Fig. 2.
Rep-PCR analysis of 30 colonies picked from kimchi inoculated with L. mesenteroides 11251and L. brevis B151. From kimchi inoculated with L. mesenteroides 11251. Using (GTG)5 primer (A), Lane: 1–100 bp marker, Lane: 2–16 (colonies KM1-15), Lane: 17-strain 11251, Lane: 18–100 bp marker, Lower half of the Gel—Lane: 19–100 bp marker, Lane: 20–34 (colonies KM16-30), Lane: 35-strain 11251, Lane: 36–100 bp marker. Using REP primer (B), Lane: 1–100 bp marker, Lane: 2–16 (colonies KM1-15), Lane: 17-strain 11251, Lane: 18–100 bp marker, Lane: 19–1 kb marker, lower half of the Gel—Lane: 20–100 bp marker, Lane: 21–35 (colonies KM16-30), Lane: 36-strain 11251, Lane: 37–100 bp marker, Lane: 38–1 kb marker. Using ERIC primer (C), Lane: 1–100 bp marker, Lane: 2–16 (colonies KM1-15), Lane: 17-strain 11251, Lane: 18–100 bp marker, Lower half of the Gel—Lane: 19–100 bp marker, Lane: 20–34 (colonies KM16-30), Lane: 35-strain 11251, Lane: 36–100 bp marker. From kimchi inoculated with L. brevis B151. Using (GTG)5 primer (D), Lane: 1–100 bp marker, Lane: 2–16 (colonies KB1-15), Lane: 17-strain B151, Lane: 18–100 bp marker, Lower half of the Gel—Lane: 19–100 bp marker, Lane: 20–34 (colonies KB16-30), Lane: 35-strain B151, Lane: 36–100 bp marker. Using REP primer (E), Lane: 1–100 bp marker, Lane: 2–16 (colonies KB1-15), Lane: 17-strain B151, Lane: 18–100 bp marker, Lane: 19–1 kb marker, Lower half of the Gel—Lane: 20–100 bp marker, Lane: 21–35(colonies KB16-30), Lane: 36-strain B151, Lane: 37–100 bp marker, Lane: 38–1 kb marker. Using ERIC primer (F), Lane: 1–1 kb marker, Lane: 2–100 bp marker, Lane: 3–17 (colonies KB1-15), Lane: 18-strain B151, Lane: 19–100 bp marker, Lower half of the Gel—Lane: 20–1 kb marker, Lane: 21–100 bp marker, Lane: 22–36 (colonies KB16-30), Lane: 37-strain B151, Lane: 38–100 bp marker. Positive controls-11251 and B151