Temporal and Spatial Distribution and Fluorescence Spectra of Dissolved Organic Matter in Plateau Lakes: A Case Study of Qinghai Lake

Dissolved organic matter (DOM) has a great impact on the main pollution indicators of lakes (such as chemical oxygen demand, COD). Therefore, DOM is the research basis for understanding the meaning of the water environment and the laws of the migration and transformation of pollutants. Qinghai Lake is one of the world’s typical inland plateau lake wetlands. It plays important roles in improving and regulating the climate and in promoting a virtuous regional ecological cycle. In recent years, with the acceleration of urbanization and the rapid development of tourism, under the background of climate change, and with grassland degradation and precipitation change, the whole basin of Qinghai Lake has been facing great ecological pressure. In order to comprehensively explore the water environment of Qinghai Lake and to protect the sustainable development of the basin, a systematic study was carried out on the whole basin of Qinghai Lake. The results show the following: (1) from 2010 to 2020, the annual average value of CODCr in Qinghai Lake fluctuated in the range from class III to class V according to the surface water environmental quality standard, showing first a downward trend and then an upward trend. (2) The concentration of CDOM in Qinghai Lake had obvious temporal and spatial changes. (3) The spatial distribution of the total fluorescence intensity of FDOM in water was also different in different seasons. However, in the three surveys, the area with the highest total fluorescence intensity of FDOM in the water body appeared near Erlangjian in the south of Qinghai Province, indicating that anthropogenic sources are the main controlling factors of dissolved organic matter in the lake.

Evaluation of Hydrophilic and Lipophilic Antioxidant Capacity in Spanish Tomato Paste: Usefulness of Front-Face Total Fluorescence Signal Combined with Parafac

The hydrophilic and lipophilic antioxidant activities due to the main bioactive components present in Spanish tomato paste samples were studied, using standardized and fluorescent methods. After extraction, phenolic antioxidants (Folin-Ciocalteu method) and total antioxidant activity (TEAC assay) were evaluated, examining differences between hydrophilic and lipophilic extracts corresponding to different samples. Total fluorescence spectra of extracts (excitation-emission matrices, EEMs) were recorded in the front-face mode at two different ranges: 210–300 nm/310–390 nm, and 295–350 nm/380–480 nm, for excitation and emission, respectively, in the hydrophilic extracts. In the lipophilic extracts, the first range was 230–283 nm/290–340 nm, while the second range was 315–383 nm/390–500 nm for excitation and emission, respectively. EEMs from a set of 22 samples were analyzed by the second-order multivariate technique Parallel Factor Analysis (PARAFAC). Tentative assignation of the different components to the various fluorophores of tomato was tried, based on literature. Correlation between the antioxidant activity and score values retrieved for different components in PARAFAC model was obtained. The possibility of using EEMs-PARAFAC to evaluate antioxidant activity of hydrophilic and lipophilic compounds in these samples was examined, obtaining good results in accordance with the Folin-Ciocalteu and TEAC assays.

Discharge and Temperature Controls of Dissolved Organic Matter (DOM) in a Forested Coastal Plain Stream

Streams in the southeastern United States Coastal Plains serve as an essential source of energy and nutrients for important estuarine ecosystems, and dissolved organic matter (DOM) exported from these streams can have profound impacts on the biogeochemical and ecological functions of fluvial networks. Here, we examined hydrological and temperature controls of DOM during low-flow periods from a forested stream located within the Coastal Plain physiographic region of Alabama, USA. We analyzed DOM via combining dissolved organic carbon (DOC) analysis, fluorescence excitation–emission matrix combined with parallel factor analysis (EEM-PARAFAC), and microbial degradation experiments. Four fluorescence components were identified: terrestrial humic-like DOM, microbial humic-like DOM, tyrosine-like DOM, and tryptophan-like DOM. Humic-like DOM accounted for ~70% of total fluorescence, and biodegradation experiments showed that it was less bioreactive than protein-like DOM that accounted for ~30% of total fluorescence. This observation indicates fluorescent DOM (FDOM) was controlled primarily by soil inputs and not substantially influenced by instream production and processing, suggesting that the bulk of FDOM in these streams is transported to downstream environments with limited in situ modification. Linear regression and redundancy analysis models identified that the seasonal variations in DOM were dictated primarily by hydrology and temperature. Overall, high discharge and shallow flow paths led to the enrichment of less-degraded DOM with higher percentages of microbial humic-like and tyrosine-like compounds, whereas high temperatures favored the accumulation of high-aromaticity, high-molecular-weight, terrestrial, humic-like compounds in stream water. The flux of DOC and four fluorescence components was driven primarily by water discharge. Thus, the instantaneous exports of both refractory humic-like DOM and reactive protein-like DOM were higher in wetter seasons (winter and spring). As high temperatures and severe precipitation are projected to become more prominent in the southeastern U.S. due to climate change, our findings have important implications for future changes in the amount, source, and composition of DOM in Coastal Plain streams and the associated impacts on downstream carbon and nutrient supplies and water quality.

