Influence of Bacteriophage PBS1 and φW-14 Deoxyribonucleic Acids on Homologous Deoxyribonucleic Acid Uptake and Transformation in Competent Bacillus subtilis

Author:

López Paloma1,Espinosa Manuel1,Piechowska Mirosława2,Shugar David2

Affiliation:

1. Consejo Superior de Investigaciones Cientificas, Instituto de Immunologia y Biologia Microbiana, Velasquez 144, Madrid 6, Spain

2. Institute of Biochemistry and Biophysics, Academy of Sciences, 02-532 Warsaw, Poland

Abstract

Both bacteriophage PBS1 deoxyribonucleic acid (DNA) (in which all the thymine residues are replaced by uracil) and phage φW-14 DNA [in which half the thymine residues are replaced by 5-(aminobutylaminomethyl)uracil or 5-putrescinylthymine] exhibit comparable competing abilities for uptake of homologous DNA in a Bacillus subtilis competent system. But, whereas PBS1 DNA leads to a decrease in transformation frequencies compatible with its competing ability for DNA uptake, φW-14 DNA decreases transformation frequencies by a factor up to eightfold higher. The effect of φW-14 DNA on transformation frequencies is visible even at a concentration level that does not decrease transforming DNA uptake. No such effect was observed with heterologous DNA containing presumably ionically bound putrescine. Low concentrations of φW-14 DNA decreased the number of double (nonlinked) transformants more than single transformants. The influence on transformation was abolished when φW-14 DNA was added 20 min after addition of transforming DNA, i.e., when the recombination process was terminated. The putrescine-containing DNA also decreased retention of trichloroacetic acid-precipitable radioactivity of homologous DNA taken up. We conclude that φW-14 DNA inhibits some intracellular process(es) at the level of recombination. In addition, there is evidence that φW-14 DNA, but not heterologous DNA with ionically bound putrescine, binds also to site(s) on the cell surface other than receptors for homologous DNA.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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