DNA Replication in Engineered Escherichia coli Genomes with Extra Replication Origins

被引:12
|
作者
Milbredt, Sarah [1 ]
Farmani, Neda [1 ]
Sobetzko, Patrick [1 ]
Waldminghaus, Torsten [1 ]
机构
[1] Philipps Univ, SYNMIKRO, LOEWE Ctr Synthet Microbiol, Hans Meerwein Str 6, D-35043 Marburg, Germany
来源
ACS SYNTHETIC BIOLOGY | 2016年 / 5卷 / 10期
关键词
genetic engineering; bacteria; synthetic chromosomes; synthetic genomes; genome design; VIBRIO-CHOLERAE CHROMOSOMES; GENE-EXPRESSION; SEQA PROTEIN; INITIATION; CYCLE; TRANSCRIPTION; INACTIVATION; CELLS;
D O I
10.1021/acssynbio.6b00064
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The standard outline of bacterial genomes is a single circular chromosome with a single replication origin. From the bioengineering perspective, it appears attractive to extend this basic setup. Bacteria with split chromosomes or multiple replication origins have been successfully constructed in the last few years. The characteristics of these engineered strains will largely depend on the respective DNA replication patterns. However, the DNA replication has not been investigated systematically in engineered bacteria with multiple origins or split replicons. Here we fill this gap by studying a set of strains consisting of (i) E. coli strains with an extra copy of the native replication origin (oriC), (ii) E. coli strains with an extra copy of the replication origin from the secondary chromosome of Vibrio cholerae (oriII), and (iii) a strain in which the E. coli chromosome is split into two linear replicons. A combination of flow cytometry, microarray-based comparative genomic hybridization (CGH), and modeling revealed silencing of extra oriC copies and differential timing of ectopic orill copies compared to the native oriC. The results were used to derive construction rules for future multiorigin and multireplicon projects.
引用
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页码:1167 / 1176
页数:10
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