Literature DB >> 22686940

Generation of thiocillin ring size variants by prepeptide gene replacement and in vivo processing by Bacillus cereus.

Albert A Bowers1, Michael G Acker, Travis S Young, Christopher T Walsh.   

Abstract

The thiocillins from Bacillus cereus ATCC 14579 are natural products from the broader class of thiazolyl peptides. Their biosynthesis proceeds via extensive post-translational modification of a ribosomally encoded precursor peptide. This post-translational tailoring involves a key step formal cycloaddition between two distal serine residues. In the wild-type structure, this cycloaddition forms a major macrocycle circumscribed by 26-atoms (shortest path). Results presented herein demonstrate the promiscuity of this last step by means of a set of "competition" experiments. Cyclization proceeds in many cases to provide altered ring sizes, giving access to several variant rings sizes that have not previously been observed in nature.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22686940      PMCID: PMC3387813          DOI: 10.1021/ja302820x

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  40 in total

1.  The thiazole ylide: a frequently invoked intermediate is a stable species in the gas phase.

Authors:  G A McGibbon; J Hrušák; D J Lavorato; H Schwarz; J K Terlouw
Journal:  Chemistry       Date:  1997-02       Impact factor: 5.236

Review 2.  Biosynthesis of nonribosomal peptides1.

Authors:  Robert Finking; Mohamed A Marahiel
Journal:  Annu Rev Microbiol       Date:  2004       Impact factor: 15.500

Review 3.  Intramolecular cyclizations of polyketide biosynthesis: mining for a "Diels-Alderase"?

Authors:  Wendy L Kelly
Journal:  Org Biomol Chem       Date:  2008-11-04       Impact factor: 3.876

4.  Thiostrepton binds to malarial plastid rRNA.

Authors:  B Clough; M Strath; P Preiser; P Denny; I R Wilson
Journal:  FEBS Lett       Date:  1997-04-07       Impact factor: 4.124

5.  Revised structure of the antibiotic GE 2270A.

Authors:  P Tavecchia; P Gentili; M Kurz; C Sottani; R Bonfichi; S Lociuro; E Selva
Journal:  J Antibiot (Tokyo)       Date:  1994-12       Impact factor: 2.649

Review 6.  Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates.

Authors:  Joel O Melby; Nathan J Nard; Douglas A Mitchell
Journal:  Curr Opin Chem Biol       Date:  2011-03-21       Impact factor: 8.822

7.  Heterologous production of thiostrepton A and biosynthetic engineering of thiostrepton analogs.

Authors:  Chaoxuan Li; Feifei Zhang; Wendy L Kelly
Journal:  Mol Biosyst       Date:  2010-11-25

8.  Thiostrepton and derivatives exhibit antimalarial and gametocytocidal activity by dually targeting parasite proteasome and apicoplast.

Authors:  Makoah N Aminake; Sebastian Schoof; Ludmilla Sologub; Monika Leubner; Marc Kirschner; Hans-Dieter Arndt; Gabriele Pradel
Journal:  Antimicrob Agents Chemother       Date:  2011-01-18       Impact factor: 5.191

Review 9.  The long-overlooked enzymology of a nonribosomal peptide synthetase-independent pathway for virulence-conferring siderophore biosynthesis.

Authors:  Daniel Oves-Costales; Nadia Kadi; Gregory L Challis
Journal:  Chem Commun (Camb)       Date:  2009-09-14       Impact factor: 6.222

Review 10.  Follow the leader: the use of leader peptides to guide natural product biosynthesis.

Authors:  Trent J Oman; Wilfred A van der Donk
Journal:  Nat Chem Biol       Date:  2010-01       Impact factor: 15.040

View more
  19 in total

1.  Characterization of a novel plasmid-borne thiopeptide gene cluster in Staphylococcus epidermidis strain 115.

Authors:  Philip R Bennallack; Scott R Burt; Michael J Heder; Richard A Robison; Joel S Griffitts
Journal:  J Bacteriol       Date:  2014-10-13       Impact factor: 3.490

Review 2.  Elucidating and engineering thiopeptide biosynthesis.

Authors:  Philip R Bennallack; Joel S Griffitts
Journal:  World J Microbiol Biotechnol       Date:  2017-05-11       Impact factor: 3.312

3.  In Vitro Biosynthesis and Substrate Tolerance of the Plantazolicin Family of Natural Products.

Authors:  Caitlin D Deane; Brandon J Burkhart; Patricia M Blair; Jonathan I Tietz; Alice Lin; Douglas A Mitchell
Journal:  ACS Chem Biol       Date:  2016-06-16       Impact factor: 5.100

Review 4.  Dehydroamino acids: chemical multi-tools for late-stage diversification.

Authors:  Jonathan W Bogart; Albert A Bowers
Journal:  Org Biomol Chem       Date:  2019-04-10       Impact factor: 3.876

5.  Characterization of Leader Peptide Binding During Catalysis by the Nisin Dehydratase NisB.

Authors:  Lindsay M Repka; Kenton J Hetrick; See Hyun Chee; Wilfred A van der Donk
Journal:  J Am Chem Soc       Date:  2018-03-20       Impact factor: 15.419

Review 6.  RiPP antibiotics: biosynthesis and engineering potential.

Authors:  Graham A Hudson; Douglas A Mitchell
Journal:  Curr Opin Microbiol       Date:  2018-03-10       Impact factor: 7.934

Review 7.  Recent advances of Diels-Alderases involved in natural product biosynthesis.

Authors:  Atsushi Minami; Hideaki Oikawa
Journal:  J Antibiot (Tokyo)       Date:  2016-06-15       Impact factor: 2.649

8.  Thiopeptide Pyridine Synthase TbtD Catalyzes an Intermolecular Formal Aza-Diels-Alder Reaction.

Authors:  Jonathan W Bogart; Albert A Bowers
Journal:  J Am Chem Soc       Date:  2019-01-22       Impact factor: 15.419

9.  Engineering unnatural variants of plantazolicin through codon reprogramming.

Authors:  Caitlin D Deane; Joel O Melby; Katie J Molohon; Aziz R Susarrey; Douglas A Mitchell
Journal:  ACS Chem Biol       Date:  2013-07-03       Impact factor: 5.100

10.  Interception of the Bycroft-Gowland Intermediate in the Enzymatic Macrocyclization of Thiopeptides.

Authors:  Jonathan W Bogart; Nicholas J Kramer; Aneta Turlik; Rachel M Bleich; Daniel S Catlin; Frank C Schroeder; Satish K Nair; R Thomas Williamson; K N Houk; Albert A Bowers
Journal:  J Am Chem Soc       Date:  2020-07-16       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.