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J Bacteriol. 1968 July; 96(1): 146-153
Copyright © 1968 American Society for Microbiology. All Rights Reserved.

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

Microbial Genetics in the School of Biology, The University of Sussex, Brighton, Sussex, England
Biophysics Department, The Pennsylvania State University, University Park, Pennsylvania 16802

ABSTRACT

Previously, arginine revertants of Escherichia coli WWU, a derivative of E. 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 defining normal revertants and a thin, irregular line defining aberrant 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.

¹ Present address: Microbiology Department, Indiana University Medical School, Indianapolis 46202.

² Present address: Biological Laboratories, Harvard University, Cambridge, Mass. 02138.