Influence of partial inactivation on growth of Listeria monocytogenes under sub-optimal conditions of increased NaCl concentration or increased acidity

2009 ◽  
Vol 10 (2) ◽  
pp. 267-271 ◽  
Author(s):  
Andreja Rajkovic ◽  
Mieke Uyttendaele ◽  
Nancy Van Houteghem ◽  
Sandra Maria Osés Gómez ◽  
Johan Debevere ◽  
...  
1996 ◽  
Vol 59 (1) ◽  
pp. 16-23 ◽  
Author(s):  
R. H. LINTON ◽  
W. H. CARTER ◽  
M. D. PIERSON ◽  
C. R. HACKNEY ◽  
J. D. EIFERT

The heat resistance of Listeria monocytogenes was determined in infant formula for all possible combinations of temperature (50, 55, and 60°C), pH level (5, 6, and 7), and NaCl concentration (0, 2, and 4%). Survival curves were fit using nonlinear regression with a Gompertz equation. The Gompertz equation was flexible enough to fit the three most commonly observed survival curves: linear curves, those with an initial lag region followed by a linear region, and sigmoidal shaped. Parameter estimates obtained by the method of nonlinear least squares were used to describe the effect(s) of different heating treatments on the lag region, death rate, and tailing region of survival curves. These estimates were further used to predict single and interactive effects of temperature, pH, and percentage of NaCl on the log of the surviving fraction (LSF) of bacteria. Interactions among these variables significantly (P ≤ .05) affected the LSF. Generally, increased pH or NaCl concentration lead to an increased LSF, whereas increased time or temperature lead to a decreased LSF. All multiple-factor interactions significantly (P ≤ .05) affected the LSF. The correlation of observed LSF versus predicted LSF (R2 = .92) indicated that the estimated Gompertz equation was in close agreement with the observation. This study demonstrated that the Gompertz equation and nonlinear regression can be used as an effective means to predict survival curve shape and response to heat of L. monocytogenes under many different environmental conditions.


2010 ◽  
Vol 28 (No. 4) ◽  
pp. 326-332 ◽  
Author(s):  
S. Purkrtová ◽  
H. Turoňová ◽  
T. Pilchová ◽  
K. Demnerová ◽  
J. Pazlarová

We studied the optimal conditions for the biofilm development by Listeria monocytogenes on a model system represented by microtiter plates, and also for determined some effective disinfectant agents. Listeria monocytogenes ATCC 13932 and an industrial isolate of Listeria monocytogenes Lm-24 were compared as to their abilities to form biofilms. The starting concentration of the cells leading to the most reproducible results was 0.5 McFarland. The temperatures tested ranged between 8°C to 37°C, the optimal values to form biofilm in buffered peptone water (BPW) with 0.05% glucose were 25°C and 30°C. Under comparable conditions the persistent strain L. monocytogenes Lm-24 constituted more massive biofilm than did the reference strain. The following disinfectants were applied: Savo, Merades Alco, benzalalkonium chloride. A persistent industry in isolate Listeria monocytogenes Lm-24 was used as the model organism for these tests. Benzalalkonium chloride treatment was found to be the most efficient way to damage the biofilm. One minute treatment with 500 mg/l was lethal for the biofilm cells, and that with 125 mg/l for planctonic cells. Savo suppresed the viability of the biofilm cells only by about 20% on average while being lethal for planctonic cells. Merades Alco exhibited only a weak effect on both the biofilm and planctonic cells.


