ABSTRACT
We investigated feeding and fecundity of the two-spotted spider mite, Tetranychus urticae (Acari: Tetranychidae), on leaves of cucumber (Cucumis sativus) seedlings that had been acclimatized to different light intensities. Based on these data, we analyzed the relationships between mite performance (feeding and fecundity) and leaf properties. The cucumber seedlings were grown in controlled-environment chambers under different light intensities at a photosynthetic photon flux density of 50, 100, 150, 300, or 450 µmol m- 2 s- 1 until the first true leaves had expanded. Adult females were released on the adaxial surfaces of excised leaf samples from the seedlings of each treatment group and held under standardized light intensity (200 µmol m- 2 s- 1). Fecundity and leaf damage area increased and decreased, respectively, as the acclimatization light intensity increased, indicating indirect effects of light intensity on feeding and fecundity through changes in the host leaf properties. Leaf mass per area (LMA) and photosynthetic capacity, which increased as the acclimatization light intensity increased, was positively related to the fecundity, but was negatively related to the leaf damage area. The higher LMA and photosynthetic capacity results in an increased amount of mesophyll per unit leaf area. This would allow the mites to feed efficiently from a limited area, which may explain the increased fecundity on these leaves.
Subject(s)
Cucumis sativus , Mites , Tetranychidae , Animals , Female , Fertility , Plant LeavesABSTRACT
BACKGROUND/AIM: In recent years, the Geriatric Nutritional Risk Index (GNRI) has been reported as a predictor of prognosis in many patients with cancer. This study investigated the association of preoperative GNRI with the occurrence of adverse events and duration of treatment with capecitabine plus oxaliplatin (CAPOX), a postoperative adjuvant chemotherapy, in 59 patients with colorectal cancer from September 2019 to April 2022. PATIENTS AND METHODS: A cut-off value of 100.9 was used to categorize patients into high and low GNRI groups. RESULTS: The incidence of grade ≥2 leukopenia (p=0.03), and all grades peripheral neuropathy (p=0.04) were significantly more frequent in the low GNRI group. Analysis of factors influencing treatment duration by univariate and multivariate Cox regression proportional hazards models showed a significant difference in GNRI (p=0.0097). CONCLUSION: GNRI, a nutritional indicator assessed before the start of treatment, influences the occurrence of adverse events and duration of treatment with CAPOX as adjuvant chemotherapy. To complete CAPOX therapy, preoperatively, it is important to assess the patients' nutritional status using the GNRI and to actively intervene in nutritional therapy.
Subject(s)
Colorectal Neoplasms , Duration of Therapy , Humans , Aged , Nutritional Status , Prognosis , Oxaliplatin/adverse effects , Colorectal Neoplasms/drug therapy , Chemotherapy, Adjuvant/adverse effects , Nutrition Assessment , Risk Factors , Retrospective StudiesABSTRACT
Monoclonal antibodies are widely used for the treatment of various diseases, and because therapeutic monoclonal antibodies are stored in an aqueous solution or in a lyophilized state, the preparation of a stabilizing formulation that prevents their deterioration (degradation and aggregation) is crucial. Given the structural similarities of the immunoglobulin G (IgG) framework regions and a diversity of only four subclasses, we aimed to find common conditions that stabilize many different antibodies. In this study, we analyzed the effect of pH (the most critical factor in establishing a stable formulation) on human monoclonal antibodies from subclasses IgG1, IgG2, and IgG4, all of which have been utilized in antibody therapeutics. We found that human IgGs are stable with minimal heat-induced degradation and aggregation at pH 5.0-5.5 irrespective of their subclass. We also found that IgG1 is more susceptible to fragmentation, whereas IgG4 is more susceptible to aggregation. This basic information emphasizing the influence of pH on IgG stability should facilitate the optimization of formulation conditions tailored to individual antibodies for specific uses.
Subject(s)
Antibodies, Monoclonal/chemistry , Immunoglobulin G/chemistry , Animals , Antibodies, Monoclonal/genetics , CHO Cells , Calorimetry, Differential Scanning , Cell Culture Techniques , Chromatography, Gel , Circular Dichroism , Cricetinae , Cricetulus , Drug Stability , Drug Storage , Hot Temperature , Hydrogen-Ion Concentration , Immunoglobulin G/genetics , Pharmaceutical Solutions/chemistry , Protein StabilityABSTRACT
The goal of this study was to establish a system for co-culturing microalgae and crop plants with biogas digestate. We examined growth performances of E. gracilis and L. sativa co-cultured using a commercial liquid fertilizer designed for soilless culture supplemented with vitamins and ammonium. This solution simulated the filtrate of nitrified biogas digestate derived from the organic fraction of municipal solid waste but was supplemented with insufficient plant nutrients (Mg, Fe and Mn). The specific growth rate of the co-cultured E. gracilis was 0.761 ± 0.081â d-1 (mean ± SE), which was the same rate that E. gracilis achieved when grown as a sole culture. There were no significant differences between L. sativa cultured with E. gracilis until the stationary growth phase of E. gracilis was reached and those cultured alone relative to biomass, RGRs (relative growth rates), or relative to SPAD values of leaves. These results suggest that E. gracilis and L. sativa could be co-cultured with the biogas digestate after being nitrified and filtered. In addition, considering concentrations of plant macronutrients in the residual solution after the co-culturing E. gracilis and L. sativa, it could be re-used as the nutrient solution for co-culturing E. gracilis and L. sativa.
