Development and PFGE monitoring of dominance among spoilage lactic acid bacteria from cured meats

Citation
Gp. Zhang et Ra. Holley, Development and PFGE monitoring of dominance among spoilage lactic acid bacteria from cured meats, FOOD MICROB, 16(6), 1999, pp. 633-644
Citations number
16
Categorie Soggetti
Food Science/Nutrition
Journal title
FOOD MICROBIOLOGY
ISSN journal
07400020 → ACNP
Volume
16
Issue
6
Year of publication
1999
Pages
633 - 644
Database
ISI
SICI code
0740-0020(199912)16:6<633:DAPMOD>2.0.ZU;2-T
Abstract
Strains of lactic acid bacteria (LAB), isolated from intact vacuum-packaged cured meats obtained at retail were subjected to single inhibitory factor and mixed-culture dominance tests during challenge with different condition s of pH and temperature in the presence of NaCl and NaNO2 to study reasons for strain dominance. Bacteria were checked for bacteriocin production Both initial pH and temperature had a significant effect on the growth of spoil age LAB isolates in modified MRS broth. Lactobacilli generally grew better than Lc. mesenteroides at pH 5.5. it appeared that L. curvatus and L. sakei grew faster at elevated temperature (12 degrees C) than Lc. mesenteroides. it was also noted that there was a similar response for strains within the same species to the challenges of NaCl, NaNO2, pH and temperature. When pr esent in mixed cultures, Leuconostoc strains did not grow well at 2 degrees C and at an initial pH of 5.5 compared with lactobacilli, but performed be tter at this low temperature as pure cultures than when mixed with lactobac illi. At normal cured meat pH (6.0 and 6.5) and higher temperatures (6 degr ees C and 12 degrees C), dominant bacteria always grew from the originally larger bacterial population. When leuconostocs and lactobacilli were presen t in equal initial numbers, leuconostocs generally did not grow as well as lactobacilli. Lc mesenteroides grew faster than L. curvatus at 6 degrees C but did not out-compete L. sakei at this temperature (pH greater than or eq ual to 6.0). Pulsed field gel electrophoresis (PFGE) of Smal digested genom ic DNA successfully distinguished all the strains under study Difficulties associated with enumeration of LAB having similar biochemical properties we re addressed by the development of a composite-simultaneous PFGE method for interspecies qualification using single colonies from agar plates to gener ate digested DNA for analysis. (C) 1999 Academic Press.