scispace - formally typeset
Open AccessJournal ArticleDOI

Phage-induced fucosidases hydrolysing the exopolysaccharide of Klebsiella arogenes type 54 [A3(S1)].

IW Sutherland
- 01 Jul 1967 - 
- Vol. 104, Iss: 1, pp 278-285
Reads0
Chats0
TLDR
Several strains of bacteriophage have been isolated that induce the formation of a polysaccharide hydrolase after infection of Klebsiella aerogenes type 54 [A3(S1]], and a study of the products released by enzyme action has shown it to be a fucosidase splitting the fucOSylglucose linkages found in the intact poly Saccharide.
Abstract
Several strains of bacteriophage have been isolated that induce the formation of a polysaccharide hydrolase after infection of Klebsiella aerogenes type 54 [A3(S1)]. The action of this enzyme on polysaccharide solutions was to decrease their viscosity and increase their reducing value. These effects were associated with the release of two oligosaccharides (O1 and O2) from the polysaccharide. These two substances are not identical with any of the four oligosaccharides isolated from autohydrolysates. The two enzymically isolated fractions have been tentatively identified as tetrasaccharides, and oligosaccharide O2 is probably an acetylated version of oligosaccharide O1. This latter oligosaccharide differs in some way, still unknown, from the tetrasaccharide cellobiosylglucuronosylfucose found in acid hydrolysates of the slime polysaccharide. The enzyme is limited in its activity to the polysaccharide excreted by the A3 strain of K. aerogenes type 54 or by similar strains. It is also active on the polysaccharides altered by acid or alkaline treatment. The enzyme has optimum activity at pH6·5. A study of the products released by enzyme action has shown it to be a fucosidase splitting the fucosylglucose linkages found in the intact polysaccharide.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Preventing biofilms of clinically relevant organisms using bacteriophage

TL;DR: Bacteriophage has been used to treat infectious diseases in humans and there is interest in phage to control biofilms, and Lytic bacteriophages could become a new class of anti-biofilm agents.
Journal ArticleDOI

Structure-function relationships in microbial exopolysaccharides.

TL;DR: Microbial exopolysaccharides frequently carry acyl groups which may profoundly affect their interactive properties although these groups often have relatively little effect on solution viscosity, and recent work in the laboratory suggests that deacetylation of certain bacterial alginates also significantly increases ion binding by these polysaccharide, making them more similar in their properties to algalAlginates even although the alginate species lack poly-L-guluronic acid sequences.
Book ChapterDOI

Biosynthesis of Microbial Exopolysaccharides

TL;DR: This chapter explores that numerous microorganisms produce exopolysaccharides, which have been most studied are those produced by Enterobacter aerogenes, Escherichia coli and Streptococcus (Dipfococcus) pneumoniae.
Journal ArticleDOI

Bacteriophage and associated polysaccharide depolymerases: Novel tools for study of bacterial biofilms

TL;DR: The bacteriophage and their associated enzymes provide very useful highly specific tools for studies of biofilms incorporating the bacterial host strains, and their potential applications in studies on bacterial biofilmms are discussed.
Journal ArticleDOI

Controlling bacterial biofilms.

TL;DR: The ubiquitous nature of bacteria in the environment, and the role they play in infectious disease has been one of the most extensively researched areas in biomedical science, and upwards of 75 % of microbial infections that occur in the human body are underpinned by the formation and persistence of biofilms.
Related Papers (5)