Abstract

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.

Highlights

  • In the framework of synthetic biology, it has become an intriguing question what would be the minimal representation of cell division machinery

  • Recent works revealed the important roles of the archaeal homologs to the eukaryotic vacuolar protein sorting 4 (Vps4, Saci_1372, called CdvC) and endosomal sorting complex required for transport-III (ESCRT-III, Saci_1373, called CdvB) proteins together with the protein Cell Division A (CdvA) (Saci_1374) for cell division in Sulfolobus acidocaldarius (Obita et al, 2007; Lindas et al, 2008; Samson et al, 2008, 2011; Wollert et al, 2009a,b; Wollert and Hurley, 2010) and for secretion of vesicles (Ellen et al, 2009)

  • After the segregation of the nucleoids, a ring formed of CdvA is supposed to precede the appearance of the ESCRT-III rings, which are later disassembled by the Vps4 (Samson et al, 2011)

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Summary

Introduction

In the framework of synthetic biology, it has become an intriguing question what would be the minimal representation of cell division machinery. 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.

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