Wheat Bran Modifications for Enhanced Nutrition and Functionality in Selected Food Products
Abstract
:1. Introduction
2. Wheat Bran Modifications/Pre-Treatments
2.1. Mechanical Treatment
2.2. Thermal Treatment
2.2.1. Dry Heat Treatment
2.2.2. Wet Heat Treatment
Autoclaving
Extrusion
Steam Treatment
2.3. Bioprocessing
2.3.1. Fermentation
2.3.2. Enzymatic Modification
2.3.3. Dephytinization Effects of Bioprocessing
2.4. Combination of Pre-Treatment Methods
2.4.1. Enzymatic and Fermentation Treatment
2.4.2. Thermomechanical and Bioprocessing
3. Modified Wheat Bran as a Functional Ingredient in Selected Food Products
3.1. Bread
3.2. Cookies and Cakes
3.3. Noodles and Pasta
3.4. Fried Dough
3.5. Gluten-Free Products
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Conflicts of Interest
References
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Fibre Component | Description | Food Sources |
---|---|---|
Cellulose | Polysaccharides comprising up to 10,000 closely packed glucose units arranged linearly. | Grains, vegetables, fruit, nuts, cereal bran. |
Hemicellulose | Polysaccharides containing sugars other than glucose. | Cereal grains, vegetables, fruit, legumes (for example peas, beans, chickpeas, lentils) and nuts. |
Lignin | A non-carbohydrate component associated with plant walls. | Foods with a woody component, for example, celery and the outer layers of cereal grains. |
Beta-glucans | Glucose polymers that (unlike cellulose) have a branched structure | Mainly found in cell wall of oats and barley. |
Pectins | A non-starch polysaccharide common to all cell walls. | Fruits and vegetables, legumes, nuts, and potatoes. |
Gums and mucilages | Non-starch polysaccharides are thick gel-forming fibres that help hold plant cell walls together. | Gums: seeds and seaweed extracts; Mucilages: pysillium seeds. Gums and mucillages are used as gelling agents, thickeners, stabilisers, and emulsifying agents. |
Resistant starch | Starch and the products of starch digestion that are not absorbed by the small intestine. | Legumes, potatoes, cereal grains |
Oligosaccharides | Short-chain carbohydrates of 3–9 monomers. These include fructo-oligosaccharides and galacto-oligosaccharides. | Onions, chicory, Jerusalem artichokes |
Micro components (waxes, cutin and suberin) | Micro components of the plant structures. | Cereal grains |
Disease | Number of Studies in Meta-Analysis | Findings | Reference |
---|---|---|---|
Cardiovascular disease | 10 | Inverse association—RR of 0.91 (95% CI 0.88–0.94) for each 7 g/day increase at p < 0.001 | [11] |
Coronary events | 12 | Inverse association—RR 0.91 (95% CI 0.87–0.94) for each 7 g/day increase at p < 0.001 | [11] |
Stroke | 7 | Inverse association with incidence of haemorrhagic plus ischemic stroke RR 0.93 (95% CI 0.88, 0.98) for each 7 g/day increase at p = 0.002 | [12] |
Colorectal cancer | 8 | Inverse association with the incidence of colorectal cancer RR = 0.88 (95% CI 0.83–0.97) for each 10 g/day at increase; p < 0.05. | [13] |
Type 2 diabetes | 10 | Inverse association RR 0.87 (95% CI 0.90, 0.97) for each 7 g/day increase; p = 0.001 | [14] |
Modification Type | Impact on Functionality | Effect on Nutritional Properties | Reference |
---|---|---|---|
Thermomechanical Treatment | |||
Milling (900, 750, 500 and 355 µm) | ND | Bound total phenolic content (TPC) and total flavonoid increased by 1.5-fold, total anthocyanin by 2-fold. Zeaxanthin and beta carotene increased in medium bran and lutein in fine bran fraction. Milling did not affect the DPPH content of wheat bran (WB). | [29] |
Autoclaving (121 °C for 0.5–2 h pH: 3.5–6.2) | ND | At native pH (6–6.2) no change in phytic acid (PA) occurred. Maximum reduction * (96%) at pH 3.5 and 2 h autoclaving was reported. | [30] |
Autoclaving (121 °C for 0.5–1.5 h, pH: 3.5–6.6) | ND | A 96% decrease * of PA at pH 4 and 1 h processing time. Significant increase in insoluble dietary fibre (IDF) and soluble dietary fibre (SDF). Autoclaving increased the bound and total TPC of wheat bran. | [31] |
