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使用固相萃取(SPE)和反相高效液相色谱(RP-HPLC)组合对清洁过程后的乳蛋白残留进行浓缩、纯化和定量分析。

Concentration, purification and quantification of milk protein residues following cleaning processes using a combination of SPE and RP-HPLC.

作者信息

Kürzl Christian, Wohlschläger Heidi, Schiffer Simon, Kulozik Ulrich

机构信息

Chair of Food and Bioprocess Engineering, TUM School of Life Sciences, Technical University of Munich, Germany.

出版信息

MethodsX. 2022 Apr 8;9:101695. doi: 10.1016/j.mex.2022.101695. eCollection 2022.

Abstract

Detection and quantification of milk protein residues can be of utmost importance for validation of cleaning process efficiency in removing even traces of residues as well as quality assurance and product safety. However, currently available assays cannot provide a combination of high sensitivity and a simultaneous quantification of the individual milk proteins. Furthermore, a low protein-to-protein-variability and high compatibility with other reagents such as residual cleaning agents (e.g. surfactants) cannot be ensured. Therefore, a new method was developed comprised of a pre-concentration of proteins by solid-phase extraction and optimisation of the sensitivity of an existing reversed-phase high performance liquid chromatography method for the separate quantification of bovine milk proteins κ-Casein, α-Casein, α-Casein, β-Casein, α-Lactalbumin, and β-Lactoglobulin. Hereby, solid-phase extraction enables robust and reproducible purification and concentration of protein residues with a high protein recovery rate and flexible adjustment of concentration factors. The increased sensitivity of the reversed-phase high performance liquid chromatography method was achieved by changes in the measurement wavelength and guanidine buffer concentration. This new method enables reproducible concentration, purification and quantification of protein concentrations below 7 ng mL and thus can be used to detect milk protein residues in highly diluted aqueous systems.•Concentration, purification and quantification of milk protein residues with a high recovery rate of proteins (> 94%) and high reproducibility (coefficient of variation (CV) < 3.0%)•Flexible adjustment of sample volumes allows the utilisation of high concentration factors (≤ 500) without compromising the recovery rate of proteins (recovery rate of proteins decreases by 2.74% per 100 CF).

摘要

检测和定量乳蛋白残留对于验证清洗过程去除哪怕痕量残留的效率以及质量保证和产品安全至关重要。然而,目前可用的检测方法无法同时提供高灵敏度和对单个乳蛋白的定量。此外,无法确保低蛋白间变异性以及与其他试剂(如残留清洗剂,如表面活性剂)的高兼容性。因此,开发了一种新方法,该方法包括通过固相萃取对蛋白质进行预浓缩,并优化现有的反相高效液相色谱法的灵敏度,以分别定量牛乳中的蛋白质κ-酪蛋白、α-酪蛋白、α-酪蛋白、β-酪蛋白、α-乳白蛋白和β-乳球蛋白。在此,固相萃取能够以高蛋白回收率稳健且可重复地纯化和浓缩蛋白质残留,并灵活调整浓缩因子。反相高效液相色谱法灵敏度的提高是通过改变测量波长和胍缓冲液浓度实现的。这种新方法能够对低于7 ng/mL的蛋白质浓度进行可重复的浓缩、纯化和定量,因此可用于检测高度稀释水体系中的乳蛋白残留。

•以高蛋白回收率(>94%)和高重现性(变异系数(CV)<3.0%)对乳蛋白残留进行浓缩、纯化和定量

•灵活调整样品体积允许使用高浓缩因子(≤500)而不影响蛋白质回收率(每100个浓缩因子蛋白质回收率降低2.74%)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83ef/9043403/e3b737d02b6d/ga1.jpg

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