Related Experiment Video
Updated: Aug 19, 2026

Studying DNA Looping by Single-Molecule FRET
Published on: June 28, 2014
DNA enzymology above 100 degrees C. Topoisomerase V unlinks circular DNA at 80-122 degrees C
S A Kozyavkin1, A V Pushkin, F A Eiserling
1Laboratory of Molecular Biology, NIDDK, National Institutes of Health, Bethesda, Maryland, 20892-0540, USA.
Abstract:
The widespread application of polymerase chain reaction and related techniques in biology and medicine has led to a heightened interest in thermophilic enzymes of DNA metabolism. Some of these enzymes are stable for hours at 100 degrees C, but no enzymatic activity on duplex DNA at temperatures above 100 degrees C has so far been demonstrated. Recently, we isolated topoisomerase V from the hyperthermophile Methanopyrus kandleri, which grows up to 110 degrees C. This novel enzyme is similar to eukaryotic topoisomerase I and acts on duplex DNA regions. We now show that topoisomerase V catalyzes the unlinking of double-stranded circular DNA at temperatures up to 122 degrees C. In this in vitro system, maximal DNA unlinking occurs at 108 degrees C and corresponds to complementary strands being linked at most once. These results further imply that in the presence of sufficient positive supercoiling DNA can exist as a double helix even at 122 degrees C.
Related Concept Videos
Proofreading
DNA Helicases
DNA Topoisomerases
Types and Mechanism of action
Topoisomerases are divided into two main types. Type I...
Translesion DNA Polymerases
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
Conservative Site-specific Recombination and Phase Variation
The recognition sites for Cre recombinase called LoxP...
Proofreading
Errors During Replication are Corrected by the DNA Polymerase Enzyme

