首页> 外国专利> A NOVEL PROCESS OF SPORULATION, ACTIVATION AND GERMINATION IN THERMOPHILIC BACTERIA FOR RAPID DETECTION OF ANTIBIOTIC RESIDUES IN MILK

A NOVEL PROCESS OF SPORULATION, ACTIVATION AND GERMINATION IN THERMOPHILIC BACTERIA FOR RAPID DETECTION OF ANTIBIOTIC RESIDUES IN MILK

机译:快速检测牛奶中抗生素残留的嗜热菌中孢子形成,活化和萌发的新过程

摘要

This invention relates to a novel analytical process of detection of antibiotic residues in milk system involving sporulation upto 80-90% in thermophillic strains B. stearothermophilus seeded in selective sporulation medium containing Beef extract 0.15-0.30% preferably 0.3%; peptone 0.25-0.5% preferably 0.5%; tryptone .09-0.17% preferably 0.17%; sodium chloride 0.025-0.5% preferably 0.05%; agar 1.5+0.2% preferably 1.5%; brombcresol purple .004-.008% preferably .006% as color indicator, followed by activation of dormant spores of B. stearothermophilus in BPTS medium at 55±5°C for 12+3 hours preferably at 55°C for 14 hours incubation, wherein the activated spores are forced for germination and out growth using 0.5+0.05mg D-dextrose preferably 0.5 mg; 5.0+0.5mg skimmed milk powder preferably 5.0 mg; 2.0±0.2mg whey powder preferably 2.0 mg at incubation temp. 64±2°C preferably at 64°C as germinant, wherein change of colour of the medium from purple to yellow within 2-3 hours is taken as criteria of dormant spores into vegetative cells and finally mixing germinant mixture 55+5.0 mg preferably 60 mg in milk and heated to 95 to 105°C preferably 100°C for 2-3 minutes and adding .01-.02 ml preferably .015 ml of milk in BPTS medium and incubating at 64±2°C preferably 64°C for 2.30-3 hours and observing the change of color of the medium.
机译:本发明涉及一种检测牛奶系统中抗生素残留的新分析方法,该方法涉及在嗜热菌株B.stearothermophilus中形成高达80-90%的孢子形成,所述嗜热脂肪芽孢杆菌接种在含有0.15-0.30%,优选0.3%的牛肉提取物的选择性孢子培养基中。蛋白ept0.25-0.5%,优选0.5%;胰蛋白。.09-0.17%,优选0.17%;氯化钠0.025-0.5%,优选0.05%;琼脂1.5 + 0.2%,优选1.5%;溴甲酚紫.004-.008%,优选.006%作为颜色指示剂,然后在BPTS培养基中将嗜热脂肪芽孢杆菌的休眠孢子在55±5°C活化12 + 3小时,优选在55°C孵育14小时,其中使用0.5 + 0.05mg D-葡萄糖,优选0.5mg,迫使活化的孢子萌发并生长。 5.0 + 0.5mg脱脂奶粉,优选5.0 mg;在温育温度下为2.0±0.2mg乳清粉,优选为2.0mg。最好在64°C下以64±2°C作为杀菌剂,其中培养基的颜色在2-3小时内从紫色变为黄色是休眠孢子进入营养细胞的标准,最后将杀菌剂混合物55 + 5.0 mg优选60将其在牛奶中加热至95至105°C(优选100°C)2-3分钟,然后在BPTS培养基中添加0.01-.02 ml(优选.015 ml)牛奶,并在64±2°C(优选64°C)下孵育2.30-3小时,观察培养基的颜色变化。

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