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Recognition of 2-keto-3-deoxyoctonate in bacterial cells and lipopolysaccharides by the sialic acid binding lectin from the horseshoe crab Carcinoscorpiusrotundacauda
Authors:DThambi Dorai  Subita Srimal  S Mohan  BK Bachhawat  TS Balganesh
Institution:1. Enzyme Engineering laboratory, Indian Institute of Chemical Biology, Calcutta 700 032 India.;2. Microbiology laboratory, Indian Inatitute of Chemical Biology, Calcutta 700 032 India.
Abstract:The sialic acid binding loctin carcinoscorpin agglutinates Escharichiacoli K12 andSalmonellaminnesots R595 cells. This interaction can be inhibited by the saccharides namely 2-keto-3-deoxyoctonate and the disaccharide D-(N-acetylneuraminyl) (2→6)2-acetamide-2-deoxy-D-galactitol. N-acetylneuraminic acid is shown to be a poor inhibitor. The same behaviour is seen when purified lipopolysaccharides from these two Gram negative bacteria are used. Vibriocholerae, a Grum negative bectarium devoid of 2-keto-3-deoxyoctonate and Staphylococcussureus a typical Gram positive bacterium failed to agglutinate in the presence of the lectin. The results suggest that the 2-keto-3-deoxyoctonate residues might represent the physiological substrate for the sialic acid binding lectin from the horseshoa crab.
Keywords:CSN  Carcinoscorpin  KDO  2-keto-3-deoxyoctonate  NANA  N-acetylneuraminic acid  Disaccheride-O-(N-acetylneuraminyl)(2→6)  2-acetamido-2-deoxy-D-galactiol  LPS  Lipepolysaccharide  Sialic acid binding lectin/2-keto-3-deoxyoctonate/lipopolysaccharides/recognition
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