Purification, structural elucidation and bioactivity of tryptophan containing diketopiperazines, from Comamonas testosteroni associated with a rhabditid entomopathogenic nematode against major human-pathogenic bacteria
•Isolated five tryptophan containing cyclic dipeptideswere from Comamonas testosteroni associated with Rhabditis sp.•The compounds were identified as Cyclo-(L-Trp-L-Pro), Cyclo-(L-Trp-L-Tyr), Cyclo-(L-Trp-L-Ile), Cyclo-(L-Trp-L-Leu) and Cyclo-(L-Trp-L-Phe), respectively.•To our knowledge this is the...
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description | •Isolated five tryptophan containing cyclic dipeptideswere from Comamonas testosteroni associated with Rhabditis sp.•The compounds were identified as Cyclo-(L-Trp-L-Pro), Cyclo-(L-Trp-L-Tyr), Cyclo-(L-Trp-L-Ile), Cyclo-(L-Trp-L-Leu) and Cyclo-(L-Trp-L-Phe), respectively.•To our knowledge this is the first report of antibacterial activity of the diketopiperazines against the human pathogenic bacteria.•Thus C. testosteroni is promising sources of natural bioactive secondary metabolites which may receive great benefit in the field of human medicine in near future.
The cell free culture filtrate of a Comamonas testosteroni associated with an Entomopathogenic nematode (EPN), Rhabditis (Oscheius) sp. exhibited promising antimicrobial activity. The ethyl acetate extract of the bacterial culture filtrate was purified by silica gel column chromatography to obtain five diketopiperazines or cyclic dipeptides (DKP 1–5). The structure and absolute stereochemistry of the compounds were determined based on extensive spectroscopic analyses (HR-MS, 1HNMR, 13CNMR, 1H–1H COSY, 1H–13C HMBC) and Marfey's method. Based on the spectral data the compounds were identified as Cyclo-(L-Trp-L-Pro) (1), Cyclo-(L-Trp-L-Tyr) (2), Cyclo-(L-Trp-L-Ile) (3), Cyclo-(L-Trp-L-Leu) (4) and Cyclo-(L-Trp-L-Phe) (5), respectively. Three diketopiperazines (DKP 2, 3 and 5) were active against all the ten bacteria tested. The highest activity of 0.5μg/ml by Cyclo-(L-Trp-L-Phe) was recorded against Vibrio cholerae followed by Salmonella typhi (1μg/ml) a human pathogen responsible for life threatening diseases like profuse watery diarrhea and typhoid or enteric fever. The activity of this compound against V. cholerae and S. typhi is more effective than ciprofloxacin and ampicillin, the standard antibiotics. Cyclo-(L-Trp-L-Phe) recorded significant antibacterial activity against all the test bacteria when compared to other compounds. Five diketopiperazines were active against all the test fungi and are more effective than bavistin the standard fungicide. Diketopiperazines recorded no cytotoxicity to FS normal fibroblast and VERO cells (African green monkey kidney) except DKP 3 and 4. To our best knowledge this is the first report of antimicrobial activity of the tryptophan containing diketopiperazines against the human pathogenic microbes. The production of cyclic dipeptides by C. testosteroni is also reported here for the first time. We conclude that the C. testosteroni is promising sources of natural |
doi_str_mv | 10.1016/j.peptides.2013.09.019 |
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The cell free culture filtrate of a Comamonas testosteroni associated with an Entomopathogenic nematode (EPN), Rhabditis (Oscheius) sp. exhibited promising antimicrobial activity. The ethyl acetate extract of the bacterial culture filtrate was purified by silica gel column chromatography to obtain five diketopiperazines or cyclic dipeptides (DKP 1–5). The structure and absolute stereochemistry of the compounds were determined based on extensive spectroscopic analyses (HR-MS, 1HNMR, 13CNMR, 1H–1H COSY, 1H–13C HMBC) and Marfey's method. Based on the spectral data the compounds were identified as