Related Experiment Video
Updated: May 4, 2026

Genetic Manipulation in Δku80 Strains for Functional Genomic Analysis of Toxoplasma gondii
Published on: July 12, 2013
Insertions, deletions and mismatches in heteroduplex DNA made by recA protein
Abstract:
E. coli recA protein promotes the pairing of circular single strands with linear duplex DNA and the subsequent formation of large heteroduplex joints. From fd and M13 DNA, recA protein can make heteroduplex joints that include every kind of single base-pair mismatch. Aided by E. coli single-strand binding protein (SSB) and ATP regeneration, recA protein can incorporate into heteroduplex DNA insertions that are hundreds of base pairs long, whether the extra DNA is located initially in either the single-stranded or the double-stranded substrate. The ability of recA protein to span large insertions in the duplex DNA indicates that it unwinds a sizeable number of turns in advance of the growing heteroduplex joint. These observations show that an enzymatic basis exists in E. coli for forming extensively mismatched heteroduplex DNA, which might be involved in conversion-like events associated with recombination.
Related Concept Videos
Nucleotide Excision Repair
Homologous Recombination
Gene Conversion
Conservative Site-specific Recombination and Phase Variation
The recognition sites for Cre recombinase called LoxP...
Restriction Enzymes
The host bacteria protect their own genomic DNA from these enzymes by methylating these sites. Some...
Nucleotide Excision Repair
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...

