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<title>Oral communications</title>
<link>http://depot.umc.edu.dz/handle/123456789/14448</link>
<description/>
<pubDate>Tue, 02 Jun 2026 05:53:18 GMT</pubDate>
<dc:date>2026-06-02T05:53:18Z</dc:date>
<item>
<title>AO-16: Study of Camel Milk Coagulation Induced by Cardosins: Enzymes  Purified from Wild Cardoon Flowers</title>
<link>http://depot.umc.edu.dz/handle/123456789/14672</link>
<description>AO-16: Study of Camel Milk Coagulation Induced by Cardosins: Enzymes  Purified from Wild Cardoon Flowers
ZIKIOU, Abdellah; SACI, Fairouz; FIALA, Samah; HADJADJ, Nasreddine
Subject description: Camel milk transformation poses significant challenges due to its unique &#13;
composition and perceived difficulties in coagulation. This research explores the feasibility of &#13;
coagulating camel milk using proteases derived from wild cardoon flowers, Cynara cardunculus Var. &#13;
sylvestris. &#13;
 &#13;
Objectives: The primary objective of this study is to investigate the potential of cardoon flower &#13;
proteases for coagulating camel milk and compare their performance to a recombinant chymosin &#13;
enzyme designed specifically for camel milk coagulation. &#13;
 &#13;
Methods: Our methodology consisted of several key steps. Initially, cardosins were extracted, &#13;
purified, and characterized using chromatographic and electrophoretic techniques. Subsequently, we &#13;
measured their coagulating and proteolytic activities, cheese yields, and syneresis ability using camel &#13;
milk as the substrate. Additionally, we assessed the textural properties of the coagulums obtained with &#13;
the Optigraph by measuring firmness parameters (A20, A30, A40) and coagulation velocity (R and &#13;
OK20). The study was conducted by comparing the cardoon-derived proteases with a commercially &#13;
available recombinant enzyme developed specifically for camel milk coagulation. &#13;
 &#13;
Results and discussion: Our purification protocol allowed us to obtain three types of cardosins: &#13;
Cardosins A0, A, and B. All three are heterodimeric proteins composed of two chains, large and small, &#13;
with molecular weights ranging from 42 to 36 kDa for the large chains and 16 to 13 kDa for the small &#13;
chains. The analysis of coagulation properties and theoretical cheese yields demonstrated that the &#13;
purified cardosins exhibit promising coagulation potential for camel milk. Cardosins A and B displayed &#13;
activities similar to those of the commercial recombinant chymosin (23 ± 2 IUMC and 21 ± 1 for &#13;
cardosins A and B, respectively, compared to 25 ± 2 for the commercial enzyme). However, cardosin &#13;
A0 exhibited lower activity (9 ± 2 IUMC). Regarding textural properties assessed with the Optigraph, &#13;
no significant differences were observed between cardosins A and B and the commercial enzyme, &#13;
whereas cardosin A0 generated a friable and less firm coagulum. &#13;
 &#13;
Conclusion: Based on these findings, we believe that proteases from cardoon flowers can be &#13;
applied as coagulation agents for camel milk transformation into cheese. The cardoon-derived &#13;
proteases, particularly cardosins A and B, exhibit coagulation capabilities comparable to those of the &#13;
commercially available recombinant chymosin. This research contributes to the potential development &#13;
of more sustainable and cost-effective methods for camel milk processing in the cheese industry
</description>
<pubDate>Thu, 05 Oct 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://depot.umc.edu.dz/handle/123456789/14672</guid>
<dc:date>2023-10-05T00:00:00Z</dc:date>
</item>
<item>
<title>AO-15: Comparative study of the chemical and biological aspects of spend coffee  grounds recovered by the filtration and decoction methods</title>
<link>http://depot.umc.edu.dz/handle/123456789/14671</link>
<description>AO-15: Comparative study of the chemical and biological aspects of spend coffee  grounds recovered by the filtration and decoction methods
TENIOU, Fatima El Batoul; AGGOUN, Moufida; BENAHMED, Chaima; BELKHAIRI, Chahinez; AMOKRANE, Serine; BENSOUICI, Chawki; ARHAB, Rabah
Subject description: Two types of coffee grounds has been studied; the first type was extracted &#13;
