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Bioinformatics Vol. 17 no. 90001 2001
Pages S253-S261
© 2001 Oxford University Press

Designing better phages

Steven S. Skiena

Applied Algorithm Laboratory, Dept. of Computer Science, State University of New York, Stony Brook, NY, 11794-4400, USA

Received on February 5, 2001 ; revised on March 30, 2001 ; accepted on March 30, 2001

We propose a method to engineer the genome of bacteriophages to increase their effectiveness as antibacterial agents. Specifically, we exploit the redundancy of the triplet code to design genomes that avoid restriction sites while producing the same proteins as wild-type phages. We give an efficient algorithm to minimize the number of restriction sites against sets of cutter sequences, and demonstrate that that phage genomes can be significantly protected against surprisingly large sets of enzymes with no loss of function. Finally, we develop a model to explain why evolution has failed to eliminate many possible restriction sites despite selective pressure, thus motivating the need for genome-level sequence engineering.

Contact: skiena{at}cs.sunysb.edu


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