Lethality of Heat to Listeria monocytogenes Scott A: D-Value and Z-Value Determinations in Ground Beef and Turkey

1991 ◽  
Vol 54 (10) ◽  
pp. 756-761 ◽  
Author(s):  
ALFRED R. FAIN ◽  
J. ERIC LINE ◽  
ALICE B. MORAN ◽  
L. MICHELE MARTIN ◽  
RICHARD V. LECHOWICH ◽  
...  
Keyword(s):  
Listeria Monocytogenes ◽  
Ground Beef ◽  
Ground Meat ◽  
Circulating Water ◽  
Death Time ◽  
Lean Beef ◽  
Z Value ◽  
D Values ◽  
Thermal Death Time ◽  
D Value

D-Values and z-values for Listeria monocytogenes strain Scott A were determined in lean (2.0% fat) and fatty (30.5%) ground beef inoculated with approximately 107cells/g. Inoculated ground meat was sealed in glass thermal death time tubes which were completely immersed in a circulating water bath and held at prescribed temperatures for predetermined lengths of time. Survival was determined by enumeration on Columbia CNA agar base containing 1% sodium pyruvate with a CNA + 4% horse blood overlay (CBNA) and on Listeria Plating Medium (LPM). D-values for L. monocytogenes in lean and fatty ground beef at 125° were 81.3 and 71.1 min, respectively, as enumerated on CBNA plus pyruvate. D-values at 135°F were 2.6 and 5.8 min in lean and fatty beef. At 145°F, D-values were determined to be 0.6 and 1.2 min. D-values calculated from LPM recovery data from fatty ground beef at 125°F were 56.1 and 34.5 min, respectively. D-values at 135°F were 2.4 and 4.6 min in lean and fatty beef. At 145°F a D-value of 0.5 min was calculated in lean beef and a D-value of 1.1 min was determined in fatty beef. The z-values determined in lean beef and fatty beef using CBNA recovery data were 9.3 and 11.4°F, respectively. The z-value in lean beef using LPM recovery data was 9.8°F. The z-value in fatty beef using LPM recovery data was 13.2°F. A D-value for ground turkey meat at 160°F could not be determined under the conditions of this study. Problems encountered are discussed.

Lethality of Heat to Escherichia coli 0157:H7: D-Value and Z-Value Determinations in Ground Beef

1991 ◽  
Vol 54 (10) ◽  
pp. 762-766 ◽  
Author(s):  
J. ERIC LINE ◽  
ALFRED R. FAIN ◽  
ALICE B. MORAN ◽  
L. MICHELE MARTIN ◽  
RICHARD V. LECHOWICH ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Ground Beef ◽  
Plate Count ◽  
Ground Meat ◽  
Plate Count Agar ◽  
Death Time ◽  
Lean Beef ◽  
Z Value ◽  
D Values ◽  
D Value

D-values and z-values were determined for lean (2.0% fat) and fatty (30.5% fat) ground beef inoculated with approximately 107 Escherichia coli 0157:H7 cells per g. Inoculated ground meat was sealed in glass thermal death time tubes which were completely immersed in a circulating water bath and held at prescribed temperatures for predetermined lengths of time. Survival was determined by enumeration on plate count agar (PCA) containing 1% sodium pyruvate and by the 2-h indole test of Lee and McClain (7). D-values for fatty ground beef exceeded those for lean ground beef at the temperatures tested. D-values for lean and fatty ground beef at 125°F were 78.2 and 115.5 min, respectively, as enumerated on PCA plus pyruvate. D-values at 135°F were 4.1 and 5.3 min for lean and fatty beef. At 145°F D-values were determined to be 0.3 and 0.5 min. D-values calculated from 2-h indole test data for lean and fatty ground beef at 125°F were 80.1 and 121.0 min, respectively. D-values at 135°F were 4.0 and 7.4 min for lean and fatty beef and at 145°F a D-value of 0.2 min was calculated for lean beef only, due to insufficient survival of E. coli 0157:H7 in fatty beef at this temperature. The z-values determined for lean beef and fatty beef using PCA were 8.3 and 8.4°F respectively. The z-value for lean beef using the 2-h indole data was 7.8°F. No z-value for fatty beef using 2-h indole data could be determined.

