<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">FNS</journal-id><journal-title-group><journal-title>Food and Nutrition Sciences</journal-title></journal-title-group><issn pub-type="epub">2157-944X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fns.2019.103026</article-id><article-id pub-id-type="publisher-id">FNS-91477</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Physiochemical Properties, Volatile Compounds and Sensory Evaluation of Chili Sauce Shrimp Paste from Different Regions in Indonesia
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Wildan</surname><given-names>Suhartini</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Fang</surname><given-names>Yang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Wenshui</surname><given-names>Xia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, China</addr-line></aff><pub-date pub-type="epub"><day>04</day><month>03</month><year>2019</year></pub-date><volume>10</volume><issue>03</issue><fpage>333</fpage><lpage>348</lpage><history><date date-type="received"><day>6,</day>	<month>March</month>	<year>2019</year></date><date date-type="rev-recd"><day>25,</day>	<month>March</month>	<year>2019</year>	</date><date date-type="accepted"><day>28,</day>	<month>March</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Chili sauce shrimp paste (CSSP) is an exotic traditional sauce prepared using mainly fresh chili and shrimp paste well known as 
  <em>sambal terasi</em> (Indonesia) and 
  <em>sambal belacan</em> (Malaysia and Brunei). This study aims to evaluate CSSP from different regions in Indonesia on physiochemical properties, volatile compounds, and sensory evaluation. Evaluation in free amino acid (FAA) and volatile compounds were analyzed using HPLC and GC-MS. CSSP had no significant (
  <em>p</em> &gt; 0.05) on proximate (except for moisture), salinity, pH, microbial counts and the redness index (
  <em>a*/b*</em>) compared to control. The identified volatiles can be grouped into hydrocarbon, carbonyl, sulfur, alcohol, nitrogen, fatty acid, and ester compounds. The CSSP A, B, C, D, and E (control) contained 9, 21, 12, 29, and 6 volatile compounds respectively. The total FAA ranged from 44.32 to 67.03 g/100 g, and histidine (his) was found as the most abundant in each CSSP. The rheological properties (yield stress, viscosity, and consistency) of CSSP and control values were significantly, except for CSSP B. The intensities perceived of saltiness, sweetness, and bitterness were greatly varied among CSSP. Although there is no correlation between sweetness and bitterness this is indicated by the negative correlation.
 
</p></abstract><kwd-group><kwd>Chili Sauce Shrimp Paste</kwd><kwd> Volatile Compound</kwd><kwd> Rheological Properties</kwd><kwd>  &lt;i&gt;Sambal Terasi&lt;/i&gt;</kwd><kwd> Free Amino Acid</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Chili sauce shrimp paste (CSSP) is an exotic traditional Southeast Asian sauce condiment prepared using mainly fresh chilies and shrimp paste [<xref ref-type="bibr" rid="scirp.91477-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.91477-ref2">2</xref>] well known as sambal terasi (Indonesia), sambal belacan (Malaysia and Brunei. Shrimp paste known by different names such as terasi (Indonesia), nappi (Bangladesh), kapi (Thailand and Cambodia), belacan (Malaysia and Brunei), shajiang (China), jeotgal/jeo (Korea), bagoong-alamang (Philippines), mam ruoc or mam tom (Vietnam), and hmyinnga-pi (Myanmar) [<xref ref-type="bibr" rid="scirp.91477-ref3">3</xref>]. Shrimp paste is one of the most common methods of shrimp preservation on the Asian countries [<xref ref-type="bibr" rid="scirp.91477-ref4">4</xref>] which attributed to strong and pungent fishy odor [<xref ref-type="bibr" rid="scirp.91477-ref2">2</xref>].</p><p>The raw material of fermented shrimp paste used the planktonic shrimps of genera; Acetes, Mesopodopsis, Lucifer, and Mysids are usually [<xref ref-type="bibr" rid="scirp.91477-ref5">5</xref>]. The genus Acetes, species of japonicas, vulgaris and erythraeus are the most common raw material to produce fermented shrimp in Southeast Asian countries, locally known as rebon in Indonesia and geragau in Malaysia and Brunei [<xref ref-type="bibr" rid="scirp.91477-ref6">6</xref>]. Shrimp paste involves the use of high salt concentration and incubation at ambient temperature [<xref ref-type="bibr" rid="scirp.91477-ref7">7</xref>] , and the major processing is salting, fermenting, and aging. Shrimp paste has radish brown to blackish brown color depending on the raw materials and the naturally occurring microbes which involve during fermentation [<xref ref-type="bibr" rid="scirp.91477-ref2">2</xref>] , a strong distinctive smell or odor which upon heating or cooking releases volatile compounds [<xref ref-type="bibr" rid="scirp.91477-ref8">8</xref>]. Shrimp paste from different regions have not the same odor, color, nutritional, and amino acid as a result of processing variety such as length of sun exposure for drying and of fermentation time [<xref ref-type="bibr" rid="scirp.91477-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.91477-ref9">9</xref>]. Shrimp paste has considerable level of free glutamic acid, amino acid and rich in umami taste [<xref ref-type="bibr" rid="scirp.91477-ref10">10</xref>]. Different regions have different recipes of chili sauce shrimp paste (CSSP) even though with a same combination of various ingredients. Fermented shrimp paste has been used for countries as a flavoring on dishes [<xref ref-type="bibr" rid="scirp.91477-ref11">11</xref>].