Dissipative biocatalytic cascades and gated transient biocatalytic cascades driven by nucleic acid networks.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35522744.
- Also identified by DOI 10.1126/sciadv.abn3534 and PMC identifier 9075803.
- Licence recorded as CC BY-NC.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Living systems consist of complex transient cellular networks guiding structural, catalytic, and switchable functions driven by auxiliary triggers, such as chemical or light energy inputs. We introduce two different transient, dissipative, biocatalytic cascades, the coupled glucose oxidase (GOx)/horseradish peroxidase (HRP) glucose-driven oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS<sup>2-</sup>) to the radical anion (ABTS<sup>•-</sup>) and the lactate dehydrogenase (LDH)/nicotinamide adenine dinucleotide (NAD<sup>+</sup>) lactate-driven reduction of NAD<sup>+</sup> to NADH. The transient biocatalytic systems are driven by nucleic acid reaction modules using a nucleic acid fuel strand L<sub>1</sub>' and a nicking enzyme, Nt.BbvCI, as fuel-degrading catalyst, leading to the dynamic spatiotemporal transient formation of structurally proximate biocatalysts activating the biocatalytic cascades and transient coupled processes, including the generation of chemiluminescence and the synthesis of alanine. Subjecting the mixture of biocatalysts to selective inhibitors allows the gated transient operation of the biocatalysts. The kinetics of transient biocatalytic cascades are accompanied by kinetic models and computational simulations.