Loading…

Structural characterization of allomelanin from black oat

The brown to black coloration found in plants is due to the melanins, which have been relatively poorly investigated among the plant pigments. The aim of this work was to study the dark pigment extracted from the black oat hull with respect to composition and structure. Ultraviolet–visible (UV–Vis)...

Full description

Saved in:
Bibliographic Details
Published in:Phytochemistry (Oxford) 2016-10, Vol.130, p.313-320
Main Authors: Varga, Mónika, Berkesi, Ottó, Darula, Zsuzsanna, May, Nóra Veronika, Palágyi, András
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3
cites cdi_FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3
container_end_page 320
container_issue
container_start_page 313
container_title Phytochemistry (Oxford)
container_volume 130
creator Varga, Mónika
Berkesi, Ottó
Darula, Zsuzsanna
May, Nóra Veronika
Palágyi, András
description The brown to black coloration found in plants is due to the melanins, which have been relatively poorly investigated among the plant pigments. The aim of this work was to study the dark pigment extracted from the black oat hull with respect to composition and structure. Ultraviolet–visible (UV–Vis) spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) and Fourier transform infrared (FT-IR) spectroscopy were applied for the characterization of the pigment. UV–Vis spectroscopy revealed that the extracted material displays a broadband, structureless absorption profile a common feature of melanins. MALDI-TOF MS measurements demonstrated that oat melanin is a homopolymer built up from p-coumaric acid and consists mainly of low molecular weight (527–1499 Da) oligomers of 3–9 monomer units. The tetramer oligomer proved to be dominant. The results of the FT-IR analysis indicated that oat melanin is a fully conjugated aromatic system containing tetrasubstituted aromatic rings linked by CC coupling. The in vitro preparation of melanin from p-coumaric acid by horseradish peroxidase was performed for comparison. The resulting polymer consisted of oligomers of 4–9 monomer units similarly to those in oat melanin. However, the building blocks proved to be connected to each other via COC linkages in contrast with the CC linkages in oat melanin. [Display omitted] •The pigment extracted from the black oat was identified as melanin.•Structure was determined by MALDI-TOF MS and FT-IR spectroscopy.•In vitro preparation of oat melanin was attempted.•Structure of the in vitro prepared polymer was elucidated.
doi_str_mv 10.1016/j.phytochem.2016.07.002
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1815368830</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0031942216301297</els_id><sourcerecordid>1815368830</sourcerecordid><originalsourceid>FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3</originalsourceid><addsrcrecordid>eNqFkF1LwzAUhoMobk7_gvbSm9aTjzbt5Rh-wcAL9TqkScoy22UmqTB_vRnT3QoHAofnzZs8CN1gKDDg6m5dbFe76NTKDAVJiwJ4AUBO0BTXnOaUA5yiKQDFecMImaCLENYAUJZVdY4mhLM0lE5R8xr9qOLoZZ-plfRSRePtt4zWbTLXZbLv3WB6ubGbrPNuyNpeqo_MyXiJzjrZB3P1e87Q-8P92-IpX748Pi_my1yxuoq56lJP2WiiWlZzo0uFeVOaVjLZsIbRilaay6YlhLRMaagZbSkuKaiSdJ3u6AzdHu7devc5mhDFYIMyfXqTcWMQuE50VdcUEsoPqPIuBG86sfV2kH4nMIi9N7EWR29i700AF8lbSl7_loztYPQx9ycqAfMDYNJXv6zxIihrNspo642KQjv7b8kPmDeDEA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1815368830</pqid></control><display><type>article</type><title>Structural characterization of allomelanin from black oat</title><source>Elsevier</source><creator>Varga, Mónika ; Berkesi, Ottó ; Darula, Zsuzsanna ; May, Nóra Veronika ; Palágyi, András</creator><creatorcontrib>Varga, Mónika ; Berkesi, Ottó ; Darula, Zsuzsanna ; May, Nóra Veronika ; Palágyi, András</creatorcontrib><description>The brown to black coloration found in plants is due to the melanins, which have been relatively poorly investigated among the plant pigments. The aim of this work was to study the dark pigment extracted from the black oat hull with respect to composition and structure. Ultraviolet–visible (UV–Vis) spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) and Fourier transform infrared (FT-IR) spectroscopy were applied for the characterization of the pigment. UV–Vis spectroscopy revealed that the extracted material displays a broadband, structureless absorption profile a common feature of melanins. MALDI-TOF MS measurements demonstrated that oat melanin is a homopolymer built up from p-coumaric acid and consists mainly of low molecular weight (527–1499 Da) oligomers of 3–9 monomer units. The tetramer oligomer proved to be dominant. The results of the FT-IR analysis indicated that oat melanin is a fully conjugated aromatic system containing tetrasubstituted aromatic rings linked by CC coupling. The in vitro preparation of melanin from p-coumaric acid by horseradish peroxidase was performed for comparison. The resulting polymer consisted of oligomers of 4–9 monomer units similarly to those in oat melanin. However, the building blocks proved to be connected to each other via COC linkages in contrast with the CC linkages in oat melanin. [Display omitted] •The pigment extracted from the black oat was identified as melanin.