Feng Lu, Senchenkova Sof'ya N, Yang Jinghua, Shashkov Alexander S, Tao Jiang, Guo Hongjie, Cheng Jiansong, Ren Yi, Knirel Yuriy A, Reeves Peter R, Wang Lei
TEDA School of Biological Sciences and Biotechnology, Nankai University, Tianjin Biochip Technology Corporation, Tianjin, People's Republic of China.
J Bacteriol. 2004 Jul;186(14):4510-9. doi: 10.1128/JB.186.14.4510-4519.2004.
The structural and genetic organization of the Escherichia coli O52 O antigen was studied. As identified by sugar and methylation analysis and nuclear magnetic resonance spectroscopy, the O antigen of E. coli O52 has a partially O-acetylated disaccharide repeating unit (O unit) containing D-fucofuranose and 6-deoxy-D-manno-heptopyranose, as well as a minor 6-deoxy-3-O-methylhexose (most likely, 3-O-methylfucose). The O-antigen gene cluster of E. coli O52, which is located between the galF and gnd genes, was found to contain putative genes for the synthesis of the O-antigen constituents, sugar transferase genes, and ABC-2 transporter genes. Further analysis confirmed that O52 employs an ATP-binding cassette (ABC) transporter-dependent pathway for translocation and polymerization of the O unit. This is the first report of an ABC transporter being involved in translocation of a heteropolysaccharide O antigen in E. coli. Genes specific for E. coli O52 were also identified.
对大肠杆菌O52 O抗原的结构和基因组织进行了研究。通过糖和甲基化分析以及核磁共振光谱鉴定,大肠杆菌O52的O抗原有一个部分O-乙酰化的二糖重复单元(O单元),包含D-岩藻呋喃糖和6-脱氧-D-甘露庚糖,以及少量的6-脱氧-3-O-甲基己糖(很可能是3-O-甲基岩藻糖)。发现位于galF和gnd基因之间的大肠杆菌O52的O抗原基因簇包含用于合成O抗原成分的推定基因、糖基转移酶基因和ABC-2转运蛋白基因。进一步分析证实,O52采用依赖ATP结合盒(ABC)转运蛋白的途径进行O单元的转运和聚合。这是关于ABC转运蛋白参与大肠杆菌中杂多糖O抗原转运的首次报道。还鉴定了大肠杆菌O52特有的基因。