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Bacteriocin ASM1 is an O/S-diglycosylated, plasmid-encoded homologue of glycocin F
P. Main, T. Hata, TS. Loo, P. Man, P. Novak, V. Havlíček, GE. Norris, ML. Patchett
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Medline Complete (EBSCOhost)
od 2016-05-01 do Před 1 rokem
Wiley Free Content
od 1997 do Před 1 rokem
PubMed
31829452
DOI
10.1002/1873-3468.13708
Knihovny.cz E-zdroje
- MeSH
- bakteriální geny genetika MeSH
- bakteriociny chemie genetika metabolismus MeSH
- fylogeneze MeSH
- glykosylace MeSH
- Lactobacillus plantarum chemie genetika MeSH
- novobiocin MeSH
- plazmidy genetika MeSH
- sekvence aminokyselin MeSH
- sekvence nukleotidů MeSH
- sekvenční analýza DNA MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Here, we report on the biochemical characterization of a new glycosylated bacteriocin (glycocin), ASM1, produced by Lactobacillus plantarum A-1 and analysis of the A-1 bacteriocinogenic genes. ASM1 is 43 amino acids in length with Ser18-O- and Cys43-S-linked N-acetylglucosamine moieties that are essential for its inhibitory activity. Its only close homologue, glycocin F (GccF), has five amino acid substitutions all residing in the flexible C-terminal 'tail' and a lower IC50 (0.9 nm) compared to that of ASM1 (1.5 nm). Asm/gcc genes share the same organization (asmH← →asmABCDE→F), and the asm genes reside on an 11 905-bp plasmid dedicated to ASM1 production. The A-1 genome also harbors a gene encoding a 'rare' bactofencin-type bacteriocin. As more examples of prokaryote S-GlcNAcylation are discovered, the functions of this modification may be understood.
Department of Food and Nutritional Sciences Ochanomizu University Tokyo Japan
Institute of Microbiology v v i Academy of Sciences of the Czech Republic Prague 4 Czech Republic
Maurice Wilkins Centre for Molecular Biodiscovery University of Auckland New Zealand
School of Fundamental Sciences Massey University Palmerston North New Zealand
Citace poskytuje Crossref.org
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