Subpasteurization Heat Treatment to Inactivate Lipase and Control Bacterial Growth in Raw Milk

1982 ◽  
Vol 45 (6) ◽  
pp. 513-515 ◽  
Author(s):  
G. F. SENYK ◽  
R. R. ZALL ◽  
W. F. SHIPE

Raw milk was heat-treated under subpasteurization and suprapasteurization conditions, cooled and stored for up to 72 h at 4.4 and 6.7°C. Milk lipase activity and bacteria counts were monitored in both unheated and heated milks. Inhibition of milk lipase activity ranged from 42 to 98% for treatments of 57.2°C for 10 sec to 73.9°C for 10 sec, respectively. The logs of Standard Plate Count after 72 h of storage at 6.7°C were 6.56, 4.86, 4.31, 4.00 and 2.82 for unheated and 10-sec heat treatments at 57.2, 65.6, 73.9 and 82.2°C, respectively. Psychrotrophic Bacteria Counts were also lower in the heated milks than in the unheated milk. The logs of Psychrotrophic Bacteria Counts after 72 h of storage at 6.7°C were 6.21, 2.45, 2.27, 1.33 and 1.00 for unheated and 10-sec heat treatments at 57.2, 65.6, 73.9 and 82.2°C, respectively. Heat treatment of raw milk supplies would result in limiting action of the milk lipase system and growth of bacteria.

1978 ◽  
Vol 41 (2) ◽  
pp. 93-95 ◽  
Author(s):  
E. M. MIKOLAJCIK ◽  
N. T. SIMON

Microbiological data are presented for 109 raw milk samples, and for the same samples after heat treatment at 80 C for 12 min, and upon subsequent storage at 7 C for 7, 14, and 28 days. The Standard Plate Count of the raw milk averaged 110,000/ml with 65% of these organisms being penicillin-resistant. Immediately after heat treatment, 87% of the samples had psychrotrophic spore counts< 10/ml. After 14 and 28 days of storage, 50 and 83% of the samples had psychrotrophic counts ≥ 100,000/ml. It was concluded that growth of heat-resistant psychrotrophic organisms may cause spoilage of heated milk. No relationship could be demonstrated between gram-negative counts of raw milk, or initial mesophilic spore counts of heated milk, and bacterial numbers in heated, stored milk.


1984 ◽  
Vol 47 (3) ◽  
pp. 206-208 ◽  
Author(s):  
J. J. RYAN ◽  
R. H. GOUGH ◽  
C. H. WHITE

During a 5-month period, 200 raw milk samples were collected from two Louisiana milk plants. Standard Plate Count (SPC), Psychrotrophic Bacteria Count (PBC), and Proteolytic Count (PC) of each sample were initially determined, then monitored daily during a 5-d storage period at 2.2°C. As hypothesized, all bacterial counts increased during the storage period. The magnitude of the increase in bacterial numbers during storage was further investigated by dividing the milk samples into bacteriologically acceptable and unacceptable groups based on SPC or Preliminary Incubation (PI) count. An SPC of 1.0 × 105/ml and PI counts of 1.0 × 105/ml, 1.5 × 105/ml, 2.3 × 105/ml, and 3.0 × 105/ml were used to repeatedly dichotomize the 200 raw milk samples into two groups. Median SPC, PBC, and PC for each acceptable and unacceptable group were then calculated. Dichotomization based on PI counts yielded acceptable sample groups having consistently lower bacterial counts during storage than did the acceptable sample group, which resulted from the dichotomization based on a SPC of 1.0 × 105/ml. The results of this study indicated that the PI count is of considerable value for raw milk quality control.


2000 ◽  
Vol 66 (3) ◽  
pp. 1228-1232 ◽  
Author(s):  
Thusitha S. Gunasekera ◽  
Paul V. Attfield ◽  
Duncan A. Veal

ABSTRACT Application of flow cytometry (FCM) to microbial analysis of milk is hampered by the presence of milk proteins and lipid particles. Here we report on the development of a rapid (≤1-h) FCM assay based on enzymatic clearing of milk to determine total bacteria in milk. When bacteria were added to ultra-heat-treated milk, a good correlation (r ≥ 0.98) between the FCM assay and the more conventional methods of plating and direct microscopic counting was achieved. Raw milk data showed a significant correlation (P < 0.01) and a good agreement (r = 0.91) between FCM and standard plate count methods. The detection limit of the FCM assay was ≤104 bacteria ml of milk−1. This limit is below the level of detection required to satisfy legislation in many countries and states.