Cyclo-(L-Trp-L-Pro) (1), Cyclo-(L-Trp-L-Tyr) (2), Cyclo-(L-Trp-L-Ile) (3), Cyclo-(L-Trp-L-Leu) (4) and Cyclo-(L-Trp-L-Phe) (5), respectively. Three diketopiperazines (DKP 2, 3 and 5) were active against all the ten bacteria tested. The highest activity of 0.5μg/ml by Cyclo-(L-Trp-L-Phe) was recorded against Vibrio cholerae followed by Salmonella typhi (1μg/ml) a human pathogen responsible for life threatening diseases like profuse watery diarrhea and typhoid or enteric fever. The activity of this compound against V. cholerae and S. typhi is more effective than ciprofloxacin and ampicillin, the standard antibiotics. Cyclo-(L-Trp-L-Phe) recorded significant antibacterial activity against all the test bacteria when compared to other compounds. Five diketopiperazines were active against all the test fungi and are more effective than bavistin the standard fungicide. Diketopiperazines recorded no cytotoxicity to FS normal fibroblast and VERO cells (African green monkey kidney) except DKP 3 and 4. To our best knowledge this is the first report of antimicrobial activity of the tryptophan containing diketopiperazines against the human pathogenic microbes. The production of cyclic dipeptides by C. testosteroni is also reported here for the first time. We conclude that the C. testosteroni is promising sources of natural bioactive secondary metabolites against human pathogenic bacteria which may receive great benefit in the field of human medicine in near future.</description><identifier>ISSN: 0196-9781</identifier><identifier>EISSN: 1873-5169</identifier><identifier>DOI: 10.1016/j.peptides.2013.09.019</identifier><identifier>PMID: 24120705</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - isolation & purification ; Anti-Bacterial Agents - pharmacology ; Antibacterial ; Antiinfectives and antibacterials ; Bacteria ; Calorimetry, Differential Scanning ; Cercopithecus aethiops ; Chromatography, Thin Layer ; Comamonas testosteroni ; Culture ; Cyclic dipeptide ; Diketopiperazines - chemistry ; Diketopiperazines - isolation & purification ; Diketopiperazines - pharmacology ; Fungicides ; Human ; Magnetic Resonance Spectroscopy ; Microbial Sensitivity Tests ; Nematoda ; Nematodes ; Phylogeny ; Rhabditis ; Rhabditoidea - metabolism ; Salmonella typhi ; Tryptophan ; Tryptophan - chemistry ; Vibrio cholerae</subject><ispartof>Peptides (New York, N.Y. : 1980), 2014-03, Vol.53, p.48-58</ispartof><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-814edf75cdce7950212c9eee14953616277c40612582b7a46fdedcc31ef1cb1e3</citedby><cites>FETCH-LOGICAL-c434t-814edf75cdce7950212c9eee14953616277c40612582b7a46fdedcc31ef1cb1e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.peptides.2013.09.019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24120705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishanth Kumar, S.</creatorcontrib><creatorcontrib>Mohandas, C.</creatorcontrib><creatorcontrib>Nambisan, Bala</creatorcontrib><title>Purification, structural elucidation and bioactivity of tryptophan containing diketopiperazines, from Comamonas testosteroni associated with a rhabditid entomopathogenic nematode against major human-pathogenic bacteria</title><title>Peptides (New York, N.Y. : 1980)</title><addtitle>Peptides</addtitle><description>•Isolated five tryptophan containing cyclic dipeptideswere from Comamonas testosteroni associated with Rhabditis sp.•The compounds were identified as Cyclo-(L-Trp-L-Pro), Cyclo-(L-Trp-L-Tyr), Cyclo-(L-Trp-L-Ile), Cyclo-(L-Trp-L-Leu) and Cyclo-(L-Trp-L-Phe), respectively.•To our knowledge this is the first report of antibacterial activity of the diketopiperazines against the human pathogenic bacteria.•Thus C. testosteroni is promising sources of natural bioactive secondary metabolites which may receive great benefit in the field of human medicine in near future.
