Pierce D C, Butler K D, Roer R D
Department of Biological Sciences, University of North Carolina at Wilmington, 601 South College Road, Wilmington, NC 28403-3297, USA.
Comp Biochem Physiol B Biochem Mol Biol. 2001 Apr;128(4):691-700. doi: 10.1016/s1096-4959(00)00362-6.
A cuticular glycosidase with characteristics of N-acetyl-beta-D-hexosaminidase (HexNAcase) was identified in post-ecdysial crab cuticle. Its appearance coincided with changes in cuticular glycoproteins and the onset of mineralization. To test if HexNAcase might be the causative agent in the alteration of the glycans and initiation of calcification, newly molted crab cuticle was treated with exogenous HexNAcase. Treating cuticular extracts from crabs at 0 h post-ecdysis with exogenous HexNAcase mimicked those changes observed in vivo. Specifically, the enzyme decreased the concanavalin A affinity of an 83-kDa glycoprotein that binds to calcite crystals in vitro. Treating pieces of 0 h post-ecdysial cuticle with HexNAcase rendered them capable of nucleating calcite in vitro (similar to 5 h post-ecdysial cuticle), while untreated, 0 h controls remained uncalcified. The data imply a role of the cuticular HexNAcase-like enzyme in the initiation of calcite nucleation in the newly formed exoskeleton.
在蜕皮后的蟹壳中鉴定出一种具有N-乙酰-β-D-己糖胺酶(HexNAcase)特征的表皮糖苷酶。它的出现与表皮糖蛋白的变化以及矿化的开始相吻合。为了测试HexNAcase是否可能是聚糖改变和钙化起始的致病因素,用外源性HexNAcase处理新蜕皮的蟹壳。用外源性HexNAcase处理蜕皮后0小时蟹的表皮提取物,模拟了体内观察到的那些变化。具体而言,该酶降低了一种83 kDa糖蛋白的伴刀豆球蛋白A亲和力,该糖蛋白在体外与方解石晶体结合。用HexNAcase处理蜕皮后0小时的表皮碎片,使其能够在体外成核方解石(类似于蜕皮后5小时的表皮),而未处理的0小时对照仍未钙化。数据表明表皮HexNAcase样酶在新形成的外骨骼中方解石成核起始中起作用。