Your browser doesn't support javascript.
loading
A dual cellular-heterogeneous catalyst strategy for the production of olefins from glucose.
Wang, Zhen Q; Song, Heng; Koleski, Edward J; Hara, Noritaka; Park, Dae Sung; Kumar, Gaurav; Min, Yejin; Dauenhauer, Paul J; Chang, Michelle C Y.
Affiliation
  • Wang ZQ; Department of Chemistry, University of California, Berkeley, Berkeley, CA, USA. zhenw@buffalo.edu.
  • Song H; Department of Biological Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA. zhenw@buffalo.edu.
  • Koleski EJ; Department of Chemistry, University of California, Berkeley, Berkeley, CA, USA.
  • Hara N; College of Chemistry & Molecular Science, Wuhan University, Wuhan, P. R. China.
  • Park DS; Department of Chemistry, University of California, Berkeley, Berkeley, CA, USA.
  • Kumar G; Department of Chemistry, University of California, Berkeley, Berkeley, CA, USA.
  • Min Y; Department of Chemical Engineering & Materials Science, University of Minnesota, Minneapolis, MN, USA.
  • Dauenhauer PJ; Korea Research Institute of Chemical Technology, Daejeon, South Korea.
  • Chang MCY; Department of Chemical Engineering & Materials Science, University of Minnesota, Minneapolis, MN, USA.
Nat Chem ; 13(12): 1178-1185, 2021 12.
Article de En | MEDLINE | ID: mdl-34811478
ABSTRACT
Living systems provide a promising approach to chemical synthesis, having been optimized by evolution to convert renewable carbon sources, such as glucose, into an enormous range of small molecules. However, a large number of synthetic structures can still be difficult to obtain solely from cells, such as unsubstituted hydrocarbons. In this work, we demonstrate the use of a dual cellular-heterogeneous catalytic strategy to produce olefins from glucose using a selective hydrolase to generate an activated intermediate that is readily deoxygenated. Using a new family of iterative thiolase enzymes, we genetically engineered a microbial strain that produces 4.3 ± 0.4 g l-1 of fatty acid from glucose with 86% captured as 3-hydroxyoctanoic and 3-hydroxydecanoic acids. This 3-hydroxy substituent serves as a leaving group that enables heterogeneous tandem decarboxylation-dehydration routes to olefinic products on Lewis acidic catalysts without the additional redox input required for enzymatic or chemical deoxygenation of simple fatty acids.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Alcènes / Acides gras / Glucose Langue: En Journal: Nat Chem Sujet du journal: QUIMICA Année: 2021 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Alcènes / Acides gras / Glucose Langue: En Journal: Nat Chem Sujet du journal: QUIMICA Année: 2021 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
...