PubMed · 4120378
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
1973-03-03. Pathways of complement activation.. https://pubmed.ncbi.nlm.nih.gov/4120378/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
The dissemination of antibiotic resistance genes (ARGs) in wastewater environments poses a severe threat to public health. Extracellular ARGs (eARGs) persist as free DNA fragments that are refractory to efficient removal by conventional physicochemical treatment technologies. Here, we isolated Stutzerimonas stutzeri CHY07 from municipal sewage and demonstrated that extracellular DNA fragments, including eARGs, can serve as chemoattractants for environmental bacteria. Through genomic mining, molecular docking, surface plasmon resonance (SPR), isothermal titration calorimetry (ITC) and protein-ligand interaction profiling, we identified the chemoreceptor Mcp16 as the primary sensor of extracellular DNA and revealed that it achieves sequence-independent recognition of the DNA phosphate backbone. We further established the endogenous pentapeptide VRSVR as a methylation substrate for CheR and constructed the engineered strain CHY07-2 (mcp16::VRSVR) using an SSB/CRISPR-Cas9 ribonucleoprotein (RNP) system. This strain exhibited significantly enhanced chemotactic responsiveness, achieving 72-h removal efficiencies of 96.56% and 91.60% for low- and high-molecular-weight eARGs in non-sterile WWTP secondary effluent; conversely, mcp16 deletion markedly attenuated both chemotaxis and removal, whereas in situ complementation restored them. These findings reveal a "chemotaxis-contact-removal" cascade - with a proposed self-reinforcing loop - in eARG-removing bacteria, providing both a theoretical framework and a technical paradigm for enhancing pollutant removal through targeted amplification of microbial chemotaxis.
Explore the source record for details and available documents.
A mathematical model was developed to simulate the movement of chemotactic bacteria into and within a capillary tube containing a metabolizable chemoattractant. The model was based on a material balance that accounts for the transport of bacteria and chemoattractant as well as consumption of the substrate throughout the capillary assay system. By solving the model with a numerical method, it was possible to predict the concentration of substrate and bacteria at points within the capillary and throughout the chamber. The model was tested for its ability to simulate the results of capillary assay experiments performed with Pseudomonas putida G7 and one of its chemoattractants, naphthalene, under conditions wherein naphthalene consumption was expected to affect the flux of bacteria into the capillary. While variations in the chemotactic responses were evident among different experiments, the model could simulate the accumulation of cells in the capillary using previously determined parameters, including the chemotactic sensitivity and random motility coefficients, chi(0) and mu. In particular, model predictions were consistent with the experimental observation that the chemotactic response in the capillary is diminished under conditions wherein consumption would be expected to be significant.