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Journal of Applied Sciences 13 (3): 401-408, 2013
ISSN 1812-5654 I DOI: QP N SYRSX。ウ N RP Q SNTPQNTセ@
0 2013
Asian
Network for Scientific InformationCharacterization of Redistilled Liquid Smoke ofOil-pabn Shells and
its
Application as Fish Preservatives
1
$.S.
Achmadi,2N.R. Mubarik. 'R.
Nursyamsi and'P.
Septiaji1Department of Chemistry,
2Department of Biology, Bogor Agricultural University, Kampus
Dramaga,
Bogor 16680, IndonesiaAbstract: Oil-pahn shells as an agricultural waste can be pyrolysed producing gaseous material that can
be
condensed into liquid smoke. Redistilled liquid smoke has been proven effective
as
freshfish
preservativedue
to its antibacterial activity. In the present study, the redistilled liquid smoke is evaluated as fish preservative
of fresh catch and as
fly
repellentin
fish salting-fem1enting process. The tests inc.luded total volatilebase-nitrogen levels in fish muscle
and
antibacterial activity using agar diffusion methcxl The content of variousorganic acids in liquid smoke reached 9.2%, mainly consisting of acetic acid and phenolics, at pH of 3.2. There
were no harmful compounds such as tar
and
polycyclic aromatic hydrocarbons. The redistilled liquid smokeconcentrations of 8, 9, and 10% were able to maintain the freslmess of porn.fret fish up to 24 h In these levels
of redistilled liquid smoke solution, diameters of clear zone formed on the antibacterial test ranged 10-20 mm,
meaning
that
the liquid smoke fell intostrong
antibacterial category. It is suggested that the contentof
carboxylic acids, phenolic compounds and carbonyl serve as a natural preservative to replace th.e use of
synthetic preservatives in sahing fermented
fish.
1Key words: Antinucrobe, fish preservative, flies repellant, liquid smoke, oil-palm shells
INTRODUCTION
.
,
'CUrreritly,
charcoal mdustries in Indonesia usecharcoal' as the main product,
and
the rest ofapprox.tmately 70-80% is
in
the form of wasted gas that isreleased to the atmosphere as air pollutant. AUempt to
increase added value of the smoke to be an
environmentally friendly has been done, in various
studies on the liquid smoke, which is commonly called as wood vinegar or liquid smoke. The prcxluction of liquid
smoke can
pe
integratedwith
charcoal making(Nurhayati.and Sofyan, 2005). The liqllld smoke is widely used as antibactenal and antioxidant by many food technologists.
Pyrolysis of coconut shells bas been reported to
produce liquid smoke with phenolic level of 9.36%, carbonyls 8.34%, and organic acids 6.38i>/o. The clistiJled
liquid smoke at lower than l 00°C yields lower quantity of
phenolics (3.90%) and lower tar (0.290/o) as compared with
the distilled products at higher temperatures
(Darmadj i, 2002). Solution of 2.5% liquid smoke made of
coconut shell extends the shelf life of fish ball from I 6
to 32 hours at room temperature (Zuraida et al., 2011 ) .
Liquid smoke of oil-palm shells has been stated
to inhibit the growth ·of
Psedoumonas f111orescens ,
Staphylococcus aureus, Escherichia coli and
Bacillus suhtilis bacteria. The activity of biopreservative
toward S. aureus is exhibited at 0.6% concentration and
towardE. coli at 0.8%
(Halim
et al., 2006). Tamaela (2003)and Yanti and Rochima (2009) also found that liquid
smoke of coconut shells is potential as an altemative in
fish preservation. The potency can be used for various
processing and storage technology
for
fish products, sothat Ll1e potency of liquid smoke derived from oil-pahn
shells, which is abmdanlly found in oil pahn plantation, should be evaluated as fish preservative of fresh catch
and as fly repellent in fish ウ。ャエゥョァ M ヲッイュ・ョエャセ@ process.