</p><p>The use of additional ingredients, with specific functionality may therefore help in modulating CSSP properties, sensory attributes, and stability as well as to product tailor which made product for specific application (i.e. multicomponent and complex product) [<xref ref-type="bibr" rid="scirp.91477-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.91477-ref13">13</xref>]. To meet consumers quality requirements, some quality parameters and shelf-life of CSSP products are to be considered important such as chemical qualities, microbial, and also rheological and appearance indicators (i.e. consistency and color) [<xref ref-type="bibr" rid="scirp.91477-ref14">14</xref>]. However, so far the study on the potential of shrimp paste as chili sauce fortification from different regions in Indonesia has not been carried out. This study was conducted to formulation and process improvement for chili sauce shrimp paste based on physiochemical properties, volatile compounds, and sensory evaluation. Therefore, the objectives of this study were to 1) investigate the feasibility of chili sauce fortification using fermented shrimp paste, 2) determine the physiochemical properties, 3) evaluate volatile compounds, and 4) evaluate the sensory attributes of CSSP.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Materials</title><p>The shrimp of genera Acetes, locally known as rebon (Indonesia) was purchased from four different regions in Indonesia. Whole part of the shrimp and salt was used to fermentation in this study. Ingredients for chili sauce shrimp paste (CSSP) preparation i.e. chili (Capsicum annum), sugar, oil, shrimp paste, salt, monosodium glutamate as flavor enhancer, modified starch, preservative potassium sorbet, and kalamansi as acid source were all of food grade obtained from local wholesale market in Wuxi, Jiangsu, China.</p></sec><sec id="s2_2"><title>2.2. Processing of Shrimp Paste</title><p>Four different types of shrimp paste production from different regions in Indonesia. They were codes as A (from Jakarta), B (from West java), C (from Central Java), and D (from East Java). In the processing of fermented shrimp, firstly fresh shrimp is washed, drained and dried until half dried. During drying, impurities such as small fish, mussel shells and coral are removed. After that, semi dried shrimp is sifted to spare to separate sand and other undesirable materials. The shrimp is then left overnight at ambient temperature and pounded the next day. During the first pounding salt is added (around half of the total salt required during processing). Total amount of salt used in shrimp fermentation processing is 20% of shrimp weight which should be added as solution. Pounded shrimp is oven dried and subsequently kept in a container at ambient temperature for 2 - 3 days. The stored shrimp is then pounded for a second time, while the remaining salt is added. After that, the pounded shrimp is oven dried and kept at ambient temperature for 3 - 5 weeks until soft. It is the ground by many passes through a meat grinder until fine [<xref ref-type="bibr" rid="scirp.91477-ref15">15</xref>].</p></sec><sec id="s2_3"><title>2.3. Preparation and Production of CSSP</title><p>A formulation of chili sauce shrimp paste (CSSP) was developed in the laboratory. The basic recipes were obtained from regions where shrimp samples are taken and the basic recipes are the same. The stem of the chilies were removed before washing. The chilies were drained to remove excess water. The shrimp paste was heated in the oven at 100˚C for 10 min. This grilled step is critical for flavor which will result in a flavorful CSSP. Kalamansi were cut into half and the juice was squeezed from the fruit. All ingredients were ground using food processor (Philips―HR7776) for 15 min, then fried in low heat for 30 minutes. The chili sauce shrimp paste was ready for analysis. CSSP was codes accordance to code of shrimp paste which are A (for shrimp paste from Jakarta), B (for shrimp paste from West Java), C (for shrimp paste from Central Java), D (for Shrimp paste from East Java) and E is control (without shrimp paste).</p></sec><sec id="s2_4"><title>2.4. Physiochemical Analysis</title><p>Moisture content, protein, fat, ash, and carbohydrate content were analyzed according to Association Official of Analytical Chemists (AOAC 2000) [<xref ref-type="bibr" rid="scirp.91477-ref16">16</xref>]. The pH of chili sauce shrimp paste (CSSP) was measured using a digital bench top pH meter (Mettler Toledo<sup>TM</sup> FE20 FiveEasy<sup>TM</sup>, Schwerzenbach, Switzerland) [<xref ref-type="bibr" rid="scirp.91477-ref17">17</xref>]. Sodium content was determined by Mohr titration method. By knowing the amount of chloride ions that need to be titrated with AgNO<sub>3</sub> will find the sodium ions content of CSSP [<xref ref-type="bibr" rid="scirp.91477-ref18">18</xref>].</p><p>Volatile compounds of CSSP was analyze with a gas chromatograph-mass spectrometer (GC-MS). Deodorized distilled water was by boiling glass-distilled water to two-thirds of its original volume. A mixture 35 g of CSSP and 315 ml of deodorized distilled water was homogenized using a blender (Joyoung JYL-C012, China) at low speed for 3 min. Five ml of the mixture was placed in the 20 ml headspace vial. Vial was heated at 80˚C for 45 min while shaking at high speed using headspace sampler. Sample was transferred to a gas chromatograph (GC-2010, Shimadzu, Kyoto, Japan) for separation. The loop and transfer line temperature were 90˚C and 100˚C respectively. The injector temperature was maintained at 250˚C. For identification, the gas chromatograph was coupled to a mass spectrometer.