Literature DB >> 28809560

Recombinant Macrocyclic Lanthipeptides Incorporating Non-Canonical Amino Acids.

Claudio Zambaldo1, Xiaozhou Luo1, Angad P Mehta1, Peter G Schultz1.   

Abstract

Nisin is a complex lanthipeptide that has broad spectrum antibacterial activity. In efforts to broaden the structural diversity of this ribosomally synthesized lantibiotic, we now report the recombinant expression of Nisin variants that incorporate noncanonical amino acids (ncAAs) at discrete positions. This is achieved by expressing the nisA structural gene, cyclase (nisC) and dehydratase (nisB), together with an orthogonal nonsense suppressor tRNA/aminoacyl-tRNA synthetase pair in Escherichia coli. A number of ncAAs with novel chemical reactivity were genetically incorporated into NisA, including an α-chloroacetamide-containing ncAA that allowed for the expression of Nisin variants with novel macrocyclic topologies. This methodology should allow for the exploration of lanthipeptide variants with new or enhanced activities.

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Year:  2017        PMID: 28809560      PMCID: PMC5847277          DOI: 10.1021/jacs.7b04159

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


  25 in total

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Review 4.  Adding amino acids to the genetic repertoire.

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5.  Facile Removal of Leader Peptides from Lanthipeptides by Incorporation of a Hydroxy Acid.

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8.  Facile chemoselective synthesis of dehydroalanine-containing peptides.

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Journal:  Biochemistry       Date:  2013-02-27       Impact factor: 3.162

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  15 in total

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8.  Expanding the Genetic Code of Lactococcus lactis and Escherichia coli to Incorporate Non-canonical Amino Acids for Production of Modified Lantibiotics.

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10.  Specificity and Application of the Lantibiotic Protease NisP.

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Journal:  Front Microbiol       Date:  2018-02-09       Impact factor: 5.640

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