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Thermal Inactivation of Pseudomonas Aeruginosa 1244 in Salted Sardinella Fimbriata Meat Homogenate
Thermal Inactivation of Pseudomonas Aeruginosa 1244 in Salted Sardinella Fimbriata Meat Homogenate
homogenate
homogenate suspending medium. The food matrix was determined to have a pH equal
to 5.85 and a w of 0.73. The moisture and NaCl contents were 38.25% and 13.81%,
0.90) at all heating temperatures. Thermal inactivation rates decreased with increasing
temperatures. The D values established were 70.94 s (60°C), 60.46 s (75°C), 31.11 s
(80°C) and 22.14 s (90°C).The thermal resistance parameter z value of 57.10°C was
determined. The results provide information on the behavior of the test organism in
heated salted herring meat, and could provide a basis for challenge studies involving
other microbial species and strains in similar food matrices. The thermal inactivation
schedules for salted herring meats, including mechanical dehydration and sun drying
This study determined the ultraviolet-C (UV-C) dose necessary to reduce 90% population
(DUV-C) of 17 spoilage yeasts and their composited inoculum in orange juice (pH 3.71,
11.60 °Brix, 0.55% citric acid, 2.46% w/v insoluble solids). Growth parameters of all test
yeasts were first established to standardize the growth stage of the cells prior to
harvesting and eventual UV-C challenge studies. Approximately 4–5 log CFU/ml cells in
the mid-stationary growth phase (30.3 t0 39.9 h, 25 °C) were suspended in 4 ml turbulent
flowing juice and subjected to UV-C irradiation at an incident surface irradiance of 3.64–
4.97 mW/cm². The inactivation rates of each yeast and their composited inoculum were
determined using 2 methods namely, the linear regression and Baranyi and Roberts
(1994) model-fitting. Results showed that the yeasts exhibited either log-linear or biphasic
(p < 0.05) UV-C resistance with DUV-C values of 1924.31 and 2174.63 mJ/cm². On the
other hand, Candida parapsilosis was determined to be least resistant with a DUV-C
values of 245.83 and 357.88 mJ/cm². Majority of the DUV-C values determined from the
model-fitting were greater than those calculated from linear regression. However, only
those determined for the composited inoculum were significantly different. The results of
this study address knowledge gaps pertinent to the UV-C resistance of less studied
spoilage yeast, and help in better understanding the utility of this non-thermal food
processing technology.
Decimal reduction energies of UV-C-irradiated spoilage yeasts in coconut liquid endosperm
yeasts and their composited inoculum were determined in coconut liquid endosperm (pH
5.26, 5.8 °Brix, 0.04% malic acid, 0.17% w/v insoluble solids). Growth kinetic parameters
of all the test yeast strains were first established to standardize the growth stage of the
cells prior to inactivation studies. Approximately 4.0 to 5.0 log CFU/mL cells in the mid-
stationary growth phase (30.3 to 39.9 h, 25 °C) were suspended in 4 mL turbulent flowing
juice and subjected to UV-C irradiation at a surface irradiance range of 3.42 to 4.99
enumerated, and were used to derive the DUV-C values using the linear regression and
Baranyi and Roberts (1994) model fitting. Results show that the yeast strains exhibited
either log-linear or biphasic inactivation behavior with inactivation lag. The most UV-C
resistant spoilage yeast was found to be Cryptococcus albidus (LJY1) with DUV-C values
of 122.72 and 214.89 mJ/cm² determined from linear regression and model-fitting,
respectively. The least UV-C resistant was Torulaspora delbrueckii (LYJ5) with a DUV-C
of 17.34 (linear regression) and 17.35 mJ/cm² (model-fitting). The DUV-C values
determined from the model fitting were generally greater than those calculated from linear
regression, although only those determined for C. albidus were significantly different. To
the investigators' knowledge, this is the first report of the UV-C inactivation kinetic
Individual and combined efficacies of mild heat and ultraviolet-c radiation against
Escherichia coli O157:H7, Salmonella enterica , and Listeria monocytogenes in coconut liquid
