4.7 Article

Efficient Biosynthesis of Acidic/Lactonic Sophorolipids and Their Application in the Remediation of Cyanobacterial Harmful Algal Blooms

Journal

Publisher

MDPI
DOI: 10.3390/ijms241512389

Keywords

sophorolipids; Starmerella bombicola; metabolic engineering; cyanobacteria degradation; cyanobacterial harmful algal blooms

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Cyanobacterial harmful algal blooms (CyanoHABs) are a global threat to human health and natural ecosystems caused by water eutrophication, increased surface water temperature, and co-occurring microorganisms. This study constructed recombinant strains capable of producing acidic or lactonic sophorolipids (SLs) using the CRISPR-Cas9 gene editing system. The yields of acidic and lactonic SLs reached 53.64 g/L and 45.32 g/L, respectively. The addition of 5 mg/L lactonic SLs effectively degraded cyanobacteria within 30 min, and a specific ratio of lactonic to acidic SLs showed the highest degradation efficiency. This study offers a safe and promising solution for the treatment of CyanoHABs.
Cyanobacterial harmful algal blooms (CyanoHABs) pose significant threats to human health and natural ecosystems worldwide, primarily caused by water eutrophication, increased surface water temperature, and co-occurring microorganisms. Urgent action is needed to develop an eco-friendly solution to effectively curb the proliferation of CyanoHABs. Sophorolipids (SLs) are fully biodegradable biosurfactants synthesized by Starmerella bombicola. They can be classified into lactone and acid types. The lactone type displays strong antimicrobial activity, while the acid type exhibits good solubility, which make them ideal agents for mitigating CyanoHABs. Nevertheless, the broad utilization of SLs are hindered by their expensive production costs and the absence of effective genetic editing tools in the native host. In this study, we constructed recombinant strains capable of producing either acidic or lactonic SLs using the CRISPR-Cas9 gene editing system. The yields of acidic and lactonic SLs reached 53.64 g/L and 45.32 g/L in a shaking flask, respectively. In a 5 L fermenter, acidic SLs reached 129.7 g/L using low-cost glucose and rapeseed oil as substrates. The addition of 5 mg/L lactonic SLs effectively degraded cyanobacteria within 30 min, and a ratio of 8.25:1.75 of lactonic to acidic SLs showed the highest degradation efficiency. This study offers a safe and promising solution for CyanoHABs treatment.

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