Macromolecular crowding potently stimulates DNA supercoiling activity of Mycobacterium tuberculosis DNA gyrase.

Mtb DNA gyrase PEG PVA excluded volume macromolecular crowding molecular dynamics simulation water activity

Journal

The Journal of biological chemistry
ISSN: 1083-351X
Titre abrégé: J Biol Chem
Pays: United States
ID NLM: 2985121R

Informations de publication

Date de publication:
07 Nov 2023
Historique:
received: 15 09 2023
revised: 19 10 2023
accepted: 30 10 2023
pubmed: 10 11 2023
medline: 10 11 2023
entrez: 9 11 2023
Statut: aheadofprint

Résumé

Macromolecular crowding, manifested by high concentrations of proteins and nucleic acids in living cells, significantly influences biological processes such as enzymatic reactions. Studying these reactions in vitro, using agents such as polyetthylene glycols (PEGs) and polyvinyl alcohols (PVAs) to mimic intracellular crowding conditions, is essential due to the notable differences from enzyme behaviors observed in diluted aqueous solutions. In this article, we studied Mycobacterium tuberculosis (Mtb) DNA gyrase under macromolecular crowding conditions by incorporating PEGs and PVAs into the DNA supercoiling reactions. We discovered that high concentrations of potassium glutamate, glycine betaine, PEGs, and PVA substantially stimulated the DNA supercoiling activity of Mtb DNA gyrase. Steady-state kinetic studies showed that glycine betaine and PEG400 significantly reduced the K

Identifiants

pubmed: 37944619
pii: S0021-9258(23)02467-5
doi: 10.1016/j.jbc.2023.105439
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105439

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that they have no conflicts of interest with the contents of this article.

Auteurs

Zifang Deng (Z)

Biomolecular Science Institute, Florida International University, Miami, Florida, USA; Department of Chemistry & Biochemistry, Florida International University, Miami, Florida, USA.

Prem Chapagain (P)

Biomolecular Science Institute, Florida International University, Miami, Florida, USA; Department of Physics, Florida International University, Miami, Florida, USA.

Fenfei Leng (F)

Biomolecular Science Institute, Florida International University, Miami, Florida, USA; Department of Chemistry & Biochemistry, Florida International University, Miami, Florida, USA. Electronic address: lengf@fiu.edu.

Classifications MeSH