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疫霉菌中的菌丝尖端生长。酶的梯度分布与超微组织化学

Hyphal tip growth in Phytophthora. Gradient distribution and ultrahistochemistry of enzymes.

作者信息

Meyer R, Parish R W, Hohl H R

出版信息

Arch Microbiol. 1976 Nov 2;110(23):215-24. doi: 10.1007/BF00690230.

Abstract

Germinating cysts and isolated walls from germinating cysts incorporated 14C-UDPG into wall material of which 22.5 and 15% respectively were insoluble in boiling 1 N HCl, indicating that part of the synthetase activity is located in the wall itself. A combination of Urografin and Ficoll density gradients was used to separate various intracellular fractions. A consistent separation of beta-glucanase and UDPG-transferase enriched fractions was achieved. The beta-glucanase fraction contained dictyosome vesicles and fragments along with some plasma membranes. The UDPG-transferase fraction was relatively rich in membranes resembling rough and smooth ER. The results suggest the two enzymes are transported to the wall by different intracellular routes, and two types of vesicle may be involved. Alkaline phosphatase, beta-glucosidase and acid phosphatase were found extracellularly and their distribution in density gradients determined. The results of histochemical staining for acid phosphatase, alkaline phosphatase and polysaccharide are described and compared with the biochemical data. beta-1,3-glucanase, found intra- and extracellularly, induced distorted growth of germ tubes and also removed most of the apical wall when added to the incubation medium. None of these responses were observed with cellulase. Determinations of the osmotic pressure of germinating cysts and incubation medium revealed that the turgor of germinating cysts amounts to about 1.8 at under the conditions used.

摘要

萌发的囊肿以及从萌发囊肿分离出的囊壁将14C-UDPG掺入壁物质中,其中分别有22.5%和15%不溶于沸腾的1N盐酸,这表明部分合成酶活性位于壁本身。采用泛影葡胺和聚蔗糖密度梯度相结合的方法分离各种细胞内组分。实现了β-葡聚糖酶和富含UDPG-转移酶的组分的一致分离。β-葡聚糖酶组分包含高尔基体囊泡和碎片以及一些质膜。UDPG-转移酶组分相对富含类似于糙面内质网和滑面内质网的膜。结果表明这两种酶通过不同的细胞内途径转运至壁,可能涉及两种类型的囊泡。在细胞外发现了碱性磷酸酶、β-葡萄糖苷酶和酸性磷酸酶,并测定了它们在密度梯度中的分布。描述了酸性磷酸酶、碱性磷酸酶和多糖的组织化学染色结果,并与生化数据进行了比较。细胞内和细胞外均发现的β-1,3-葡聚糖酶诱导芽管生长畸变,当添加到孵育培养基中时还去除了大部分顶端壁。用纤维素酶未观察到这些反应。对萌发囊肿和孵育培养基渗透压的测定表明,在所使用的条件下,萌发囊肿的膨压约为1.8。

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