Pheophytin a isolated from the seagrass Syringodium isoetifolium plausibly blocks umuC proteins of select bacterial pathogens, in silico
Aims This investigation is designed to evaluate the antibacterial efficiency of the noodle grass Syringodium isoetifolium, which is commonly found in the Indian coastal waters. Also, this study characterizes the active compound and predicts the mode of action in silico. Methods and Results Human pat...
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Veröffentlicht in: | Journal of applied microbiology 2016-12, Vol.121 (6), p.1592-1602 |
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creator | Sathyanathan, C.V. Jyothirmayi, B. Sundaram, L.R. Abhinand, P.A. Eswaramoorthy, R. Gnanambal, K.M.E. |
description | Aims
This investigation is designed to evaluate the antibacterial efficiency of the noodle grass Syringodium isoetifolium, which is commonly found in the Indian coastal waters. Also, this study characterizes the active compound and predicts the mode of action in silico.
Methods and Results
Human pathogenic bacteria were treated with crude metabolites of S. isoetifolium. The potent fraction b was analysed by UV/VIS, Spectroscopy RP‐HPLC, FT‐IR, ESI‐Mass and 1H and 13C NMRs and determined to be a hydrate of pheophytin a (C55H74N4O6). The isolated compound Pheo had MIC values of 6·2 ± 0·7 (Salmonella typhi) and 12·5 ± 0·8 (Escherichia coli and Pseudomonas aeruginosa) μg ml−1. Molecular docking studies of the compound were done to find the binding sites on the pathogens using a Molegro Virtual Docker platform. Pheo targets umuC proteins by binding compactly to five amino acid residues with interaction energy of −3·66 and a Moldock score of −160·175.
Conclusions
Hence, we conclude that pheophytin a, besides being an accessory photosynthetic pigment, also has proven to be antibacterial against human pathogens. Lesser MIC values with definite binding sites predicted in silico are suggestive of a precise of action for this compound.
Significance and Impact of the Study
Easy extraction methods of the active compound that has a definite target render this under‐explored seagrass a good source of antibacterial compound against human pathogenic bacteria. This learning may favour more researches in this unexplored area to build up Pheo‐based natural products as antibiotic therapies. |
doi_str_mv | 10.1111/jam.13312 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1850771938</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4266734061</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3862-6951c29992f9dcd7844a44adae1111cfc538178ed31e3cfd2f28dc6c6386d9c93</originalsourceid><addsrcrecordid>eNqNkd-K1DAUxoMo7h-98AUk4I2C3W2SNmkul0FXZUVBvS6Z5GQmY9p0kxTpG_jYpjurF4JgCCQHfvnynfMh9IzUF6Ssy4MaLghjhD5Ap4TxtqJc0Id396Zqa0FP0FlKh7omrG75Y3RCBZdScnKKfn7eQ5j2S3YjVtil4FUGg20MA857wAnULqqU8JclunEXjJuHFYPsbPBrMXk1J7f1C976oL8nPA_zBk8xZHBjwsEWDQ86463SGaJTHk8q78MOxvQal2-T806HJ-iRVT7B0_vzHH17--br5l118-n6_ebqptKs47TisiWaFvPUSqON6JpGlW0UrJPQVresI6IDwwgwbQ21tDOaa15eG6klO0cvj7rF4e0MKfeDSxq8VyOEOfWkKwMTRLLuP1DWslY0oinoi7_QQ5jjWBopVNNIKSRfqVdHSseQUgTbT9ENKi49qfvVf1-S7O-SLOzze8V5O4D5Q_6OrgCXR-CH87D8W6n_cPXxKPkLRqqpeA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1844997964</pqid></control><display><type>article</type><title>Pheophytin a isolated from the seagrass Syringodium isoetifolium plausibly blocks umuC proteins of select bacterial pathogens, in silico</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Sathyanathan, C.V. ; Jyothirmayi, B. ; Sundaram, L.R. ; Abhinand, P.A. ; Eswaramoorthy, R. ; Gnanambal, K.M.E.</creator><creatorcontrib>Sathyanathan, C.V. ; Jyothirmayi, B. ; Sundaram, L.R. ; Abhinand, P.A. ; Eswaramoorthy, R. ; Gnanambal, K.M.E.</creatorcontrib><description>Aims
This investigation is designed to evaluate the antibacterial efficiency of the noodle grass Syringodium isoetifolium, which is commonly found in the Indian coastal waters. Also, this study characterizes the active compound and predicts the mode of action in silico.