Autoclaving conditions (121 °C for 20–21 min) | Increase in water retention capacity (WRC) and water holding capacity (WHC). No change in microstructure. | Reduction in TPC, PA and IDF. An increase in alkylresorcinol, water-extractable arabinoxylan (WEAX) was observed. | [32,33] |
Microwave (800 W, 2 min) and hot air oven, (150 °C for 20 min) | Water absorption capacity and swelling capacity (SC) markedly increased in both treatments by up to 11%. Hot air treatment increased bran lightness. | Both methods increased protein and total dietary fibre content. A decrease in moisture and PA content was also observed | [34] |
Extrusion (temperature: 80 and 120℃, screw speed: 120 and 250 rpm) | ND | Extrusion increased WEAX content, SDF content. Fermentable carbohydrates and short-chain fatty acid (SCFA) content were higher in extruded bran. | [35] |
Extrusion (temperature:140 °C, screw speed: 150 rpm, 45% moisture) + size reduction (830, 380, 250 and 180 µm) | The surface of extruded bran was full of holes and had an irregular surface structure. WHC < ORC and SC increased with extrusion and size reduction | SDF of extruded WB increased by 70% *. Antioxidant properties increased as dosage (mg/mL) increased. | [36] |
Extrusion (temperature: 120 and 145 °C, moisture: 23, 27 and 33% screw speed: 310 rpm) | A greater extent of degradation of pericarp and aleurone layer of WB was caused by very high shear than low shear extrusion using light microscopy. | A 1.8-fold and 3.5-fold increase in WEAX and free ferulic acid. PA content decreased by 19% * andA small increase in SCFA was reported after 48 h fermentation. | [6] |
Milling (420, 280, 170 and 90 µm) Hydrothermal (acetate buffer (pH 4.8) at 55 °C, 60 min and incubation at 5 5°C for 24 h) Yeast fermentation (8 h at 30 °C) | Reduced WHC and swelling power and increase in water solubility index of fermented and hydrothermal bran. Size reduction increased L * values of WB. | 34, 57 and 76% reduction * in PA content in milled, fermented, and hydrothermal WB. Hydrothermal and fermentation treatments increased the total dietary fibre (TDF), SDF and reduced the IDF content of WB. Mineral contents reduced with all treatments. | [37] |
Super-heated steam (15.0 m3/h, 170 °C for 20 min) Hot air processing in an electro-thermostatic blast oven (170 °C for 20 min) | ND | Superheated steam was more efficient in enzyme inactivation, enhancement of non-starch nutrients, reduction of peroxide value, higher soluble phenolic content, and better sensory profile than hot air treatment. | [38] |
Milling + Steam explosion (120–160 °C for 5–10 min) | Lightness values of WB treated with steam explosion decreased. Severe disruption of bran cell wall by grinding and steam explosion was reported. | Milling and steam explosion alone and in combination increased AX solubilisation in fine bran. Loaf volume, SDF increased, and PA content reduced in breads with pre-treated WB. | [39] |
Steam explosion (0.8 MPa, 170 °C, 5 min) + grinding (425–75 µm) | Steam explosion and milling increased WB porosity, WHC and SC. | Fat, starch, protein, SDF, TPC, total flavonoids and DPPH contents increased with steam explosion and size reduction. | [40] |
Steam explosion (0.3, 0.5 & 0.8 MPa, at 170 °C, for 5 min) | Lipase and peroxidase activity reduced and shelf life increased. | Protein, and lipid content remain unchanged. SDF, TPC, TFC and DPPH values increased at maximum steam (0.8 MPa). | [41] |
Microwave (2450 MHz at 1.5–2.5 min) Hot air oven (100 & 110 °C, 15, 20 & 25 min) Steaming (100, 110 & 115 °C, 15, 20 at 25 min) | All treatments increased bulk density and darkened the bran samples. | Microwave treatment at 2.5 min caused a significant reduction of PA, polyphenols, saponins, trypsin inhibitors and toxicants | [42] |
Milling (ultra-centrifugal mill-500 µm) + Extrusion | Structural modification of WEAX was more distinct in extruded bran. | Milling increased WEAX content (26% *) and reduced molecular weight of WB. No significant change in TPC, but 38% * increase in free TPC of milled bran. | [43] |
Milling + Extrusion | About 1.5-fold increase in WHC and IDF content of bran fractions and a decrease in SDF content after extrusion process. | Antioxidant capacity increased as the particle sizes of the milled bran reduced up to 180µm. | [44] |
