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Updated: Aug 18, 2026

Design and Use of a Low Cost, Automated Morbidostat for Adaptive Evolution of Bacteria Under Antibiotic Drug Selection
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On the origin of the DNA sequence selectivity of the azinomycins
Rachel C LePla1, Cyrille A S Landreau, Michael Shipman
1Department of Chemistry, University of Warwick, Coventry, UK CV4 7AL.
Abstract:
Simplified synthetic azinomycins preferentially induce in vitro DNA interstrand cross-links at the same 5'-d(GCC)-3' site as the natural products revealing that non-covalent interactions are relatively unimportant in defining sequence specificity.
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