Canadian Journal of Microbiology · 1993 · 28 citations · 17 references
Life SciencesGeneticsMicrobiologyBacteriologyEnzymologyMicrobial GeneticsBacteriophage GeneticsBacteriophage VectorsPhage GeneticsAlternative Start CodonsAlternative Translation InitiationBacteriophage BiologyBacteriophagesEscherichia ColiOpen Reading Frame IdentificationPhage Gene TransferUpstream Open Reading Frames
Approximately 80% of the genome of the prolate-headed lactococcal bacteriophage c2 was cloned into shuttle vectors pSA3 and pFX3 in Escherichia coli and transferred to Lactococcus lactis. A 1.67-kilobase EcoRV fragment containing the gene for the phage lysin was identified and the position and orientation of the phage lysin gene in the physical map of the phage were determined. The phage lysin was expressed in E. coli and its sequence was determined and compared with the sequences of other bacteriophage lytic genes. The sequence was similar, but not identical, to that of the related lactococcal phage m13, having a number of silent substitutions and an apparent deletion that altered the carboxy terminus of the protein. Possible alternative translation initiation codons for the lysin gene and two possible alternative mechanisms for access of the lysin enzyme to the cell wall are discussed. An open reading frame upstream of the putative lysin gene was found to be 177 base pairs longer than that reported for phage m13. A codon usage table for the lysin genes of several phages as well as for reported gene sequences from L. lactis and lactococcal bacteriophages is presented.
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A comprehensive set of sequence analysis programs for the VAX
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