endosperm
heat, ultraviolet-C and combined heat-UV-C treated coconut liquid endosperm. Separate
monocytogenes strains were inoculated into coconut liquid endosperm (pH 5.15, TSS
4.4oBx, TA 0.062% malic acid, extinction coefficient (ε) at 254 nm of 0.0154 cm-1) for
inactivation studies. Result showed that all organisms generally exhibited a log-linear heat
inactivation behavior (R2 0.81-0.99). The E. coli O157:H7 cocktail (D55 = 19.75 min, D57
= 10.79 min, D60 = 3.38 min, and D63 = 0.46 min) was found to be significantly more
resistant (P > 0.05) than the tested cocktail of L. monocytogenes (D55 = 11.68 min, D57
= 4.53 min, D60 = 1.82 min and D63 = 0.26 min) and S. enterica cocktail (D55 = 3.08 min,
D57 = 2.60 min, D60 = 0.89 min and D63 = 0.25 min). Despite the differences in DT
values, computed z values for L. monocytogenes cocktail (5.12 ± 0.43 °C) and E. coli
O157:H7 cocktail (4.95 ± 0.12 °C) were not significantly different (P > 0.05), but were both
significantly (P < 0.05) lower than that of S. enterica cocktail (7.10 ± 0.15 °C). All test
organisms also exhibited a generally log-linear UV-C inactivation behavior (R2 0.90-0.99)
with E. coli O157:H7 cocktail (DUV-C = 25.26 mJ/cm2) demonstrating greatest resistance
17.30 mJ/cm2) cocktails. The D55 values of each organism cocktail were used to
calculate for the 3-log reduction heating process schedules, during which UV-C
combined processes revealed that within the 3-log reduction heating processes, co-
exposure of UV-C resulted in 5.62 to 6.20 log reductions in the test organism populations.
Heating caused 69.3, 97.2, and 67.4% of the reduction in E. coli O157:H7, S. enterica
data in the establishment of mild heat treatment in combination with UV-C process
A Candida parapsilosis inactivation-based UV-C process for calamansi (Citrus microcarpa ) juice
drink
Spoilage yeasts were isolated from ready-to-drink calamansi juice stored at room
isolates were Candida parapsilosis. Known population of each of the two isolates was
separately inoculated to freshly prepared juice drink and individually subjected to UV-C
inactivation challenge. Both isolates (BC1 and SC1) exhibited a biphasic inactivation
behavior, with an inactivation curve with upward concavity. The inactivation curves of both
isolates had an initial inactivation lag time with minimal or no population change (7.78–
14.64 s), followed by fast log-linear population decay (0.03–0.09 log CFU/s). Despite
exhibiting the same inactivation behavior, the inactivation kinetic parameters of the two
isolates were significantly different, with the SC1 isolate being more resistant. The
inactivation kinetic parameter of the SC1 isolate was therefore used as basis for the
establishment of UV-C process for the same calamansi juice drink with a lethal rate
against the test organism equal to 99.999%. Application and evaluation of the process
showed that the processed juice drink had sensory quality attributes not significantly
different from non-processed samples. These results provide baseline information on the
application of UV-C as a non-thermal processing technology for calamansi juice drink and
stainless steel surfaces commonly used as food contact surfaces. Two types of stainless steel
namely 304 and 316, were used as test surfaces with each type having three different finishes:
2B, Hair line (HL), and Mirror (MR). A cocktail of 7 serovars of S. enterica at mid stationary phase
(17 h) cells were allowed to adhere onto the surfaces (4h) prior to UV-C and plasma treatment.
Results showed that the test organism exhibited a biphasic UV-C inactivation composed of a fast
log linear inactivation phase followed by a slower inactivation tail on all test surfaces. The D
values calculated from the faster log linear inactivation phase ranged from 2.54 (316 2B and 316
HL) to 4.31 s (304 2B). The maximum population reduction calculated before the inactivation tail
ranged from 3.32 (316 HL) to 4.97 log CFU/in² (304 MR). Plasma treatment of metal surfaces
treatment, and led to log linear inactivation in all surfaces treated with atmospheric plasma jet.
