Streptomyces can produce a wealth of pharmaceutically valuable antibiotics and other bioactive compounds. Production of most antibiotics is generally low due to the rigorously controlled regulatory networks, in which global/pleiotropic and cluster-situated regulatory proteins coordinate with various intra- and extracellular signals. Thus, mining new antibiotic regulatory proteins, particularly the ones that are widespread, is essential for understanding the regulation of antibiotic biosynthesis. Here, in the biopesticide milbemycin producing strain Streptomyces bingchenggensis, a novel global/pleiotropic regulatory protein, SspH, a single domain protein containing only the HATPase domain, was identified as being involved in controlling antibiotic biosynthesis. The sspH overexpression inhibited milbemycin production by repressing the expression of milbemycin biosynthetic genes. The sspH overexpression also differentially influenced the expression of various antibiotic biosynthetic core genes. Site-directed mutagenesis revealed that the HATPase domain was essential for SspH’s function, and mutation of the conserved amino acid residues N54A and D84A led to the loss of SspH function. Moreover, cross-overexpression experiments showed that SspH and its orthologs, SCO1241 from Streptomyces coelicolor and SAVERM_07097 from Streptomyces avermitilis, shared identical functionality, and all exerted a positive effect on actinorhodin production but a negative effect on avermectin production, indicating that SspH-mediated differential control of antibiotic biosynthesis may be widespread in Streptomyces. This study extended our understanding of the regulatory network of antibiotic biosynthesis and provided effective targets for future antibiotic discovery and overproduction.

In this work, a stable silver nanoparticle (AgNPs) with strong surface plasmon resonance absorption (Abs) signals was synthesized using light-wave technology. In the absence of aptamers, AgNPs can aggregate in a given concentration of salt solution, resulting in significant changes in color. After adding the aptamer (Apt), it was observed that the aptamer can coordinate with AgNPs and adsorb on the surface of AgNPs, thereby maintaining the stability of the nanosol. In the presence of mercury ions (Hg²⁺), their high-affinity reaction with the aptamer compromised the latter’s protective effect on AgNPs, causing the color of the system to change again. Based on this, a simple and rapid new Abs method for detecting Hg²⁺ can be constructed. The linear range was 2.5 × 10⁻³–10.00 μmol/L, and the detection limit (DL) of the system was 2.03 nmol/L.