</p><p>Free amino acid (FAA) was determination performed base on the method followed in the key laboratory of food science and technology, Jiangnan University, Wuxi, Jiangsu, China. CSSP sample 1 g weighed into tubes and hydrolyzed in 8 ml 5 M NaOH in alkaline hydrolysis tube containing sample, then treatment by nitrogen filling in 3 min, put the tube into the oven for 22 h at 105˚C. Transferred the sample from the tube to the 25 ml volumetric flask and added 6.67 ml 6 M HCl. Washed the wall of the flask by small amount of water, then diluted with water to 25 ml, after that filtrated out of 2 slices filter paper. Taken 1 ml of filtrate and centrifuged at 10,000 rpm for 10 min. Taken 400 μl of the supernatant into HPLC sample bottle. Net height of each peak representing individual FAA produced by chart in recorder of analyzer were measured, calculated, and recorded. Values of FAA were reported as g/100 g of sample. Twenty amino acid for FAA determination with IUPAC symbol i.e. aspartic acid (asp), glutamic acid (glu), asparagine (asn), serine (ser), glutamine (gln), histidine (his), glycine (gly), threonine (thr), citruline (cit), arginine (arg), alanine (ala), tyrosine (tyr), valine (val), methionine (met), tryptophan (trp), phenylalanine (phe), isoleucine (ile), leucine (leu), and lysine (lys), proline (pro) and internal standard (norvaline and sarcosine) were HPLC grade.</p></sec><sec id="s2_5"><title>2.5. Microbial Analysis</title><p>Microbiological evaluation of CSSP was carried out immediately after storage treatment, sample were analyzed for the aerobic plate count (APC). The determination of APC was done using the pour-plate method on plate count agar in accordance to the ISO 4833:2003 standard protocol [<xref ref-type="bibr" rid="scirp.91477-ref19">19</xref>].</p></sec><sec id="s2_6"><title>2.6. Rheological Properties</title><p>The rheological characterization of CSSP were investigated using a rheometer (Discovery<sup>HR-3</sup>, hybrid rheometer, TA instrument, UK) connected to computing applications (TRIOS). Serrated plates are measured according to geometry PP35S to avoid slippage. Oscillation frequency sweep tests applied in the frequency range from 1.00 to 30.00 Hz with a shear stress of 50.00 Pa at 25˚C &#177; 0.1˚C and the loss tangent values in 20 Hz were used for paste preference evaluating.</p></sec><sec id="s2_7"><title>2.7. Color Properties</title><p>The color of CSSP sample was measured using a UltraScan PRO 5 nm optical resolution at wavelength range from 250 to 1100 nm (Hunter Associate Laboratory Inc., Reston, USA). Easy Match QC software is attached to the equipment. The ultraScan PRO measures the reflected color of food products, measured color represented by Hunter’s color value, L (lightness), a (redness), and b (yellowness). The instrument was calibrated on a white standard tile before analysis (L* = 98.82; a* = −0.18; b* = 0.31).</p></sec><sec id="s2_8"><title>2.8. Sensory Evaluation</title><p>Twenty-one (21) semi-trained panelists are Indonesian living in Wuxi, Jiangsu, China, the age of panelist between 18 - 40 years old. These panelists had received a brief explanation of each of the sensory attributes (<xref ref-type="table" rid="table5">Table 5</xref>). Intensity evaluation of the perception by the panel was carried out by use of unstructured linear scale with the anchor point 0-not perceptible and 10-strongly perceptible. The chili sauce shrimp paste (CSSP) was put in the glass bottle container, and samples were coded with three digit random numbers to storage in refrigerator (4˚C). Duplicate samples were served each panelist in different seasons in a randomized order. Mineral water was provided to cleanse the palate between samples during evaluation. The study was performed in tasting booths with properly controlled environment conditions [<xref ref-type="bibr" rid="scirp.91477-ref20">20</xref>].</p></sec><sec id="s2_9"><title>2.9. Statistical Analysis</title><p>Statistical analysis for physiochemical, microbial, rheological, color, and sensory analysis of different chili sauce shrimp paste (CSSP) was performed using two-way analysis of variance (ANOVA) and Duncan test to determine the significant difference among means at the level of p = 0.05 using statistical package of SPSS version 16 (SPSS Inc., Chicago).</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Physiochemical Properties of CSSP</title><p>The proximate composition of CSSP is shown in <xref ref-type="table" rid="table1">Table 1</xref>. The fat and moisture content of the CSSP tended to be higher in CSSP than control (p &lt; 0.05). The protein, moisture, ash and carbohydrate content of CSSP compared to control was no significant (p &gt; 0.05). However, the result of this study was in agreement with the previous study that traditional chili shrimp paste in Malaysia indicated approximately 70% moisture content [<xref ref-type="bibr" rid="scirp.91477-ref21">21</xref>] , the percentage of fat in CSP is around 0.41% and the protein content is around 7.67% [<xref ref-type="bibr" rid="scirp.91477-ref22">22</xref>].