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Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens

Serratia marcescens is an opportunistic pathogen that can utilize chitin as a carbon source, through its ability to produce chitin-degrading enzymes to digest chitin and membrane transporters to transport the degradation products (chitooligosaccharides) into the cells. Further characterization of th...

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Autores principales: Soysa, H. Sasimali M., Kumsaoad, Sawitree, Amornloetwattana, Rawiporn, Watanabe, Takeshi, Suginta, Wipa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582717/
https://www.ncbi.nlm.nih.gov/pubmed/36113582
http://dx.doi.org/10.1016/j.jbc.2022.102487
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author Soysa, H. Sasimali M.
Kumsaoad, Sawitree
Amornloetwattana, Rawiporn
Watanabe, Takeshi
Suginta, Wipa
author_facet Soysa, H. Sasimali M.
Kumsaoad, Sawitree
Amornloetwattana, Rawiporn
Watanabe, Takeshi
Suginta, Wipa
author_sort Soysa, H. Sasimali M.
collection PubMed
description Serratia marcescens is an opportunistic pathogen that can utilize chitin as a carbon source, through its ability to produce chitin-degrading enzymes to digest chitin and membrane transporters to transport the degradation products (chitooligosaccharides) into the cells. Further characterization of these proteins is important to understand details of chitin metabolism. Here, we investigate the properties and function of the S. marcescens chitoporin, namely SmChiP, a chitooligosaccharide transporter. We show that SmChiP is a monomeric porin that forms a stable channel in artificial phospholipid membranes, with an average single-channel conductance of 0.5 ± 0.02 nS in 1 M KCl electrolyte. Additionally, we demonstrated that SmChiP allowed the passage of small molecules with a size exclusion limit of <300 Da and exhibited substrate specificity toward chitooligosaccharides, both in membrane and detergent-solubilized forms. We found that SmChiP interacted strongly with chitopentaose (K(d) = 23 ± 2.0 μM) and chitohexaose (K(d) = 17 ± 0.6 μM) but did not recognize nonchitose oligosaccharides (maltohexaose and cellohexaose). Given that S. marcescens can use chitin as a primary energy source, SmChiP may serve as a target for further development of nutrient-based antimicrobial therapies directed against multidrug antibiotic-resistant S. marcescens infections.
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spelling pubmed-95827172022-10-21 Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens Soysa, H. Sasimali M. Kumsaoad, Sawitree Amornloetwattana, Rawiporn Watanabe, Takeshi Suginta, Wipa J Biol Chem Research Article Serratia marcescens is an opportunistic pathogen that can utilize chitin as a carbon source, through its ability to produce chitin-degrading enzymes to digest chitin and membrane transporters to transport the degradation products (chitooligosaccharides) into the cells. Further characterization of these proteins is important to understand details of chitin metabolism. Here, we investigate the properties and function of the S. marcescens chitoporin, namely SmChiP, a chitooligosaccharide transporter. We show that SmChiP is a monomeric porin that forms a stable channel in artificial phospholipid membranes, with an average single-channel conductance of 0.5 ± 0.02 nS in 1 M KCl electrolyte. Additionally, we demonstrated that SmChiP allowed the passage of small molecules with a size exclusion limit of <300 Da and exhibited substrate specificity toward chitooligosaccharides, both in membrane and detergent-solubilized forms. We found that SmChiP interacted strongly with chitopentaose (K(d) = 23 ± 2.0 μM) and chitohexaose (K(d) = 17 ± 0.6 μM) but did not recognize nonchitose oligosaccharides (maltohexaose and cellohexaose). Given that S. marcescens can use chitin as a primary energy source, SmChiP may serve as a target for further development of nutrient-based antimicrobial therapies directed against multidrug antibiotic-resistant S. marcescens infections. American Society for Biochemistry and Molecular Biology 2022-09-14 /pmc/articles/PMC9582717/ /pubmed/36113582 http://dx.doi.org/10.1016/j.jbc.2022.102487 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Soysa, H. Sasimali M.
Kumsaoad, Sawitree
Amornloetwattana, Rawiporn
Watanabe, Takeshi
Suginta, Wipa
Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens
title Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens
title_full Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens
title_fullStr Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens
title_full_unstemmed Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens
title_short Single-channel characterization of the chitooligosaccharide transporter chitoporin (SmChiP) from the opportunistic pathogen Serratia marcescens
title_sort single-channel characterization of the chitooligosaccharide transporter chitoporin (smchip) from the opportunistic pathogen serratia marcescens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582717/
https://www.ncbi.nlm.nih.gov/pubmed/36113582
http://dx.doi.org/10.1016/j.jbc.2022.102487
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