Sadovskaya I, Brisson J R, Lam J S, Richards J C, Altman E
Institute for Biological Sciences, National Research Council of Canada, Ottawa, Ontario.
Eur J Biochem. 1998 Aug 1;255(3):673-84. doi: 10.1046/j.1432-1327.1998.2550673.x.
Lipopolysaccharide (LPS) of the Pseudomonas aeruginosa serotype O5 wild-type strain PAO1 and derived rough-type mutant strains AK1401 and AK1012 was isolated by a modified phenol/chloroform/petroleum-ether extraction method. Deoxycholate/PAGE of the LPS from the rough mutant AK1401 indicated two bands near the dye front with mobilities similar to those of the parent strain, indicating that both LPS contain a complete core and a species comprising a core and one repeating unit. Composition analysis of the LPS from strains PAO1 and AK1401 indicated that the complete core oligosaccharide was composed of D-glucose (four units), L-rhamnose (one unit), 2-amino-2-deoxy-D-galactose (one unit), L-glycero-D-manno-heptose (Hep; two units), 3-deoxy-D-manno-octulosonic acid (Kdo; two units), L-alanine (one unit) and phosphate (three units). The glycan structure of the LPS was determined by one-dimensional and two-dimensional (2D) NMR techniques in combination with MS-based methods on oligosaccharide samples obtained from the LPS by delipidation procedures. The locations of three phosphomonoester groups on the first heptose residue were established by a two-dimensional 31P (omega1)-half-filtered COSY experiment on the reduced core oligosaccharide sample of the LPS from the wild-type strain. The presence of a 7-O-carbamoyl substituent was observed on the second heptose. The structure of the core region of the O-chain-deficient LPS from P. aeruginosa serotype 05 is as follows: [structure: see text] where R1 is beta-D-Glcp-(1-->2)-alpha-L-Rhap-(1-->6)-alpha-D-Glcp-(1--> and R2 is alpha-D-Glcp-(1-->6)-beta-D-Glcp-(1->. A structural model is presented that is also representative of that for P. aeruginosa serotype O6 LPS. A revised structure for the serotype O6 mutant strain A28 is presented.
采用改良的苯酚/氯仿/石油醚萃取法,从铜绿假单胞菌血清型O5野生型菌株PAO1以及衍生的粗糙型突变菌株AK1401和AK1012中分离出脂多糖(LPS)。对粗糙突变体AK1401的LPS进行脱氧胆酸盐/聚丙烯酰胺凝胶电泳(Deoxycholate/PAGE)分析,结果显示在染料前沿附近有两条带,其迁移率与亲本菌株相似,这表明两种LPS均含有完整的核心以及一种包含核心和一个重复单元的物质。对菌株PAO1和AK1401的LPS进行组成分析表明,完整的核心寡糖由D-葡萄糖(四个单元)、L-鼠李糖(一个单元)、2-氨基-2-脱氧-D-半乳糖(一个单元)、L-甘油-D-甘露庚糖(Hep;两个单元)、3-脱氧-D-甘露辛酮酸(Kdo;两个单元)、L-丙氨酸(一个单元)和磷酸盐(三个单元)组成。LPS的聚糖结构通过一维和二维(2D)核磁共振技术,并结合基于质谱的方法,对通过脱脂程序从LPS获得的寡糖样品进行测定。通过对野生型菌株LPS的还原核心寡糖样品进行二维31P(ω1)-半滤波COSY实验,确定了第一个庚糖残基上三个磷酸单酯基团的位置。在第二个庚糖上观察到7-O-氨基甲酰基取代基的存在。铜绿假单胞菌血清型05的O链缺陷型LPS核心区域的结构如下:[结构:见原文],其中R1为β-D-葡萄糖基-(1→2)-α-L-鼠李糖基-(1→6)-α-D-葡萄糖基-(1→,R2为α-D-葡萄糖基-(1→6)-β-D-葡萄糖基-(1→。本文提出了一个结构模型,该模型也代表了铜绿假单胞菌血清型O6 LPS的结构模型。还给出了血清型O6突变菌株A28的修订结构。