The transcription factor MYB156 controls the polar stiffening of guard cell walls in poplar.

The mechanical properties of guard cells have major effects on stomatal functioning. Reinforced stiffness in the stomatal polar regions was recently proposed to play an important role in stomatal function, but the underlying molecular mechanisms remain elusive. Here, we used genetic and biochemical approaches in poplar (Populus spp.) to show that the transcription factor MYB156 controls pectic homogalacturonan-based polar stiffening through the downregulation of the gene encoding pectin methylesterase 6 (PME6). Loss of MYB156 increased the polar stiffness of stomata, thereby enhancing stomatal dynamics and response speed to various stimuli. In contrast, overexpression of MYB156 resulted in decreased polar stiffness and impaired stomatal dynamics, accompanied by smaller leaves. Polar stiffening functions in guard cell dynamics in response to changing environmental conditions by maintaining normal stomatal morphology during stomatal movement. Our study revealed the structure-function relationship of the cell wall of guard cells in stomatal dynamics, providing an important means for improving the stomatal performance and drought tolerance of plants.

Contamination status, source analysis and exposure assessments of quinolone antibiotics in the south of Yancheng Coastal Wetland, China.

Yancheng coastal wetland, the largest coastal wetland in the west coast of the Pacific Ocean and the margin of the Asian continent, has significant environmental, economic and social effects on local human beings. The extensive contamination and potential risk of quinolone antibiotics (QNs) on local aquaculture and human health are still not clear until now. In this study, 52 surface sediment samples were collected to investigate the contamination status and polluted sources, and evaluate ecological risks of QNs in the south of Yancheng coastal wetland. The total contents of QNs ranged from 0.33 to 21.60 ng/g dw (mean value of 4.51 ng/g dw), following the detection frequencies of QNs ranging from 19.23 to 94.23%. The highest content of QNs occurred around an aquaculture pond dominated by flumequine. The total organic carbon contents of sediment were positively correlated with sarafloxacin and lomefloxacin (p < 0.05), indicating the enhanced absorption of these QNs onto sediments. Partial QNs, such as lomefloxacin, enrofloxacin, sarafloxacin and flumequine, presented the homology features originating from the emission of medical treatment and aquaculture. There was no potential risk of QNs to human beings but a potential risk to aquatic organisms (algae > plant > invertebrate). Totally, the management and protection of Yancheng coastal wetland should be of concern with aquaculture as the important industry.

Time- and dose-dependent allelopathic effects and mechanisms of kaempferol on toxigenic Microcystis growth.

This study determined time-dependent IC50 and confirmed 3.5 mg/L as IC50 value for kaempferol inhibiting toxigenic Microcystis growth, based on which algicidal effects and mechanisms against toxigenic Microcystis exposed to various kaempferol doses (0.5-2 × IC50) were explored along 14 day-test. Results showed that growth inhibition ratio (GIR) almost elevated with increasing kaempferol dose, and at each dose GIR elevated firstly and fluctuated around 17.8%- > 40%, 53.6%-65.6% and 84.8%-89.3% at 1.75, 3.5 and 7 mg/L kaempferol during mid-late stage, respectively. With rising kaempferol dose, photosynthetic pigments contents (chlorophyll-a, phycobiliproteins), antioxidant response (superoxide dismutase and catalase (CAT) activities, glutathione (GSH) contents) and microcystins (MCs) production were almost increasingly stimulated as cellular protective responses during early-mid stage. However, these parameters (excluding CAT and GSH) were almost increasingly inhibited at late stage by prolonged stress and Microcystis cell was still more severely damaged as dose elevated along test, which could be reasons for increasing GIR with rising kamepferol dose. Persistent stimulation of CAT and GSH at each dose could alleviate cell damage until late stage, thus GIR no longer increased at late stage at each kaempferol dose. Moreover, fewer MCs release under kaempferol stress than control suggested kaempferol as eco-safe algaecide for migrating toxigenic Microcystis-dominated blooms (MCBs) and decreasing MCs risks. Compared with our previous data for luteolin inhibiting toxigenic Microcystis, this study supported formerly-proposed 'flavonoids structure - algicidal activity' relationship that the only OH-location difference between kaempferol and luteolin could affect algicidal activity and mechanisms against toxigenic Microcystis. Also, kaempferol and luteolin was revealed to exert additive effect on toxigenic Microcystis growth at equitoxic ratio. Our findings gave novel algicidal scenario of flavonoids and were greatly implicated in eco-friendly migrating toxigenic MCBs.

Long-term tracking robust removal of Microcystis-dominated bloom and microcystin-pollution risk by luteolin continuous-release microsphere at different nitrogen levels-Mechanisms from proteomics and gene expression.

