Dieckol is a brown algal phlorotannin with potent bioactivities such as hepatoprotective effects. This study aimed to produce dieckol-rich extract from Eisenia bicyclis and apply them as a functional ingredient for a novel bacterial cellulose (BC)-based dessert. The modeling and optimization of the ultrasound-assisted extraction (UAE) process were performed. The developed model showed that at least one of the linear or quadratic terms of all variables (amplitude, solvent concentration, temperature, and time) affected dieckol recovery (p < 0.05). Following numerical optimization, dieckol recovery achieved 17.3 mg/g biomass under optimal conditions (62 % amplitude, 35 % solvent concentration, 70 °C, and 6 min), similar to the model-predicted value (18.3 mg/g). Then, BC-dieckol (BC-D) pellicles were fabricated by ex situ loading 25, 50, 75, and 100 % of the liquid extract with 9.954 mg dieckol (recommended intake level). All BC-D pellicles showed high dieckol loading (98.16 - 100 %), and BC-D100 meets the acceptable level. The FTIR and SEM analyses confirmed the impregnation of the extract, especially the signature peaks of dieckol, related to aromatic ether stretch and aromatic ring structure of phlorotannin by the FTIR spectra. The crystallinity index and water absorption capacity of BC-D100 were determined to be about 83.9 % and 415.6 %, respectively, which were slightly decreased compared to BC-control, but not significantly. In addition, BC-D100 has shown antioxidant activity making it valuable as a food material. This study provides valuable information for the food industry, paving the way for developing novel BC-based foods using brown algal extracts.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.ijbiomac.2025.140044 | DOI Listing |
Int J Biol Macromol
January 2025
Department of Biotechnology, Sangmyung University, Seoul 03016, Republic of Korea. Electronic address:
Dieckol is a brown algal phlorotannin with potent bioactivities such as hepatoprotective effects. This study aimed to produce dieckol-rich extract from Eisenia bicyclis and apply them as a functional ingredient for a novel bacterial cellulose (BC)-based dessert. The modeling and optimization of the ultrasound-assisted extraction (UAE) process were performed.
View Article and Find Full Text PDFFood Chem X
December 2024
Department of Food and Nutrition, Sangmyung University, 20, Hongjimun 2-Gil, Jongno-Gu, Seoul 03016, Republic of Korea.
This study aimed to develop a novel functional jelly by incorporating dieckol-rich extracts from (). In the extraction process, a high dieckol yield (16.5 mg/g biomass) was achieved by response surface optimization (optimum conditions: 55.
View Article and Find Full Text PDFJ Microbiol Biotechnol
October 2024
KOICA-PKNU International Graduate Program of Fisheries Science, Pukyong National University, Busan 48513, Republic of Korea.
Food Funct
June 2024
Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, Seoul, 02447, Republic of Korea.
Obesity requires treatment to mitigate the potential development of further metabolic disorders, including diabetes, hyperlipidemia, tumor growth, and non-alcoholic fatty liver disease. We investigated the anti-obesity effect of a 30% ethanol extract of (Kjellman) Setchell (EEB) on 3T3-L1 preadipocytes and high-fat diet (HFD)-induced obese C57BL/6 mice. Adipogenesis transcription factors including peroxisome proliferator-activated receptor (PPAR)γ, CCAAT/enhancer-binding protein-alpha (C/EBPα), and sterol regulatory element-binding protein-1 (SREBP-1) were ameliorated through the AMP-activated protein kinase (AMPK) pathway by EEB treatment in differentiated 3T3-L1 cells.
View Article and Find Full Text PDFChemistry
August 2024
Institut des Biomolécules Max Mousseron, IBMM, Université de Montpellier, CNRS, ENSCM., 1919 route de Mende, 34293, Montpellier, France.
Ecklonialactones, Eiseniachlorides, and Egregiachlorides are synthesized in living organisms via the lipoxygenase-mediated oxidation of polyunsaturated fatty acids. Originally isolated and identified from brown seaweed (Ecklonia stolonifera, Eisenia bicyclis, and Egregia menziesii), and later replicated on milligram scale through chemical synthesis, the full biological activities of these compounds remain to be elucidated. To bridge this gap in knowledge, we propose a unified methodology to synthesize the 14-membered macrocyclic structures of Ecklonialactones, Eiseniachlorides and analogs using a versatile and convergent approach.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!