylfurfural (HMF) content and mineral content, including sodium (Na), potassium (K), magnesium (Mg) and calcium (Ca). Fructose, glucose and disaccharide content were also identified and fructose/glucose ratio was calculated. In addition melissopalynological analyses were carried out for characterization of honeys. The mean values of analyzed honeys were: pH 3.8; moisture 17.3%; free acidity 20.4 mmol/kg; electrical conductivity 0.2 mS/cm; diastase activity 23.1 DN and HMF was below 3.8 mg/kg. Within the mineral content, potassium was quantitatively the most important mineral in the range of 125.79 to 1381.53 mg/kg followed by calcium of 20.37-63.65 mg/kg, magnesium 5.53-25.49 mg/kg and sodium 4.77- 19.44 mg/kg. The predominant sugar in honey samples was fructose having the mean value of 35.91 g/100 g followed by glucose 35.00 g/100 g. The disaccharide average content was 6.00 g/100 g. The melissopalynological analyzes showed that the most dominant pollens in honey samples were cruciferous (Cruciferae)-mainly rape (Brassica napus); rosacean (Rosaceae)-mainly raspberry (Rubus idaeus); white clover (Trifolium repens); sweet clover (Melilotus officinalis) and willow (Salix). The results of honey pollen profile analysis and calculated fructose/glucose ratios (0.89-1.17) both indicated to flower honeys. All of the analyzed honeys were found to meet European Legislation (EC Directive 2001/110) for all parameters.     

HPLC flavonoid profiles as markers for the botanical origin of European unifloral honeys

The HPLC phenolic profiles of 52 selected unifloral honey samples produced in Europe were analysed to detect possible markers for the floral origin of the different honeys. Lime‐tree (five markers), chestnut (five markers), rapeseed (one marker), eucalyptus (six markers) and heather (three markers) honeys had specific markers with characteristic UV spectra. In addition, the flavanone hesperetin was confirmed as a marker for citrus honey, as well as kaempferol for rosemary honey and quercetin for sunflower honey. Abscisic acid, which had been reported to be a possible marker for heather honey, was also detected in rapeseed, lime‐tree and acacia honeys. Ellagic acid in heather honey and the hydroxycinnamates caffeic, p‐coumaric and ferulic acids in chestnut, sunflower, lavender and acacia honeys were also detected. The characteristic propolis‐derived flavonoids pinocembrin, pinobanksin and chrysin were present in most samples in variable amounts. © 2001 Society of Chemical Industry     

Effects of microwaves,hot air and freeze-drying on the phenolic compounds,antioxidant capacity,enzyme activity and microstructure of cacao pod husks (Theobroma cacao L.)

The cacao pod husk (CPH) is the primary waste byproduct of the chocolate industry. One ton of cacao beans generate approximately ten times that amount of fresh CPH. The husk is rich in phenolic compounds. The aim of this study is to determine the effects of microwaves, hot air and freeze-drying on the phenolic compound content, antioxidant capacity, enzyme activity and microstructure of CPH. The results showed that fresh CPH contain 323.7 ± 26.5 mg gallic acid equivalents (GAE)/100 g dry mass (d.m.) of total phenolic compounds, and dehydration had a positive effect on the CPH phenolic content and antioxidant capacity. Catechin, quercetin, and (−)-epicatechin and gallic, coumaric and protocatechuic acids were identified in fresh and dried CPH. Drying the material using a microwave and freeze-drying preserved the husk microstructure. The results showed that microwave drying was a better drying method than hot air and as good as freeze-drying.Industrial relevanceThe food industry is currently searching for new sources of natural antioxidants. The cacao pod husk (CPH) is a good source of phenolic compounds that can function as antioxidants and could be used as ingredients in functional foods. However, due to their high water content, fresh CPH are perishable products, and for this reason, the first step would be dry the pod husk to improve its shelf life. The findings of this study showed that the use of microwaves to dry CPH may release polyphenols, thereby enhancing the antioxidant capacity and decreasing the polyphenol oxidase (PPO) activity while maintaining the microstructure. Thus, microwave drying could be of interest as a method for enhancing the extractability of phenolic compounds from CPH.     

