| Literature DB >> 34453343 |
Marina Mefleh1, Antonella Pasqualone1, Francesco Caponio1, Michele Faccia1.
Abstract
Research into dairy-free alternative products, whether plant-based or cell-based, is growing fast and the food industry is facing a new challenge of creating innovative, nutritious, accessible, and natural dairy-free cheese alternatives. The market demand for these products is continuing to increase owing to more people choosing to reduce or eliminate meat and dairy products from their diet for health, environmental sustainability, and/or ethical reasons. This review investigates the current status of dairy product alternatives. Legume proteins have good technological properties and are cheap, which gives them a strong commercial potential to be used in plant-based cheese-like products. However, few legume proteins have been explored in the formulation, development, and manufacture of a fully dairy-free cheese because of their undesirable properties: heat stable anti-nutritional factors and a beany flavor. These can be alleviated by novel or traditional and economical techniques. The improvement and diversification of the formulation of legume-based cheese alternatives is strongly suggested as a low-cost step towards more sustainable food chains.Entities:
Keywords: anti-nutritional factors; dairy-free products; legume proteins; technological properties; vegan; sustainability
Mesh:
Substances:
Year: 2021 PMID: 34453343 PMCID: PMC9293078 DOI: 10.1002/jsfa.11502
Source DB: PubMed Journal: J Sci Food Agric ISSN: 0022-5142 Impact factor: 4.125
The percentage of globulin fraction in the total grain proteins, the denomination of globulin subunits 11S and 7S, the ratio of globulin subunits 11S over 7S and the protein digestibility‐corrected amino acid scores (PDCAAS) of chickpea, lentil, lupin, pea and, soybean. , , ,
| Legume | Globulin (% of total proteins) | 11S and 7S subunit denomination | 11S/7S ratio | PDCAAS |
|---|---|---|---|---|
| Chickpea | 60 | Legumin and vicilin | 1.60–3.70 | 0.59–0.82 |
| Lentil | 80 | Legumin and vicilin | 0.49–0.70 | 0.50–0.70 |
| Lupin | 85 |
| 0.77 | 0.80 |
| Pea | 60 | Legumin and vicilin | 0.50–4.20 | 0.79 |
| Soybean | 90 | Glycinin and β‐conglycinin | 0.6 0–3.00 | 0.90 |
Effects of processing technologies on beany flavor and anti‐nutritional factors of various legumes and legumes‐based products
| Technique | Legumes | Treatment parameters | Inference | References |
|---|---|---|---|---|
| Micronization or infrared treatment | Lentils | Previously tempered to 33 g/100 g moisture for 16 h, heating to up to 138 °C internal temp. | Decreased the phytic acid level, improved digestibility, and reduced trypsin inhibitors |
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| Cowpea, kidney bean and pea | Previously tempered to 24 g/100 g, heating at 90 °C using tubular quartz infrared lamp (115 V) for 2.5 min for cowpea and pea and 3 min for kidney beans | Reduced the phytic acid level, oligosaccharides, and trypsin inhibitors |
| |
| High hydrostatic pressure (HHP) | Soymilk enriched with calcium | 614 MPa, 85.5 °C, and 8.53 mmol Ca L–1 | Inhibited trypsin inhibitors and lipoxygenase enzymes |
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| High and ultra‐high pressure homogenization (HPH) and (UHPH) | Soy milk | 200 MPa, 55–75 °C and thermal pasteurization at 90 °C for 30 s | Reduced hydroperoxide index values and trypsin activity |
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| Pulsed electric field (PEF) | Soybean LOX | 20–42 kV cm–1; 2 μs pulse width; 1036 μs treatment time | Inactivated LOX (88%) at 42 kV cm–1 when treated for 1036 μs. |
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| Soybean LOX | 20–40 kV cm–1; 25–100 μs; 23, 35, 50 °C | Inactivated LOX (85%) at the highest processing conditions |
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| Pea LOX | 2.5–20 kV cm–1; 1 μs pulse width; 100–400 pulses | No inactivation |
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| Ultrasonication | Soy milk | 20 kHz, 15–20 min, 600 W | Decreased trypsin inhibitors (52%) after 16 min of the treatment |
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| Radio frequency (RF) | Soybean | 27.12 MHz and the electrode gap was set at 45 mm during RF heating period. Soybeans were stored at 30 °C and heated for different time from 30 to 180 s at 2.1 kW, and then were maintained at those temperatures for 120 s. Technique was compared with conventional hot‐air‐heating at 132 °C for different times | Reduced LOX (95.2%), urease (93.4%) and trypsin inhibitor (89.4%) activities. Compared with the conventional thermal treatment, RF heating efficiently inactivated ANFs with a shorter time and a lower treatment temperature |
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| Combined high temperature pre‐treatment heating and enzymatic hydrolysis | Soybean isolates (SPI) | Temperature was increased to 121 °C at a heating rate of 17 °C min–1. After heating, the temperature was held for 3 min at 121 °C and cooled for 2 h at room temperature. SPI was then hydrolyzed by | Reduced LOX activity and some volatile compounds e.g., hexanol, hexanal, and pentanol |
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