Bench-scale fermentation of Trichoderma viride on wastewater sludge: Rheology, lytic enzymes and biocontrol activity

Conidiation and lytic enzyme production by Trichoderma viride at different solids concentration of pre-treated municipal wastewater sludge was examined in a 15-L fermenter. The maximum conidia concentration (5.94 × 10⁷ CFU mL⁻¹ at 96 h) was obtained at 30 g L⁻¹ suspended solids. The maximum lytic enzyme activities were achieved around 12–30 h of fermentation. Bioassay against a fungal phytopathogen, Fusarium sp. showed maximum activity in the sample drawn around 96 h of fermentation at 30 g L⁻¹ suspended solids concentration. Entomotoxicity against spruce budworm larvae showed maximum value ≈17290 SBU μL⁻¹ at 30 g L⁻¹ suspended solids concentration at the end of fermentation (96 h). Plant bioassay showed dual action of T. viride, i.e., disease prevention and growth promotion. The rheological analyses of fermentation sludges showed the pseudoplastic behaviour. In order to maintain required dissolved oxygen concentration ≥30%, the agitation and aeration requirements significantly increased at 35 g L⁻¹ compared to 30 and 25 g L⁻¹. The oxygen uptake rate and volumetric oxygen mass transfer coefficient, k_La at 35 g L⁻¹ did not increase in comparison to 30 g L⁻¹ due to rheological complexity of the broth during fermentation. Thus, the successful fermentation operation of the biocontrol fungus T. viride is a rational indication of its potential for mass-scale production for agriculture and forest sector as a biocontrol agent.     

高浓度臭氧对大豆生长发育及产量的影响

采用开顶式同化箱(open-top chambers,OTCs)装置,设置活性碳过滤大气(CF,［O₃］<10 μg·kg^-1)和高臭氧(O₃)浓度(HO,约为80 μg·kg^-1)两个处理,研究开花后高浓度O₃对大豆农艺性状、叶面积、叶绿素、抗氧化系统与产量的影响.结果表明： 与对照(CF)同期相比,HO处理植株的叶面积和叶绿素含量显著降低(P<0.05);过氧化物酶、过氧化氢酶和超氧化物歧化酶活性极显著增强(P<0.01),但随着处理时间的延长,其活性逐渐降低;HO处理下植株叶片中可溶性蛋白质和抗坏血酸(AsA)含量降低,丙二醛含量显著升高,表明膜脂过氧化进程加快;大豆的单株干物质量、有效结荚数、籽粒数、百粒重和产量都有所降低,其中产量降低了47%,差异达极显著水平(P<0.01).     

The response of sweet corn to HF and SO2 under field conditions

“Marcorss” sweet corn plants grown in field plots were exposed continuously in open-top chambers for 32 days to ambient air, charcoal-filtered air or charcoal-filtered air containing HF (ca. 0.5 μgF m⁻³), SO₂ (ca. 235 μg m⁻³), or the two pollutants combined. Elliptical chlorotic leasions appeared after 23 days on leaves of plants exposed to SO₂/HF, and shortly thereafter on plants exposed to all other treatments. At harvest, the number of plants with lesions was significantly greater in chambers supplied with SO₂/HF than in chambers with SO₂, HF, or filtered air.

The different treatments had no effect on fresh or dry weights of leaves, husks, or tassels, height of plants, or number of kernels per ear. Exposure to SO₂/HF reduced the fresh and dry weights of stalks. There were fewer mature ears in the SO₂/HF and unfiltered air treatments than in the others. The reduction in yield from SO₂/HF was about the same as that ascribed to ambient photochemical oxidants in the unfiltered air treatment.

HF combined with SO₂ had no effect on accumulation of S as compared with SO₂ alone, but there was a striking reduction in accumulation of foliar F in plants exposed to SO₂/HF as compared with HF alone.     

