» Articles » PMID: 21770392

Nine Post-translational Modifications During the Biosynthesis of Cinnamycin

Overview
Journal J Am Chem Soc
Specialty Chemistry
Date 2011 Jul 21
PMID 21770392
Citations 57
Authors
Affiliations
Soon will be listed here.
Abstract

Lantibiotics are ribosomally synthesized and post-translationally modified antimicrobial peptides that are characterized by the thioether cross-linked amino acids lanthionine (Lan) and methyllanthionine (MeLan). Cinnamycin is a 19 amino acid lantibiotic that contains one Lan and two MeLan. Cinnamycin also contains an unusual lysinoalanine (Lal) bridge formed from the ε-amino group of lysine 19 and a serine residue at position 6, and an erythro-3-hydroxy-L-aspartic acid resulting from the hydroxylation of L-aspartate at position 15. These modifications are critical in mediating the interactions of cinnamycin with its target, phosphatidylethanolamine. Recently, the cinnamycin biosynthetic gene cluster (cin) from Streptomyces cinnamoneus cinnamoneus DSM 40005 was reported. Herein, we investigated the biosynthetic machinery using both in vitro studies and heterologous expression in Escherichia coli. CinX is an α-ketoglutarate/iron(II)-dependent hydroxylase that carries out the hydroxylation of aspartate 15 of the precursor peptide CinA. In addition, CinM catalyzes dehydration of four Ser and Thr residues and subsequent cyclization of Cys residues to form the three (Me)Lan bridges. The order of the post-translational modifications catalyzed by CinM and CinX is interchangeable in vitro. CinX did not require the leader sequence at the N-terminus of CinA for activity, but the leader peptide was necessary for CinM function. Although CinM dehydrated serine 6, it did not catalyze the formation of Lal. A small protein encoded by cinorf7 is critical for the formation of the cross-link between Lys19 and dehydroalanine 6 as shown by coexpression studies of CinA, CinM, CinX, and Cinorf7 in E. coli.

Citing Articles

Bibacillin 1: a two-component lantibiotic from .

Moreira R, Yang Y, Luo Y, Gilmore M, van der Donk W RSC Chem Biol. 2024; .

PMID: 39268544 PMC: 11385697. DOI: 10.1039/d4cb00192c.


Genome Mining of CCNP1313 Indicates a New Scope in the Search for Antiproliferative and Antiviral Agents.

Grabski M, Gawor J, Ceglowska M, Gromadka R, Mazur-Marzec H, Wegrzyn G Microorganisms. 2024; 12(8).

PMID: 39203471 PMC: 11356792. DOI: 10.3390/microorganisms12081628.


Bibacillin 1: A two-component lantibiotic from .

Moreira R, Yang Y, Luo Y, Gilmore M, van der Donk W bioRxiv. 2024; .

PMID: 39185197 PMC: 11343131. DOI: 10.1101/2024.08.13.607848.


Use of the mCherry fluorescent protein to optimize the expression of class I lanthipeptides in Escherichia coli.

Van Zyl W, Van Staden A, Dicks L, Trindade M Microb Cell Fact. 2023; 22(1):149.

PMID: 37559122 PMC: 10413542. DOI: 10.1186/s12934-023-02162-7.


Engineering lanthipeptides by introducing a large variety of RiPP modifications to obtain new-to-nature bioactive peptides.

Fu Y, Xu Y, Ruijne F, Kuipers O FEMS Microbiol Rev. 2023; 47(3).

PMID: 37096385 PMC: 10373908. DOI: 10.1093/femsre/fuad017.


References
1.
Li B, Sher D, Kelly L, Shi Y, Huang K, Knerr P . Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria. Proc Natl Acad Sci U S A. 2010; 107(23):10430-5. PMC: 2890784. DOI: 10.1073/pnas.0913677107. View

2.
Willey J, van der Donk W . Lantibiotics: peptides of diverse structure and function. Annu Rev Microbiol. 2007; 61:477-501. DOI: 10.1146/annurev.micro.61.080706.093501. View

3.
Paul M, Patton G, van der Donk W . Mutants of the zinc ligands of lacticin 481 synthetase retain dehydration activity but have impaired cyclization activity. Biochemistry. 2007; 46(21):6268-76. PMC: 2517114. DOI: 10.1021/bi7000104. View

4.
Nagao J, Harada Y, Shioya K, Aso Y, Zendo T, Nakayama J . Lanthionine introduction into nukacin ISK-1 prepeptide by co-expression with modification enzyme NukM in Escherichia coli. Biochem Biophys Res Commun. 2005; 336(2):507-13. DOI: 10.1016/j.bbrc.2005.08.125. View

5.
Hosoda K, Ohya M, Kohno T, Maeda T, Endo S, Wakamatsu K . Structure determination of an immunopotentiator peptide, cinnamycin, complexed with lysophosphatidylethanolamine by 1H-NMR1. J Biochem. 1996; 119(2):226-30. DOI: 10.1093/oxfordjournals.jbchem.a021226. View