Effect of light- and dark-germination on the phenolic biosynthesis, phytochemical profiles, and antioxidant activities in sweet corn (Zea mays L.) sprouts

Sweet corn is one of the most widely planted crops in China. Sprouting of grains is a new processes to increase the nutritional value of grain products. The present study explores the effects of light on the nutritional quality of sweet corn sprouts. Gene expression of phenolic biosynthesis, phytochemical profiles and antioxidant activity were studied. Two treatments (light and dark) were selected and the morphological structure of sweet corn sprouts, as well as their biochemical composition were investigated to determine the effects of light on the regulation of genes responsible for nutritional compounds. Transcription analyses for three key-encoding genes in the biosynthesis of the precursors of phenolic were studied. Results revealed a negative regulation in the expression of ZmPAL with total phenolic content (TPC) in the light group. TPC and total flavonoid content (TFC) increased during germination and this was correlated with an increase in antioxidant activity (r = 0.95 and 1.0). The findings illustrate that the nutritional value of sweet corn for the consumer can be improved through germination to the euphylla stage

Quantifying spin Hall topological Hall effect in ultrathin Tm 3 Fe 5 O 12 / Pt bilayers

Recent reports have shown that thulium iron garnet (TmIG) based bilayers are promising material platforms for realizing small, room-temperature skyrmions. For potential applications, it is impera- tive to accurately evaluate electrical read-out signals of skyrmions. In this context, the topological Hall effect has been considered as a characteristic signature of skyrmion formation. Unlike previous studies that have modeled the anomalous Hall effect in ultrathin TmIG/Pt bilayers, we isolate its contribution to the electrical read-out signal by directly measuring the magnetic hysteresis loops using a sensitive Sagnac magneto-optical Kerr effect technique. Our combined optical and electrical measurements reveal that the spin-Hall topological Hall resistivity is considerably larger than previ- ously estimated values. Our finding further indicates that skyrmions can exist at room-temperature and near-zero applied magnetic fields.This research was primarily supported by the National Science Foundation through the Center for Dynamics and Control of Materials: an NSF MRSEC under Coopera- tive Agreement No. DMR-1720595, and the Center for Emergent Materials, an NSF MRSEC under Grant No. DMR-2011876. Additional support was provided by the Welch Foundation F-1662. Facilities provided by MR- SEC DMR-1720595 and by NSF MRI DMR-2019130 are gratefully acknowledged. Partial funding for L. J. Chang while visiting UT-Austin was provided by a Portugal-UT collaboration grant. The collaboration between S,F. Lee and X. Li is facilitated by the AFOSR grant FA2386-21- 1-4067.Center for Dynamics and Control of Material

Quantifying spin Hall topological Hall effect in ultrathin Tm 3 Fe 5 O 12 / Pt bilayers

Recent reports have shown that thulium iron garnet (TmIG) based bilayers are promising material platforms for realizing small, room-temperature skyrmions. For potential applications, it is imperative to accurately evaluate electrical readout signals of skyrmions. In this context, the topological Hall effect has been considered as a characteristic signature of skyrmion formation. Unlike previous studies that have modeled the anomalous Hall effect in ultrathin TmIG/Pt bilayers, we isolate its contribution to the electrical readout signal by directly measuring the magnetic hysteresis loops using a sensitive Sagnac magneto-optical Kerr effect technique. Our combined optical and electrical measurements reveal that the spin Hall topological Hall resistivity is considerably larger than previously estimated values. Our finding further indicates that skyrmions can exist at room-temperature and near-zero applied magnetic fields.This research was primarily supported by the National Science Foundation through the Center for Dynamics and Control of Materials: an NSF MRSEC under Coopera- tive Agreement No. DMR-1720595, and the Center for Emergent Materials, an NSF MRSEC under Grant No. DMR-2011876. Additional support was provided by the Welch Foundation F-1662. Facilities provided by MR- SEC DMR-1720595 and by NSF MRI DMR-2019130 are gratefully acknowledged. Partial funding for L. J. Chang while visiting UT-Austin was provided by a Portugal-UT collaboration grant. The collaboration between S,F. Lee and X. Li is facilitated by the AFOSR grant FA2386-21- 1-4067.Center for Dynamics and Control of Material

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.