MATERIALS AND MEIBODS
Materials: Materials used were crude Jjquid smoke of
oil-palm shells extracted from pyrolysis product at the
temperature of 400°C (provided by PT Global Deorub
Indusuy), Staphyloooccus aureus and Escherichia coli
(available from the Laboratory of 1.ficrobiology Culture Collection, the Department of Biology, Boger Agricultural U niversity), fresh water pomfret fish, patin fish
(Pangasi11s hypophthalmus), Ch1ysoma megalocephoda
flies and bnne shrimp larvae Artemia salina. The
experiment was done in 201 I -2012. Chemicals used were
Corresponding Author: S.S. Achmadi, Department of Chemistry, Bogor Agricultural University, Kampus Dramaga, Bogor 16680, Indonesia
J.AppliedSci., 13 (3): 401-408, 2013
Folin-Ciocalteau reagent, Tashiro indicator solution, cblorampbenicol in powder
form,
liquid media ofTxyptic Soy Broth (TSB) and solid medium of Nutrient Agar (NA).Preparation of
liquid
smoke: Crude liquid smokeof oil-pahn shells (20 L) was placed in a large container and distilled
using
a concentration boule type TA62D at 80±5°C.The
distil.latein
the fonn of liquid smoke was then collectedin
a closed container. Total Acid Assaywas
measured by titration (AOAC, 2005). Phenolics Determination was canied out using Folin-Ciocalteau reagent (Waterhouse, 2002).
GC-MS analysis: Chemical compounds in the redistilled liquid smoke were identified
using
gas chromatography· mass spectrometry (GC-MS) instrument equipped with 60-meter HP5 column Detector temperature, initial column temperature and final column temperature were 250, 280 and 290°C, respectively. The carrier gas was helium with flow rate of 23.7 mL min-'. at 17.56 psi pressure. The liquid smoke sample injectedwas
lµL.
Toxicity assay was performed on A. salina and calculat.ed based on the percent mortality using probit scale (Manila! et al., 2009).l・ カ セ i@ of T VB-N Assay (Standar Nasional Indonesia 2354.8:2009): Samples of fresh-cut pomfret fish (10 g each)
that
had been immersedin
various concentrations G_セ@ liquid smoke were placed in beaker glass. To each beaker glass was added 90 mL perchloric acid 6%: TI1e content of the beaker glass was stirred for 2min
and filtered.The
filtrate (50mL)was
transferred into a dis ti Uationtube,
added afew
drops of phenolphthaJein indicator and antifoaming silicon. The distillation tube was mourited one steam distillation apparatus and I 0 mL NaOII 200/owas
added A collecting erleruneyer was prepared, containmgl
00mL H
3B0
4 3%ru"l<l
3-5 drops ofTashiro indicator (violet solution). Steam distillation was performed
for
ap{lroximately 10min
until 100mL
distillate was collected and thefinal
volume was approximately200 mL
(green solution). Distillation of blank solution wasperformed
in
a
similarway
using 50mL
perchloric acid 6%.The distilled samples as well as the blank were titrated
using solution ofHCl 0.02 N. The end point of titration was indicated by reforming the violet color. The analysis was carried out every 8
h
until the permissible total vo!aule base nitrogen (TVB-N) value was reached. The experiment was repeated twice.QvbMn H セ I M Hv」Mv「Iクn@ X14.007x100
LOOg w
where,
v.
is the volume of HCI for titration on sample, Vb1s the volume of HCl for bJank titration, N is the normahty of HCl solution, Wis sample weight (g), 14.007 is the atomic weight of nitrogen
and
2 is the dilution factor.Inhibition Assay on Bacteria was carried out as reported by Fitrial et al.
(2008). The
NA medium containing bacteria (S. aureus and E. coli, ±J 5 mL) was poured into the petri dish that already coll18ined solid NA medium (the first layer). The mixture was homogenized and the second layer was left to solidify. In the first step, five wells were conditioned aseptically, 6 mm diameter each. Into each weU, the liquid smoke solution (8, 9 and 10% concentrations), a positive control (solution of 100 PF!Il chlorarnphenicol) and negative control (sterilized distilled water) were transferred,60
µL each. Each of the bacteria, i.e . were tested with five replicatiom. Diameters of the measurab le inhibition zone (replicatedthree
times) were converted to inhibition index. P reparation of Dried -fermented Fish followed Ariyaniet al.
(2007) method Patin fish was used in this experiment.In
thesalting
process, 30% of salt (basedon
the
fish
weight), was applied. Some salts were put into thefah abdominal cavity and the rest of salts were dlssolved
into a saturated solution and fermented for 48
h.
