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Growth medium-dependent glycine incorporation into the peptidoglycan of Caulobacter crescentus
The peptidoglycan (PG) is a macromolecular component of the bacterial cell wall that maintains the shape and integrity of the cell. The PG of Caulobacter crescentus, unlike that of many other Gram-negative bacteria, has repeatedly been shown to contain significant amounts of glycine. This compositio...
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Published in: | PloS one 2013-02, Vol.8 (2), p.e57579-e57579 |
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description | The peptidoglycan (PG) is a macromolecular component of the bacterial cell wall that maintains the shape and integrity of the cell. The PG of Caulobacter crescentus, unlike that of many other Gram-negative bacteria, has repeatedly been shown to contain significant amounts of glycine. This compositional peculiarity has been deemed an intrinsic characteristic of this species. By performing a comprehensive qualitative and quantitative analysis of the C. crescentus PG by high-performance liquid chromatography (HPLC) and mass spectrometry (MS), we show here that glycine incorporation into the C. crescentus PG depends on the presence of exogenous glycine in the growth medium. High levels of glycine were detected at the fifth position of the peptide side chains of PG isolated from C. crescentus cells grown in the complex laboratory medium PYE or in defined medium (M2G) supplemented with casamino acids or glycine alone. In contrast, glycine incorporation was undetectable when cells were grown in M2G medium lacking glycine. Remarkably, glycine incorporation into C. crescentus peptidoglycan occurred even in the presence of low millimolar to sub-millimolar concentrations of free glycine. High glycine content in the PG had no obvious effects on growth rates, mode of PG incorporation or cell morphology. Hence, the C. crescentus PG is able to retain its physiological functions in cell growth and morphogenesis despite significant alterations in its composition, in what we deem to be unprecedented plasticity. |
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The PG of Caulobacter crescentus, unlike that of many other Gram-negative bacteria, has repeatedly been shown to contain significant amounts of glycine. This compositional peculiarity has been deemed an intrinsic characteristic of this species. By performing a comprehensive qualitative and quantitative analysis of the C. crescentus PG by high-performance liquid chromatography (HPLC) and mass spectrometry (MS), we show here that glycine incorporation into the C. crescentus PG depends on the presence of exogenous glycine in the growth medium. High levels of glycine were detected at the fifth position of the peptide side chains of PG isolated from C. crescentus cells grown in the complex laboratory medium PYE or in defined medium (M2G) supplemented with casamino acids or glycine alone. In contrast, glycine incorporation was undetectable when cells were grown in M2G medium lacking glycine. Remarkably, glycine incorporation into C. crescentus peptidoglycan occurred even in the presence of low millimolar to sub-millimolar concentrations of free glycine. High glycine content in the PG had no obvious effects on growth rates, mode of PG incorporation or cell morphology. Hence, the C. crescentus PG is able to retain its physiological functions in cell growth and morphogenesis despite significant alterations in its composition, in what we deem to be unprecedented plasticity.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0057579</identifier><identifier>PMID: 23469030</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Amino acids ; Antibiotics ; Bacteria ; Bacterial proteins ; Biology ; Biosynthesis ; Caulobacter crescentus - growth & development ; Caulobacter crescentus - metabolism ; Cell morphology ; Cell walls ; Chromatography ; Chromatography, High Pressure Liquid ; Culture Media ; Cytology ; Developmental biology ; Enzymes ; Glycine ; Glycine - metabolism ; Gram-negative bacteria ; Growth rate ; Helicobacter pylori ; High performance liquid chromatography ; Lipids ; Lipoproteins ; Liquid chromatography ; Macromolecules ; Mass spectrometry ; Mass spectroscopy ; Microscopy, Electron, Transmission ; Morphogenesis ; Penicillin ; Peptides ; Peptidoglycan - metabolism ; Peptidoglycans ; Qualitative analysis ; Quantitative analysis ; Scientific imaging ; Staphylococcus aureus ; Staphylococcus infections</subject><ispartof>PloS one, 2013-02, Vol.8 (2), p.e57579-e57579</ispartof><rights>2013 Takacs et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Takacs et al 2013 Takacs et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-f8966b5d0af28e22016856b828456f39b2fbb3087f2a0fe29a4bb991d45baa193</citedby><cites>FETCH-LOGICAL-c526t-f8966b5d0af28e22016856b828456f39b2fbb3087f2a0fe29a4bb991d45baa193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1330882844/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1330882844?