The cell free culture filtrate of a Comamonas testosteroni associated with an Entomopathogenic nematode (EPN), Rhabditis (Oscheius) sp. exhibited promising antimicrobial activity. The ethyl acetate extract of the bacterial culture filtrate was purified by silica gel column chromatography to obtain five diketopiperazines or cyclic dipeptides (DKP 1–5). The structure and absolute stereochemistry of the compounds were determined based on extensive spectroscopic analyses (HR-MS, 1HNMR, 13CNMR, 1H–1H COSY, 1H–13C HMBC) and Marfey's method. Based on the spectral data the compounds were identified as Cyclo-(L-Trp-L-Pro) (1), Cyclo-(L-Trp-L-Tyr) (2), Cyclo-(L-Trp-L-Ile) (3), Cyclo-(L-Trp-L-Leu) (4) and Cyclo-(L-Trp-L-Phe) (5), respectively. Three diketopiperazines (DKP 2, 3 and 5) were active against all the ten bacteria tested. The highest activity of 0.5μg/ml by Cyclo-(L-Trp-L-Phe) was recorded against Vibrio cholerae followed by Salmonella typhi (1μg/ml) a human pathogen responsible for life threatening diseases like profuse watery diarrhea and typhoid or enteric fever. The activity of this compound against V. cholerae and S. typhi is more effective than ciprofloxacin and ampicillin, the standard antibiotics. Cyclo-(L-Trp-L-Phe) recorded significant antibacterial activity against all the test bacteria when compared to other compounds. Five diketopiperazines were active against all the test fungi and are more effective than bavistin the standard fungicide. Diketopiperazines recorded no cytotoxicity to FS normal fibroblast and VERO cells (African green monkey kidney) except DKP 3 and 4. To our best knowledge this is the first report of antimicrobial activity of the tryptophan containing diketopiperazines against the human pathogenic microbes. The production of cyclic dipeptides by C. testosteroni is also reported here for the first time. We conclude that the C. testosteroni is promising sources of natural bioactive secondary metabolites against human pathogenic bacteria which may receive great benefit in the field of human medicine in near future.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - isolation & purification</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterial</subject><subject>Antiinfectives and antibacterials</subject><subject>Bacteria</subject><subject>Calorimetry, Differential Scanning</subject><subject>Cercopithecus aethiops</subject><subject>Chromatography, Thin Layer</subject><subject>Comamonas testosteroni</subject><subject>Culture</subject><subject>Cyclic dipeptide</subject><subject>Diketopiperazines - chemistry</subject><subject>Diketopiperazines - isolation & purification</subject><subject>Diketopiperazines - pharmacology</subject><subject>Fungicides</subject><subject>Human</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Microbial Sensitivity Tests</subject><subject>Nematoda</subject><subject>Nematodes</subject><subject>Phylogeny</subject><subject>Rhabditis</subject><subject>Rhabditoidea - metabolism</subject><subject>Salmonella typhi</subject><subject>Tryptophan</subject><subject>Tryptophan - chemistry</subject><subject>Vibrio cholerae</subject><issn>0196-9781</issn><issn>1873-5169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks9u1DAQxiMEokvhFSofOTSLnThxcgOt-CdVggOcrYk92Z1lYwfbKVoetU9Tl20Rt3Ia6dNv5psZfUVxIfhacNG-2a9nnBNZjOuKi3rN-zUX_ZNiJTpVl41o-6fFKitt2atOnBUvYtxzzqXsu-fFWSVFxRVvVsXN1yXQSAYSeXfJYgqLSUuAA8PDYsj-0Rk4ywbyYBJdUzoyP7IUjnPy8w4cM94lIEduyyz9wKzSjAF-k8N4ycbgJ7bxE0zeQWQJY_IxYfCOGMToDUFCy35R2jFgYQeDpXwYQ5f85GdIO79FR4Y5nCB5iwy22S0mNsHeB7ZbJnDlP9yQ18RA8LJ4NsIh4qv7el58__D-2-ZTefXl4-fNu6vSyFqmshMS7agaYw2qvuGVqEyPiEL2Td2KtlLKSN6KqumqQYFsR4vWmFrgKMwgsD4vXp_mzsH_XPJ5eqJo8HAAh36JWrRK9W1T9fJxtJGSC96J-j_QPLeqhGoz2p5QE3yMAUc9B5ogHLXg-i4teq8f0qLv0qJ5r3M2cuPFvccyTGj_tj3EIwNvTwDm_10TBh0NoTNoKaBJ2np6zOMWsy_cUw</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Nishanth Kumar, S.