Emerging roles and mechanisms of lncRNAs in fruit and vegetables.

With the development of genome sequencing technologies, many long non-coding RNAs (lncRNAs) have been identified in fruit and vegetables. lncRNAs are primarily transcribed and spliced by RNA polymerase II (Pol II) or plant-specific Pol IV/V, and exhibit limited evolutionary conservation. lncRNAs intricately regulate various aspects of fruit and vegetables, including pigment accumulation, reproductive tissue development, fruit ripening, and responses to biotic and abiotic stresses, through diverse mechanisms such as gene expression modulation, interaction with hormones and transcription factors, microRNA regulation, and involvement in alternative splicing.

In Situ SERS Detection of Photocatalytic Degradation of Aminothiophenol on Carbon-Nanotubes/CoPt Hollow Nanoparticles Composite.

The phenol derivatives, as one kind of hormone, are analogous to endocrine disruptors with high carcinogenicity. The photocatalytic technology is an effective approach to mitigate environmental pollution by utilizing solar energy to degrade organic pollutants. In this work, CoPt hollow nanoparticles (NPs) attached to carbon nanotubes (CNTs) are employed to catalytically decompose the -aminothiophenol (PATP) molecules under light irradiation, which is monitored by using surface-enhanced Raman scattering spectra.

[Drought-resistance evaluation of marigold cultivars based on multiple statistics analysis].

By the methods of principal component analysis, subordinate function, and cluster analysis, a comprehensive evaluation was conducted on the drought-resistance of 16 physiological indices of nine marigold cultivars. Under drought stress, the 16 physiological indices had different responses, among which, free proline (Pro), H2O2, and ascorbate peroxidase (APX) showed the greatest sensitivity. There existed significant correlations in the drought-resistance coefficients of parts of the physiological indices.

Theoretical study on contribution of charge transfer effect to surface-enhanced Raman scattering spectra of pyridine adsorbed on Ag(n) (n = 2-8) clusters.

We investigate surface-enhanced Raman scattering (SERS) spectra of pyridine-Ag(n) (n = 2-8) complexes by density functional theory (DFT) and time-dependent DFT (TDDFT) methods. In simulated normal Raman scattering (NRS) spectra, profiles of pyridine-Ag(n) (n = 2-8) complexes are analogical with that of isolated pyridine. Nevertheless, calculated pre-SERS spectra are strongly dependent on electronic transition states of new complexes.

Electronic structure and optical properties of dianionic and dicationic pi-dimers.

The absorption spectra of dianionic tetrocyanoethylene and dicationic tetrathiafulvalene dimers have been studied theoretically with the time-dependent density functional theory and the recently proposed Coulomb-attenuated model. The nature of the excited states was further explored by means of the two-dimensional (2D) site (transition density matrix) and three-dimensional (3D) cube (transition density and charge difference density) representations. By use of the 3D transition density and charge difference density, we visualized the orientation of transition dipole moment and also explained charge-transfer characteristics occurring in the dianionic/dicationic pi-dimers system.

Density functional theory study on Herzberg-Teller contribution in Raman scattering from 4-aminothiophenol-metal complex and metal-4-aminothiophenol-metal junction.

Density functional theory (DFT) and time-dependent DFT calculations have been performed to investigate the Raman scattering spectra of metal-molecule complex and metal-molecule-metal junction architectures interconnected with 4-aminothiophenol (PATP) molecule. The simulated profiles of normal Raman scattering (NRS) spectra for the two complexes (Ag(2)-PATP and PATP-Au(2)) and the two junctions (Ag(2)-PATP-Au(2) and Au(2)-PATP-Ag(2)) are similar to each other, but exhibit obviously different Raman intensities. Due to the lager static polarizabilities of the two junctions, which directly influence the ground state chemical enhancement in NRS spectra, the calculated normal Raman intensities of them are stronger than those of two complexes by the factor of 10(2).