We report an ingestible, millimeter-sized microbial fuel cell (MFC) capsule that can provide a realistic and practical power solution for ingestible electronics. The capsule integrates a pH-sensitive enteric membrane, a germinant-containing layer, and a microfluidic hydrogel-based anodic channel pre-inoculated with Bacillus subtilis spores as dormant biocatalysts, which are directly connected to an integrated MFC. When the pH-sensitive membrane dissolves in a designated gut location with a specific pH, the hydrophilic hydrogel in the anodic channel absorb the gut fluids washing the germinant to trigger the spore germination and generate microbial metabolic electricity in our world’s smallest MFC. When the capsule is designed to work in the human intestine, it generates electricity only in the neutral pH solution achieving maximum power and current densities of 64μW/cm2 and 435 μA/cm2, respectively, which are substantially higher than the other energy harvesting techniques. 
                        more » 
                        « less   
                    
                            
                            Revolutionary self-powered transducing mechanism for long-lasting and stable glucose monitoring: achieving selective and sensitive bacterial endospore germination in microengineered paper-based platforms
                        
                    
    
            Abstract We introduce a groundbreaking proof-of-concept for a novel glucose monitoring transducing mechanism, marking the first demonstration of a spore-forming microbial whole-cell sensing platform. The approach uses selective and sensitive germination ofBacillus subtilisspores in response to glucose in potassium-rich bodily fluids such as sweat. As the rate of germination and the number of metabolically active germinating cells are directly proportional to glucose concentration, the electrogenic activity of these cells—manifested as electricity—serves as a self-powered transducing signal for glucose detection. Within a microengineered, paper-based microbial fuel cell (MFC), these electrical power outputs are measurable and can be visually displayed through a compact interface, providing real-time alerts. The dormant spores extend shelf-life, and the self-replicating bacteria ensure robustness. The MFC demonstrated a remarkable sensitivity of 2.246 µW·(log mM)−1·cm−2to glucose concentrations ranging from 0.2 to 10 mM, with a notably lower limit of detection at ~0.07 mM. The sensor exhibited exceptional selectivity, accurately detecting glucose even in the presence of various interferents. Comparative analyses revealed that, unlike conventional enzymatic biosensors whose performance degrades significantly through time even when inactive, the spore-based MFC is stable for extended periods and promptly regains functionality when needed. This preliminary investigation indicates that the spore-forming microbial whole-cell sensing strategy holds considerable promise for efficient diabetes management and can be extended toward noninvasive wearable monitoring, overcoming critical challenges of current technologies and paving the way for advanced biosensing applications. 
        more » 
        « less   
        
    
    
                            - PAR ID:
- 10559863
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Microsystems & Nanoengineering
- Volume:
- 10
- Issue:
- 1
- ISSN:
- 2055-7434
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
- 
            
