Immethun Cheryl M, Ng Kenneth M, DeLorenzo Drew M, Waldron-Feinstein Ben, Lee Ying-Chiang, Moon Tae Seok
Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, Missouri.
Biotechnol Bioeng. 2016 Feb;113(2):433-42. doi: 10.1002/bit.25722. Epub 2015 Sep 4.
As photoautotrophic prokaryotes, cyanobacteria are promising platforms for producing value-added bioproducts. However, few regulatory genetic parts and devices (e.g., inducible promoters and regulatory circuits) have been developed for these potential hosts. Furthermore, the devices that have been created respond only to a single input. To address these issues, we developed an inducible genetic circuit that generates heterologous proteins in response to oxygen, an environmental signal. To test its performance and utility in Synechocystis sp. PCC 6803, a model cyanobacterial strain, we connected this circuit to either heterologous nifHDK genes, which encode oxygen-sensitive nitrogenase's structural proteins, or a fluorescent protein gene. The circuit was transcriptionally activated to generate nifHDK transcripts or fluorescent output only in low oxygen conditions. We expanded the oxygen-responsive circuit into a more complex circuit by building a two-input AND gate, which allows Synechocystis to specifically control expression of the fluorescent reporter in response to two signals, low oxygen and high anhydrotetracycline. To our knowledge, the AND gate is the first complex logic circuit built in a cyanobacterial strain. This work expands the synthetic biology tools available for complex gene expression in cyanobacteria, increasing their potential as biotechnology platforms.
作为光合自养原核生物,蓝细菌是生产增值生物产品的有前景的平台。然而,针对这些潜在宿主开发的调控基因元件和装置(如诱导型启动子和调控回路)很少。此外,已创建的装置仅对单一输入作出响应。为了解决这些问题,我们开发了一种诱导型基因回路,其可响应环境信号氧气产生异源蛋白。为了测试其在模式蓝细菌菌株集胞藻PCC 6803中的性能和效用,我们将该回路连接到编码对氧敏感的固氮酶结构蛋白的异源nifHDK基因或荧光蛋白基因上。该回路仅在低氧条件下被转录激活以产生nifHDK转录本或荧光输出。我们通过构建一个双输入与门将氧响应回路扩展为一个更复杂的回路,该与门使集胞藻能够响应低氧和高脱水四环素这两个信号特异性地控制荧光报告基因的表达。据我们所知,该与门是在蓝细菌菌株中构建的首个复杂逻辑回路。这项工作扩展了可用于蓝细菌中复杂基因表达的合成生物学工具,增加了它们作为生物技术平台的潜力。