Self-entrapment of Azotobacter vinelandii cultures by gelation of their exopolysaccharides: A way towards next-generation bioinoculants
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
40399005
DOI
10.1016/j.carbpol.2025.123607
PII: S0144-8617(25)00388-1
Knihovny.cz E-resources
- Keywords
- Alginate, Azotobacter vinelandii, Bioinoculants, Hydrogels, Polyhydroxyalkanoates,
- MeSH
- Alginates * chemistry MeSH
- Azotobacter vinelandii * metabolism chemistry MeSH
- Polysaccharides, Bacterial * chemistry MeSH
- Phosphates metabolism MeSH
- Hydrogels * chemistry MeSH
- Indoleacetic Acids metabolism MeSH
- Calcium chemistry MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Alginates * MeSH
- Polysaccharides, Bacterial * MeSH
- Phosphates MeSH
- Hydrogels * MeSH
- indoleacetic acid MeSH Browser
- Indoleacetic Acids MeSH
- Calcium MeSH
Encapsulation of Plant Growth-Promoting Rhizobacteria (PGPR) in hydrogel carriers is a cutting-edge approach in developing agricultural bioinoculants, aiming to improve soil fertility and crop yield. Hydrogels provide protection against environmental stress, though traditional methods using external gel-forming agents limit economic viability. This study presents a novel approach, demonstrating the entrapment of Azotobacter vinelandii, a promising PGPR, within a gel matrix formed by Ca2+-induced crosslinking of its own exopolysaccharide, alginate. Among the five strains evaluated, A. vinelandii DSM 87, DSM 720, and DSM 13529 showed the highest alginate production, peaking at 4.9 ± 0.6 g/L, 3.5 ± 0.5 g/L, 3.8 ± 0.8 g/L, and enabling stable gel formation by the fourth day of cultivation. These strains also exhibited molecular weights and chemical structures of alginate suitable for effective gelation upon Ca2+addition. Additionally, these strains demonstrated significant plant growth-promoting activities, including indole acetic acid production (up to 10.5 μg/mL), siderophore release, and phosphate solubilization, further validating their potential for sustainable bioinoculant production. Finally, the viability of the A.vinelandii cells released from the gels was experimentally verified. Our findings support a feasible, cost-effective method for bioinoculant production that leverages A. vinelandii's intrinsic capabilities, offering a sustainable alternative to conventional agricultural practices.
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