Heat Resistance of an Outbreak Strain of Listeria monocytogenes in Hot Dog Batter

2001 ◽  
Vol 64 (3) ◽  
pp. 321-324 ◽  
Author(s):  
ALEJANDRO S. MAZZOTTA ◽  
DAVID E. GOMBAS
Keyword(s):  
Listeria Monocytogenes ◽  
Heat Resistance ◽  
Outbreak Strain ◽  
Death Time ◽  
Thermal Death ◽  
Z Value ◽  
D Values ◽  
Hot Dog ◽  
Thermal Death Time ◽  
Phosphate Buffered Saline

The heat resistance of a strain of Listeria monocytogenes responsible for a listeriosis outbreak in hot dogs was not higher than the heat resistance of other L. monocytogenes strains when tested in tryptic soy broth and in laboratory-prepared hot dog batter. For the thermal death time experiments, the cells were grown to stationary phase or were starved in phosphate-buffered saline, pH 7, for 6 h at 30°C. Starvation increased the heat resistance of L. monocytogenes in broth but not in hot dog batter. D-values in hot dog batter were higher than in broth. For the hot dog formulation used in this study, cooking the hot dog batter for 30 s at 71.1°C (160°F), or its equivalent using a z-value of 6°C (11°F), would inactivate 5 logs of L. monocytogenes.

Carvacrol and Cinnamaldehyde Facilitate Thermal Destruction of Escherichia coli O157:H7 in Raw Ground Beef†

2008 ◽  
Vol 71 (8) ◽  
pp. 1604-1611 ◽  
Author(s):  
VIJAY K. JUNEJA ◽  
MENDEL FRIEDMAN
Keyword(s):  
Escherichia Coli ◽  
Ground Beef ◽  
Inactivation Kinetics ◽  
Escherichia Coli O157 ◽  
Internal Temperature ◽  
Circulating Water ◽  
Critical Control Points ◽  
Thermal Death ◽  
D Values ◽  
D Value

The heat resistance of a four-strain mixture of Escherichia coli O157:H7 in raw ground beef in both the absence and presence of the antimicrobials carvacrol and cinnamaldehyde was tested at temperatures ranging from 55 to 62.5°C. Inoculated meat packaged in bags was completely immersed in a circulating water bath, cooked for 1 h to an internal temperature of 55, 58, 60, or 62.5°C, and then held for predetermined lengths of time ranging from 210 min at 55°C to 5 min at 62.5°C. The surviving bacteria were enumerated by spiral plating onto tryptic soy agar overlaid with sorbitol MacConkey agar. Inactivation kinetics of the pathogens deviated from first-order kinetics. D-values (time for the bacteria to decrease by 90%) in the control beef ranged from 63.90 min at 55°C to 1.79 min at 62.5°C. D-values determined by a logistic model ranged from 43.18 min (D1, the D-value of a major population of surviving cells) and 89.84 min (D2, the D-value of a minor subpopulation) at 55°C to 1.77 (D1) and 0.78 min (D2) at 62.5°C. The thermal death times suggested that to achieve a 4-D reduction, contaminated processed ground beef should be heated to an internal temperature of 60°C for at least 30.32 min. Significantly increased sensitivity to heat (P < 0.05) was observed with the addition and/or increasing levels of carvacrol or cinnamaldehyde from 0.5 to 1.0%. The observed thermal death times may facilitate the design of acceptance limits at critical control points for ground beef at lower times and temperatures of heating.

Thermal Destruction of Escherichia coli O157:H7 in Sous-Vide Cooked Ground Beef as Affected by Tea Leaf and Apple Skin Powders†

2009 ◽  
Vol 72 (4) ◽  
pp. 860-865 ◽  
Author(s):  
VIJAY K. JUNEJA ◽  
M. L. BARI ◽  
Y. INATSU ◽  
S. KAWAMOTO ◽  
MENDEL FRIEDMAN
Keyword(s):  
Escherichia Coli ◽  
Ground Beef ◽  
Inactivation Kinetics ◽  
Skin Extract ◽  
Escherichia Coli O157 ◽  
Circulating Water ◽  
Sous Vide ◽  
D Values ◽  
A Minor ◽  
D Value

