Londoño-Vallejo J A, Fréhel C, Stragier P
Institut de Biologie Physico-Chimique, Paris, France.
Mol Microbiol. 1997 Apr;24(1):29-39. doi: 10.1046/j.1365-2958.1997.3181680.x.
A crucial step in converting an actively growing Bacillus subtilis cell into a dormant spore is the formation of a cell within a cell. This unusual structure is created by a phagocytosis-like process in which the larger mother cell progressively engulfs the adjacent smaller forespore. Only mutations blocking engulfment at an early stage and affecting genes expressed in the mother cell have been identified. Here we describe a new locus, spoIIQ, which is transcribed in the forespore and which encodes a membrane-bound protein required at a late stage of engulfment. Immunofluorescence microscopy analysis have shown that SpoIIQ is initially targeted to the septum at the boundary between the two cells and then spreads around the entire membrane of the forespore. Septum targeting requires only the first 52 residues of SpoIIQ as well as unidentified forespore-specific components. Electron-microscopy studies of cells engineered to activate the mother-cell program of gene expression independently of the forespore indicate that other as yet uncharacterized genes are involved in engulfment and that this morphological process is driven from both sides of the forespore envelope.
将活跃生长的枯草芽孢杆菌细胞转化为休眠孢子的关键步骤是形成细胞内细胞结构。这种不同寻常的结构是通过类似吞噬作用的过程形成的,在这个过程中,较大的母细胞逐渐吞噬相邻的较小的前芽孢。目前仅鉴定出了在早期阶段阻断吞噬作用并影响母细胞中表达基因的突变。在此,我们描述了一个新的基因座spoIIQ,它在前芽孢中被转录,并且编码一种在吞噬作用后期所需的膜结合蛋白。免疫荧光显微镜分析表明,SpoIIQ最初定位于两个细胞之间边界处的隔膜,然后扩散到前芽孢的整个膜周围。隔膜靶向仅需要SpoIIQ的前52个残基以及未鉴定的前芽孢特异性成分。对经工程改造以独立于前芽孢激活母细胞基因表达程序的细胞进行的电子显微镜研究表明,其他尚未表征的基因参与了吞噬作用,并且这种形态发生过程是从前芽孢包膜的两侧驱动的。