4.7 Article

Cost-effective production of alginate oligosaccharides from Laminaria japonica roots by Pseudoalteromonas agarivorans A3

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MICROBIAL CELL FACTORIES
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12934-023-02170-7

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Alginate oligosaccharides; Pseudoalteromonas; Laminaria japonica; Fermentation; Alginate lyase

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An efficient and cost-effective process for the production of alginate oligosaccharides (AOs) directly from Laminaria japonica roots was established using the strain Pseudoalteromonas agarivorans A3. The study showed that A3 could secrete alginate lyases to degrade L. japonica, and by optimizing the production and hydrolysis parameters, AOs were efficiently produced from the fermentation broth supernatant. The generated AOs had a wide range in size and showed potential for industrial and agricultural applications.
Background Alginate oligosaccharides (AOs) are the degradation products of alginate, a natural polysaccharide abundant in brown algae. AOs generated by enzymatic hydrolysis have diverse bioactivities and show broad application potentials. AOs production via enzymolysis is now generally with sodium alginate as the raw material, which is chemically extracted from brown algae. In contrast, AOs production by direct degradation of brown algae is more advantageous on account of its cost reduction and is more eco-friendly. However, there have been only a few attempts reported in AOs production from direct degradation of brown algae. Results In this study, an efficient Laminaria japonica-decomposing strain Pseudoalteromonas agarivorans A3 was screened. Based on the secretome and mass spectrum analyses, strain A3 showed the potential as a cell factory for AOs production by secreting alginate lyases to directly degrade L. japonica. By using the L. japonica roots, which are normally discarded in the food industry, as the raw material for both fermentation and enzymatic hydrolysis, AOs were produced by the fermentation broth supernatant of strain A3 after optimization of the alginate lyase production and hydrolysis parameters. The generated AOs mainly ranged from dimers to tetramers, among which trimers and tetramers were predominant. The degradation efficiency of the roots reached 54.58%, the AOs production was 33.11%, and the AOs purity was 85.03%. Conclusion An efficient, cost-effective and green process for AOs production directly from the underutilized L. japonica roots by using strain A3 was set up, which differed from the reported processes in terms of the substrate and strain used for fermentation and the AOs composition. This study provides a promising platform for scalable production of AOs, which may have application potentials in industry and agriculture.

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