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The effects of processing on sodium-potassium and calcium-phosphorus ratios in foodsRonan, Kathleen M. 04 June 1981 (has links)
The objective of this study was to determine the effects of processing
on sodium - potassium and calcium - phosphorus ratios in tuna canned in
oil and in water, peanut butter, white and whole wheat flours. Mineral
levels were determined by atomic absorption spectrophotometry in food
samples at various stages in the production of these finished products.
The average sodium - potassium ratios of the tuna samples were: 1.37
raw, 1.24 precooked, 1.87 canned in oil and 1.61 canned in water.
Processing did not significantly effect sodium and potassium ratios in
canned tuna. The average calcium - phosphorus ratios of the tuna samples
were: 0.034 raw, 0.024 precooked, 0.034 canned in oil and 0.065 canned
in water. The ratio of the canned in water meat was significantly
effected by processing.
The average sodium - potassium ratios of the peanut samples were:
0.034 raw, 0.043 roasted, 0.031 blanched and 0.781 peanut butter. The
ratio of peanut butter was significantly greater than the ratios of
the other peanut samples. The average calcium - phosphorus ratios of
the peanut samples were: 0.148 raw, 0.121 roasted, 0.141 blanched and
0.128 peanut butter. These ratios were not significantly effected by
processing.
The average sodium - potassium ratio was 0.16 in white flours,
0.84 in whole wheat flour and 0.89 in the kernel. The average calcium -
phosphorus ratio was 0.14 in white flours, 0.07 in whole wheat flour
and 0.07 in the kernel. The ratios of the kernel and whole wheat
flour were not significantly different. Processing significantly effected
the ratios of the white flour.
The preferred concentration of sodium chloride and a 1:1 sodium -
potassium chloride mixture in white and whole wheat breads was also
studied. Bread samples were made with 1.0%, 0.75% and 0.5% levels of
both salt treatments. They were evaluated by an untrained flavor panel
for overall desirability with a nine point hedonic scale. The judges
preferred a sodium chloride white bread with a 7.0 sodium - potassium
ratio, and a sodium chloride whole wheat bread with a 3.29 ratio. These
ratios were both lower than those found in commercial products. White
and whole wheat breads made with 0.75% sodium chloride were as acceptable
as breads made with 1.0% 1:1 sodium - potassium chloride mixture.
The sodium - potassium ratio of the salt mixture white bread was 1.20 and
the ratio of the whole wheat bread was 0.91.
The addition of salt to finished products for flavor had an effect
on the sodium - potassium ratio of the foods studied. Also, reducing
the amount of added salt to commercial breads and replacing some sodium
chloride with potassium chloride were acceptable means of lowering
the sodium - potassium ratios of white and whole wheat breads. / Graduation date: 1982
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Mineral content of sweet corn and broccoli cooked in waters of varying hardnessBohn, Lorraine Kay, 1959- January 2011 (has links)
Vita. / Digitized by Kansas Correctional Industries
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BINDING OF COPPER, ZINC AND IRON BY SIX DIETARY FIBER SOURCESThompson, Sue Angele January 1980 (has links)
Six dietary fiber sources, wheat bran, corn bran, soy bran, oat hulls, rice bran, and cellulose were examined with regard to their abilities to bind copper, zinc, and iron. Their chemical composition, some of their physical properties, and their in vivo action on mineral status in tissues of chicks were investigated. Also, a comparison of the physicochemical properties of neutral detergent treated (NDF) and pepsin-pancreatin treated (EIR) residues was made. The release of endogenous copper, zinc, and iron from the fiber sources was pH dependent. Greater amounts of minerals were released into solution at pH 0.65 than into solution at pH 6.8. After a sequential treatment of pH 0.65 solution, neutralization, then pH 6.8 buffer, the mineral levels in the residues were similar to those remaining in the residues after the near neutral treatment. This indicated that the minerals were rebound after the pH of the solution was raised from acidic to near neutral. The amount of zinc in the residues from the sequential treatment correlated positively to protein and phytic acid contents and negatively to NDF and EIR contents. Neither copper nor iron showed any significant correlations. Hydrogen ion buffering capacities were determined for three preparations of the six fiber sources: (1) untreated, original material; (2) NDF-treated; and (3) EIR-treated materials. The buffering capacities were expressed as functions of the slopes of titration curves, where the smaller the slope, the greater the buffering capacity. The treated preparations had lower buffering capacities than did the untreated preparation. The treatments reduced the amounts of digestible/soluble components, especially protein in the fiber sources. Protein content was strongly correlated to buffering capacity for the untreated and the EIR-treated preparations but not for the NDF-treated preparation. Wheat bran, soy bran, oat hulls, and cellulose were subjected to NDF and EIR treatments, and the residues were used as column material for cation exchange experiments. A factorial experiment was performed using fibers by treatments by three solutions. The solutions were copper alone, zinc alone, and copper-zinc in combination. Cation exchange capacities (CEC) and protein contents were also determined. The CEC values for the residues from the two treatments for wheat bran and cellulose were similar but were very different for the soy bran (EIR-treated CEC was higher than NDF-treated) and oat hulls (NDF much greater than EIR). More mmoles of copper were bound than zinc whether presented alone or in equimolar combination. Protein content correlated to mmoles mineral bound for only the NDF-treated residues and only when the minerals were presented singly. These in vitro experiments demonstrated the intrinsic differences of the fiber sources. One fiber source may be beneficial to nutritional status while another may be detrimental. The fiber isolation technique produced residues with different compositions and different physical properties. Future biochemical investigations of dietary fiber must acknowledge the possible divergence from physiological reality which results from the isolation methodology. The chick feeding study used diets which had the fiber sources added to be equivalent to the addition of 6% dietary fiber (as NDF). At this level, all the fiber sources, except rice bran, resulted in adequate growth and adequate deposition of tissue minerals. The chicks on the rice bran diet had lowered feed intakes, significantly reduced growth and significantly lower tibia zinc, iron, and manganese levels. One factor in the rice bran diet, which may have influenced the status of the chicks, was its phytic acid content which was the highest of the fiber sources. This in vivo experiment again indicates the dissimilarity in effects of the dietary fiber sources.
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