African Journal of Biotechnology

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Afr. J. Biotechnol.


Vol. 6 No.19



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Khalil R

Omar SH

 


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African Journal of Biotechnology Vol. 6 (19), pp. 2280-2286, 4 October 2007   

ISSN 1684–5315 © 2007 Academic Journals        

 

 

Full Length Research Paper

 

Inhibition of phage infection in capsule-producing Streptococcus thermophilus using   concanavalin A, lysozyme and saccharides

 

Rowaida Khalil1*, Joseph F. Frank2, Ashraf N. Hassan3, and Sanaa H. Omar1

 

1Botany Department, Faculty of Science, Alexandria University, Alexandria, Egypt.

2Department of Food Science and Technology, University of Georgia, Athens, GA 30602 USA.

3Dairy Science Department, South Dakota State University, Brookings, SD 57007, USA.

 

*Corresponding author. E-mail: rowaida_georgia1@hotmail.com. Tel: 002-3921595. Mobile. 002 0123772803. Fax: 002-3911794.

 

Accepted 16 July, 2007

 
    Abstract

 

 

 

Lactic cultures that produce capsular polysaccharides are widely used in the dairy industry. However, little information is available on their phage-cell interactions.  Concanavalin A (Con A), lysozyme, and saccharides were investigated for their ability to modify phage-cell interactions in such a manner as to inhibit phage infection. The ability of phage to infect cells was determined by measuring acid production in Elliker broth. Acid production by capsule-producing Streptococcus thermophilus was inhibited less by bacteriophage when cells were pretreated with Con. A than was acid production by a capsule-free variant. The presence of 0.5 mg/ml lysozyme in Elliker broth significantly reduced phage infection. However, there was no increased effect when lysozyme and Con A were combined in the growth medium. The addition of 5 g/L of glucosamine to Elliker broth also inhibited phage infection. The results of this study indicate that it is possible to reduce phage infection of capsule-forming S. thermophilus by blocking or modifying phage adsorption sites.

 

Key words: Capsular polysaccharides, Concanavalin A, bacteriophage adsorption, adsorption sites, phage inhibition.

 

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