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Abstract Key messageBiolistic particle bombardment was used to deliver CRISPR-Cas9 ribonucleoprotein complexes (RNP) into the shoot apical meristem tissue of citrus and axillary meristem tissue of poplar, generating directed mutations in target genes. AbstractThe use of meristematic tissues offers a strategic approach to genome editing in woody species, especially those that are recalcitrant to conventional tissue culture, as these regions contain totipotent, highly regenerative cells capable of giving rise to whole plants. Here, we employed biolistic delivery of genome-editing reagents into theshoot apical meristem (SAM) of citrus and the axillary meristems (AXM) of poplar. The system was first validated using a GFP expression construct and subsequently applied for targeted genome editing. In citrus, edited plants were obtained at the CsNPR3 locus exclusively through the delivery of CRISPR/Cas9 ribonucleoproteins (RNPs), whereas plasmid-based vectors were unsuccessful. Similarly, genome editing in poplar was achieved using RNPs targeting the Pt4CL1 gene. Although chimeric events were detected, this approach provides a feasible and innovative framework for producing transgene-free edited perennial plants. 

In recent years, there has been increasing interest in the understanding and application of nanoparticle assemblies driven by external fields. Although these systems can exhibit marked transitions in behavior compared to non-interacting counterparts, it has often proven challenging to connect their dynamics with underlying physical mechanisms or even to verifiably establish their structure under realistic experimental conditions. We have studied colloidal iron oxide nanoparticles that assemble into ordered, few-particle linear chains under the influence of oscillating and pulsed magnetic fields. In this work, our goal has been to answer the following question: by what physical mechanisms does the magnetic switching of a linear chain evolve from the switching of its constituent particles? Cryo-TEM has been used to flash freeze and image the structures formed by oscillatory drive fields, and magnetic relaxometry has been used to extract the multiple time constants associated with magnetic switching of the short chains. Armed with the physical structure from microscopy and the field-dependent switching times from magnetic measurements, we have conducted extensive micromagnetic simulations, revealing probable physical mechanisms for each time constant regime spanning$$10^{6}$$($$\approx$$1 μs to 1 s) in time. These types of magnetic nanomaterials have great potential for biomedical technologies, particularly magnetic particle imaging and hyperthermia, and rigorous elucidation of their physics will hasten their optimization.