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Bicarbonate inhibition of carbonic anhydrase mimics hinders catalytic efficiency: Elucidating the mechanism and gaining insight toward improving speed and efficiency
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ACS Catalysis manuscript - carbonic anhydrase mimics FINAL 12.10.18.docx | Accepted version | 1.07 MB | Microsoft Word | View/Open |
Title: | Bicarbonate inhibition of carbonic anhydrase mimics hinders catalytic efficiency: Elucidating the mechanism and gaining insight toward improving speed and efficiency |
Authors: | Rains, JGD O’Donnelly, K Oliver, T Woscholski, R Long, NJ Barter, LMC |
Item Type: | Journal Article |
Abstract: | Carbonic anhydrase (CA) mimics are often studied with a focus on the hydration of CO2 for atmospheric carbon capture. Consequently, the reverse reaction (dehydration of HCO3–) has received minimal attention, so much so that the rate-limiting step of the dehydration reaction in CA mimics is currently unknown. The rate-limiting step of the hydration reaction is reported to be the bicarbonate-bound intermediate step, and thus is susceptible to product inhibition. It is not, however, clear if this inhibition is a consequence of an increase in the rate of the competing dehydration reaction or resulting from the strong affinity of bicarbonate to the mimic. To address this, insight into the dehydration reaction kinetics is needed. We therefore report the most comprehensive study of a CA mimic to date. The dehydration profile of the fastest small-molecule CA mimic, ZnL1S, was characterized, and consequently evidence for the rate-limiting step for the dehydration reaction was seen to be the bicarbonate-bound intermediate step, much like the hydration reaction. This experimental validation of the rate-limiting step was achieved through a variety of methods including NMR experiments and the effect of inhibitors, substrate concentration, and metal center on activity. With this understanding, an improvement in the favorability of the rate-limiting step was achieved, resulting in decreased bicarbonate inhibition. Thus, an increase in the mimic’s kcat for both reactions was observed, resulting in the largest rate constants of any small-molecule CA mimic reported to date (28 093 and 579 M–1 s–1 for hydration and dehydration, respectively). Enzyme-like kcat/km values were obtained for ZnL1S (5.9 × 105 M–1 s–1 for CO2 hydration), and notably there is only a difference of 2.5 orders of magnitude from the enzyme, the closest of any CA mimic reported in the literature. The results from this work can be applied to the development and improvement of future and existing mimics toward attaining increased activities. |
Issue Date: | 1-Feb-2019 |
Date of Acceptance: | 3-Jan-2019 |
URI: | http://hdl.handle.net/10044/1/66624 |
DOI: | 10.1021/acscatal.8b04077 |
ISSN: | 2155-5435 |
Publisher: | American Chemical Society (ACS) |
Start Page: | 1353 |
End Page: | 1365 |
Journal / Book Title: | ACS Catalysis |
Volume: | 9 |
Issue: | 2 |
Copyright Statement: | © 2019 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, after peer review and technical editing by the publisher. To access the final edited and published work see https://dx.doi.org/10.1021/acscatal.8b04077 |
Sponsor/Funder: | Engineering & Physical Science Research Council (E |
Funder's Grant Number: | EP/I037180/1 |
Keywords: | Science & Technology Physical Sciences Chemistry, Physical Chemistry carbonic anhydrase biomimetic HCO3- dehydration CO2 hydration rate-limiting step stopped-flow METAL-ORGANIC FRAMEWORKS CO2 HYDRATION ZINC(II) COMPLEXES SMALL-MOLECULE ACTIVE-SITE MODEL DEHYDRATION DIOXIDE CAPTURE KINETICS 0302 Inorganic Chemistry 0305 Organic Chemistry 0904 Chemical Engineering |
Publication Status: | Published |
Online Publication Date: | 2019-01-03 |
Appears in Collections: | Chemistry Biological and Biophysical Chemistry Catalysis and Advanced Materials Faculty of Natural Sciences |