Solid-state fermentation of brown seaweeds for the production of alginate lyase using marine bacterium Enterobacter tabaci RAU2C
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
KARE/VC/R&D/SMPG/2023-2024/01
Kalasalingam Academy of Research and Education
PubMed
38401040
DOI
10.1007/s12223-024-01150-7
PII: 10.1007/s12223-024-01150-7
Knihovny.cz E-zdroje
- Klíčová slova
- Enterobacter tabaci RAU2C, Alginate lyase, Seaweeds, Solid-state fermentation,
- MeSH
- algináty * metabolismus MeSH
- biomasa MeSH
- Enterobacter * metabolismus enzymologie izolace a purifikace růst a vývoj MeSH
- fermentace * MeSH
- koncentrace vodíkových iontů MeSH
- kyselina glukuronová metabolismus MeSH
- mořské řasy * mikrobiologie MeSH
- Phaeophyceae mikrobiologie MeSH
- polysacharid-lyasy * metabolismus MeSH
- Sargassum * mikrobiologie metabolismus MeSH
- teplota MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- algináty * MeSH
- kyselina glukuronová MeSH
- poly(beta-D-mannuronate) lyase MeSH Prohlížeč
- polysacharid-lyasy * MeSH
Alginate lyases have countless potential for application in industries and medicine particularly as an appealing biocatalyst for the production of biofuels and bioactive oligosaccharides. Solid-state fermentation (SSF) allows improved production of enzymes and consumes less energy compared to submerged fermentation. Seaweeds can serve as the most promising biomass for the production of biochemicals. Alginate present in the seaweed can be used by alginate lyase-producing bacteria to support growth and can secrete alginate lyase. In this perspective, the current study was directed on the bioprocessing of brown seaweeds for the production of alginate lyase using marine bacterial isolate. A novel alginate-degrading marine bacterium Enterobacter tabaci RAU2C which was previously isolated in the laboratory was used for the production of alginate lyase using Sargassum swartzii as a low-cost solid substrate. Process parameters such as inoculum incubation period and moisture content were optimized for alginate lyase production. SSF resulted in 33.56 U/mL of alginate lyase under the static condition maintained with 75% moisture after 4 days. Further, the effect of different buffers, pH, and temperature on alginate lyase activity was also analyzed. An increase in alginate lyase activity was observed with an increase in moisture content from 60 to 75%. Maximum enzyme activity was perceived with phosphate buffer at pH 7 and 37 °C. Further, the residual biomass after SSF could be employed as biofertilizer for plant growth promotion based on the preliminary analysis. To our knowledge, this is the first report stating the usage of seaweed biomass as a substrate for the production of alginate lyase using solid-state fermentation.
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