Literature DB >> 27206099

Total Synthesis of Circular Bacteriocins by Butelase 1.

Xinya Hemu1, Yibo Qiu1, Giang K T Nguyen1, James P Tam1.   

Abstract

Circular bacteriocins, ranging from 35 to 70 amino acids, are the largest cyclic peptides produced by lactic acid bacteria to suppress growth of other bacteria. Their end-to-end cyclized backbone that enhances molecular stability is an advantage to survive in pasteurization and cooking processes in food preservation, but becomes a disadvantage and challenge in chemical synthesis. They also contain unusually long and highly hydrophobic segments which pose an additional synthetic challenge. Here we report the total synthesis of the three largest circular bacteriocins, AS-48, uberolysin, and garvicin ML, by an efficient chemoenzymatic strategy. A key feature of our synthetic scheme is the use of an Asn-specific butelase-mediated cyclization of their linear precursors, prepared by microwave stepwise synthesis. Antimicrobial assays showed that the AS-48 linear precursor is inactive at concentrations up to 100 μM, whereas the macrocyclic AS-48 is potently active against pathogenic and drug-resistant bacteria, with minimal inhibitory concentrations in a sub-micromolar range.

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Year:  2016        PMID: 27206099     DOI: 10.1021/jacs.6b04310

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


  31 in total

Review 1.  General lack of structural characterization of chemically synthesized long peptides.

Authors:  Jean A Boutin; André L Tartar; Alain van Dorsselaer; Hubert Vaudry
Journal:  Protein Sci       Date:  2019-03-25       Impact factor: 6.725

2.  Characterization of the macrocyclase involved in the biosynthesis of RiPP cyclic peptides in plants.

Authors:  Jonathan R Chekan; Paola Estrada; Patrick S Covello; Satish K Nair
Journal:  Proc Natl Acad Sci U S A       Date:  2017-06-05       Impact factor: 11.205

3.  One-Pot Dual Labeling of IgG 1 and Preparation of C-to-C Fusion Proteins Through a Combination of Sortase A and Butelase 1.

Authors:  Thibault J Harmand; Djenet Bousbaine; Alix Chan; Xiaohong Zhang; David R Liu; James P Tam; Hidde L Ploegh
Journal:  Bioconjug Chem       Date:  2018-09-21       Impact factor: 4.774

4.  Structural determinants for peptide-bond formation by asparaginyl ligases.

Authors:  Xinya Hemu; Abbas El Sahili; Side Hu; Kaho Wong; Yu Chen; Yee Hwa Wong; Xiaohong Zhang; Aida Serra; Boon Chong Goh; Dina A Darwis; Ming Wei Chen; Siu Kwan Sze; Chuan-Fa Liu; Julien Lescar; James P Tam
Journal:  Proc Natl Acad Sci U S A       Date:  2019-05-23       Impact factor: 11.205

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

6.  Enterocin AS-48 as Evidence for the Use of Bacteriocins as New Leishmanicidal Agents.

Authors:  María Ángeles Abengózar; Rubén Cebrián; José María Saugar; Teresa Gárate; Eva Valdivia; Manuel Martínez-Bueno; Mercedes Maqueda; Luis Rivas
Journal:  Antimicrob Agents Chemother       Date:  2017-03-24       Impact factor: 5.191

7.  Improved Handling of Peptide Segments Using Side Chain-Based "Helping Hand" Solubilizing Tools.

Authors:  Michael T Jacobsen; Paul Spaltenstein; Riley J Giesler; Danny Hung-Chieh Chou; Michael S Kay
Journal:  Methods Mol Biol       Date:  2022

Review 8.  Biosynthetic Proteases That Catalyze the Macrocyclization of Ribosomally Synthesized Linear Peptides.

Authors:  Chayanid Ongpipattanakul; Satish K Nair
Journal:  Biochemistry       Date:  2018-03-27       Impact factor: 3.162

Review 9.  Cyclotides, a versatile ultrastable micro-protein scaffold for biotechnological applications.

Authors:  Julio A Camarero
Journal:  Bioorg Med Chem Lett       Date:  2017-10-21       Impact factor: 2.823

Review 10.  Plant asparaginyl endopeptidases and their structural determinants of function.

Authors:  Samuel G Nonis; Joel Haywood; Joshua S Mylne
Journal:  Biochem Soc Trans       Date:  2021-04-30       Impact factor: 5.407

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