Acetanisole (4'-methoxyacetophenone) (AC), benzaldehyde (BE), cinnamal
dehyde (CI), diacetyl (DI), phenylpropionaldehyde (PH), and pyruvaldeh
yde (PY) were tested against growth of S. aureus WRRC B124 in brain he
art infusion broth. Activity was assessed in the presence and absence
of oxygen at 12, 19 and 37C, and in combination with mild (20 min at 5
0 or 60C) heat treatments. The carbonyl compounds limited S. aureus gr
owth. at minimal inhibitory concentrations (MIG) of less than or equal
to 0.5-8.0 mM. After 4 h at 37C, a 2 to 3-log(10) CFU/ml population r
eduction was observed with cultures containing 8.0 mM PH, PY, DI or Cl
. Activity was O-2-tension independent, with CI (0.5 mM), DI(2.0 mM) a
nd PY(2.0 mM) being most active. The MIC for CI was temperature indepe
ndent, while PY was most effective at 19C, and PH and DI at 12C. Mild
heat treatment of carbonyl-supplemented samples reduced previously obs
erved MICs. At 60C, for example, the MICs for AC and BE, 4.0 and 8.0 m
M respectively, were both reduced to less than or equal to 0.5 mM. The
decimal reduction times for S. aureus exposed to both UV-light and 8
mM flavor compounds were 3.3 and 4.3 s for CI and DI, respectively. Ho
wever, the other compounds were not as effective in the presence of UV
since the decimal reduction rimes ranged from 77 to 9.0 s. The carbon
yl compounds tested were effective antistaphylococcal agents and their
use in combination with thermal processing may serve as a new approac
h to control S. aureus growth and other gram-positive foodborne pathog
ens.