The phenolic compounds and the antioxidant potential of infusion of herbs from the Brazilian Amazonian region

The consumption of tea increased significantly in the past few years as a result of its health benefits as potent antioxidants in the diet. However, studies on the antioxidant compounds from Brazilian tea are scarce. Thus, the aim of this work was to evaluate the total phenolic compounds (TPC) and total flavonoids (TF) contents and the antioxidant capacity (DPPH and β-carotene/linoleic acid system) of nine herb infusions from the Amazonian region, namely agirú (Chrysobalanus icaco), açoita-cavalo (Luehea speciosa), capim-santo (Cymbopogon citratus), erva-cidreira (Lippia alba), graviola (Annona muricata L.), jucá (Libidibia ferrea), pata-de-vaca (Bauhinia ungulata), parirí (Fridericia chica) and sacaca comum (Croton spp.). These herbs were chosen based on popular knowledge and consumption. C. ferrea (68.13 mg GAE/g), L. speciosa (47.54 mg GAE/g) and C. icaco (51.30 mg GAE/g) presented the highest TPC contents, while L. speciosa (12.85 mg CE/g) and L. alba (15.42 mg CE/g) showed the highest TF contents. The highest antioxidant capacity, using both assays, was shown by L. ferrea. The three herbs with the highest TPC contents were selected to be analyzed by high performance liquid chromatography (HPLC) coupled to a diode array detector (DAD). A commercial green tea (Camellia sinensis) was also analyzed as a reference. The main compounds tentatively identified were gallic acid (0.45 mg/g), myricetin (0.78 mg/g) and quercetin (0.14 mg/g) in C. icaco; (+)-catechin (1.20 mg/g) and quercetin (0.14 mg/g) in L. speciosa; gallic acid (0.59 mg/g) and quercetin (0.13 mg/g) in C. ferrea; and gallic acid (0.24 mg/g), (−)-epicatechin (2.44 mg/g), (+)-catechin (0.68 mg/g) and quercetin (0.66 mg/g) in green tea. Among the nine studied herbs, the importance of L. ferrea should be pointed out since it presented the highest TPC content and antioxidant capacity and its gallic acid content was much higher than that of green tea.     

Inhibition of the decrease of volatile esters and terpenes during storage of a white wine and a model wine medium by caffeic acid and gallic acid

Caffeic acid and gallic acid were tested as inhibitors of the decrease of volatile acetate esters, ethyl esters and terpenes during storage of a white wine and a model wine medium. Wine and model wine samples were analysed by SPME along with GC–MS. At t = 0, no effect on the concentration of any volatile was observed as a result of adding each phenolic acid in any of wine or model wine samples. Many esters, such as isoamyl acetate, ethyl hexanoate, ethyl octanoate, ethyl decanoate, and linalool decreased during storage of Debina-white wine for up to 20 months. Caffeic acid and gallic acid at 60 mg/L inhibited the decrease of these volatiles. Isoamyl acetate, ethyl hexanoate and linalool decreased during storage of the model wine medium containing 0, 20 or 40 mg/L SO₂. Caffeic acid and gallic acid inhibited the decrease of three volatiles; SO₂ inhibited the decrease of isoamyl acetate and ethyl hexanoate. In some cases, SO₂ increased the inhibitory action of two phenolic acids. The inhibitory action of caffeic acid and gallic acid was dose dependent in the range 0–60 mg/L. Caffeic acid was active at 7.5 mg/L while gallic acid at 15 mg/L.Present results indicate that caffeic acid and gallic acid may be taken into account as potent inhibitors of the disappearance of aromatic volatile esters and terpenes in wines at concentrations similar to those existing in wines.     

Yerba mate tea (Ilex paraguariensis): Phenolics,antioxidant capacity and in vitro inhibition of colon cancer cell proliferation

Mate tea (MT) is a rich source of phenolic compounds that vary depending on geographical origin and mode of preparation. Total phenolic concentration and antioxidant capacity of Mate tea (Ilex paraguariensis) products were determined in this work. In addition, a representative MT was tested for in vitro inhibition of human colon carcinoma cell proliferation. Total polyphenol concentration, was measured using Folin–Ciocalteau method, ranged from 90 to 176 mg gallic acid eq (GAE)/g dry leaves (DL) in traditional MT and from 40 to 113 mg GAE/g DL in MT added with other flavouring ingredients. It was estimated that a cup of tea (250 ml) containing one teaspoon (5 g) of instant MT could provide an average intake of 1.5 g GAE. Fresh tea (FT) from Mate leaves displayed high antioxidant capacity (85 ± 1%) and preferentially inhibited 50% of net growth of human colorectal adenocarcinoma cells CaCo-2 (GI₅₀ = 1.0 ± 0.03 μg/ml) and HT-29 (GI₅₀ = 105.2 ± 15.2 μg/ml) when compared with the CCD-33Co normal colon fibroblast cell line (GI₅₀ > 300 μg/ml). MT inhibited in vitro colon cancer cell proliferation possibly mediated via pro-oxidant activities, therefore represents a potential source of chemopreventive agents that deserve further investigation.     