1978 ◽  
Vol 41 (11) ◽  
pp. 902-906 ◽  
Author(s):  
DARRELL L. BIGALKE

Milking equipment on four farms each in the St. Paul. Minnesota area and the Ithaca, New York area was cleaned at wash solution starting temperatures of 120, 130, 140, 150, and 160 F. The effect of wash solution temperature on raw milk microbiological quality was determined by the Standard Plate Count (SPC), Psychrotrophic Bacteria Count (PBC). Coliform Count (CC) and Laboratory Pasteurized Count (LPC). Cleanliness of the farm milking equipment was determined by microbiological counts (SPC, PBC, CC) of circulated sterile water, visual examination and determination of residual calcium on the equipment. Statistical analysis of the data indicated that Klenzade farm detergents and Agway farm detergents can be used at temperatures such that the final wash solution temperature does not drop below 105 F and have no significant effect on cleaning performance, microbiological quality of raw milk or microbiological status of the milking equipment.


1990 ◽  
Vol 53 (7) ◽  
pp. 610-623 ◽  
Author(s):  
ERIC A JOHNSON ◽  
JOHN H. NELSON ◽  
MARK JOHNSON

Heat treatment or pasteurization does not adversely affect the cheesemaking process or the resulting physical properties of the cheese. Both types of heat-treatments can correct chemical changes that occur in cold stored raw milk. Thermization on the farm may help control psychrotrophic bacteria in cold stored milk. Some denaturation of whey protein does occur during pasteurization. Heat treatments slightly above current minimum pasteurization requirements can cause body/texture and moisture control problems in cheese. Loss of functionality can adversely affect the marketing of whey protein products. Cheeses made from pasteurized milk ripen more slowly and usually do not exhibit the flavor intensity of cheeses made from raw or heat-treated milk. Swiss and hard Italian type cheese, whose traditional flavor results in part from native milk enzymes and microflora, would also be adversely affected if milk pasteurization for cheesemaking were mandatory. The quality of cheese made from pasteurized milk is consistently better than cheese made from raw milk as evidenced by fewer body and flavor defects consequent to the growth of undesirable bacteria. Either pasteurization or heat-treatment enables improved uniform process control and quality during cheesemaking. Pathogens were prioritized as high, medium, or low risk in cheese. Three organisms, Salmonella, Listeria monocytogenes and enteropathogenic Escherichia coli were judged to be high risk threats to the cheese industry. Staphylococcus aureus was listed as low risk because growth and toxin production is readily suppressed by lactic cultures and acidity (pH) control in cheese. Three actions are recommended:Establish a guideline for minimum heat-treatment of milk for cheesemaking: 64.4°C (148°F) for 16 s or equivalent with adequate process control.Evaluate current safety technology and practices used for cheese manufacture. Support research with primary emphasis on the combined effect of heat-treatment and other current cheese technologies.Evaluate technologies not currently utilized in cheese manufacture for safety potential.


1966 ◽  
Vol 29 (5) ◽  
pp. 156-160 ◽  
Author(s):  
W. R. Thomas ◽  
G. W. Reinbold ◽  
F. E. Nelson

Summary Plating media of different pH were studied as to effects on enumeration of pasteurization-resistant bacteria in milk. After heat treatment, thermoduric bacteria were more tolerant of pH levels above rather than below 7, and maximum mean thermoduric counts were obtained at pH 7.5. There were some exceptions, but usually the pH levels that yielded the highest counts also produced the largest and most easily discernible colonies. Pure cultures of thermoduric bacteria grew over a much wider range of pH before than they did after laboratory pasteurization. Results indicate that, although seemingly adequate for enumeration in raw milk, the medium pH currently recommended for the standard plate count may not be satisfactory for the determination of the maximum viable bacteria population of pasteurized milk.


