4 °C - the National Sea Grant Library
4 °C - the National Sea Grant Library 4 °C - the National Sea Grant Library
in a stainless steel tank (SOL) with iced water at a ratio of 1 part flesh to 3 parts water (W/W). Water was used for the fourth wash cycle contained 0.15% (w/w) NaCl to facilitate de-watering. Hand whipper was used to stir the slurry for 5 min and excess water was removed between washes using cheesecloth. A basket centrifuge (Wastem States, Hamilton, ON) was used for the final de-watering to the extent that water was no longer visibly being extracted from the washed mince. Raw surimi was either directly vacuum-packaged or chopped with cryoprotectants (4% sucrose, 4% sorbitol and 0.25% sodium tripolyphosphate, STPP) for 2 min using a Hobart silent cutter and then vacuumpackaged. Oxygen barrier-bags (Surlyn, oxygen transmission rate = 5cc/m2/24hr/atm, at 4.4 “C and 0% Rk, Cryovac Co. Duncan, SC) and a Multivac AG 900 vacuum packaging machine (Multivac, Sepp Haggenenmuller KG, Germany) were used to pack all samples. Praximate Composition Moisture, crude protein, fat and ash content were determined according to AOAC (1984) methods. Protein in Washing Water Washing water in different washing cycles were filtrated using Whatman No.2 filter papers. The filtrate was used for protein analysis (Douglas-schwarz and Lee, 1988). Expressible Water A 3mm thick and 20mm diameter slice of surimi gel was pressed between four sheets of No. 1 f&r paper under a weight of lO.Skg for 1 min. The weight loss of a gel slice after pressing was expressed as percent of the original sample weight (Hennigar et al., 1988). Expressible water for a surimi sample was determined according to Alvarez et al. (1992). A 2g of a surimi sample was folded with one sheet of filter paper Watman No. 1 and centrifuged at 3000 r-pm for 15 min at room temperature (Servall angel centrifuge type SPX., Ivan Servall Inc. Norwalk, Corn.). Preweighed nylon screen was placed between the surimi sample and the filter paper sheet. This was used to aid in removing the sticky “cake” rapidly from the filter paper after wntrifugath (W5nberg et al., 1984). Values reported represent an average of six samples per treatment. I I I Whole Fish I I I I I Filleting Frame Fillet
I Minced fish I I I I I At a ratio of 1:3(w/w) minced muscle to iced water for 5 min Washing 4 times First washing Second washing Third washing Excess water removed between washes 1 by draining the slurry in cheesecloth Mixing with cryoprotectants (4% sucrose, 4% sorbitol and 0.25% TSPP) (for 2 min) I Surimi I I I I Packaging under vacuum I I Storing at - 27OC Fig. 1 A flowchart of processing surimi from tilapia Hunter Color Values Hunter color values (L, “a”, “b”) of fish mince during washing steps and final surimi products were measured using a colorimeter (Minolta Chroma Meter CR-200, Minolta Camera, Ltd., Osaka, Japan). The value L was the lightness ranged from 0 to 100; ‘*a” was chromaticity where positive value indicating redness and negative value indicating greenness; while positive value of “b” indicating yellowness and negative value indicating blueness. Three random spots on each sample were measured and the average data were recorded.