INFLUENCE OF NEUROTROPIC AND METABOLIC DRUGS ON STRUCTURAL AND FUNCTIONAL STATE OF LIPID MATRIX OF THE CELL MEMBRANE

Lately, more and more often to stimulate the reproductive function of animals people use biochemical products, which are based on neurotropic and metabolic compounds and trace elements of nanobiotechnological origin. In order to new biotechnical drugs search and development, and more effective and safe combinations of dietary supplements in them, one should know Biochemical mechanisms of membranotropic action of these substances on a cell. Since these substances can lead to physiological changes in the cell and trigger nonspecific toxic effects on the body of animals depending on dose and period of action. The article presents the results of studies on the effects of neurotropic and metabolic drugs on structural and functional state of lipid matrix of the cell membrane. In experiment were used four drugs: hlutam 1-M (Sodium Glutaminate), stymulin (Sodium Glutaminate, Sodium Succinate), nanovulin-VHR (Sodium Glutaminate, Sodium Succinate, Copper Citrate), nanovulin-R (Sodium Glutaminate, Sodium Succinate, L-arginine, Copper Citrate). The main task of the experiment was to investigate the concentration effects and primary mechanisms of membranotropic influence of the components of investigated drugs in the range of physiological concentrations of the active substance on the structural and functional state of the lipid matrix of cell membranes. According to research results, it was found that Sodium Glutaminate, which is part of all the investigational drugs, affects the polarity of the hydrophobic zone of the membrane and increases the polarity of the lipid surround. An application of Sodium glutaminate with Succinate in same drug (stimulin, nanovulin-VHR, nanovulin-R) reduces the destructive effects of Sodium Glutamate on the lipid membrane of cells. Also, it should be noted that Copper Citrate in combination with Glutaminate and Succinate (nanovulin-VHR, nanovolin-R) excludes the membrane-stabilizing and membrane-disruptive effects of their influence on the structure of lipid packing in the bilayer. From the results of the research we can suggest, that aquachelates penetrate the hydrophobic lipid bilayer zone, as evidenced by the total fluorescence quenching of pyrene.

Fluorescence Emission Behaviors of the L-Cysteine/Au(I) Complex in a Cyclodextrin-Based Metal-Organic Framework

Aggregation-induced emission (AIE) molecules are nonemissive in dilute solution but emit intensely upon aggregation in complete contrast to aggregation-caused quenching (ACQ) molecules. The emission of ACQ molecules, such as fluorescein, that have been encapsulated into the hydrophilic nanopores in a cyclodextrin-based metal-organic framework (CD-MOF) was reported to be enhanced due to the disappearance of concentration quenching and the restriction of thermal motion. However, the contribution of the restriction of thermal motion in CD-MOF could not be elucidated. In this study, an AIE-active L-cysteine/Au(I) (L-Cys/Au(I)) complex was synthesized and introduced into the nanopores of CD-MOF via a co-crystallization method. We determined the amount and chemical composition of the L-Cys/Au(I) complex in CD-MOF. The fluorescence intensity of the L-Cys/Au(I)@CD-MOF composite was investigated. The L-Cys/Au(I) complex that was synthesized from Au(III) chloride and L-cysteine was found to be a linear oligomer consisting of Cys5Au4. For the L-Cys/Au(I)@CD-MOF composite with a L-Cys/Au(I) complex of 0.45 per hydrophilic nanopore, the total fluorescence intensity of the isolated L-Cys/Au(I) complex in CD-MOF exceeded that of the L-Cys/Au(I) complex in the solid-state due to the restriction of the thermal motion without the aggregation of the complex.

mGreenLantern: a bright monomeric fluorescent protein with rapid expression and cell filling properties for neuronal imaging

Although ubiquitous in biological studies, the enhanced green and yellow fluorescent proteins (EGFP and EYFP) were not specifically optimized for neuroscience, and their underwhelming brightness and slow expression in brain tissue limits the fidelity of dendritic spine analysis and other indispensable techniques for studying neurodevelopment and plasticity. We hypothesized that EGFP’s low solubility in mammalian systems must limit the total fluorescence output of whole cells, and that improving folding efficiency could therefore translate into greater brightness of expressing neurons. By introducing rationally selected combinations of folding-enhancing mutations into GFP templates and screening for brightness and expression rate in human cells, we developed mGreenLantern, a fluorescent protein having up to sixfold greater brightness in cells than EGFP. mGreenLantern illuminates neurons in the mouse brain within 72 h, dramatically reducing lag time between viral transduction and imaging, while its high brightness improves detection of neuronal morphology using widefield, confocal, and two-photon microscopy. When virally expressed to projection neurons in vivo, mGreenLantern fluorescence developed four times faster than EYFP and highlighted long-range processes that were poorly detectable in EYFP-labeled cells. Additionally, mGreenLantern retains strong fluorescence after tissue clearing and expansion microscopy, thereby facilitating superresolution and whole-brain imaging without immunohistochemistry. mGreenLantern can directly replace EGFP/EYFP in diverse systems due to its compatibility with GFP filter sets, recognition by EGFP antibodies, and excellent performance in mouse, human, and bacterial cells. Our screening and rational engineering approach is broadly applicable and suggests that greater potential of fluorescent proteins, including biosensors, could be unlocked using a similar strategy.