Methods and Results
Human pathogenic bacteria were treated with crude metabolites of S. isoetifolium. The potent fraction b was analysed by UV/VIS, Spectroscopy RP‐HPLC, FT‐IR, ESI‐Mass and 1H and 13C NMRs and determined to be a hydrate of pheophytin a (C55H74N4O6). The isolated compound Pheo had MIC values of 6·2 ± 0·7 (Salmonella typhi) and 12·5 ± 0·8 (Escherichia coli and Pseudomonas aeruginosa) μg ml−1. Molecular docking studies of the compound were done to find the binding sites on the pathogens using a Molegro Virtual Docker platform. Pheo targets umuC proteins by binding compactly to five amino acid residues with interaction energy of −3·66 and a Moldock score of −160·175.
Conclusions
Hence, we conclude that pheophytin a, besides being an accessory photosynthetic pigment, also has proven to be antibacterial against human pathogens. Lesser MIC values with definite binding sites predicted in silico are suggestive of a precise of action for this compound.
Significance and Impact of the Study
Easy extraction methods of the active compound that has a definite target render this under‐explored seagrass a good source of antibacterial compound against human pathogenic bacteria. This learning may favour more researches in this unexplored area to build up Pheo‐based natural products as antibiotic therapies.</description><identifier>ISSN: 1364-5072</identifier><identifier>EISSN: 1365-2672</identifier><identifier>DOI: 10.1111/jam.13312</identifier><identifier>PMID: 27699961</identifier><identifier>CODEN: JAMIFK</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Alismatales - chemistry ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - isolation & purification ; Anti-Bacterial Agents - pharmacology ; antibacterial ; Bacterial Proteins - antagonists & inhibitors ; Bacterial Proteins - chemistry ; Computer Simulation ; DNA-Directed DNA Polymerase - chemistry ; Escherichia coli ; Escherichia coli - drug effects ; Escherichia coli Proteins - chemistry ; in silico ; Microbiology ; Molecular Docking Simulation ; Pathogens ; pheophytin a ; Pheophytins - chemistry ; Pheophytins - isolation & purification ; Pheophytins - pharmacology ; Proteins ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - drug effects ; Salmonella typhi ; Salmonella typhi - drug effects ; Syringodium isoetifolium ; umuC proteins</subject><ispartof>Journal of applied microbiology, 2016-12, Vol.121 (6), p.1592-1602</ispartof><rights>2016 The Society for Applied Microbiology</rights><rights>2016 The Society for Applied Microbiology.</rights><rights>Copyright © 2016 The Society for Applied Microbiology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3862-6951c29992f9dcd7844a44adae1111cfc538178ed31e3cfd2f28dc6c6386d9c93</citedby><cites>FETCH-LOGICAL-c3862-6951c29992f9dcd7844a44adae1111cfc538178ed31e3cfd2f28dc6c6386d9c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjam.13312$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjam.13312$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27699961$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sathyanathan, C.V.</creatorcontrib><creatorcontrib>Jyothirmayi, B.</creatorcontrib><creatorcontrib>Sundaram, L.R.</creatorcontrib><creatorcontrib>Abhinand, P.A.</creatorcontrib><creatorcontrib>Eswaramoorthy, R.</creatorcontrib><creatorcontrib>Gnanambal, K.M.E.</creatorcontrib><title>Pheophytin a isolated from the seagrass Syringodium isoetifolium plausibly blocks umuC proteins of select bacterial pathogens, in silico</title><title>Journal of applied microbiology</title><addtitle>J Appl Microbiol</addtitle><description>Aims
This investigation is designed to evaluate the antibacterial efficiency of the noodle grass Syringodium isoetifolium, which is commonly found in the Indian coastal waters. Also, this study characterizes the active compound and predicts the mode of action in silico.
