Construction of improved tools for protein localization studies in Streptococcus pneumoniae.

We have constructed a set of plasmids that allow efficient expression of both N- and C-terminal fusions of proteins of interest to fluorescent proteins mCherry, Citrine, CFP and GFP in the Gram-positive pathogen Streptococcus pneumoniae. In order to improve expression of the fluorescent fusions to l...

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Main Authors: Mafalda X Henriques, Maria João Catalão, Joana Figueiredo, João Paulo Gomes, Sergio R Filipe
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349996/?tool=EBI
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author Mafalda X Henriques
Maria João Catalão
Joana Figueiredo
João Paulo Gomes
Sergio R Filipe
author_facet Mafalda X Henriques
Maria João Catalão
Joana Figueiredo
João Paulo Gomes
Sergio R Filipe
author_sort Mafalda X Henriques
collection DOAJ
description We have constructed a set of plasmids that allow efficient expression of both N- and C-terminal fusions of proteins of interest to fluorescent proteins mCherry, Citrine, CFP and GFP in the Gram-positive pathogen Streptococcus pneumoniae. In order to improve expression of the fluorescent fusions to levels that allow their detection by fluorescence microscopy, we have introduced a 10 amino acid tag, named i-tag, at the N-terminal end of the fluorescent proteins. This caused increased expression due to improved translation efficiency and did not interfere with the protein localization in pneumococcal bacteria. Localizing fluorescent derivatives of FtsZ, Wzd and Wze in dividing bacteria validated the developed tools. The availability of the new plasmids described in this work should greatly facilitate studies of protein localization in an important clinical pathogen.
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spelling doaj.art-67e49e3fb303480195140563280101342022-12-21T21:33:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5504910.1371/journal.pone.0055049Construction of improved tools for protein localization studies in Streptococcus pneumoniae.Mafalda X HenriquesMaria João CatalãoJoana FigueiredoJoão Paulo GomesSergio R FilipeWe have constructed a set of plasmids that allow efficient expression of both N- and C-terminal fusions of proteins of interest to fluorescent proteins mCherry, Citrine, CFP and GFP in the Gram-positive pathogen Streptococcus pneumoniae. In order to improve expression of the fluorescent fusions to levels that allow their detection by fluorescence microscopy, we have introduced a 10 amino acid tag, named i-tag, at the N-terminal end of the fluorescent proteins. This caused increased expression due to improved translation efficiency and did not interfere with the protein localization in pneumococcal bacteria. Localizing fluorescent derivatives of FtsZ, Wzd and Wze in dividing bacteria validated the developed tools. The availability of the new plasmids described in this work should greatly facilitate studies of protein localization in an important clinical pathogen.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349996/?tool=EBI
spellingShingle Mafalda X Henriques
Maria João Catalão
Joana Figueiredo
João Paulo Gomes
Sergio R Filipe
Construction of improved tools for protein localization studies in Streptococcus pneumoniae.
PLoS ONE
title Construction of improved tools for protein localization studies in Streptococcus pneumoniae.
title_full Construction of improved tools for protein localization studies in Streptococcus pneumoniae.
title_fullStr Construction of improved tools for protein localization studies in Streptococcus pneumoniae.
title_full_unstemmed Construction of improved tools for protein localization studies in Streptococcus pneumoniae.
title_short Construction of improved tools for protein localization studies in Streptococcus pneumoniae.
title_sort construction of improved tools for protein localization studies in streptococcus pneumoniae
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349996/?tool=EBI
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