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JBC, Vol. 252, Issue 20, 7023-7030, Oct, 1977
G. H. Yoakum and R. S. Cole
Removal of interstrand cross-linked from DNA was examined in Escherichia
coli permeabilized by treatment with toluene. Under these conditions, the
reaction requires ATP and Mg2+, and the mechanism appears to be similar to
that occurring in whole cells. Under optimum conditions, the rate constant
was 0.06 min-1. Genetical, physical, and biochemical analysis of the repair
process suggest the following mechanism. In an ATP-dependent reaction, the
uvrA and uvrB gene products cleave a phosphodiester bond on the 5' side of
one arm of the cross-link, producing a 3'-OH terminus. Subsequently, DNA
polymerase I (5'-3' exonuclease activity) makes a second strand cut on the
3' side of the cross-link in the same DNA strand, completing removal of the
covalent link between complementary strands. The second reaction did not
occur in a uvrD- strain, which had normal levels of DNA polymerizing
activity. The uvrD gene may regulate the specificity or activity of the
5'-3' exonuclease of DNA polymerase I in vivo.
Role of ATP in removal of psoralen cross-links from DNA of Escherichia coli permeabilized by treatment with toluene
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