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通过凝胶过滤色谱法从人乳中分离非蛋白氮组分,并通过快速蛋白质液相色谱法对其进行分离。

Isolation of the nonprotein nitrogen fraction from human milk by gel-filtration chromatography and its separation by fast protein liquid chromatography.

作者信息

Donovan S M, Lönnerdal B

机构信息

Department of Nutrition, University of California, Davis.

出版信息

Am J Clin Nutr. 1989 Jul;50(1):53-7. doi: 10.1093/ajcn/50.1.53.

Abstract

Human milk (HM) is unique compared with the milk of other species in that nonprotein nitrogen (NPN) constitutes 20-25% of the total N. The NPN fraction consists of a diverse group of compounds with molecular masses less than 10,000 Da (in the picogram to microgram per milliliter range), which have only been partially characterized. We developed a methodology to separate and concentrate the NPN fraction for further analysis. NPN was initially separated from other milk components by Sephadex G-25 gel filtration. Further isolation and separation was carried out by fast protein liquid chromatography gel filtration and ion-exchange chromatography. Molecular masses of unknown peaks were determined by using known molecular mass markers and standards. The methodologies developed lead to the discrete separation of NPN from other milk compounds and can be particularly valuable for isolating peptides in HM.

摘要

与其他物种的乳汁相比,人乳(HM)具有独特性,即非蛋白氮(NPN)占总氮的20%-25%。NPN部分由一组分子量小于10,000道尔顿(每毫升皮克至微克范围)的多种化合物组成,这些化合物仅得到部分表征。我们开发了一种方法来分离和浓缩NPN部分以便进一步分析。NPN最初通过Sephadex G-25凝胶过滤从其他乳汁成分中分离出来。进一步的分离通过快速蛋白质液相色谱凝胶过滤和离子交换色谱进行。未知峰的分子量通过使用已知分子量标志物和标准物来确定。所开发的方法能够将NPN与其他乳汁化合物离散分离,对于分离人乳中的肽可能特别有价值。

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