Antimicrobial resistance poses a great threat and challenge to humanity. Therefore, the search for alternative ways to target and eliminate microbes from plant, animal, and marine microorganisms is one of the world’s concerns today.

Fucoidan is one of the main polysaccharides of brown algae and echinoderm, which has nutritional and pharmacological functions. Due to the low molecular weight and exposure of more sulfate groups, oligo-fucoidan or fucoidan oligosaccharides have potential for broader applications. In this research, a novel endo-α-1,4-L-fucoidanase OUC-FaFcn1 which can degrade fucoidan into oligo-fucoidan was discovered from the fucoidan-digesting strain Flavobacterium algicola 12,076. OUC-FaFcn1 belongs to glycoside hydrolases (GH) family 107 and shows highest activity at 40 °C and pH 9.0. It can degrade the α-1,4 glycosidic bond, instead of α-1,3 glycosidic bond, of the fucoidan with a random tangent way to generate the principal product of disaccharide, which accounts for 49.4% of the total products. Therefore, OUC-FaFcn1 is a promising bio-catalyst for the preparation of fucoidan-derived disaccharide. These results further enrich the resource library of fucoidanase and provide the basis for the directional preparation of fucoidan-derived oligosaccharide with specific polymerization.

In an attempt to produce bioethanol as a renewable and natural energy resource and as a promising alternative/complement to conventional petrol (i.e., gasoline), 44 microbial isolates (12 yeast and 32 bacterial strains) were isolated from molasses samples obtained from some of the sugar factories in Egypt. Among the microbial isolates obtained, only two yeast isolates (HSC-22 and HSC-24) were selected from sugarcane molasses (SCM) for their high bioethanol fermentation capabilities, recording bioethanol production of ≈9.6 and 8.2 g/L with actual yield of 0.48 and 0.41 g ethanol/g SCM, respectively, within 48-h incubation period at 30°C. Phylogenetic identification of these isolates was performed based on the analysis of the nucleotide sequence of the 18S rDNA gene, which indicated that these isolates can be identified as Pichia veronae and Candida tropicalis, respectively, with similarity of 99%.