Biodegradation of allethrin, a pyrethroid insecticide, by an Acidomonas sp
Allethrin is a major mosquito repellent agent. To degrade allethrin present in used mats and the environment, a bacterium capable of utilizing allethrin was isolated. This isolate, an Acidomonas sp., grew in minimal medium with 16 mM: allethrin as sole source of carbon and degraded >70% of it in...
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| Veröffentlicht in: | Biotechnology letters 2005-12, Vol.27 (23-24), p.1909-1913 |
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| container_end_page | 1913 |
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| container_issue | 23-24 |
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| container_title | Biotechnology letters |
| container_volume | 27 |
| creator | PAINGANKAR, Mandar JAIN, Manish DEOBAGKAR, Dileep |
| description | Allethrin is a major mosquito repellent agent. To degrade allethrin present in used mats and the environment, a bacterium capable of utilizing allethrin was isolated. This isolate, an Acidomonas sp., grew in minimal medium with 16 mM: allethrin as sole source of carbon and degraded >70% of it in 72 h, with negligible residual metabolites in the medium. Culture filtrates collected after 48 h and 72 h showed presence of (i) cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl), (ii) 2-ethyl-1,3-dimethyl-cyclopent-2-ene-carboxylic acid (iii) chrysanthemic acid and (iv) allethrolone [2-cyclopenten-l-one, 4-hydroxy-3-methyl-2(-2-propenyl)] as the major metabolites with 2 minor metabolites. Allethrin is thus metabolized by a hydrolytic pathway followed by oxidation and dehydrogenation. |
| doi_str_mv | 10.1007/s10529-005-3902-3 |
| format | Article |
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To degrade allethrin present in used mats and the environment, a bacterium capable of utilizing allethrin was isolated. This isolate, an Acidomonas sp., grew in minimal medium with 16 mM: allethrin as sole source of carbon and degraded >70% of it in 72 h, with negligible residual metabolites in the medium. Culture filtrates collected after 48 h and 72 h showed presence of (i) cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl), (ii) 2-ethyl-1,3-dimethyl-cyclopent-2-ene-carboxylic acid (iii) chrysanthemic acid and (iv) allethrolone [2-cyclopenten-l-one, 4-hydroxy-3-methyl-2(-2-propenyl)] as the major metabolites with 2 minor metabolites. Allethrin is thus metabolized by a hydrolytic pathway followed by oxidation and dehydrogenation.</description><identifier>ISSN: 0141-5492</identifier><identifier>EISSN: 1573-6776</identifier><identifier>DOI: 10.1007/s10529-005-3902-3</identifier><identifier>PMID: 16328989</identifier><identifier>CODEN: BILED3</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Acetobacteraceae - cytology ; Acetobacteraceae - isolation & purification ; Acetobacteraceae - metabolism ; Acidomonas ; Allethrin - chemistry ; Allethrin - metabolism ; Biodegradation ; Biodegradation, Environmental ; Biological and medical sciences ; Biotechnology ; Carbon ; Carboxylic acids ; Cell Division ; Culture ; Cyclopentanes - metabolism ; Degradation ; Fundamental and applied biological sciences. Psychology ; Gas Chromatography-Mass Spectrometry ; Insecticides ; Insecticides - metabolism ; Mats ; Metabolites ; Microbiology ; Molecular Structure ; Pathways ; Pyrethrins - metabolism ; Pyrethroids ; Sole</subject><ispartof>Biotechnology letters, 2005-12, Vol.27 (23-24), p.1909-1913</ispartof><rights>2006 INIST-CNRS</rights><rights>Springer 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c587t-1f3159a6eed94d66e016c7fa405971804937bc3abb1ceebc7b02ceeb6ae1ea233</citedby><cites>FETCH-LOGICAL-c587t-1f3159a6eed94d66e016c7fa405971804937bc3abb1ceebc7b02ceeb6ae1ea233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17349007$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16328989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PAINGANKAR, Mandar</creatorcontrib><creatorcontrib>JAIN, Manish</creatorcontrib><creatorcontrib>DEOBAGKAR, Dileep</creatorcontrib><title>Biodegradation of allethrin, a pyrethroid insecticide, by an Acidomonas sp</title><title>Biotechnology letters</title><addtitle>Biotechnol Lett</addtitle><description>Allethrin is a major mosquito repellent agent. To degrade allethrin present in used mats and the environment, a bacterium capable of utilizing allethrin was isolated. This isolate, an Acidomonas sp., grew in minimal medium with 16 mM: allethrin as sole source of carbon and degraded >70% of it in 72 h, with negligible residual metabolites in the medium. Culture filtrates collected after 48 h and 72 h showed presence of (i) cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl), (ii) 2-ethyl-1,3-dimethyl-cyclopent-2-ene-carboxylic acid (iii) chrysanthemic acid and (iv) allethrolone [2-cyclopenten-l-one, 4-hydroxy-3-methyl-2(-2-propenyl)] as the major metabolites with 2 minor metabolites. Allethrin is thus metabolized by a hydrolytic pathway followed by oxidation and dehydrogenation.