A conversion of the global terrestrial carbon sink to a source is critically dependent on the microbially mediated decomposition of soil organic matter (SOM). We have developed a detailed, process-based, mechanistic model for simulating SOM decomposition and its associated processes, based on Microbial Kinetics and Thermodynamics, called the MKT model. We formulated the sequential oxidation-reduction potential (ORP) and chemical reactions undergoing at the soil-water zone using dual Michaelis-Menten kinetics. Soil environmental variables, as required in the MKT model, are simulated using one of the most widely used watershed-scale models - the soil water assessment tool (SWAT). The MKT model was calibrated and validated using field-scale data of soil temperature, soil moisture, and NO emissions from three locations in the province of Saskatchewan, Canada. The model evaluation statistics show good performance of the MKT model for daily soil NO simulations. The results show that the proposed MKT model can perform better than the more widely used process-based and SWAT-based models for soil NO simulations. This is because the multiple processes of microbial activities and environmental constraints, which govern the availability of substrates to enzymes were explicitly represented. Most importantly, the MKT model represents a step forward from conceptual carbon pools at varying rates.
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http://dx.doi.org/10.1016/j.envpol.2019.01.062 | DOI Listing |
Commun Med (Lond)
January 2025
Dyne Therapeutics Inc, Waltham, MA, USA.
Background: We developed the FORCE platform to overcome limitations of oligonucleotide delivery to muscle and enable their applicability to neuromuscular disorders. The platform consists of an antigen-binding fragment, highly specific for the human transferrin receptor 1 (TfR1), conjugated to an oligonucleotide via a cleavable valine-citrulline linker. Myotonic dystrophy type 1 (DM1) is a neuromuscular disorder caused by expanded CUG triplets in the DMPK RNA, which sequester splicing proteins in the nucleus, lead to spliceopathy, and drive disease progression.
View Article and Find Full Text PDFInt J Pharm
December 2024
University Institute of Pharmaceutical Sciences, UGC-centre of Advanced Studies, Panjab University, Chandigarh 160014, India. Electronic address:
Nat Aging
November 2024
Division of Cancer Cell Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Phys Chem Chem Phys
August 2024
Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, USA.
Understanding the structural dynamics of covalent organic frameworks (COFs) in response to external temperature change is necessary for these materials' application at cryogenic temperatures. Herein, we report reversible structural dynamics observed in covalent organic frameworks as the temperature varies from 298 K to 30 K. A series of frameworks (COF-300, COF-300-amine, and COF-V) was studied using a cryogenic infrared spectroscopy system.
View Article and Find Full Text PDFCell Metab
July 2024
Eli Lilly and Company, Indianapolis, IN 46285, USA. Electronic address:
Tirzepatide, a glucose-dependent insulinotropic polypeptide/glucagon-like peptide 1 receptor (GIPR/GLP-1R) agonist, has, in clinical trials, demonstrated greater reductions in glucose, body weight, and triglyceride levels compared with selective GLP-1R agonists in people with type 2 diabetes (T2D). However, cellular mechanisms by which GIPR agonism may contribute to these improved efficacy outcomes have not been fully defined. Using human adipocyte and mouse models, we investigated how long-acting GIPR agonists regulate fasted and fed adipocyte functions.
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