We investigated the heat resistance of a four-strain mixture of Escherichia coli O157:H7 in raw ground beef in both the absence and presence of white and green tea powders and an apple skin extract. Inoculated meat was cooked using the sous-vide technique, i.e., the meat was packaged in sterile bags and completely immersed in a circulating water bath at low temperature for a period of time. The bags were cooked for 1 h to an internal temperature of 55, 58, 60, or 62.5°C, and then held from 240 min at 55°C to 10 min at 62.5°C. The surviving bacteria were enumerated by spiral plating onto tryptic soy agar overlaid with sorbitol-MacConkey agar. Inactivation kinetics of the pathogens deviated from first-order kinetics. D-values (time, in minutes, required for the bacteria to decrease by 90%) in the control beef ranged from 67.79 min at 55°C to 2.01 min at 62.5°C. D-values determined by a logistic model ranged from 36.22 (D1, the D-value of a major population of surviving cells) and 112.79 (D2, the D-value of a minor subpopulation) at 55°C to 1.39 (D1) and 3.00 (D2) at 62.5°C. A significant increase (P < 0.05) in the sensitivity of the bacteria to heat was observed with the addition of 3% added antimicrobials. D-value reductions of 62 to 74% were observed with apple powder and 18 to 58% with tea powders. Thermal death times from this study will assist the retail food industry to design cooking regimes that ensure the safety of beef contaminated with E. coli O157:H7.

Heat Resistance of Juice Spoilage Microorganisms

2002 ◽  
Vol 65 (8) ◽  
pp. 1271-1275 ◽  
Author(s):  
ADRIENNE E. H. SHEARER ◽  
ALEJANDRO S. MAZZOTTA ◽  
ROLENDA CHUYATE ◽  
DAVID E. GOMBAS
Keyword(s):  
Heat Resistance ◽  
Process Conditions ◽  
Citrate Buffer ◽  
Ph Values ◽  
Death Time ◽  
High Fructose ◽  
Thermal Death ◽  
Challenge Tests ◽  
D Values ◽  
Thermal Death Time

The heat resistance of various yeasts (Saccharomyces cerevisiae, Rhodotorula mucilaginosa, Torulaspora delbrueckii, and Zygosaccharomyces rouxii), molds (Penicillium citrinum, Penicillium roquefortii, and Aspergillus niger), and lactic acid bacteria (Lactobacillus fermentum and Lactobacillus plantarum) obtained from spoiled acid or acidified food products was determined in 0.1 M citrate buffer at pH values of 3.0, 3.5, and 4.0. S. cerevisiae was the most heat resistant of the microorganisms in citrate buffer, and its heat resistance was further evaluated in apple, grapefruit, calcium-fortified apple, and tomato juices as well as in a juice base with high fructose corn syrup. Decimal reduction times (D-values) and changes in temperature required to change the D-value (z-values) for S. cerevisiae were higher in the juices than in citrate buffer at all pH values tested. The D57°C(135°F)-values varied from 9.4 min in the juice product with pH 2.8 to 32 min in a calcium-added apple juice with pH 3.9. The S. cerevisiae strain used in this study can be used in thermal-death-time experiments in acidic products to calculate process conditions and in challenge tests to validate the calculated temperatures and hold times during processing.

Thermal Inactivation of Escherichia coli O157: H7, Salmonella senftenberg, and Enzymes with Potential as Time-Temperature Indicators in Ground Beef

1997 ◽  
Vol 60 (5) ◽  
pp. 471-475 ◽  
Author(s):  
ALICIA ORTA-RAMIREZ ◽  
JAMES F. PRICE ◽  
YIH-CHIH HSU ◽  
GIRIDARAN J. VEERAMUTHU ◽  
JAMIE S. CHERRY-MERRITT ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Thermal Inactivation ◽  
Ground Beef ◽  
Escherichia Coli O157 ◽  
E Coli ◽  
Triose Phosphate ◽  
Beef Products ◽  
Z Value ◽  
D Values ◽  
Salmonella Senftenberg

