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A New Na<sup>+</sup>‐Dependent RNA‐Cleaving DNAzyme with over 1000‐fold Rate Acceleration by Ethanol
76
Citations
34
References
2015
Year
GeneticsMolecular BiologyMolecular GeneticsRate AccelerationTranscriptional RegulationNucleic Acid ChemistryOrganic SolventsBiochemical EngineeringAnalytical ChemistryAlcohol DehydrogenasesRna ProcessingBiochemistryRna BiologyDna ReplicationOligonucleotideGene ExpressionNatural SciencesEnzyme CatalysisNucleic Acid BiochemistryConcentrated Organic SolventsMedicineNon-coding Rna
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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