Related Experiment Video
Updated: Jun 4, 2025

Composition and Properties of Aquafaba: Water Recovered from Commercially Canned Chickpeas
Published on: February 10, 2018
Oleogelation for saturated fat replacement in vegan cheese
J Noon1, D Rousseau2, S R Euston3
1Institute of Biological Chemistry, Biophysics and Bioengineering, School of Engineering and Physical Sciences, Heriot-Watt University, Edinburgh, UK.
Abstract:
Oleogelation was investigated to reduce the saturated fat content of vegan cheese. Oleogels were formulated using a range of oleogelators, oleogelator concentrations and oil phase compositions to study the effect that adjusting these parameters had on both oleogel and vegan cheese properties. Comparing oleogels at an equivalent mass basis of 20 wt%, phytosterol oleogels exhibited greater hardness (5.9 N) than either monoglyceride (1.7 N), stearic acid (0.7 N) or carnauba wax (4.3 N) oleogels. Oleogels generally exhibited lower oxidative stability than the coconut and sunflower oil controls, with phytosterol oleogelators exhibiting a pro-oxidant effect. Oleogel-based vegan cheese properties were highly tuneable, with hardness and adhesiveness levels which could be in excess or below that of the control samples. Furthermore, oleogelled vegan cheese samples exhibited superior meltability whilst offering major reductions in saturated fat content from 28 % in the control to as low as 2 % in oleogel-based vegan cheese samples.
More Related Videos
06:31Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators
Published on: November 27, 2015
08:02Author Spotlight: Innovative Ice Cream Melting Behavior Analysis Through a Computer Vision System
Published on: October 4, 2024
Related Concept Videos
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Nonenolizable Aldehydes to Acids and Alcohols: The Cannizzaro Reaction
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Fats as Energy Storage Molecules
Loss of Carboxy Group as CO2: Decarboxylation of β-Ketoacids