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Microbial phototrophs, key primary producers on Earth, use HO, H, HS and other reduced inorganic compounds as electron donors. Here we describe a form of metabolism linking anoxygenic photosynthesis to anaerobic respiration that we call 'syntrophic anaerobic photosynthesis'. We show that photoautotrophy in the green sulfur bacterium Prosthecochloris aestaurii can be driven by either electrons from a solid electrode or acetate oxidation via direct interspecies electron transfer from a heterotrophic partner bacterium, Geobacter sulfurreducens. Photosynthetic growth of P. aestuarii using reductant provided by either an electrode or syntrophy is robust and light-dependent. In contrast, P. aestuarii does not grow in co-culture with a G. sulfurreducens mutant lacking a trans-outer membrane porin-cytochrome protein complex required for direct intercellular electron transfer. Syntrophic anaerobic photosynthesis is therefore a carbon cycling process that could take place in anoxic environments. This process could be exploited for biotechnological applications, such as waste treatment and bioenergy production, using engineered phototrophic microbial communities.
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http://dx.doi.org/10.1038/ncomms13924 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Northeast Normal University, Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education, Institute of Functional Material Chemistry, Local United Engineering Lab for Power Battery, CHINA.
Construction of metal-organic cages (MOCs) with internal modifications is a promising avenue to build enzyme-like cavities and unlocking the mystery of highly catalytic activity and selectivity of enzymes. However, current interests are mainly focused on single-metal-node cages, little achievement has been expended to metalloclusters-based architectures, and the in situ endogenous generation of metal clusters. Herein, based on the hard-soft-acids-bases (HSAB), the metalloclusters-based heterometallic MOC (Cu3VMOP) constructed of [Cu3OPz3]+ and [V6O6(OCH3)9(SO4)(CO2)3]2- clusters was obtained by one-pot method.
View Article and Find Full Text PDFLangmuir
December 2024
School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai 200093, China.
To address the limitations of carbon nitride in photocatalysis, we propose constructing a three-dimensional interwoven SiC/g-CN composite structure. Utilizing the strong microwave-thermal conversion characteristics of SiC whiskers, localized "hot spots" are generated, which induce rapid thermal gradients, promoting rapid polymerization of urea and in situ formation of the interwoven network. This unique structure strengthens the interaction between these two components, creates multiple electron transport pathways, enhances CO adsorption, and effectively improves charge separation while reducing photogenerated carrier recombination.
View Article and Find Full Text PDFAnal Chem
December 2024
Guangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Center for Drug Research and Development, Guangdong Pharmaceutical University, Guangzhou, Guangdong 510006, China.
Among the various aflatoxin B1 (AFB1) assays, performing accurate detection is difficult because false positives and false negatives are frequent due to limited sensitivity, expensive equipment, or inadequate pretreatment during operation. Here, an "off-on" switch-type electrochemiluminescence (ECL) aptasensor armed with cobalt-sulfur quantum dots was encapsulated in hollow cobalt-layered double hydroxide nanocages as an enhanced luminescent probe (Co-LDH@QDs), and a ferrocene-modified aptamer (Fc-APT) was used as a luminescent quencher. In general, when Fc-APT was hybridized with complementary DNA modified with a DNA nanotetrahedron, electron transfer between ferrocene and Co-LDH@QDs was facilitated, leading to efficient quenching of the ECL intensity into an "off" state in the absence of AFB1.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Hubei Key Lab on Organic and Polymeric Optoelectronic Materials, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
Artificial photosynthesis of hydrogen peroxide (HO) from ambient air, water, and sunlight has attracted considerable attention recently. Despite being extremely challenging to synthesis, sp carbon-conjugated covalent organic frameworks (COFs) can be powerful and efficient materials for the photosynthesis of HO due to desirable properties. Herein, we report the designed synthesis of an sp carbon-conjugated COF, BTD-spc-COF, from benzothiadiazole and triazine units with high crystallinity and ultralarge mesopores (∼4 nm).
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
December 2024
Department of Materials Science, University of Milano-Bicocca, Via Roberto Cozzi 55, 20125 Milano, Italy.
The adsorption of (X = Ni, Pd, and Pt) nanoclusters is simulated by using first-principles methods on MgO(100) and on a MgO monolayer supported on Ag(100), considering the presence of interfacial oxygen. On both the free-standing MgO surface and MgO/Ag, all clusters exhibit robust adhesion and negative charge transfer. molecular dynamics calculations at 200 K demonstrate the stability of the nanoparticles on the MgO/Ag support.
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