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3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures

3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures

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Chem. Listy, 102, s265–s1311 (2008) Food Chemistry & Biotechnology<br />

P49 EVALuATION OF ANTIOxIDANT AND<br />

ANTIMICRObIAL ACTIVITIES OF NATuRAL<br />

hONEyS<br />

MIROSLAVA KAČánIOVá, MARTInA FIKSELOVá,<br />

SOňA FELŠÖCIOVá, VLADIMíRA KňAZOVICKá,<br />

KATARínA FATRCOVá-ŠRAMKOVá, JAnKA<br />

nôŽKOVá and IVETA UBREŽIOVá<br />

Faculty of Biotechnology and Food Sciences, Slovak University<br />

of Agriculture, Tr. A.Hlinku 2, Nitra, 949 76 Slovakia,<br />

miroslava.kacaniova@uniag.sk<br />

Introduction<br />

In general, the antioxidant capacity of honey appeared to<br />

be a result of the compounds including phenolics, peptides,<br />

organic acids, enzymes and other phytochemicals (Gheldof et<br />

al., 2002). The phenolic compounds contribute significantly<br />

to the antioxidant capacity in many studies. Reports on honey<br />

as antifungal agent were comprehensively reviewed by Molan<br />

(1992). The “inhibine number” is the degree of dilution to<br />

which a honey retains its antibacterial activity, representing a<br />

sequential dilution of honey in steps of 5 %, from 25 to 5 %.<br />

Allen et al., (1991) found many honeys with low activity and<br />

36 % of samples with activity near or below detectable levels.<br />

In this study, antioxidant effects (by DPPH method) as well<br />

as the antifungal effects of natural honeys on five species of<br />

fungi collected, were tested.<br />

Experimental<br />

Honey was extracted from the hives of bees and kept at<br />

4 °C away from direct light before use. Samples were derived<br />

from different plant species of Acacia (2 samples), Brassica<br />

(1 sample), Thyme (1 sample) and the rest of samples (5 samples)<br />

were of floral origin. Samples originated from different<br />

places of Slovakia and one sample came from Rodos<br />

A n t i o x i d a n t A c t i v i t y<br />

A method was adapted according to Sanches Moreno<br />

et al. (1998) and Brand-Wiliams et al. (1995). Honey (10 g)<br />

was dissolved in 100 ml of ethanol (90%), and 0.1 ml of<br />

solution was taken to <strong>3.</strong>9 ml of DPPH methanolic solution<br />

(25 mg dm −3 ) and mixed. Absorbance at 515 nm was measured<br />

at different time intervals. The blank reference cuvette<br />

contained DPPH methanolic solution. Results were expressed<br />

as % inhibition.<br />

A n t i f u g a l A c t i v i t y<br />

All samples were prepared aseptically and handled protected<br />

from direct sunlight. Honey solutions were prepared in<br />

three fractions: 50, 25 and 10 % (by mass per volume). Five<br />

species of fungi were isolated from wheat samples collected<br />

from different locations in Slovakia: Penicillium crustosum,<br />

P. expansum, P. griseofulvum P. raistrickii and P. verrucosum<br />

by the agar well diffusion method. All fungal isolates were<br />

identified microscopically, and samples of each fungus were<br />

deposited in the fungal collection bank. The strains of fungi<br />

s680<br />

were maintained on Czapek yeast extract agar (CYA, HiMedia).<br />

All plates were incubated at 25 °C in the dark and inhibition<br />

zones were measured after 3 days. The statistical processing<br />

of the data obtained was implemented by means with<br />

SAS software.<br />

Results<br />

In term of antioxidant activity of honeys the best results<br />

were found at thyme honey from Rodos (11.84 %) and floral<br />

honeys from different places of Lučenec (10.09 %, 10.19 %).<br />

The lowest antiradical activity was determined at Acacia<br />

honey (7.615 %). Kücük et al. (2007) studied three different<br />

Turkish honeys and found high levels of polyphenolics and<br />

high antioxidant activity in three antioxidant assays. Radical<br />

scavenging assay was the highest at chestnut honey, then followed<br />

heterofloral honey and the least at rododendron one.<br />

Table I<br />

Antioxidant activity [%] of honey samples<br />

Honey/Place of origin Inhibition [%] ± SD<br />

Acacia/nitra 8.53 ± 0.08<br />

Brassica/nitra 9.89 ± 0.33<br />

Floral/Smrečany 8.39 ± 0.11<br />

Thyme/Rodos 11.84 ± 0.35<br />

Floral/nitra 8.98 ± 0.24<br />

Floral/Hlohovec 9.96 ± 0.40<br />

Floral/Lučenec 10.19 ± 0.53<br />

Acacia/Lučenec 7.62 ± 0.56<br />

Floral/Lučenec 10.09 ± 0.34<br />

All 9.50 ± 1.25<br />

Al-Mamary et al. (2002) showed a linear positive relationship<br />

with the extract concentration. The antioxidant activity<br />

of diluted honey samples increased with increasing the<br />

levels (50 μl, 100 μl, 200 μl) of honey samples. The total<br />

antioxidant activities of diluted samples varied from −6.48 %<br />

(prooxidant activity) to 65.44 % inhibition. In our case determined<br />

antioxidant activity (Table I) was low, varied from<br />

7.62 % (Acacia/Lučenec) to 11.84 % (Thyme/Rodos).<br />

The results obtained characterize honey samples as<br />

a product with a broad antimicrobial effect. The strongest<br />

antifungal effect was shown by honey samples of 50 % concentration<br />

against Penicillium raistricki strains. The least<br />

antifungal effect was shown by honey samples of 10 % concentration<br />

against to Penicillium expansum strains. no inhibitory<br />

activity was detected with any of the seven species<br />

with the pasture honey at any concentration up to the highest<br />

tested 50 % (v/v). Maughrabi (2003) found that wild honey<br />

was effective against Alternaria solani and Phytophthora<br />

infestanns, also against Rhizoctonia solani and Fusarium<br />

oxysporum, and to a less extent against Stemphylium solani<br />

and Colletotrichum sp.

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