Bhat U R, Forsberg L S, Carlson R W
Complex Carbohydrate Research Center, University of Georgia, Athens 30605.
J Biol Chem. 1994 May 20;269(20):14402-10.
The structure of lipid A from the lipopolysaccharide of Rhizobium leguminosarum bv. phaseoli (wild type strain CE3) was investigated by alkylation analysis, nuclear magnetic resonance spectroscopy, and electrospray and fast atom bombardment mass spectrometry of the de-O-acylated lipid A. The lipid A carbohydrate backbone was shown to be a trisaccharide containing galacturonic acid, glucosamine, and the unique sugar 2-amino-2-deoxygluconic acid, previously unreported in lipopolysaccharides. Nuclear magnetic resonance spectroscopy and ethylation analyses revealed that the galacturonic acid is alpha-1,4-linked to the glucosamine, while the amino aldonic acid residue, which may exist as the 1,5-lactone, is attached as an aglycone to the glucosamine and, thus, occupies the reducing end of the molecule. The resulting backbone is hydrophilic and analogous to the commonly observed bisphosphorylated glucosamine disaccharide from enteric bacterial lipopolysaccharides in that both the nonreducing and reducing ends carry negatively charged substituents. The fatty acids of the R. leguminosarum lipid A are attached both as O- and N-acyl substituents to glucosamine and 2-aminogluconate. All fatty acids are hydroxylated consisting of 3-hydroxymyristate (3-OH-C14.0), 3-hydroxypentadecanoate (3-OH-C15.0), 3-hydroxypalmitate (3-OH-C16.0), 3-hydroxystearate (3-OH-C18.0), and 27-hydroxyoctacosanoate (27-OH-C28.0) in the approximate mole ratio 3:0.2:1:0.6:1. Unlike lipid As from enteric bacteria, the R. leguminosarum lipid A lacks 3-acyloxyacyl substituents; however, the long chain 27-hydroxy fatty acid carries ester-linked beta-hydroxybutyrate at the 27-hydroxy position. Fast atom bombardment mass spectrometry of the de-O-acylated lipid A demonstrated the presence of 2 molecular species that differ by 28 mass units due to fatty acid heterogeneity at the two amide linkages. One species carries amide-linked 3-OH-C14.0 and 3-OH-C16.0; the second species carries 3-OH-C14.0 and 3-OH-C18.0. Each molecular species also exists as the aldonolactone, yielding molecular ions at ((M+H)+)-18. The heterogeneity in the amide-linked fatty acids further distinguishes the Rhizobium lipid A from enteric lipid As.
通过烷基化分析、核磁共振光谱以及对脱O-酰化脂质A进行电喷雾和快原子轰击质谱分析,对菜豆根瘤菌(Rhizobium leguminosarum bv. phaseoli)(野生型菌株CE3)脂多糖中的脂质A结构进行了研究。脂质A碳水化合物主链被证明是一种三糖,包含半乳糖醛酸、葡萄糖胺以及独特的糖2-氨基-2-脱氧葡糖酸,此前在脂多糖中未报道过这种糖。核磁共振光谱和乙基化分析表明,半乳糖醛酸通过α-1,4连接到葡萄糖胺上,而氨基醛糖酸残基(可能以1,5-内酯形式存在)作为糖苷配基连接到葡萄糖胺上,因此占据分子的还原端。由此产生的主链是亲水性的,类似于在肠道细菌脂多糖中常见观察到的双磷酸化葡萄糖胺二糖,因为非还原端和还原端都带有带负电荷的取代基。菜豆根瘤菌脂质A的脂肪酸以O-和N-酰基取代基的形式连接到葡萄糖胺和2-氨基葡糖酸上。所有脂肪酸都被羟基化,由3-羟基肉豆蔻酸(3-OH-C14.0)、3-羟基十五烷酸(3-OH-C15.0)、3-羟基棕榈酸(3-OH-C16.0)、3-羟基硬脂酸(3-OH-C18.0)和27-羟基二十八烷酸(27-OH-C28.0)组成,其摩尔比约为3:0.2:1:0.6:1。与肠道细菌的脂质A不同,菜豆根瘤菌脂质A缺乏3-酰氧基酰基取代基;然而,长链27-羟基脂肪酸在27-羟基位置带有酯连接的β-羟基丁酸。对脱O-酰化脂质A进行快原子轰击质谱分析表明存在两种分子种类,由于两个酰胺键处脂肪酸的异质性,它们的质量相差28个质量单位。一种分子种类带有酰胺连接的3-OH-C14.0和3-OH-C16.0;第二种分子种类带有3-OH-C14.0和3-OH-C18.0。每种分子种类也以醛糖内酯形式存在,在((M+H)+)-18处产生分子离子。酰胺连接的脂肪酸的异质性进一步将根瘤菌脂质A与肠道脂质A区分开来。