Assay for Repellency toward Chrysoma megalocephoda Flies (Yuliani
et al.,
2005). The testing was performed using 25 llies that were caged in a 60x40x30cm
glass tank.The
treatedfish
were put into this glasstank.
Observation was started after l min by counting the number of fly perch on the dried-fenneotedfish
every minuteuntil 60 min
The e>.-periments werereplicated three times for each concentration of 5, I 0, 15 and 200/o and the percem repellency was calcuJated.
Statistical analysis: The observed data on inhibition index and fly repellency were subjected to arialysis of variance (ANOVA). If there was any significant difference, the difference among treatment mean'> was determined by Duncan' s multiple range test at
p"'
0 .05.RESULTS
The redistilled liquid smoke of oil-palm shells at 80"C gave clear acidic liquid, containing 63% of simple carboxylic acids and to
a
lesser extern were pbenolics, with no indication of tox ic polyaromatic hydrocarbons. The liquid was also a strong antibactenal toward S. aureus and E. coli, which would be a beneficial property for fish preservative. The low TVB-N valuesof
fish muscles immersed in the Liquid indicated good inhibition of protein putrefaction until 24 h and l 0% concentration of the gave significant effect on avoiding fly infestation in salting-fermentation process.
J.
ApplitdSci., 13 (3): 401-408, 2013 [image:9.622.22.553.102.474.2](•)
Fig. 1
(a-b): (a)Appearance of
crudeliquid smoke and
(b)Redistilled
liquidsmoke of oil-
palm
shells at 8<1'C
Table l : GC-MS anaJ!sill oo li!J!!id smoke of oil-l!alm sbclls wi1h 90o/osimilarity
Retettioo lime Hュセス@ aイ・。セ@ MW
.s.o.s
4147 60.S.31 1.00 74
6.24 3.31 96
7.03 0.66 82
7.99 26.13 94
8.73 1.33 !OS
8.9.5 l.06 109
9.11
s . .so
124972 032 Ill
10.04 0.21 138
10.19' 2.42 138
11.04 U9 1.52
Jl.72 0.43 154
11.89 016 166
MW= molecular weiaht
'
yellowish brown liquid (Fig. 1 ). The liquid smoke of
oil-palm shells has specific
odorand volatile. There
is an
indication
that the redistillation of
the liquid smokeat
80±5°C
ISable
toreduce P
AHs content that has boil mg
point
ofmore
than300CC.
Three parameters
o fliquid
smokewere
ob<lervcd
organic acid
content,
total phcnolics and pl I. Theredistilled
liquid,smoke of the
oil-palmshells exhibits
organic acids of
9.14%,
total phenolics of 2.6% endpH 3.2. The GC-MS
analysis on the redisuJledliquid
smoke identified some
chemicals asshown
Ul Table I .These compounds have more than 90% simiJarily with
those
in
theGC-MS instrument's
library.The highest
constituenl (
41
%)was
acetic acid. followedby
phenol (260/o). Other consutuents with sumlantymore
than 95% beloog tophenol.Jes,
i.e. 3-methylphenol, 2-methylphenol,2-methoxyphenol and 3,
5-dimethylphenol.Toxicity of the l"edistilled liquid smoke: Dat.11 of the toxicity
test toward
brine shrimp larvae and the correspondingLCse
areexh1b1ted
in
Fig2.
