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A cell wall synthase accelerates plasma membrane partitioning in mycobacteria

Lateral partitioning of proteins and lipids shapes membrane function. In model membranes, partitioning can be influenced both by bilayer-intrinsic factors like molecular composition and by bilayer-extrinsic factors such as interactions with other membranes and solid supports. While cellular membrane...

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Autores principales: Kado, Takehiro, Akbary, Zarina, Motooka, Daisuke, Sparks, Ian L, Melzer, Emily S, Nakamura, Shota, Rojas, Enrique R, Morita, Yasu S, Siegrist, M Sloan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547480/
https://www.ncbi.nlm.nih.gov/pubmed/37665120
http://dx.doi.org/10.7554/eLife.81924
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author Kado, Takehiro
Akbary, Zarina
Motooka, Daisuke
Sparks, Ian L
Melzer, Emily S
Nakamura, Shota
Rojas, Enrique R
Morita, Yasu S
Siegrist, M Sloan
author_facet Kado, Takehiro
Akbary, Zarina
Motooka, Daisuke
Sparks, Ian L
Melzer, Emily S
Nakamura, Shota
Rojas, Enrique R
Morita, Yasu S
Siegrist, M Sloan
author_sort Kado, Takehiro
collection PubMed
description Lateral partitioning of proteins and lipids shapes membrane function. In model membranes, partitioning can be influenced both by bilayer-intrinsic factors like molecular composition and by bilayer-extrinsic factors such as interactions with other membranes and solid supports. While cellular membranes can departition in response to bilayer-intrinsic or -extrinsic disruptions, the mechanisms by which they partition de novo are largely unknown. The plasma membrane of Mycobacterium smegmatis spatially and biochemically departitions in response to the fluidizing agent benzyl alcohol, then repartitions upon fluidizer washout. By screening for mutants that are sensitive to benzyl alcohol, we show that the bifunctional cell wall synthase PonA2 promotes membrane partitioning and cell growth during recovery from benzyl alcohol exposure. PonA2’s role in membrane repartitioning and regrowth depends solely on its conserved transglycosylase domain. Active cell wall polymerization promotes de novo membrane partitioning and the completed cell wall polymer helps to maintain membrane partitioning. Our work highlights the complexity of membrane–cell wall interactions and establishes a facile model system for departitioning and repartitioning cellular membranes.
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spelling pubmed-105474802023-10-04 A cell wall synthase accelerates plasma membrane partitioning in mycobacteria Kado, Takehiro Akbary, Zarina Motooka, Daisuke Sparks, Ian L Melzer, Emily S Nakamura, Shota Rojas, Enrique R Morita, Yasu S Siegrist, M Sloan eLife Cell Biology Lateral partitioning of proteins and lipids shapes membrane function. In model membranes, partitioning can be influenced both by bilayer-intrinsic factors like molecular composition and by bilayer-extrinsic factors such as interactions with other membranes and solid supports. While cellular membranes can departition in response to bilayer-intrinsic or -extrinsic disruptions, the mechanisms by which they partition de novo are largely unknown. The plasma membrane of Mycobacterium smegmatis spatially and biochemically departitions in response to the fluidizing agent benzyl alcohol, then repartitions upon fluidizer washout. By screening for mutants that are sensitive to benzyl alcohol, we show that the bifunctional cell wall synthase PonA2 promotes membrane partitioning and cell growth during recovery from benzyl alcohol exposure. PonA2’s role in membrane repartitioning and regrowth depends solely on its conserved transglycosylase domain. Active cell wall polymerization promotes de novo membrane partitioning and the completed cell wall polymer helps to maintain membrane partitioning. Our work highlights the complexity of membrane–cell wall interactions and establishes a facile model system for departitioning and repartitioning cellular membranes. eLife Sciences Publications, Ltd 2023-09-04 /pmc/articles/PMC10547480/ /pubmed/37665120 http://dx.doi.org/10.7554/eLife.81924 Text en © 2023, Kado et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Kado, Takehiro
Akbary, Zarina
Motooka, Daisuke
Sparks, Ian L
Melzer, Emily S
Nakamura, Shota
Rojas, Enrique R
Morita, Yasu S
Siegrist, M Sloan
A cell wall synthase accelerates plasma membrane partitioning in mycobacteria
title A cell wall synthase accelerates plasma membrane partitioning in mycobacteria
title_full A cell wall synthase accelerates plasma membrane partitioning in mycobacteria
title_fullStr A cell wall synthase accelerates plasma membrane partitioning in mycobacteria
title_full_unstemmed A cell wall synthase accelerates plasma membrane partitioning in mycobacteria
title_short A cell wall synthase accelerates plasma membrane partitioning in mycobacteria
title_sort cell wall synthase accelerates plasma membrane partitioning in mycobacteria
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547480/
https://www.ncbi.nlm.nih.gov/pubmed/37665120
http://dx.doi.org/10.7554/eLife.81924
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