Liang Xiquan, Baek Chang-Ho, Katzen Federico
Life Technologies , 5791 Van Allen Way, Carlsbad, California 92008, United States.
ACS Synth Biol. 2013 Dec 20;2(12):734-40. doi: 10.1021/sb400079u. Epub 2013 Nov 11.
A number of attempts have been made to simplify the synthesis of whole chromosomes to generate artificial microorganisms. However, the sheer size of the average bacterial genome makes the task virtually impracticable. A major limitation is the maximum assembly DNA size imposed by the current available technologies. We propose to fragment the bacterial chromosome into autonomous replicating units so that (i) each episome becomes small enough to be assembled in its entirety within an assembly host and (ii) the complete episome set should be able to generate a viable cell. In this work, we used the telN/tos system of bacteriophage N1 to show that the circular genome of Escherichia coli can be split into two linear chromosomes that complement each other to produce viable cells.
人们已经进行了多次尝试来简化全染色体的合成以产生人工微生物。然而,细菌平均基因组的巨大规模使得这项任务几乎无法实现。一个主要限制是当前可用技术所施加的最大组装DNA大小。我们建议将细菌染色体片段化为自主复制单元,以便(i)每个附加体变得足够小,能够在组装宿主内完整组装,并且(ii)完整的附加体集合应该能够产生一个活细胞。在这项工作中,我们使用噬菌体N1的telN/tos系统表明大肠杆菌的环状基因组可以被分裂成两条相互补充以产生活细胞的线性染色体。