</p><p>The CSSP and control had pH range of 5.73 - 6.40, shown in <xref ref-type="table" rid="table1">Table 1</xref> that no</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Physiochemical properties of CSSP and control</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Sample</th><th align="center" valign="middle"  colspan="5"  >Proximate (%)</th><th align="center" valign="middle"  rowspan="2"  >Salinity (%)</th><th align="center" valign="middle"  rowspan="2"  >pH</th></tr></thead><tr><td align="center" valign="middle" >Fat</td><td align="center" valign="middle" >Protein</td><td align="center" valign="middle" >Moisture</td><td align="center" valign="middle" >Ash</td><td align="center" valign="middle" >Carbohydrate</td></tr><tr><td align="center" valign="middle" >A</td><td align="center" valign="middle" >5.00<sup>a</sup></td><td align="center" valign="middle" >6.00<sup>a</sup></td><td align="center" valign="middle" >68.34<sup>a</sup></td><td align="center" valign="middle" >12.73<sup>a</sup></td><td align="center" valign="middle" >9.07<sup>a</sup></td><td align="center" valign="middle" >3.01<sup>a</sup></td><td align="center" valign="middle" >6.40<sup>a</sup></td></tr><tr><td align="center" valign="middle" >B</td><td align="center" valign="middle" >2.09<sup>b</sup></td><td align="center" valign="middle" >1.90<sup>b</sup></td><td align="center" valign="middle" >70.06<sup>a</sup></td><td align="center" valign="middle" >13.96<sup>a</sup></td><td align="center" valign="middle" >5.00<sup>b</sup></td><td align="center" valign="middle" >3.92<sup>a</sup></td><td align="center" valign="middle" >6.29<sup>a</sup></td></tr><tr><td align="center" valign="middle" >C</td><td align="center" valign="middle" >4.31<sup>a</sup></td><td align="center" valign="middle" >2.62<sup>b</sup></td><td align="center" valign="middle" >69.37<sup>a</sup></td><td align="center" valign="middle" >13.04<sup>a</sup></td><td align="center" valign="middle" >4.10<sup>b</sup></td><td align="center" valign="middle" >3.08<sup>a</sup></td><td align="center" valign="middle" >6.35<sup>a</sup></td></tr><tr><td align="center" valign="middle" >D</td><td align="center" valign="middle" >4.08<sup>a</sup></td><td align="center" valign="middle" >1.76<sup>b</sup></td><td align="center" valign="middle" >70.20<sup>a</sup></td><td align="center" valign="middle" >10.98<sup>a</sup></td><td align="center" valign="middle" >2.84<sup>b</sup></td><td align="center" valign="middle" >4.06<sup>a</sup></td><td align="center" valign="middle" >6.30<sup>a</sup></td></tr><tr><td align="center" valign="middle" >E</td><td align="center" valign="middle" >2.11<sup>b</sup></td><td align="center" valign="middle" >3.25<sup>ab</sup></td><td align="center" valign="middle" >89.11<sup>b</sup></td><td align="center" valign="middle" >11.70<sup>a</sup></td><td align="center" valign="middle" >5.02<sup>ab</sup></td><td align="center" valign="middle" >4.74<sup>a</sup></td><td align="center" valign="middle" >5.73<sup>a</sup></td></tr></tbody></table></table-wrap><p>Means with different letters are significantly different (p &lt; 0.05) for each parameter (column).</p><p>significant (p &gt; 0.05) between CSSP and control. However, pH of CSSP decreased compared to pH of shrimp paste which had pH 7.62 for Indonesian dried shrimp paste, and pH 6.83 - 7.23 for Korean dried shrimp paste [<xref ref-type="bibr" rid="scirp.91477-ref3">3</xref>]. Kalamansi (Citrfortunella microcarpa) as acid sources of CSSP had dominant organic acid and it impart as a tangy citrus flavor [<xref ref-type="bibr" rid="scirp.91477-ref23">23</xref>] , that might decreased pH in the final product. The salinity of CSSP had no significant (p &gt; 0.05) compared to control, even though control had salinity of 4.74%, which was higher than CSSP (3.01% - 4.06%). In general, salinity of chili shrimp paste is 4.4% [<xref ref-type="bibr" rid="scirp.91477-ref21">21</xref>]. The salinity of CSSP depends on the quality and type of salt used during manufacturing process [<xref ref-type="bibr" rid="scirp.91477-ref24">24</xref>].</p><sec id="s3_1_1"><title>3.1.1. Volatile Compounds</title><p>The chromatogram of GC-MS result was dentified based on the retention time and the area of the peaks (<xref ref-type="fig" rid="fig1">Figure 1</xref>). <xref ref-type="table" rid="table2">Table 2</xref> showed the result of each class of volatile compounds in each CSSP containing shrimp paste from different area. The identified volatiles can be grouped into hydrocarbon, carbonyl, sulfur, alcohol, nitrogen, fatty acid, and ester compounds which showed similarities with other research volatile compounds of shrimp paste [<xref ref-type="bibr" rid="scirp.91477-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.91477-ref26">26</xref>]. The CSSP A, B, C, D, and E (control) are contained 9, 21, 12, 29, and 6 volatile compounds respectively. Sample E (control) has the lowest and CSSP D has the highest of volatile compounds. Dimethyl sulfide as an organosulfur which are formed from the degradation of methionine (met) amino acid in food product [<xref ref-type="bibr" rid="scirp.91477-ref27">27</xref>]. This volatile compound have cabbage aroma respectively. Alcohol and aldehydes are an important role in chilies flavor [<xref ref-type="bibr" rid="scirp.91477-ref28">28</xref>] , and conferring the freshness of products [<xref ref-type="bibr" rid="scirp.91477-ref29">29</xref>]. Ester usually provides the aroma of food with fruity notes [<xref ref-type="bibr" rid="scirp.91477-ref30">30</xref>].