Phenolic acid composition and antioxidant properties of Malaysian honeys

Abstract: The phenolic acid and flavonoid contents of Malaysian Tualang, Gelam, and Borneo tropical honeys were compared to those of Manuka honey. Ferric reducing/antioxidant power assay (FRAP) and the 1,1‐diphenyl‐2‐picryl‐hydrazyl (DPPH) radical‐scavenging activities were also quantified. All honey extracts exhibited high phenolic contents (15.21 ± 0.51– 42.23 ± 0.64 mg/kg), flavonoid contents (11.52 ± 0.27– 25.31 ± 0.37 mg/kg), FRAP values (892.15 ± 4.97– 363.38 ± 10.57 μM Fe[II]/kg), and high IC₅₀ of DPPH radical‐scavenging activities (5.24 ± 0.40– 17.51 ± 0.51 mg/mL). Total of 6 phenolic acids (gallic, syringic, benzoic, trans‐cinnamic, p‐coumaric, and caffeic acids) and 5 flavonoids (catechin, kaempferol, naringenin, luteolin, and apigenin) were identified. Among the Malaysian honey samples, Tualang honey had the highest contents of phenolics, and flavonoids, and DPPH radical‐scavenging activities. We conclude that among Malaysian honey samples, Tualang honey is the richest in phenolic acids, and flavonoid compounds, which have strong free radical‐scavenging activities.     

A comparative study of the phenolic compounds and the in vitro antioxidant activity of different Brazilian teas using multivariate statistical techniques

A total of 51 Brazilian teas from the species Camellia sinensis, Peumus boldus, Matricaria recutita, Baccharis trimera, Cymbopogon citratus, Pimpinella anisum, Mentha piperita, and Ilex paraguariensis were analyzed in terms of phenolic compounds, color and in vitro antioxidant capacity using ferric reducing antioxidant power (FRAP) and 1,1-diphenyl-2-picrylhydrazyl (DPPH) assays. Data were processed using principal component analysis (PCA), hierarchical cluster analysis (HCA) and linear discriminant analysis (LDA). Significant (P < 0.01) correlations between antioxidant activity measured by DPPH and FRAP assays with the total phenolic compounds (r = 0.87; r = 0.90, respectively) and flavonoids (r = 0.79; r = 0.77, respectively) were attained. The compounds that displayed significant (P < 0.05) correlations with the antioxidant activity were gallic acid, catechin, epicatechin, procyanidin B2, quercetrin, and caffeine. PCA was a suitable approach to check for similarities among tea samples, explaining up to 50% of data variability. Four groups were suggested using HCA, in which cluster 3 showed the highest content of total phenolic compounds, flavonoids, antioxidant activity, gallic acid, and caffeine. All samples included in this group were from C. sinensis. The overall classification capacity obtained by LDA was 82.00%, in which 100% of samples from I. paraguariensis, C. citratus, M. recutita, and P. boldus were adroitly classified, while 60% of teas from P. anisum, 80% of M. piperita teas, and 88.24% of C. sinensis teas were correctly classified.     

Tea and herbal infusions: Their antioxidant activity and phenolic profile

Tea and herbal infusions have been studied for their polyphenolic content, antioxidant activity and phenolic profile. The total phenolics recovered by ethyl acetate from the water extract, were determined by the Folin–Ciocalteu procedure and ranged from 88.1 ± 0.42 (Greek mountain tea) to 1216 ± 32.0 mg (Chinese green tea) GAE (Gallic acid equivalents)/cup. The antioxidant activity was evaluated by two methods, DPPH and chemiluminescence assays, using Trolox and quercetin as standards. The EC₅₀ of herbal extracts ranged from 0.151 ± 0.002 mg extract/mg DPPH (0.38 quercetin equivalents and 0.57 Trolox equivalents), for Chinese green tea, to 0.77 ± 0.012 mg extract/mg DPPH (0.08 quercetin equivalents and 0.13 Trolox equivalents), for Greek mountain tea. Chemiluminescence assay results showed that the IC₅₀ ranged from 0.17 ± 3.4 × 10⁻³ μg extract/ml of the final solution in the measuring cell (1.89 quercetin and 5.89 Trolox equivalents) for Chinese green tea, to 1.10 ± 1.86 × 10⁻² g extract/ml of the final solution in the measuring cell (0.29 quercetin and 0.90 Trolox equivalents) for Greek mountain tea. The phenolic profile in the herbal infusions was investigated by LC-DAD-MS in the positive electrospray ionization (ESI⁺) mode. About 60 different flavonoids, phenolic acids and their derivatives have been identified.     