by pressure, while the second was obtained by decoction. &#13;
Objectives: The aim of our work is to compare the recovered ground using these two methods &#13;
on both, chemical and biological scales. &#13;
Methods: The chemical study concerns primary compounds (dry, mineral and fatty matter) and &#13;
secondary compounds (phenols, flavonoïds), the biological study however, is about assessing the &#13;
antioxidant potential (DPPH, CUPRAC, FRAP, Phenanthroline) as well as the enzymatic one (Anti&#13;
Alzheimer’s and Anti-diabetic) of the two samples. For valuation purposes, and by choosing the most &#13;
active coffee ground, we simultaneously elaborate the effect of the preparation method on the quality &#13;
of the recovered coffee ground. &#13;
Results and discussion: The results show a difference between the two extracts in the primary &#13;
composition (DM, MM, FM) and a similarity in the secondary composition for phenols and flavonoids’ &#13;
levels. The evaluation of the antioxidant activity shows that the two extracts have a low and similar &#13;
antioxidant potential; and that both had no activity against Alzheimer's disease. In return, the two &#13;
substrates possess a detectable activity against the therapeutic enzyme responsible for the development &#13;
of diabetes. &#13;
Conclusion: Espresso coffee grounds seem to be richer in fat source than decoction grounds. &#13;
Therefore, the two beverage preparation methods discussed herein did not greatly influence the quality &#13;
of the coffee grounds. In addition, given its phenolic and chemical composition, the coffee ground &#13;
presents an important source of natural compounds of biological and therapeutic interest
</description>
<pubDate>Thu, 05 Oct 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://depot.umc.edu.dz/handle/123456789/14671</guid>
<dc:date>2023-10-05T00:00:00Z</dc:date>
</item>
<item>
<title>AO-14: Insects oil a promising ingredient for cosmetic formulations: Fatty acid  profile, antioxidant and antibacterial activity of pressed Locusta migratoria oil</title>
<link>http://depot.umc.edu.dz/handle/123456789/14670</link>
<description>AO-14: Insects oil a promising ingredient for cosmetic formulations: Fatty acid  profile, antioxidant and antibacterial activity of pressed Locusta migratoria oil
TEBIB, Nacira; ACHEUK, Fatma
Subject description: Edible insects represent an interesting alternative source of proteins and &#13;
lipids for human and animal consumption and have the potential to play a significant role in a circular &#13;
economy to meet current societal challenges. There is growing interest in the use of insects in the &#13;
manufacture of biomaterials and the valorization of secondary waste products. &#13;
Objectives: The potential of locust (Locusta migratoria) oil, adapted to intensive breeding using &#13;
by-products as feed, for incorporation as an ingredient in cosmetic formulations is investigated. &#13;
Methods: Locusts are mass-reared under controlled conditions. Firstly, techniques for obtaining &#13;
good oil extraction yields from dried locust biomass were tested. Extraction using hexane as a solvent &#13;
(soxhlet) and traditional pressing. Fatty acid composition (%) and profile (%) and the major groups of &#13;
fatty acids of the migratory locust were determined (gas chromatography-mass spectrometry (GC-MS)). &#13;
For antioxidant capacity, two different methodologies were used (DPPH, FRAP), and agar diffusion &#13;
tests were performed for antibacterial activity. &#13;
Results and discussion: Migratory locust is rich in lipids (≈33% of dry weight), and traditional &#13;
pressing was found to be the best system for maximizing oil yield (26.90g/100g vs. 24.75g/100g for &#13;
hexane). The most abundant saturated fatty acid was palmitic acid, 16:0 (30.5%) followed by stearic &#13;
acid, 18:0 (9.3%TFA), while oleic acid, C18:1n9c (40.53%), was the main monounsaturated fatty acid, &#13;
and linolenic acid, C18:3n3 (13.7%) was the most abundant polyunsaturated fatty acid. Unsaturated &#13;
fatty acids (UFAs) make up 59% of TFA. MUFA are the most predominant fatty acids in locust tissues, &#13;
