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PROCEEDING
The
I't
International
Seminar
onAnimal Industry
2009'osustainable
Animal
Production
for
Food Security and Safety"
Published: Faculty of Animal Science, Bogor
Agriculturat
University (IPB)Jl. Agatis Kampus IPB Darmaga 16680 T el. + 625 | 86228 I
l,
86228 Il,
862281.2Fax. +62518622842
http: I I fapet.ipb. ac. id
P.rp*tukuun Nasional RI: Katalog Dalam Terbitan (KDT) Faculty of Animal Science
PROCEEDING.
The 1't lnternational Seminar on Animal lndustry 2009."sustainable Animal Production for Food Security and Safety"
Published: Faculty of Animal Science, Bogor Agricultural University' Bogor' 2010
Ed.1. 2010. 210 x297 mm. 411 P.
ISBN: 978-96530-0-7
Language English
Layout and Printed bY:
KANZ SARANA RAHARJO (KSR)
Bogor
-
Jawa Barate-Mail: ksrcenter@ gmail.com
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etuosFeed Nutrition
physico-chemical properties
of meat and
meat product.Due
to
the negative effect of sucrose 8oloand sorbitol, this study investigated the effects
of
sucroselevel
under 8o/oas
a
single agentof
cryioprotectant
on the
physico-chemicalproperties of surimi-like from beef meat.
MATERIALS
AND METHODSSurimi Preparation
The round meat of beef was obtained from traditional market in Bengkulu. The muscle tissue
was
separatedfrom
fat and
connective tissuemanually and then was cut into 3 cm size of meat
for
mincingby
using meat mincer. Then, theminced meat was washed three times
by
using chilling water (5-10"C) which the final washing usedchilling 05%
NaCl solution. The ratioof
water
to
minced meatin
washing was 3:1. Thefinal
stepof
surimi preparation was dewatering by pressing washed minced meat in the screenof
linen
mesh manually.Finally, raw
surimi wasstirred
with
sucrose 3%(Pl),
4% (P2) and 5oh (P3) and added sodium tripolyphosphate 0.2o/o foreach treatment. Each treatment was replicated
three times.
pH and Water Holding Capacity (WHC)
Surimi pH was measured by using pH-meter
(TOA
HM-11p).At
first,
the elechodeof
pH-meterwas
calibratedto
pH
4
and
7.
Aftercalibrating,
the
electrodeof
pH-meter
wasinserted into sample and the pH indicator rose on
the monitor
of
pH-meter. WHC was determinedby
using Hamm method (Soepamo, 2005). Thesteps of WHC determination are below:
a)
A
0.3g
sample was placedon filter
paperWhatman
4l
and pressed at 3,000 psifor
3 minutes by using Carver Press.b)
Two distinct areas are produced: a meat area and a water area and measured by using plainmater. The area between water and meat area is wet area (mm2). The weight of water (mg) is counted by using formula:
wet area _* 0.0948
c)
Converting
weight
of
free
water
intopercentage
of
sample: ratio of weight of freewater to weight
of
sample (known as %o freewater).
d)
To
determine WHC, the percentageof
free water in the moisture of sample is counted b1 using formula:t00
,n"ir1"*
X
(o/o free water)e)
Finally, WHC (%) is counted by the formula:(100
-
percent free water in the moisture).Gel Strength
Gel
strength was determined according to method describedby
Tan et al., (1988). Surimiwas mixed with3o/o smooth salt and 30% chillin-e
water by using food processor until sticky surim-r
formed. Then, sticky surimi was cased and was heated
with
double step heating: 40"Cin
20 minutes and 90"Cin
20 minutes. This surimi's gel strength was measured by using anvil instron1140 and expressed as gf/cm2.
Chemical Composition
The procedures used to determine proximate composition was similar to that of Apriyantono e/
al.
(1989). Moisturewas
determined through oven drying methodat
110"Cfor 24 h;
crudeprotein
was determined
by
using
Kjeldhal method; crudefat
was evaluatedby
using the soxhlet method; and ash content was measuredby
ashingthe
samplein
a muffle
furnace at600'C. Using a modified method used by Park er
al.
(1996), Salt-Soluble Protein was measured afterit
was homogenizedby
using20 ml
salt solution for a minute in an ice bath. Homogenatewas centrifuged
for
10 minutes at 3020xg
andthe filtrate was separated. Filtrate was centrifuged
for
l0
minutes at 3020xg
and supernatant was decanted.A
ml
of
supematantwas
used todetermined Salt-Soluble
Protein
by
usingKjehdahl method.
Statistical AnalYsis
One-way ANOVA was used to compare the
treatments effects. Duncan's Multiple Range Test
was set
to
determined significant differencesamong mean values. The
level
of
significancewas P<0.05.
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Feed Nutrition
The interesting here was that crude protein and salt-soluble protein of surimi' The crude
protein was decline distinctly
betweenPl
Qe.teyi
andP3
(1339%),while P2
(14'63 wasno
different,but the
salt-soluble proteinresponse was no different. This fact indicated
thx
the incrementof
sucrose added could notprotect protein content of the surimi although
it
was no change the salt soluble contentof
thesurimi.
The
decline
of
the
crude
protein correspondedto the
decrementof
the WHC' Oneof
the
factor affectingWHC
is
protein content which the protein moleculesbind
the water molecule (Aberle et-a\.,2001)' This study resulted that 3o/oThis
study resulted that 30sucrose added had
the
highest valueof
thevariables.
CONCLUSIONS
The increase ofsucrose level added to beef surimi decreased pH, WHC and crude protein,
but
it
couldnot
change the responsesof
gelstrength, ash content, and crude
fat
and salt-soluble protein. The suitable sucrose level forthe best characteristic
of
beef surimi was 3o/osucrose as a single agent of cryoprotectant'
REF'FERENCES
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D. E'
Gerrard, E' W. Mills, H. B' Hendrick,M'
D' Judge, R'A.
Merkel.
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A.,
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J' Bechtel, andM.
C.Keith.
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Protein:Processing Technology' Applied Science, London.
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M., M.
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T.
Fujiwara, H' Kok Kuang and H. Hasegawa. 1988' Handbookon the processing of forzen surimi and fish
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