Aerosolised fluorescein can quantify FFP mask faceseal leakage: a cost-effective adaptation to the existing point of care fit-test.

Background Filtering facepiece (FFP) respirators must provide an adequate faceseal to protect healthcare workers from harmful particles. A qualitative fit-test using bitter-tasting aerosols the commonest way to determine if an FFP mask is safe enough for clinical use. This taste-test is subjective and can be biased by placebo. We propose a cheap and quantitative modification of the taste-test, by measuring the amount of fluorescein staining filter paper behind the FFP mask after a fit-test protocol, using digital image analysis. Methods Medical grade fluorescein was added to bitter-tasting denatonium benzoate solution and Aerosolised during a mask fit-testing protocol. Scientific filter paper was placed on the inner surface of the mask. Participants were asked if they could taste the solution to determine their qualitative ‘pass’ or ‘fail’ result. Filter paper photographs were analysed after the test to quantify total fluorescence (TF). TF levels in the taste-test ‘pass’ and ‘fail’ groups were compared.Results Fifty-six healthcare professionals completed the fluorescein mask fit-test protocol. 32 (57%) ‘passed’ the qualitative (taste) test and the remainder ‘failed’. There was a significant difference in TF between the groups based on their qualitative results (p <0.001). A cut-off of TF = 5.0 x 106 fluorescence units was determined by analysing the precision (78%) and recall (84%) of the fluorescein test. Applying this cut-off resulted in 5 out of 56 participants (9%) being reclassified from ‘pass’ to ‘fail’ by the fluorescein test. 7 out of 56 (12%) participants were reclassified from ‘fail’ to ‘pass’.Conclusions Fluorescein is detectable and sensitive to identify faceseal leaks in FFP masks. The fluorescein fit-test is discriminating in its ability to divide people into ‘pass’ and ‘fail’ groups similarly to the taste-test. The adaptations are low-cost and could be incorporated in the point-of-care setting. After further validation the fluorescein test could increase safety for staff by reducing the number of false ‘pass’ by the taste-test. It could also reassure people who have ‘failed’ the taste-test that they have low levels of fluorescein leak, enabling them to return to clinical practice safely.

5-aminolevulinic acid-guided surgery for focal pediatric brainstem gliomas: A preliminary study

Background: There is a growing body of literature supporting the use of 5-aminolevulinic acid (5-ALA) in the pediatric population, however, its use is still considered “off label” in this setting. In this retrospective study, we report our experience using 5-ALA in pediatric patients with focal brainstem gliomas (BSGs). Methods: Patients younger than 16 years presenting with a newly diagnosed BSG that was focal in nature were considered suitable for treatment with 5-ALA-assisted surgery. Exclusion criteria included MRI features suggestive of a diffuse intrinsic pontine glioma. A single dose of 5-ALA was administered preoperatively. Intraoperative fluorescence was recorded as “solid,” “vague,” or “none.” The effectiveness of the fluorescence was graded as “helpful” or “unhelpful.” Results: Eight patients underwent 5-ALA-assisted surgery. There were four tumors located in the pons, two midbrain tumors, and two cervicomedullary tumors. Histological analysis demonstrated three diffuse astrocytomas, three pilocytic astrocytomas, and two anaplastic astrocytomas. Solid fluorescence was found in three of the eight cases, vague fluorescence was found in two cases, and no fluorescence was found in three cases. Fluorescence was useful in 3 (37%) cases. No patients experienced any complications attributable to the administration of the 5-ALA. Conclusion: With a total fluorescence rate of 62.5% but a subjectively assessed “usefulness” rate of only 37.5%, the role of 5-ALA in BSG surgery is limited. Given the toxicological safety, however, of the agent, caution is perhaps needed before dismissing the use of 5-ALA entirely.

Morphology Manipulation and Upconversion Luminescence Enhancement of β-NaLuF4: Er3+ Hexagonal Microtubes via Sr2+ Doping

A new and facile strategy to enhance the upconversion luminescence (UCL) emission of NaLuF4: Er3+ microcrystals (MCs) using strontium (Sr) as a dopant has been reported. With the introduction of Sr2+, the products change from long NaLuF4: Er3+ hexagonal microtubes to short hexagonal microtubes and finally to hexagonal microprisms. The growth mechanism is profoundly discussed according to the different reaction time-dependent morphologies. More importantly, the total fluorescence intensity is significantly reinforced by doping Sr2+ ions. When 18% Sr2+ is doped into NaLuF4: Er3+ hexagonal microtubes, the maximum green and red luminescence intensities are about 5.8 and 4.4 times higher than those of Sr2+-free samples, respectively. The influences of Sr2+ ion doping content on the phase, the morphology, and the local crystal field symmetry of the as-synthesized NaLuF4 crystals are investigated.