Cloning and expression of the human N-acetylneuraminic acid phosphate synthase gene with 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid biosynthetic ability

被引:80
作者
Lawrence, SM
Huddleston, KA
Pitts, LR
Nguyen, N
Lee, YC
Vann, WF
Coleman, TA
Betenbaugh, MJ [1 ]
机构
[1] Johns Hopkins Univ, Dept Chem Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
[3] US FDA, Lab Bacterial Toxins, Bethesda, MD 20892 USA
[4] US FDA, Lab Bacterial Polysaccharides, Bethesda, MD 20892 USA
[5] Human Genome Sci, Prot Dev, Rockville, MD 20850 USA
关键词
D O I
10.1074/jbc.M000217200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sialic acids participate in many important biological recognition events, yet eukaryotic sialic acid biosynthetic genes are not well characterized. In this study, we have identified a novel human gene based on homology to the Escherichia coli sialic acid synthase gene (neuB), The human gene is ubiquitously expressed and encodes a 40-kDa enzyme. The gene partially restores sialic acid synthase activity in a neuB-negative mutant of E. coli and results in N-acetylneuraminic acid (Neu5Ac) and 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid (KDN) production in insect cells upon recombinant baculovirus infection. In vitro the human enzyme uses N-acetylmannosamine 6-phosphate and mannose 6-phosphate as substrates to generate phosphorylated forms of Neu5Ac and KDN, respectively, but exhibits much higher activity toward the Neu5Ac phosphate product.
引用
收藏
页码:17869 / 17877
页数:9
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