Carbohydrate composition of honey from different floral sources and their influence on growth of selected intestinal bacteria: An in vitro comparison

Five human intestinal Bifidobacterium spp. (B. longum, B. adolescentis, B. breve, B. bifidum, and B. infantis) and intestinal microorganism (Bacteriodes thetaiotaomicron, Clostridium perfringens, Eubacterium aerofaciens, and Enterococcus faecalis) were cultured in De Man Rogosa Sharpe (MRS) medium or thioglycollate medium supplemented (5% w/v) with different unifloral honeys (sourwood, alfalfa, or sage). Inoculated samples were incubated anaerobically at 37 °C for 48 h. Samples were collected at 12 h intervals and examined for specific growth rate. Levels of fermentation end products (lactic and acetic acids) produced by Bifidobacterium spp. were measured by high-pressure liquid chromatography. Growth of intestinal microorganisms co-cultured with Bifidobacterium spp. in the presence of different unifloral honeys were also examined. All three honeys enhanced (p < 0.05) growth and activity of the five intestinal Bifidobacterium spp. Their effect on other organisms of the intestinal microflora was selective. Growth of C. perfringens and E. aerofaciens was inhibited (p < 0.05) in the presence of honey and further inhibited when co-cultured with Bifidobacterium spp. Bifidobacterium spp. was not affected.     

Determination of Viscosity of Some Australian Honeys Based on Composition

Abstract

Rheological properties of four unprocessed unifloral Australian honeys (heath, tea tree, yapunya, and yellow box) and an artificial honey were analysed at 20°C. A model previously used to describe viscosity data of various sugar and sugar mixtures was used to describe the concentration dependence of the viscosity of honey samples with varying moisture contents. The model successfully described the sugar concentration dependence of the unadulterated and medium moisture (70–85% solids) range honey samples.     

Phenolic Profile and Antioxidant Activity of Polish Meads

The purpose of this study was to evaluate phenolic profile and antioxidant activity of ten different meads of 1:1 and 1:2 types, produced with addition of fruit juices, root spices, and herbs. The total phenolic content in meads varied from 15.27 to 70.80 mg/dm³. The meads originated from dark honeys exhibited the highest antioxidant activity. The predominant phenolic compounds in meads were hydroxybenzoic acids, especially gallic and protocatechuic acid, originated mainly from honeys. Whereas, among the hydroxycinnamic acids, the major phenolic was chlorogenic acid, derived mainly from plant additives used in meads production. A principal component analysis was applied in order to differentiate the investigated meads. The 1:2 meads type could be best described by chlorogenic acid. Among the 1:1 meads type, those made from the dark honeys could be best described by gallic, p-coumaric, and protocatechuic acid while those made with addition of blackcurrant and raspberry juice could be described by caffeic and ferulic acid.     

Caffeic acid derivatives in dried Lamiaceae and Echinacea purpurea products

The concentrations of caffeic acid derivatives within Lamiaceae and Echinacea (herb, spice, tea, and dietary supplement forms) readily available in the US marketplace (n = 72) were determined. After the first identification of chicoric acid in Ocimum basilicum (basil), the extent to which chicoric acid could be found within the family Lamiaceae was investigated. The dominant phenolic acid in all Lamiaceae samples was rosmarinic acid, which ranged from 2.04 mg/100 g (one of 12 oregano samples) to 622.28 mg/100 g (lemon balm). Of the herbs tested in this study (marjoram, oregano, peppermint, rosemary, sage, spearmint, and thyme from the family Lamiaceae), only basil and lemon balm (Melissa officinalis) contained chicoric acid. Basil samples (starting material and resulting end product) obtained from an industry cooperator, showed substantial phenolic deficiency as a result of processing (approximately 78% loss).     

Antibacterial phenolic components of New Zealand manuka honey

This paper describes several methods for isolation of the antibacterially active phenolic fraction of honey derived from the native New Zealand manuka tree, Leptospermum scoparium (Myrtaceae). This fraction consists of phenolic derivatives of benzoic acids, cinnamic acids and flavonoids, all of which have been identified previously in honeys which do not exhibit non-peroxide residual antibacterial activity. The flavonoids had not previously been identified in manuka honey. Furthermore, the flavonoids were different from those found in the leaves of manuka trees but were the same as those found in European honeys and propolis. While most of these phenolic products possess antibiotic activity, they do not individually or collectively account for the antibacterial activity of `active' manuka honey. Essentially all of this activity is associated with the carbohydrate fraction of the honey.