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Summary The biosynthesis of metal nanoparticles from precious metals has been of wide concern. Their antibacterial activity is a main bottleneck restricting the bacterial activity and reduction performance. Here, bio-electrochemical systems were used to harvest electroactive biofilms (EABs), where bacteria were naturally protected by extracellular polymeric substances to keep activity. The biofilm was further encapsulated with polydopamine (PDA) as additional shield. Silver nanoparticles (AgNPs) were biosynthesized on EABs, whose electroactivity could be fully recovered after Ag+ reduction. The PDA increased bacterial viability by 90%–105%, confirmed as an effective protection against antibacterial activity of Ag+/AgNPs. The biosynthetic process changed the component and function of the microbial community, shifting from bacterial Fe reduction to archaeal methanogenesis. These results demonstrated that the electrochemical acclimation of EABs and encapsulation with PDA were effective protective measures during the biosynthesis of AgNPs. These approaches have a bright future in the green synthesis of nanomaterials, biotoxic wastewater treatment, and sustainable bio-catalysis., Graphical abstract, Highlights • The EABs formed using BESs had an efficient ability to recover Ag+ to AgNPs • The bio-reduction efficiencies of AgNPs reached more than 94% • The PDA increased by 90%–105% of the bacterial viability • The biosynthesis process changed the microbial community, Electrochemistry; Microbiofilms; Nanoparticles

The recovery of precious metals by biosynthesis of metal nanoparticles (NPs) has been a wide concern. The biotoxicity of metal ions and metal NPs is the main bottleneck restricting the bacterial activity and reduction performance. Here, bio-electrochemical systems were used to harvest electroactive biofilms (EABs), where cells were naturally protected by extracellular polymeric substances to keep the activity of the bacteria during this process. The biofilm with polydopamine (PDA) was further encapsulated as additional shield. Silver nanoparticles (AgNPs) were formed on the surface of bacterial cells, while the electroactivity of the biofilm could be fully recovered after Ag+ reduction. The PDA increased the bacterial viability by 90%–105%, confirmed as an effective protection against biotoxic Ag+ and AgNPs. The exposure to Ag+ and AgNPs changed the component and the main function of the microbial community, shifting from bacterial Fe reduction to archaeal methanogenesis. These results demonstrated that the electrochemical acclimation of EABs and encapsulation with PDA were effective in protecting bacteria from being inhibited by toxic metal ions. These approaches have a bright future in the green synthesis of nanomaterials, biotoxic wastewater treatment, and sustainable bio-catalysis.

Artificial sweeteners (ASs) are emerging polar organic contaminants, which can chelate with heavy metals in the environment. Recently, the ASs have been widely detected in the aquatic environment. However, little is known about the influence of ASs on the mobility and toxicity of heavy metals associated in sediment. In the present study, the release of heavy metals from a lake sediment and the toxicity to a green algae Scenedesmus obliquus were examined in the presence of two most frequently detected ASs, acesulfame and sucralose, and humic acid (HA), respectively. The existence of 1.00–100 mg/L of acesulfame, sucralose, and HA enhanced the release rates (Rrelease) of Cd, Cu, and Pb from the virgin lake sediment significantly by up to 46.7%, 86.0%, and 79.9%, respectively. Further, the results from microcosm experiments revealed that the existence of 1.00–10.0 mg/L of acesulfame, sucralose, and HA in the water phase prompted the release and toxicity of heavy metals associated with Cd- and Cu-spiked sediment, and the promotion capacity followed the order of HA > acesulfame > sucralose. The inhibitions on cell-specific growth rate (μ) of the algae were found increasing significantly with the elevated levels of acesulfame and HA (p

Escherichia coli O157:H7 associated with food has caused many serious public health problems in recent years. However, only viable cells of this pathogen can cause infections, and false-positive detection caused by dead cells can lead to unnecessary product recalls. The objective of this study was to develop and optimize a method that combines propidium monoazide (PMA) staining with real-time PCR to detect only viable cells of E. coli O157:H7 in ground beef. PMA is a DNA intercalating dye that can penetrate compromised membranes of dead cells and bind to cellular DNA, preventing its amplification via a subsequent PCR. Three strains of E. coli O157:H7 (505B, G5310 and C7927) at concentrations of 10(0) to 10(8)CFU/mL were used as live cells. Dead cells were obtained by heating cell suspensions at 85°C for 15 min. Suspensions were treated with PMA and the optimized assay was applied to artificially contaminated ground beef with two different fat contents (10% and 27%). DNA was extracted and amplified by TaqMan® real-time PCR assay targeting the uidA gene for detection of E. coli O157:H7. Plasmid pUC19 was added as an internal amplification control (IAC). A treatment of 25 μM PMA with a 10-min light exposure on ice was sufficient to eliminate DNA from 10(8) dead E. coli O157:H7 cells/mL. The optimized assay could detect as low as 10(2) CFU/mL viable E. coli O157:H7 in pure culture and 10(5) CFU/g in ground beef, in the presence of 10(6)/mL or g of dead cells. With an 8-h enrichment, 1 CFU/g viable E. coli O157:H7 in ground beef was detectable without interference from 10(6) dead cells/g. In conclusion, the PMA real-time PCR could effectively detect viable E. coli O157:H7 without being compromised by dead cells.