Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Hakozaki 6-10-1, Higashi-ku, Fukuoka 812-8581, Japan.
Glycobiology. 2009 Dec;19(12):1446-51. doi: 10.1093/glycob/cwp118. Epub 2009 Aug 21.
Endoglycoceramidase (EGCase; EC 3.2.1.123) is a glycohydrolase that hydrolyzes the glycosidic linkage between the oligosaccharide and ceramide of various glycosphingolipids. We previously reported that hydra produced EGCase to digest glycosphingolipids of brine shrimp (Artemia salina), a type of aquatic crustacean used as a diet for the culture of hydra (Horibata Y, Sakaguchi K, Okino N, Iida H, Inagaki M, Fujisawa T, Hama Y, Ito M. 2004. J Biol Chem. 279:33379-33389). We report here that a major glycosphingolipid of brine shrimp is unique in structure and highly sensitive to EGCase. The glycosphingolipid was extracted from freshly hatched brine shrimp by Folch's partition, followed by mild alkaline hydrolysis and purification with a Sep-Pak plus silica cartridge. The structure of brine shrimp glycosphingolipid was determined by gas chromatography, gas chromatography-mass spectrometry, fast-atom bombardment mass spectrometry, and (1)H-NMR spectrometry to be GlcNAcalpha1-2Fucalpha1-3Manbeta1-4Glcbeta1-1'Cer. Two major molecular species of the glycosphingolipid were identified; the sugar and sphingoid base of each were the same but the major fatty acid was C22:0 and 2-hydroxy C22:0, respectively. This is the first report describing the glycosphingolipid that has an internal fucosyl residue substituted with alpha1-2 N-acetylglucosaminyl residue. This study also suggests the biological relevance of the glycosphingolipid as a dietary source of hydra which possesses EGCase as a digestion enzyme.
内切糖苷神经酰胺酶(EGCase;EC 3.2.1.123)是一种糖苷水解酶,可水解各种糖脂的寡糖和神经酰胺之间的糖苷键。我们之前曾报道过,水螅产生 EGCase 来消化盐水虾(Artemia salina)的糖脂,盐水虾是一种用于水螅培养的水生甲壳类动物(饲料)(Horibata Y,Sakaguchi K,Okino N,Iida H,Inagaki M,Fujisawa T,Hama Y,Ito M. 2004. J Biol Chem. 279:33379-33389)。我们在这里报告,盐水虾的一种主要糖脂在结构上是独特的,并且对 EGCase 高度敏感。该糖脂是通过 Folch 分配法从刚孵化的盐水虾中提取的,然后通过温和的碱性水解和 Sep-Pak plus 硅胶柱纯化。盐水虾糖脂的结构通过气相色谱、气相色谱-质谱、快原子轰击质谱和(1)H-NMR 光谱确定为 GlcNAcalpha1-2Fucalpha1-3Manbeta1-4Glcbeta1-1'Cer。鉴定出两种主要的糖脂分子种类;每个糖脂的糖和神经酰胺碱基相同,但主要脂肪酸分别为 C22:0 和 2-羟基 C22:0。这是第一个描述具有内部岩藻糖残基取代为α1-2 N-乙酰葡萄糖胺残基的糖脂的报告。这项研究还表明,作为水螅消化酶的消化酶,这种糖脂作为水螅的饮食来源具有生物学意义。