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Lipid Flippases for Bacterial Peptidoglycan Biosynthesis
The biosynthesis of cellular polysaccharides and glycoconjugates often involves lipid-linked intermediates that need to be translocated across membranes. Essential pathways such as N-glycosylation in eukaryotes and biogenesis of the peptidoglycan (PG) cell wall in bacteria share a common strategy wh...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Libertas Academica
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714577/ https://www.ncbi.nlm.nih.gov/pubmed/26792999 http://dx.doi.org/10.4137/LPI.S31783 |
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author | Ruiz, Natividad |
author_facet | Ruiz, Natividad |
author_sort | Ruiz, Natividad |
collection | PubMed |
description | The biosynthesis of cellular polysaccharides and glycoconjugates often involves lipid-linked intermediates that need to be translocated across membranes. Essential pathways such as N-glycosylation in eukaryotes and biogenesis of the peptidoglycan (PG) cell wall in bacteria share a common strategy where nucleotide-sugars are used to build a membrane-bound oligosaccharide precursor that is linked to a phosphorylated isoprenoid lipid. Once made, these lipid-linked intermediates must be translocated across a membrane so that they can serve as substrates in a different cellular compartment. How translocation occurs is poorly understood, although it clearly requires a transporter or flippase. Identification of these transporters is notoriously difficult, and, in particular, the identity of the flippase of lipid II, an intermediate required for PG biogenesis, has been the subject of much debate. Here, I will review the body of work that has recently fueled this controversy, centered on proposed flippase candidates FtsW, MurJ, and AmJ. |
format | Online Article Text |
id | pubmed-4714577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-47145772016-01-20 Lipid Flippases for Bacterial Peptidoglycan Biosynthesis Ruiz, Natividad Lipid Insights Review The biosynthesis of cellular polysaccharides and glycoconjugates often involves lipid-linked intermediates that need to be translocated across membranes. Essential pathways such as N-glycosylation in eukaryotes and biogenesis of the peptidoglycan (PG) cell wall in bacteria share a common strategy where nucleotide-sugars are used to build a membrane-bound oligosaccharide precursor that is linked to a phosphorylated isoprenoid lipid. Once made, these lipid-linked intermediates must be translocated across a membrane so that they can serve as substrates in a different cellular compartment. How translocation occurs is poorly understood, although it clearly requires a transporter or flippase. Identification of these transporters is notoriously difficult, and, in particular, the identity of the flippase of lipid II, an intermediate required for PG biogenesis, has been the subject of much debate. Here, I will review the body of work that has recently fueled this controversy, centered on proposed flippase candidates FtsW, MurJ, and AmJ. Libertas Academica 2016-01-13 /pmc/articles/PMC4714577/ /pubmed/26792999 http://dx.doi.org/10.4137/LPI.S31783 Text en © 2015 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 license. |
spellingShingle | Review Ruiz, Natividad Lipid Flippases for Bacterial Peptidoglycan Biosynthesis |
title | Lipid Flippases for Bacterial Peptidoglycan Biosynthesis |
title_full | Lipid Flippases for Bacterial Peptidoglycan Biosynthesis |
title_fullStr | Lipid Flippases for Bacterial Peptidoglycan Biosynthesis |
title_full_unstemmed | Lipid Flippases for Bacterial Peptidoglycan Biosynthesis |
title_short | Lipid Flippases for Bacterial Peptidoglycan Biosynthesis |
title_sort | lipid flippases for bacterial peptidoglycan biosynthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714577/ https://www.ncbi.nlm.nih.gov/pubmed/26792999 http://dx.doi.org/10.4137/LPI.S31783 |
work_keys_str_mv | AT ruiznatividad lipidflippasesforbacterialpeptidoglycanbiosynthesis |