Plomp Marco, Carroll Alicia Monroe, Setlow Peter, Malkin Alexander J
Biosciences and Biotechnology Division, Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, California, United States of America.
Department of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut, United States of America.
PLoS One. 2014 Sep 26;9(9):e108560. doi: 10.1371/journal.pone.0108560. eCollection 2014.
Bacillus spores are encased in a multilayer, proteinaceous self-assembled coat structure that assists in protecting the bacterial genome from stresses and consists of at least 70 proteins. The elucidation of Bacillus spore coat assembly, architecture, and function is critical to determining mechanisms of spore pathogenesis, environmental resistance, immune response, and physicochemical properties. Recently, genetic, biochemical and microscopy methods have provided new insight into spore coat architecture, assembly, structure and function. However, detailed spore coat architecture and assembly, comprehensive understanding of the proteomic composition of coat layers, and specific roles of coat proteins in coat assembly and their precise localization within the coat remain in question. In this study, atomic force microscopy was used to probe the coat structure of Bacillus subtilis wild type and cotA, cotB, safA, cotH, cotO, cotE, gerE, and cotE gerE spores. This approach provided high-resolution visualization of the various spore coat structures, new insight into the function of specific coat proteins, and enabled the development of a detailed model of spore coat architecture. This model is consistent with a recently reported four-layer coat assembly and further adds several coat layers not reported previously. The coat is organized starting from the outside into an outermost amorphous (crust) layer, a rodlet layer, a honeycomb layer, a fibrous layer, a layer of "nanodot" particles, a multilayer assembly, and finally the undercoat/basement layer. We propose that the assembly of the previously unreported fibrous layer, which we link to the darkly stained outer coat seen by electron microscopy, and the nanodot layer are cotH- and cotE- dependent and cotE-specific respectively. We further propose that the inner coat multilayer structure is crystalline with its apparent two-dimensional (2D) nuclei being the first example of a non-mineral 2D nucleation crystallization pattern in a biological organism.
芽孢杆菌的孢子被包裹在一个多层的、蛋白质自组装的外壳结构中,该结构有助于保护细菌基因组免受压力,并且由至少70种蛋白质组成。阐明芽孢杆菌孢子外壳的组装、结构和功能对于确定孢子致病机制、环境抗性、免疫反应以及物理化学性质至关重要。最近,遗传学、生物化学和显微镜方法为孢子外壳的结构、组装、结构和功能提供了新的见解。然而,详细的孢子外壳结构和组装、对外壳层蛋白质组组成的全面理解以及外壳蛋白在外壳组装中的具体作用及其在外壳内的精确定位仍存在疑问。在本研究中,原子力显微镜被用于探测枯草芽孢杆菌野生型以及cotA、cotB、safA、cotH、cotO、cotE、gerE和cotE gerE孢子的外壳结构。这种方法提供了各种孢子外壳结构的高分辨率可视化,对特定外壳蛋白的功能有了新的认识,并促成了一个详细的孢子外壳结构模型的建立。该模型与最近报道的四层外壳组装一致,并进一步增加了几个以前未报道的外壳层。外壳从外到内依次组织为最外层的无定形(硬壳)层、小杆层、蜂窝层、纤维层、“纳米点”颗粒层、多层组装体,最后是内壳/基层。我们提出,以前未报道的纤维层(我们将其与电子显微镜下看到的深色外被联系起来)和纳米点层的组装分别依赖于cotH和cotE,且是cotE特异性的。我们进一步提出,内壳多层结构是晶体状的,其明显的二维(2D)核是生物体内非矿物二维成核结晶模式的首个例子。