2012
DOI: 10.1016/j.carres.2012.02.002
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Structural characterization of surface glycans from Clostridium difficile

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Cited by 66 publications
(71 citation statements)
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“…This cell biological function, i.e., the markings of new and old peptidoglycan or of discrete subcellular sites, may explain the essential contributions of teichoic acids to bacterial growth. Technological advances such as NMR and mass spectrometry have provided the means of identifying and characterizing the structures of new amphiphiles from Gram-positive bacteria (44,135). Yet we remain unable to build models for the synthesis of many different types of LTA molecules.…”
Section: Discussionmentioning
confidence: 99%
“…This cell biological function, i.e., the markings of new and old peptidoglycan or of discrete subcellular sites, may explain the essential contributions of teichoic acids to bacterial growth. Technological advances such as NMR and mass spectrometry have provided the means of identifying and characterizing the structures of new amphiphiles from Gram-positive bacteria (44,135). Yet we remain unable to build models for the synthesis of many different types of LTA molecules.…”
Section: Discussionmentioning
confidence: 99%
“…A Gal-Gal-GroP-repeating unit was detected in Lactococcus garvieae (formerly Streptococcus lactis ) [22, 27, 29, 31,32,33,34]. Several rare repeating units have been identified in Clostridium difficile [35], Clostridium innocuum ATCC 14501 T [34], Streptococcus oralis Uo5 [36], and Streptococcus pneumoniae R6 (ATCC BAA-225) [34, 37,38,39,40] and R36A (ATCC 12214) [37] (see Table 1 for detailed structures).…”
Section: Structural Diversity In Ltasmentioning
confidence: 99%
“…We were unable to isolate staphylococcal mutants with resistance against compound 1771, suggesting that LTA synthesis may display target attributes similar to peptidoglycan synthesis. Some Gram-positive bacteria, for example, C. difficile and S. pneumoniae, synthesize LTA with distinct phosphate-polymer structures (42,43); however, their mechanisms of synthesis and possible inhibition by compound 1771 are not yet known. Future work must develop compound 1771 further to generate molecules that are stable in mammalian tissues and display antibiotic activity against many different bacteria.…”
Section: Selecting For S Aureus Variants With Increased Resistance Tmentioning
confidence: 99%