Department of Biology and Biochemistry, University of Houston, Houston, TX 77204-5001, USA.
Mol Microbiol. 2018 May;108(4):424-442. doi: 10.1111/mmi.13945. Epub 2018 Mar 23.
In starving Bacillus subtilis cells, the accDA operon encoding two subunits of the essential acetyl-CoA carboxylase (ACC) has been proposed to be tightly regulated by direct binding of the master regulator Spo0A to a cis element (0A box) in the promoter region. When the 0A box is mutated, biofilm formation and sporulation have been reported to be impaired. Here, we present evidence that two 0A boxes, one previously known (0A-1) and another newly discovered (0A-2) in the accDA promoter region are positively and negatively regulated by Spo0A∼P respectively. Cells with mutated 0A boxes experience slight delays in sporulation, but eventually sporulate with high efficiency. In contrast, cells harboring a single mutated 0A-2 box are deficient for biofilm formation, while cells harboring either a mutated 0A-1 box or both mutated 0A boxes form biofilms. We further show that the essential ACC enzyme localizes on or near the cell membrane by directly observing a functional GFP fusion to one of the enzyme's subunits. Collectively, we propose a revised model in which accDA is primarily transcribed by a major σ -RNA polymerase, while Spo0A∼P plays an additional role in the fine-tuning of accDA expression upon starvation to support proper biofilm formation and sporulation.
在饥饿的枯草芽孢杆菌细胞中,编码必需乙酰辅酶 A 羧化酶(ACC)两个亚基的 accDA 操纵子被提议通过主调控因子 Spo0A 与启动子区域中顺式元件(0A 盒)的直接结合而受到紧密调控。当 0A 盒发生突变时,据报道生物膜形成和孢子形成受损。在这里,我们提供的证据表明,accDA 启动子区域中的两个 0A 盒,一个先前已知的(0A-1)和另一个新发现的(0A-2),分别被 Spo0A∼P 正向和负向调控。具有突变 0A 盒的细胞在孢子形成方面略有延迟,但最终仍以高效率进行孢子形成。相比之下,携带单个突变 0A-2 盒的细胞缺乏生物膜形成能力,而携带突变 0A-1 盒或两个突变 0A 盒的细胞则形成生物膜。我们进一步表明,通过直接观察到一个酶的亚基的功能性 GFP 融合,必需的 ACC 酶定位于细胞膜上或附近。总的来说,我们提出了一个修正的模型,其中 accDA 主要由主要的 σ-RNA 聚合酶转录,而 Spo0A∼P 在饥饿时对 accDA 表达的微调中发挥额外作用,以支持适当的生物膜形成和孢子形成。