Department of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry Martinsried, Germany.
Front Microbiol. 2014 Jun 4;5:257. doi: 10.3389/fmicb.2014.00257. eCollection 2014.
In the framework of synthetic biology, it has become an intriguing question what would be the minimal representation of cell division machinery. Thus, it seems appropriate to compare how cell division is realized in different microorganisms. In particular, the cell division system of Crenarchaeota lacks certain proteins found in most bacteria and Euryarchaeota, such as FtsZ, MreB or the Min system. The Sulfolobaceae family encodes functional homologs of the eukaryotic proteins vacuolar protein sorting 4 (Vps4) and endosomal sorting complex required for transport-III (ESCRT-III). ESCRT-III is essential for several eukaryotic pathways, e.g., budding of intraluminal vesicles, or cytokinesis, whereas Vps4 dissociates the ESCRT-III complex from the membrane. Cell Division A (CdvA) is required for the recruitment of crenarchaeal ESCRT-III proteins to the membrane at mid-cell. The proteins polymerize and form a smaller structure during constriction. Thus, ESCRT-III mediated cell division in Sulfolobus acidocaldarius shows functional analogies to the Z ring observed in prokaryotes like Escherichia coli, which has recently begun to be reconstituted in vitro. In this short perspective, we discuss the possibility of building such an in vitro cell division system on basis of archaeal ESCRT-III.
在合成生物学的框架内,细胞分裂机制的最小代表性是什么,这已成为一个有趣的问题。因此,比较不同微生物中细胞分裂的实现方式似乎是合适的。特别是,古菌的细胞分裂系统缺乏大多数细菌和真细菌中发现的某些蛋白质,如 FtsZ、MreB 或 Min 系统。硫微菌科编码真核蛋白液泡蛋白分选 4(Vps4)和内体分选复合物需要运输 III(ESCRT-III)的功能同源物。ESCRT-III 对于几种真核途径是必不可少的,例如,腔内囊泡的出芽或胞质分裂,而 Vps4 将 ESCRT-III 复合物从膜上解离。细胞分裂 A(CdvA)是将古菌 ESCRT-III 蛋白募集到中膜的必需条件。这些蛋白质在收缩过程中聚合并形成较小的结构。因此,在嗜酸热硫化叶菌中,ESCRT-III 介导的细胞分裂与在大肠杆菌等原核生物中观察到的 Z 环具有功能相似性,最近已开始在体外重建。在这篇短评中,我们讨论了基于古菌 ESCRT-III 构建这种体外细胞分裂系统的可能性。