The D values ranged from 2.66 (304 2B) to 3.43 s (316 MR). Both metal type and surface finish
were observed not to affect the efficacies of UV-C inactivation and atmospheric pressure plasma
jet treatment. The results obtained in the study demonstrated the potential of the tested physical
treatments as alternatives to commonly used food contact surface chemical sanitation protocols.
A model for the influences of soluble and insoluble solids, and treated volume on the
characteristics namely insoluble solids (IS, 0-3 %w/v), and soluble solids (SS, 0-70 °Brix),
and extrinsic process parameter treated volume (250-1000 mL) on the UV-C inactivation
of the test variables, while Response Surface Methodology (RSM) was used to
characterize and quantify the influences of the test variables on microbial inactivation.
The heat-stressed cells exhibited log-linear UV-C inactivation behavior (R² 0.952 to
0.999) in all CCRD combinations with DUV-C values ranging from 10.0 to 80.2 mJ/cm².
The DUV-C values obtained from the CCRD significantly fitted into a quadratic model (P
<0.0001). RSM results showed that individual linear (IS, SS, volume), individual quadratic
(IS² and volume²), and factor interactions (IS×volume and SS×volume) were found to
combinations not included in the CCRD showed that the predictions were within
gradual acidification (final pH 4.5), abrupt desiccation (aw 0.96), or heat stress at 40 °C
for 24 h, after which the test strains were cocktailed and subjected to UV-C challenge.
Cells were also exposed to all possible combinations of the individual stresses and
thereafter subjected to UV-C challenge. Cells exposed to all individual and combinations
of stresses exhibited 1st order, log-linear inactivation behavior (R² 0.903 to 0.998). Cells
previously exposed to singular heat stress had the highest UV-C resistance (DUV-C 43.8
mJ/cm²), while cells exposed to all simultaneous pH, aw, and heat stresses had the least
enterica cells were exposed to acid, acid + desiccation, heat, and acid + heat, with
individual heat stress exposure resulting in the significantly most UV-C resistant cells.
Results obtained in this study provide baseline information on the selection of appropriate
challenge organism for establishment of UV-C process schedule for coconut liquid
aqueous garlic bulb- (GBE), ethanolic lemon peel- (ELPE), and ethanolic orange peel
(EOPE) extracts against Escherichia coli K-12, E. coli O157:H7, Salmonella enterica
sauce. The maximum permissible supplementation (MPS) levels of GBE, ELPE, and
EOPE in the meat sauce formulation determined through sensory evaluations were 6.0%,
3.0%, and 3.0%, respectively. However, the MPS values of ELPE and EOPE did not
inhibit any of the test organisms in the subsequent antibacterial assays, with minimum
inhibitory concentration (MIC) values of 6.0 – 9.0% (ELPE) and 7.5 – 10.0% (EOPE). On
the other hand, GBE had an MIC values range of 1.0 – 2.5%. Thus, the study also
MICo values of 3.0% GBE +3.0% ELPE and 3.0% GBE +3.0% EOPE. Supplementation
of the meat sauce with these MICo resulted in products with similar consumer
meat sauce with the MICo of the test extracts exhibited bacteriostatic effect on selected
selected bacteria in UV-C treated human breast milk. Multi strain mixtures of Salmonella
Listeria monocytogenes, and a lone strain of Staphylococcus aureus were inoculated into
donated breast milk prior to UV-C inactivation studies. Results showed that the test
log-linear inactivation pattern within the 60-min UV-C treatment period. All other challenge
linear inactivation, followed by a slower inactivation tailing. Sublethal injury rates were
small in all test organisms except for S. aureus, which developed total sublethal injury
throughout the UV-C exposure. Despite the injury rates, S. aureus had the least total
population reduction (2.63 log CFU) after the 60-min treatment, while S. enterica had the
greatest reduction (3.88 log CFU). The inactivation behaviors established in this work