2012
DOI: 10.1074/jbc.m111.324012
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O-antigen and Core Carbohydrate of Vibrio fischeri Lipopolysaccharide

Abstract: Background:The structure and function of the Vibrio fischeri O-antigen were unknown. Results: The O-antigen structure was determined using an O-antigen ligase mutant. Conclusion: This mutant had a motility defect, and comparison of its LPS with wild-type LPS showed that the O-antigen contains some unusual sugars. Significance: The O-antigen mutation results in a significantly slower rate of bacterial colonization of the squid light organ.

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Cited by 58 publications
(36 citation statements)
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“…The addition of this LPS extract significantly inhibited biofilm growth in a concentration-dependent manner ( Figure 1B), as previously shown by Kim et al (2007). To further evaluate the inhibitory role of LPS in biofilm formation, the lipid moiety of LPS was removed by acidic hydrolysis (Post et al 2012). The resultant dLPS, which does not include the lipid A part of LPS ( Figure 1A, right lane), was added to the biofilm assay at time zero.…”
Section: Effects Of the Exogenous Addition Of Lps Dlps Lps Core Comsupporting
confidence: 69%
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“…The addition of this LPS extract significantly inhibited biofilm growth in a concentration-dependent manner ( Figure 1B), as previously shown by Kim et al (2007). To further evaluate the inhibitory role of LPS in biofilm formation, the lipid moiety of LPS was removed by acidic hydrolysis (Post et al 2012). The resultant dLPS, which does not include the lipid A part of LPS ( Figure 1A, right lane), was added to the biofilm assay at time zero.…”
Section: Effects Of the Exogenous Addition Of Lps Dlps Lps Core Comsupporting
confidence: 69%
“…Since the LPS fraction was found to be slightly contaminated with another type of exopolysaccharide that is tightly bound to membranes, such as CPS, the wbpP mutant defective in CPS production (Lee et al 2013) was used to prepare CPS-free LPS. Lipid A components in the extracted LPS were removed by treating LPS with 1% acetic acid at 100°C for 2 h, as described by Post et al (2012). The resulting dLPS was precipitated with ethanol and resuspended in distilled water.…”
Section: Extraction and Deacylation Of Lpsmentioning
confidence: 99%
“…In contrast to the ompU mutant, neither colonization by the waaL mutant nor treatment with waaL mutant-derived OMV resulted in a detectable difference in phenotypic responses from that of wild-type cells (see Fig. S2 in the supplemental material), even though the waaL mutant colonizes at a lower level (18). These results suggest that OMV recognition is not dependent on O-antigen recognition.…”
Section: Resultsmentioning
confidence: 82%
“…fischeri has been reported to express an unusual O antigen on its LPS, so we next asked whether this major envelope surface element plays a role in OMV recognition. Specifically, we determined how host development was affected by symbionts carrying a mutation in the waaL gene, which eliminates the bacterium's ability to ligate the O antigen to the core LPS (18). In contrast to the ompU mutant, neither colonization by the waaL mutant nor treatment with waaL mutant-derived OMV resulted in a detectable difference in phenotypic responses from that of wild-type cells (see Fig.…”
Section: Resultsmentioning
confidence: 99%
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