TY - JOUR
T1 - Phenotypic and reversion analysis of a Salmonella typhimurium constructed to have an arginine codon at the hisG46 missense codon
AU - Kelvin Miller, Judith
AU - Barnes, Wayne M.
N1 - Funding Information:
This work was supported by National Institutes of Health grant GM24956 to W.M.B., who acknowledges Faculty Research support from the American Cancer Society. J.K.M. received support from the Division of Biology and Biomedical sciences, Washington University, and from the Training Program in Cellular and Molecular Biology, National Institutes of Health GM 07067.
PY - 1988/9
Y1 - 1988/9
N2 - Of the 6 single-base mutations that would be predicted to change the missense mutation hisG46 away from a proline codon in the Salmonella/microsome mutagen selection assay for histidine-independent revertants, only 5 have been observed. We have used site-specific mutagenesis to make the unobserved mutant [CCC (proline) → CGC (arginine)] codon in the Salmonella genome. Experiments with this arginine mutant demonstrate that, like bacteria containing the hisG46 mutation, bacteria with the arginine missense mutation are histidine auxotrophs which are capable of reversion to histidine independence. However, unlike the ATP phosphoribosyltransferase coded by the hisG46 hisG gene (with a proline), the arginine mutant enzyme is partially active. This is indicated by a histidine-independent phenotype when the arginine hisG gene is present in multiple copies.
AB - Of the 6 single-base mutations that would be predicted to change the missense mutation hisG46 away from a proline codon in the Salmonella/microsome mutagen selection assay for histidine-independent revertants, only 5 have been observed. We have used site-specific mutagenesis to make the unobserved mutant [CCC (proline) → CGC (arginine)] codon in the Salmonella genome. Experiments with this arginine mutant demonstrate that, like bacteria containing the hisG46 mutation, bacteria with the arginine missense mutation are histidine auxotrophs which are capable of reversion to histidine independence. However, unlike the ATP phosphoribosyltransferase coded by the hisG46 hisG gene (with a proline), the arginine mutant enzyme is partially active. This is indicated by a histidine-independent phenotype when the arginine hisG gene is present in multiple copies.
KW - Arginine codon
KW - HisG46 missense codon
KW - Histidine-independent revertants
KW - Salmonella typhimurium, phenotypic and reversion analysis
UR - http://www.scopus.com/inward/record.url?scp=0023715971&partnerID=8YFLogxK
U2 - 10.1016/0027-5107(88)90125-X
DO - 10.1016/0027-5107(88)90125-X
M3 - Article
C2 - 3047572
AN - SCOPUS:0023715971
SN - 0027-5107
VL - 201
SP - 189
EP - 194
JO - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
JF - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
IS - 1
ER -