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Importance of processing for physico-chemical and physiological properties of dietary fibre

Published online by Cambridge University Press:  05 March 2007

E. Margareta*
Affiliation:
Applied Nutrition and Food Chemistry, Center for Chemistry and Chemical Engineering, Lund University, PO Box 124, SE-221 00-Lund, Sweden
G.-L. Nyman
Affiliation:
Applied Nutrition and Food Chemistry, Center for Chemistry and Chemical Engineering, Lund University, PO Box 124, SE-221 00-Lund, Sweden
*
Corresponding author: Professor Margareta Nyman, fax +46 46 222 4532, Margareta.Nyman@inl.lth.se
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Abstract

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There is considerable loss of DM during wet heat treatment of vegetables, leading to an increase in dietary fibre. Correction for the loss of DM indicates that the effects on total dietary fibre are minor. There is, however, depolymerization of the dietary fibre polysaccharides. The degradation is related to the severity of the heat treatment. Souring, freezing and mild microwave treatment have no effects. The viscosity is in general related to the extent of polymerisation. Microwave treatment has different effects on various cultivars of green beans, and the addition of salt (NaCl and CaCl2) to the boiling water changes the physico-chemical properties of soluble fibre in carrots, depending on the cation. The higher viscosity of the soluble fibre in raw carrots may partly explain the lower glucose and hormonal responses observed in healthy subjects when compared with blanched and microwave-cooked carrots. In studies on rats the amount of butyric acid in the distal colon has been shown to be higher with dietary components containing high amounts of resistant starch. Further, the fermentability is lower and the butyric acid concentration higher with composite foods than with the corresponding purified fibre fractions. In human studies the faecal concentration of butyric acid has been shown to increase in patients with ulcerative colitis when β-glucan-enriched oat bran (20 g fibre) is added to the diet for 12 weeks. Also, an improvement of symptoms was reported.

Type
Session: Nutrients contributing to the fibre effect
Copyright
Copyright © The Nutrition Society 2003