</p></sec><sec id="s3_1_2"><title>3.1.2. Free Amino Acid (FAA)</title><p>The free amino acid (FAA) content of CSSP is shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>. The FAA content of CSSP and control ranged from 44.32 to 67.03 g/100 g respectively. His was found as the most abundant and varied FAA in each CSSP, which consisting more than 15% of total FAA, followed by asp, met, and lys. Lys tended to be dominant in the long fermented fish product [<xref ref-type="bibr" rid="scirp.91477-ref31">31</xref>]. These result are comparable to fish sauce production in Southeast and East Asian countries, as asp, glu, and</p><table-wrap-group id="2"><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Volatile compounds in chili sauce shrimp paste (CSSP) and control</title></caption><table-wrap id="2_1"><table><tbody><thead><tr><th align="center" valign="middle" >Compound</th><th align="center" valign="middle" >A</th><th align="center" valign="middle" >B</th><th align="center" valign="middle" >C</th><th align="center" valign="middle" >D</th><th align="center" valign="middle" >E</th></tr></thead><tr><td align="center" valign="middle" >Hydrocarbon</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Hexadecane</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >1,4-octadiene</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >7-hexadecane</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1,11-dodecadiene</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2-Methylbutylidene 2-phenylethyl</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >Cyclododecane</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >3-Tetradecene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1.3-cyclooctadicene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1-pentadecene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Cyclotetradecene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Cyclodecene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1,2-dimethyl cyclooctane</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Bicyclo [2.2.1] heptane</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1.4-cyclononadiene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2-metoxy naphthalene</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Subtotal</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Carbonyl</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >5z,8z,11z-tetra-decatrien-2-one</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2-Undecanon</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2-Tridecanon</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1-Finil-Etenon</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Benzaldehyde</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >3,4,5-methyl Cyclopentene-1-one</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Subtotal</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >Sulfur</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Dimethyl trisulfide</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Dinonil trisulfide, isomer mix</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Subtotal</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >Alcohol</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Phenol, 2,6-bis (1,1-dimethylethyl)</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Phenol</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >1-pentadecanol</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Phenyl ethyl alcohol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2.2-oxibis Ethanol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >4-methyl phenol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1-Heptadecanol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1-Octadecanol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >p-Mentha-1 (7), 8 (10)-dien-9-ol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >9,12,15-octadeca-trien-1-ol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Mentionol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr></tbody></table></table-wrap><table-wrap id="2_2"><table><tbody><thead><tr><th align="center" valign="middle" >Subtotal</th><th align="center" valign="middle" >3</th><th align="center" valign="middle" >4</th><th align="center" valign="middle" >2</th><th align="center" valign="middle" >7</th><th align="center" valign="middle" >1</th></tr></thead><tr><td align="center" valign="middle" >Nitrogen</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Indole</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >2.6-dimethyl-3-N-butilpyrazine</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2.6-dimethyl pirazin</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >2,5-dimethyl-3-(3-methyl) pirazin</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >4-Phenyl Piridine</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >4-methyl-2-phenyl pyrimidine</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Benzeamine</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >1-Benzeneetamine, N-(Fenilmetil)</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >5-metiloxiindol</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Subtotal</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Fatty acid</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >1,2 Benzene-dicarboxylic acid</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Pentanoic acid</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Hexadecanoic acid</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Tetradecanoic acid</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Subtotal</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >Ester</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Hexadecanoic acid, Methyl ester</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Ethyl linoleic</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >−</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >29</td><td align="center" valign="middle" >6</td></tr></tbody></table></table-wrap></table-wrap-group><p>lys are more the most abundant FAA [<xref ref-type="bibr" rid="scirp.91477-ref32">32</xref>] , glu, ala, and ieu are predominantly found in shrimp sauce [<xref ref-type="bibr" rid="scirp.91477-ref33">33</xref>]. Asp, ser, arg, thr, pro val, iso, and lys are related to taste and flavor. Free amino acid related to sweetness are gly, ala, ser, thr, and tyr, while the related to bitterness are val, met, iso, leu, try, phe, his, and arg [<xref ref-type="bibr" rid="scirp.91477-ref34">34</xref>]. The proportion of FAA related to flavor/taste was similar for each CSSP.