•Structure was determined by MALDI-TOF MS and FT-IR spectroscopy.•In vitro preparation of oat melanin was attempted.•Structure of the in vitro prepared polymer was elucidated.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2016.07.002</identifier><identifier>PMID: 27427433</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Avena - chemistry ; Avena sativa (Poaceae) ; Coumaric Acids - chemistry ; FT-IR spectroscopy ; MALDI-TOF MS ; Melanin ; Melanins - analysis ; Molecular Weight ; Oat ; p-Coumaric acid ; Pigmentation ; Propionates ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Spectroscopy, Fourier Transform Infrared</subject><ispartof>Phytochemistry (Oxford), 2016-10, Vol.130, p.313-320</ispartof><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3</citedby><cites>FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27427433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Varga, Mónika</creatorcontrib><creatorcontrib>Berkesi, Ottó</creatorcontrib><creatorcontrib>Darula, Zsuzsanna</creatorcontrib><creatorcontrib>May, Nóra Veronika</creatorcontrib><creatorcontrib>Palágyi, András</creatorcontrib><title>Structural characterization of allomelanin from black oat</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>The brown to black coloration found in plants is due to the melanins, which have been relatively poorly investigated among the plant pigments. The aim of this work was to study the dark pigment extracted from the black oat hull with respect to composition and structure. Ultraviolet–visible (UV–Vis) spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) and Fourier transform infrared (FT-IR) spectroscopy were applied for the characterization of the pigment. UV–Vis spectroscopy revealed that the extracted material displays a broadband, structureless absorption profile a common feature of melanins. MALDI-TOF MS measurements demonstrated that oat melanin is a homopolymer built up from p-coumaric acid and consists mainly of low molecular weight (527–1499 Da) oligomers of 3–9 monomer units. The tetramer oligomer proved to be dominant. The results of the FT-IR analysis indicated that oat melanin is a fully conjugated aromatic system containing tetrasubstituted aromatic rings linked by CC coupling. The in vitro preparation of melanin from p-coumaric acid by horseradish peroxidase was performed for comparison. The resulting polymer consisted of oligomers of 4–9 monomer units similarly to those in oat melanin. However, the building blocks proved to be connected to each other via COC linkages in contrast with the CC linkages in oat melanin. [Display omitted] •The pigment extracted from the black oat was identified as melanin.•Structure was determined by MALDI-TOF MS and FT-IR spectroscopy.•In vitro preparation of oat melanin was attempted.•Structure of the in vitro prepared polymer was elucidated.</description><subject>Avena - chemistry</subject><subject>Avena sativa (Poaceae)</subject><subject>Coumaric Acids - chemistry</subject><subject>FT-IR spectroscopy</subject><subject>MALDI-TOF MS</subject><subject>Melanin</subject><subject>Melanins - analysis</subject><subject>Molecular Weight</subject><subject>Oat</subject><subject>p-Coumaric acid</subject><subject>Pigmentation</subject><subject>Propionates</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkF1LwzAUhoMobk7_gvbSm9aTjzbt5Rh-wcAL9TqkScoy22UmqTB_vRnT3QoHAofnzZs8CN1gKDDg6m5dbFe76NTKDAVJiwJ4AUBO0BTXnOaUA5yiKQDFecMImaCLENYAUJZVdY4mhLM0lE5R8xr9qOLoZZ-plfRSRePtt4zWbTLXZbLv3WB6ubGbrPNuyNpeqo_MyXiJzjrZB3P1e87Q-8P92-IpX748Pi_my1yxuoq56lJP2WiiWlZzo0uFeVOaVjLZsIbRilaay6YlhLRMaagZbSkuKaiSdJ3u6AzdHu7devc5mhDFYIMyfXqTcWMQuE50VdcUEsoPqPIuBG86sfV2kH4nMIi9N7EWR29i700AF8lbSl7_loztYPQx9ycqAfMDYNJXv6zxIihrNspo642KQjv7b8kPmDeDEA</recordid><startdate>201610</startdate><enddate>201610</enddate><creator>Varga, Mónika</creator><creator>Berkesi, Ottó</creator><creator>Darula, Zsuzsanna</creator><creator>May, Nóra