Electrochemical quartz crystal impedance study on the overoxidation of polypyrrole-carbon nanotubes composite film for amperometric detection of dopamine

The electrochemical quartz crystal impedance (EQCI) method was used to study the overoxidation of polypyrrole (PPy)–multiwalled carbon nanotubes (MWCNT) nanocomposite film in neutral and alkaline solutions. The values of molar mass per electron transferred (M/n) obtained during the overoxidation of PPy in 0.10 mol L⁻¹ Na₂SO₄ and 0.20 mol L⁻¹ NaOH aqueous solutions were estimated to be ca. 17 and 22 g mol⁻¹, respectively, suggesting the nucleophilic attack of solution OH⁻ to the pyrrole units during the overoxidation, and the possible partial formation of carboxylic groups after the overoxidation in the NaOH solution. Also, the overoxidized PPy–MWCNT composite film prepared in the NaOH solution showed a notably larger affinity to dopamine (DA) dissolved in a neutral phosphate buffer than that prepared in the Na₂SO₄ solution. The modification of the overoxidized nanocomposite film improved substantially the sensitivity for DA assay in a neutral phosphate buffer, as compared with the modification of overoxidized PPy or MWCNT alone. At a −6 kHz (201-nm thickness) nanocomposite film prepared in a polymerization bath containing 1.0 mg mL⁻¹ MWCNT and overoxidized in 0.20 mol L⁻¹ aqueous NaOH, the peak current response from differential pulse voltammetric assay of DA was linear with DA concentration from 4.0 × 10⁻⁸ to 1.4 × 10⁻⁶ mol L⁻¹, with a lower limit of detection of 1.7 nmol L⁻¹, good anti-interferent ability, as well as good stability and reproducibility.     

Removal of lead (Pb(2+)) by the cyanobacterium Gloeocapsa sp

Pb²⁺ removal ability of the viable-freshwater cyanobacterium Gloeocapsa sp. was studied in batch experiments. Gloeocapsa sp. was cultured in the Medium 18 with pH adjusted to 3, 4, 5, 6 and 7. Growth was subsequently determined based on the increase of chlorophyll-a content. Gloeocapsa sp. was able to grow at all pH levels tested, except at pH 3. Removal of Pb²⁺ was then further studied under pH 4. The results showed that Pb²⁺ concentration in the range of 0–20 mg L⁻¹ was not inhibitory to Gloeocapsa sp. growth but reduced its Pb²⁺ removal efficiency (by 4.5% when Pb²⁺ concentration increased from 2.5 to 20 mg L⁻¹). Pb²⁺ removal characteristics followed the Langmuir adsorption isotherm with the maximum removal capacity (q_max) of 232.56 mg g⁻¹. Adsorption of Pb²⁺ by this cyanobacterium followed the second order rate reaction and intraparticle diffusion was likely the rate-determining step. The initial rate of Pb²⁺adsorption during intraparticle diffusion was slower under light than under dark conditions, indicating that light probably slowed down the initial rate of intraparticle diffusion through the repulsion effects on cell membrane.     

Actual and potential dark respiration rates and different electron transport pathways in freshwater aquatic plants

The rates of respiratory O₂ uptake have been studied in leaves, stems and whole shoots of several freshwater plants: 6 angiosperms, 2 bryophytes and one alga. For angiosperm leaves, rates varied widely with species (30–142 μmol O₂ (gDW)⁻¹ h⁻¹), were correlated with chlorophyll content and were higher than those of the stems (13–71 μmol O₂ (gDQ)⁻¹ h⁻¹). The rates for the shoots of bryophytes (53–66 μmol O₂ (gDW)⁻¹ h⁻¹) and for the alga Cladophora glomerata (L.) Kütz. (96 μmol O₂ (gDW)⁻¹ h⁻¹) were slightly higher than those of most angiosperm stems, but lower than those for most leaves.

These plants had a significant cyanide-resistant respiration, suggesting the existence of an alternative pathway to the “classic” cytochrome system. This pathway was found to be active in all the species studied, as judged by responses to a specific inhibitor, SHAM (salicylhydroxamic acid). Measurement of electron-transport system (ETS) activity showed that there is a large electron-transport capacity which is not normally used by respiration in vivo.     

Atmospheric nitric oxide stimulates plant growth and improves the quality of spinach (Spinacia oleracea)

Nitric oxide (NO) is an endogenous signalling molecule implicated in a growing number of plant processes and has been recognised as a plant hormone. The present research employed spinach plant ( Spinacia oleracea cv. Huangjia) and closed growth chambers to investigate the effects of gaseous NO application on vegetable production in greenhouses. Treatment of low concentration of NO gas (ambient atmosphere with 200 nL L⁻¹ NO gas) significantly increased the shoot biomass of the soil-cultivated plants as compared with the control treatment (ambient atmosphere). In addition, the NO treatment also increased the photosynthetic rate of leaves, indicating that the enhancement of photosynthesis is an important reason leading to more biomass accumulation induced by NO gas. Furthermore, the NO treatment decreased nitrate concentration but increased the concentrations of soluble sugar, protein, antioxidants (vitamin C, glutathione and flavonoids), and ferric reducing-antioxidant power (FRAP) in shoots of the plants grown in soil, suggesting that the gaseous NO treatment can not only increase vegetable production but also improve vegetable quality. In addition, the effects of the combined application of NO and CO₂ (NO 200 nL L⁻¹ and CO₂ 800 μL L⁻¹) on shoot biomass was even greater than the effects of elevated CO₂ (CO₂ 800 μL L⁻¹) or the NO treatment alone, implying that gaseous NO treatment can be used in CO₂-elevated greenhouses as an effective strategy in improving vegetable production.     

