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Antimicrobial and antioxidant activities of different propolis samples from north‐western Algeria

Identifieur interne : 001574 ( Istex/Corpus ); précédent : 001573; suivant : 001575

Antimicrobial and antioxidant activities of different propolis samples from north‐western Algeria

Auteurs : Mokhtar Benhanifia ; Wessam M. Mohamed ; Yuva Bellik ; Hama Benbarek

Source :

RBID : ISTEX:1AF6E50A0A987340AA1DCB0C6576A84E7AF5DF12

Abstract

The aim of this study was the investigation of antimicrobial and antioxidant activities of different ethanolic extracts of propolis (EEP) collected from north‐western Algeria. Total polyphenols and flavonoids contents of extracts were measured. The UV absorption spectrum showed and confirmed their polyphenols constituents. All EEPs exerted antibacterial activity against Gram‐positive bacteria, but no effect on Gram‐negative bacteria. The minimum inhibitory concentration (MIC) of EEPs ranged from 0.01% to 2.6% v/v. The antioxidant activity was measured using ferric‐reducing power (FRAP), 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) free radical‐scavenging and ESR methods. Propolis TIA‐2 and MOH‐MAS samples showed the highest antioxidative capacity, after 35 min, while TIA‐1, NED‐TL and SFS‐SBA samples showed the highest antioxidative potential of measured EEPs, after 3 min. TIA‐2 sample showed the highest antibacterial, antioxidant activity and highest DPPH free radical‐scavenging activity as well as the highest polyphenols and flavonoids content, compared with other propolis samples.

Url:
DOI: 10.1111/ijfs.12244

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ISTEX:1AF6E50A0A987340AA1DCB0C6576A84E7AF5DF12