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23469030$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takacs, Constantin N</creatorcontrib><creatorcontrib>Hocking, Jason</creatorcontrib><creatorcontrib>Cabeen, Matthew T</creatorcontrib><creatorcontrib>Bui, Nhat Khai</creatorcontrib><creatorcontrib>Poggio, Sebastian</creatorcontrib><creatorcontrib>Vollmer, Waldemar</creatorcontrib><creatorcontrib>Jacobs-Wagner, Christine</creatorcontrib><title>Growth medium-dependent glycine incorporation into the peptidoglycan of Caulobacter crescentus</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The peptidoglycan (PG) is a macromolecular component of the bacterial cell wall that maintains the shape and integrity of the cell. The PG of Caulobacter crescentus, unlike that of many other Gram-negative bacteria, has repeatedly been shown to contain significant amounts of glycine. This compositional peculiarity has been deemed an intrinsic characteristic of this species. By performing a comprehensive qualitative and quantitative analysis of the C. crescentus PG by high-performance liquid chromatography (HPLC) and mass spectrometry (MS), we show here that glycine incorporation into the C. crescentus PG depends on the presence of exogenous glycine in the growth medium. High levels of glycine were detected at the fifth position of the peptide side chains of PG isolated from C. crescentus cells grown in the complex laboratory medium PYE or in defined medium (M2G) supplemented with casamino acids or glycine alone. In contrast, glycine incorporation was undetectable when cells were grown in M2G medium lacking glycine. Remarkably, glycine incorporation into C. crescentus peptidoglycan occurred even in the presence of low millimolar to sub-millimolar concentrations of free glycine. High glycine content in the PG had no obvious effects on growth rates, mode of PG incorporation or cell morphology. Hence, the C. crescentus PG is able to retain its physiological functions in cell growth and morphogenesis despite significant alterations in its composition, in what we deem to be unprecedented plasticity.</description><subject>Amino acids</subject><subject>Antibiotics</subject><subject>Bacteria</subject><subject>Bacterial proteins</subject><subject>Biology</subject><subject>Biosynthesis</subject><subject>Caulobacter crescentus - growth & development</subject><subject>Caulobacter crescentus - metabolism</subject><subject>Cell morphology</subject><subject>Cell walls</subject><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Culture Media</subject><subject>Cytology</subject><subject>Developmental biology</subject><subject>Enzymes</subject><subject>Glycine</subject><subject>Glycine - metabolism</subject><subject>Gram-negative bacteria</subject><subject>Growth rate</subject><subject>Helicobacter pylori</subject><subject>High performance liquid chromatography</subject><subject>Lipids</subject><subject>Lipoproteins</subject><subject>Liquid chromatography</subject><subject>Macromolecules</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Microscopy, Electron, Transmission</subject><subject>Morphogenesis</subject><subject>Penicillin</subject><subject>Peptides</subject><subject>Peptidoglycan - 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The PG of Caulobacter crescentus, unlike that of many other Gram-negative bacteria, has repeatedly been shown to contain significant amounts of glycine. This compositional peculiarity has been deemed an intrinsic characteristic of this species. By performing a comprehensive qualitative and quantitative analysis of the C. crescentus PG by high-performance liquid chromatography (HPLC) and mass spectrometry (MS), we show here that glycine incorporation into the C. crescentus PG depends on the presence of exogenous glycine in the growth medium. High levels of glycine were detected at the fifth position of the peptide side chains of PG isolated from C. crescentus cells grown in the complex laboratory medium PYE or in defined medium (M2G) supplemented with casamino acids or glycine alone. In contrast, glycine incorporation was undetectable when cells were grown in M2G medium lacking glycine. Remarkably, glycine incorporation into C. crescentus peptidoglycan occurred even in the presence of low millimolar to sub-millimolar concentrations of free glycine. High glycine content in the PG had no obvious effects on growth rates, mode of PG incorporation or cell morphology. Hence, the C. crescentus PG is able to retain its physiological functions in cell growth and morphogenesis despite significant alterations in its composition, in what we deem to be unprecedented plasticity.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23469030</pmid><doi>10.1371/journal.pone.0057579</doi><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Antibiotics Bacteria Bacterial proteins Biology Biosynthesis Caulobacter crescentus - growth & development Caulobacter crescentus - metabolism Cell morphology Cell walls Chromatography Chromatography, High Pressure Liquid Culture Media Cytology Developmental biology Enzymes Glycine Glycine - metabolism Gram-negative bacteria Growth rate Helicobacter pylori High performance liquid chromatography Lipids Lipoproteins Liquid chromatography Macromolecules Mass spectrometry Mass spectroscopy Microscopy, Electron, Transmission Morphogenesis Penicillin Peptides Peptidoglycan - metabolism Peptidoglycans Qualitative analysis Quantitative analysis Scientific imaging Staphylococcus aureus Staphylococcus infections |
title | Growth medium-dependent glycine incorporation into the peptidoglycan of Caulobacter crescentus |
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