Vinogradov E V, Müller-Loennies S, Petersen B O, Meshkov S, Thomas-Oates J E, Holst O, Brade H
Division of Medical and Microbiology, Center for Medicine and Biosciences, Research Center Borstel, Germany.
Eur J Biochem. 1997 Jul 1;247(1):82-90. doi: 10.1111/j.1432-1033.1997.00082.x.
The structure of the lipopolysaccharide (LPS) from Acinetobacter haemolyticus strain NCTC 10305 (DNA group 4) was elucidated by means of analytical chemistry, NMR spectroscopy and fast-atom-bombardment mass spectrometry. Several oligosaccharides were obtained after deacylation or successive de-O-acylation, dephosphorylation, reduction, and de-N-acylation of LPS. In the major fraction of the LPS, the core is attached to the lipid A through D-glycero-D-talo-2-octulopyranosonic acid (Ko), whereas in a minor fraction (<20%) Ko is replaced by 3-deoxy-D-manno-octulopyranosonic acid (Kdo). The structures of the phosphorylated carbohydrate backbones of these LPS fractions are [structure: see text] with Dha = 3-deoxy-D-lyxo-2-heptulosaric acid, Sug = sugar and is Ko in a major fraction and Kdo in a minor fraction. All sugar residues have the D-configuration and are present in the pyranose form. Mass spectrometry of de-O-acylated LPS revealed the presence of an additional hexose residue in minor amounts, the position and nature of which could not be identified.
通过分析化学、核磁共振光谱法和快原子轰击质谱法阐明了溶血不动杆菌菌株NCTC 10305(DNA群4)的脂多糖(LPS)结构。对LPS进行脱酰基或连续脱O-酰基、去磷酸化、还原和脱N-酰基后,得到了几种寡糖。在LPS的主要部分中,核心通过D-甘油-D-塔罗-2-辛酮糖醛酸(Ko)与脂质A相连,而在一小部分(<20%)中,Ko被3-脱氧-D-甘露-辛酮糖醛酸(Kdo)取代。这些LPS组分的磷酸化碳水化合物主链结构为[结构:见正文],其中Dha = 3-脱氧-D-木酮糖-2-庚酮糖酸,Sug = 糖,在主要部分为Ko,在次要部分为Kdo。所有糖残基均为D-构型,且以吡喃糖形式存在。脱O-酰基LPS的质谱分析显示存在少量额外的己糖残基,但其位置和性质无法确定。