Divided we stand: splitting synthetic cells for their proliferation.

Systems and Synthetic Biology Pub Date : 2014-09-01 Epub Date: 2014-05-27 DOI:10.1007/s11693-014-9145-7
Yaron Caspi, Cees Dekker
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引用次数: 37

Abstract

With the recent dawn of synthetic biology, the old idea of man-made artificial life has gained renewed interest. In the context of a bottom-up approach, this entails the de novo construction of synthetic cells that can autonomously sustain themselves and proliferate. Reproduction of a synthetic cell involves the synthesis of its inner content, replication of its information module, and growth and division of its shell. Theoretical and experimental analysis of natural cells shows that, whereas the core synthesis machinery of the information module is highly conserved, a wide range of solutions have been realized in order to accomplish division. It is therefore to be expected that there are multiple ways to engineer division of synthetic cells. Here we survey the field and review potential routes that can be explored to accomplish the division of bottom-up designed synthetic cells. We cover a range of complexities from simple abiotic mechanisms involving splitting of lipid-membrane-encapsulated vesicles due to physical or chemical principles, to potential division mechanisms of synthetic cells that are based on prokaryotic division machineries.

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我们分裂了:分裂合成细胞使其增殖。
随着最近合成生物学的兴起,人造生命的旧观念重新引起了人们的兴趣。在自下而上方法的背景下,这需要从头构建能够自主维持自身和增殖的合成细胞。合成细胞的繁殖包括其内部内容物的合成、其信息模块的复制以及其外壳的生长和分裂。对自然细胞的理论和实验分析表明,虽然信息模块的核心合成机制是高度保守的,但为了实现分裂,已经实现了广泛的解决方案。因此,可以预期有多种方法来设计合成细胞的分裂。在此,我们综述了这一领域,并回顾了可以探索完成自下而上设计的合成细胞分裂的潜在途径。我们涵盖了一系列复杂的问题,从简单的非生物机制,包括由于物理或化学原理导致脂质膜包裹的囊泡分裂,到基于原核分裂机制的合成细胞的潜在分裂机制。
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