Taxonomic group: bacteria / Proteobacteria
(Phylum: Proteobacteria)
Associated disease: infection due to Acinetobacter baumannii [ICD11:
XN8LS 
]
NCBI PubMed ID: 27230482Publication DOI: 10.1099/mic.0.000313Journal NLM ID: 0376646Publisher: Washington, DC: Kluwer Academic/Plenum Publishers
Correspondence: Johanna J. Kenyon <johanna.kenyon
qut.edu.au>
Institutions: N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia, School of Molecular Bioscience, University of Sydney, Sydney, Australia, M. M. Shemyakin & Y. A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia, Interdisciplinary Center for Proteomics Research, Kazan (Volga region) Federal University, Kazan, Russian Federation, Moscow Institute of Physics and Technology, Dolgoprudny, Moscow Region, Russian Federation, State Research Center for Applied Microbiology and Biotechnology, Obolensk, Moscow Region, Russian Federation
Polymerization of the oligosaccharides (K units) of complex capsular polysaccharides (CPSs) requires a Wzy polymerase, which is usually encoded in the gene cluster that directs K unit synthesis. Here, a gene cluster at the Acinetobacter K locus (KL) that lacks a wzy gene, KL19, was found in Acinetobacter baumannii ST111 isolates 28 and RBH2 recovered from hospitals in the Russian Federation and Australia, respectively. However, these isolates produced long-chain capsule, and a wzy gene was found in a 6.1 kb genomic island (GI) located adjacent to the cpn60 gene. The GI also includes an acetyltransferase gene, atr25, which is interrupted by an insertion sequence (IS) in RBH2. The capsule structure from both strains was →3)-α-d-GalpNAc-(1→4)-α-d-GalpNAcA-(1→3)-β-d-QuipNAc4NAc-(1→, determined using NMR spectroscopy. Biosynthesis of the K unit was inferred to be initiated with QuiNAc4NAc, and hence the Wzy forms the β-(1→3) linkage between QuipNAc4NAc and GalpNAc. The GalpNAc residue is 6-O-acetylated in isolate 28 only, showing that atr25 is responsible for this acetylation. The same GI with or without an IS in atr25 was found in draft genomes of other KL19 isolates, as well as ones carrying a closely related CPS gene cluster, KL39, which differs from KL19 only in a gene for an acyltransferase in the QuiNAc4NR synthesis pathway. Isolates carrying a KL1 variant with the wzy and atr genes each interrupted by an ISAba125 also have this GI. To our knowledge, this study is the first report of genes involved in capsule biosynthesis normally found at the KL located elsewhere in A. baumannii genomes.
Acinetobacter baumannii, capsule, Wzy polymerase, K locus, genomic island
Structure type: polymer chemical repeating unit
Location inside paper: p.1485, fig.6, K1 AB307-0294
Compound class: CPS
Contained glycoepitopes: IEDB_137340,IEDB_141807,IEDB_151531
Methods: 13C NMR, 1H NMR, NMR-2D, DNA sequencing, SDS-PAGE, sugar analysis, acid hydrolysis, GLC, de-O-acetylation, bioinformatic analysis, SEC
Enzymes that release or process the structure: Wzy(K1)(ItrA1), Gtr2, Gtr1, Wzy(K1)
Biosynthesis and genetic data: genetic data
Comments, role: Ac or (S)-3-hydroxybutanoyl (~1 : 1)
Related record ID(s): 11281, 11644, 11645
NCBI Taxonomy refs (TaxIDs): 557600
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
report error