2 research outputs found
Preparation and Characterization of Maillard Reaction Products from a Trinary System Composed of the Soy Protein Isolate, Chitosan Oligosaccharide, and Gum Arabic
To
extend the application of chitosan oligosaccharide (COS) in complex
coacervation
between the soy protein isolate (SPI) and gum Arabic (GA), Maillard
reaction among SPI, COS, and GA was induced under different conditions.
High-performance gel permeation chromatography and sodium dodecyl
sulfate polyacrylamide gel electrophoresis illustrated that products
with high molecular weights (1.17 × 106 and 2.79 ×
106 Da) were generated in the trinary system, and the Maillard
reaction promoted the cross-linking of SPI, COS, and GA. The Maillard
reaction was observed the most under conditions where SPI, COS, and
GA (4:2:4, w/w) were kept at 80 °C for 12 h, and the results
of thermogravimetry indicated that Maillard reaction products (MRPs)
with the best thermal stability, which were positively charged, were
generated. The results revealed that the extent of Maillard reaction
was enhanced with the increase of time SPI being involved in the complex
rather than GA. X-ray diffraction and Fourier transform infrared analysis
indicated that Maillard reactions between SPI, COS, and GA under different
conditions did not impact the crystal particle structures among them.
Even though the extent of Maillard reaction among SPI, COS, and GA
was lower than that between SPI and COS, MRPs with various viscoelastic
properties were obtained under different conditions. Thus, as one
kind of difunctional reactant in Maillard reaction, COS could react
with either proteins or polysaccharides, and the MRPs have potential
utilization in the food industry
Additional file 1: of Preparation and Characterization of Tadpole- and Sphere-Shaped Hemin Nanoparticles for Enhanced Solubility
Figure S1. TEM images of hemin nanoparticles prepared by dialyzing for one day with various hemin/water volume ratios, including 1:3 (A), 1:5 (B), 1:10 (C), and 1:50 (D) at 25 °C. The concentration of hemin was 0.5 mg/mL. Figure S2. TEM images of hemin nanoparticles prepared by dialyzing for two days with various hemin/water volume ratios, including 1:3 (A), 1:5 (B), 1:10 (C), and 1:50 (D) at 25 °C. The concentration of hemin was 0.5 mg/mL. Figure S3. TEM images of hemin nanoparticles prepared by dialyzing for five days with various hemin/water volume ratios, including 1:3 (A), 1:5 (B), 1:10 (C), and 1:50 (D) at 25 °C. The concentration of hemin was 0.5 mg/mL. Figure S4. TEM images of hemin nanoparticles prepared by dialyzing for three days with the hemin/water volume ratio of 1:10 at various temperatures, including 4 °C (A) and 25 °C (B). The concentration of hemin was 0.5 mg/mL. Figure S5. UV–Vis spectrum of free hemin. The free hemin was dissolved in acidified aqueous acetone solution. (DOC 1146 kb
