novel hydroxamic acid‐containing antibiotic produced by a Saharan soil‐living Streptomyces strain
During screening for potentially antimicrobial actinobacteria, a highly antagonistic strain, designated WAB9, was isolated from a Saharan soil of Algeria. A polyphasic approach characterized the strain taxonomically as a member of the genus Streptomyces. The strain WAB9 exhibited a broad spectrum of...
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description | During screening for potentially antimicrobial actinobacteria, a highly antagonistic strain, designated WAB9, was isolated from a Saharan soil of Algeria. A polyphasic approach characterized the strain taxonomically as a member of the genus Streptomyces. The strain WAB9 exhibited a broad spectrum of antimicrobial activity toward various multidrug‐resistant micro‐organisms. A PCR‐based assay of genomic potential for producing bioactive metabolites revealed the presence of PKS‐II gene. After 6 days of strain fermentation, one bioactive compound was extracted from the remaining aqueous phase and then purified by HPLC. The chemical structure of the compound was determined by spectroscopic (UV–visible, and¹H and¹³C NMR) and spectrometric analysis. The compound was identified to be 2‐amino‐N‐(2‐amino‐3‐phenylpropanoyl)‐N‐hydroxy‐3‐phenylpropanamide, a novel hydroxamic acid‐containing molecule. The pure molecule showed appreciable minimum inhibitory concentration values against a selection of drug‐resistant bacteria, filamentous fungi and yeasts. SIGNIFICANCE AND IMPACT OF THE STUDY: This study presents the isolation of a Streptomyces strain, named WAB9, from a Saharan soil in Algeria. This strain was found to produce a new hydroxamic acid‐containing molecule with interesting antimicrobial activities towards various multidrug‐resistant micro‐organisms. Although hydroxamic acid‐containing molecules are known to exhibit low toxicities in general, only real evaluations of the toxicity levels could decide on the applications for which this new molecule is potentially most appropriate. Thus, this article provides a new framework of research. |
doi_str_mv | 10.1111/lam.12412 |
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A polyphasic approach characterized the strain taxonomically as a member of the genus Streptomyces. The strain WAB9 exhibited a broad spectrum of antimicrobial activity toward various multidrug‐resistant micro‐organisms. A PCR‐based assay of genomic potential for producing bioactive metabolites revealed the presence of PKS‐II gene. After 6 days of strain fermentation, one bioactive compound was extracted from the remaining aqueous phase and then purified by HPLC. The chemical structure of the compound was determined by spectroscopic (UV–visible, and¹H and¹³C NMR) and spectrometric analysis. The compound was identified to be 2‐amino‐N‐(2‐amino‐3‐phenylpropanoyl)‐N‐hydroxy‐3‐phenylpropanamide, a novel hydroxamic acid‐containing molecule. The pure molecule showed appreciable minimum inhibitory concentration values against a selection of drug‐resistant bacteria, filamentous fungi and yeasts. SIGNIFICANCE AND IMPACT OF THE STUDY: This study presents the isolation of a Streptomyces strain, named WAB9, from a Saharan soil in Algeria. This strain was found to produce a new hydroxamic acid‐containing molecule with interesting antimicrobial activities towards various multidrug‐resistant micro‐organisms. Although hydroxamic acid‐containing molecules are known to exhibit low toxicities in general, only real evaluations of the toxicity levels could decide on the applications for which this new molecule is potentially most appropriate. Thus, this article provides a new framework of research.</description><identifier>ISSN: 0266-8254</identifier><identifier>EISSN: 1472-765X</identifier><identifier>DOI: 10.1111/lam.12412</identifier><identifier>PMID: 25754683</identifier><identifier>CODEN: LAMIE7</identifier><language>eng</language><publisher>England: Published for the Society for Applied Bacteriology by Blackwell Scientific Publications [c1985-]</publisher><subject>Algeria ; Anti-Bacterial Agents - biosynthesis ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; anti-infective properties ; antibiotics ; antimicrobial activity ; bacteria ; Bacteria - drug effects ; Bacteriology ; Biodiversity ; Biotechnology ; Chemical and Process Engineering ; chemical structure ; Chromatography, High Pressure Liquid ; Drug Resistance, Multiple, Bacterial - drug effects ; Drug Resistance, Multiple, Fungal - drug effects ; Engineering Sciences ; fermentation ; genes ; high performance liquid chromatography ; hydroxamic acid ; Hydroxamic Acids - chemistry ; Hydroxamic Acids - metabolism ; Hydroxamic Acids - pharmacology ; Life Sciences ; metabolites ; Microbial Sensitivity Tests ; Microbiology and Parasitology ; minimum inhibitory concentration ; multiple drug resistance ; nuclear magnetic resonance spectroscopy ; polymerase chain reaction ; screening ; Soil ; Soil Microbiology ; Streptomyces ; Streptomyces - genetics ; Streptomyces - isolation & purification ; Streptomyces - metabolism ; structure elucidation ; Systematics, Phylogenetics and taxonomy ; taxonomy ; toxicity ; yeasts ; Yeasts - drug effects</subject><ispartof>Letters in applied microbiology, 2015-06, Vol.60 (6), p.589-596</ispartof><rights>2015 The Society for Applied Microbiology</rights><rights>2015 The Society for Applied Microbiology.