4 °C - the National Sea Grant Library
4 °C - the National Sea Grant Library 4 °C - the National Sea Grant Library
6 Antioxidants were dissolved in a small amount of water added to unwashed mince and were added to the washed mince in powdered form. All treatments including controls were mixed for 3 min to evenly disperse the antioxidants. Replication 1 used a household mixer (Model K45 Kitchenaid Division, Hobart Manufacturing CO., Troy OH) and replications 2 and 3 used an industrial size mixer (Model A200, Hobart Manufacturing Co.). Mince was then placed in 20 0.45 kg wax coated cardboard boxes (Packaging Production Corp., New Bedford, MA) and frozen to -40°C in a plate freezer (Dole Freeze-Cell Model 2735-6A, Dole Refrigerating Co., Lewisburg, TN). Frozen mince was stored in a storage freezer overnight (- 20°C), packed in dry ice, and transported to Mississippi St&e University for chemical analyses. Samples were stored at - 14°C -r- 2°C for the duration of the study. Analyses Oxidative rancidity was determined by the 2-thiobarbituric acid reactive substances (TBARS) test (Tarladgis et al, 1960). Optical density was multiplied by a factor of 7.8 to express the results as mg malonaldehyde/kg mince according to Sinnhuber and Yu (1958). Enzymatic rancidity (free fatty acids, FFA) was determined by the method described by Woyewoda et al (1986). Color was determined by a Hunterlab Model D25 Color Meter (Hunter Associates Laboratory, Inc., Reston, VA), standardized with a white plate standard no. LS-13601. All preceding tests were performed in duplicate after 0, 1, 2, 3, and 4 mo. of frozen storage. Moisture, fat, protein, ash, copper, iron, phosphorus, and erythorbate contents were determined at time 0 for each experimental observations by the Mississippi State Chemical Laboratory. All analyses, with the exception of erythorbate, used AOAC (1990) methods. A standard curve was set up to evaluate erythorbate results using Vitamin C (ascorbate) procedures (Strohecker and Henning, 1966). In addition to AOAC methods, the phosphate analysis used procedures from Clesceri et al. (1989). Statistical Analysis The data were analyzed using analyses of variance for a split-plot in a radomized complete block design. Wash treatment (w and u), whole plot and antioxidant treatment (5), and storage time (0 to 4 mo.) were the subplots. Data was analyzed using PROC GLM of the Statistical Analysis System (SAS, 1985). If significant differences were found, means were separated using Fisher’s Protected least significant difference (LSD) (Steel and Torrie, 1980) at the 5% level of significance. RESULTS AND DISCUSSION washed mince had lower (P
Table 1. Effect of wash treatment on proximate composition and selected nutrients (wet basis) in catfish mince averaged over antioxidant treatment. Nutrient Washed Unwashed Phosphorous (%) Copper (mg/kg) Iron (mg/kg) Erythorbate (mg/g)_ Moisture (%) Fat (%) - Ash (%) Protein (%) 0.22 b 0.65 a 5.29 a 0.57 a 82.20 a 3.24 b 0.51 b 14.20 a 0.30 a 0.58 a 5.21 a 0.58 a 74.25 b 14.09 a 0.66 a 11.22 b ab - Means within row not followed by same letter differ (P
- Page 134 and 135: 48,693 mt/yr in 198690. The primary
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- Page 138 and 139: Christmas, J., D. Etzold, T. McIlwa
- Page 140 and 141: Perkins, G. 1977. Potential for exp
- Page 142 and 143: EFFECT OF WASHING WATER pH ON COLOR
- Page 144 and 145: Figure 1, Whole Fish I Dehead (M-07
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- Page 148 and 149: Table 1. Mean carotenoids, hematin,
- Page 150 and 151: Table 2. Treatments Mean moisture v
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- Page 154 and 155: Siggia S. 1963. Methods for trace q
- Page 156 and 157: work on combining acetates and phos
- Page 158 and 159: untreated fresh fillets and treated
- Page 160 and 161: Fig. 3. 10 0 m control tJ 0.1% MKP-
- Page 162 and 163: negative bacteria such as Pseudomon
- Page 164 and 165: concentrations up to 1% could be us
- Page 166 and 167: Fey, M.S., and Regenstein, J.M. 198
- Page 168 and 169: Schaack, M.M., and Marth E.H. 1988.
