A 300 bp DNA fragment of Lactobacillus plantarum isolated by randomly
amplified polymorphic DNA (RAPD) analysis was cloned and sequenced. Th
is fragment was tested using a dot-blot DNA hybridization technique fo
r its ability to identify Lact. plantarum strains. This probe hybridiz
ed with all Lact. plantarum strains tested and with some strains of La
ct. pentosus, albeit more weakly. Two internal primers of this probe w
ere selected (LbP11 and LbP12) and polymerase chain reaction (PCR) was
carried out, All Lact. plantarum strains tested amplified a 250 bp fr
agment contrary to the other LAB species tested, This specific PCR for
Lact. plantarum was also performed from colonies grown on MRS medium
with similar results. These methods enabled the rapid and specific det
ection and identification of Lact. plantarum.