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<note>Figure S1. Kinetics study of the reduction of the DPPH‐ESR signal by ethanolic extract of propolis (EEP). Figure S2. Determination of antioxidative potential of ethanolic extract of propolis (EEP) against DPPH. Figure S3. Determination of antioxidative capacity of ethanolic extract of propolis (EEP) against DPPH.</note>
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<orgName>University of Ibn Khaldoun</orgName>
<address>
<city>Tiaret</city>
<postCode>14000</postCode>
<country>Algeria</country>
</address>
</affiliation>
<affiliation countryCode="JP" type="organization" xml:id="ijfs12244-aff-0002">
<orgDiv>Graduate School of Pure and Applied Sciences</orgDiv>
<orgName>University of Tsukuba</orgName>
<address>
<street>1‐1‐1 Tennodai</street>
<city>Tsukuba</city>
<countryPart>Ibaraki</countryPart>
<postCode>305‐8573</postCode>
<country>Japan</country>
</address>
</affiliation>
<affiliation countryCode="DZ" type="organization" xml:id="ijfs12244-aff-0003">
<orgDiv>Department of Agricultural Sciences</orgDiv>
<orgDiv>Faculty of life and natural Sciences</orgDiv>
<orgName>University of Mascara</orgName>
<address>
<postCode>29000</postCode>
<country>Algeria</country>
</address>
</affiliation>
</affiliationGroup>
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<keyword xml:id="ijfs12244-kwd-0001">2,2‐diphenyl‐1‐picrylhydrazyl</keyword>
<keyword xml:id="ijfs12244-kwd-0002">
<fc>A</fc>
lgerian propolis</keyword>
<keyword xml:id="ijfs12244-kwd-0003">antibacterial activity</keyword>
<keyword xml:id="ijfs12244-kwd-0004">antioxidants</keyword>
<keyword xml:id="ijfs12244-kwd-0005">electron spin resonance</keyword>
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<fundingAgency>Ministry of higher education and Scientific Research</fundingAgency>
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<caption>
<p>
<b>Figure S1.</b>
Kinetics study of the reduction of the DPPH‐ESR signal by ethanolic extract of propolis (EEP).</p>
<p>
<b>Figure S2.</b>
Determination of antioxidative potential of ethanolic extract of propolis (EEP) against DPPH.</p>
<p>
<b>Figure S3.</b>
Determination of antioxidative capacity of ethanolic extract of propolis (EEP) against DPPH.</p>
</caption>
</supportingInfoItem>
</supportingInformation>
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<abstract type="main" xml:id="ijfs12244-abs-0001">
<title type="main">Summary</title>
<p>The aim of this study was the investigation of antimicrobial and antioxidant activities of different ethanolic extracts of propolis (
<fc>EEP</fc>
) collected from north‐western
<fc>A</fc>
lgeria. Total polyphenols and flavonoids contents of extracts were measured. The
<fc>UV</fc>
absorption spectrum showed and confirmed their polyphenols constituents. All
<fc>EEP</fc>
s exerted antibacterial activity against Gram‐positive bacteria, but no effect on Gram‐negative bacteria. The minimum inhibitory concentration (
<fc>MIC</fc>
) of
<fc>EEP</fc>
s ranged from 0.01% to 2.6% v/v. The antioxidant activity was measured using ferric‐reducing power (
<fc>FRAP</fc>
), 1,1‐diphenyl‐2‐picrylhydrazyl (
<fc>DPPH</fc>
) free radical‐scavenging and
<fc>ESR</fc>
methods. Propolis
<fc>TIA</fc>
‐2 and
<fc>MOH</fc>
<fc>MAS</fc>
samples showed the highest antioxidative capacity, after 35 min, while
<fc>TIA</fc>
‐1,
<fc>NED</fc>
<fc>TL</fc>
and
<fc>SFS</fc>
<fc>SBA</fc>
samples showed the highest antioxidative potential of measured
<fc>EEP</fc>
s, after 3 min.
<fc>TIA</fc>
‐2 sample showed the highest antibacterial, antioxidant activity and highest
<fc>DPPH</fc>
free radical‐scavenging activity as well as the highest polyphenols and flavonoids content, compared with other propolis samples.</p>
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<title>Antimicrobial and antioxidant activities of different propolis samples from north‐western Algeria</title>
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<title>Antimicrobial and antioxidant activities of different propolis samples from north‐western Algeria</title>
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<name type="personal">
<namePart type="given">Mokhtar</namePart>
<namePart type="family">Benhanifia</namePart>
<affiliation>Laboratory of Research on Local Animal Products, Institute of Veterinary Sciences, University of Ibn Khaldoun, 14000, Tiaret, Algeria</affiliation>
<affiliation>Graduate School of Pure and Applied Sciences, University of Tsukuba, 1‐1‐1 Tennodai, Ibaraki, 305‐8573, Tsukuba, Japan</affiliation>
<description>Correspondence: Correspondent: E‐mails: ; </description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Wessam M.</namePart>
<namePart type="family">Mohamed</namePart>
<affiliation>Graduate School of Pure and Applied Sciences, University of Tsukuba, 1‐1‐1 Tennodai, Ibaraki, 305‐8573, Tsukuba, Japan</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
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<name type="personal">
<namePart type="given">Yuva</namePart>
<namePart type="family">Bellik</namePart>
<affiliation>Laboratory of Research on Local Animal Products, Institute of Veterinary Sciences, University of Ibn Khaldoun, 14000, Tiaret, Algeria</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Hama</namePart>
<namePart type="family">Benbarek</namePart>
<affiliation>Laboratory of Research on Local Animal Products, Institute of Veterinary Sciences, University of Ibn Khaldoun, 14000, Tiaret, Algeria</affiliation>
<affiliation>Department of Agricultural Sciences, Faculty of life and natural Sciences, University of Mascara, 29000, Algeria</affiliation>
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<dateIssued encoding="w3cdtf">2013-12</dateIssued>
<dateCreated encoding="w3cdtf">2013-06-19</dateCreated>
<dateCaptured encoding="w3cdtf">2012-12-26</dateCaptured>
<dateValid encoding="w3cdtf">2013-06-08</dateValid>
<copyrightDate encoding="w3cdtf">2013</copyrightDate>
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<abstract>The aim of this study was the investigation of antimicrobial and antioxidant activities of different ethanolic extracts of propolis (EEP) collected from north‐western Algeria. Total polyphenols and flavonoids contents of extracts were measured. The UV absorption spectrum showed and confirmed their polyphenols constituents. All EEPs exerted antibacterial activity against Gram‐positive bacteria, but no effect on Gram‐negative bacteria. The minimum inhibitory concentration (MIC) of EEPs ranged from 0.01% to 2.6% v/v. The antioxidant activity was measured using ferric‐reducing power (FRAP), 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) free radical‐scavenging and ESR methods. Propolis TIA‐2 and MOH‐MAS samples showed the highest antioxidative capacity, after 35 min, while TIA‐1, NED‐TL and SFS‐SBA samples showed the highest antioxidative potential of measured EEPs, after 3 min. TIA‐2 sample showed the highest antibacterial, antioxidant activity and highest DPPH free radical‐scavenging activity as well as the highest polyphenols and flavonoids content, compared with other propolis samples.</abstract>
<note type="additional physical form">Figure S1. Kinetics study of the reduction of the DPPH‐ESR signal by ethanolic extract of propolis (EEP). Figure S2. Determination of antioxidative potential of ethanolic extract of propolis (EEP) against DPPH. Figure S3. Determination of antioxidative capacity of ethanolic extract of propolis (EEP) against DPPH.</note>
<note type="funding">Ministry of higher education and Scientific Research</note>
<subject>
<genre>keywords</genre>
<topic>2,2‐diphenyl‐1‐picrylhydrazyl</topic>
<topic>Algerian propolis</topic>
<topic>antibacterial activity</topic>
<topic>antioxidants</topic>
<topic>electron spin resonance</topic>
</subject>
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<title>International Journal of Food Science & Technology</title>
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<titleInfo type="abbreviated">
<title>Int J Food Sci Technol</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>article-category</genre>
<topic>Original Article</topic>
</subject>
<identifier type="ISSN">0950-5423</identifier>
<identifier type="eISSN">1365-2621</identifier>
<identifier type="DOI">10.1111/(ISSN)1365-2621</identifier>
<identifier type="PublisherID">IJFS</identifier>
<part>
<date>2013</date>
<detail type="volume">
<caption>vol.</caption>
<number>48</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>12</number>
</detail>
<extent unit="pages">
<start>2521</start>
<end>2527</end>
<total>7</total>
</extent>
</part>
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<identifier type="DOI">10.1111/ijfs.12244</identifier>
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<accessCondition type="use and reproduction" contentType="copyright">International Journal of Food Science and Technology © 2013 Institute of Food Science and Technology© 2013 The Authors. International Journal of Food Science and Technology © 2013 Institute of Food Science and Technology</accessCondition>
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