Li Biao, Sun Jia-Dong, Tang Chen, Zhou Jun, Wu Xia-Yuan, Jia Hong-Hua, Wei Ping, Zhang Yi-Feng, Yong Xiao-Yu
College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China; Department of Environmental Engineering, Technical University of Denmark, DK, 2800, Lyngby, Denmark.
College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China.
Water Res. 2021 Feb 1;189:116589. doi: 10.1016/j.watres.2020.116589. Epub 2020 Nov 2.
Electroactive biofilms (EABs) can be integrated with conductive nanomaterials to boost extracellular electron transfer (EET) for achieving efficient waste treatment and energy conversion in bioelectrochemical systems. However, the in situ nanomaterial-modified EABs of mixed-culture, and their response under environmental stress are rarely revealed. Here, two nanocatalyst-decorated EABs were established by self-assembled Au nanoparticles-reduced graphene oxide (Au-NPs/rGO) in mixed-biofilms with different maturities, then their multi-property were analyzed under long-term phenolic shock. Results showed that the power density of Au-NPs/rGO decorated EABs was significantly enhanced by 28.66-42.82% due to the intensified EET pathways inside biofilms. Meanwhile, the electrochemical and catalytic performance of EABs were controllably regulated by 0.3-3.0 g/L phenolic compounds, which, however, resulted in differential alterations in their architecture, composition, and viability. EABs originated with higher maturity displayed more compact structure, lower thickness (110 μm), higher biomass (8.67 mg/cm) and viability (0.85-0.91), endowing it better antishock ability to phenolic compounds. Phenolic-shock also induced the heterogeneous distribution of extracellular polymeric substances in terms of both spatial and bonding degrees of the decorated EABs, which could be regarded as an active response to strike a balance between self-protection and EET under environmental pressure. Our findings provide a broader understanding of microbe-electrode interactions in the micro-ecology interface and improve their performance in the removal of complex contaminants for sustainable remediation and new-energy development.
电活性生物膜(EABs)可与导电纳米材料结合,以促进细胞外电子转移(EET),从而在生物电化学系统中实现高效的废物处理和能量转换。然而,混合培养的原位纳米材料修饰的EABs及其在环境压力下的响应鲜有报道。在此,通过在不同成熟度的混合生物膜中自组装金纳米颗粒还原氧化石墨烯(Au-NPs/rGO),建立了两种纳米催化剂修饰的EABs,然后在长期酚类冲击下分析它们的多种特性。结果表明,由于生物膜内部EET途径的增强,Au-NPs/rGO修饰的EABs的功率密度显著提高了28.66%-42.82%。同时,0.3-3.0 g/L的酚类化合物可可控地调节EABs的电化学和催化性能,然而,这也导致了它们的结构、组成和活力的不同变化。起源于较高成熟度的EABs显示出更紧凑的结构、更低的厚度(110μm)、更高的生物量(8.67 mg/cm)和活力(0.85-0.91),使其对酚类化合物具有更好的抗冲击能力。酚类冲击还在修饰的EABs的空间和结合程度方面诱导了细胞外聚合物的异质分布,这可被视为在环境压力下在自我保护和EET之间取得平衡的一种积极响应。我们的研究结果为微生态界面中微生物-电极相互作用提供了更广泛的理解,并提高了它们在去除复杂污染物方面的性能,以实现可持续修复和新能源开发。