Literature DB >> 23518239

Alkylating enzymes.

Ludger A Wessjohann1, Jeanette Keim, Benjamin Weigel, Martin Dippe.   

Abstract

Chemospecific and regiospecific modifications of natural products by methyl, prenyl, or C-glycosyl moieties are a challenging and cumbersome task in organic synthesis. Because of the availability of an increasing number of stable and selective transferases and cofactor regeneration processes, enzyme-assisted strategies turn out to be promising alternatives to classical synthesis. Two categories of alkylating enzymes become increasingly relevant for applications: firstly prenyltransferases and terpene synthases (including terpene cyclases), which are used in the production of terpenoids such as artemisinin, or meroterpenoids like alkylated phenolics and indoles, and secondly methyltransferases, which modify flavonoids and alkaloids to yield products with a specific methylation pattern such as 7-O-methylaromadendrin and scopolamine.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23518239     DOI: 10.1016/j.cbpa.2013.02.016

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  12 in total

1.  Site-directed mutagenesis switching a dimethylallyl tryptophan synthase to a specific tyrosine C3-prenylating enzyme.

Authors:  Aili Fan; Georg Zocher; Edyta Stec; Thilo Stehle; Shu-Ming Li
Journal:  J Biol Chem       Date:  2014-12-04       Impact factor: 5.157

2.  Functional AdoMet Isosteres Resistant to Classical AdoMet Degradation Pathways.

Authors:  Tyler D Huber; Fengbin Wang; Shanteri Singh; Brooke R Johnson; Jianjun Zhang; Manjula Sunkara; Steven G Van Lanen; Andrew J Morris; George N Phillips; Jon S Thorson
Journal:  ACS Chem Biol       Date:  2016-07-14       Impact factor: 5.100

3.  Methionine Adenosyltransferase Engineering to Enable Bioorthogonal Platforms for AdoMet-Utilizing Enzymes.

Authors:  Tyler D Huber; Jonathan A Clinger; Yang Liu; Weijun Xu; Mitchell D Miller; George N Phillips; Jon S Thorson
Journal:  ACS Chem Biol       Date:  2020-03-03       Impact factor: 5.100

Review 4.  AdoMet analog synthesis and utilization: current state of the art.

Authors:  Tyler D Huber; Brooke R Johnson; Jianjun Zhang; Jon S Thorson
Journal:  Curr Opin Biotechnol       Date:  2016-08-06       Impact factor: 9.740

Review 5.  Building Bridges: Biocatalytic C-C-Bond Formation toward Multifunctional Products.

Authors:  Nina G Schmidt; Elisabeth Eger; Wolfgang Kroutil
Journal:  ACS Catal       Date:  2016-06-08       Impact factor: 13.084

6.  Biocatalytic Friedel-Crafts Acylation and Fries Reaction.

Authors:  Nina G Schmidt; Tea Pavkov-Keller; Nina Richter; Birgit Wiltschi; Karl Gruber; Wolfgang Kroutil
Journal:  Angew Chem Int Ed Engl       Date:  2017-05-23       Impact factor: 15.336

7.  Rational Reprogramming of O-Methylation Regioselectivity for Combinatorial Biosynthetic Tailoring of Benzenediol Lactone Scaffolds.

Authors:  Xiaojing Wang; Chen Wang; Lixin Duan; Liwen Zhang; Hang Liu; Ya-Ming Xu; Qingpei Liu; Tonglin Mao; Wei Zhang; Ming Chen; Min Lin; A A Leslie Gunatilaka; Yuquan Xu; István Molnár
Journal:  J Am Chem Soc       Date:  2019-02-27       Impact factor: 15.419

8.  Rational Engineered C-Acyltransferase Transforms Sterically Demanding Acyl Donors.

Authors:  Anna Żądło-Dobrowolska; Lucas Hammerer; Tea Pavkov-Keller; Karl Gruber; Wolfgang Kroutil
Journal:  ACS Catal       Date:  2019-12-27       Impact factor: 13.084

9.  Engineered Enzymes Enable Selective N-Alkylation of Pyrazoles With Simple Haloalkanes.

Authors:  Ludwig L Bengel; Benjamin Aberle; Alexander-N Egler-Kemmerer; Samuel Kienzle; Bernhard Hauer; Stephan C Hammer
Journal:  Angew Chem Int Ed Engl       Date:  2021-01-21       Impact factor: 15.336

Review 10.  Methyltransferase-Directed Labeling of Biomolecules and its Applications.

Authors:  Jochem Deen; Charlotte Vranken; Volker Leen; Robert K Neely; Kris P F Janssen; Johan Hofkens
Journal:  Angew Chem Int Ed Engl       Date:  2017-04-10       Impact factor: 15.336

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.