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为两种模式蓝细菌集胞藻PCC 6803和PCC 7942建立丙二酰辅酶A生物传感器。

Establishing a Malonyl-CoA Biosensor for the Two Model Cyanobacteria sp. PCC 6803 and PCC 7942.

作者信息

Cengic Ivana, Hudson Elton P

机构信息

School of Engineering Sciences in Chemistry, Biotechnology and Health, Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm 106 91, Sweden.

出版信息

ACS Synth Biol. 2025 Jul 18;14(7):2865-2877. doi: 10.1021/acssynbio.5c00320. Epub 2025 Jun 30.

Abstract

Malonyl-CoA, produced by the first committed step of fatty acid biosynthesis, is a precursor for many valuable bioproducts, making it an important metabolic engineering target. Here, we establish a malonyl-CoA biosensor for the model cyanobacteria sp. PCC 6803 and PCC 7942. The developed biosensor utilizes FapR, a malonyl-CoA-regulated transcriptional repressor from , and novel FapR-regulated and cyanobacteria-compatible hybrid promoters for expressing Yfp, the biosensor output reporter. A l-rhamnose-inducible promoter , characterized in combination with ribosome binding sites of varied strengths, was evaluated for titratable FapR expression. Additionally, the placement and quantity of the FapR-recognized operator within the hybrid promoter was evaluated for its effect on biosensor performance. The optimal operator placement was found to differ for the biosensor variants that achieved maximum reporter expression in the two considered model cyanobacteria. Overall, this biosensor provides new opportunities for further development of cyanobacterial cell factories.

摘要

丙二酰辅酶A是脂肪酸生物合成第一步的产物,是许多有价值生物产品的前体,使其成为重要的代谢工程靶点。在此,我们为模式蓝藻集胞藻PCC 6803和PCC 7942建立了一种丙二酰辅酶A生物传感器。所开发的生物传感器利用来自的丙二酰辅酶A调节转录阻遏物FapR,以及新型的FapR调节且与蓝藻兼容的杂交启动子来表达生物传感器输出报告基因Yfp。对与不同强度核糖体结合位点结合表征的L-鼠李糖诱导型启动子进行了可滴定FapR表达的评估。此外,还评估了杂交启动子内FapR识别的操纵子的位置和数量对生物传感器性能的影响。发现在两种模式蓝藻中实现最大报告基因表达的生物传感器变体的最佳操纵子位置不同。总体而言,这种生物传感器为蓝藻细胞工厂的进一步开发提供了新机会。

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