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Alginate is an important polysaccharide in the ocean that supports the growth of marine microorganisms. Many widespread species possess alginate lyases and can utilize alginate as a carbon source, but the detailed alginate degradation mechanism in remains to be further explored. In this study, we obtained a highly efficient alginate-degrading strain, Vibrio pelagius WXL662, with 11 alginate lyases (VpAly-I to -XI) and further elucidated its molecular mechanism of alginate degradation. Three alginate utilization loci (AUL) were identified in different parts of WXL662's genome, comprising six alginate lyases (VpAly-I, -II, -VIII, -IX, -X, and -XI) and other genes related to alginate degradation. Most of the alginate-degrading genes are strongly induced when alginate is provided as the sole carbon source. Ten alginate lyases (VpAly-I to -X) had been purified and characterized, including six from polysaccharide lyase family 7 (PL7), three from PL17, and one from PL6. These recombinant alginate lyases existing in different cellular locations were active at a wide temperature (10 to 50°C) and pH (4.0 to 9.0) range, with different substrate preferences and diverse degradation products, enabling WXL662 to efficiently utilize alginate in a changing marine environment. Importantly, outer membrane vesicles (OMVs) can act as vectors for alginate lyases (VpAly-II, -V, and -VI) in WXL662. Further investigations of public genomes revealed that most alginate-degrading vibrios possess one AUL instead of previously reported "scattered" system. These results emphasize the specific alginate degradation strategy in Vibrio pelagius WXL662, which can be used as a model strain to study the ecological importance of effective alginate-degrading vibrios in the ocean. Alginate is an important carbon source in the marine environment, and vibrios are major alginate utilizers. Previous studies focused only on the characteristics of individual alginate lyases in vibrios, but few of them discussed the comprehensive alginate-degrading strategy. Here, we depicted the alginate utilization mechanism and its ecological implications of a highly efficient alginate-degrading strain, WXL662, which contained 11 alginate lyases with distinct enzymatic characteristics. Importantly, unlike other vibrios with only one alginate utilization locus (AUL) or the previously reported "scattered" system, three AUL were identified in WXL662. Additionally, the involvement of outer membrane vesicles (OMVs) in the secretion of alginate lyases is proposed for the first time.
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http://dx.doi.org/10.1128/aem.01389-22 | DOI Listing |
Appl Biochem Biotechnol
September 2025
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
Marine-derived enzymes often show distinct physiological properties and great potential for industrial use. Salt ions may improve the stability and expression efficiency of marine enzymes, which requires salt-resistant host based expression platform. Aspergillus oryzae of good protein expression and secretion was evaluated and explored for this purpose.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
College of Food Science and Light Industry, Nanjing Tech University, Nanjing, 211816, China. Electronic address:
Cellulases and glucanases can effectively degrade the seaweed polysaccharides, and the resulting oligosaccharides may be subsequently fermented or used as feed additives. To improve the utilization of marine algae, the study identified and characterized Cel5B, a novel bifunctional cellulase-glucanase from Cellulophaga lytica. Phylogenetic tree analysis indicated that Cel5B belongs to the GH5_2 subfamily.
View Article and Find Full Text PDFBiosci Biotechnol Biochem
July 2025
Laboratory of Basic and Applied Molecular Biotechnology, Division of Food Science and Biotechnology, Graduate School of Agriculture, Kyoto University, Japan.
Acidic polysaccharides such as alginate, a key component of brown algae, have unique properties conferred by their carboxyl groups. Alginate is degraded by alginate lyases, a class of polysaccharide lyases (PLs) that cleave uronic acid glycoside bonds via β-elimination. These enzymes, which are classified into various PL families, differ in structure and substrate specificity but frequently share structural motifs including β-helices, β-jelly rolls, and (α/α)6 barrels coupled with antiparallel β-sheets.
View Article and Find Full Text PDFPrep Biochem Biotechnol
July 2025
School of Bioscience and Biotechnology, University of Jinan, Jinan, China.
A marine bacterial strain, sp. E, capable of producing alginate lyases, was isolated from seawater. Three alginate lyase genes from this strain were cloned and expressed in .
View Article and Find Full Text PDFEnhanced drug testing efficiency has driven the prominence of high-content and high-throughput screening (HCHTS) in drug discovery and development. However, traditional HCHTS in well-plates often lack complexity of in vivo conditions. 3D cell cultures, like cellular spheroids/organoids, offer a promising alternative by replicating in vivo conditions and improving the reliability of drug responses.
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