Reactive oxygen species and the Antarctic macroalgal wound response

Reactive oxygen species ( ROS ) are commonly produced by algal, vascular plant, and animal cells involved in the innate immune response as cellular signals promoting defense and healing and/or as a direct defense against invading pathogens. The production of reactive species in macroalgae upon injur...

Full description

Bibliographic Details
Published in:Journal of Phycology
Main Authors: McDowell, Ruth E., Amsler, Charles D., Dickinson, Dale A., McClintock, James B., Baker, Bill J.
Other Authors: Graham, M., National Science Foundation, Antarctic Organisms and Ecosystems
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2013
Subjects:
Online Access:http://dx.doi.org/10.1111/jpy.12127
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fjpy.12127
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jpy.12127
id crwiley:10.1111/jpy.12127
record_format openpolar
spelling crwiley:10.1111/jpy.12127 2024-09-15T17:44:25+00:00 Reactive oxygen species and the Antarctic macroalgal wound response McDowell, Ruth E. Amsler, Charles D. Dickinson, Dale A. McClintock, James B. Baker, Bill J. Graham, M. National Science Foundation Antarctic Organisms and Ecosystems 2013 http://dx.doi.org/10.1111/jpy.12127 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fjpy.12127 https://onlinelibrary.wiley.com/doi/pdf/10.1111/jpy.12127 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Phycology volume 50, issue 1, page 71-80 ISSN 0022-3646 1529-8817 journal-article 2013 crwiley https://doi.org/10.1111/jpy.12127 2024-08-09T04:31:51Z Reactive oxygen species ( ROS ) are commonly produced by algal, vascular plant, and animal cells involved in the innate immune response as cellular signals promoting defense and healing and/or as a direct defense against invading pathogens. The production of reactive species in macroalgae upon injury, however, is largely uncharacterized. In this study, we surveyed 13 species of macroalgae from the W estern A ntarctic P eninsula and show that the release of strong oxidants is common after macroalgal wounding. Most species released strong oxidants within 1 min of wounding and/or showed cellular accumulation of strong oxidants over an hour post‐wounding. Exogenous catalase was used to show that hydrogen peroxide was a component of immediate oxidant release in one of five species, but was not responsible for the entire oxidative wound response as is common in vascular plants. The other component(s) of the oxidant cocktail released upon wounding are unknown. We were unable to detect protein nitration in extracts of four oxidant‐producing species flash frozen 30 s after wounding, but a role for reactive nitrogen species such as peroxynitrite cannot be completely ruled out. Two species showed evidence for the production of a catalase‐activated oxidant, a mechanism previously known only from the laboratory and from the synthetic drug isoniazid used to kill the human pathogen Mycobacterium tuberculosis . The rhodophyte Palmaria decipiens , which released strong oxidants after wounding, also produced strong oxidants upon grazing by a sympatric amphipod, suggesting that oxidants are involved in the response to grazing. Article in Journal/Newspaper Antarc* Antarctic Wiley Online Library Journal of Phycology 50 1 71 80
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Reactive oxygen species ( ROS ) are commonly produced by algal, vascular plant, and animal cells involved in the innate immune response as cellular signals promoting defense and healing and/or as a direct defense against invading pathogens. The production of reactive species in macroalgae upon injury, however, is largely uncharacterized. In this study, we surveyed 13 species of macroalgae from the W estern A ntarctic P eninsula and show that the release of strong oxidants is common after macroalgal wounding. Most species released strong oxidants within 1 min of wounding and/or showed cellular accumulation of strong oxidants over an hour post‐wounding. Exogenous catalase was used to show that hydrogen peroxide was a component of immediate oxidant release in one of five species, but was not responsible for the entire oxidative wound response as is common in vascular plants. The other component(s) of the oxidant cocktail released upon wounding are unknown. We were unable to detect protein nitration in extracts of four oxidant‐producing species flash frozen 30 s after wounding, but a role for reactive nitrogen species such as peroxynitrite cannot be completely ruled out. Two species showed evidence for the production of a catalase‐activated oxidant, a mechanism previously known only from the laboratory and from the synthetic drug isoniazid used to kill the human pathogen Mycobacterium tuberculosis . The rhodophyte Palmaria decipiens , which released strong oxidants after wounding, also produced strong oxidants upon grazing by a sympatric amphipod, suggesting that oxidants are involved in the response to grazing.
author2 Graham, M.
National Science Foundation
Antarctic Organisms and Ecosystems
format Article in Journal/Newspaper
author McDowell, Ruth E.
Amsler, Charles D.
Dickinson, Dale A.
McClintock, James B.
Baker, Bill J.
spellingShingle McDowell, Ruth E.
Amsler, Charles D.
Dickinson, Dale A.
McClintock, James B.
Baker, Bill J.
Reactive oxygen species and the Antarctic macroalgal wound response
author_facet McDowell, Ruth E.
Amsler, Charles D.
Dickinson, Dale A.
McClintock, James B.
Baker, Bill J.
author_sort McDowell, Ruth E.
title Reactive oxygen species and the Antarctic macroalgal wound response
title_short Reactive oxygen species and the Antarctic macroalgal wound response
title_full Reactive oxygen species and the Antarctic macroalgal wound response
title_fullStr Reactive oxygen species and the Antarctic macroalgal wound response
title_full_unstemmed Reactive oxygen species and the Antarctic macroalgal wound response
title_sort reactive oxygen species and the antarctic macroalgal wound response
publisher Wiley
publishDate 2013
url http://dx.doi.org/10.1111/jpy.12127
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fjpy.12127
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jpy.12127
genre Antarc*
Antarctic
genre_facet Antarc*
Antarctic
op_source Journal of Phycology
volume 50, issue 1, page 71-80
ISSN 0022-3646 1529-8817
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1111/jpy.12127
container_title Journal of Phycology
container_volume 50
container_issue 1
container_start_page 71
op_container_end_page 80
_version_ 1810491993723240448