Abstract:
:Klebsiella pneumoniae strain KK207-2 was isolated in 2010 from a bloodstream infection of an inpatient at an Italian hospital. It was previously found to produce the KPC-2 carbapenemase and to belong to clade 1 of sequence type 258. Genotyping of the conserved wzi and wzc genes from strain KK207-2 yielded contrasting results: the wzc-based method assigned the cps207-2 to a new K-type, while the wzi-based method assigned it to the known K41 K-type. In order to resolve this contradiction, the capsular polysaccharide of K. pneumoniae KK207-2 was purified and its structure determined by using GLC-MS of appropriate carbohydrate derivatives, ESI-MS of both partial hydrolysis and Smith degradation derived oligosaccharides, and NMR spectroscopy of oligosaccharides, and the lithium degraded, native and de-O-acetylated polysaccharide. All the collected data demonstrated the following repeating unit for the K. pneumoniae KK207-2 capsular polysaccharide: The polysaccharide contains about 0.60 acetyl groups per repeating unit on C6 of the Gal residue. The reactions catalyzed by each glycosyltransferase in the cpsKK207-2 gene cluster were assigned on the basis of structural homology with other Klebsiella K antigens.
journal_name
Int J Biol Macromoljournal_title
International journal of biological macromoleculesauthors
Bellich B,Ravenscroft N,Rizzo R,Lagatolla C,D'Andrea MM,Rossolini GM,Cescutti Pdoi
10.1016/j.ijbiomac.2019.02.128subject
Has Abstractpub_date
2019-06-01 00:00:00pages
536-544eissn
0141-8130issn
1879-0003pii
S0141-8130(18)37388-4journal_volume
130pub_type
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