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Use chitosan as protein stabilizer for fish during frozen storage.


Protecting proteins is a primary concern when attempting to maintain quality during the freezing and frozen storage of fish. Currently, a 4%-sucrose/5%-sorbitol mixture is used in conjunction with phosphate as the industry standard.

In order to improve quality, new alternatives, which prevent protein denaturation denaturation, term used to describe the loss of native, higher-order structure of protein molecules in solution. Most globular proteins exhibit complicated three-dimensional folding described as secondary, tertiary, and quarternary structures. , are continually being explored. The goal of scientists at Oregon State University Oregon State University, at Corvallis; land-grant and state supported; coeducational; chartered 1858 as Corvallis College, opened 1865. In 1868 it was designated Oregon's land-grant agricultural college and was taken over completely by the state in 1885.  was to measure the effects of chitosan as a replacement for phosphate. They wanted to see what effects chitosan had on the functional and biochemical properties of fish proteins during their frozen storage, and compare those results to a commercial control and screw-pressed meat. Their efforts indicate that chitosan may be a suitable phosphate replacement that can stabilize fish proteins during the product's frozen storage.

Researchers prepared four samples: a screw-pressed (SP) product, a commercial control with 0.3% STP STP or standard temperature and pressure, standard conditions for measurement of the properties of matter. The standard temperature is the freezing point of pure water, 0°C; or 273.15°K;. , a 0.3% chitosan (T1) mix and a 1% chitosan (T2) mixture. Raw surimi su·ri·mi  
n.
Minced, processed fish used in the preparation of imitation seafood, especially imitation shellfish.



[Japanese : suru, to process, mash + mi, meat.]
 was mixed with the respective ingredients at 5 C and packed in approximately 500-g portions. Then the samples were vacuum-packaged and frozen at -18 C, except the 0 month samples, which were stored at 5 C until they were tested.

Investigators tested the samples at 0, 1, 4, 8, 12 months of frozen storage to evaluate changes in salt extractable protein, turbidity turbidity /tur·bid·i·ty/ (ter-bid´i-te) cloudiness; disturbance of solids (sediment) in a solution, so that it is not clear.tur´bid
Turbidity
The cloudiness or lack of transparency of a solution.
, water retention ability, gelation gelation /ge·la·tion/ (je-la´shun) conversion of a sol into a gel.

ge·la·tion
n.
1. Solidification by cooling or freezing.

2. The process of forming a gel.

3.
 properties, pH and color. For evaluating the gel, the samples were prepared with 2% salt and 1% BPP (Bits Per Pixel) See bit depth.

bpp - bits per pixel
. They were adjusted to a 78% moisture content using ice and water. They were then cooked in stainless steel tubes at 95 C for 15 minutes.

The texture values of T1 after four months of frozen storage were equal to or better than those of the control. In addition, the T2 samples yielded salt extractable proteins greater than the control, supporting the role of chitosan as a stabilizer of proteins during frozen storage.

The color values of T1 and T2 were also comparable to the control, and the water retention ability of the chitosan samples (T1 and T2) was greater than or equal to that of the control after four months of frozen storage.

Further information. Jae Park, Department of Food Science and Technology, Oregon State University, Seafood Research Laboratory, 2001 Marine Dr., Room 253, Astoria, OR 97103; phone: 503-325-4531; fax: 503-325-2753; email: jae.park@orst.edu.
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Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Emerging Food R&D Report
Date:Aug 1, 2004
Words:384
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