Fernandez-Rodriguez Jesus, Yang Lei, Gorochowski Thomas E, Gordon D Benjamin, Voigt Christopher A
Synthetic Biology Center, Department of Biological Engineering, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
Broad Institute of MIT and Harvard , Cambridge, Massachusetts 02142, United States.
ACS Synth Biol. 2015 Dec 18;4(12):1361-72. doi: 10.1021/acssynbio.5b00170. Epub 2015 Nov 24.
Genetic memory can be implemented using enzymes that catalyze DNA inversions, where each orientation corresponds to a "bit". Here, we use two DNA invertases (FimE and HbiF) that reorient DNA irreversibly between two states with opposite directionality. First, we construct memory that is set by FimE and reset by HbiF. Next, we build a NOT gate where the input promoter drives FimE and in the absence of signal the reverse state is maintained by the constitutive expression of HbiF. The gate requires ∼3 h to turn on and off. The evolutionary stabilities of these circuits are measured by passaging cells while cycling function. The memory switch is stable over 400 h (17 days, 14 state changes); however, the gate breaks after 54 h (>2 days) due to continuous invertase expression. Genome sequencing reveals that the circuit remains intact, but the host strain evolves to reduce invertase expression. This work highlights the need to evaluate the evolutionary robustness and failure modes of circuit designs, especially as more complex multigate circuits are implemented.
遗传记忆可以通过催化DNA倒位的酶来实现,其中每个方向对应一个“位”。在这里,我们使用两种DNA转化酶(FimE和HbiF),它们能使DNA在两个具有相反方向性的状态之间不可逆地重新定向。首先,我们构建由FimE设置并由HbiF重置的记忆。接下来,我们构建一个非门,其中输入启动子驱动FimE,并且在没有信号的情况下,通过HbiF的组成型表达维持反向状态。该门需要约3小时来开启和关闭。这些电路的进化稳定性通过在循环功能时传代细胞来测量。记忆开关在400小时(17天,14次状态变化)内是稳定的;然而,由于转化酶的持续表达,该门在54小时(>2天)后失效。基因组测序表明电路保持完整,但宿主菌株进化以降低转化酶的表达。这项工作强调了评估电路设计的进化稳健性和故障模式的必要性,特别是在实施更复杂的多门电路时。