- 
            Abstract Transient electronics, which can operate only for short‐lived applications and then be eco‐friendly disintegrated, create opportunities in environmental sensing, healthcare, and hardware security. Paper‐based electronics, or papertronics, recently have rapidly advanced the physically transient device platform because paper as a foundation offers an environmentally sustainable and cost‐effective option for those increasingly pervasive and fast‐updated single‐use applications. Paper‐based power supplies are indispensable to realize a fully papertronic paradigm and are a critical enabler of environmentally benign power solutions. Microbial fuel cells (MFCs) hold great potential as power sources for such green papertronic applications. This work reports the design, operation, and optimization of a high‐power papertronic MFC by biosynthesizing microbe‐mediated tin oxide nanoparticles (SnO2NPs) on dormant Bacillus subtilis endospores. They form an electrical conduit that improves electron harvesting during the spore germination and power generation. The MFC is packaged in a sub‐microporous alginate to minimize the potential risk of bacteria leakage. Upon the introduction of water, the paper‐based MFC generates a significantly enhanced power density of 140 µW cm−2, which is more than two orders of magnitude greater than their previously reported counterparts. Six MFCs connected in series generate more than sufficient power to run an on‐chip, light‐emitting diode.more » « less
- 
            Abstract Paenibacillus larvae, a Gram-positive bacterium, causes American foulbrood (AFB) in honey bee larvae (Apis mellifera Linnaeus [Hymenoptera: Apidae]). P. larvae spores exit dormancy in the gut of bee larvae, the germinated cells proliferate, and ultimately bacteremia kills the host. Hence, spore germination is a required step for establishing AFB disease. We previously found that P. larvae spores germinate in response to l-tyrosine plus uric acid in vitro. Additionally, we determined that indole and phenol blocked spore germination. In this work, we evaluated the antagonistic effect of 35 indole and phenol analogs and identified strong inhibitors of P. larvae spore germination in vitro. We further tested the most promising candidate, 5-chloroindole, and found that it significantly reduced bacterial proliferation. Finally, feeding artificial worker jelly containing anti-germination compounds to AFB-exposed larvae significantly decreased AFB infection in laboratory-reared honey bee larvae. Together, these results suggest that inhibitors of P. larvae spore germination could provide another method to control AFB.more » « less
- 
            Abstract BackgroundThe Spacecraft Assembly Facility (SAF) at the NASA’s Jet Propulsion Laboratory is the primary cleanroom facility used in the construction of some of the planetary protection (PP)-sensitive missions developed by NASA, including the Mars 2020 Perseverance Rover that launched in July 2020. SAF floor samples (n=98) were collected, over a 6-month period in 2016 prior to the construction of the Mars rover subsystems, to better understand the temporal and spatial distribution of bacterial populations (total, viable, cultivable, and spore) in this unique cleanroom. ResultsCleanroom samples were examined for total (living and dead) and viable (living only) microbial populations using molecular approaches and cultured isolates employing the traditional NASA standard spore assay (NSA), which predominantly isolated spores. The 130 NSA isolates were represented by 16 bacterial genera, of which 97% were identified as spore-formers via Sanger sequencing. The most spatially abundant isolate wasBacillus subtilis, and the most temporally abundant spore-former wasVirgibacillus panthothenticus. The 16S rRNA gene-targeted amplicon sequencing detected 51 additional genera not found in the NSA method. The amplicon sequencing of the samples treated with propidium monoazide (PMA), which would differentiate between viable and dead organisms, revealed a total of 54 genera: 46 viable non-spore forming genera and 8 viable spore forming genera in these samples. The microbial diversity generated by the amplicon sequencing corresponded to ~86% non-spore-formers and ~14% spore-formers. The most common spatially distributed genera wereSphinigobium,Geobacillus, andBacilluswhereas temporally distributed common genera wereAcinetobacter,Geobacilllus, andBacillus. Single-cell genomics detected 6 genera in the sample analyzed, with the most prominent beingAcinetobacter. ConclusionThis study clearly established that detecting spores via NSA does not provide a complete assessment for the cleanliness of spacecraft-associated environments since it failed to detect several PP-relevant genera that were only recovered via molecular methods. This highlights the importance of a methodological paradigm shift to appropriately monitor bioburden in cleanrooms for not only the aeronautical industry but also for pharmaceutical, medical industries, etc., and the need to employ molecular sequencing to complement traditional culture-based assays.more » « less
- 
            Although the evolution of spores was critical to the diversification of plants on land, sporogenesis is incompletely characterized for model plants such as Physcomitrium patens . In this study, the complete process of P. patens sporogenesis is detailed from capsule expansion to mature spore formation, with emphasis on the construction of the complex spore wall and proximal aperture. Both diploid (sporophytic) and haploid (spores) cells contribute to the development and maturation of spores. During capsule expansion, the diploid cells of the capsule, including spore mother cells (SMCs), inner capsule wall layer (spore sac), and columella, contribute a locular fibrillar matrix that contains the machinery and nutrients for spore ontogeny. Nascent spores are enclosed in a second matrix that is surrounded by a thin SMC wall and suspended in the locular material. As they expand and separate, a band of exine is produced external to a thin foundation layer of tripartite lamellae. Dense globules assemble evenly throughout the locule, and these are incorporated progressively onto the spore surface to form the perine external to the exine. On the distal spore surface, the intine forms internally, while the spiny perine ornamentation is assembled. The exine is at least partially extrasporal in origin, while the perine is derived exclusively from outside the spore. Across the proximal surface of the polar spores, an aperture begins formation at the onset of spore development and consists of an expanded intine, an annulus, and a central pad with radiating fibers. This complex aperture is elastic and enables the proximal spore surface to cycle between being compressed (concave) and expanded (rounded). In addition to providing a site for water intake and germination, the elastic aperture is likely involved in desiccation tolerance. Based on the current phylogenies, the ancestral plant spore contained an aperture, exine, intine, and perine. The reductive evolution of liverwort and hornwort spores entailed the loss of perine in both groups and the aperture in liverworts. This research serves as the foundation for comparisons with other plant groups and for future studies of the developmental genetics and evolution of spores across plants.more » « less
 An official website of the United States government
An official website of the United States government 
				
			 
					 
					