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- Page 240 and 241: SAS Institute Inc. 1987. “SAS/STA
- Page 242 and 243: with a color chart. In this paper,
- Page 244 and 245: TABLE 1 Comparison of Histamine Tes
- Page 246 and 247: 11, Chassande, O., Renard, S., Barb
- Page 248 and 249: FIGURE 1 Time Course for Histamine
- Page 250 and 251: BACKGROUND A Rapid, Easily Used Tes
- Page 252 and 253: We acknowledge with thanks the inte
- Page 254 and 255: AOAC Add 1 ml Extract to 8 cm Prepa
- Page 256 and 257: 248 . Fig. 4 pnitroaniline in HCl N
- Page 258 and 259: 1 O .’ REFLECTANCE (arbitrary uni
- Page 260 and 261: 552 650 600 Salt Effects in the Fig
- Page 262 and 263: IMMUNOLOGIC APPROACHES TO THE IDENT
- Page 264 and 265: Table 1. Fish collected in Biscayne
- Page 266 and 267: Based on unpublished data comparing
- Page 268 and 269: 2. 3. 4. Hartmann, J.X., Poyer, J.C
- Page 270 and 271: irradiated foods look like. After t
- Page 272 and 273: silver carp Wpophthalmichthys molit
- Page 274 and 275: ,$mory Analysis. Sensory data were
- Page 276 and 277: Table 3. Percentage of panelists wh
- Page 278 and 279: Table 5. Percent response of paneli
- Page 280 and 281: McNulty, T, 1996. Personal communic
- Page 284 and 285: Mineral Content Five macro-elements
- Page 286 and 287: TBble 1 _ Yield of surimi made from
- Page 288 and 289: Table 4 - Proximate composition of
- Page 290 and 291: goatfish lizardfish, ponyfish, ther
- Page 292 and 293: Table 7 - Amino acid composition of
- Page 294 and 295: Gel Strength For surimi gels, stres
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- Page 298 and 299: CONSUMER SURVEY OF POND RAISED CATF
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- Page 315 and 316: 100000 10000 P 12 > 1000 10 1 � T
- Page 317 and 318: THE EFFECT OF IONIZING Kvulnificus
- Page 319 and 320: io Vulnificus: Past, Present, and F
- Page 321 and 322: conce op on Vibrio vulnificus in 19
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- Page 325 and 326: isregard include the education of o
- Page 327 and 328: USE OF “COOL PASTEURIZATION” TO
- Page 329 and 330: Survival rate of V: vuZnificus in o
- Page 331 and 332: REFERENCES BAM. 1992. Bacteriologic
in a stainless steel tank (SOL) with iced water at a ratio of 1 part flesh to 3 parts water (W/W). Water<br />
was used for <strong>the</strong> fourth wash cycle contained 0.15% (w/w) NaCl to facilitate de-watering. Hand<br />
whipper was used to stir <strong>the</strong> slurry for 5 min and excess water was removed between washes using<br />
cheesecloth. A basket centrifuge (Wastem States, Hamilton, ON) was used for <strong>the</strong> final de-watering<br />
to <strong>the</strong> extent that water was no longer visibly being extracted from <strong>the</strong> washed mince. Raw surimi<br />
was ei<strong>the</strong>r directly vacuum-packaged or chopped with cryoprotectants (4% sucrose, 4% sorbitol and<br />
0.25% sodium tripolyphosphate, STPP) for 2 min using a Hobart silent cutter and <strong>the</strong>n vacuumpackaged.<br />
Oxygen barrier-bags (Surlyn, oxygen transmission rate = 5cc/m2/24hr/atm, at 4.4 “C and<br />
0% Rk, Cryovac Co. Duncan, SC) and a Multivac AG 900 vacuum packaging machine (Multivac,<br />
Sepp Haggenenmuller KG, Germany) were used to pack all samples.<br />
Praximate Composition<br />
Moisture, crude protein, fat and ash content were determined according to AOAC (1984)<br />
methods.<br />
Protein in Washing Water<br />
Washing water in different washing cycles were filtrated using Whatman No.2 filter papers.<br />
The filtrate was used for protein analysis (Douglas-schwarz and Lee, 1988).<br />
Expressible Water<br />
A 3mm thick and 20mm diameter slice of surimi gel was pressed between four sheets of<br />
No. 1 f&r paper under a weight of lO.Skg for 1 min. The weight loss of a gel slice after<br />
pressing was expressed as percent of <strong>the</strong> original sample weight (Hennigar et al., 1988).<br />
Expressible water for a surimi sample was determined according to Alvarez et al. (1992).<br />
A 2g of a surimi sample was folded with one sheet of filter paper Watman No. 1 and centrifuged at<br />
3000 r-pm for 15 min at room temperature (Servall angel centrifuge type SPX., Ivan Servall Inc.<br />
Norwalk, Corn.). Preweighed nylon screen was placed between <strong>the</strong> surimi sample and <strong>the</strong> filter<br />
paper sheet. This was used to aid in removing <strong>the</strong> sticky “cake” rapidly from <strong>the</strong> filter paper after<br />
wntrifugath (W5nberg et al., 1984). Values reported represent an average of six samples per<br />
treatment.<br />
I<br />
I I<br />
Whole Fish<br />
I I<br />
I<br />
I I<br />
Filleting Frame<br />
Fillet