The USDA has established processing schedules for beef products based on the destruction of pathogens. Several enzymes have been suggested as potential indicators of heat processing. However, no relationship between the inactivation rates of these enzymes and those of pathogenic microorganisms has been determined. Our objective was to compare the thermal inactivation of Escherichia coli O157:H7 and Salmonella senftenberg to those of endogenous muscle proteins. Inoculated and noninoculated ground beef samples were heated at four temperatures for predetermined intervals of time in thermal-death-time studies. Bacterial counts were determined and enzymes were assayed for residual activity. The D values for E. coli O157:H7 were 46.10, 6.44, 0.43, and 0.12 min at 53, 58, 63, and 68°C, respectively, with a z value of 5.60°C. The D values for S. senftenberg were 53.00, 15.17, 2.08, and 0.22 min at 53, 58, 63, and 68°C, respectively, with a z value of 6.24°C. Apparent D values at 53, 58, 63, and 68°C were 352.93, 26.31, 5.56, and 3.33 min for acid phosphatase; 6968.64, 543.48, 19.61, and 1.40 min for lactate dehydrogenase; and 3870.97, 2678.59, 769.23, and 42.92 min for peroxidase; with z values of 7.41,3.99, and 7.80°C, respectively. Apparent D values at 53, 58, 63, and 66°C were 325.03, 60.07, 3.07, and 1.34 min for phosphoglycerate mutase; 606.72, 89.86, 4.40, and 1.28 min for glyceraldehyde-3-phosphate dehydrogenase; and 153.06, 20.13, 2.25, and 0.74 min for triose phosphate isomerase; with z values of 5.18, 4.71, and 5.56°C, respectively. The temperature dependence of triose phosphate isomerase was similar to those of both E. coli O157 :H7 and S. senftenberg, suggesting that this enzyme could be used as an endogenous time-temperature indicator in beef products.

Thermal Inactivation of Listeria monocytogenes in Chicken Gravy

1992 ◽  
Vol 55 (7) ◽  
pp. 492-496 ◽  
Author(s):  
I-PING D. HUANG ◽  
AHMED E. YOUSEF ◽  
ELMER H. MARTH ◽  
M. EILEEN MATTHEWS
Keyword(s):  
Heat Treatment ◽  
Listeria Monocytogenes ◽  
Heat Resistance ◽  
Thermal Inactivation ◽  
Refrigerated Storage ◽  
Department Of Agriculture ◽  
Large Numbers ◽  
Z Value ◽  
D Values ◽  
The U.S

Heat resistance of Listeria monocytogenes strains V7 and Scott A in chicken gravy and changes in heat resistance during refrigerated storage were studied. After chicken gravy was made, it was cooled to 40°C, inoculated with 105 CFU L. monocytogenes per ml of gravy, and then stored at 7°C for 10 d. Gravy was heated at 50, 55, 60, and 65°C immediately after inoculation and after 1, 3, 5, and 10 d of refrigerated storage. The D values for strains Scott A and V7 in gravy heated at 50°C at day 0 were 119 and 195 min and at day 10 they were 115 and 119 min, respectively, whereas at 65°C comparable values at day 0 were 0.48 and 0.19 min and at day 10 they were 0.014 and 0.007 min. Heat resistance (expressed as D values) was greater at day 0 than at the end of refrigerated storage. The z values ranged from 3.41 to 6.10°C and were highest at the early stages of chill storage and then decreased at the later stages. Strain V7 was more heat resistant than Scott A at 50°C. Strain Scott A always had a higher z value than did strain V7 at the same storage interval. A heat treatment greater than the 4-D process recommended by the U.S. Department of Agriculture was required to inactivate the large numbers of L. monocytogenes that developed in chicken gravy during refrigerated storage.

Application of the Bigelow (z-Value) Model and Histamine Detection to Determine the Time and Temperature Required to Eliminate Morganella morganii from Seafood

2000 ◽  
Vol 63 (2) ◽  
pp. 277-280 ◽  
Author(s):  
CAROLYN M. OSBORNE ◽  
PHILIP J. BREMER
Keyword(s):  
Morganella Morganii ◽  
Death Time ◽  
Time Graph ◽  
Heat Treated ◽  
Thermal Death ◽  
Amino Acid Histidine ◽  
Z Value ◽  
Value Model ◽  
Thermal Death Time ◽  
Death Determination

In New Zealand, the product most frequently implicated in cases of scombroid or histamine poisoning is the hot-smoked fish, kahawai (Arripis trutta). A properly controlled heating step in the production of hot-smoked seafood could eliminate bacteria able to convert the amino acid histidine to histamine. In this study, we determined the core temperatures and times required during hot smoking of kahawai to eliminate histamine-forming bacteria and to ensure a final product that will not produce histamine if subsequent temperature abuse occurs. Morganella morganii strains previously isolated from portions of hot-smoked kahawai with elevated histamine levels were inoculated onto product to be tested. A variation of the Bigelow or z-value model was used to generate a thermal death time graph, where the production of histamine, in a heat-treated and subsequently temperature-abused sample, was scored as a positive value (growth) and the absence of histamine was scored as a negative value (no growth). From a line fitted to the data, calculated times for the elimination of histamine-forming bacteria at test temperatures of 58, 59, 60, 61, and 62°C were estimated to be 15.27, 8.81, 4.79, 2.68, and 1.46 min, respectively, giving a z value of 3.85°C. This approach to thermal death determination, based on the presence or absence of a bacterial metabolite, proved to be an efficient way to determine the thermal regime required to eliminate bacteria capable of converting histidine to histamine on kahawai.