Veronika</creator><creator>Palágyi, András</creator><general>Elsevier Ltd</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></search><sort><creationdate>201610</creationdate><title>Structural characterization of allomelanin from black oat</title><author>Varga, Mónika ; Berkesi, Ottó ; Darula, Zsuzsanna ; May, Nóra Veronika ; Palágyi, András</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Avena - chemistry</topic><topic>Avena sativa (Poaceae)</topic><topic>Coumaric Acids - chemistry</topic><topic>FT-IR spectroscopy</topic><topic>MALDI-TOF MS</topic><topic>Melanin</topic><topic>Melanins - analysis</topic><topic>Molecular Weight</topic><topic>Oat</topic><topic>p-Coumaric acid</topic><topic>Pigmentation</topic><topic>Propionates</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Varga, Mónika</creatorcontrib><creatorcontrib>Berkesi, Ottó</creatorcontrib><creatorcontrib>Darula, Zsuzsanna</creatorcontrib><creatorcontrib>May, Nóra Veronika</creatorcontrib><creatorcontrib>Palágyi, András</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Varga, Mónika</au><au>Berkesi, Ottó</au><au>Darula, Zsuzsanna</au><au>May, Nóra Veronika</au><au>Palágyi, András</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural characterization of allomelanin from black oat</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2016-10</date><risdate>2016</risdate><volume>130</volume><spage>313</spage><epage>320</epage><pages>313-320</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>The brown to black coloration found in plants is due to the melanins, which have been relatively poorly investigated among the plant pigments. The aim of this work was to study the dark pigment extracted from the black oat hull with respect to composition and structure. Ultraviolet–visible (UV–Vis) spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) and Fourier transform infrared (FT-IR) spectroscopy were applied for the characterization of the pigment. UV–Vis spectroscopy revealed that the extracted material displays a broadband, structureless absorption profile a common feature of melanins. MALDI-TOF MS measurements demonstrated that oat melanin is a homopolymer built up from p-coumaric acid and consists mainly of low molecular weight (527–1499 Da) oligomers of 3–9 monomer units. The tetramer oligomer proved to be dominant. The results of the FT-IR analysis indicated that oat melanin is a fully conjugated aromatic system containing tetrasubstituted aromatic rings linked by CC coupling. The in vitro preparation of melanin from p-coumaric acid by horseradish peroxidase was performed for comparison. The resulting polymer consisted of oligomers of 4–9 monomer units similarly to those in oat melanin. However, the building blocks proved to be connected to each other via COC linkages in contrast with the CC linkages in oat melanin. [Display omitted] •The pigment extracted from the black oat was identified as melanin.•Structure was determined by MALDI-TOF MS and FT-IR spectroscopy.•In vitro preparation of oat melanin was attempted.•Structure of the in vitro prepared polymer was elucidated.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27427433</pmid><doi>10.1016/j.phytochem.2016.07.002</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0031-9422
ispartof Phytochemistry (Oxford), 2016-10, Vol.130, p.313-320
issn 0031-9422
1873-3700
language eng
recordid cdi_proquest_miscellaneous_1815368830
source Elsevier
subjects Avena - chemistry
Avena sativa (Poaceae)
Coumaric Acids - chemistry
FT-IR spectroscopy
MALDI-TOF MS
Melanin
Melanins - analysis
Molecular Weight
Oat
p-Coumaric acid
Pigmentation
Propionates
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spectroscopy, Fourier Transform Infrared
title Structural characterization of allomelanin from black oat
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T01%3A38%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structural%20characterization%20of%20allomelanin%20from%20black%20oat&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=Varga,%20M%C3%B3nika&rft.date=2016-10&rft.volume=130&rft.spage=313&rft.epage=320&rft.pages=313-320&rft.issn=0031-9422&rft.eissn=1873-3700&rft_id=info:doi/10.1016/j.phytochem.2016.07.002&rft_dat=%3Cproquest_cross%3E1815368830%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c486t-cf43359d2cb487ed5c1795eba4a94943636d7a9b222b4cd0843b31530c52ffdf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1815368830&rft_id=info:pmid/27427433&rfr_iscdi=true