Díaz J A, Monteiro-Leal L H, de Souza W
Laboratorio de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Brazil.
Exp Parasitol. 1996 Jul;83(2):174-83. doi: 10.1006/expr.1996.0064.
An effective methodology to isolate and characterize the Golgi complex of Tritrichomonas foetus is described in this work. Using sucrose density gradient centrifugation, two highly enriched Golgi fractions (GF1 and GF2) were obtained. Enzymatic assays of GF1 and GF2 showed a strong enrichment in galactosyltransferase activity (20- and 7-fold, respectively), with minimal contamination with other organelles. The GF fraction was further subfractionated by alkaline treatment, which resulted in the production of Golgi content and membrane subfractions. Electron microscopic observations of intact cells or Golgi fractions fixed in solutions containing glutaraldehyde and tannic acid, as well as of deep-etched replicas of isolated fractions, revealed the presence of discrete bridges only between closely apposed cisternae.
本研究描述了一种分离和鉴定胎儿三毛滴虫高尔基体复合物的有效方法。通过蔗糖密度梯度离心,获得了两个高度富集的高尔基体组分(GF1和GF2)。对GF1和GF2的酶活性分析表明,半乳糖基转移酶活性有很强的富集(分别为20倍和7倍),其他细胞器的污染极少。GF组分通过碱性处理进一步细分,产生了高尔基体内容物和膜亚组分。对固定在含有戊二醛和单宁酸的溶液中的完整细胞或高尔基体组分,以及对分离组分的深度蚀刻复制品进行电子显微镜观察,发现仅在紧密相邻的扁平囊之间存在离散的桥。