Improving spent fowl meat tenderness with calcium chloride /

Four experiments were conducted to determine the optimal

Bibliographic Details
Main Author: Nurmahmudi, 1961-
Format: Thesis Book
Language:English
Published: [Place of publication not identified] : [publisher not identified] ; 1994.
Subjects:
Online Access:http://proxy.library.tamu.edu/login?url=http://proquest.umi.com/pqdweb?did=741965901&sid=1&Fmt=2&clientId=2945&RQT=309&VName=PQD
Description
Summary:Four experiments were conducted to determine the optimal
method of introduction and concentration of calcium solution
into spent fowl meat as a tenderizing agent. Calpain
activities, heat stable collagen content, and sarcomere
length were measured to characterize the mechanism of
tenderization. In experiment 1, numbers of chickens were
slaughtered under commercial procedures; Pectoralis major
were excised and injected to 10% (w/w) with 0.1, 0.2, or 0.3M
CaCI2 solutions; 0.3M ZnCl2 solution; deionizedwater; or left
uninjected as control, then aged for 1 or 3 days. results
indicated that injection was not a successful delivery method
to improve the tenderness. In experiment 2, using 0.2M or
0.3M CaCI2 solutions, hot-boned fillets were treated with
combinations of injection, soaking, and tumbling.
Introduction of 0.2M CaCI2 using all methods was not
sufficient to improve the tenderness. Injection of 0.3M
CaCI2 followed by tumbling reduced the shear value to near
the level acceptable to consumers. Therefore, tumbling with
injection of O.3M CaCl2 is essential for maximum
tenderization of spent fowl meat. In experiment 3, hot-boned
fillets were injected with or soaked in 0.3M CaCI2 or 0.6M
NaCl to 10% (w/w) followed by tumbling. Calcium treatment
was delayed 24 hr postmortem for some fillets while others
had fresh CaCI2 added after tumbling. Calcium chloride and
NaCl reduced the shear values equally, suggesting that
conductivity may play a major role in the calcium-induced
tenderization. Replenishing the 0.3M CaCI2 after tumbling
did not exert further tenderization. Additional
tenderization was achieved by both solutions when the
injection and tumbling were applied at 24 hr postmortem. In
experiment 4, the hot-boned fillets were injected to 10%
(w/w) with 0.3M CaCI2 or 0.6M NaCl and tumbled. Results
indicated that calcium treatment activated m-calpain. The
decreased collagen stability. Similar shear values at 24 hr
postmortem for CaCl2- and NaCl-injected fillets indicated
that the calcium tenderization was conductivity effect,
despite CaCI2 activated calpain.
Item Description:Vita.
"Major Subject: Food Science and Technology".
Physical Description:xi, 97 leaves ; 28 cm.
Issued also on microfiche from University Microfilms Inc.
Bibliography:Includes bibliographical references.