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A mutant LexA repressor harboring a cleavage motif cysteine‐glycine remains inducible
[摘要]

Using site-directed mutagenesis of the lexA gene we have changed the amino acid Ala-84 of the LexA repressor for a cysteine. The reason for this change was the striking homology between LexA and UmuD and the comparable size of the two amino acid side chains. Using an in vivo repression/induction assay it is shown that the LexA-Cys-84 mutant remains inducible by mitomycin C and UV irradiation essentially in the same way as the wild-type repressor.

[发布日期]  [发布机构] 
[效力级别]  [学科分类] 生物化学/生物物理
[关键词] LexA repressor;UmuD protein;SOS induction;Genotoxic agent;Site-directed mutagenesis [时效性] 
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