</rights><rights>Copyright © 2015 The Society for Applied Microbiology</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4112-480ef7d063c004ecb9ec8d0e6908186f5fe64abc5c721e665a86d7fe6fae14113</citedby><cites>FETCH-LOGICAL-c4112-480ef7d063c004ecb9ec8d0e6908186f5fe64abc5c721e665a86d7fe6fae14113</cites><orcidid>0000-0003-3989-3021 ; 0000-0003-3071-9561</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Flam.12412$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Flam.12412$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25754683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01938007$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Yekkour, A</creatorcontrib><creatorcontrib>Meklat, A</creatorcontrib><creatorcontrib>Bijani, C</creatorcontrib><creatorcontrib>Toumatia, O</creatorcontrib><creatorcontrib>Errakhi, R</creatorcontrib><creatorcontrib>Lebrihi, A</creatorcontrib><creatorcontrib>Mathieu, F</creatorcontrib><creatorcontrib>Zitouni, A</creatorcontrib><creatorcontrib>Sabaou, N</creatorcontrib><title>novel hydroxamic acid‐containing antibiotic produced by a Saharan soil‐living Streptomyces strain</title><title>Letters in applied microbiology</title><addtitle>Lett Appl Microbiol</addtitle><description>During screening for potentially antimicrobial actinobacteria, a highly antagonistic strain, designated WAB9, was isolated from a Saharan soil of Algeria. A polyphasic approach characterized the strain taxonomically as a member of the genus Streptomyces. The strain WAB9 exhibited a broad spectrum of antimicrobial activity toward various multidrug‐resistant micro‐organisms. A PCR‐based assay of genomic potential for producing bioactive metabolites revealed the presence of PKS‐II gene. After 6 days of strain fermentation, one bioactive compound was extracted from the remaining aqueous phase and then purified by HPLC. The chemical structure of the compound was determined by spectroscopic (UV–visible, and¹H and¹³C NMR) and spectrometric analysis. The compound was identified to be 2‐amino‐N‐(2‐amino‐3‐phenylpropanoyl)‐N‐hydroxy‐3‐phenylpropanamide, a novel hydroxamic acid‐containing molecule. The pure molecule showed appreciable minimum inhibitory concentration values against a selection of drug‐resistant bacteria, filamentous fungi and yeasts. SIGNIFICANCE AND IMPACT OF THE STUDY: This study presents the isolation of a Streptomyces strain, named WAB9, from a Saharan soil in Algeria. This strain was found to produce a new hydroxamic acid‐containing molecule with interesting antimicrobial activities towards various multidrug‐resistant micro‐organisms. Although hydroxamic acid‐containing molecules are known to exhibit low toxicities in general, only real evaluations of the toxicity levels could decide on the applications for which this new molecule is potentially most appropriate. Thus, this article provides a new framework of research.</description><subject>Algeria</subject><subject>Anti-Bacterial Agents - biosynthesis</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>anti-infective properties</subject><subject>antibiotics</subject><subject>antimicrobial activity</subject><subject>bacteria</subject><subject>Bacteria - drug effects</subject><subject>Bacteriology</subject><subject>Biodiversity</subject><subject>Biotechnology</subject><subject>Chemical and Process Engineering</subject><subject>chemical structure</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Drug Resistance, Multiple, Bacterial - drug effects</subject><subject>Drug Resistance, Multiple, Fungal - drug effects</subject><subject>Engineering Sciences</subject><subject>fermentation</subject><subject>genes</subject><subject>high performance liquid chromatography</subject><subject>hydroxamic acid</subject><subject>Hydroxamic Acids - chemistry</subject><subject>Hydroxamic Acids - metabolism</subject><subject>Hydroxamic Acids - pharmacology</subject><subject>Life Sciences</subject><subject>metabolites</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbiology and Parasitology</subject><subject>minimum inhibitory concentration</subject><subject>multiple drug resistance</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>polymerase chain reaction</subject><subject>screening</subject><subject>Soil</subject><subject>Soil Microbiology</subject><subject>Streptomyces</subject><subject>Streptomyces - genetics</subject><subject>Streptomyces - isolation & purification</subject><subject>Streptomyces - metabolism</subject><subject>structure elucidation</subject><subject>Systematics, Phylogenetics and taxonomy</subject><subject>taxonomy</subject><subject>toxicity</subject><subject>yeasts</subject><subject>Yeasts - drug effects</subject><issn>0266-8254</issn><issn>1472-765X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9u1DAQhy0EokvhwAtAJE4c0tqO_-W4qihFWsRhqcTNmjiTrqskXuzsQm59BJ6RJ8HLtuXEXEYaf_Np_CPkNaNnLNd5D8MZ44LxJ2TBhOalVvLbU7KgXKnScClOyIuUbimlhvH6OTnhUkuhTLUgOIY99sVmbmP4CYN3BTjf_r775cI4gR_9eFPAOPnGhyk_bmNodw7bopkLKNawgQhjkYLv80rv9wd8PUXcTmGYHaYiTTFbXpJnHfQJX933U3J9-eHrxVW5-vLx08VyVTrBGC-FodjplqrKUSrQNTU601JUdT7cqE52qAQ0TjrNGSolwahW52EHyLKhOiXvj94N9HYb_QBxtgG8vVqu7GFGWV0ZSvX-wL47svlP33eYJnsbdnHM51mmdG24lsz8M7oYUorYPWoZtYfwbQ7f_g0_s2_ujbtmwPaRfEg7A-dH4Ifvcf6_ya6Wnx-Ub48bHQQLN9Ene73mlElKmTFC8uoPlXyZkg</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Yekkour, A</creator><creator>Meklat, A</creator><creator>Bijani, C</creator><creator>Toumatia, O</creator><creator>Errakhi, R</creator><creator>Lebrihi, A</creator><creator>Mathieu, F</creator><creator>Zitouni, A</creator><creator>Sabaou, N</creator><general>Published for the Society for Applied Bacteriology by Blackwell Scientific Publications [c1985-]</general><general>Oxford University Press</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-3989-3021</orcidid><orcidid>https://orcid.org/0000-0003-3071-9561</orcidid></search><sort><creationdate>201506</creationdate><title>novel hydroxamic acid‐containing antibiotic produced by a Saharan soil‐living Streptomyces strain</title><author>Yekkour, A ; 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A polyphasic approach characterized the strain taxonomically as a member of the genus Streptomyces. The strain WAB9 exhibited a broad spectrum of antimicrobial activity toward various multidrug‐resistant micro‐organisms. A PCR‐based assay of genomic potential for producing bioactive metabolites revealed the presence of PKS‐II gene. After 6 days of strain fermentation, one bioactive compound was extracted from the remaining aqueous phase and then purified by HPLC. The chemical structure of the compound was determined by spectroscopic (UV–visible, and¹H and¹³C NMR) and spectrometric analysis. The compound was identified to be 2‐amino‐N‐(2‐amino‐3‐phenylpropanoyl)‐N‐hydroxy‐3‐phenylpropanamide, a novel hydroxamic acid‐containing molecule. The pure molecule showed appreciable minimum inhibitory concentration values against a selection of drug‐resistant bacteria, filamentous fungi and yeasts. SIGNIFICANCE AND IMPACT OF THE STUDY: This study presents the isolation of a Streptomyces strain, named WAB9, from a Saharan soil in Algeria. This strain was found to produce a new hydroxamic acid‐containing molecule with interesting antimicrobial activities towards various multidrug‐resistant micro‐organisms. Although hydroxamic acid‐containing molecules are known to exhibit low toxicities in general, only real evaluations of the toxicity levels could decide on the applications for which this new molecule is potentially most appropriate. Thus, this article provides a new framework of research.</abstract><cop>England</cop><pub>Published for the Society for Applied Bacteriology by Blackwell Scientific Publications [c1985-]</pub><pmid>25754683</pmid><doi>10.1111/lam.12412</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-3989-3021</orcidid><orcidid>https://orcid.org/0000-0003-3071-9561</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals; Alma/SFX Local Collection |
subjects | Algeria Anti-Bacterial Agents - biosynthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology anti-infective properties antibiotics antimicrobial activity bacteria Bacteria - drug effects Bacteriology Biodiversity Biotechnology Chemical and Process Engineering chemical structure Chromatography, High Pressure Liquid Drug Resistance, Multiple, Bacterial - drug effects Drug Resistance, Multiple, Fungal - drug effects Engineering Sciences fermentation genes high performance liquid chromatography hydroxamic acid Hydroxamic Acids - chemistry Hydroxamic Acids - metabolism Hydroxamic Acids - pharmacology Life Sciences metabolites Microbial Sensitivity Tests Microbiology and Parasitology minimum inhibitory concentration multiple drug resistance nuclear magnetic resonance spectroscopy polymerase chain reaction screening Soil Soil Microbiology Streptomyces Streptomyces - genetics Streptomyces - isolation & purification Streptomyces - metabolism structure elucidation Systematics, Phylogenetics and taxonomy taxonomy toxicity yeasts Yeasts - drug effects |
title | novel hydroxamic acid‐containing antibiotic produced by a Saharan soil‐living Streptomyces strain |
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