Eckner Karl F
Silliker Laboratories Group, Inc., 1304 Halsted Avenue, Chicago Heights, Illinois 60411.
J Food Prot. 1992 Dec;55(12):960-963. doi: 10.4315/0362-028X-55.12.960.
The correlation between alkaline phosphatase (ALP) inactivation and bacterial pathogen inactivation in raw milk was studied using a newly Association of Official Analytical Chemists-approved fluorometric assay (AOAC 991.24). Fresh, raw milk was inoculated with Listeria monocytogenes Scott A and Salmonella senftenberg 775W at levels of approximately 1 × 10 and 1 × 10 CFU/g milk, respectively. Milk was heat treated to target temperatures of 63 ± 0.5°C, 65 ± 0.5°C, 67 ± 0.5°C, 68 ± 0.5°C, or 71 ± 0.5°C in five trials. The D values calculated for S. senftenberg 775W ranged from 4.6 at 63°C to 0.17 at 71 °C with z values of 5.0 to 6.7. The D values calculated for L. monocytogenes Scott A ranged from 8.4 at 63°C to 0.19 at 71°C with z value of 4.8 to 6.1. Concomitantly, ALP concentration was monitored using a fluorometric assay. The inactivation rates of the test microbes were greater than or equal to that of alkaline phosphatase over the temperature range tested. The fluorometric assay exhibited excellent accuracy, precision, reproducibility, and repeatability under the test conditions. Viable test pathogens were isolated from milk samples with ALP levels corresponding to legal pasteurization requirements of < 500 milli-Units/L ALP activity assayed fluorometrically (=1.0μg phenol per mL/15 min) when inoculated with 1 × 10 CFU/g milk.
采用美国官方分析化学家协会新批准的荧光测定法(AOAC 991.24)研究了生乳中碱性磷酸酶(ALP)失活与细菌病原体失活之间的相关性。分别以约1×10⁵和1×10⁶CFU/g牛奶的水平,将单核细胞增生李斯特菌斯科特A和肠炎沙门氏菌775W接种到新鲜生乳中。在五项试验中,将牛奶加热至目标温度63±0.5°C、65±0.5°C、67±0.5°C、68±0.5°C或71±0.5°C。计算得出肠炎沙门氏菌775W的D值范围为63°C时的4.6至71°C时的0.17,z值为5.0至6.7。计算得出单核细胞增生李斯特菌斯科特A的D值范围为63°C时的8.4至71°C时的0.19,z值为4.8至6.1。同时,使用荧光测定法监测ALP浓度。在所测试的温度范围内,测试微生物的失活率大于或等于碱性磷酸酶的失活率。在测试条件下,荧光测定法表现出优异的准确性、精密度、重现性和可重复性。当接种1×10⁵CFU/g牛奶时,从ALP水平符合法定巴氏杀菌要求(荧光法测定的ALP活性<500毫单位/L = 每毫升1.0微克苯酚/15分钟)的牛奶样品中分离出了活的测试病原体。