Frirdich Emilisa, Vinogradov Evgeny, Whitfield Chris
Department of Microbiology, University of Guelph, 50 Stone Road East, Guelph, Ontario N1G 2W1, Canada.
J Biol Chem. 2004 Jul 2;279(27):27928-40. doi: 10.1074/jbc.M402549200. Epub 2004 Apr 15.
The core oligosaccharide region of Klebsiella pneumoniae lipopolysaccharide contains some novel features that distinguish it from the corresponding lipopolysaccharide region in other members of the Enterobacteriaceae family, such as Escherichia coli and Salmonella. The conserved Klebsiella outer core contains the unusual trisaccharide 3-deoxy-d-manno-oct-2-ulosonic acid (Kdo)-(2,6)-GlcN-(1,4)-GalUA. In general, Kdo residues are normally found in the inner core, but in K. pneumoniae, this Kdo residue provides the ligation site for O polysaccharide. The outer core Kdo residue can also be non-stoichiometrically substituted with an l-glycero-d-manno-heptopyranose (Hep) residue, another component more frequently found in the inner core. To understand the genetics and biosynthesis of core oligosaccharide synthesis in Klebsiella, the gene products involved in the addition of the outer core GlcN (WabH), Kdo (WabI), and Hep (WabJ) residues as well as the inner core HepIII residue (WaaQ) were identified. Non-polar mutations were created in each of the genes, and the resulting mutant lipopolysaccharide was analyzed by mass spectrometry. The in vitro glycosyltransferase activity of WabI and WabH was verified. WabI transferred a Kdo residue from CMP-Kdo onto the acceptor lipopolysaccharide. The activated precursor required for GlcN addition has not been identified. However, lysates overexpressing WabH were able to transfer a GlcNAc residue from UDP-GlcNAc onto the acceptor GalUA residue in the outer core.
肺炎克雷伯菌脂多糖的核心寡糖区域具有一些新颖的特征,使其有别于肠杆菌科其他成员(如大肠杆菌和沙门氏菌)的相应脂多糖区域。保守的肺炎克雷伯菌外核心包含不寻常的三糖3-脱氧-D-甘露糖-辛-2-酮糖酸(Kdo)-(2,6)-GlcN-(1,4)-GalUA。一般来说,Kdo残基通常存在于内核心中,但在肺炎克雷伯菌中,这个Kdo残基为O多糖提供连接位点。外核心Kdo残基也可以非化学计量地被L-甘油-D-甘露庚糖(Hep)残基取代,Hep是另一种更常见于内核心的成分。为了了解肺炎克雷伯菌核心寡糖合成的遗传学和生物合成过程,鉴定了参与添加外核心GlcN(WabH)、Kdo(WabI)和Hep(WabJ)残基以及内核心HepIII残基(WaaQ)的基因产物。在每个基因中产生了非极性突变,并通过质谱分析所得突变体脂多糖。验证了WabI和WabH的体外糖基转移酶活性。WabI将一个Kdo残基从CMP-Kdo转移到受体脂多糖上。尚未鉴定出添加GlcN所需的活化前体。然而,过表达WabH的裂解物能够将UDP-GlcNAc中的一个GlcNAc残基转移到外核心中的受体GalUA残基上。