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Extracellular fibrils and contact-mediated cell interactions in Myxococcus xanthus.

机译:粘球菌中的细胞外原纤维和接触介导的细胞相互作用。

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摘要

Contact-mediated cell-cell interactions play an important role in the social life-style of Myxococcus xanthus. Previous investigations have demonstrated that fimbriae (also referred to as pili) and extracellular fibrils are involved in these social interactions (L. J. Shimkets, Microbiol. Rev. 54:473-501, 1990). We have used the relatively new technique of low-voltage scanning electron microscopy (an ultra-high-resolution scanning technique that allows for the nanometer resolution of biological materials) to observe the topological details of cell-cell interactions in M. xanthus. Our observations indicated that the fibrils (which measure approximately 30 nm in diameter) are produced most extensively by cells that are in close contact with each other and are aberrantly produced by the cohesion-deficient dsp mutants. Immunogold analysis identified an antigen which is located exclusively on the extracellular fibrils. Western blots (immunoblots) of this antigen (designated FA-1 for fibrillar antigen 1) indicated that it is composed of several immunoreactive bands (molecular size range, 90 to 14 kDa), all of which are sensitive to protease digestion. A technique for fibril isolation was developed by using FA-1 as a fibril-specific marker. Low-voltage scanning electron microscope observations of swarming cells demonstrated that the expression of fibrils is differentially regulated between adventurous (individual) and socially (group) motile cells. The differential expression of fibrils suggests the existence of a mechanism for the regulation of fibril biosynthesis that functions within the overall system governing social interactions in M. xanthus.
机译:接触介导的细胞-细胞相互作用在粘多糖球菌的社会生活方式中起着重要作用。先前的研究表明,菌毛(也称为菌毛)和细胞外原纤维参与这些社交相互作用(L.J.Shimkets,Microbiol.Rev.54:473-501,1990)。我们已经使用了相对较新的低压扫描电子显微镜技术(一种超高分辨率的扫描技术,可以对生物材料进行纳米分辨率)来观察黄单胞菌中细胞间相互作用的拓扑细节。我们的观察结果表明,原纤维(直径约30 nm)是由彼此紧密接触的细胞产生的,并且是由内聚力不足的dsp突变体异常产生的。免疫金分析鉴定出仅位于细胞外原纤维上的抗原。该抗原(原纤维抗原1的FA-1)的Western印迹(免疫印迹)表明,它由几个免疫反应带(分子大小范围为90至14 kDa)组成,所有这些带均对蛋白酶消化敏感。通过使用FA-1作为原纤维特异性标记物开发了原纤维分离技术。低电压扫描电子显微镜对成群细胞的观察表明,原动力细胞(个体)和社交细胞(群体)的原纤维表达受到差异调节。原纤维的差异表达表明存在调节原纤维生物合成的机制,该机制在支配黄单胞菌社会相互作用的整个系统中起作用。

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  • 作者

    Behmlander, R M; Dworkin, M;

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  • 年度 1991
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  • 正文语种 en
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