2005 ◽  
Vol 68 (11) ◽  
pp. 2356-2361 ◽  
Author(s):  
JIN KYUNG KIM ◽  
ELAINE M. D'SA ◽  
MARK A. HARRISON ◽  
JUDY A. HARRISON ◽  
ELIZABETH L. ANDRESS

Listeria monocytogenes can survive and grow in refrigerated foods with pH values of approximately 4.0 to 5.0 and salt concentrations of 3 to 4%. Home-fermented refrigerator dill pickles fit this description. Contamination of this product with L. monocytogenes could cause serious problems because these items are not heated prior to consumption. L. monocytogenes survival and growth patterns were investigated in refrigerator dill pickles at 1.3, 3.8, and 7.6% salt concentrations. Pickling cucumbers were dipped into an inoculum of L. monocytogenes, brine mixtures were added, and cucumbers were held at room temperature for 1 week and then refrigerated for up to 3 months. The pH, NaCl percentage, titratable acidity percentage, and total populations of Listeria and aerobic, psychrotrophic, and lactic acid bacteria were measured at the addition of brine, after 2, 4, and 7 days of storage at room temperature, and then weekly during refrigerated storage. The initial Listeria population was 5.4 to 5.6 log CFU/cm2 on cucumber surfaces and 3.9 to 4.6 log CFU/g internally. There was an approximate 0.3- to 1-log increase during room temperature fermentation followed by a population decline during refrigerator storage, with a greater decrease in the brines with the highest NaCl concentration. Up to 49 days, the internal tissue of pickles with 1.3, 3.8, or 7.6% salt concentrations were presumptively positive for L. monocytogenes by the enrichment method, and at 91 days the surfaces of such pickles were still positive for L. monocytogenes. Populations of total aerobes and lactic acid bacteria increased during room temperature storage and decreased gradually during refrigerated storage.


2019 ◽  
Vol 12 (1) ◽  
pp. 103-107
Author(s):  
Marta Ostrihoňová ◽  
Jana Adamíková ◽  
Tomáš Molnár ◽  
Monika Antošová ◽  
Milan Polakovič

Abstract This work deals with the capture of human recombinant erythropoietin (rhEPO) from a mixture of proteins in a concentrated postcultivation supernatant. Cation-exchange multimodal adsorbent Capto MMC ImpRes was selected as potential chromatographic separation material. Its equilibrium properties were investigated in batch adsorption experiments. The effect of pH in the range of 5.5—7.5 and NaCl concentration in the range of 0—300 mM on the adsorption of rhEPO and contaminant proteins was examined. Optimal conditions found in these equilibrium experiments were applied to rhEPO adsorption in a chromatographic column. Several experiments were carried out at different elution conditions to optimize the rhEPO yield and selectivity.


1995 ◽  
Vol 58 (9) ◽  
pp. 1031-1033 ◽  
Author(s):  
LOWELL L. ISOM ◽  
ZUBIN S. KHAMBATTA ◽  
JON L. MOLUF ◽  
DANIEL F. AKERS ◽  
SCOTT E. MARTIN

Listeria monocytogenes strains SLCC 5764 cells were challenged with various NaCl concentrations and levels of pH. Cells were propagated in tryptic soy broth containing 250 to 1,500 mM NaCl or TSB at pH values ranging from 3.5 to 9.5.Microscopic analyses of the listerial cells following incubation revealed morphological changes under several adverse conditions. Filament formation occurred at NaCl concentrations above 1,000 mM with an increase in filament length as NaCl concentration increased. The same phenomenon was observed at pH values of 5.0 to 6.0 (adjusted with citric acid) and at pH > 9.0 (NaOH). The length of the filaments increased as the growth environment became more challenging. Cellular elongation of L. monocytogenes cells grown under these conditions suggests that an adaptation mechanism for survival may be involved. Since long filament structures may form under certain stressful conditions, these observations may be useful in preventing misidentification of L. monocytogenes.


1993 ◽  
Vol 56 (11) ◽  
pp. 938-943 ◽  
Author(s):  
MARK E. PETERSON ◽  
GRETCHEN A. PELROY ◽  
ROHINEE N. PARANJPYE ◽  
FRANK T. POYSKY ◽  
JAMIE S. ALMOND ◽  
...  

