The genomic cleavage map of Salmonella paratyphi B was determined thro
ugh digestion with endonucleases and separation of the fragments by pu
lsed-field gel electrophoresis. The chromosome has 19 XbaI sites, 10 B
lnI sites, and 7 CeuI sites. The fragments were arranged in order thro
ugh excision of fragments from the gel, redigestion with a second enzy
me, end labelling with P-32, and reelectrophoresis. Tn10 transposons i
nserted in 61 different genes of S. typhimurium LT2 were transduced by
use of bacteriophage P22 into S. paratyphi B. The locations of Tn10 i
nsertions on the chromosome of S. paratyphi B were determined by use o
f,E;bal and BlnI sites in Tn10, revealing the positions of genes with
Tn10 insertions in S. paratyphi B. All seven CeuI sites (in rrl genes
for 23S rRNA) and most of the XbaI and BlnI sites in rm genes for Glt-
tRNA are conserved, but only about half of the XbaI and BlnI sites out
side rm genes are conserved. Gene order is identical in the 68 genes t
hat we could compare between S. paratyphi B and S. typhimurium LT2, an
d the lengths of intervals between the genes are often the same, but t
here are several instances of differences in interval lengths, indicat
ing that insertions or deletions of DNA have occurred during the evolu
tionary divergence of these bacteria.