The genome of the Bacillus subtilis 168-type strain contains 10 ribosomal R
NA (rRNA) operons. In the intergenic spacer region (ISR) between the 16S an
d 23S rRNA genes, five rRNA operons, rrnl-H-G and rrnJ-W, lack a trinucleot
ide signature region. Precise determination of molecular weight (MW), using
electrospray mass spectrometry (MS), of the polymerase chain reaction (PCR
) products from a segment of the ISR from the 168-type strain and B. subtil
is 168-like strain 23071 demonstrated 114 and 111 basepair (bp) PCR product
s (due to the presence or absence of the insert in the operons) as predicte
d from sequence. However, PCR of the ISR segment for five other B. subtilis
168 isolates generated only a 114bp PCR product, suggesting the presence o
f the trinucleotide signature region in all rRNA operons for these strains.
Additional genetic variability between the seven B. subtilis 168 isolates
was demonstrated by restriction fragment length polymorphism (RFLP) of the
rRNA operons, with three distinct patterns found upon Southern blot analysi
s. The 168-type strain and three others (23066, 23067, and 23071) exhibited
the same Southern pattern. Thus, operon deletion is not responsible for th
e absence of a 111 bp product on MS analysis for strains 23066 and 23067. R
estriction analysis confirmed the presence of the trinucleotide signature r
egion in the ISR of all rRNA operons for five B. subtilis 168 isolates; seq
uencing of rrnW/H from a representative strain also upheld this finding. Th
ese results help provide a better understanding of variations in sequence,
operon number and chromosomal organization, both within a genome and among
isolates of B. subtilis subgroup 168. It is also hypothesized that the pres
ence of the trinucleotide insert in certain rRNA operons may play a role in
rRNA maturation and protein synthesis.