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The structural characteristics and physiological activities of reduced glutathione （GSH）, as well as its metabolic pathways in vivo were reviewed, and the research progress in preparation, extraction, purification, application and industrial production of GSH were summarized. Moreover, the future research directions in functional activity, industrial production and product application of GSH were prospected.

Species diversity can be underestimated due to a lack of regional studies and limitations in research methods. China is widely recognized as one of the primary hotspots for the biodiversity of freshwater mussels as it harbours a wealth of endemic species. Pseudocuneopsis was recently established to belong to the Unioninae subfamily within Unionidae and is endemic to China. Recent research has expanded the diversity and range of distribution of this genus. However, sufficient data is required to precisely determine the phylogenetic relationships within Pseudocuneopsis. This study conducted an integrative taxonomy using morphological, COI barcode, and complete maternal mitogenome data to clarify the taxonomy of Pseudocuneopsis. Both morphological and COI barcode data supported the validity of all Pseudocuneopsis species. Furthermore, a new species, Pseudocuneopsis yemaoi sp. n. was described from a tributary of the Man River in Hubei, China. Mitochondrial phylogenomic analyses showed that P. yemaoi was closely related to P. sichuanensis and resolved phylogenetic relationship as (P. capitata + (P. yangshuoensis + (P. sichuanensis + P. yemaoi))). Our results highlight the significance of utilizing integrative classification methods. Moreover, we propose enhancing the research and preservation measures of minor streams in China, as these streams may house distinctive species. [ABSTRACT FROM AUTHOR]

Freshwater mussels are one of the most diverse and endangered faunas worldwide. Owing to the continuing global biodiversity loss, it is essential to identify and protect populations that are not severely affected by human disturbances and ensure that natural genetic diversity is not inevitably lost. The generation of baseline genetic diversity data will help guide species conservation and restoration plans in the Yangtze River Basin where freshwater mussels are facing multiple threats and where strong declines have been observed.The genetic diversity of freshwater mussels was assessed using 818 mtDNA cytochrome c oxidase subunit 1 (COI), 565 28S rRNA and 509 COI + 28S datasets, and refuge areas in the Yangtze River floodplain were predicted using a Maxent habitat suitability model.The results showed that the genetic diversity of Aculamprotula spp., Sinosolenaia carinata, Cuneopsis rufescens, Lamprotula cornuumlunae, Lanceolaria lanceolata, Ptychorhynchus pfisteri, Schistodesmus spp. and Sinohyriopsis cumingii was lower than that of other freshwater mussels, which indicated that the conservation status of these species should be prioritized.The habitat suitability modelling showed that Poyang Lake and Dongting Lake basins (lakes and tributary rivers connected to the Yangtze River mainstem) present the most suitable habitats for freshwater mussels, indicating that lateral hydrological connectivity may be the most important factor in maintaining the genetic diversity of Chinese freshwater mussels. Consequently, Poyang Lake and Dongting Lake basins should be established as protected areas.This study provides valuable information for the conservation and management of freshwater mussel biodiversity in the Yangtze River basin, which will not only help conserve this vulnerable group but will also provide wider benefits to freshwater ecosystems. [ABSTRACT FROM AUTHOR]

Background and Aims Whole-genome duplication (WGD) events are considered important driving forces of diversification. At least 11 out of 52 Brassicaceae tribes had independent mesopolyploid WGDs followed by diploidization processes. However, the association between mesopolyploidy and subsequent diversification is equivocal. Herein we show the results from a family-wide diversification analysis on Brassicaceae, and elaborate on the hypothesis that polyploidization per se is a fundamental driver in Brassicaceae evolution. Methods We established a time-calibrated chronogram based on whole plastid genomes comprising representative Brassicaceae taxa and published data spanning the entire Rosidae clade. This allowed us to set multiple calibration points and anchored various Brassicaceae taxa for subsequent downstream analyses. All major splits among Brassicaceae lineages were used in BEAST analyses of 48 individually analysed tribes comprising 2101 taxa in total using the internal transcribed spacers of nuclear ribosomal DNA. Diversification patterns were investigated on these tribe-wide chronograms using BAMM and were compared with family-wide data on genome size variation and species richness. Key Results Brassicaceae diverged 29.9 million years ago (Mya) during the Oligocene, and the majority of tribes started diversification in the Miocene with an average crown group age of about 12.5 Mya. This matches the cooling phase right after the Mid Miocene climatic optimum. Significant rate shifts were detected in 12 out of 52 tribes during the Mio- and Pliocene, decoupled from preceding mesopolyploid WGDs. Among the various factors analysed, the combined effect of tribal crown group age and net diversification rate (speciation minus extinction) is likely to explain sufficiently species richness across Brassicaceae tribes. Conclusions The onset of the evolutionary splits among tribes took place under cooler and drier conditions. Pleistocene glacial cycles may have contributed to the maintenance of high diversification rates. Rate shifts are not consistently associated with mesopolyploid WGD. We propose, therefore, that WGDs in general serve as a constant 'pump' for continuous and high species diversification. [ABSTRACT FROM AUTHOR]

A novel magnetic plasticizer molecularly imprinted polymer adsorbing material (MIP@mSiO2‐β‐CD@Fe3O4) was successfully synthesized for the determination of six phthalic acid esters in water, milk, and wine samples. The molecularly imprinted polymers were prepared via precipitation polymerization and a surface molecular imprinting technique, using a cyclodextrin‐modified magnetic meso‐porous material (mSiO2‐β‐CD@Fe3O4) as a magnetic supporter, dibutyl phthalate and butyl benzyl phthalate as the dual template molecules, methacrylic acid as the functional monomer, and ethyleneglycol dimethacrylate as the cross‐linking agent. The polymers were characterized by scanning electron microscopy, IR spectroscopy, and X‐ray powder diffraction. Thermogravimetric analysis and static and dynamic adsorption experiments were carried out to assay its stability and selectivity. Under optimal experimental conditions, a magnetic solid‐phase extraction with MIP@mSiO2‐β‐CD@Fe3O4 coupled to gas chromatography and mass spectrometry method was successfully developed for the determination of phthalic acid esters. The established method achieved a good linear range of 0.10∼8.00 μg/mL (R > 0.99) and a low detection limit within the range of 1.0∼5.0 μg/L. An average recovery rate of 80.2∼103% with relative standard deviation < 6.7% was obtained upon the application of the developed method to detect phthalic acid esters in actual aqueous samples. [ABSTRACT FROM AUTHOR]