Methods and Results
Human pathogenic bacteria were treated with crude metabolites of S. isoetifolium. The potent fraction b was analysed by UV/VIS, Spectroscopy RP‐HPLC, FT‐IR, ESI‐Mass and 1H and 13C NMRs and determined to be a hydrate of pheophytin a (C55H74N4O6). The isolated compound Pheo had MIC values of 6·2 ± 0·7 (Salmonella typhi) and 12·5 ± 0·8 (Escherichia coli and Pseudomonas aeruginosa) μg ml−1. Molecular docking studies of the compound were done to find the binding sites on the pathogens using a Molegro Virtual Docker platform. Pheo targets umuC proteins by binding compactly to five amino acid residues with interaction energy of −3·66 and a Moldock score of −160·175.
Conclusions
Hence, we conclude that pheophytin a, besides being an accessory photosynthetic pigment, also has proven to be antibacterial against human pathogens. Lesser MIC values with definite binding sites predicted in silico are suggestive of a precise of action for this compound.
Significance and Impact of the Study
Easy extraction methods of the active compound that has a definite target render this under‐explored seagrass a good source of antibacterial compound against human pathogenic bacteria. This learning may favour more researches in this unexplored area to build up Pheo‐based natural products as antibiotic therapies.</description><subject>Alismatales - chemistry</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - isolation & purification</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antibacterial</subject><subject>Bacterial Proteins - antagonists & inhibitors</subject><subject>Bacterial Proteins - chemistry</subject><subject>Computer Simulation</subject><subject>DNA-Directed DNA Polymerase - chemistry</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli Proteins - chemistry</subject><subject>in silico</subject><subject>Microbiology</subject><subject>Molecular Docking Simulation</subject><subject>Pathogens</subject><subject>pheophytin a</subject><subject>Pheophytins - chemistry</subject><subject>Pheophytins - isolation & purification</subject><subject>Pheophytins - pharmacology</subject><subject>Proteins</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas aeruginosa - drug effects</subject><subject>Salmonella typhi</subject><subject>Salmonella typhi - drug effects</subject><subject>Syringodium isoetifolium</subject><subject>umuC proteins</subject><issn>1364-5072</issn><issn>1365-2672</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkd-K1DAUxoMo7h-98AUk4I2C3W2SNmkul0FXZUVBvS6Z5GQmY9p0kxTpG_jYpjurF4JgCCQHfvnynfMh9IzUF6Ssy4MaLghjhD5Ap4TxtqJc0Id396Zqa0FP0FlKh7omrG75Y3RCBZdScnKKfn7eQ5j2S3YjVtil4FUGg20MA857wAnULqqU8JclunEXjJuHFYPsbPBrMXk1J7f1C976oL8nPA_zBk8xZHBjwsEWDQ86463SGaJTHk8q78MOxvQal2-T806HJ-iRVT7B0_vzHH17--br5l118-n6_ebqptKs47TisiWaFvPUSqON6JpGlW0UrJPQVresI6IDwwgwbQ21tDOaa15eG6klO0cvj7rF4e0MKfeDSxq8VyOEOfWkKwMTRLLuP1DWslY0oinoi7_QQ5jjWBopVNNIKSRfqVdHSseQUgTbT9ENKi49qfvVf1-S7O-SLOzze8V5O4D5Q_6OrgCXR-CH87D8W6n_cPXxKPkLRqqpeA</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Sathyanathan, C.V.</creator><creator>Jyothirmayi, B.</creator><creator>Sundaram, L.R.</creator><creator>Abhinand, P.A.</creator><creator>Eswaramoorthy, R.</creator><creator>Gnanambal, K.M.E.</creator><general>Oxford University Press</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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201612</creationdate><title>Pheophytin a isolated from the seagrass Syringodium isoetifolium plausibly blocks umuC proteins of select bacterial pathogens, in silico</title><author>Sathyanathan, C.V. ; Jyothirmayi, B. ; Sundaram, L.R. ; Abhinand, P.A. ; Eswaramoorthy, R. ; Gnanambal, K.M.