</creator><creator>Mohandas, C.</creator><creator>Nambisan, Bala</creator><general>Elsevier Inc</general><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>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>P64</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>20140301</creationdate><title>Purification, structural elucidation and bioactivity of tryptophan containing diketopiperazines, from Comamonas testosteroni associated with a rhabditid entomopathogenic nematode against major human-pathogenic bacteria</title><author>Nishanth Kumar, S. ; 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The cell free culture filtrate of a Comamonas testosteroni associated with an Entomopathogenic nematode (EPN), Rhabditis (Oscheius) sp. exhibited promising antimicrobial activity. The ethyl acetate extract of the bacterial culture filtrate was purified by silica gel column chromatography to obtain five diketopiperazines or cyclic dipeptides (DKP 1–5). The structure and absolute stereochemistry of the compounds were determined based on extensive spectroscopic analyses (HR-MS, 1HNMR, 13CNMR, 1H–1H COSY, 1H–13C HMBC) and Marfey's method. Based on the spectral data the compounds were identified as Cyclo-(L-Trp-L-Pro) (1), Cyclo-(L-Trp-L-Tyr) (2), Cyclo-(L-Trp-L-Ile) (3), Cyclo-(L-Trp-L-Leu) (4) and Cyclo-(L-Trp-L-Phe) (5), respectively. Three diketopiperazines (DKP 2, 3 and 5) were active against all the ten bacteria tested. The highest activity of 0.5μg/ml by Cyclo-(L-Trp-L-Phe) was recorded against Vibrio cholerae followed by Salmonella typhi (1μg/ml) a human pathogen responsible for life threatening diseases like profuse watery diarrhea and typhoid or enteric fever. The activity of this compound against V. cholerae and S. typhi is more effective than ciprofloxacin and ampicillin, the standard antibiotics. Cyclo-(L-Trp-L-Phe) recorded significant antibacterial activity against all the test bacteria when compared to other compounds. Five diketopiperazines were active against all the test fungi and are more effective than bavistin the standard fungicide. Diketopiperazines recorded no cytotoxicity to FS normal fibroblast and VERO cells (African green monkey kidney) except DKP 3 and 4. To our best knowledge this is the first report of antimicrobial activity of the tryptophan containing diketopiperazines against the human pathogenic microbes. The production of cyclic dipeptides by C. testosteroni is also reported here for the first time. We conclude that the C. testosteroni is promising sources of natural bioactive secondary metabolites against human pathogenic bacteria which may receive great benefit in the field of human medicine in near future.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24120705</pmid><doi>10.1016/j.peptides.2013.09.019</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - isolation & purification Anti-Bacterial Agents - pharmacology Antibacterial Antiinfectives and antibacterials Bacteria Calorimetry, Differential Scanning Cercopithecus aethiops Chromatography, Thin Layer Comamonas testosteroni Culture Cyclic dipeptide Diketopiperazines - chemistry Diketopiperazines - isolation & purification Diketopiperazines - pharmacology Fungicides Human Magnetic Resonance Spectroscopy Microbial Sensitivity Tests Nematoda Nematodes Phylogeny Rhabditis Rhabditoidea - metabolism Salmonella typhi Tryptophan Tryptophan - chemistry Vibrio cholerae |
title | Purification, structural elucidation and bioactivity of tryptophan containing diketopiperazines, from Comamonas testosteroni associated with a rhabditid entomopathogenic nematode against major human-pathogenic bacteria |
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