Pyruvate Substitutions on Glycoconjugates
Glycoconjugates are the most diverse biomolecules of life. Mostly located at the cell surface, they translate into cell-specific “barcodes” and offer a vast repertoire of functions, including support of cellular physiology, lifestyle, and pathogenicity. Functions can be fine-tune...
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doaj-293e2de3c59b4273b03e658f666451d22020-11-25T01:34:56ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-10-012019492910.3390/ijms20194929ijms20194929Pyruvate Substitutions on GlycoconjugatesFiona F. Hager0Leander Sützl1Cordula Stefanović2Markus Blaukopf3Christina Schäffer4Department of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Wien, Muthgasse 11, A-1190 Vienna, AustriaDepartment of Food Science and Technology, Food Biotechnology Laboratory, Muthgasse 11, Universität für Bodenkultur Wien, A-1190 Vienna, AustriaDepartment of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Wien, Muthgasse 11, A-1190 Vienna, AustriaDepartment of Chemistry, Division of Organic Chemistry, Universität für Bodenkultur Wien, Muthgasse 18, A-1190 Vienna, AustriaDepartment of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Wien, Muthgasse 11, A-1190 Vienna, AustriaGlycoconjugates are the most diverse biomolecules of life. Mostly located at the cell surface, they translate into cell-specific “barcodes” and offer a vast repertoire of functions, including support of cellular physiology, lifestyle, and pathogenicity. Functions can be fine-tuned by non-carbohydrate modifications on the constituting monosaccharides. Among these modifications is pyruvylation, which is present either in enol or ketal form. The most commonly best-understood example of pyruvylation is enol-pyruvylation of <i>N</i>-acetylglucosamine, which occurs at an early stage in the biosynthesis of the bacterial cell wall component peptidoglycan. Ketal-pyruvylation, in contrast, is present in diverse classes of glycoconjugates, from bacteria to algae to yeast—but not in humans. Mild purification strategies preventing the loss of the acid-labile ketal-pyruvyl group have led to a collection of elucidated pyruvylated glycan structures. However, knowledge of involved pyruvyltransferases creating a ring structure on various monosaccharides is scarce, mainly due to the lack of knowledge of fingerprint motifs of these enzymes and the unavailability of genome sequences of the organisms undergoing pyruvylation. This review compiles the current information on the widespread but under-investigated ketal-pyruvylation of monosaccharides, starting with different classes of pyruvylated glycoconjugates and associated functions, leading to pyruvyltransferases, their specificity and sequence space, and insight into pyruvate analytics.https://www.mdpi.com/1422-0067/20/19/4929pyruvylationpyruvyltransferaseexopolysaccharidescapsular polysaccharidescell wall glycopolymers<i>n</i>-glycanslipopolysaccharidesbiosynthesissequence spacepyruvate analytics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fiona F. Hager Leander Sützl Cordula Stefanović Markus Blaukopf Christina Schäffer |
spellingShingle |
Fiona F. Hager Leander Sützl Cordula Stefanović Markus Blaukopf Christina Schäffer Pyruvate Substitutions on Glycoconjugates International Journal of Molecular Sciences pyruvylation pyruvyltransferase exopolysaccharides capsular polysaccharides cell wall glycopolymers <i>n</i>-glycans lipopolysaccharides biosynthesis sequence space pyruvate analytics |
author_facet |
Fiona F. Hager Leander Sützl Cordula Stefanović Markus Blaukopf Christina Schäffer |
author_sort |
Fiona F. Hager |
title |
Pyruvate Substitutions on Glycoconjugates |
title_short |
Pyruvate Substitutions on Glycoconjugates |
title_full |
Pyruvate Substitutions on Glycoconjugates |
title_fullStr |
Pyruvate Substitutions on Glycoconjugates |
title_full_unstemmed |
Pyruvate Substitutions on Glycoconjugates |
title_sort |
pyruvate substitutions on glycoconjugates |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2019-10-01 |
description |
Glycoconjugates are the most diverse biomolecules of life. Mostly located at the cell surface, they translate into cell-specific “barcodes” and offer a vast repertoire of functions, including support of cellular physiology, lifestyle, and pathogenicity. Functions can be fine-tuned by non-carbohydrate modifications on the constituting monosaccharides. Among these modifications is pyruvylation, which is present either in enol or ketal form. The most commonly best-understood example of pyruvylation is enol-pyruvylation of <i>N</i>-acetylglucosamine, which occurs at an early stage in the biosynthesis of the bacterial cell wall component peptidoglycan. Ketal-pyruvylation, in contrast, is present in diverse classes of glycoconjugates, from bacteria to algae to yeast—but not in humans. Mild purification strategies preventing the loss of the acid-labile ketal-pyruvyl group have led to a collection of elucidated pyruvylated glycan structures. However, knowledge of involved pyruvyltransferases creating a ring structure on various monosaccharides is scarce, mainly due to the lack of knowledge of fingerprint motifs of these enzymes and the unavailability of genome sequences of the organisms undergoing pyruvylation. This review compiles the current information on the widespread but under-investigated ketal-pyruvylation of monosaccharides, starting with different classes of pyruvylated glycoconjugates and associated functions, leading to pyruvyltransferases, their specificity and sequence space, and insight into pyruvate analytics. |
topic |
pyruvylation pyruvyltransferase exopolysaccharides capsular polysaccharides cell wall glycopolymers <i>n</i>-glycans lipopolysaccharides biosynthesis sequence space pyruvate analytics |
url |
https://www.mdpi.com/1422-0067/20/19/4929 |
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