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
Hauptverfasser: Sathyanathan, C.V., Jyothirmayi, B., Sundaram, L.R., Abhinand, P.A., Eswaramoorthy, R., Gnanambal, K.M.E.
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container_end_page 1602
container_issue 6
container_start_page 1592
container_title Journal of applied microbiology
container_volume 121
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
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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 &amp; purification ; Anti-Bacterial Agents - pharmacology ; antibacterial ; Bacterial Proteins - antagonists &amp; 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 &amp; 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. 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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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source MEDLINE; Access via Wiley Online Library; Oxford University Press Journals All Titles (1996-Current)
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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