Kennedy Agata, Griffin Guy, Freemont Paul S, Polizzi Karen M, Moore Simon J
School of Biosciences University of Kent Canterbury UK.
Centre for Synthetic Biology and Innovation South Kensington Campus London UK.
Eng Biol. 2022 Aug 18;6(2-3):62-68. doi: 10.1049/enb2.12024. eCollection 2022 Jun-Sep.
In synthetic biology, biosensors are routinely coupled with a gene expression system for detecting small molecules and physical signals. We reveal a fluorescent complex, based on the interaction of an coli double bond reductase (CurA), as a detection unit with its substrate curcumin-we call this a direct protein (DiPro) biosensor. Using a cell-free synthetic biology approach, we use the CurA DiPro biosensor to fine tune 10 reaction parameters (cofactor, substrate, and enzyme levels) for cell-free curcumin biosynthesis, assisted through acoustic liquid handling robotics. Overall, we increase CurA-curcumin DiPro fluorescence within cell-free reactions by 78-fold. This finding adds to the growing family of protein-ligand complexes that are naturally fluorescent and potentially exploitable for a range of applications, including medical imaging to engineering high-value chemicals.
在合成生物学中,生物传感器通常与基因表达系统相结合,用于检测小分子和物理信号。我们揭示了一种基于大肠杆菌双键还原酶(CurA)与其底物姜黄素相互作用的荧光复合物,作为一个检测单元——我们将其称为直接蛋白质(DiPro)生物传感器。使用无细胞合成生物学方法,我们利用CurA DiPro生物传感器,通过声学液体处理机器人辅助,对无细胞姜黄素生物合成的10个反应参数(辅因子、底物和酶水平)进行微调。总体而言,我们使无细胞反应中CurA-姜黄素DiPro荧光增加了78倍。这一发现为不断壮大的天然荧光且可能用于一系列应用(包括医学成像到工程高价值化学品)的蛋白质-配体复合物家族增添了新成员。