The occurrence of non-epileptic hyperkinetic movements in the context of developmental epileptic encephalopathies is an increasingly recognized phenomenon. Identification of causative mutations provides an important insight into common pathogenic mechanisms that cause both seizures and abnormal motor control. We report bi-allelic loss-of-function CACNA1B variants in six children from three unrelated families whose affected members present with a complex and progressive neurological syndrome. All affected individuals presented with epileptic encephalopathy, severe neurodevelopmental delay (often with regression), and a hyperkinetic movement disorder. Additional neurological features included postnatal microcephaly and hypotonia. Five children died in childhood or adolescence (mean age of death: 9 years), mainly as a result of secondary respiratory complications. CACNA1B encodes the pore-forming subunit of the pre-synaptic neuronal voltage-gated calcium channel Cav2.2/N-type, crucial for SNARE-mediated neurotransmission, particularly in the early postnatal period. Bi-allelic loss-of-function variants in CACNA1B are predicted to cause disruption of Ca2+ influx, leading to impaired synaptic neurotransmission. The resultant effect on neuronal function is likely to be important in the development of involuntary movements and epilepsy. Overall, our findings provide further evidence for the key role of Cav2.2 in normal human neurodevelopment.MAK is funded by an NIHR Research Professorship and receives funding from the Wellcome Trust, Great Ormond Street Children's Hospital Charity, and Rosetrees Trust. E.M. received funding from the Rosetrees Trust (CD-A53) and Great Ormond Street Hospital Children's Charity. K.G. received funding from Temple Street Foundation. A.M. is funded by Great Ormond Street Hospital, the National Institute for Health Research (NIHR), and Biomedical Research Centre. F.L.R. and D.G. are funded by Cambridge Biomedical Research Centre. K.C. and A.S.J. are funded by NIHR Bioresource for Rare Diseases. The DDD Study presents independent research commissioned by the Health Innovation Challenge Fund (grant number HICF-1009-003), a parallel funding partnership between the Wellcome Trust and the Department of Health, and the Wellcome Trust Sanger Institute (grant number WT098051). We acknowledge support from the UK Department of Health via the NIHR comprehensive Biomedical Research Centre award to Guy's and St. Thomas' National Health Service (NHS) Foundation Trust in partnership with King's College London. This research was also supported by the NIHR Great Ormond Street Hospital Biomedical Research Centre. J.H.C. is in receipt of an NIHR Senior Investigator Award. The research team acknowledges the support of the NIHR through the Comprehensive Clinical Research Network. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, Department of Health, or Wellcome Trust. E.R.M. acknowledges support from NIHR Cambridge Biomedical Research Centre, an NIHR Senior Investigator Award, and the University of Cambridge has received salary support in respect of E.R.M. from the NHS in the East of England through the Clinical Academic Reserve. I.E.S. is supported by the National Health and Medical Research Council of Australia (Program Grant and Practitioner Fellowship)

Enantioselective organocatalytic synthesis of axially chiral aldehyde-containing styrenes via SNAr reaction-guided dynamic kinetic resolution

Abstract The precise and efficient construction of axially chiral scaffolds, particularly toward the aryl-alkene atropoisomers with impeccably full enantiocontrol and highly structural diversity, remains greatly challenging. Herein, we disclose an organocatalytic asymmetric nucleophilic aromatic substitution (SNAr) reaction of aldehyde-substituted styrenes involving a dynamic kinetic resolution process via a hemiacetal intermediate, offering a novel and facile way to significant axial styrene scaffolds. Upon treatment of the aldehyde-containing styrenes bearing (o-hydroxyl)aryl unit with commonly available fluoroarenes in the presence of chiral peptide-phosphonium salts, the SNAr reaction via an exquisite bridged biaryl lactol intermediate undergoes smoothly to furnish a series of axially chiral aldehyde-containing styrenes decorated with various functionalities and bioactive fragments in high stereoselectivities (up to >99% ee) and complete E/Z selectivities. These resulting structural motifs are important building blocks for the preparation of diverse functionalized axial styrenes, which have great potential as efficient and privileged chiral ligands/catalysts in asymmetric synthesis

Responsive hydrogel microfibers for biomedical engineering

Abstract Responsive hydrogel microfibers can realize multiple controllable changes in shapes or properties under the stimulation of the surrounding environment, and are called as intelligent biomaterials. Recently, these responsive hydrogel microfibers have been proved to possess significant biomedical values, and remarkable progress has been achieved in biomedical engineering applications, including drug delivery, biosensors and clinical therapy, etc. In this review, the latest research progress and application prospects of responsive hydrogel microfibers in biomedical engineering are summarized. We first introduce the common preparation strategies of responsive hydrogel microfibers. Subsequently, the response characteristics and the biomedical applications of these materials are discussed. Finally, the present opportunities and challenges as well as the prospects for future development are critically analyzed