Burkholderia cenocepacia lectin A binding to heptoses from the bacterial lipopolysaccharide

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Publikace nespadá pod Ekonomicko-správní fakultu, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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MARCHETTI Roberta MALINOVSKÁ Lenka LAMEIGNERE Emilie ADAMOVÁ Lenka DE CASTRO Cristina CIOCI Gianluca STANETTY Christian KOSMA Paul MOLINARO Antonio WIMMEROVÁ Michaela IMBERTY Anne SILIPO Alba

Rok publikování 2012
Druh Článek v odborném periodiku
Časopis / Zdroj Glycobiology
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www http://glycob.oxfordjournals.org/content/22/10/1387.abstract
Doi http://dx.doi.org/10.1093/glycob/cws105
Obor Biochemie
Klíčová slova bacterial lectin;heptose;lipopolysaccharide;NMR;titration microcalorimetry
Přiložené soubory
Popis Bacteria from the Burkholderia cepacia complex (Bcc) cause highly contagious pneumonia among cystic fibrosis (CF) patients. Among them, Burkholderia cenocepacia is one of the most dangerous in the Bcc and is the most frequent cause of morbidity and mortality in CF patients. Indeed, it is responsible of “cepacia syndrome”, a deadly exacerbation of infection, that is the main cause of poor outcomes in lung transplantation. Burkholderia cenocepacia produces several soluble lectins with specificity for fucosylated and mannosylated glycoconjugates. These lectins are present on the bacterial cell surface and it has been proposed that they bind to lipopolysaccharide epitopes. In this work, we report on the interaction of one B. cenocepacia lectin, BC2L-A, with heptose and other manno configured sugar residues. Saturation transfer difference NMR spectroscopy studies of BC2L-A with different mono- and disaccharides demonstrated the requirement of manno configuration with the hydroxyl or glycol group at C6 for the binding process. The crystal structure of BC2L-A complexed with the methyl-heptoside confirmed the location of the carbohydrate ring in the binding site and elucidated the orientation of the glycol tail, in agreement with NMR data. Titration calorimetry performed on monosaccharides, heptose disaccharides and bacterial heptose-containing oligosaccharides and polysaccharides confirmed that bacterial cell wall contains carbohydrate epitopes that can bind to BC2L-A. Additionally, the specific binding of fluorescent BC2L-A lectin on B. cenocepacia bacterial surface was demonstrated by microscopy.
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