PROMOTERS OF THE PHR GENE IN ESCHERICHIA-COLI K-12

被引:3
作者
MA, CP [1 ]
RUPERT, CS [1 ]
机构
[1] UNIV TEXAS,PROGRAM MOLEC & CELL BIOL,RICHARDSON,TX 75083
来源
MOLECULAR & GENERAL GENETICS | 1995年 / 248卷 / 01期
关键词
PHL; PHOTOLYASE; DNA REPAIR; SULA;
D O I
10.1007/BF02456613
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have identified two promoters of the Escherichia coli phl gene by DNA deletion mapping, S1 mapping of transcripts and sequence homology. The weaker promoter, P2, located approximately 530 bp upstream from the start codon, extends beyond the previously known nucleotide sequence. The stronger, P1, lies 90 bp from the gene and is distinct from three previously described promoter-like sequences nearby. beta-Galactosidase production from a plasmid-borne gene, promoted by a synthetic copy of P1, increases after DNA damage, but the increase does not depend on the SOS-box-like sequences normally present in the vicinity of P1. Induction still requires intact recA and lexA genes, and also intact sulA.
引用
收藏
页码:52 / 58
页数:7
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