Chilliard Y
J Dairy Res. 1979 Nov;46(4):599-605. doi: 10.1017/s0022029900020653.
Mammary lipoprotein lipase of lactating goats was extracted by 3 methods: homogenization of tissue acetone-ether powders; aqueous homogenization of crude tissue using an Ultra-Turrax apparatus; aqueous homogenization of crude tissue using a Sorvall Omni-mixer microhomogenizer. Although there were differences between absolute values obtained by the 3 methods, each type of homogenate had a lipolytic activity with lipoprotein lipase characteristics (i.e. more than 90% inhibition by serum omission or NaCl addition). Furthermore, the 3 methods were highly correlated and presented similar variations with the stage of lactation, in parallel with long-chain fatty acid secretion into milk. Repeatability of the measure of homogenate lipolytic activities was about 8%, whereas day-to-day repeatability of enzyme extraction and assay was about 20% for each method.
采用3种方法提取泌乳山羊的乳腺脂蛋白脂肪酶:组织丙酮 - 乙醚粉末匀浆法;使用Ultra - Turrax仪器对粗组织进行水相匀浆法;使用Sorvall Omni - mixer微量匀浆器对粗组织进行水相匀浆法。尽管这3种方法获得的绝对值存在差异,但每种匀浆物都具有脂蛋白脂肪酶特征的脂解活性(即通过血清缺失或添加氯化钠可抑制90%以上)。此外,这3种方法高度相关,并且随着泌乳阶段呈现出相似的变化,与长链脂肪酸分泌到乳汁中的情况平行。匀浆物脂解活性测量的重复性约为8%,而每种方法酶提取和测定的每日重复性约为20%。