- Page 170 and 171: MATERIALS AND METHODS Materials Liv
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- Page 187 and 188: Table 2. Effect of antioxidant trea
- Page 189 and 190: (1993) for whole dressed catfish. C
- Page 191 and 192: Anonymous. 1992. Processing up 11%
- Page 193 and 194: Sin&_&x, R. O. and Yu, T. C. 1958.
- Page 195 and 196: 1. Materials MATERIALS AND METHODS
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- Page 208 and 209: STORAGE CHARACTERISTICS OF FROZEN B
- Page 210 and 211: OPTIMUM CONDITIONS FOR THE PREPARAT
- Page 212 and 213: 3 BUILDING STRATEGIC PARTNERSHIPS F
- Page 214 and 215: for aquaculture supporting developm
- Page 216 and 217: problem solving of complex regional
- Page 218 and 219: DESIGN OF AN AUTOMAT EVALUATION DEV
- Page 220 and 221: sides of the shrimp were averaged.
- Page 222 and 223: Ammonia Measurements Figure 2 shows
- Page 224 and 225: REFERENCES Balaban, M. O., Yeralan,
- Page 226 and 227: QUALITIES OF FRESH AND PREVIOUSLY F
- Page 228 and 229: For the samples stored for six mont
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- Page 232 and 233: Table 1. Psychrotrophic bacterial p
6<br />
Antioxidants were dissolved in a small amount of water added to unwashed mince and were<br />
added to <strong>the</strong> washed mince in powdered form. All treatments including controls were mixed for 3<br />
min to evenly disperse <strong>the</strong> antioxidants. Replication 1 used a household mixer (Model K45 Kitchenaid<br />
Division, Hobart Manufacturing CO., Troy OH) and replications 2 and 3 used an industrial size<br />
mixer (Model A200, Hobart Manufacturing Co.). Mince was <strong>the</strong>n placed in 20 0.45 kg wax coated<br />
cardboard boxes (Packaging Production Corp., New Bedford, MA) and frozen to -40<strong>°C</strong> in a plate<br />
freezer (Dole Freeze-Cell Model 2735-6A, Dole Refrigerating Co., Lewisburg, TN). Frozen mince<br />
was stored in a storage freezer overnight (- 20<strong>°C</strong>), packed in dry ice, and transported to Mississippi<br />
St&e University for chemical analyses. Samples were stored at - 14<strong>°C</strong> -r- 2<strong>°C</strong> for <strong>the</strong> duration of <strong>the</strong><br />
study.<br />
Analyses<br />
Oxidative rancidity was determined by <strong>the</strong> 2-thiobarbituric acid reactive substances (TBARS)<br />
test (Tarladgis et al, 1960). Optical density was multiplied by a factor of 7.8 to express <strong>the</strong> results<br />
as mg malonaldehyde/kg mince according to Sinnhuber and Yu (1958). Enzymatic rancidity (free<br />
fatty acids, FFA) was determined by <strong>the</strong> method described by Woyewoda et al (1986). Color was<br />
determined by a Hunterlab Model D25 Color Meter (Hunter Associates Laboratory, Inc., Reston,<br />
VA), standardized with a white plate standard no. LS-13601. All preceding tests were performed<br />
in duplicate after 0, 1, 2, 3, and 4 mo. of frozen storage.<br />
Moisture, fat, protein, ash, copper, iron, phosphorus, and erythorbate contents were<br />
determined at time 0 for each experimental observations by <strong>the</strong> Mississippi State Chemical<br />
Laboratory. All analyses, with <strong>the</strong> exception of erythorbate, used AOAC (1990) methods. A<br />
standard curve was set up to evaluate erythorbate results using Vitamin C (ascorbate) procedures<br />
(Strohecker and Henning, 1966). In addition to AOAC methods, <strong>the</strong> phosphate analysis used<br />
procedures from Clesceri et al. (1989).<br />
Statistical Analysis<br />
The data were analyzed using analyses of variance for a split-plot in a radomized complete<br />
block design. Wash treatment (w and u), whole plot and antioxidant treatment (5), and storage time<br />
(0 to 4 mo.) were <strong>the</strong> subplots. Data was analyzed using PROC GLM of <strong>the</strong> Statistical Analysis<br />
System (SAS, 1985). If significant differences were found, means were separated using Fisher’s<br />
Protected least significant difference (LSD) (Steel and Torrie, 1980) at <strong>the</strong> 5% level of significance.<br />
RESULTS AND DISCUSSION<br />
washed mince had lower (P