4.7 Article

Structure of β-lactoglobulin microgels formed during heating as revealed by small-angle X-ray scattering and light scattering

期刊

FOOD HYDROCOLLOIDS
卷 25, 期 7, 页码 1766-1774

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.foodhyd.2011.03.020

关键词

beta-Lactoglobulin; Aggregation; Microgel; Small-angle X-ray scattering; Dynamic light scattering

资金

  1. Nestle Research Center, Lausanne, Switzerland
  2. University of Fribourg, Switzerland
  3. Adolphe Merkle Foundation

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We have investigated the structure of microgels formed during heating of demineralized beta-lactoglobulin (beta lg) solutions at pH 5.9 by small-angle X-ray scattering (SAXS) and light scattering. First, unheated blg solutions were characterized at different pH values between 2.0 and 7.0. At pH 5.9, beta lg solutions contain mainly dimers (with a radius of approx. 2 nm), which coexist with a small number of larger oligomers (approx. 4 nm). Afterwards, beta lg microgels, which form upon heating, were studied. They exhibit an average hydrodynamic radius around 130 +/- 20 nm and an average molar mass around 7 x 10(8) g mol(-1). We followed the temporal evolution of the various structures that form after different heating times using subsequent SAXS measurements of the entire sample, the soluble fraction where the beta lg microgels were removed, and the solvent. After an hour of heating at 85 degrees C the maximum yield of the beta lg microgels (ca. 70%) is almost reached. Interestingly, the SAXS data show a correlation peak corresponding to a characteristic distance of about 9 nm, indicating an internal organization of the microgels. During the heating procedure the pH increases from pH 5.9 to approximately 6.6, which is induced by the partial conversion of beta lg into beta lg microgels that exhibit less buffering capacity than native protein. The remaining soluble fraction consists of native beta lg and some small aggregates, whose number increases on the cost of native beta lg as heating time proceeds. We propose that the formation of these lower molecular mass aggregates is triggered by the increased pH. (C) 2011 Elsevier Ltd. All rights reserved.

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