Centro di Endocrinologia ed Oncologia Sperimentale del CNR, II Istituto di Patologia Generale, 2a Facoltà di Medicina, Via Sergio Pansini 5, 80131, Naples, Italy
Laboratory of Chemical Biology, National Institute of Arthritis, Metabolism and Digestive Diseases, Bethesda, Maryland 20014
ABSTRACT
The defective prophage
80i
cI857dhis has been mapped through both marker rescue and deletion analysis. Deletions have been isolated which put residual his genes close to trp genes. Analysis of these deletions shows that the histidine operon on the prophage is oriented clockwise as on the bacterial chromosome, thus opposite to the orientation of the trp operon. The presence of the his promoter-operator region is inferred by the ability of the prophage-carrying strain to derepress sequentially under conditions in which the histidine concentration is limiting. In addition to his, the gnd gene is also present on the prophage and is located between his and trp operons. The bacterial genes are inserted in the right arm of the prophage and substitute for all of the late function genes, except for the first three. These data indicate that the "sense" strand for transcription of the his operon in vivo must be the "R" strand.
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