Knirel Y A, Widmalm G, Senchenkova S N, Jansson P E, Weintraub A
Karolinska Institute, Clinical Research Centre, Huddinge University Hospital, Sweden.
Eur J Biochem. 1997 Jul 1;247(1):402-10. doi: 10.1111/j.1432-1033.1997.00402.x.
A Vibrio cholerae O139 strain, MO10-T4, lacking capsular polysaccharide, produces a short-chain lipopolysaccharide (LPS), similar to enterobacterial SR strains. It was studied by acidic and alkaline degradation, dephosphorylation, sugar and methylation analysis, high-performance anion-exchange chromatography, one- and two-dimensional 1H-, 13C-, and 31P-NMR spectroscopy, and electrospray ionization mass spectrometry. The following structure was proposed for the core region of the LPS: [structure: see text] where PEtn stands for 2-aminoethyl phosphate, Fru for fructose, Hep for L-glycero-D-manno-heptose, and Kdo for 3-deoxy-D-manno-octulosonic acid; unless otherwise stated, the monosaccharide residues are D and present in the pyranose form. An O-acetyl group is present on a secondary position, tentatively O4 of the alpha-linked glucosyl group. Some LPS species contain an additional putative fructose residue whose location remains unknown. An O139-negative mutant strain, Bengal-2R, derived from V. cholerae O139, has also been investigated and shown to produce an O-antigen-lacking LPS similar to those from enterobacterial R strains, some of the LPS species containing the same core region as the strain MO10-T4 LPS and the other lacking the lateral heptose residue. The carbohydrate backbone core structure is the same for the V. cholerae O139 and V. cholerae O1 LPS, thus confirming the close relation between these bacteria; however, the 2-aminoethyl phosphate, the O-acetyl group, and the second fructose residue have not been reported for the O1 LPS. In the V. cholerae O139 strain MO10-T4 LPS, a short O-side chain is attached at position 3 of the 7-substituted heptose residue and has the same structure as one repeating unit of the V. cholerae O139 capsular polysaccharide. Some details of the structure proposed are at variance with those recently published for another V. cholerae O139 strain [Cox, A. D., Brisson, J.-R., Varma, V. & Perry, M. B. (1996) Carbohydr. Res. 290, 43-58; Cox, A. D. & Perry, M. B. (1996) Carbohydr. Res. 290, 59-65.]
一株霍乱弧菌O139菌株MO10-T4,缺乏荚膜多糖,产生一种短链脂多糖(LPS),类似于肠道杆菌SR菌株。通过酸碱性降解、去磷酸化、糖和甲基化分析、高效阴离子交换色谱、一维和二维1H-、13C-和31P-NMR光谱以及电喷雾电离质谱对其进行了研究。针对LPS的核心区域提出了以下结构:[结构:见原文],其中PEtn代表2-氨基乙基磷酸,Fru代表果糖,Hep代表L-甘油-D-甘露庚糖,Kdo代表3-脱氧-D-甘露辛酮糖酸;除非另有说明,单糖残基为D型且以吡喃糖形式存在。一个O-乙酰基位于二级位置,暂定为α-连接葡萄糖基的O4位。一些LPS种类含有一个额外的推定果糖残基,其位置尚不清楚。一株源自霍乱弧菌O139的O139阴性突变菌株Bengal-2R也已被研究,结果表明它产生一种缺乏O抗原的LPS,类似于肠道杆菌R菌株的LPS,其中一些LPS种类含有与MO10-T4菌株LPS相同的核心区域而另一些则缺少侧链庚糖残基。霍乱弧菌O139和霍乱弧菌O1的LPS的碳水化合物主链核心结构相同,从而证实了这些细菌之间的密切关系;然而,O1 LPS尚未报道有2-氨基乙基磷酸、O-乙酰基和第二个果糖残基。在霍乱弧菌O139菌株MO10-T4的LPS中,一个短的O侧链连接在7-取代庚糖残基的3位,并且与霍乱弧菌O139荚膜多糖的一个重复单元具有相同的结构。所提出结构的一些细节与最近发表的另一株霍乱弧菌O139菌株的结构细节不同[考克斯,A.D.,布里松,J.-R.,瓦尔马,V. & 佩里,M.B.(199