Dawra R K, Makkar H P, Singh B
Indian Veterinary Research Institute, Palampur.
Anal Biochem. 1988 Apr;170(1):50-3. doi: 10.1016/0003-2697(88)90088-7.
The physiological effect of tannins is studied in terms of their protein-binding or precipitation capacity. A number of assays based on binding of hemoglobin or bovine serum albumin (BSA) and subsequent determination of unbound protein in supernatant or tannin in a protein-tannin complex are available but with various limitations. These methods are unable to estimate protein-binding capacity, if the quantity of tannin available is low. In the method reported here, tannins or other phenolics were applied on chromatography paper and reacted with BSA and unbound BSA was washed off. The protein in the tannin-protein complex was measured spectrophotometrically after staining with Ponceau S. It required microquantities of sample. Using this method the protein-binding capacity of total leaf extract and hydrolyzable and condensed tannins of Quercus incana, Q. semecarpofolia, and Q. dilatata was determined. The protein binding capacities of ellagic acid and quercetin (microgram BSA/mg) were 297.3 and 78.0, respectively.
单宁的生理效应是根据其蛋白质结合或沉淀能力来研究的。有许多基于血红蛋白或牛血清白蛋白(BSA)结合以及随后测定上清液中未结合蛋白质或蛋白质 - 单宁复合物中单宁的分析方法,但各有局限性。如果可用单宁的量很低,这些方法无法估计蛋白质结合能力。在本文报道的方法中,将单宁或其他酚类物质应用于色谱纸上,使其与BSA反应,然后洗去未结合的BSA。用丽春红S染色后,通过分光光度法测定单宁 - 蛋白质复合物中的蛋白质。该方法需要微量样品。使用该方法测定了灰毛栎、喜马拉雅栎和阔叶栎总叶提取物以及可水解单宁和缩合单宁的蛋白质结合能力。鞣花酸和槲皮素的蛋白质结合能力(微克BSA/毫克)分别为297.3和78.0。