Journal
FOOD ENGINEERING REVIEWS
Volume 13, Issue 1, Pages 36-53Publisher
SPRINGER
DOI: 10.1007/s12393-020-09225-0
Keywords
Food microstructure; High-pressure processing; Calcium; Infusion; Cell permeabilization
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Funding
- New Jersey Agricultural Experiment Station (NJAES)
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The study evaluated the influence of food microstructure, particularly cell diameter and cell breakage, on high-pressure-assisted calcium infusion. Higher levels of cell breakage were found to result in more infusion, with the amount of calcium infused being variable across different food matrices.
The influence of food microstructure on high-pressure-assisted infusion of calcium was evaluated. Calcium was infused in baby carrots, celery pieces, and peeled mango cuboids, under varying pressures (100 to 500 MPa) using 6% calcium lactate gluconate. Microstructures of a baby carrot, celery, and mango were quantified before HPP in terms of their cell wall thickness (CWT) and cell diameter (CD). All samples had comparable CWT (4.5 to 5.5 mu m), but differed in their CDs. CD and the amount of calcium infused were correlated. Mango had the largest cells (76 mu m +/- 8 mu m) and the highest level of calcium infusion (111.02 +/- 14.03 mg/100 g fruit). Cell breakage under high pressure, calculated as cell permeabilization index (Z(P)), significantly influenced the infusion, with higher cell breakage resulting in more infusion. However, the influence of Z(P)was observed within a given fruit/vegetable matrix but not across all the food matrices. This indicated that the microstructure, particularly CD and Z(P)together, played a role in calcium infusion under high pressure. The infused calcium was found to be concentrated around the transport tubes in the baby carrot and celery samples, while it was uniformly distributed in the mango samples, which indicated that the calcium uptake took place via the transport tubes and diffused into the surrounding cells. Following HPP-assisted calcium infusion, the cutting force (N) and the energy (J) required to cut the samples decreased, while the color of the processed samples became slightly darker (lower L* values) for all samples.
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