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A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens

Pathogenic bacteria adapt to their environment and manipulate the biochemistry of hosts by secretion of effector molecules. Serratia marcescens is an opportunistic pathogen associated with healthcare-acquired infections and is a prolific secretor of proteins, including three chitinases (ChiA, ChiB,...

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Autores principales: Hamilton, Jaeger J., Marlow, Victoria L., Owen, Richard A., Costa, Marília de Assis Alcoforado, Guo, Manman, Buchanan, Grant, Chandra, Govind, Trost, Matthias, Coulthurst, Sarah J., Palmer, Tracy, Stanley-Wall, Nicola R., Sargent, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259817/
https://www.ncbi.nlm.nih.gov/pubmed/25488919
http://dx.doi.org/10.1083/jcb.201404127
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author Hamilton, Jaeger J.
Marlow, Victoria L.
Owen, Richard A.
Costa, Marília de Assis Alcoforado
Guo, Manman
Buchanan, Grant
Chandra, Govind
Trost, Matthias
Coulthurst, Sarah J.
Palmer, Tracy
Stanley-Wall, Nicola R.
Sargent, Frank
author_facet Hamilton, Jaeger J.
Marlow, Victoria L.
Owen, Richard A.
Costa, Marília de Assis Alcoforado
Guo, Manman
Buchanan, Grant
Chandra, Govind
Trost, Matthias
Coulthurst, Sarah J.
Palmer, Tracy
Stanley-Wall, Nicola R.
Sargent, Frank
author_sort Hamilton, Jaeger J.
collection PubMed
description Pathogenic bacteria adapt to their environment and manipulate the biochemistry of hosts by secretion of effector molecules. Serratia marcescens is an opportunistic pathogen associated with healthcare-acquired infections and is a prolific secretor of proteins, including three chitinases (ChiA, ChiB, and ChiC) and a chitin binding protein (Cbp21). In this work, genetic, biochemical, and proteomic approaches identified genes that were required for secretion of all three chitinases and Cbp21. A genetic screen identified a holin-like protein (ChiW) and a putative l-alanyl-d-glutamate endopeptidase (ChiX), and subsequent biochemical analyses established that both were required for nonlytic secretion of the entire chitinolytic machinery, with chitinase secretion being blocked at a late stage in the mutants. In addition, live-cell imaging experiments demonstrated bimodal and coordinated expression of chiX and chiA and revealed that cells expressing chiA remained viable. It is proposed that ChiW and ChiX operate in tandem as components of a protein secretion system used by gram-negative bacteria.
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spelling pubmed-42598172015-06-08 A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens Hamilton, Jaeger J. Marlow, Victoria L. Owen, Richard A. Costa, Marília de Assis Alcoforado Guo, Manman Buchanan, Grant Chandra, Govind Trost, Matthias Coulthurst, Sarah J. Palmer, Tracy Stanley-Wall, Nicola R. Sargent, Frank J Cell Biol Research Articles Pathogenic bacteria adapt to their environment and manipulate the biochemistry of hosts by secretion of effector molecules. Serratia marcescens is an opportunistic pathogen associated with healthcare-acquired infections and is a prolific secretor of proteins, including three chitinases (ChiA, ChiB, and ChiC) and a chitin binding protein (Cbp21). In this work, genetic, biochemical, and proteomic approaches identified genes that were required for secretion of all three chitinases and Cbp21. A genetic screen identified a holin-like protein (ChiW) and a putative l-alanyl-d-glutamate endopeptidase (ChiX), and subsequent biochemical analyses established that both were required for nonlytic secretion of the entire chitinolytic machinery, with chitinase secretion being blocked at a late stage in the mutants. In addition, live-cell imaging experiments demonstrated bimodal and coordinated expression of chiX and chiA and revealed that cells expressing chiA remained viable. It is proposed that ChiW and ChiX operate in tandem as components of a protein secretion system used by gram-negative bacteria. The Rockefeller University Press 2014-12-08 /pmc/articles/PMC4259817/ /pubmed/25488919 http://dx.doi.org/10.1083/jcb.201404127 Text en © 2014 Hamilton et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Hamilton, Jaeger J.
Marlow, Victoria L.
Owen, Richard A.
Costa, Marília de Assis Alcoforado
Guo, Manman
Buchanan, Grant
Chandra, Govind
Trost, Matthias
Coulthurst, Sarah J.
Palmer, Tracy
Stanley-Wall, Nicola R.
Sargent, Frank
A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens
title A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens
title_full A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens
title_fullStr A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens
title_full_unstemmed A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens
title_short A holin and an endopeptidase are essential for chitinolytic protein secretion in Serratia marcescens
title_sort holin and an endopeptidase are essential for chitinolytic protein secretion in serratia marcescens
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259817/
https://www.ncbi.nlm.nih.gov/pubmed/25488919
http://dx.doi.org/10.1083/jcb.201404127
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