</p></sec></sec><sec id="s3_2"><title>3.2. Microbial Analysis</title><p>The observation of the microbial count (total plate count and yeast and mold) of CSSP and control is shown in <xref ref-type="table" rid="table3">Table 3</xref>. The results showed that microbial counts of CSSP no significant (p &gt; 0.05) in all sample of CSSP compared to control. However, the total plate count (TPC) which is the highest is CSSP C and the lowest is CSSP B, colony count of yeast and mold the highest is CSSP D and the lowest is CSSP C. However, to reduce microbial growth for extending the shelf life of food product to an acceptable level of microorganism, chemical and physical methods can be used [<xref ref-type="bibr" rid="scirp.91477-ref35">35</xref>]. Chemical methods usually used such as dimethyl dicarbonate (DMDC), sodium metabisulfite, sodium benzoate, and potassium sorbate. DMDC is not a suitable processing aid to be used for microbial reduction in a fat containing food system such as CSSP [<xref ref-type="bibr" rid="scirp.91477-ref36">36</xref>]. On the other hand, using 300 ppm sodium hypochlorite (NaOCl) with acetic acid in the ratio 1:1 for 10 min in spice products considers less production time, less amount of acetic acid usage and higher microbial reduction [<xref ref-type="bibr" rid="scirp.91477-ref35">35</xref>].</p><p>Physical methods to reduce microbial growth of food product are used such as irradiation treatment. Electron beam irradiation at 10 kGy is an effective irradiation dose in reaching good level decontamination in chili shrimp paste for total pathogenic enterobacteriaceae, mesophilic bacteria, yeast and mold [<xref ref-type="bibr" rid="scirp.91477-ref2">2</xref>] , another research reported that electron beam irradiation of 3.0 kGy on sun-dried apricots was sufficient to suppress the growth of yeast and mold, and bacterial to below detection limits for a storage for 10 months [<xref ref-type="bibr" rid="scirp.91477-ref37">37</xref>]. On the other hand, physical methods cannot always be applied owing restriction such as temperature safety</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Microbial count and rheological properties of CSSP and control</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Sample</th><th align="center" valign="middle"  colspan="2"  >Microbial count</th><th align="center" valign="middle"  colspan="3"  >Rheological properties</th></tr></thead><tr><td align="center" valign="middle" >TPC (CFU/mL)</td><td align="center" valign="middle" >Yeast and Mold (CFU/mL)</td><td align="center" valign="middle" >Yield stress, τ 0 (Pa)</td><td align="center" valign="middle" >Viscosity (Pa∙s)</td><td align="center" valign="middle" >Consistency, K (Pa∙s<sup>n</sup>)</td></tr><tr><td align="center" valign="middle" >A</td><td align="center" valign="middle" >2.3 &#215; 10<sup>3 </sup></td><td align="center" valign="middle" >3.9 &#215; 10<sup>2</sup></td><td align="center" valign="middle" >1657.63 &#177; 1.43<sup>a </sup></td><td align="center" valign="middle" >20.20 &#177; 0.01<sup>a </sup></td><td align="center" valign="middle" >978.64 &#177; 0.13<sup>a </sup></td></tr><tr><td align="center" valign="middle" >B</td><td align="center" valign="middle" >1.1 &#215; 10<sup>3</sup></td><td align="center" valign="middle" >4.0 &#215; 10<sup>2 </sup></td><td align="center" valign="middle" >763.89 &#177; 0.09<sup>b </sup></td><td align="center" valign="middle" >8.62 &#177; 0.30<sup>b </sup></td><td align="center" valign="middle" >512.76 &#177; 0.02<sup>b </sup></td></tr><tr><td align="center" valign="middle" >C</td><td align="center" valign="middle" >4.2 &#215; 10<sup>3 </sup></td><td align="center" valign="middle" >2.7 &#215; 10<sup>2</sup></td><td align="center" valign="middle" >1796.72 &#177; 0.65<sup>a </sup></td><td align="center" valign="middle" >21.34 &#177; 0.09<sup>a </sup></td><td align="center" valign="middle" >1109.07 &#177; 0.04<sup>a </sup></td></tr><tr><td align="center" valign="middle" >D</td><td align="center" valign="middle" >3.5 &#215; 10<sup>3 </sup></td><td align="center" valign="middle" >4.2 &#215; 10<sup>2 </sup></td><td align="center" valign="middle" >1495.12 &#177; 0.13<sup>a </sup></td><td align="center" valign="middle" >18.40 &#177; 0.01<sup>a </sup></td><td align="center" valign="middle" >692.49 &#177; 0.09<sup>a </sup></td></tr><tr><td align="center" valign="middle" >E</td><td align="center" valign="middle" >1.6 &#215; 10<sup>3 </sup></td><td align="center" valign="middle" >3.7 &#215; 10<sup>2</sup></td><td align="center" valign="middle" >31.94 &#177; 0.66<sup>b</sup></td><td align="center" valign="middle" >0.35 &#177; 0.07<sup>b </sup></td><td align="center" valign="middle" >32.31 &#177; 0.02<sup>b </sup></td></tr></tbody></table></table-wrap><p>All data are expressed as the mean &#177; SD from three independent replication. Means with different letters are significantly different (p &lt; 0.05) for each parameter (column).</p><p>of personnel and design of the process flow [<xref ref-type="bibr" rid="scirp.91477-ref38">38</xref>] , considering on chili composition are enriched in essential oil to gives the value of spices, which essential oils are sensitive to temperature.