Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2049774 | FEBS Letters | 2009 | 6 Pages |
Abstract
We have studied the naturally split αα subunit of the DNA polymerase III (DnaE) intein from Nostoc punctiforme PCC73102 (Npu) using purified proteins and determined an apparent first-order rate constant of (1.1±0.2)×10-2(1.1±0.2)×10-2 s−1 at 37 °C. This represents the highest rate reported for the protein trans -splicing reaction so far (t1/2t1/2 of ∼∼ 60 s). Furthermore, the reaction was very robust and high-yielding with respect to different extein sequences, temperatures from 6 to 37 °C, and the presence of up to 6 M urea. Given these outstanding properties, the Npu DnaE intein appears to be the intein of choice for many applications in protein and cellular chemistry.
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Authors
Joachim Zettler, Vivien Schütz, Henning D. Mootz,