Here, we report a distinct approach for regulating the substrate specificity of enzymes immobilized in microgels by a phase transition in polymer networks. The finding is demonstrated on glucose oxidase that is immobilized in thermoresponsive poly(N-isopropylacrylamide)-based microgels. Laser light scattering and enzymatic oxidation tests indicate that the broadened specificity appears at low temperatures, at which the gel matrix is in the relatively swollen state relative to its state at microgel synthesis temperature; upon heating to the relative higher temperatures, the gel matrix is not able to shrink further that offers a tight space in which the enzyme resides to retain high glucose specificity. It is proposed that polymer phase transition in the gel matrix mainly alter protein gates that control passage of substrates into active sites, making them open or close to a certain extent that enable reversible regulating the substrate specificity. The finding is also observed on bulk gels under a rational design, making it of potential interest in enzymatic biofuel cell applications.
Pyridinium-containing
polyheterocycles exhibit distinctive biological
properties and interesting electrochemical and optical properties
and thus are widely used as drugs, functional materials, and photocatalysts.
Here, we describe a unified two-step strategy by merging Rh-catalyzed
C–H vinylation with two switchable electrocyclizations, including
aza-6π-electrocyclization and all-carbon-6π-electrocyclization,
for rapid and divergent access to dihydropyridoisoquinoliniums and
dihydrobenzoquinolines. Through computation, the high selectivity
of aza-electrocyclization in the presence of an appropriate “HCl”
source under either thermal conditions or photochemical conditions
is shown to result from the favorable kinetics and symmetries of frontier
orbitals. We further demonstrated the value of this protocol by the
synthesis of several complex pyridinium-containing polyheterocycles,
including the two alkaloids berberine and chelerythrine.
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