Bacterial Lipopolysaccharide, OPS, and Lipid A

2013 ◽  
pp. 161-162
Author(s):  
Antonio Molinaro ◽  
Michelangelo Parrilli ◽  
Cristina Castro
1981 ◽  
Vol 90 (2) ◽  
pp. C8-C11 ◽  
Author(s):  
Makoto Kiso ◽  
Yasuhiko Goh ◽  
Eiji Tanahashi ◽  
Akira Hasegawa ◽  
Hiroyuki Okumura ◽  
...  

Author(s):  
Antonio Molinaro ◽  
Cristina De Castro ◽  
Michelangelo Parrilli

1975 ◽  
Vol 31 (1) ◽  
pp. 83-92 ◽  
Author(s):  
Nelda M. Marecki ◽  
S.G. Bradley ◽  
A.E. Munson ◽  
D.C. Drummond

1996 ◽  
Vol 3 (3) ◽  
pp. 173-178 ◽  
Author(s):  
Klaus Brandenburg ◽  
Ulrich Seydel ◽  
Andra B. Schromm ◽  
Harald Loppnow ◽  
Michel H.J. Koch ◽  
...  

2013 ◽  
Vol 59 (10) ◽  
pp. 645-655 ◽  
Author(s):  
Jolanta Lodowska ◽  
Daniel Wolny ◽  
Ludmiła Węglarz

The sugar 3-deoxy-d-manno-oct-2-ulosonic acid (Kdo) is a characteristic component of bacterial lipopolysaccharide (LPS, endotoxin). It connects the carbohydrate part of LPS with C6 of glucosamine or 2,3-diaminoglucose of lipid A by acid-labile α-ketosidic linkage. The number of Kdo units present in LPS, the way they are connected, and the occurrence of other substituents (P, PEtn, PPEtn, Gal, or β-l-Ara4N) account for structural diversity of the inner core region of endotoxin. In a majority of cases, Kdo is crucial to the viability and growth of bacterial cells. In this paper, the biosynthesis of Kdo and the mechanism of its incorporation into the LPS structure, as well as the location of this unique component in the endotoxin core structures, have been described.


1979 ◽  
Vol 25 (2) ◽  
pp. 124-129 ◽  
Author(s):  
John N. Saddler ◽  
John G. Coote ◽  
Alastair C. Wardlaw

A strain of the acellular slime mould Physarum polycephalum degraded lipopolysaccharides (LPS) from a variety of bacteria. The anticomplementary (AC) activity of LPS was greatly reduced, as was the content of lauric, myristic, and palmitic acids, and the ability to sensitize erythrocytes to agglutination by antibody. These results indicate that Physarum has enzymes which reduce the lipid A moiety of LPS. In contrast. 2-keto-3-deoxy-D-manno-actanoic acid (KDO), immunodominant sugars, and β-hydroxymyristic acid were scarcely affected. Both supernates and plasmodial extracts of Physarum had LPS-degradative activity and were able to attack both purified LPS and LPS in killed bacteria.


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