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Polyaniline is a kind of polymer material with excellent electrochemical performance, and it stands out among a number of conductive polymer materials owing to its low cost, easy availability of raw materials, and excellent physical and chemical properties. However, the poor processability of polyaniline impedes its broad application. Preparing nanosized structure and introducing big molecular organic acids as dopant are practical strategies to solve this problem. Here using ammonium persulfate as oxidant, sodium dodecyl sulfate as surfactant, and 3,5-dinitrobenzoic acid as doping acid, polyaniline nanotubes were successfully prepared via emulsion polymerization method and characterized by various measurements. The influence of aniline concentration on the morphology and property of the product was explored. The polymerization mechanism of polyaniline nanotubes was discussed in detail based on the analysis of the microscopic morphology. As the concentration of aniline monomer increases, the position of the characteristic absorption peak in the infrared spectrum of the polyaniline main chain remains almost unchanged, but the ratio of benzene to quinone gradually increases. Along with the increasing aniline concentration, the crystallinity of polyaniline gradually decreases from 56.21% to 40.37%. In addition, the optimal conductivity is 2.05×10−2 S/cm when the concentration of aniline monomer is 0.5 mol/L. [ABSTRACT FROM AUTHOR]

Trehalose-6-phosphate synthase (TPS) is essential for plant growth and development, linking trehalose-6-phosphate (T6P) to carbon metabolism. However, little is known about the TPS gene family in peaches and their potential roles in regulating carbohydrates in peach fruit. In this study, nine TPS genes were identified in the peach genome and named according to the homologous genes in Arabidopsis. Phylogenetic analysis showed that three subfamilies were identified, including TPSI, TPSII-1, and TPSII-2, which were also consistent with gene structure analysis. Considerable cis-elements were enriched in the promoters, including plant hormone-related elements. Tissue-specific analysis showed that these TPS genes were mainly expressed in leaves, stems, and fruit, showing different expression patterns for each gene. In addition, during fruit development, the content of trehalose-6-phosphate (T6P) was positively correlated with the expression of PpTPS7a and negatively with sucrose non-fermenting-1-related kinase 1 (SnRK1) activity. Transient overexpression and silencing of PpTPS7a in peach fruit validated its function in regulating T6P content and SnRK1 activity. [ABSTRACT FROM AUTHOR]

This document is a correction notice for an article titled "Waterlogging resistance and evaluation of physiological mechanism of three peach (Prunus persica) rootstocks" published in the journal Protoplasma. The correction addresses the incorrect numbering of Figures 5, 6, and 7 in the published proof. The corrected figures depict the effects of waterlogging on cell death and ROS accumulation in the leaves of peach rootstocks and grafted seedlings. The original article has been corrected. The publisher, Springer Nature, remains neutral regarding jurisdictional claims and institutional affiliations. [Extracted from the article]

LATERAL ORGAN BOUNDARIES DOMAIN/ASYMMETRIC LEAVES2-LIKEs (LBDs/ASLs) are plant-specific transcription factors that function downstream of auxin-regulated lateral root (LR) formation. Our previous research found that PpLBD16 positively regulates peach (Prunus persica) LR formation. However, the downstream regulatory network and target genes of PpLBD16 are still largely unknown. Here, we constructed a PpLBD16 homologous overexpression line and a PpLBD16 silenced line. We found that overexpressing PpLBD16 promoted peach root initiation, while silencing PpLBD16 inhibited peach root formation. Through RNA sequencing (RNA-seq) analysis of roots from PpLBD16 overexpression and silenced lines, we discovered that genes positively regulated by PpLBD16 were closely related to cell wall synthesis and degradation, ion/substance transport, and ion binding and homeostasis. To further detect the binding motifs and potential target genes of PpLBD16, we performed DNA-affinity purification sequencing (DAP-seq) analysis in vitro. PpLBD16 preferentially bound to CCNGAAANNNNGG (MEME-1), [C/T]TTCT[C/T][T/C] (MEME-2), and GCGGCGG (ABR1) motifs. By combined analysis of RNA-seq and DAP-seq data, we screened candidate target genes for PpLBD16. We demonstrated that PpLBD16 bound and activated the cell wall modification-related genes EXPANSIN-B2 (PpEXPB2) and SUBTILISIN-LIKE PROTEASE 1.7 (PpSBT1.7), the ion transport-related gene CYCLIC NUCLEOTIDE-GATED ION CHANNEL 1 (PpCNGC1) and the polyphenol oxidase (PPO)-encoding gene PpPPO, thereby controlling peach root organogenesis and promoting LR formation. Moreover, our results displayed that PpLBD16 and its target genes are involved in peach LR primordia development. Overall, this work reveals the downstream regulatory network and target genes of PpLBD16, providing insights into the molecular network of LBD16-mediated LR development. A plant-specific transcription factor controls root organogenesis, promotes lateral root formation, and participates in lateral root primordia development in peach. [ABSTRACT FROM AUTHOR]