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表面多孔反相高效液相色谱柱上的角蛋白分离。

Separation of kafirins on surface porous reversed-phase high-performance liquid chromatography columns.

机构信息

Center for Grain and Animal Health Research (CGAHR), Agricultural Research Service (ARS), United States Department of Agriculture (USDA), Manhattan, Kansas 66502, USA.

出版信息

J Agric Food Chem. 2011 Jan 12;59(1):85-91. doi: 10.1021/jf1036195. Epub 2010 Dec 9.

Abstract

Surface porous high-performance liquid chromatography (HPLC) columns were investigated for the separation of kafirins, storage proteins of grain sorghum. Kafirins were successfully separated using C3, C8, and C18 surface porous stationary phases in less than 17 min. Separations using a monolithic C18 stationary phase were also developed and were slightly faster than those achieved on the surface porous C18 stationary phase. However, the resolution was higher on the latter column. Using an ammonium hydroxide/acetonitrile mobile phase, separations were performed on a novel, alkaline stable surface porous C18 stationary phase. The resolution at alkaline pH was not as high, however, as with the traditional acidic acetonitrile mobile phases. In comparison to fully porous stationary phases, the surface porous phases provided higher resolution with much lower separation times (17 versus 40 min). Total peak areas were correlated to total protein content of sorghum (r(2) = 0.96; n = 10), and a method to measure in vitro pepsin digestibility using reversed-phase (RP)-HPLC peak areas showed good correlation to the traditional nitrogen combustion method (r(2) = 0.82; n = 20). Thus, the surface porous stationary phases could be used not only for more rapid separations but also to provide simultaneous information on total protein content and digestibility.

摘要

表面多孔高效液相色谱(HPLC)柱被用于分离高粱的储存蛋白——高粱醇溶蛋白。使用 C3、C8 和 C18 表面多孔固定相,在不到 17 分钟的时间内成功地分离了高粱醇溶蛋白。还开发了使用整体式 C18 固定相的分离方法,其速度略快于表面多孔 C18 固定相。然而,后者的分辨率更高。使用氨/乙腈流动相,在新型碱性稳定的表面多孔 C18 固定相上进行了分离。然而,在碱性 pH 下的分辨率不如传统的酸性乙腈流动相高。与全多孔固定相相比,表面多孔相提供了更高的分辨率,分离时间更短(17 分钟与 40 分钟)。总峰面积与高粱的总蛋白含量相关(r(2) = 0.96;n = 10),使用反相(RP)-HPLC 峰面积测量体外胃蛋白酶消化率的方法与传统的氮燃烧法相关性良好(r(2) = 0.82;n = 20)。因此,表面多孔固定相不仅可以用于更快速的分离,还可以提供总蛋白含量和消化率的同时信息。

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