Literature DB >> 18414736

How to tailor non-ribosomal peptide products--new clues about the structures and mechanisms of modifying enzymes.

Stefan A Samel1, Mohamed A Marahiel, Lars-Oliver Essen.   

Abstract

Non-ribosomal peptide products often contain modified building blocks or post-assembly line alterations of their peptide scaffolds with some of them being crucial for biological activity. These reactions such as halogenation, hydroxylation or glycosylation are mostly catalyzed by individual enzymes associated with the respective biosynthesis cluster. The versatile nature of these chemical modifications gives rise to a high degree of structural and functional diversity. Recent progress in this area enhances our insight about the mechanisms of these enzymes. Biotechnological applications might include the synthesis of novel, non-ribosomal peptide products or modified amino acid building blocks for pharmaceutical research.

Mesh:

Substances:

Year:  2008        PMID: 18414736     DOI: 10.1039/b717538h

Source DB:  PubMed          Journal:  Mol Biosyst        ISSN: 1742-2051


  14 in total

1.  Insights into an unusual nonribosomal peptide synthetase biosynthesis: identification and characterization of the GE81112 biosynthetic gene cluster.

Authors:  Tina M Binz; Sonia I Maffioli; Margherita Sosio; Stefano Donadio; Rolf Müller
Journal:  J Biol Chem       Date:  2010-08-14       Impact factor: 5.157

Review 2.  Structure and noncanonical chemistry of nonribosomal peptide biosynthetic machinery.

Authors:  Heather L Condurso; Steven D Bruner
Journal:  Nat Prod Rep       Date:  2012-06-25       Impact factor: 13.423

3.  Structure determination of the functional domain interaction of a chimeric nonribosomal peptide synthetase from a challenging crystal with noncrystallographic translational symmetry.

Authors:  Jesse A Sundlov; Andrew M Gulick
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2013-07-18

4.  Structures of a Nonribosomal Peptide Synthetase Module Bound to MbtH-like Proteins Support a Highly Dynamic Domain Architecture.

Authors:  Bradley R Miller; Eric J Drake; Ce Shi; Courtney C Aldrich; Andrew M Gulick
Journal:  J Biol Chem       Date:  2016-09-05       Impact factor: 5.157

5.  Amidoligases with ATP-grasp, glutamine synthetase-like and acetyltransferase-like domains: synthesis of novel metabolites and peptide modifications of proteins.

Authors:  Lakshminarayan M Iyer; Saraswathi Abhiman; A Maxwell Burroughs; L Aravind
Journal:  Mol Biosyst       Date:  2009-10-13

6.  Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis.

Authors:  Brian D Ames; Xinyu Liu; Christopher T Walsh
Journal:  Biochemistry       Date:  2010-09-08       Impact factor: 3.162

7.  Characterization of a novel type of oxidative decarboxylase involved in the biosynthesis of the styryl moiety of chondrochloren from an acylated tyrosine.

Authors:  Shwan Rachid; Ole Revermann; Christina Dauth; Uli Kazmaier; Rolf Müller
Journal:  J Biol Chem       Date:  2010-01-15       Impact factor: 5.157

Review 8.  Ribosomal peptide natural products: bridging the ribosomal and nonribosomal worlds.

Authors:  John A McIntosh; Mohamed S Donia; Eric W Schmidt
Journal:  Nat Prod Rep       Date:  2009-04       Impact factor: 13.423

9.  Stereospecific synthesis of threo- and erythro-beta-hydroxyglutamic acid during kutzneride biosynthesis.

Authors:  Matthias Strieker; Elizabeth M Nolan; Christopher T Walsh; Mohamed A Marahiel
Journal:  J Am Chem Soc       Date:  2009-09-23       Impact factor: 15.419

10.  Phylogenomics reveals subfamilies of fungal nonribosomal peptide synthetases and their evolutionary relationships.

Authors:  Kathryn E Bushley; B Gillian Turgeon
Journal:  BMC Evol Biol       Date:  2010-01-26       Impact factor: 3.260

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.