There areincreasing numbers of dead
laivae with theincreasing
concentrations of
the liquidsmoke. Afterwards,
thevalues are derived
in
the fonn ofrelation
between-logComoound sゥュゥャセセャ@
Acetic acid 90
Propmx>ic acid 90
Furfural 91
RMセ」ャッーュエ・ョMQMッッ@ 91
Alcnol 91
2-Methylphenol 97
3-Methylphenol 96
2· Mcthoxyphenol 97
3,.S·Dimdhylphenol
en
2-Mdhoxy-3-methyl pht:ool 91
2-Mdhoxy-4-mdhyl phenol 9S
4-Elllyl-l-mctlloxy phenol 9S
2,6-Dimdhoicyphr:nol 93
2-Mdhoxy-4-propyl phmol 91
concentration
of the
hqwdsmoke and
percentof
dead larvae.The LCso
valueof
0.2147%
is obtainedfrom
a line equationy
=
-1 6662x + 4. 9456with
R1=
0.8527TVB-N
values:TVB-N values of pomfret fish that
havebeen preserved for 30 min
using the red.isrilled
hqmdsmoke
are shown in Fig. 3. The
concentrationsof
theliquid
smokewere 0, 8, 9 and 1
()''loa.nd
theTVB-N values
were determined every 8 hours at room-temperature
storage. Increasn'l; TVB-N
valuesare
caused by theacuon
of
degradmgbactena
on thefish muscular tissues
thal produces mainly ammorua, tnmethylamine and
dimethylamine. With prolonging the storage time, the TVB-N
values
also increasing.Analysis
onbour-8
shows that immersion in I 0% concentrauooof
liqU1d ウュッォ セ@produces !he
lowest TVB-N value ( 4 mg/I 00 g) among
thethree
other treatments,
aswell as those observed at
hour-16 Analysis on hour-24 showsthat
TVB-N value for the control (38 mg/I 00 g) has exceeded the max imwnpermissible
value,whereas
those treatments with the8-10% concentration of liquid
smokeare still below
theJ. Applied Sci., 13 (3): 401-408. 2013
:!
.3
11
..
"Cl...
0セ@
120
100
go
60
40
20
0
y -166.6>ct494.5
R'-O.a51
0. 0.50 J.00 I.SO 2-00 2.50 3.00 3.SO
-20 -lo! conccnrraticn
Fig. 2: Relation between -log concentration of liquid
smoke
and
percent of dead larvaeso
-4540
セオ@
セ@
30l
1sセ@
20セ@ 15 10
'
8 16 24 32
• ' • Siotagc tim.: (h)
Fig. 3: Total volatile base rutrogen (TVB-N) values of
pomfret
fish
preserved with variousconcentrations of
liquid
smoke8%, 9%, I 00/o and
control
values that are lower than that without liquid smoke
treatment, indicating that the fish arc well preserved by
the
redisulledhq1.11d
smoke.Antibacterial properties: Two species for assay on
anlibact.enal activity were used, namely S. aureus
(rcp-esenu.ng Gram positive) and £. coli (representing
Gram negative).1\ntibecterial activity of the liquid smoke
can
be
seen from
the clear rone formed surrounding thecorresponding
well (Fig. 4). The clear
zone fonned onS. aureus is more clistinct es compared with that on
E. coli Tlus is related to the effects of the
hquid
smoke onthe bacterial growth. Based on the diameter of formed
clear zooe, tbe
hquid
of oil -palm shells has antibacterialac11v1ty in strong category The strength of antibactenal
activity
is designated as follow:inhibition
area >20 mm isvery strong,
inhibition
area of I 0-20 mm is strong,inhibition area of 5-10 mm
is
moderate and inhibition area<5 mm 1s in weak category (Dav.is
and
Stout, 1971).Fig.
4(
a-b ): A nu bacterial acllv ity of rcd.istl lied liquidsmoke derived from oil-palm shells toward (a)
S. aureus and (b) E. coli
Table 2· lnhibiticn indices of liCJlid smoke of oil-palm shells as compared With C0011'1lCJCiaJ •lllbiot1CS
Avcngcofimibition index
Treauncnt Sltlp/rvlocOCl'u..r nurtur Escl1trichia coli
Blank O O' O O'
8% liquid woke l 'i' 0 セ@
9% liquid smoke l.'i' 1.1'
ャセャゥアオゥ、@ smoke 14' l.Z'
Chl<n!!!lhcnicol IOO ppm 1.8' - --'0--'0' _ _ _ _
Value widl different lctt# m the same column is significantly different at
p<0.05
Data of the formed clear zone diameter were further
cor.verted into inhibition
mdex
(Table 2>.The
カ。ャオセ@ o finhibition
index exhibited
by theliquid smoke
ofconcenl.ration 0, 8, 9 and I 00/. are also compared with lhat
of 100 ppm chloramphenicol. The average of inhibi11on
index by the liquid smoke toward S. aureus shows higher
value than
that
toward E . coli for the same concentration.The value is also compared
with mhib1t1on by common
antibiotics chloramphemcol 100 ppm. Test on dオョ」。ョᄋセ@
multiple range gives three calegones of results,
designated as a,
b
and c. The same letter means that thetreatments
do
not give significantly clifferent results. OnS. aureus, the use of8, 9 and 10% liquid smoke give the
[image:10.634.23.312.96.735.2] [image:10.634.293.557.122.723.2]J. Applied Sci., 13 (3): 401-408, 2013
100 セ@
-セ@
so
-セ@
60t
.!It
..