1990 ◽  
Vol 53 (2) ◽  
pp. 176-177 ◽  
Author(s):  
P. L. HARRIS ◽  
S. L. CUPPETT ◽  
L. B. BULLERMAN

Three different agar diffusion screening methods, employing two growth media, standard plate count agar (SPCA) and 1% peptone enriched trypticase soy agar (TSA), were used to isolate psychrotrophic bacteria from raw milk which produce lipase. Clarified butterfat and nile blue sulfate served as the substrate and dye, respectively, in all methods. Although a double-overlay method yielded slightly greater numbers of lipolytic bacteria than a single-layered method with comparable media, better visual clarity was achieved with the single-layered method. Peptone enriched TSA medium supported better growth of lipolytic bacteria than SPCA.


1984 ◽  
Vol 47 (10) ◽  
pp. 753-755 ◽  
Author(s):  
R. E. GINN ◽  
V. S. PACKARD ◽  
T. L. FOX

The 3M Company has developed a sample-ready system (Petrifilm ™ SM) for enumerating bacteria in milk and other food products. The testing unit consists of Standard Methods culture medium coated onto a base film and overlaid with a second film coated with a cold-water-soluble gelling agent and tetrazolium indicator dye. As such, the system is ready to accept samples of product. A pipette or 0.001-ml plate loop continuous pipetting syringe can be used for applying samples. In this study, both methods of sample addition were used and results compared with those of the Standard Plate Count (SPC) and standard Plate Loop (PL) methods for determining bacteria numbers in raw milk. In total, 108 samples were analyzed in duplicate by each of the four methods. The correlation coefficients (r) between the 3M-SPC and SPC, 3M-PL and PL, 3M-PL and SPC and PL and SPC were 0.946, 0.935, 0.941, and 0.974, respectively. Repeatability, as measured by mean log10 variance for duplicate determinations, was essentially the same for the four methods, and in all instances less than 0.005. The mean log10 differences between the SPC and 3M-SPC, and SPC and 3M-PL were, respectively, −0.177 and −0.168. The preceding statistical criteria suggest the Petrifilm™ SM method to be a suitable alternative to the SPC or the PL procedure.


1974 ◽  
Vol 37 (8) ◽  
pp. 435-437 ◽  
Author(s):  
V. S. Packard ◽  
Roy E. Ginn

The 3M Brand Automatic Colony Counter, Model 620, was evaluated and compared with three laboratory technicians on raw milk Standard Plate Count (SPC) cultures over the range of counts from 0–300 colonies per culture plate. Overall, the estimated total variance for the three technicians was 15.07, for the 3M unit 17.82. On plates averaging greater than 150 colonies the 3M unit and hand counts were about equal in Variability. On lower counts the 3M device was somewhat more variable, although within what would appear to be acceptable limits. For the range of data studied, 99.4% of the variance (for the average of three counts by either method) could be accounted for by a similar average of observations using the other method. The 3M unit averaged 2.33 counts higher than technician counts.


1966 ◽  
Vol 29 (4) ◽  
pp. 118-121 ◽  
Author(s):  
S. P. Ohri ◽  
W. L. Slatter

Summary An 8-month survey of the bacteriological quality of bulk tank produced fluid milk supplies for four major markets in Ohio, was made utilizing the Standard Plate Count (SPC), the preliminary incubation count (PI), the thermoduric (pasteurized milk) count, and the coliform count. In terms of maximum standards of 200,000 and 100,000 organisms/ml, the SPC would have eliminated 13% and 20% of the milk samples, respectively. A SPC of 50,000/ml, a PI count of 200,000/ml, a thermoduric count of 500/ml, and a coliform count of 100/ml would have eliminated 37%, 34%, 40%, and 40%, respectively, of the samples but not all of the samples eliminated by one test were eliminated by another test. All of the tests employed showed a seasonal trend especially in the high count categories but the trend was less noticeable in the results of the preliminary incubation count. A combination of two of the methods was superior to any single bacteriological method employed in detecting unsatisfactory milk. Of the tests used, the combination of the thermoduric count (500/ml) and the coliform count (100/ml) was the most effective in the detection of unsatisfactory milk samples.


Sign in / Sign up

Export Citation Format

Share Document