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Ultralight Ultrafast Enzymes.

Authors :
Zhang X
Meng Z
Beusch CM
Gharibi H
Cheng Q
Lyu H
Di Stefano L
Wang J
Saei AA
Végvári Á
Gaetani M
Zubarev RA
Source :
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2024 Jan 15; Vol. 63 (3), pp. e202316488. Date of Electronic Publication: 2023 Dec 07.
Publication Year :
2024

Abstract

Inorganic materials depleted of heavy stable isotopes are known to deviate strongly in some physicochemical properties from their isotopically natural counterparts. Here we explored for the first time the effect of simultaneous depletion of the heavy carbon, hydrogen, oxygen and nitrogen isotopes on the bacterium E. coli and the enzymes expressed in it. Bacteria showed faster growth, with most proteins exhibiting higher thermal stability, while for recombinant enzymes expressed in depleted media, faster kinetics was discovered. At room temperature, luciferase, thioredoxin and dihydrofolate reductase and Pfu DNA polymerase showed up to a 250 % increase in activity compared to the native counterparts, with an additional ∼50 % increase at 10 °C. Diminished conformational and vibrational entropy is hypothesized to be the cause of the accelerated kinetics. Ultralight enzymes may find an application where extreme reaction rates are required.<br /> (© 2023 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1521-3773
Volume :
63
Issue :
3
Database :
MEDLINE
Journal :
Angewandte Chemie (International ed. in English)
Publication Type :
Academic Journal
Accession number :
38009610
Full Text :
https://doi.org/10.1002/anie.202316488