Ajunwa Obinna M, Minero Gabriel Antonio S, Jensen Sissel D, Meyer Rikke L
Interdisciplinary Nanoscience Center (iNANO), Aarhus University, Gustav Wieds Vej 14, 8000 Aarhus, Denmark.
Center for Electromicrobiology, Department of Biology, Aarhus University, Ny Munkegade 114, DK-8000 Aarhus C, Denmark.
Nucleic Acids Res. 2025 Aug 11;53(15). doi: 10.1093/nar/gkaf790.
Non-canonical DNA structures have been recently identified in bacterial biofilms, but their functional roles remain poorly understood. Here, we demonstrate that G-quadruplex (G4) DNA structures complexed with hemin enable extracellular electron transfer (EET) in biofilms. Using Staphylococcusepidermidis as a model organism, we show that extracellular DNA and hemin are essential for EET, with surface-associated G4-DNA/hemin complexes transferring electrons from bacteria to electrodes under anoxic conditions. Adding G4-DNA and hemin to growing biofilms promoted stable EET for days, demonstrating that these complexes serve as robust electrical conduits. The structural properties of G4-DNA, with its stacked guanine quartets facilitating π-π interactions with hemin's porphyrin ring, create an effective electron transfer pathway. Additionally, the G4-DNA/hemin complex functions as a peroxidase-like DNAzyme, transferring electrons from bacteria to H2O2. This study reveals a previously unknown functional role for G4-DNA structures in biofilms, establishing them as components of bacterial EET. Our findings provide new insights into how non-canonical DNA structures contribute to bacterial energy conservation under oxygen limitation, and potentially also to their defense against oxidative stress during infection.
非经典DNA结构最近在细菌生物膜中被发现,但其功能作用仍知之甚少。在此,我们证明与血红素复合的G-四链体(G4)DNA结构能够在生物膜中实现细胞外电子转移(EET)。以表皮葡萄球菌作为模式生物,我们表明细胞外DNA和血红素对EET至关重要,表面相关的G4-DNA/血红素复合物在缺氧条件下将电子从细菌转移到电极。向生长中的生物膜中添加G4-DNA和血红素可促进数天的稳定EET,表明这些复合物可作为强大的电导体。G4-DNA的结构特性,其堆叠的鸟嘌呤四重体促进与血红素卟啉环的π-π相互作用,创造了一条有效的电子转移途径。此外,G4-DNA/血红素复合物作为一种类似过氧化物酶的脱氧核酶,将电子从细菌转移到H2O2。这项研究揭示了G4-DNA结构在生物膜中以前未知的功能作用,将它们确立为细菌EET的组成部分。我们的发现为非经典DNA结构如何在氧气限制下促进细菌能量守恒以及在感染期间对氧化应激的防御提供了新的见解。