Bioprocessing (Fermentation and Enzymatic Treatments) | |||
Fermentation at 2–8 h with Saccharomyces. cerevisiae (3–9%). | ND | A reduction (≤96%) in phytic acid content with an increase in fermentation time and yeast concentration. | [30] |
Lactobacillus brevis and Kazachstania exigua (20 °C for24 h) + enzymes (xylanase, endoglucanase and β-glucanase) | Partial degradation of bran cell wall. | A sixfold increase * in WEAX in fermented bran and up to 11.5-fold increase * when fermentation was combined with enzymes. A 50% increase * in peptide content was observed in bioprocessed bran compared to native bran | [45] |
Fermentation with L. rhamnosus (37 °C for 24–48 h) | ND | Free TPC and WEAX increased significantly. Caffeic acid was notable in fermented bran. A reduction in phytic acid (PA) content was observed. | [33] |
Fermentation with S. cerevisiae (30 °C for 6 h) | Increase in water absorption capacity of WB. | An 86% decrease * of PA at pH 4 and 1 h processing time. TDF of bran was not affected by fermentation. | [26] |
Fermentation with S. cerevisiae at (30 °C for 6 days) | ND | A significant increase in the TPC, DPPH, antioxidant activity of WB was observed on day 3 of fermentation. | [46] |
Spontaneous and yeast fermentation (20 & 32 °C for 20 h) | ND | Significant increase (≥40% *) in folates, free ferulic acid and soluble AX in yeast-fermented bran. Acidification of bran slurries at maximum fermentation temperature. | [47] |
Fermentation with L. brevis (28 °C for 16 h) | An increase in gas retention of dough and bread volume was observed with the inclusion of fermented WB. Significant reduction in bread staling compared to bread with unfermented WB. Improved viscoelasticity of dough | There was a two- and four-fold increase * in WEAX and SDF of fermented WB compared to native bran. | [48] |
Enzymatic treatment (cellulase and xylanase) | WRC increased by 16%. Enzymatic treatment improved oil holding and swelling capacity. Glucose adsorption capacity improved by 1.4-fold. Loose structure, wall structure damaged/degradation of wall PS. | A twofold increase of TPC, and antioxidant properties of enzyme-treated WB compared to the control sample. | [49] |
Treatment with Lactobacillus bulgaricus, Streptococcus thermophiles and Saccharomyces cerevisiae (alone and in combination)–37 °C for 24 h & 48 h | The WHC and WRC improved significantly in fermented WB. Partial degradation of aleurone cells. | Five-fold increase in WEAX content, 60% increase in phenolic lipids, 2-fold increase in SDF, 23–27% reduction in PA. | [32] |
Extrusion (115 and 130 °C; screw speeds: 16, 20, and 25 rpm) + fermentation (L. plantarum and L. uvarum) | ND | Combination of both treatments lowered mycotoxin content by 80.6% * and increased biogenic amines by 42.9% * of bran samples. Fructose content increased by 15% * after fermentation. | [50] |
Enzymatic treatment (β-endoxylanase and α-L-arabinofuranosidase) | WRC and fat binding capacity increased in single and combined enzyme-treated WB. Improved porosity of enzyme-treated bran dough | TPC and DPPH content increased in single and combined enzyme-treated WB. pH reduced in WB treated with xylanase and combined enzymes. | [51] |
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Onipe, O.O.; Ramashia, S.E.; Jideani, A.I.O. Wheat Bran Modifications for Enhanced Nutrition and Functionality in Selected Food Products. Molecules 2021, 26, 3918. https://doi.org/10.3390/molecules26133918
Onipe OO, Ramashia SE, Jideani AIO. Wheat Bran Modifications for Enhanced Nutrition and Functionality in Selected Food Products. Molecules. 2021; 26(13):3918. https://doi.org/10.3390/molecules26133918
Chicago/Turabian StyleOnipe, Oluwatoyin O., Shonisani E. Ramashia, and Afam I. O. Jideani. 2021. "Wheat Bran Modifications for Enhanced Nutrition and Functionality in Selected Food Products" Molecules 26, no. 13: 3918. https://doi.org/10.3390/molecules26133918
APA StyleOnipe, O. O., Ramashia, S. E., & Jideani, A. I. O. (2021). Wheat Bran Modifications for Enhanced Nutrition and Functionality in Selected Food Products. Molecules, 26(13), 3918. https://doi.org/10.3390/molecules26133918