</p></sec><sec id="s3_3"><title>3.3. Rheological Properties</title><p><xref ref-type="table" rid="table3">Table 3</xref> showed that the rheological properties (yield stress, viscosity, and consistency) of CSSP and control values were significantly (p &lt; 0.05) compared to control (sample E) except for CSSP B and no significant (p &gt; 0.05) between samples of CSSP. Viscosity dependence of sauce on pulp or total solids content and naturally occurring pectic substances was already noticed [<xref ref-type="bibr" rid="scirp.91477-ref39">39</xref>] [<xref ref-type="bibr" rid="scirp.91477-ref40">40</xref>]. The sample was heated and mixed for 30 min, generally heated of CSSP for 15 min [<xref ref-type="bibr" rid="scirp.91477-ref36">36</xref>] , processing conditions changed particles shape from spheroidal to elongated leading to greater resistance flow [<xref ref-type="bibr" rid="scirp.91477-ref39">39</xref>]. Yield stress showed that system parameter was dominated by the content of total solid. In comparison to chili shrimp paste (CSP) by processing time for 15 min [<xref ref-type="bibr" rid="scirp.91477-ref2">2</xref>] was characterized by lowest consistency values. For purpose of the standard manufacturing process in industrial conditions on the existing equipment, it was necessary to adjust the consistency of CSSP. This consistency caused that the viscosity of the produced sauce corresponded to the one characteristic for chili sauce, which in the case of independent marketing had to be packed in jars.</p></sec><sec id="s3_4"><title>3.4. Color Properties</title><p>The effect different recipes and shrimp paste from four regions in Indonesia on the color of CSSP is shown in <xref ref-type="table" rid="table4">Table 4</xref>. Shrimp paste and recipes of CSSP have significant impact to the lightness was found in all samples, as compared to control and differ within CSSP samples (p &lt; 0.05). CSSP have significant (p &lt; 0.05) except for CSSP A in redness, and sample B only in yellowness compared to control was observed. The redness index (a*/b*) was not affected by the different CSSP with a significantly higher a*/b* in all samples compared to control (p &gt; 0.05).</p><p>Redness index enhancement might be associated to a limited alteration of</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Color properties of CSSP and control</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sample</th><th align="center" valign="middle" >Lightness (L)</th><th align="center" valign="middle" >Redness (a)</th><th align="center" valign="middle" >Yellowness (b)</th><th align="center" valign="middle" >a*/b*</th></tr></thead><tr><td align="center" valign="middle" >A</td><td align="center" valign="middle" >32.50 &#177; 0.09<sup>b</sup></td><td align="center" valign="middle" >13.61 &#177; 0.11<sup>b</sup></td><td align="center" valign="middle" >12.32 &#177; 0.05<sup>b</sup></td><td align="center" valign="middle" >1.10 &#177; 0.32<sup>a</sup><sup> </sup></td></tr><tr><td align="center" valign="middle" >B</td><td align="center" valign="middle" >29.32 &#177; 0.76<sup>a</sup></td><td align="center" valign="middle" >10.91 &#177; 0.23<sup>a</sup></td><td align="center" valign="middle" >7.63 &#177; 0.09<sup>a</sup></td><td align="center" valign="middle" >1.43 &#177; 0.31<sup>a </sup></td></tr><tr><td align="center" valign="middle" >C</td><td align="center" valign="middle" >32.41 &#177; 0.17<sup>b</sup></td><td align="center" valign="middle" >17.52 &#177; 0.06<sup>c</sup></td><td align="center" valign="middle" >12.91 &#177; 0.04<sup>b</sup></td><td align="center" valign="middle" >1.36 &#177; 0.02<sup>a </sup></td></tr><tr><td align="center" valign="middle" >D</td><td align="center" valign="middle" >33.16 &#177; 0.13<sup>c</sup></td><td align="center" valign="middle" >15.27 &#177; 0.32<sup>d</sup></td><td align="center" valign="middle" >13.54 &#177; 0.12<sup>bc</sup></td><td align="center" valign="middle" >1.13 &#177; 0.08<sup>a </sup></td></tr><tr><td align="center" valign="middle" >E</td><td align="center" valign="middle" >38.23 &#177; 0.04<sup>d</sup></td><td align="center" valign="middle" >13.58 &#177; 0.11<sup>b</sup></td><td align="center" valign="middle" >12.62 &#177; 0.44<sup>b</sup></td><td align="center" valign="middle" >1.08 &#177; 0.07<sup>a </sup></td></tr></tbody></table></table-wrap><p>All data are expressed as the mean &#177; SD from three independent replication. Means with different letters are significantly different (p &lt; 0.05) for each parameter (column).</p><p>lycopene during the cooking [<xref ref-type="bibr" rid="scirp.91477-ref41">41</xref>]. The lightness, redness and yellowness of product relate to the food composition, food density, equipment capability as well as packaging materials [<xref ref-type="bibr" rid="scirp.91477-ref42">42</xref>]. Irradiation and thermal treatment had no significantly of chili shrimp paste on color [<xref ref-type="bibr" rid="scirp.91477-ref2">2</xref>].