</description><subject>Acetobacteraceae - cytology</subject><subject>Acetobacteraceae - isolation & purification</subject><subject>Acetobacteraceae - metabolism</subject><subject>Acidomonas</subject><subject>Allethrin - chemistry</subject><subject>Allethrin - metabolism</subject><subject>Biodegradation</subject><subject>Biodegradation, Environmental</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Carbon</subject><subject>Carboxylic acids</subject><subject>Cell Division</subject><subject>Culture</subject><subject>Cyclopentanes - metabolism</subject><subject>Degradation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Insecticides</subject><subject>Insecticides - metabolism</subject><subject>Mats</subject><subject>Metabolites</subject><subject>Microbiology</subject><subject>Molecular Structure</subject><subject>Pathways</subject><subject>Pyrethrins - metabolism</subject><subject>Pyrethroids</subject><subject>Sole</subject><issn>0141-5492</issn><issn>1573-6776</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0U1r3DAQBmBRWpLNxw_opYhC0x7idkaf1jEJaZsQyKU9C1mWWwWvtZW8h_33ldmFQA_pSRp4ZgbmJeQtwmcE0F8KgmSmAZANN8Aa_oqsUGreKK3Va7ICFNhIYdgxOSnlCQCMBn1EjlFx1prWrMj9dUx9-JVd7-aYJpoG6sYxzL9znC6po5tdXooUexqnEvwcfezDJe121E30qhZpnSZXaNmckTeDG0s4P7yn5OfX2x8335uHx293N1cPjZetnhscOErjVAi9Eb1SAVB5PTgB0mhsQRiuO89d16EPofO6A7Z8lAsYHOP8lHzcz93k9GcbymzXsfgwjm4KaVuslkIqbBX7vxQcWs0ZVHnxokTNOBhpKvz0MlSCMcOFlpW-_4c-pW2e6mms5qLuVS1WhHvkcyolh8Fucly7vLMIdgnZ7kO2NWS7hGyXA7w7DN5269A_dxxSreDDAbji3ThkN_lYnl1db-po_hc_2a00</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>PAINGANKAR, Mandar</creator><creator>JAIN, Manish</creator><creator>DEOBAGKAR, Dileep</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</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>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TB</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7QO</scope><scope>7ST</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>SOI</scope></search><sort><creationdate>20051201</creationdate><title>Biodegradation of allethrin, a pyrethroid insecticide, by an Acidomonas sp</title><author>PAINGANKAR, Mandar ; JAIN, Manish ; DEOBAGKAR, Dileep</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c587t-1f3159a6eed94d66e016c7fa405971804937bc3abb1ceebc7b02ceeb6ae1ea233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acetobacteraceae - cytology</topic><topic>Acetobacteraceae - isolation & purification</topic><topic>Acetobacteraceae - metabolism</topic><topic>Acidomonas</topic><topic>Allethrin - chemistry</topic><topic>Allethrin - metabolism</topic><topic>Biodegradation</topic><topic>Biodegradation, Environmental</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Carbon</topic><topic>Carboxylic acids</topic><topic>Cell Division</topic><topic>Culture</topic><topic>Cyclopentanes - metabolism</topic><topic>Degradation</topic><topic>Fundamental and applied biological sciences. 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To degrade allethrin present in used mats and the environment, a bacterium capable of utilizing allethrin was isolated. This isolate, an Acidomonas sp., grew in minimal medium with 16 mM: allethrin as sole source of carbon and degraded >70% of it in 72 h, with negligible residual metabolites in the medium. Culture filtrates collected after 48 h and 72 h showed presence of (i) cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl), (ii) 2-ethyl-1,3-dimethyl-cyclopent-2-ene-carboxylic acid (iii) chrysanthemic acid and (iv) allethrolone [2-cyclopenten-l-one, 4-hydroxy-3-methyl-2(-2-propenyl)] as the major metabolites with 2 minor metabolites. Allethrin is thus metabolized by a hydrolytic pathway followed by oxidation and dehydrogenation.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>16328989</pmid><doi>10.1007/s10529-005-3902-3</doi><tpages>5</tpages></addata></record> |
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| ispartof | Biotechnology letters, 2005-12, Vol.27 (23-24), p.1909-1913 |
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| subjects | Acetobacteraceae - cytology Acetobacteraceae - isolation & purification Acetobacteraceae - metabolism Acidomonas Allethrin - chemistry Allethrin - metabolism Biodegradation Biodegradation, Environmental Biological and medical sciences Biotechnology Carbon Carboxylic acids Cell Division Culture Cyclopentanes - metabolism Degradation Fundamental and applied biological sciences. Psychology Gas Chromatography-Mass Spectrometry Insecticides Insecticides - metabolism Mats Metabolites Microbiology Molecular Structure Pathways Pyrethrins - metabolism Pyrethroids Sole |
| title | Biodegradation of allethrin, a pyrethroid insecticide, by an Acidomonas sp |
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