Institute of Microbiology, University of Stuttgart, Stuttgart, Germany.
Department of Microbiology, University Bayreuth, Bayreuth, Germany.
Microb Physiol. 2022;32(3-4):71-82. doi: 10.1159/000521970. Epub 2022 Feb 15.
Agrobacterium tumefaciens has two polyphosphate (polyP) kinases, one of which (PPK1AT) is responsible for the formation of polyP granules, while the other (PPK2AT) is used for replenishing the NTP pools by using polyP as a phosphate donor to phosphorylate nucleoside diphosphates. Fusions of eYFP with PPK2AT or of the polyP granule-associated phosin PptA from Ralstonia eutropha always co-localized with polyP granules in A. tumefaciens and allowed the tracking of polyP granules in time-lapse microscopy experiments without the necessity to label the cells with the toxic dye DAPI. Fusions of PPK1AT with mCherry formed fluorescent signals often attached to, but not completely co-localizing with, polyP granules in wild-type cells. Time-lapse microscopy revealed that polyP granules in about one-third of a cell population migrated from the old pole to the new cell pole shortly before or during cell division. Many cells de novo formed a second (nonmigrating) polyP granule at the opposite cell pole before cell division was completed, resulting in two daughter cells each having a polyP granule at the old pole after septum formation. Migration of polyP granules was disordered in mitomycin C-treated or in PopZ-depleted cells, suggesting that polyP granules can associate with DNA or with other molecules that are segregated during the cell cycle.
根瘤农杆菌有两种多磷酸盐(polyP)激酶,其中一种(PPK1AT)负责多磷酸盐颗粒的形成,而另一种(PPK2AT)则利用多磷酸盐作为磷酸供体磷酸化核苷二磷酸来补充 NTP 池。eYFP 与 PPK2AT 的融合,或来自恶臭假单胞菌的多磷酸盐颗粒相关磷酸酶 PptA 的融合,在根瘤农杆菌中总是与多磷酸盐颗粒共定位,并允许在延时显微镜实验中跟踪多磷酸盐颗粒,而无需用有毒染料 DAPI 标记细胞。与 mCherry 的融合 PPK1AT 形成的荧光信号通常附着在多磷酸盐颗粒上,但不完全与多磷酸盐颗粒共定位。延时显微镜显示,在细胞群体的约三分之一中,多磷酸盐颗粒在细胞分裂前不久或期间从旧极迁移到新的细胞极。许多细胞在完成细胞分裂之前,在相反的细胞极新形成第二个(非迁移)多磷酸盐颗粒,导致在隔膜形成后,每个子细胞在旧极都有一个多磷酸盐颗粒。在用丝裂霉素 C 处理或 PopZ 耗尽的细胞中,多磷酸盐颗粒的迁移是无序的,这表明多磷酸盐颗粒可以与 DNA 或在细胞周期中分离的其他分子结合。