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The diversity of marine biomasses is a set of exploitable and renewable resources with application in several sectors. In this context, a co-culture based on three protease-producing bacterial isolates, namely Aeribacillus pallidus VP3, Lysinibacillus fusiformis C250R, and Anoxybacillus kamchatkensis M1V strains, was carried out in a medium based on the blue swimming crab Portunus segnis bio-waste. Proteases production was optimized using a central composite design (CCD). The highest level of proteases production obtained was 8,809 U/mL in a medium comprising 75 g/L of Portunus segnis by-product powder (P). The biological value of P and its obtained derivatives were evidenced via accredited protocols. The recovered protein hydrolysate (P) was found to be active towards radical scavenging power and against angiotensin I-converting enzyme (ACE). The blue crab chitin (BC) extraction efficiency was achieved with a yield of 32%. Afterwards, chitosan was prepared through chitin N-deacetylation with a yield of 52%, leading to an acetylation degree (AD) of 19% and solubility of 90%. In addition, chitosan is found to be active against the growth of all pathogenic bacteria tested.
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http://dx.doi.org/10.1007/s11356-021-18398-y | DOI Listing |
Vet Res Forum
June 2025
Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, Iran.
This study investigated the antioxidant and apoptotic systems of blue swimmer crabs at various reproductive stages, providing valuable insights into their potential as biological markers, particularly in the polluted Persian Gulf. Our research along the coasts of Hendijan County, Iran, involved capturing live crabs (167 ± 52.07 g), examining their morphological traits and determining their reproductive stages through dissection and histological analysis.
View Article and Find Full Text PDFEnviron Monit Assess
February 2025
Laboratory of Fisheries Sciences, University of Carthage, National Institute of Marine Sciences and Technologies (INSTM), 28 Rue du 2 Mars 1934, Salammbô 2025, Tunis, Tunisia.
The current study aims to examine the concentrations of eight trace elements (TE) (nickel, aluminum, copper, cadmium, lead, cobalt, chromium, and zinc) in the edible tissue of the invasive blue crab Portunus segnis in two southern Mediterranean lagoons (i.e., Bizerte Lagoon (BL) and Ghar El-Melh Lagoon (GML)) between 2020 and 2021.
View Article and Find Full Text PDFFoods
December 2024
Department of Chemical Engineering, Faculty of Chemistry, Universidad de Sevilla, 41012 Seville, Spain.
Eco-friendly, bioactive and edible films from renewable resources are increasingly regarded as viable replacements for petroleum-based packaging. This study investigates the application of macroalgae powder (ULP) as an active additive in crab () chitosan-based films for natural food packaging. Films with ULP concentrations of 0.
View Article and Find Full Text PDFSci Total Environ
December 2024
Post-Graduation Program in Conservation of Cerrado Natural Resources, Goiano Federal Institute, Urutaí, GO, Brazil; Post-Graduation Program in Ecology, Conservation, and Biodiversity, Federal University of Uberlˆandia, Uberlˆandia, MG, Brazil; Post-Graduation Program in Biotechnology and Biodiver
Environ Sci Pollut Res Int
July 2024
Laboratory of Microbial and Enzymatic Biotechnologies and Biomolecules (LMEBB), Centre of Biotechnology of Sfax (CBS), University of Sfax (USF), Road of Sidi Mansour Km 6, P.O. Box 1177, 3018, Sfax, Tunisia.
In accordance with the framework of the Circular Blue Bioeconomy in the Mediterranean region, the objective of this study was to evaluate the biotransformation of blue swimming crab (Portunus segnis) residues obtained from the port of Sfax by an extracellular chitinase produced by Nocardiopsis halophila strain TN-X8 isolated from Chott El Jerid (Tozeur, Tunisia). From the analysis of multiple extremophilic Actinomycetota, it was determined that strain TN-X8 exclusively utilized 60 g/L of raw blue swimming crab as its carbon and energy source, achieving a chitinase activity of approximately 950 U/mL following a 6-day incubation period at 40 °C. Pure chitinase, designated as ChiA-Nh30, was obtained after heat treatment, followed by ammonium sulfate fractionation and Sephacryl® S-200 column chromatography.
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