</p></sec><sec id="s3_5"><title>3.5. Sensory Evaluation</title><p>The sensory evaluation of CSSP tended to be different (<xref ref-type="fig" rid="fig3">Figure 3</xref>) indicating some interaction between shrimp paste and the CSSP. The interaction was probably shown through the correlation among each flavor (<xref ref-type="table" rid="table5">Table 5</xref>). The intensities perceived of saltiness, sweetness, and bitterness were greatly varied among CSSP. Although there is no correlation between sweetness and bitterness this is indicated by the negative correlation. The highest bitterness from CSSP containing shrimp paste A was probably due to the lowest salt content of CSSP A. NaCl might elicit sweet, sour, and bitterness, especially at higher concentration [<xref ref-type="bibr" rid="scirp.91477-ref43">43</xref>]. The sea salt has different umami and astringency intensity [<xref ref-type="bibr" rid="scirp.91477-ref44">44</xref>] , as salt may contain different concentration of calcium, potassium, magnesium, iron, sodium, and zinc. Food containing seafood has fishy flavor could enhance the saltiness intensity [<xref ref-type="bibr" rid="scirp.91477-ref45">45</xref>]. This is confirmed by the correlation of shrimp flavor which was positively correlated to saltiness, and umami but negatively correlated to the sourness. The free amino acids in shrimp paste were found contributing to the flavor of CSSP.</p><p>These free amino acids were also indicated from protein content, which were found to be higher and varied than other major composition of shrimp paste. The major contributor was generally derived from the glutamic acid, alanine, glycine, leucine, and lysine [<xref ref-type="bibr" rid="scirp.91477-ref9">9</xref>]. Some cultures add sour tasting ingredients such as kalamansi to improve the overall flavor of CSSP. The sourness tended to enhance the sweetness of CSSP thereby this sweetness might enhance the umami taste. Umami sometimes linked to sweetness and saltiness [<xref ref-type="bibr" rid="scirp.91477-ref46">46</xref>] , along with the actual flavor of compatible food, increase the body or mouthfulness of food, and it makes food taste more pleasant [<xref ref-type="bibr" rid="scirp.91477-ref47">47</xref>]. To suppress the sweetness and bitterness intensity adds chili [<xref ref-type="bibr" rid="scirp.91477-ref48">48</xref>]. Each chili type has its own taste, aftertaste and burning sensation, differentiated by Scoville Heat Units (SHU) [<xref ref-type="bibr" rid="scirp.91477-ref49">49</xref>].</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Spearman Correlation of CSSP and control among each flavor</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Sourness</th><th align="center" valign="middle" >Bitterness</th><th align="center" valign="middle" >Sweetness</th><th align="center" valign="middle" >Saltiness</th><th align="center" valign="middle" >Umami</th><th align="center" valign="middle" >Shrimp</th></tr></thead><tr><td align="center" valign="middle" >Sourness</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Bitterness</td><td align="center" valign="middle" >0.401*</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Sweetness</td><td align="center" valign="middle" >0.264*</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Saltiness</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.426*</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Umami</td><td align="center" valign="middle" >0.301*</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.347*</td><td align="center" valign="middle" >0.549*</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Shrimp</td><td align="center" valign="middle" >0.542*</td><td align="center" valign="middle" >0.431*</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.311*</td><td align="center" valign="middle" >1</td></tr></tbody></table></table-wrap><p>Correlation is significant at the 0.05 level.</p></sec></sec><sec id="s4"><title>4. Conclusion</title><p>Chili sauce shrimp paste from different regions in Indonesia had no significant (p &gt; 0.05) in proximate (except for moisture), salinity, and pH. However, the range content is of fat 2.09% - 5.11%, protein 1.76% - 6.00%, moisture 68.34% - 89.11%, ash 10.98% - 13.96%, carbohydrate 2.84% - 9.07%, and pH 5.73 - 6.40. The identified volatiles can be grouped into hydrocarbon, carbonyl, sulfur, alcohol, nitrogen, fatty acid, and ester compounds. The CSSP A, B, C, D, and E (control) contained 9, 21, 12, 29, and 6 volatile compounds respectively. The total FAA ranged from 44.32 to 67.03 g/100 g, and histidine (his) was found as the most abundant and varied FAA in each CSSP. The microbial counts and the redness index (a*/b*) of CSSP are not significant (p &gt; 0.05) compared to control. The rheological properties (yield stress, viscosity, and consistency) of CSSP and control values were significantly (p &lt; 0.05) except for CSSP B. The intensities perceived of saltiness, sweetness, and bitterness were greatly varied among CSSP. Although there is no correlation between sweetness and bitterness this is indicated by the negative correlation.</p></sec><sec id="s5"><title>Acknowledgements</title><p>This research was supported by the earmarked fund for China Agriculture Research system (CARS-46), Jiangsu Project for Fisheries, and Collaborative innovation center of food safety and quality control in Jiangsu Province, China.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Suhartini, W., Yang, F. and Xia, W.S. (2019) Physiochemical Properties, Volatile Compounds and Sensory Evaluation of Chili Sauce Shrimp Paste from Different Regions in Indonesia. Food and Nutrition Sciences, 10, 333-348. https://doi.org/10.4236/fns.2019.103026</p></sec></body><back><ref-list><title>References</title><ref id="scirp.91477-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Jinap, S., Ilya-Nur, A.R., Tang, S.C., Hajeb, P., Shahrim, K. and Khairunnisak, M. (2010) Sensory Attributes of Dishes Containing Shrimp Paste with Different Concentrations of Glutamate and 5’-Nucleotides. Appetite, 55, 238-244.  
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