Evaluating Pediococcus acidilactici and Enterococcus faecium NRRL B-2354 as Thermal Surrogate Microorganisms for Salmonella for In-Plant Validation Studies of Low-Moisture Pet Food Products

2015 ◽  
Vol 78 (5) ◽  
pp. 934-939 ◽  
Author(s):  
ERDOGAN CEYLAN ◽  
DERRICK A. BAUTISTA
Keyword(s):  
Enterococcus Faecium ◽  
Thermal Inactivation ◽  
Food Product ◽  
Food Products ◽  
Pediococcus Acidilactici ◽  
Pet Food ◽  
Death Time ◽  
Salmonella Serovars ◽  
D Values ◽  
Thermal Death Time

Pediococcus acidilactici ATCC 8042 and Enterococcus faecium NRRL B-2354 were investigated as potential surrogates for Salmonella serovars using thermal death time kinetics in products such as dry pet foods. The D-values of P. acidilactici ATCC 8042, E. faecium NRRL B-2354, and a cocktail of seven Salmonella serovars associated with low-moisture products were determined in a preservative-free dry pet food product at moisture levels of 9.1, 17.9, and 27.0% and heated between 76.7 and 87.8°C. The D-values were calculated by least squares linear regression. The D-values of P. acidilactici ATCC 8042 were higher than those for the Salmonella serovar cocktail but lower than those for E. faecium NRRL 2354. At 9.1% moisture, D-values of 6.54, 11.51, and 11.66 min at 76.7°C, 2.66, 3.22, and 4.08 min at 82.2°C, and 1.07, 1.29, and 1.69 min at 87.8°C were calculated for Salmonella serovars, P. acidilactici ATCC 8042, and E. faecium NRRL B-2354, respectively. The data suggest that the thermal inactivation characteristics of P. acidilactici ATCC 8042 can be utilized as a surrogate to predict the response of Salmonella in dry pet food products that are thermally processed at <90°C.

Thermal Resistance of Nonproteolytic Type B and Type E Clostridium botulinum Spores in Phosphate Buffer and Turkey Slurry†

1995 ◽  
Vol 58 (7) ◽  
pp. 758-763 ◽  
Author(s):  
VIJAY K. JUNEJA ◽  
BRIAN S. EBLEN ◽  
BENNE S. MARMER ◽  
AARON C. WILLIAMS ◽  
SAMUEL A. PALUMBO ◽  
...  
Keyword(s):  
Heat Resistance ◽  
Phosphate Buffer ◽  
Clostridium Botulinum ◽  
Thermal Processes ◽  
Type B ◽  
Concomitant Increase ◽  
Death Time ◽  
Thermal Death ◽  
D Values ◽  
Thermal Death Time

The heat resistance of nonproteolytic type B and type E Clostridium botulinum spores in phosphate buffer and turkey slurry was determined from 70 to 90°C. Thermal-death times were determined in vials heated using a water bath. Recovery of heat-injured spores was on reinforced clostridial medium (RCM) and tryptic soy agar (TSA) with and without added lysozyme (10 μg/ml). Decimal-reduction times (D-values) were determined by fitting a survival model to the data using a curve-fitting program. The apparent or measured heat resistance was maximum with RCM supplemented with lysozyme. The D-values at 80°C for type E spores in buffer ranged from 1.03 min for strain Whitefish to 4.51 min for strain Saratoga. The D-value for the most heat-resistant nonproteolytic type B strain KAP B5 in buffer was 4.31 min at 80°C. The z-values in buffer for all strains were very similar, ranging from 8.35 to 10.08°C.Turkey slurry offered protection to the spores with a concomitant increase in heat resistance. The D-values in turkey slurry ranged from 51.89 min at 70°C to 1.18min at 85°C for type E strain Alaska (z = 9.90°C) and from 32.53 min at 75°C to 0.80 min at 90°C for nonproteolytic type B strain KAP B5 (z = 9.43°C). Thermal-death-time values from this study will assist food processors to design thermal processes that ensure safety against nonproteolytic C. botulinum in cook/chill foods.

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