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The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research
BACKGROUND: The mBFP is an improved variant of NADPH-dependent blue fluorescent protein that was originally identified from the non-bioluminescent pathogenic bacteria Vibrio vulnificus CKM-1. To explore the application of mBFP in plants, the mBFP gene expression was driven by one of the three promot...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432841/ https://www.ncbi.nlm.nih.gov/pubmed/28510958 http://dx.doi.org/10.1186/s40529-014-0079-x |
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author | Tu, Jin-Min Chang, Ming-Chung Huang, Lynn LH Chang, Ching-Dong Huang, Hao-Jen Lee, Ruey-Hua Chang, Ching-Chun |
author_facet | Tu, Jin-Min Chang, Ming-Chung Huang, Lynn LH Chang, Ching-Dong Huang, Hao-Jen Lee, Ruey-Hua Chang, Ching-Chun |
author_sort | Tu, Jin-Min |
collection | PubMed |
description | BACKGROUND: The mBFP is an improved variant of NADPH-dependent blue fluorescent protein that was originally identified from the non-bioluminescent pathogenic bacteria Vibrio vulnificus CKM-1. To explore the application of mBFP in plants, the mBFP gene expression was driven by one of the three promoters, namely, leaf-specific (RbcS), hypoxia-inducible (Adh) or auxin-inducible (DR5) promoters, in different plant tissues such as leaves, roots and flowers under diverse treatments. In addition, the expressed mBFP protein was targeted to five subcellular compartments such as cytosol, endoplasmic reticulum, apoplast, chloroplast and mitochondria, respectively, in plant cells. RESULTS: When the mBFP was transiently expressed in the tobacco leaves and floral tissues of moth orchid, the cytosol and apoplast exhibited brighter blue fluorescence than other compartments. The recombinant mBFP-mS(1)C fusion protein exhibited enhanced fluorescence intensity that was correlated with more abundant RNA transcripts (1.8 fold) as compared with a control. In the root tips of horizontally grown transgenic Arabidopsis, mBFP could be induced as a reporter under hypoxia condition. Furthermore, the mBFP was localized to the expected subcellular compartments, except that dual targeting was found when the mBFP was fused with the mitochondria-targeting signal peptide. Additionally, the brightness of mBFP blue fluorescence was correlated with NADPH concentration. CONCLUSION: The NADPH-dependent blue fluorescent protein could serve as a useful reporter in plants under aerobic or hypoxic condition. However, to avoid masking the mitochondrial targeting signal, fusing mBFP as a fusion tag in the C-terminal will be better when the mBFP is applied in mitochondria trafficking study. Furthermore, mBFP might have the potential to be further adopted as a NADPH biosensor in plant cells. Future codon optimization of mBFP for plants could significantly enhance its brightness and expand its potential applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40529-014-0079-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5432841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-54328412017-05-31 The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research Tu, Jin-Min Chang, Ming-Chung Huang, Lynn LH Chang, Ching-Dong Huang, Hao-Jen Lee, Ruey-Hua Chang, Ching-Chun Bot Stud Research BACKGROUND: The mBFP is an improved variant of NADPH-dependent blue fluorescent protein that was originally identified from the non-bioluminescent pathogenic bacteria Vibrio vulnificus CKM-1. To explore the application of mBFP in plants, the mBFP gene expression was driven by one of the three promoters, namely, leaf-specific (RbcS), hypoxia-inducible (Adh) or auxin-inducible (DR5) promoters, in different plant tissues such as leaves, roots and flowers under diverse treatments. In addition, the expressed mBFP protein was targeted to five subcellular compartments such as cytosol, endoplasmic reticulum, apoplast, chloroplast and mitochondria, respectively, in plant cells. RESULTS: When the mBFP was transiently expressed in the tobacco leaves and floral tissues of moth orchid, the cytosol and apoplast exhibited brighter blue fluorescence than other compartments. The recombinant mBFP-mS(1)C fusion protein exhibited enhanced fluorescence intensity that was correlated with more abundant RNA transcripts (1.8 fold) as compared with a control. In the root tips of horizontally grown transgenic Arabidopsis, mBFP could be induced as a reporter under hypoxia condition. Furthermore, the mBFP was localized to the expected subcellular compartments, except that dual targeting was found when the mBFP was fused with the mitochondria-targeting signal peptide. Additionally, the brightness of mBFP blue fluorescence was correlated with NADPH concentration. CONCLUSION: The NADPH-dependent blue fluorescent protein could serve as a useful reporter in plants under aerobic or hypoxic condition. However, to avoid masking the mitochondrial targeting signal, fusing mBFP as a fusion tag in the C-terminal will be better when the mBFP is applied in mitochondria trafficking study. Furthermore, mBFP might have the potential to be further adopted as a NADPH biosensor in plant cells. Future codon optimization of mBFP for plants could significantly enhance its brightness and expand its potential applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40529-014-0079-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-12-17 /pmc/articles/PMC5432841/ /pubmed/28510958 http://dx.doi.org/10.1186/s40529-014-0079-x Text en © Tu et al.; licensee Springer. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Tu, Jin-Min Chang, Ming-Chung Huang, Lynn LH Chang, Ching-Dong Huang, Hao-Jen Lee, Ruey-Hua Chang, Ching-Chun The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research |
title | The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research |
title_full | The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research |
title_fullStr | The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research |
title_full_unstemmed | The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research |
title_short | The blue fluorescent protein from Vibrio vulnificus CKM-1 is a useful reporter for plant research |
title_sort | blue fluorescent protein from vibrio vulnificus ckm-1 is a useful reporter for plant research |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432841/ https://www.ncbi.nlm.nih.gov/pubmed/28510958 http://dx.doi.org/10.1186/s40529-014-0079-x |
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