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Journal of Bacteriology, October 2004, p. 6560-6574, Vol. 186, No. 19
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.19.6560-6574.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Complete Genomic Sequence of Bacteriophage B3, a Mu-Like Phage of Pseudomonas aeruginosa{dagger}

Michael D. Braid,1 Jennifer L. Silhavy,1 Christopher L. Kitts,1 Raul J. Cano,1 and Martha M. Howe2*

Biological Sciences Department and Environmental Biotechnology Institute, California Polytechnic State University, San Luis Obispo, California,1 Department of Molecular Sciences, University of Tennessee Health Science Center, Memphis, Tennessee2

Received 24 March 2004/ Accepted 9 July 2004

Bacteriophage B3 is a transposable phage of Pseudomonas aeruginosa. In this report, we present the complete DNA sequence and annotation of the B3 genome. DNA sequence analysis revealed that the B3 genome is 38,439 bp long with a G+C content of 63.3%. The genome contains 59 proposed open reading frames (ORFs) organized into at least three operons. Of these ORFs, the predicted proteins from 41 ORFs (68%) display significant similarity to other phage or bacterial proteins. Many of the predicted B3 proteins are homologous to those encoded by the early genes and head genes of Mu and Mu-like prophages found in sequenced bacterial genomes. Only two of the predicted B3 tail proteins are homologous to other well-characterized phage tail proteins; however, several Mu-like prophages and transposable phage D3112 encode approximately 10 highly similar proteins in their predicted tail gene regions. Comparison of the B3 genomic organization with that of Mu revealed evidence of multiple genetic rearrangements, the most notable being the inversion of the proposed B3 immunity/early gene region, the loss of Mu-like tail genes, and an extreme leftward shift of the B3 DNA modification gene cluster. These differences illustrate and support the widely held view that tailed phages are genetic mosaics arising by the exchange of functional modules within a diverse genetic pool.


* Corresponding author. Mailing address: Department of Molecular Sciences, University of Tennessee Health Science Center, 858 Madison Ave., Memphis, TN 38163. Phone: (901) 448-8215. Fax: (901) 448-8462. E-mail: mhowe{at}utmem.edu.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.


Journal of Bacteriology, October 2004, p. 6560-6574, Vol. 186, No. 19
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.19.6560-6574.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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