The filamentous fungus Aspergillus niger is widely employed in the production of citric acid and some industrial enzymes such as phytase, glucoamylase, and glucose oxidase. Currently, several genetic modification tools have been developed and applied to this fungal species. However, the RNA silencing technique is less used for A. niger. In the present study, an RNA silencing binary vector integrated with the Gateway recombination cloning technology was evaluated in A. niger. The integration of Gateway recombination cloning technology in binary vectors for rapid generation of hairpin RNA structure allowed the assessment of inhibition of target gene expression through mRNA degradation. The RNA silencing constructs were successfully transferred into A. nigervia Agrobacterium tumefaciens. Results showed that the RNA silencing vectors were effective in downregulating the expression of the DsRed fluorescent reporter gene and the stuA regulatory gene. Interestingly, the silenced mutants of stuA exhibited a significant reduction in fungal sporulation. This finding revealed that the RNA silencing technique with the examined Gateway binary vector represents a potential genetic tool for functional studies of target genes in A. niger.

Cordyceps militaris is a valuable medicinal mushroom that contains numerous bioactive ingredients such as cordycepin, adenosine, pentostatin, polysaccharides, and carotenoids. However, the contents of these substances in wild-type strains of C. militaris are relatively low. Recently, the genome of C. militaris has been fully sequenced, and genes involved in the biosynthesis of beneficial constituents have been identified. Therefore, research on enhancing the biosynthesis of the bioactive compounds in this fungus by recombinant DNA technology has advantages. In the present study, the authors have successfully generated a binary vector with a T-DNA region carrying a construct regulated by the native rpb1 promoter that can enhance gene expression in C. militaris. The T-DNA structure from the binary vector was then transferred into the C. militaris genome by Agrobacterium tumefaciens-mediated transformation. Analysis of some fungal transformants by PCR using the specific primer pairs indicated that the T-DNA structure was successfully integrated into the fungal genome. Observation of the transformants under fluorescence microscopy confirmed the overexpression of the DsRed fluorescent protein under the regulation of the rpb1promoter. The binary vector carrying the rpb1 promoter constructed in this study can be employed to promote the expression of target genes in the medicinal mushroom C. militaris.