Hwang D L, Yang W K, Foard D E
The University of Tennessee-Oak Ridge Graduate School of Biomedical Sciences and Biology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830.
Plant Physiol. 1978 Jan;61(1):30-4. doi: 10.1104/pp.61.1.30.
Specific antisera were prepared against the Bowman-Birk trypsin inhibitor and four other trypsin inhibitors of low molecular weight isolated from soybeans (Glycine max L. cv. Tracy). These antisera were used to detect the presence and amount of the inhibitors in: (a) seeds and protein extracts of soybean meal; (b) seedlings; and (c) the water surrounding the seeds and roots of seedlings. Lectin activities in seeds, seedlings, and water were also determined at the same time as the protease inhibitor activities. By competitive inhibition of immunoprecipitation, the combined five low molecular weight protease inhibitors were found to constitute the following percentages of proteins (w/w): 6.3% in defatted soybean meal; 8.1% of the protein extracted from the meal by a buffer of pH 8.6; 8.3, 14.7, 15.2, 16.1, 17.2, and 18.9% of the protein in a lyophilisate of water in which seeds were incubated for 4, 8, 12, 16, 20, and 24 hours, respectively; 8.2% in a lyophilisate of water in which roots of seedlings grew for 20 days; 1.5% in cotyledons; and less than 0.1% in epicotyls, hypocotyls, and roots of 12-day-old seedlings. Hemagglutination activities, expressed as the lowest amount of protein required to give a positive agglutination of 0.2 ml of 2% rabbit red blood cells, were as follows: purified soybean lectin, 0.08 mug; lyophilisate of water in which seeds were incubated for 4, 8, 12, 16, 20, and 24 hours, 10, 2.5, 5, 5, and 2.5 mug, respectively; lyophilisate of water in which roots grew for 20 days, 5 mug; 12-day-old cotyledons, roots, epicotyls, and hypocotyls, 12.5, 100, >1,000, and >500 mug, respectively. The results indicate that a large amount of protease inhibitors as well as lectins are released from seeds during the first 8 hours of imbibition. Neither lima bean trypsin inhibitor (mol wt, 10,000) nor Kunitz soybean trypsin inhibitor (mol wt, 21,500) showed competitive inhibition in tests with antisera against low molecular weight soybean protease inhibitors.
制备了针对鲍曼-伯克胰蛋白酶抑制剂以及从大豆(Glycine max L. cv. Tracy)中分离出的其他四种低分子量胰蛋白酶抑制剂的特异性抗血清。这些抗血清用于检测抑制剂在以下物质中的存在和含量:(a) 大豆粕的种子和蛋白质提取物;(b) 幼苗;以及 (c) 幼苗种子和根部周围的水。在测定蛋白酶抑制剂活性的同时,还测定了种子、幼苗和水中的凝集素活性。通过免疫沉淀的竞争性抑制发现,这五种低分子量蛋白酶抑制剂组合占蛋白质的百分比(w/w)如下:脱脂大豆粕中为6.3%;用pH 8.6的缓冲液从粕中提取的蛋白质中为8.1%;分别将种子在水中孵育4、8、12、16、20和24小时后冻干物中的蛋白质含量分别为8.3%、14.7%、15.2%、16.1%、17.2%和18.9%;幼苗根在水中生长20天后冻干物中的蛋白质含量为8.2%;子叶中为1.5%;12日龄幼苗的上胚轴、下胚轴和根中含量小于0.1%。凝集素活性以使0.2 ml 2%兔红细胞产生阳性凝集所需的最低蛋白质含量表示,结果如下:纯化的大豆凝集素为0.08 μg;种子在水中孵育4、8、12、16、20和24小时后的冻干物分别为10、2.5、5、5和2.5 μg;根在水中生长20天后的冻干物为5 μg;12日龄的子叶、根、上胚轴和下胚轴分别为12.5、100、>1000和>500 μg。结果表明,在吸水的最初8小时内,种子会释放大量的蛋白酶抑制剂和凝集素。利马豆胰蛋白酶抑制剂(分子量10,000)和库尼茨大豆胰蛋白酶抑制剂(分子量21,500)在用针对低分子量大豆蛋白酶抑制剂的抗血清进行的试验中均未表现出竞争性抑制作用。