40Cf.
セ@
0
0 g Q lO
Conaaiioo of liquid セ@ {%)
Fig, 5: Fly
repellency on the dried-fermented fish withdifferent application o f redistilled Jiqujd smoke
T@ble 3: Sjcnjficanct of fly rq>el!ency based oo Dwcao's ®lliP!c Cl!12C
Level of liguid smoke(%) A verase af rcpellcncy
0 71.7.:S'
8 Yセ N PRG@
9 セセ@
JO
<.»fd-Value will! different lct1cr 111 lhc same column is signi6i:a11tly diffcrctt al p<0.0.:S
diffe,ent with that of chlorampherucol l 00 ppm (letter c)
and the blank (letter a) The 8% concentration of
liquid
smoke (letter b) glves mh.ibition differently with that of 9
and I
0'% concentration(Jetter c)
toward£ coli. Thell$e
ofchlorampher;iicol·
foo
ppm. does notinhibit
the growth ofthis panJ<;ular bacteria, just similar to the blank (letter a).
Repellenc:y to flies: Observation on repellency of the
liquid smoke toward flies
is
slLown in Fig. 5. lncrc.asingrepellency is linearly correl.ited wilh the mcreasing concent.rauon o f the applied liquid smoke ' I he best repellency of the liquid smoke applied on the fermented salted fish was analy1.ed using Duncan's mulLiple range (Table 3). The first step was to determine the highest
value of all treatments. The highest value was 99.69, obtallled from concentration of I 00.4 hquid smoke. The
next step considers the letters corres1xmding to the
treatment. All of lhe average of rcpcllcocy is followed by
different letter. This cneans that every tr.:atment
bas
sigruficant effect, differently from one to another. Therefore, the average of the highest repellent. (10%
conccnlration of liquid smoke) is the best treat.mcnl
DISCUSS I OK
Physical and chemical properties and toxicity: From the
appearance aspect, color of the reclistilled liquid smoke is
no longer dark. The recbstillation turns the previous dark
color liquid
smoke
to brightyellowish-browrL
Thisphysical property shall give good effect for its utilization
iri
foodstuff.The redistiJled
liquid
smoke of oil-palm shellsmainly
contains organic acids and phenolics. Lower organic
acids are weak acids with pK. of approxID1ately 5.
However, the crganic
ac1<h
are more acidicas compared
with the phenolics, particularly due to resonance
stabilization of the carboxylic
anioos
(RCO;).
These acidiccompounds play important role in creating the low pH of
the liquid smoke (pH 3.2). In addition, the low pH value
reiresents a
high
quality
of
liquid smoke particularlyin
its
utilizatioo as
food
preservatives (Wijayaet al.,
2008;Theron
and Lues, 2011 ).
Furthermore, compounds ofP AHs faro
ilyare
notidentified, indicating
that theredistillation of
the
liquid
smoke al 80°Cis
effective ineliminating
the carcinogenicPAHs
contentOC.MS
anaJysis
on liquid smokeis
also perfonnedin
a previousstudy. Budijanto
et al.
(2008) onhis
investigation on thesafety of
liquid
smoke denved from cocorrut shells fcxfood products shows
that
there are 40 constituentsidentified
by
GC-MS analysis. There are phenoliccomponents, such as phenol, 2-metho.xy phenol.
3,4-dimethoxy phenol.
2-metboxy-4-methylphenol.