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3862-6951c29992f9dcd7844a44adae1111cfc538178ed31e3cfd2f28dc6c6386d9c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Alismatales - chemistry</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - isolation & purification</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>antibacterial</topic><topic>Bacterial Proteins - antagonists & inhibitors</topic><topic>Bacterial Proteins - chemistry</topic><topic>Computer Simulation</topic><topic>DNA-Directed DNA Polymerase - chemistry</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli Proteins - chemistry</topic><topic>in silico</topic><topic>Microbiology</topic><topic>Molecular Docking Simulation</topic><topic>Pathogens</topic><topic>pheophytin a</topic><topic>Pheophytins - chemistry</topic><topic>Pheophytins - isolation & purification</topic><topic>Pheophytins - pharmacology</topic><topic>Proteins</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - drug effects</topic><topic>Salmonella typhi</topic><topic>Salmonella typhi - drug effects</topic><topic>Syringodium isoetifolium</topic><topic>umuC proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sathyanathan, C.V.</creatorcontrib><creatorcontrib>Jyothirmayi, B.</creatorcontrib><creatorcontrib>Sundaram, L.R.</creatorcontrib><creatorcontrib>Abhinand, P.A.</creatorcontrib><creatorcontrib>Eswaramoorthy, R.</creatorcontrib><creatorcontrib>Gnanambal, K.M.E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sathyanathan, C.V.</au><au>Jyothirmayi, B.</au><au>Sundaram, L.R.</au><au>Abhinand, P.A.</au><au>Eswaramoorthy, R.</au><au>Gnanambal, K.M.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pheophytin a isolated from the seagrass Syringodium isoetifolium plausibly blocks umuC proteins of select bacterial pathogens, in silico</atitle><jtitle>Journal of applied microbiology</jtitle><addtitle>J Appl Microbiol</addtitle><date>2016-12</date><risdate>2016</risdate><volume>121</volume><issue>6</issue><spage>1592</spage><epage>1602</epage><pages>1592-1602</pages><issn>1364-5072</issn><eissn>1365-2672</eissn><coden>JAMIFK</coden><abstract>Aims
This investigation is designed to evaluate the antibacterial efficiency of the noodle grass Syringodium isoetifolium, which is commonly found in the Indian coastal waters. Also, this study characterizes the active compound and predicts the mode of action in silico.
Methods and Results
Human pathogenic bacteria were treated with crude metabolites of S. isoetifolium. The potent fraction b was analysed by UV/VIS, Spectroscopy RP‐HPLC, FT‐IR, ESI‐Mass and 1H and 13C NMRs and determined to be a hydrate of pheophytin a (C55H74N4O6). The isolated compound Pheo had MIC values of 6·2 ± 0·7 (Salmonella typhi) and 12·5 ± 0·8 (Escherichia coli and Pseudomonas aeruginosa) μg ml−1. Molecular docking studies of the compound were done to find the binding sites on the pathogens using a Molegro Virtual Docker platform. Pheo targets umuC proteins by binding compactly to five amino acid residues with interaction energy of −3·66 and a Moldock score of −160·175.
Conclusions
Hence, we conclude that pheophytin a, besides being an accessory photosynthetic pigment, also has proven to be antibacterial against human pathogens. Lesser MIC values with definite binding sites predicted in silico are suggestive of a precise of action for this compound.
Significance and Impact of the Study
Easy extraction methods of the active compound that has a definite target render this under‐explored seagrass a good source of antibacterial compound against human pathogenic bacteria. This learning may favour more researches in this unexplored area to build up Pheo‐based natural products as antibiotic therapies.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>27699961</pmid><doi>10.1111/jam.13312</doi><tpages>11</tpages></addata></record> |
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subjects | Alismatales - chemistry Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - isolation & purification Anti-Bacterial Agents - pharmacology antibacterial Bacterial Proteins - antagonists & inhibitors Bacterial Proteins - chemistry Computer Simulation DNA-Directed DNA Polymerase - chemistry Escherichia coli Escherichia coli - drug effects Escherichia coli Proteins - chemistry in silico Microbiology Molecular Docking Simulation Pathogens pheophytin a Pheophytins - chemistry Pheophytins - isolation & purification Pheophytins - pharmacology Proteins Pseudomonas aeruginosa Pseudomonas aeruginosa - drug effects Salmonella typhi Salmonella typhi - drug effects Syringodium isoetifolium umuC proteins |
title | Pheophytin a isolated from the seagrass Syringodium isoetifolium plausibly blocks umuC proteins of select bacterial pathogens, in silico |
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