Insights into the Function of the N -Acetyltransferase SatA That Detoxifies Streptothricin in Bacillus subtilis and Bacillus anthracis .
| Autor: | Burckhardt RM; Department of Microbiology, University of Georgia, Athens, Georgia, USA., Escalante-Semerena JC; Department of Microbiology, University of Georgia, Athens, Georgia, USA jcescala@uga.edu. |
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| Jazyk: | angličtina |
| Zdroj: | Applied and environmental microbiology [Appl Environ Microbiol] 2019 Mar 06; Vol. 85 (6). Date of Electronic Publication: 2019 Mar 06 (Print Publication: 2019). |
| DOI: | 10.1128/AEM.03029-18 |
| Abstrakt: | Acylation of epsilon amino groups of lysyl side chains is a widespread modification of proteins and small molecules in cells of all three domains of life. Recently, we showed that Bacillus subtilis and Bacillus anthracis encode the GCN5-related N -acetyltransferase (GNAT) SatA that can acetylate and inactivate streptothricin, which is a broad-spectrum antibiotic produced by actinomycetes in the soil. To determine functionally relevant residues of B. subtilis SatA ( Bs SatA), a mutational screen was performed, highlighting the importance of a conserved area near the C terminus. Upon inspection of the crystal structure of the B. anthracis Ames SatA ( Ba SatA; PDB entry 3PP9), this area appears to form a pocket with multiple conserved aromatic residues; we hypothesized this region contains the streptothricin-binding site. Chemical and site-directed mutagenesis was used to introduce missense mutations into satA , and the functionality of the variants was assessed using a heterologous host ( Salmonella enterica ). Results of isothermal titration calorimetry experiments showed that residue Y164 of Ba SatA was important for binding streptothricin. Results of size exclusion chromatography analyses showed that residue D160 was important for dimerization. Together, these data advance our understanding of how SatA interacts with streptothricin. IMPORTANCE This work provides insights into how an abundant antibiotic found in soil is bound to the enzyme that inactivates it. This work identifies residues for the binding of the antibiotic and probes the contributions of substituting side chains for those in the native protein, providing information regarding hydrophobicity, size, and flexibility of the antibiotic binding site. (Copyright © 2019 American Society for Microbiology.) |
| Databáze: | MEDLINE |
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