Liven E
Acta Vet Scand. 1976;17(2):244-54. doi: 10.1186/BF03547932.
The suitability of an agar-diffusion test (ADT) using toluidine blue deoxyribonucleic acid agar (TDA) for measuring DNase activity in pig intestinal contents was investigated. The ADT was compared with a spectrophotometrical method. Distinct metachromatic zones around wells in the DNA-containing agar, into which the intestinal content was applied, indicated DNase activity. The DNase activity was determined semiquantitatively by making serial twofold dilutions of the intestinal content. The spectrophotometrical method was optimal at pH 7.2. The ADT proved to be most sensitive at pH 5.6. The ability of the 2 methods employed to measure low concentrations of DNases was equal. However, the ADT was considered more suitable than the spectrophotometrical method because ADT measured reduced amounts of enzyme. DNase activity was demonstrated throughout the small intestine and in the large intestine. By the zymogram technique, at least 3 different DNases could be demonstrated in the lower parts of the small intestine, 1 of which could be of extrapancreatic origin.
研究了使用甲苯胺蓝脱氧核糖核酸琼脂(TDA)的琼脂扩散试验(ADT)用于测定猪肠道内容物中DNase活性的适用性。将ADT与分光光度法进行比较。在加入肠道内容物的含DNA琼脂中,孔周围出现明显的异染区表明存在DNase活性。通过对肠道内容物进行系列两倍稀释,半定量测定DNase活性。分光光度法在pH 7.2时最为适宜。ADT在pH 5.6时被证明最敏感。两种方法测定低浓度DNase的能力相当。然而,ADT被认为比分光光度法更合适,因为ADT能测定较少的酶量。在整个小肠和大肠中均证实有DNase活性。通过酶谱技术,在小肠下部至少可证实有3种不同的DNase,其中1种可能来源于胰腺外。