Division of Medical and Biochemical Microbiology, Research Center Borstel, Leibniz-Center for Medicine and Biosciences, Borstel, Germany.
Eur J Cell Biol. 2010 Jan;89(1):3-10. doi: 10.1016/j.ejcb.2009.10.002. Epub 2009 Nov 8.
The inner core of lipopolysaccharide (LPS) structures in Gram-negative bacteria is considered a highly conserved region. The sugar connecting the membrane-associated lipid A moiety with the hydrophilic saccharide moiety, 3-deoxy-alpha-d-manno-oct-2-ulosonic acid (Kdo) is present in every LPS molecule investigated but it may be partially replaced by d-glycero-alpha-d-talo-oct-2-ulosonic acid (Ko). l-Glycero-alpha-d-manno-heptose (Hep) and phosphate residues are part of most but not all LPS structures and additionally, modifications with 4-amino-4-deoxy-beta-l-arabinose (Ara4N) residues occur in some. A number of different glycosyltransferases is involved in the biosynthesis of the inner core region of different lipopolysaccharides. Here, we report the characterization of Kdo transferases, heptosyltransferases and Ara4N transferases from a variety of bacteria.
革兰氏阴性菌脂多糖(LPS)结构的核心被认为是一个高度保守的区域。连接膜相关脂酰 A 部分与亲水性糖部分的糖是 3-脱氧-α-d-甘露-oct-2-烯酸(Kdo),存在于每一种已研究的 LPS 分子中,但它可能部分被 d-甘油-α-d-塔罗-oct-2-烯酸(Ko)取代。l-甘油-α-d-甘露庚糖(Hep)和磷酸残基是大多数 LPS 结构的一部分,但并非全部,并且在某些 LPS 结构中还存在 4-氨基-4-脱氧-β-l-阿拉伯糖(Ara4N)残基的修饰。许多不同的糖基转移酶参与不同 LPS 核心区域的生物合成。在这里,我们报道了来自多种细菌的 Kdo 转移酶、庚糖转移酶和 Ara4N 转移酶的特性。