Integration of genome-wide association study, linkage analysis, and population transcriptome analysis to reveal the TaFMO1-5B modulating seminal root growth in bread wheat.

Bread wheat, one of the keystone crops for global food security, is challenged by climate change and resource shortage. The root system plays a vital role in water and nutrient absorption, making it essential for meeting the growing global demand. Here, using an association-mapping population composed of 406 accessions, we identified QTrl.Rs-5B modulating seminal root development with a genome-wide association study and validated its genetic effects with two F5 segregation populations. Transcriptome-wide association study prioritized TaFMO1-5B, a gene encoding the flavin-containing monooxygenases, as the causal gene for QTrl.Rs-5B, whose expression levels correlate negatively with the phenotyping variations among our population. The lines silenced for TaFMO1-5B consistently showed significantly larger seminal roots in different genetic backgrounds. Additionally, the agriculture traits measured in multiple environments showed that QTrl.Rs-5B also affects yield component traits and plant architecture-related traits, and its favorable haplotype modulates these traits toward that of modern cultivars, suggesting the application potential of QTrl.Rs-5B for wheat breeding. Consistently, the frequency of the favorable haplotype of QTrl.Rs-5B increased with habitat expansion and breeding improvement of bread wheat. In conclusion, our findings identified and demonstrated the effects of QTrl.Rs-5B on seminal root development and illustrated that it is a valuable genetic locus for wheat root improvement.

Solvothermal synthesis of NiCo alloy icosahedral nanocrystals.

New dimensional NiCo alloy icosahedral nanocrystals with controllable size have been first reported and synthesized through an Ostwald ripening process in a template-absent solvothermal reaction system. The proposed synthesis is corroborated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction analysis (XRD), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The as-obtained NiCo icosahedral nanocrystals exhibit the size- and component-dependent magnetic behaviors. The coercivity (H(c)) depends on both the magnetocrystalline and structure anisotropy, and the saturation magnetizations (M(s)) decided by the content of Co. H(c) decreases from 189.02 to 147.95 Oe with the increase of the icosahedral NCs size from 200 to 850 nm. Especially, the H(c) of the icosahedral NCs at 157.38 Oe is higher than that of nanospheres at 104.02 Oe. In addition, M(s) and H(c) increased with the increasing Co content. It can be an ideal building block for applications in magnetic media, sensors, and other devices.

Inducing growth of FeNi-Pt match-like magnetic nanoheterostructures on Pt nanotips and dechlorination of hydrochloric ether.

Newly designed magnetic FeNi-Pt match-like heterostructured nanorods were synthesized by means of induced growth of FeNi nanorods on Pt nanotips. The proposed synthesis mechanism is corroborated by SEM, TEM, XRD and XPS. The magnetic behavior shows that the magnetic saturation and coercivity are strongly dependent on both the shape and the alloy composition. The saturation magnetizations (Ms) and the coercivity (Hc) of nanorods synthesized are larger than those of nanoparticles because of the relatively large anisotropy of nanorods. Maximum saturation magnetization is obtained for Fe(82) Ni(15) -Pt(3) at 226.6 emu g(-1), whereas maximum coercivity is obtained for Fe(20)Ni(77)-Pt(3) at 136.8 Oe. Shape-dependent reactivity toward the reduction of chlorinated solvents was observed for the FeNi-Pt heterostructured nanomaterials. In particular, the Fe(82)Ni(15)-Pt(3) nanorods are highly reactive in the dechlorination process of 1,1,2,2-tetrachloroethane.

Pt-NiCo nanostructures with facilitated electrocatalytic activities for sensitive determination of intracellular thiols with long-term stability.

A Pt-NiCo nanomaterial has been synthesized for developing the sensitive electrochemical determination of biological thiols that include L-cysteine (CySH), homocysteine (HCySH), and gluthione (GSH) with high sensitivity and long-term stability, in which the Pt nanoparticles are well supported on amorphous NiCo nanofilms. The electrochemical oxidation of thiols has been successfully facilitated on the optimized Pt-NiCo nanostructures, that is, two oxidation peaks of CySH have been clearly observed at potentials of +0.06 and +0.45 V. The experimental results demonstrate that the first peak for CySH oxidation may be attributed to a direct oxidation from CySH to L-cystine (CySSCy), whereas the second peak possibly results from a sequential oxidation from CySSCy to cysteic acid (CySO(3)H), together with a direct oxidation of CySH into CySO(3)H. The enhanced electrocatalytic activities at the Pt(23)-NiCo nanostructures have provided a methodology to determine thiols at a very low potential of 0.0 V with relatively high sensitivity (637 nA µM cm(-2)), a low detection limit (20 nM), and a broad linear range. The striking analytical performance, together with the characteristic properties of the Pt-NiCo nanomaterial itself, including long-term stability and strong antipoisoning ability, has established a reliable and durable approach for the detection of thiols in liver cancer cells, Hep G2.

Controlled fabrication of 0 & 2D NiCu amorphous nanoalloys by the cooperation of hard-soft interfacial templates.

Assembling-controlled synthesis is carried out for fabrication 0 & 2D NiCu amorphous nanoalloys through the cooperation of hard-soft interfacial templates in different template-assist routes at room temperature. The controlled fabrication of 0D nanospheres and 2D ultrathin nanofilms of NiCu amorphous alloys is attributed to the synergistic effect between structure-inducing of hard collodion membrane and the reactor volume adjusting of reverse microemulsion as well as coordination of ethylenediamine ligand. The hard artificial active collodion membrane lost the structure-inducing activity after ligand ethylenediamine coordinated with metal ions. The phase transformation behavior recordings indicate that the replacement of Ni by Cu can delay phase transformation. And as the Cu concentration increases, the kinetic ordering temperature increases. The magnetic property shows that the saturation magnetizations (Ms) and coercivities (Hc) of annealed nanoalloys decrease with the increasing of Cu concentration in NiCu system.