6-O-Nucleotidyltransferase: an aminoglycoside-modifying enzyme specific for streptomycin/streptidine. Issue 1 (23rd November 2015)

• Record Type: Journal Article
• Authors: Latorre, Montserrat; Revuelta, Julia; García-Junceda, Eduardo; Bastida, Agatha
• Is Part Of: MedChemComm. Volume 7:Issue 1(2016:Jan.)
• Page Start: 177
• Page End: 183
• Publication Date: 2015-11-23
• Subjects: Pharmaceutical chemistry -- Periodicals; 615.19
• DOI: 10.1039/c5md00496a
• Languages: English
• ISSNs: 2040-2503

Abstract

Abstract : ANT(6) has a narrow tolerance to chemical variations in the aminoglycoside/nucleotide, making it very useful in the design of non-inactivable derivatives. Abstract : Aminoglycosides are especially useful for the treatment of hospital-acquired infections. The main problem for the application of these antibiotics is the presence of bacterial resistance enzymes, in particular, nucleotidyltransferases (ANTs). These enzymes catalyze the transfer of an adenylyl group from the MgATP complex to different positions of the antibiotic. To understand the mechanisms that lead to antibiotic inactivation, we have performed a comprehensive experimental analysis of one of those enzymes. The 6- O - nucleotidyltransferase enzyme (ANT(6)) from Bacillus subtilis was cloned, overexpressed and purified in E. coli . The kinetic parameters revealed a narrow specificity of the ANT(6) for MgATP/streptomycin as substrates. The binding epitope of the streptomycin recognized by the ANT(6) is the streptidine moiety. Therefore, the use of streptidine as a "decoy acceptor" allows the recovery of the antibiotic activity of streptomycin E. coli cells that are overexpressing the ANT(6).