Di.hydrox:ybenzoic acid, methoxybenzoic acid
and
hydroxyl benzoicacid are present as minor components
Level of organic acids, total pbenol1cs
and
pH of ourstudy are different with the study by Darmadji and
Triyudiaoa (2006)
whichalso
usedliqwd
smoke redistilledbelow
l OO°C,
producing 12.34% organic acidsand 1.1
%total phenolics. Therefore, the redisulled liquid smoke
from oil-palm
shells
gives lower orgwucac1m
(9.14%)but
higher total phenolics (2.6%). The difference is due to
cellulose-hem1cellulose
and ligrun
contents inthe raw
materials, from which the pyrolysis process would deter:mme the liquid smoke quality There seems to be a
clear correlation between hgnin
and
phenolics contents.The liqujd smoke from oil-palm shelJs is also Jess acidic
as compared with the liquid smoke from bamboo
(3.08), Leucaena
wood
(2.9) and corn cobs (3.0)(Swastawall et
al,
2007). Acids level ts also affected bydistillation temperature (Dannadji, 2002).
Titrce ma.in components of the liquid smoke from our
study are carboxylic acids, phenohcs and carbonyls
Ilem1celluloses
are
wood componentlhat
firstlyunJergo
pyrolysis to produce furfural,
furan.
acetic acid and
itshomologues h・ュゥ」・ャャオャッセ・ウ@ consist of ー・ョャッセ。ョウ@
(CsH,01 ) and hexosans (CJl,00 s). with the average
proportion depend on the raw matenals Pyrolysis of the
pentosans produces furfural, furan and the1r denvat1ves,
as well as carboxylic acids. Together with cellulose,
pyrolysis of hexosans also produces acetic acid and
its
J. Applied Sci., 13 (3): 401-408, 2013
decomposition at
300-4.SOOC
(Girard,1992).
Furtherprocess
in
the pyrolysis of cellulose will produce aceticacid and carbonyl
compounds,
suchas
acetaldehyde,glioxal and acreolin. Pyrolysis of lignin will produce
phenol, guaiacol and syringol, together with their
hcmologs and derivatives (Darmadji,
2002).
Phenolics contribute to the quality for modifying
color, flava-,
aroma
and odor (Sengulet
al., 2009). Levelof total phenolics
io
theI
iquid smoke of oil-palm shells0.26%
(bib) is moreUlan
20
times
higherthan
that
ofliquid smoke of teakwood, pine wood and
barn
boo
(Wijaya et al., RセIN@ Pheoolics with low boiling points
are
good as bacteriostatics. Organic acids are stronger
in
inhibiting bacterial
growth
as compared with phenolics,however, combination of these two categcnes of
organic acids will gave
nse to
higher inhtb1tionPheoolics, as healthy phytochemicals, are ccmmonly used
in
food mdustriesas
antiOXIdant and antibacte11aJ(Esekhiagbe
et
al., 2009).Toxicity of the liquid smoke
using BSL T
methodrevealed that no larvae survived on the concentrations of
0.3,
0.4 and 0.5%LC1t
in
this
studyis
0.2147%.A
compowd is designated to have acute toxicity if the
LC)I
is below 0.1 % (CaJ'ballo et al , 2002). Therefoce,
based
onthis assay, the redi.stilled
liqwd
smoke of oil-palm shells 1snot considered 8l} 40xic material
'
J>oten cy ·as a n ti bacterial in fresh fis h preservation:
Redistilled liquid smoke in this study act as bacteriostatics (inhibit the growth without lethal effect) on
E. coli and bacteriocidal/bactcriolitic (lethal effect) on
S. "aureus. lnlubition on bacterial gro\vth by an
antibactenal agent can be ch.ae to the inhibition of
synthesis of cell wall, protems, nucleic acids
and disruption• of the functions of cell membranes
(Jawetz et al., 2010). Resistance of E. coli which is lugher
than that of
S.
aureus
toward antibacterial agents maybe
related to the structure of cell membranes.
E.
coliis
amember of Gram ョセ。エjカ・@ bacteria with layered membrane
structure, among which are lipoproteins,
lipopolysaccabarides and pcptidoghcans (Madigan et al.,
2010).
Organic acids nre food preservatives that function ll!I
acid-taste elicitoc arxt reduce bacterial growth by reducmg
pH within the food to pH level that can inhibit bactenal
growth. Pnnciple of the mhibitioo by organic acids
is
thatthe undissociated part of the acids (anion moieties) can
penetrate into the cell wall of the bacteria and disrupt the
normal physiological function of the cells (Theron and
Lues, 2011 ).
