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The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli
Curli amyloid fibers are the major protein component of the extracellular matrix produced by Enterobacteriaceae during biofilm formation. Curli are required for proper biofilm development and environmental persistence by Escherichia coli. Here, we present a complete and vetted genetic analysis of fu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745457/ https://www.ncbi.nlm.nih.gov/pubmed/29088115 http://dx.doi.org/10.3390/biom7040075 |
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author | Smith, Daniel R. Price, Janet E. Burby, Peter E. Blanco, Luz P. Chamberlain, Justin Chapman, Matthew R. |
author_facet | Smith, Daniel R. Price, Janet E. Burby, Peter E. Blanco, Luz P. Chamberlain, Justin Chapman, Matthew R. |
author_sort | Smith, Daniel R. |
collection | PubMed |
description | Curli amyloid fibers are the major protein component of the extracellular matrix produced by Enterobacteriaceae during biofilm formation. Curli are required for proper biofilm development and environmental persistence by Escherichia coli. Here, we present a complete and vetted genetic analysis of functional amyloid fiber biogenesis. The Keio collection of single gene deletions was screened on Congo red indicator plates to identify E. coli mutants that had defective amyloid production. We discovered that more than three hundred gene products modulated curli production. These genes were involved in fundamental cellular processes such as regulation, environmental sensing, respiration, metabolism, cell envelope biogenesis, transport, and protein turnover. The alternative sigma factors, σ(S) and σ(E), had opposing roles in curli production. Mutations that induced the σ(E) or Cpx stress response systems had reduced curli production, while mutant strains with increased σ(S) levels had increased curli production. Mutations in metabolic pathways, including gluconeogenesis and the biosynthesis of lipopolysaccharide (LPS), produced less curli. Regulation of the master biofilm regulator, CsgD, was diverse, and the screen revealed several proteins and small RNAs (sRNA) that regulate csgD messenger RNA (mRNA) levels. Using previously published studies, we found minimal overlap between the genes affecting curli biogenesis and genes known to impact swimming or swarming motility, underlying the distinction between motile and sessile lifestyles. Collectively, the diversity and number of elements required suggest curli production is part of a highly regulated and complex developmental pathway in E. coli. |
format | Online Article Text |
id | pubmed-5745457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-57454572018-01-02 The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli Smith, Daniel R. Price, Janet E. Burby, Peter E. Blanco, Luz P. Chamberlain, Justin Chapman, Matthew R. Biomolecules Article Curli amyloid fibers are the major protein component of the extracellular matrix produced by Enterobacteriaceae during biofilm formation. Curli are required for proper biofilm development and environmental persistence by Escherichia coli. Here, we present a complete and vetted genetic analysis of functional amyloid fiber biogenesis. The Keio collection of single gene deletions was screened on Congo red indicator plates to identify E. coli mutants that had defective amyloid production. We discovered that more than three hundred gene products modulated curli production. These genes were involved in fundamental cellular processes such as regulation, environmental sensing, respiration, metabolism, cell envelope biogenesis, transport, and protein turnover. The alternative sigma factors, σ(S) and σ(E), had opposing roles in curli production. Mutations that induced the σ(E) or Cpx stress response systems had reduced curli production, while mutant strains with increased σ(S) levels had increased curli production. Mutations in metabolic pathways, including gluconeogenesis and the biosynthesis of lipopolysaccharide (LPS), produced less curli. Regulation of the master biofilm regulator, CsgD, was diverse, and the screen revealed several proteins and small RNAs (sRNA) that regulate csgD messenger RNA (mRNA) levels. Using previously published studies, we found minimal overlap between the genes affecting curli biogenesis and genes known to impact swimming or swarming motility, underlying the distinction between motile and sessile lifestyles. Collectively, the diversity and number of elements required suggest curli production is part of a highly regulated and complex developmental pathway in E. coli. MDPI 2017-10-31 /pmc/articles/PMC5745457/ /pubmed/29088115 http://dx.doi.org/10.3390/biom7040075 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Smith, Daniel R. Price, Janet E. Burby, Peter E. Blanco, Luz P. Chamberlain, Justin Chapman, Matthew R. The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli |
title | The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli |
title_full | The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli |
title_fullStr | The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli |
title_full_unstemmed | The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli |
title_short | The Production of Curli Amyloid Fibers Is Deeply Integrated into the Biology of Escherichia coli |
title_sort | production of curli amyloid fibers is deeply integrated into the biology of escherichia coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745457/ https://www.ncbi.nlm.nih.gov/pubmed/29088115 http://dx.doi.org/10.3390/biom7040075 |
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