Helbert W, Schülein M, Henrissat B
Centre de Recherches sur les Macromolécules Végétales, C.N.R.S., Grenoble, France.
Int J Biol Macromol. 1996 Oct;19(3):165-9. doi: 10.1016/0141-8130(96)01123-3.
A method for the direct electron microscopic observation of amylases in interaction with starch granules is presented. The technique involves immuno-gold labeling of the enzymes and cross-sectioning of hydrated starch granules. This approach allows the analysis of the internal degradation of starch with a concomitant visualization of enzymes at the sites of hydrolysis. The visualization of enzymes at the surface, inside the channel and inside the core of the degraded granules shows that the alpha-amylase molecules first proceed from the surface toward the center (centripetal hydrolysis). Then the core is completely degraded from within by erosion of its periphery (centrifugal hydrolysis). In the first case (centripetal hydrolysis), the enzymes act by progressing along the polysaccharide chains. By contrast, the centrifugal hydrolysis leads to even erosion, indicative of a more diffusive motion of the enzymes.
本文介绍了一种直接通过电子显微镜观察淀粉酶与淀粉颗粒相互作用的方法。该技术包括对酶进行免疫金标记以及对水合淀粉颗粒进行横截面切片。这种方法能够分析淀粉的内部降解情况,同时在水解位点观察到酶。在降解颗粒的表面、通道内部和核心部位观察到酶,这表明α-淀粉酶分子首先从表面向中心进行(向心水解)。然后,核心通过其外围的侵蚀从内部完全降解(离心水解)。在第一种情况(向心水解)中,酶沿着多糖链移动起作用。相比之下,离心水解导致均匀侵蚀,这表明酶的运动更具扩散性。