4.4 Article

A New Na+-Dependent RNA-Cleaving DNAzyme with over 1000-fold Rate Acceleration by Ethanol

Journal

CHEMBIOCHEM
Volume 17, Issue 2, Pages 159-163

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201500603

Keywords

biosensors; DNAzymes; organic solvents; RNA cleavage; sodium

Funding

  1. University of Waterloo
  2. Natural Sciences and Engineering Research Council of Canada (NSERC)
  3. Foundation for Shenghua Scholar of Central South University
  4. National Natural Science Foundation of China [21301195]
  5. China Scholarship Council (CSC) [201406370116]

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Enzymes working in organic solvents are important for analytical chemistry, catalysis, and mechanistic studies. Although a few protein enzymes are highly active in organic solvents, little is known regarding nucleic acid-based enzymes. Herein, we report the first RNA-cleaving DNAzyme, named EtNa, that works optimally in concentrated organic solvents containing only monovalent Na+. The EtNa DNAzyme has a rate of 2.0 h(-1) in 54% ethanol (with 120 mm NaCl and no divalent metal ions), and a Kd of 21 mm Na+. It retains activity even in 72% ethanol as well as in DMSO. With 4 mm Na+, the rate in 54% ethanol is >1000-fold higher than that in water. We also demonstrated the use of EtNa to measuring the ethanol content in alcoholic drinks. In total, this DNAzyme has three unique features: divalent metal independent activity, Na+ selectivity among monovalent metals, and acceleration by organic solvents.

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