Literature DB >> 28266745

Breaking the Dogma of Aldolase Specificity: Simple Aliphatic Ketones and Aldehydes are Nucleophiles for Fructose-6-phosphate Aldolase.

Raquel Roldán1, Israel Sanchez-Moreno2, Thomas Scheidt3, Virgil Hélaine2, Marielle Lemaire2, Teodor Parella4, Pere Clapés1, Wolf-Dieter Fessner3, Christine Guérard-Hélaine2.   

Abstract

d-Fructose-6-phosphate aldolase (FSA) was probed for extended nucleophile promiscuity by using a series of fluorogenic substrates to reveal retro-aldol activity. Four nucleophiles ethanal, propanone, butanone, and cyclopentanone were subsequently confirmed to be non-natural substrates in the synthesis direction using the wild-type enzyme and its D6H variant. This exceptional widening of the nucleophile substrate scope offers a rapid entry, in good yields and high stereoselectivity, to less oxygenated alkyl ketones and aldehydes, which was hitherto impossible.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  aldolization; biocatalysis; enzymes; fructose-6-phosphate aldolase; phosphorylated compounds

Mesh:

Substances:

Year:  2017        PMID: 28266745     DOI: 10.1002/chem.201701020

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  6 in total

1.  Complete Switch of Reaction Specificity of an Aldolase by Directed Evolution In Vitro: Synthesis of Generic Aliphatic Aldol Products.

Authors:  Sebastian Junker; Raquel Roldan; Henk-Jan Joosten; Pere Clapés; Wolf-Dieter Fessner
Journal:  Angew Chem Int Ed Engl       Date:  2018-07-04       Impact factor: 15.336

2.  Aldolase-Catalyzed Asymmetric Synthesis of N-Heterocycles by Addition of Simple Aliphatic Nucleophiles to Aminoaldehydes.

Authors:  Raquel Roldán; Karel Hernández; Jesús Joglar; Jordi Bujons; Teodor Parella; Wolf-Dieter Fessner; Pere Clapés
Journal:  Adv Synth Catal       Date:  2019-02-15       Impact factor: 5.837

Review 3.  Progress in Stereoselective Construction of C-C Bonds Enabled by Aldolases and Hydroxynitrile Lyases.

Authors:  Mi Liu; Dan Wei; Zexing Wen; Jian-Bo Wang
Journal:  Front Bioeng Biotechnol       Date:  2021-04-21

4.  Structurally Informed Mutagenesis of a Stereochemically Promiscuous Aldolase Produces Mutants That Catalyze the Diastereoselective Syntheses of All Four Stereoisomers of 3-Deoxy-hexulosonic Acid.

Authors:  Sylvain F Royer; Xuan Gao; Robin R Groleau; Marc W van der Kamp; Steven D Bull; Michael J Danson; Susan J Crennell
Journal:  ACS Catal       Date:  2022-09-06       Impact factor: 13.700

5.  Non-natural Aldol Reactions Enable the Design and Construction of Novel One-Carbon Assimilation Pathways in vitro.

Authors:  Yufeng Mao; Qianqian Yuan; Xue Yang; Pi Liu; Ying Cheng; Jiahao Luo; Huanhuan Liu; Yonghong Yao; Hongbing Sun; Tao Cai; Hongwu Ma
Journal:  Front Microbiol       Date:  2021-06-02       Impact factor: 5.640

6.  Biocatalytic Aldol Addition of Simple Aliphatic Nucleophiles to Hydroxyaldehydes.

Authors:  Raquel Roldán; Karel Hernandez; Jesús Joglar; Jordi Bujons; Teodor Parella; Israel Sánchez-Moreno; Virgil Hélaine; Marielle Lemaire; Christine Guérard-Hélaine; Wolf-Dieter Fessner; Pere Clapés
Journal:  ACS Catal       Date:  2018-08-08       Impact factor: 13.084

  6 in total

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