accounting for 41.2% of TFA, followed by SFA, which make up 41% of TFAs, and PUFA, which make &#13;
up 17.8% of TFA. The proportion of saturated/unsaturated fatty acids was (0.7). Omega-6 content was &#13;
(11.5mg/g) and omega-3 (24.8mg/g), representing (5.6% TFA) and (12.1% TFA). The N-3/N-6 ratio &#13;
was 2.2. Regarding antioxidant activity, Locusta migratoria showed values of 2.03, and 4.93 mg TE/g &#13;
of oil for DPPH and FRAP tests. Interestingly, agar diffusion tests demonstrated the sensitivity of Gram&#13;
positive Bacillus subtilis and Staphylococcus aureus to the oil, while the growth of Gram-negative &#13;
Pseudomonas aeruginosa and Escherichia coli was unaffected. This study confirms that fat and other &#13;
active compounds in pressed oil could be effective antimicrobials against bacteria.  &#13;
Conclusion: The fatty acid profile indicates a high proportion of unsaturated fatty acids, and the &#13;
antioxidant and antibacterial activity of pressed Locusta migratoria oil is promising for use in cosmetic &#13;
applications
</description>
<pubDate>Thu, 05 Oct 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://depot.umc.edu.dz/handle/123456789/14670</guid>
<dc:date>2023-10-05T00:00:00Z</dc:date>
</item>
<item>
<title>AO-13: Phenolic Compounds of algae (Ulva lactuca): Optimization of extraction by  response surface methodology and in vitro antioxidant properties</title>
<link>http://depot.umc.edu.dz/handle/123456789/14669</link>
<description>AO-13: Phenolic Compounds of algae (Ulva lactuca): Optimization of extraction by  response surface methodology and in vitro antioxidant properties
CAID, Rachida; CHAALAL, Makhlouf; YDJEDD, Siham; CHEBOUT, Afaf; LAOUABDIA  SELLAMI, Nadjette1
Subject description: Seaweeds are a rich source of natural antioxidants with potent antioxidant &#13;
properties. While the one-factor method has limitations in optimizing the phenolic extract, the use of &#13;
developed mathematical models such as Response Surface Methodology (RSM) is recommended for &#13;
more effective optimization processes. &#13;
Objectives: Given the highly bioactive nature of phenolics and their numerous therapeutic &#13;
applications, the primary objective of this investigation is to optimize their recovery using Response &#13;
Surface Methodology (RSM). &#13;
Methods: Prior to RSM, the single-factor method was applied to reveal the main factors &#13;
influencing the extraction (solvent type and concentration, sample˗to˗solvent ratio, temperature, and &#13;
time of extraction). The contents of total polyphenols (TP) and flavonoids were determined. While the &#13;
ferric reducing power (FRP) and the free radical scavenging activity (DPPH) were used to evaluate the &#13;
antioxidant activity of the extracts. &#13;
Results and discussion: The results of the preliminary optimization step through sequential &#13;
methodology revealed that solvent concentration, extraction duration, and temperature were the main &#13;
influencing factors. All these tested extraction parameters significantly influenced total phenolic &#13;
contents (TPC) and DPPH-free radical scavenging activity (FRSA) and ferric reducing power (FRP). &#13;
RSM analysis using Box˗Behnken design showed that the optimal extraction conditions of total &#13;
phenolic contents of algae were 23.07% acetone, 51.82 °C, and 118.02 min with values of 29.44 mg &#13;
GAE/g for total phenolic extracts, 59.48% and FRSA, and 123.45 mg AAE/100g for FRP. The results &#13;
obtained show that the extraction conditions have a significant effect (p&lt;0.05) on the content of total &#13;
polyphenols, flavonoids, and the antioxidant activity of the extracts. &#13;
Conclusion: The developed mathematical models have demonstrated a high level of &#13;
significance through sequential and RSM optimization processes for phenolic antioxidants of Ficus &#13;
carica leaves. This method allows us to observe the effects of different extraction conditions on the &#13;
phenolic antioxidants
</description>
<pubDate>Thu, 05 Oct 2023 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://depot.umc.edu.dz/handle/123456789/14669</guid>
<dc:date>2023-10-05T00:00:00Z</dc:date>
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