Phenolics
in
the
Liquid smoke of pelawan(Tristania obovata) wood actively attack on bacterial vegetative cells, can penetrate and disrupt cell walls and
precipitate proteins
in
the microbe cells (Panagan andSyarif, 2009). Inhibition
by
phenolics may be due tointeractioo
through
hydrogenbonding
with someimport.ant
proteinsas
enzyme constituent(Saravanakumar
et
al., 2009).Fish putrefaction
is
commonly indicated by highTVB-N
value.The
increasein TVB-N
valuesis due
tobacterial action as proved by
inclination
of bacterialpopulation Immersion
treatments
in
liquid smokesolutions are able to reduce the rate of volatile base
fonnation as compared with the cootrol. The higher the
concentration of the liqwd smoke, the
better
the
abilityto
tnhibit the formation of
the
volatilebases
The maximumTVB-N
Jevelfor fresh
fishm Japan and Australia ts 30
mgNo/o (Siagian, 2002). Dw1yitno and Riyanto (2006) in the
experiment
using
liquid smoke of coconut shellsfor
preserving fresh mackerel is able to
maintain TVB-N
valuebelow the maximum level until 12-hour storage with
treatments using
7 .5
andI 0%
concentrationsBased on
BSLT,
the LC,. for liqwd smoke of oil-palmshells is 0.22%, meaning that
il
is
safe to be mcorporatedm foodstuff. Safe limit for phenol m food p-oducts is
0
0006-0.
5%oc
0.06-5000 mg kg-1 (Girard, 1992). Therefore,unmersion in the redisulled bqwd smoke (0 18-0.26%) will
not exceed the detennined safe limit Phenol content will
also decrease
in
further fish processing such as washingand heating for products to be consumed.
Pote-ncy as
ny
r epellen t: Fly mfestat:ion on <lmxlfermented fish
during
sunchying may be due to somevolatile bases such as ammonia
and
hydrogen sulfide.These two compounds are onginated from protein degradation caused by p-oteolytic enzymes dunng
autolysis and fermentation processes (Anyani et al.,
2007). However, ttnmers1on
in
liquid smoke solution haselicited odorous phenolici1 Fセャゥォ。「ャ・@ lo flies In addition,
the presence of 30% salt is indirectly functioning a.'\
insecticide (Ariyani
et al.,
2007). Some phenolics detectedin the redistilled liquid smoke of oil-palm shells, namely
cresol, 」イッッウッセ@ guaiacol, syringol, eugenol and
xylenol, may gave specific aroma. Furfw-al as the only member of aldehydes that 1s also detected in 11l1s particular liquid smoke has been reported as a disinfectant
(Madigan et al., 2010). Furfural gives pleasant aroma that
reduces aroma of the phenohcs that have rather sharp odors. This compotmd gJVt:s specific aroma of the Liquid
smoke
that
function as repellent Action of the liquidJ. Applied Sci., 13 (3) : 401-408, 2013
working as contact insecticide. Hence, insects that do not like poison with repellent action can quickly avoid the
baits (Yul iani et al., 2005).
CONCLUSION
Liquid smoke of oil-palm shells reclistilled al 80"C
gives clear yellowish-brown in color with specific aroma
of volatile constituents. With chemical specifications of organic acids 9.1 %, total phenolics 2.6% and pH 3 .2, the
redistilled liquid smoke is potential as a safe preservative
for fresh fish By 30 min immersion in the liquid smoke
solution, the fish freshness can be longer than that
without liquid smoke treatments, i.e.
up
to 24 h at roomtemperature storage. The redi.stilled liquid smoke of
oil-palm shells is bacteriostatics
in
nature and showsstrong inhibition toward bacterial growth. The best
ITeatrnenl as antibacterial is toward S. aureus which
represents Gram posiliv.:. Immersion in the solution of
redistilled liqtnd smoke functiom as antibacterial and
fly
repellent for dl).ed-fennented
frnh
The fly-repdlency ofthe treated dried-fermented fis h is excellent, wilh the
repellcncy above 95% Thus. the redistilled Liquid smoke
of dil-pahn shells can be applied as safe fish preservative
and can be combined with other preservation methods
such 。セ@ cooling and salting.
.
'
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