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分则立:分裂合成细胞以实现其增殖。

Divided we stand: splitting synthetic cells for their proliferation.

作者信息

Caspi Yaron, Dekker Cees

机构信息

Department of Bionanoscience, Kavli Institute of Nanoscience, Delft University of Technology, Delft , 2628 CJ The Netherlands.

出版信息

Syst Synth Biol. 2014 Sep;8(3):249-69. doi: 10.1007/s11693-014-9145-7. Epub 2014 May 27.

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.

摘要

随着合成生物学的兴起,人造人工生命这一古老概念重新引发了人们的兴趣。在自下而上的方法背景下,这需要从头构建能够自主维持自身并增殖的合成细胞。合成细胞的繁殖涉及细胞内部物质的合成、信息模块的复制以及外壳的生长和分裂。对天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高度保守,但为了实现分裂已经实现了多种解决方案。因此,可以预期存在多种设计合成细胞分裂的方法。在这里,我们对该领域进行了综述,并回顾了为实现自下而上设计的合成细胞分裂可探索的潜在途径。我们涵盖了一系列复杂情况,从基于物理或化学原理导致脂质膜包裹的囊泡分裂的简单非生物机制,到基于原核分裂机制的合成细胞潜在分裂机制。

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