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Poly(ethylene glycol)

聚乙二醇)

Company: Sigma-Aldrich
Catalog#: 81310
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Quantification of Chitinase Activity in Fusarium oxysporum
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Date:
2016-08-05
[Abstract]  Fungal morphogenetic development requires modification and plasticity of the cell wall, which implies synthesis and remodelling of its components, including chitin and glucan. Thus chitinase and glucanase activities are crucial for cell-wall biogenesis and cell division. Quantification of chitinase activity might be useful to identify structural defects that could negatively influence growth and morphogenesis of some filamentous fungi like Fusarium oxysporum, which produces both intracellular and secreted chitinases. The chitinolytic enzymes are categorized based on their enzymatic action on chitin substrates. Endochitinases are defined as the enzymes catalyzing the random cleavage at internal points in the chitin chain. Exochitinases catalyze the progressive release of ... [摘要]  真菌形态发生需要细胞壁的修饰和可塑性,这意味着其组分(包括壳多糖和葡聚糖)的合成和重塑。因此几丁质酶和葡聚糖酶活性对于细胞壁生物发生和细胞分裂是至关重要的。几丁质酶活性的定量可能有助于鉴定可能负面影响一些丝状真菌如产生细胞内和分泌型几丁质酶的尖孢镰刀菌的生长和形态发生的结构缺陷。基于它们对壳多糖底物的酶作用将壳聚糖分解酶分类。内酯酶被定义为催化几丁质链中内部点的随机裂解的酶。外切球蛋白酶催化乙酰壳寡糖或N-乙酰葡糖胺从几丁质的非还原端逐步释放,因此分别称为壳聚糖酶和β-N-乙酰氨基葡糖苷酶。在这里,我们描述了一种简单的方法来轻易地纯化几丁质酶,以便比较不同的F的内切几丁质酶活性和外切几丁质酶活性。尖孢镰孢菌株。该方案可适用于任何真菌物种。

Actin Retrograde Flow in Permeabilized Cells: Myosin-II Driven Centripetal Movement of Transverse Arcs
Author:
Date:
2016-03-05
[Abstract]  Numerous biological functions such as cytokinesis, changes in cell shape and cell migration require actomyosin-driven cellular contractility. However, the detailed mechanism of how contractile forces drive cellular processes are difficult to decipher due to the complexity of the intracellular environment. In particular, the mesoscopic description of the myosin II-dependent actin retrograde flow in cell lamellum is missing. Here, we describe a methodology for detergent extraction of cell, which preserves integrity of the actin cytoskeleton. This semi-in vitro cell model allows for the observation, using light microscopy, and quantification of changes in the actin cytoskeleton resulting from the activation of cellular contractility upon addition of ATP. This assay also allows for ... [摘要]  许多生物学功能如细胞分裂,细胞形状和细胞迁移的变化需要肌动蛋白驱动的细胞收缩性。然而,由于细胞内环境的复杂性,收缩力如何驱动细胞过程的详细机制难以解读。特别是,细胞层中的肌球蛋白II依赖性肌动蛋白逆行流的介观描述缺失。在这里,我们描述了洗涤剂提取的细胞,保留肌动蛋白细胞骨架的完整性的方法。这种半体外细胞模型允许使用光学显微镜观察和定量在添加ATP时由于细胞收缩性的活化而导致的肌动蛋白细胞骨架中的变化。该测定还允许评估肌动蛋白相关蛋白和其他相关因子在肌动蛋白收缩活性的调节中的作用。在这里,我们证明逆行流动的着名的基于肌动蛋白的结构 - 横向弧,这是肌球蛋白IIA含有结构出现在lamellipodium-lamellum之间的边界和肌球蛋白II依赖的方式向心移动。

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