Vann W F, Tavarez J J, Crowley J, Vimr E, Silver R P
Laboratory of Bacterial Polysaccharides, Center for Biologics Research and Review, Bethesda, MD 20892, USA.
Glycobiology. 1997 Jul;7(5):697-701. doi: 10.1093/glycob/7.5.697.
Escherichia coli K1 produces a capsular polysaccharide of alpha(2-8) poly-N-acetylneuraminic acid. This polysaccharide is an essential virulence factor of these neuropathogenic bacteria. The genes necessary for the synthesis of neuNAc were localized to a plasmid containing the neuBAC genes of the K1 gene cluster. Cells harboring the neuB+ allele in an aldolase (nanA-) negative background produce neuNAc in vivo. Enzymatic synthesis of neuNAc could be demonstrated in extracts of cells harboring an expression plasmid (pNEUB) containing the neuB gene alone. NeuNAc synthetase was purified to homogeneity from extracts of cells harboring pNEUB. The molecular weight of the purified enzyme is 40 kDa, similar to that predicted by the nucleotide sequence of the neuB gene. The amino terminal sequence of the purified protein matches that predicted by the nucleotide sequence of the neuB gene. NeuNAc synthetase catalyzes the formation of neuNAc as indicated by its coupling to the CMP-neuNAc synthetase reaction. The enzyme condenses manNAc and PEP with the release of phosphate. The E. coli neuNAc synthetase is specific for manNAc and PEP, unlike rat liver enzyme that utilizes N-acetylmannosamine-6-phosphate to form neuNAc-9-PO4. This represents the first report of a purification of a sialic acid synthetase from either a eukaryotic or prokaryotic source to homogeneity. These experiments clearly demonstrate an aldolase-independent sialic acid synthetase activity in E. coli K1.
大肠杆菌K1产生α(2-8)聚-N-乙酰神经氨酸的荚膜多糖。这种多糖是这些神经致病性细菌的一种重要毒力因子。合成神经氨酸(neuNAc)所需的基因定位于一个含有K1基因簇的neuBAC基因的质粒上。在醛缩酶(nanA-)阴性背景下携带neuB+等位基因的细胞在体内产生神经氨酸。在仅含有neuB基因的表达质粒(pNEUB)的细胞提取物中可以证明神经氨酸的酶促合成。从携带pNEUB的细胞提取物中纯化神经氨酸合成酶至同质。纯化酶的分子量为40 kDa,与neuB基因的核苷酸序列预测的分子量相似。纯化蛋白的氨基末端序列与neuB基因的核苷酸序列预测的序列匹配。神经氨酸合成酶催化神经氨酸的形成,这通过其与CMP-神经氨酸合成酶反应的偶联得以表明。该酶将甘露糖胺和磷酸烯醇式丙酮酸缩合,释放出磷酸。与利用N-乙酰甘露糖胺-6-磷酸形成神经氨酸-9-磷酸的大鼠肝脏酶不同,大肠杆菌神经氨酸合成酶对甘露糖胺和磷酸烯醇式丙酮酸具有特异性。这是首次从真核或原核来源纯化唾液酸合成酶至同质的报告。这些实验清楚地证明了大肠杆菌K1中存在一种不依赖醛缩酶的唾液酸合成酶活性。