Pyrimidine metabolism is an appropriate model for studying bacterial genome
dynamics. Whereas pyrimidine de novo biosynthesis and salvage pathways are
the same throughout the living world, the organization of the correspondin
g pyr genes varies greatly from one organism to another. Lactobacillus plan
tarum has a large pyr biosynthesis operon and a bicistronic cluster involve
d in pyrimidine salvage. These features were the starling point of a compar
ative study of all known pyr structures. All lactic acid bacteria possess t
wo pyrD genes, both encoding a functional enzyme, except L, plantarum. Addi
tionally L. plantarum has no pyrK gene, and its pyrP and upp genes form a c
luster. pyr operonic structures are common among Gram(+) bacteria and are r
elatively well conserved, but there is greater diversity amongst the lactic
acid bacteria. This diversity could be due to adaptation to new ecological
niches, correlated with functional gains or losses. This, in turn, could g
ive rise to the differences in genome size.