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  • Kazemi, MasoudStockholms universitet,Institutionen för organisk kemi (author)

Computational Study of Mycobacterium smegmatis Acyl Transferase Reaction Mechanism and Specificity

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018-10-09
  • American Chemical Society (ACS),2018
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:su-162978
  • https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-162978URI
  • https://doi.org/10.1021/acscatal.8b03360DOI

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  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • The acyl transferase from Mycobacterium smegmatis (MsAcT) catalyzes the acyl transfer between a range of primary and secondary alcohols, whereby its outstanding ability is to perform this reaction in aqueous solution. Therefore, MsAcT opens different options for acylation reactions enabling alternatives for many conventionally hydrolytic enzymes used in biocatalysis. Nevertheless, hydrolysis is still a major side reaction of this enzyme. To provide a detailed understanding of the competition between hydrolysis and transesterification reactions, a combination of density functional theory and free energy perturbation methods have been employed. The relative binding free energies and the energy profiles of the chemical steps involved in the reaction were calculated for a number of substrates. The calculations show that the enzyme active site exhibits a higher affinity for substrates with an aromatic ring. The rate-determining step corresponds to the collapse of a negatively charged tetrahedral intermediate in the substrate acylation half-reaction. The intrinsic barriers of the transesterification and hydrolysis half-reactions are calculated to be of similar heights, suggesting that the determining factor in the MsAcT specificity is the higher binding affinity of the active site for the alcohol substrates relative to water. Finally, the influence of the acyl donor on the MsAcT-catalyzed reaction is also investigated by considering different esters in the calculations.

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  • Sheng, XiangStockholms universitet,Institutionen för organisk kemi(Swepub:su)xshen (author)
  • Kroutil, Wolfgang (author)
  • Himo, FahmiStockholms universitet,Institutionen för organisk kemi(Swepub:su)himo (author)
  • Stockholms universitetInstitutionen för organisk kemi (creator_code:org_t)

Related titles

  • In:ACS Catalysis: American Chemical Society (ACS)8:11, s. 10698-107062155-5435

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Kazemi, Masoud
Sheng, Xiang
Kroutil, Wolfgan ...
Himo, Fahmi
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NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
and Organic Chemistr ...
Articles in the publication
ACS Catalysis
By the university
Stockholm University

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