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E. coliBW25113 cells transformed with either the pBR322 empty vector or either the two pBR322-based plasmids driving the expression of the TAC operons under the control of the constitutive Ptetpromoter were challenged with 10-fold serial dilutions of BASEL23 and common laboratory coliphages. Selected phages that were countered by one or other of the TAC systems tested.
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