SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:ltu-68904"
 

Search: onr:"swepub:oai:DiVA.org:ltu-68904" > Tailoring the speci...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Antonopoulou, Io,1989-Luleå tekniska universitet,Kemiteknik (author)

Tailoring the specificity of the type C feruloyl esterase FoFaeC from Fusarium oxysporum towards methyl sinapate by rational redesign based on small molecule docking simulations

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018-05-24
  • Public Library of Science,2018
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:ltu-68904
  • https://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-68904URI
  • https://doi.org/10.1371/journal.pone.0198127DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

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

Notes

  • Validerad;2018;Nivå 2;2018-05-28 (andbra)
  • The type C feruloyl esterase FoFaeC from Fusarium oxysporum is a newly discovered enzyme with high potential for use in the hydrolysis of lignocellulosic biomass but it shows low activity towards sinapates. In this work, small molecule docking simulations were employed in order to identify important residues for the binding of the four model methyl esters of hydroxycinnamic acids, methyl ferulate/caffeate/sinapate/p-coumarate, to the predicted structure of FoFaeC. Subsequently rational redesign was applied to the enzyme’ active site in order to improve its specificity towards methyl sinapate. A double mutation (F230H/T202V) was considered to provide hydrophobic environment for stabilization of the methoxy substitution on sinapate and a larger binding pocket. Five mutant clones and the wild type were produced in Pichia pastoris and biochemically characterized. All clones showed improved activity, substrate affinity, catalytic efficiency and turnover rate compared to the wild type against methyl sinapate, with clone P13 showing a 5-fold improvement in catalytic efficiency. Although the affinity of all mutant clones was improved against the four model substrates, the catalytic efficiency and turnover rate decreased for the substrates containing a hydroxyl substitution.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Hunt, CameronLuleå tekniska universitet,Kemiteknik(Swepub:ltu)camhun (author)
  • Cerullo, GabriellaDepartment of Chemical Sciences, University of Naples "Federico II" (author)
  • Varriale, SimonaDepartment of Chemical Sciences, University of Naples “Federico II” (author)
  • Gerogianni, AlexandraLuleå tekniska universitet,Kemiteknik(Swepub:ltu)aleger (author)
  • Faraco, VincenzaDepartment of Chemical Sciences, University of Naples "Federico II" (author)
  • Rova, UlrikaLuleå tekniska universitet,Kemiteknik(Swepub:ltu)ulrok (author)
  • Christakopoulos, PaulLuleå tekniska universitet,Kemiteknik(Swepub:ltu)pauchr (author)
  • Luleå tekniska universitetKemiteknik (creator_code:org_t)

Related titles

  • In:PLOS ONE: Public Library of Science13:51932-6203

Internet link

Find in a library

  • PLOS ONE (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view