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Coral Fluorescent Proteins as Antioxidants
BACKGROUND: A wide array of fluorescent proteins (FP) is present in anthozoans, although their biochemical characteristics and function in host tissue remain to be determined. Upregulation of FP's frequently occurs in injured or compromised coral tissue, suggesting a potential role of coral FPs...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752795/ https://www.ncbi.nlm.nih.gov/pubmed/19806218 http://dx.doi.org/10.1371/journal.pone.0007298 |
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author | Palmer, Caroline V. Modi, Chintan K. Mydlarz, Laura D. |
author_facet | Palmer, Caroline V. Modi, Chintan K. Mydlarz, Laura D. |
author_sort | Palmer, Caroline V. |
collection | PubMed |
description | BACKGROUND: A wide array of fluorescent proteins (FP) is present in anthozoans, although their biochemical characteristics and function in host tissue remain to be determined. Upregulation of FP's frequently occurs in injured or compromised coral tissue, suggesting a potential role of coral FPs in host stress responses. METHODOLOGY/PRINCIPAL FINDINGS: The presence of FPs was determined and quantified for a subsample of seven healthy Caribbean coral species using spectral emission analysis of tissue extracts. FP concentration was correlated with the in vivo antioxidant potential of the tissue extracts by quantifying the hydrogen peroxide (H(2)O(2)) scavenging rates. FPs of the seven species varied in both type and abundance and demonstrated a positive correlation between H(2)O(2) scavenging rate and FP concentration. To validate this data, the H(2)O(2) scavenging rates of four pure scleractinian FPs, cyan (CFP), green (GFP), red (RFP) and chromoprotein (CP), and their mutant counterparts (without chromophores), were investigated. In vitro, each FP scavenged H(2)O(2) with the most efficient being CP followed by equivalent activity of CFP and RFP. Scavenging was significantly higher in all mutant counterparts. CONCLUSIONS/SIGNIFICANCE: Both naturally occurring and pure coral FPs have significant H(2)O(2) scavenging activity. The higher scavenging rate of RFP and the CP in vitro is consistent with observed increases of these specific FPs in areas of compromised coral tissue. However, the greater scavenging ability of the mutant counterparts suggests additional roles of scleractinian FPs, potentially pertaining to their color. This study documents H(2)O(2) scavenging of scleractinian FPs, a novel biochemical characteristic, both in vivo across multiple species and in vitro with purified proteins. These data support a role for FPs in coral stress and immune responses and highlights the multi-functionality of these conspicuous proteins. |
format | Text |
id | pubmed-2752795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27527952009-10-06 Coral Fluorescent Proteins as Antioxidants Palmer, Caroline V. Modi, Chintan K. Mydlarz, Laura D. PLoS One Research Article BACKGROUND: A wide array of fluorescent proteins (FP) is present in anthozoans, although their biochemical characteristics and function in host tissue remain to be determined. Upregulation of FP's frequently occurs in injured or compromised coral tissue, suggesting a potential role of coral FPs in host stress responses. METHODOLOGY/PRINCIPAL FINDINGS: The presence of FPs was determined and quantified for a subsample of seven healthy Caribbean coral species using spectral emission analysis of tissue extracts. FP concentration was correlated with the in vivo antioxidant potential of the tissue extracts by quantifying the hydrogen peroxide (H(2)O(2)) scavenging rates. FPs of the seven species varied in both type and abundance and demonstrated a positive correlation between H(2)O(2) scavenging rate and FP concentration. To validate this data, the H(2)O(2) scavenging rates of four pure scleractinian FPs, cyan (CFP), green (GFP), red (RFP) and chromoprotein (CP), and their mutant counterparts (without chromophores), were investigated. In vitro, each FP scavenged H(2)O(2) with the most efficient being CP followed by equivalent activity of CFP and RFP. Scavenging was significantly higher in all mutant counterparts. CONCLUSIONS/SIGNIFICANCE: Both naturally occurring and pure coral FPs have significant H(2)O(2) scavenging activity. The higher scavenging rate of RFP and the CP in vitro is consistent with observed increases of these specific FPs in areas of compromised coral tissue. However, the greater scavenging ability of the mutant counterparts suggests additional roles of scleractinian FPs, potentially pertaining to their color. This study documents H(2)O(2) scavenging of scleractinian FPs, a novel biochemical characteristic, both in vivo across multiple species and in vitro with purified proteins. These data support a role for FPs in coral stress and immune responses and highlights the multi-functionality of these conspicuous proteins. Public Library of Science 2009-10-06 /pmc/articles/PMC2752795/ /pubmed/19806218 http://dx.doi.org/10.1371/journal.pone.0007298 Text en Palmer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Palmer, Caroline V. Modi, Chintan K. Mydlarz, Laura D. Coral Fluorescent Proteins as Antioxidants |
title | Coral Fluorescent Proteins as Antioxidants |
title_full | Coral Fluorescent Proteins as Antioxidants |
title_fullStr | Coral Fluorescent Proteins as Antioxidants |
title_full_unstemmed | Coral Fluorescent Proteins as Antioxidants |
title_short | Coral Fluorescent Proteins as Antioxidants |
title_sort | coral fluorescent proteins as antioxidants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752795/ https://www.ncbi.nlm.nih.gov/pubmed/19806218 http://dx.doi.org/10.1371/journal.pone.0007298 |
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