Cloning, sequencing, and overexpression of gene 16 of Salmonella bacteriophage P22

Virology. 1992 Jun;188(2):495-501. doi: 10.1016/0042-6822(92)90503-h.

Abstract

It has been suggested that gene product 16 of bacteriophage P22 forms a pore for DNA transfer and/or that it functions as a pilot protein guiding the DNA across the membrane. We have cloned gene 16 and determined the nucleotide sequence. Within the sequenced region there is an open reading frame that could encode a protein of 609 amino acids having a molecular weight of 64,366. The hydropathic plot of this protein does not reveal putative membrane-spanning regions as expected for a protein forming a membrane pore. Overproduction of gene product 16 in Escherichia coli was successful only in a mutant in which the La protease was inactivated. Gene 16 mutants of phage P22 were not able to infect recBCD mutants of Salmonella typhimurium nor was protein 16, synthesized in E. coli from a plasmid, able to substitute for the pilot protein of phage T4. It seems that gene product 16 is not a pilot protein in the meaning of binding to the ends of linear DNA, thus protecting it from degradation by nucleases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cloning, Molecular
  • DNA, Viral / metabolism
  • Genes, Viral*
  • Genetic Complementation Test
  • Molecular Sequence Data
  • Recombinant Proteins
  • Restriction Mapping
  • Salmonella Phages / genetics*
  • Solubility
  • Viral Proteins / chemistry
  • Viral Proteins / genetics*
  • Viral Structural Proteins / genetics*

Substances

  • DNA, Viral
  • Recombinant Proteins
  • Viral Proteins
  • Viral Structural Proteins
  • gene 16 protein, Enterobacteria phage P22

Associated data

  • GENBANK/M74136