A novel recombineering technique in Bacillus subtilis for producing anti-fusarium bioagents. Enables introduction of large biosynthetic gene clusters from environmental Bacillus isolates to combat fusarium fungal pathogens that cause major agricultural crop losses. Platform supports screening for novel antifungal activities and has potential for extension to Gram-negative rhizobacteria.
Fusarium fungal pathogens cause significant losses in agricultural crop yields worldwide. This project delivers a biological control solution by engineering plant beneficial bacteria with enhanced anti-fusarium activity. The team has isolated environmental Bacillus species exhibiting strong antifungal properties and developed a novel recombineering technique to transfer large biosynthetic gene clusters into a well-characterized Bacillus subtilis host strain. The resulting recombinant strains can be deployed directly as field-ready bioagents, offering a promising alternative to conventional chemical fungicides and labor-intensive screening of native isolates.
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The recombinant B. subtilis strains have been constructed and characterized for anti-fusarium activity in laboratory settings. Near-term validation includes promoter and transcription engineering to increase antifungal yield, in planta efficacy testing, and expanded screening of environmental DNA for novel antifungal activities. Collaboration with Dr. Godoy's group is underway to adapt the platform to a Gram-negative rhizobacterial host. The technology is at an early-to-mid stage of development, progressing toward field-ready bioagent formulations.
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