Madsen P S
Acta Vet Scand. 1969;10(4):319-44. doi: 10.1186/BF03548267.
The Feulgen reaction is examined by absorption photometric measurements at 565 nm with correction for varying background absorption at 485 nm. This correction is done to improve the accuracy of measuring. Examinations of the accuracy of analysis for the Feulgen reaction and the direct microscopic cell counts show that the former is of the same order, when the cell count is made at a working factor of 17,000. The standard deviations expressed in percentage of the reaction value are greater the lower the reaction is, whereas the absolute standard deviation is reduced. It has been demonstrated that addition of a few (< 5) µg of DNA per ml milk can give Feulgen reaction. The coefficient of correlation between log added amount of DNA and log Feulgen reaction is 0.98. The coefficient of correlation between log Feulgen reaction and log cell content depends on the accuracy at which both determinations are made. In a determination of cell content at a working factor of 550, and several determinations of the Feulgen reaction the coefficient of correlation (r) is found to be 0.98. A cell content determination at a working factor of 20,000 and a single determination of Feulgen reaction on each milk sample yields r = 0.83. An examination of foremilk samples of the same cell content reveals on an average the highest reaction in mastitis-affected quarters which have been infected within the last 4 weeks. Quarters that have been infected for more than 4 weeks, on an average show the second highest reaction, whereas quarters of physiological cell number show the lowest reaction. The DNA-content in most cases is found to be too high compared with the number of cells counted microscopically. The DNA-content in centrifugated cells corresponds to the one calculated theoretically. The surplus DNA-content can be demonstrated in the cell-free skim milk fraction, probably originating from destroyed cells. The studies performed suggest that determination of the content of 2-deoxyribose in milk by means of the Feulgen reaction is a more correct measure of the cell content in the milk than is the microscopic cell count. Studies are being continued for illustration of these conditions.
通过在565nm处进行吸收光度测量来检测福尔根反应,并对485nm处变化的背景吸收进行校正。进行这种校正是为了提高测量的准确性。对福尔根反应的分析准确性和直接显微镜细胞计数的检查表明,当细胞计数在17000的工作系数下进行时,前者处于同一水平。以反应值的百分比表示的标准偏差在反应越低时越大,而绝对标准偏差则减小。已经证明,每毫升牛奶中添加几(<5)μg DNA可以产生福尔根反应。添加的DNA量的对数与福尔根反应的对数之间的相关系数为0.98。福尔根反应的对数与细胞含量的对数之间的相关系数取决于这两种测定的准确性。在工作系数为550的细胞含量测定以及几次福尔根反应测定中,发现相关系数(r)为0.98。在工作系数为20000的细胞含量测定以及对每个牛奶样品进行一次福尔根反应测定时,r = 0.83。对具有相同细胞含量的初乳样品进行检查发现,平均而言,在过去4周内感染的乳腺炎受影响乳腺区的反应最高。感染超过4周的乳腺区平均显示出第二高的反应,而生理细胞数的乳腺区显示出最低的反应。在大多数情况下,发现DNA含量与显微镜下计数的细胞数量相比过高。离心细胞中的DNA含量与理论计算的含量一致。多余的DNA含量可以在无细胞脱脂乳部分中证明,可能来自被破坏的细胞。进行的研究表明,通过福尔根反应测定牛奶中2-脱氧核糖的含量比显微镜细胞计数更能准确衡量牛奶中的细胞含量。正在继续进行研究以阐明这些情况。