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Previously, arginine revertants ofEscherichia coli WWU, a derivative ofE. coli 15T− , have been subdivided by two independent methods: (i) the streak morphology on nutrient agar, and (ii) the pattern of phage growth using amber and ochre mutants of bacteriophage T4. In the first assay, revertants were subdivided into two classes according to the appearance of streaks after incubation on nutrient agar, a thick, even line of growth definingnormal revertants and a thin, irregular line definingaberrant revertants. In the second assay, revertants were classified by the suppressors they contained. The present work demonstrates that revertants containing an amber suppressor show the aberrant morphology and are also able to catabolize thymidine for energy and carbon. This is in contrast to the parent WWU containing no suppressor, which shows a normal morphology and cannot utilize thymidine as an energy source. Revertants containing no suppressor, isolated specifically for their ability to catabolize thymidine, show an aberrant morphology. Together, these results indicate that the aberrant morphology results from suppression of an amber triplet in a gene of the thymidine catabolic pathway. Enzyme assays show the amber triplet to be in the gene specifying deoxyribomutase. It is suggested that the aberrant arginine revertants are analogous to high thymine-requiring mutants and that, in general, high and low thymine-requiring mutants differ from one another in their ability to catabolize deoxyribose-1-phosphate.

journal of bacteriology

Nonsense Suppression in a Multiauxotrophic Derivative of <i>Escherichia coli</i> 15T <sup>−</sup> : Identification and Consequences of an Amber Triplet in the Deoxyribomutase Gene

Nonsense Suppression in a Multiauxotrophic Derivative of Escherichia coli 15T − : Identification and Consequences of an Amber Triplet in the Deoxyribomutase Gene

Nonsense Suppression in a Multiauxotrophic Derivative of Escherichia coli 15T ⁻ : Identification and Consequences of an Amber Triplet in the Deoxyribomutase Gene