Subject(s)
Euglena gracilis , Microalgae , Anaerobiosis , Biofuels , Biomass , LactucaABSTRACT
Iron regulatory proteins (IRPs), regulators of iron metabolism in mammalian cells, control the translation of proteins involved in iron uptake, storage and utilization by binding to specific iron-responsive element (IRE) sequences of mRNAs. Two homologs of IRPs (IRP1 and IRP2) have a typical heme regulatory motif (HRM), a consensus sequence found in "heme-regulated proteins". However, specific heme binding to HRM has been reported only for IRP2, which is essential for oxidative modification and loss of binding to target mRNAs. In this paper, we confirmed that IRP1 also specifically binds two molar equivalents of heme, and found that the absorption and resonance Raman spectra of heme-bound IRP1 were quite similar to those of heme-bound IRP2. This shows that the heme environmental structures in IRP1 are close to those of proteins using heme as a regulatory molecule. Pulse radiolysis experiments, however, clearly revealed an axial ligand exchange from Cys to His immediately after the reduction of the heme iron to form a 5-coordinate His-ligated heme in heme-bound IRP2, whereas the 5-coordinate His-ligated heme was not observed after the reduction of heme-bound IRP1. Considering that the oxidative modification is only observed in heme-bound IRP2, but not IRP1, probably owing to the structural flexibility of IRP2, we propose that the transient 5-coordinate His-ligated heme is a prerequisite for oxidative modification of heme-bound IRP2, which functionally differentiates heme binding of IRP2 from that of IRP1.
Subject(s)
Iron-Regulatory Proteins/chemistry , Iron-Regulatory Proteins/metabolism , Heme/chemistry , Heme/metabolism , Iron/metabolism , Protein BindingABSTRACT
We investigated the possibility of using Euglena gracilis to convert digestate from methane fermentation of organic wastes into a medium for soilless crop culture. The growth of E. gracilis cultured with aqueous solutions containing filtrate of raw digestate at 1-30% (v/v) and nitrified digestate at 10-100% (v/v) was examined. Concentrations of plant macronutrient ions in nitrified digestate before and after culturing E. gracilis were also examined. Specific growth rates in aqueous solutions containing filtrate of raw digestate at 1-10% and nitrified digestate at 10-100% showed no significant differences, respectively (0.781 ± 0.031â d-1 and 0.925 ± 0.033â d-1, mean ± standard error). The rates in the filtrate of nitrified digestate were significantly higher than those in the filtrate of raw digestate. Moreover, there were no significant differences between the concentrations of plant macronutrient ions other than [Formula: see text] in the filtrate of nitrified digestate before and after culturing E. gracilis. The concentration of [Formula: see text] decreased significantly by 10.5% of the initial concentration. As a result, the constituent ratio of plant macronutrient ions other than magnesium in the solution after culturing E. gracilis was similar to that in a standard nutrient solution for soilless culture.
Subject(s)
Euglena gracilis , Methane , Culture Media , Fermentation , IonsABSTRACT
A passive light microscope system has been developed, capable of reconstructing an extended-focus 3-D cell-level image of chlorophyll fluorescence and Phi(PSII) of intact attached leaves using a limited number of focal plane images of chlorophyll fluorescence. Using this system, the relationships between the depth of the mesophyll cells in spongy tissue and the intensity of the chlorophyll fluorescence and the Phi(PSII) were investigated in sunflower leaves exposed to 300 ppb ozone for 12 h at a PPFD of 300 micromol m(-2) s(-1) actinic light. After ozone exposure, fluorescence intensity (F) largely decreased in the cells just under the epidermal cells (within approximately 20 microm of the epidermal cells), but the sites where fluorescence intensity decreased had no relationship to the position of the stomata. By contrast, the distribution of Phi(PSII) showed no change after the ozone exposure. These findings suggest that ozone-induced inhibition occurs in the cells just under the epidermal cells by reducing the light absorption of the chloroplasts, while the operating quantum efficiency of PSII photochemistry is maintained.
Subject(s)
Chlorophyll/analysis , Helianthus/drug effects , Imaging, Three-Dimensional/methods , Microscopy/methods , Ozone/pharmacology , Plant Leaves/drug effects , Plant Leaves/metabolism , Algorithms , Chlorophyll/metabolism , Fluorescence , Helianthus/cytology , Helianthus/metabolism , Plant Leaves/cytologyABSTRACT
Serious environmental degradation of aquatic ecosystems has been caused by eutrophication and by pollutants such as herbicides. Therefore, measurement of in situ algal photosynthetic activity is important for environmental monitoring. With ordinary nonimaging fluorometers, algal chlorophyll fluorescence can be measured easily, but heterogeneity within samples cannot be detected. Effects of a herbicide preparation containing 3-(3,4-dichlorophenyl)-1,1 -dimethylurea (DCMU) on photosynthetic activity at different growth stages of Spirogyra distenta were investigated by using a computer-aided microscopic imaging system for chlorophyll afluorescence. Photosystem II photochemical yield (phiPSII) images were used to diagnose photosynthetic activity of spiral filate chloroplasts in algal cells. The herbicide treatment caused a stronger decline in phiPSII values in younger than in mature algae cells. This result indicated that heterogeneity within algal samples should be considered when algae are used for environmental monitoring. Thus, measurement of chlorophyll fluorescence from young and mature chloroplasts with a microscopic imaging system makes it possible to improve the sensitivity for monitoring the environmental degradation of aquatic ecosystems.