References

Albersheim, P, Neukom, H, Deuel, H (1960) Splitting of pectin chain molecules in neutral solutions. Archives of Biochemistry and Biophysics 90, 4651.CrossRefGoogle ScholarPubMed
Berggren, AM, Bjorck, IME, Nyman, EMG-L (1993) Short-chain fatty acid content and pH in caecum of rats given various sources of carbohydrates. Journal of the Science of Food and Agriculture 63, 397406.CrossRefGoogle Scholar
Björck, I, Nyman, M, Asp, N-G (1984) Extrusion cooking and dietary fibre: effects on dietary fibre content and on degradation in the rat intestinal tract. Cereal Chemistry 61, 174179.Google Scholar
Björck, IM, Nyman, M, Pedersen, B, Siljeström, M, Asp, N-G, Eggum, BO (1986) On the digestibility of starch in wheat bread – Studies in vitro and in vivo. Journal of Cereal Science 4, 111.CrossRefGoogle Scholar
Cummings, JH (1997) Short-chain fatty acid enemas in the treatment of distal ulcerative colitis. European Journal of Gastroenterology and Hepatology 9, 149153.CrossRefGoogle ScholarPubMed
Cummings, JH, Beatty, ER, Kingman, SM, Bingham, SA, Englyst, HN (1996) Digestion and physiological properties of resistant starch in the human large bowel. British Journal of Nutrition 75, 733747.CrossRefGoogle ScholarPubMed
Eastwood, MA, Morris, ER (1992) Physical properties of dietary fiber that influence physiological function: a model for polymers along the gastrointestinal tract. American Journal of Clinical Nutrition 55, 436442.CrossRefGoogle Scholar
Englyst, HN, Hay, S, Macfarlane, GT (1987) Polysaccharide breakdown by mixed populations of human faecal bacteria. FEMS Microbial Ecology 95, 163171.CrossRefGoogle Scholar
Goodlad, JS, Mathers, JC (1992) Digestion of complex carbohydrates and large bowel fermentation in rats fed on raw and cooked peas. (Pisum sativum). British Journal of Nutrition 67, 475488.CrossRefGoogle ScholarPubMed
Greve, LC, McArdle, RN, Gohlke, JR, Labavitch, JM (1994) Impact of heating on carrot firmness: changes in cell wall components. Journal of Agricultural and Food Chemistry 42, 29002906.CrossRefGoogle Scholar
Gustafsson, K, Asp, N-G, Hagander, B, Nyman, M, Schweizer, T (1995) Influence of processing and cooking of carrots in mixed meals on satiety, glucose and hormonal response. International Journal of Food Science and Nutrition 46, 312.CrossRefGoogle ScholarPubMed
Hallert, C, Bjorck, I, Nyman, M, Pousette, A, Grännö, C, Svensson, H (2003) Increasing the fecal butyrate in ulcerative colitis patients by diet. A pilot study. Inflammatory Bowel Diseases 9 (In the Press)CrossRefGoogle Scholar
Henningsson, ÅM, Nyman, EMG-L, Björck, IME (2001) Content of short-chain fatty acids in the hindgut of rats fed processed bean (Phaseolus vulgaris) flours varying in distribution and content of indigestible carbohydrates. British Journal of Nutrition 86, 379389.CrossRefGoogle ScholarPubMed
Henningsson, ÅM, Nyman, EMG-L, Björck, IME (2002) Short-chain fatty acid content in the hindgut of rats fed various composite foods and commercial dietary fibre fractions from similar sources. Journal of the Science of Food and Agriculture 82, 385393.CrossRefGoogle Scholar
Levrat, MA, Remesy, C, Demigne, C (1991) High propionic acid fermentations and mineral accumulation in the cecum of rats adapted to different levels of inulin. Journal of Nutrition 121, 17301737.Google ScholarPubMed
Martin, LJM, Dumon, HJW, Champ, MMJ (1998) Production of short-chain fatty acids from resistant starch in a pig model. Journal of the Science of Food and Agriculture 77, 7180.3.0.CO;2-H>CrossRefGoogle Scholar
Morris, ER (1990) Shear-thinning of ‘random coil‘ polysaccharides: characterisation by two parameters from a simple linear plot. Carbohydrate Polymers 13, 8596.CrossRefGoogle Scholar
Mortensen, PB, Holtug, K, Rasmussen, HS (1988) Short-chain fatty acid production from mono-and disaccharides in a fecal incubation system: implications for colonic fermentation of dietary fiber in humans. Journal of Nutrition 118, 321325.CrossRefGoogle Scholar
Nyman, EMG-L, Svanberg, SJM (2002) Modification of physico-chemical properties of dietary fibre in carrots by mono-and divalent cations. Food Chemistry 76, 273280.CrossRefGoogle Scholar
Nyman, EMG-L, Svanberg, SJM, Asp, N-G (1994) Molecular weight distribution and viscosity of water-soluble dietary fibre isolated from green beans, Brussels sprouts and green peas following different types of processing. Journal of the Science of Food and Agriculture 66, 8391.CrossRefGoogle Scholar
Nyman, M, Asp, N-G (1982) Fermentation of dietary fibre components in the rat intestinal tract. British Journal of Nutrition 47, 357366.CrossRefGoogle ScholarPubMed
Nyman, M, Björck, I, Håkansson, B, Asp, N-G (1987a) Popping of whole-grain wheat: effect on dietary fibre degradation in the rat intestinal tract. Journal of Cereal Science 5, 6772.CrossRefGoogle Scholar
Nyman, M, Pålsson, K-E, Asp, N-G (1987b) Effects of processing on dietary fibre in vegetables. Lebensmittel Wissenschaft und Technologie 20, 2936.Google Scholar
Nyman, M, Schweizer, TF, Pålsson, KE, Asp, NG (1991) Effects of processing on fermentation of dietary fibre in vegetables by rats. Lebensmittel Wissenschaft und Technologie 24, 433441.Google Scholar
Roediger, WE (1982) Utilization of nutrients by isolated epithelial cells of the rat colon. Gastroenterology 83, 424429.CrossRefGoogle ScholarPubMed
Roland, N, Nugon-Baudon, L, Andrieux, C, Szylit, O (1995) Comparative study of the fermentative characteristics of inulin and different types of fibre in rats inoculated with a human whole faecal flora. British Journal of Nutrition 74, 239249.CrossRefGoogle ScholarPubMed
Scheppach, W, Bartram, HP, Richter, F (1995) Role of short-chain fatty acids in the prevention of colorectal cancer European Journal of Cancer 31A 10771080.CrossRefGoogle Scholar
Scheppach, W, Sommer, H, Kirchner, T, Paganelli, GM, Bartram, P, Christl, S, Richter, F, Dusel, G, Kasper, H (1992) Effect of butyrate enemas on the colonic mucosa in distal ulcerative colitis. Gastroenterology 103, 5156.CrossRefGoogle ScholarPubMed
Selvendran, RR & Robertson, JA (1994) Dietary fibre in foods: amount and type. In Physico-chemical Properties of Dietary Fibre and Effect of Processing on Micronutrients Availability, pp. 11–19 [Amadò, R Barry, JL and Frølich, W, editors]. Luxembourg: COST 92 Directorate-general XIII.Google Scholar
Siljeström, M, Björck, I (1990) Digestible and undigestible carbohydrates in autoclaved legumes, potatoes and corn. Food Chemistry 38, 145152.CrossRefGoogle Scholar
Svanberg, SJM, Gustafsson, KBH, Suortti, T, Nyman, EMG-L (1995) Molecular weight distribution, measured by HPSEC, and viscosity of water-soluble dietary fiber in carrots following different types of processing. Journal of Agricultural and Food Chemistry 43, 26922697.CrossRefGoogle Scholar
Svanberg, SJM, Nyman, EMG-L, Nilsson, R, Nilsson, T (1997a) Effects of boiling and storage on dietary fibre and digestible carbohydrates in various cultivars of carrots. Journal of the Science of Food and Agriculture 73, 245254.3.0.CO;2-P>CrossRefGoogle Scholar
Svanberg, SJM, Suortti, T, Nyman, EMG-L (1997b) Physico-chemical changes in dietary fiber of green beans after repeated microwave treatments. Journal of Food Science 62, 10061010.CrossRefGoogle Scholar
Svanberg, SJM, Suortti, T, Nyman, EMG-L (1999) Intestinal degradation of dietary fibre in green beans – effects of microwave treatments. International Journal of Food Science and Nutrition 50, 245253.Google ScholarPubMed
Tietyen, JL, Nevins, DJ, Schneeman, BO (1990) Characterization of the hypocholesterolic potential of oat bran. FASEB Journal 4, A527Google Scholar
Todesco, T, Rao, AV, Bosello, O, Jenkins, DJ (1991) Propionate lowers blood glucose and alters lipid metabolism in healthy subjects. American Journal of Clinical Nutrition 54, 860865.CrossRefGoogle ScholarPubMed
Topping, DL, Illman, RJ, Trimble, RP (1985) Volatile fatty acids concentrations in rats fed diets containing gum arabic and cellulose separately and as a mixture. Nutrition Reports International 32, 809814.Google Scholar
Torsdottir, I, Alpsten, M, Andersson, H, Einarsson, S (1989) Dietary guar gum effects on postprandial blood glucose, insulin and hydroxyproline in humans. Journal of Nutrition 119, 19251931.CrossRefGoogle ScholarPubMed