The behavior of Listeria monocytogenes (10 Scott A cells per g) in cold-process (smoked) salmon containing 3, 5, or 6% water-phase NaCl was evaluated during 30 to 40 d storage at 5 or 10°C in either oxygen-permeable film or vacuum-sealed impermeable film. At 10°C, L. monocytogenes grew to 106 to 108 CFU/g by the second week, with no differences attributed to NaCl concentration except for an initial lag in the 6% NaCl samples. Vacuum packaging suppressed growth of L. monocytogenes by 10- to 100-fold in samples with 3 or 5% NaCl. Inhibition related to NaCl concentration was most apparent at 5°C and L. monocytogenes populations were held below 102 CFU/g by 6% NaCl. Growth of a 327 CFU/g inoculum was about 10-fold greater than a 10 CFU/g inoculum at 10°C and 100-fold greater at 5°C. Growth of two strains isolated from naturally contaminated, commercially prepared, cold-smoked fish did not differ from Scott A. The use of sugar in the product did not influence growth of L. monocytogenes. Maximum populations of aerobic microorganisms reached at 5 and 10°C were similar, although the rate of growth was somewhat delayed at 5°C, and some inhibition was shown by 5 and 6% NaCl and by vacuum packaging.


1996 ◽  
Vol 29 (2-3) ◽  
pp. 201-211 ◽  
Author(s):  
S. Bajard ◽  
L. Rosso ◽  
G. Fardel ◽  
J.P. Flandrois

1994 ◽  
Vol 57 (2) ◽  
pp. 114-119 ◽  
Author(s):  
GRETCHEN PELROY ◽  
MARK PETERSON ◽  
ROHINEE PARANJPYE ◽  
JAMIE ALMOND ◽  
MEL EKLUND

The behavior of Listeria monocytogenes in relation to sodium nitrite (NaNO2) in combination with sodium chloride (NaCl) was evaluated in cold-process (smoked) salmon during storage at 5 or 10°C in either oxygen-permeable film or vacuum-sealed impermeable film. Salmon slices containing either 3 or 5% water-phase NaCl, with or without 190–200 ppm of NaNO2, were inoculated with 10 or 327 CFU/g (150 or 4.9 × 103 CFU/15-g sample) of strain Scott A. The inhibitory contribution of NaNO2 was relative to inoculum size, storage time and temperature, packaging method, and concentration of NaCl. There was less growth of L. monocytogenes in vacuum-packaged samples as compared to those packaged in oxygen-permeable film. The most inhibition was achieved in vacuum-packaged products stored at 5°C, where NaNO2 in combination with 5% water-phase NaCl prevented any increase in a 10 CFU/g-inoculum during 34 d storage. At 10°C, inhibition was initially enhanced by NaNO2, but by 32 d L. monocytogenes populations had increased from a 10 CFU/g-inoculum to the range of 106 CFU/g in vacuum-packaged products and 108 CFU/g in permeable-film packaged products, regardless of NaNO2 or NaCl concentration. Growth of naturally occurring aerobic microorganisms was also inhibited by NaNO2 but to a lesser degree than L. monocytogenes.


2012 ◽  
Vol 18 (3) ◽  
pp. 251-259 ◽  
Author(s):  
MJ Martelo-Vidal ◽  
JM Mesas ◽  
M Vázquez

Atlantic mackerel ( Scomber scombrus) is a pelagic and migratory species that is usually caught with other fish as bycatch. The aim of this work was to obtain low-salt restructured fish products from Atlantic mackerel resembling turkey breast using transglutaminase (0.2 U/g) as binder. NaCl concentration (0–20 g/kg), temperature (25–40 °C) and time of incubation (30–90 min) were assayed. The texture parameters (Warner–Bratzler force and Warner–Bratzler work) and expressible water were compared to those of turkey breast. Mathematical models were obtained to determine the effect of these variables on the texture of Atlantic mackerel restructured products. Optimal conditions to obtain a similar texture than turkey breast were found. The overall optimization point out that the treatment at 31.8 °C for 63.35 min using a NaCl concentration of 8.45 g/kg allowed to obtain restructured products from Atlantic mackerel with texture and expressible water similar to those of turkey breast. Color parameters ( L*, a* and b*) of the product were also similar to those of turkey breast. The results showed the feasibility of producing low-salt restructured products from Atlantic mackerel resembling turkey breast using transglutaminase.


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