The biological synthesis of nanoparticles (NPs) has attracted because of their non-toxic abilities.
We reported the synthesis of ZnO nanoparticles (ZnO NPs) via an extract of the Amycolatopsis roodepoortensis strain EA7.
ZnO nanoparticles (ZnO NPs) exhibited stronger antibacterial efficacy against clinical and standard Staphylococcus aureus (250 and 125 μg/mL) than Pseudomonas aeruginosa (500 μg/mL) by the MIC assay.
The anticancer effects of these nanoparticles (NPs) demonstrated a dose‒dependent relationship against HT-29, HEK-293, and HDF1BOM cell lines.
The IC 50 values were determined to be 47 , 32.88, and 81.37 μg/mL for the HT-29, HEK293, and HDF1BOM cell lines, respectively.
The biological synthesis of nanoparticles (NPs) has attracted because of their non-toxic abilities. We reported the synthesis of ZnO nanoparticles (ZnO NPs) via an extract of the Amycolatopsis roodepoortensis strain EA7. Their physical characteristics were investigated with XRD, FT-IR, SEM, TEM, DLS, EDX, and zeta potential analyses. The toxicity of nanoparticles (NPs) was investigated via antimicrobial and the MTT assays in the HT-29, HEK293, and HDF1BOM cell lines.The expression levels of genes related to apoptosis (ATM, ATR, CHK1, and CHK2), anti apoptose (MMP-9 and Bcl-2), cell death, and cell cycle distribution were determined in the HT-29 cell line. ZnO nanoparticles (ZnO NPs) exhibited stronger antibacterial efficacy against clinical and standard Staphylococcus aureus (250 and 125 μg/mL) than Pseudomonas aeruginosa (500 μg/mL) by the MIC assay. The anticancer effects of these nanoparticles (NPs) demonstrated a dose‒dependent relationship against HT-29, HEK-293, and HDF1BOM cell lines. The IC 50 values were determined to be 47 , 32.88, and 81.37 μg/mL for the HT-29, HEK293, and HDF1BOM cell lines, respectively. The levels of genes related to apoptosis (ATM = 2.35 ± 0.293, ATR = 2.87 ± 0.280, CHK1 = 3.67 ± 0.378, and CHK2 = 5.86 ± 0.495) were significantly increased compared to the control (P ≤ 0.0001). However, no significant decrease was observed in the expression of genes associated with cancer development. Flow-cytometric analysis revealed apoptosis induction (P ≤ 0.001) and cell cycle arrest in G0/G1 phase in the HT-29 cells. Given the results presented, this research could be an important step towards further investigations and the development of novel antimicrobial and anticancer therapeutics.