Luteolin continuous-release microsphere (CRM) has promising algicidal effect against Microcystis, but how nitrogen (N) level impacted CRM effects on Microcystis growth and microcystins (MCs) pollution was never tracked along long term. This study revealed that luteolin CRM exerted long-term and robust inhibitory effects on Microcystis growth and MC-pollution by sharply decreasing extracellular and total MCs content at each N level, with growth inhibition ratio of 88.18%-96.03%, 92.91%-97.17% and 91.36%-95.55% at 0.5, 5 and 50 mg/L N, respectively, during day 8-30. Further analyses revealed that CRM-stress inhibited transferase, GTPase and ATPase activities, ATP binding, metal ion binding, fatty acid biosynthesis, transmembrane transport and disrupted redox homeostasis to pose equally robust algicidal effect at each N level. At lower N level, CRM-stress tended to induce cellular metabolic mode towards stronger energy supply/acquisition but weaker energy production/consumption, while triggered a shift towards stronger energy production/storage but weaker energy acquisition/consumption as N level elevated, thus disturbing metabolic balance and strongly inhibiting Microcystis growth at each N level. Long-term robust algicidal effect of CRM against other common cyanobacteria besides Microcystis was evident in natural water. This study shed novel insights into inhibitory effects and mechanisms of luteolin CRM on Microcystis growth and MC-pollution in different N-level waters.

Long-term and strong suppression against Microcystis growth and microcystin-release by luteolin continuous-release microsphere: Optimal construction, characterization, effects and proteomic mechanisms.

Microcystis-dominated cyanobacterial blooms (MCBs) severely threaten ecological health by causing hypoxia and releasing microcystins (MCs). Luteolin has potential as low-cost eco-safe algaecide against Microcystis, but to enhance sustainability of its algicidal effect and elucidate underlying mechanisms at proteomic level are urgently desirable. This study optimally constructed continuous-release microsphere (CRM) of luteolin with strong solidity and durability even after long-term immersion. Applying luteolin CRM, this study developed a long-term algicidal option to strongly inhibit Microcystis growth and MC-release until 49 days, with inhibition ratios of growth and MC-release (both ≥ 98%) and inhibitory effect-lasting time (nearly 50 days) of CRM superior to most former reports, and long-term strong inhibitory effects of CRM on Microcystis growth and MC-release kept stable at various nitrogen levels. Also, luteolin CRM rendered extracellular MCs content decrease to nearby acceptable threshold for drinking water. These signified a promising prospect of luteolin CRM in sustained effective control against toxigenic MCBs in waters of different eutrophic states. Comparative proteomic analysis showed that luteolin CRM significantly up-regulated photosynthesis and protein homestasis, but down-regulated other processes including stress response, MC-synthesis/release, glycolysis, amino acid synthesis, fatty acid synthesis/ß-oxidation, tricarboxylic acid cycle, transcription, translation, transport, cell shaping and cell division. These implied that continuous stress of luteolin released from CRM induced Microcystis proteome towards a shift of higher energy storage but lower energy release/consumption, which largely disturbed its physiological metabolic processes and thus negatively impact its growth. Proteomics results shed newly deep insights on algicidal mechanisms of flavonoid in the form of CRM.

[Effects of three at-home bleaching agents on enamel structure and structure-related mechanical properties].

OBJECTIVE: To investigate the effects of three differently concentrated at-home bleaching agents on the structure and the structure-related mechanical properties of human enamel. METHODS: Sixty enamel specimens were randomly divided into four groups and treated with 10% carbamide peroxide (CP), 15% CP, 20% CP and distilled water, respectively. The bleaching process was 8 h/day for 14 consecutive days. Baseline and final atomic force microscopy (AFM) surface detection, Raman spectroscopy, attenuated total reflectance-infrared spectroscopy (ATR-IR), microhardness and fracture toughness (FT) measurements were carried out before and after bleaching experiments. RESULTS: CP didn't change the morphology of enamel. Meanwhile, the three bleached groups and the control group had no significant difference in root mean square detection (P = 0.774), ν(2)CO(3)(2-) : ν(1)ν(3)PO(4)(3-) (P = 0.263) and microhardness (P = 0.829). The percentage of relative Raman intensity in the three bleached groups and the control group were (105.74 ± 11.34)%, (104.46 ± 8.83)%, (99.52 ± 9.32)% and (97.62 ± 7.46)%, respectively. There was no significant difference among them (P = 0.062). However, the percentage of laser-induced fluorescence in the three bleached groups and the control group were (20.86 ± 7.23)%, (22.14 ± 7.34)%, (21.10 ± 7.59)% and (100.78 ± 3.70)%, respectively. There was significant difference between either of the bleached groups and the control group (P < 0.001). Moreover, FT declined significantly in the three groups (P = 0.024, P = 0.005, P = 0.013) when compared with the control group. CONCLUSIONS: Under in vitro condition, three differently concentrated at-home bleaching agents wouldn't induce the demineralization and the decline of microhardness on enamel. However, the decrease of FT on enamel seemed to be inevitable after bleaching.