Exogenously applied ascorbic acid alleviates salt-induced oxidative stress in wheat

Although ascorbic acid (AsA) is one of the most important and abundantly occurring water soluble antioxidants in plants, relatively little is known about its role in counteracting the adverse effects of salt stress on plant growth. To address this issue that whether exogenous application of ascorbic acid (AsA) through rooting medium could alleviate the adverse effects of salt stress on wheat plants, a hydroponic experiment was conducted under glasshouse conditions using two wheat cultivars, S-24 (salt tolerant) and MH-97 (moderately salt sensitive). Plants of both cultivars were subjected to 0 or 150 mM NaCl solution supplemented with 0, 50, or 150 mg L⁻¹ AsA for 58 days. Imposition of salt stress reduced the growth of both wheat cultivars by causing reduction in photosynthesis, and endogenous AsA level, and enhancing accumulation of Na⁺ and Cl⁻ coupled with a decrease in K⁺ and Ca²⁺ in the leaves and roots of both cultivars thereby decreasing tissue K⁺/Na⁺ ratio. However, root applied AsA counteracted the adverse effects of salt stress on the growth of cv. S-24 only, particularly at 100 mg L⁻¹ AsA level. AsA-induced enhancement in growth of salt-stressed plants of S-24 was associated with enhanced endogenous AsA level and CAT activity, and higher photosynthetic capacity, and accumulation of K⁺ and Ca²⁺ in the leaves. Although root applied AsA did not improve the growth of salt-stressed plants of MH-97, it enhanced endogenous level of AsA, CAT activity, photosynthetic capacity, and leaf K⁺ and Ca²⁺. These findings led us to conclude that root applied AsA counteracts the adverse effects of salt stress on growth of wheat by improving photosynthetic capacity of wheat plants against salt-induced oxidative stress and maintaining ion homeostasis, however, these effects were cultivar specific.     

Trehalose: Protector of antioxidant enzymes or reactive oxygen species scavenger under heat stress?

Trehalose is known to protect membranes and macromolecules. Its accumulation has been implicated in allowing plants to tolerate stress, including heat-shock. However, under heat-shock, it is not clear whether trehalose eliminates reactive oxygen species (ROS) directly or indirectly by protecting antioxidant enzymes. In this study, we initially examined the effects of trehalose on the activities of key antioxidant enzymes, including superoxide dismutases (SODs), ascorbate catalases (CATs), and ascorbate peroxidases (APX) from wheat (Triticum aestivum L.), and then measured the ability of trehalose to scavenge hydrogen peroxide (H₂O₂) and superoxide anions (O₂⁻). Our results indicated that trehalose protected SOD activity slightly. However, it inhibited CAT and APX activities under heat stress, with a little protection of CAT activity (only about 7% promotion) at 22 °C. Moreover, trehalose scavenged H₂O₂ and O₂⁻ greatly in a concentration-dependent manner, reaching the maximal scavenging H₂O₂ rate of 95% and O₂⁻ rate of 78%, respectively, at 50 mM trehalose. These results suggest that trehalose plays a direct role in eliminating H₂O₂ and O₂⁻ in wheat under heat stress.     

Effect of oxygen supply on cell growth and saponin production in bioreactor cultures of Panax ginseng

The effects of oxygen supply within the range 20.8–50% (using pure oxygen and air), on cell cultures of Panax ginseng were investigated in a balloon-type bubble bioreactor (5 L capacity, containing 4 L Murashige and Skoog medium, supplemented with 7.0 mg L⁻¹ indolebutyric acid, 0.5 mg L⁻¹ kinetin and 30 g L⁻¹ sucrose). A 40% oxygen supply was found to be optimal for the production of both cell mass and saponin yielding values of 12.8 g (DW) L⁻¹, 4.5 mg (g DW)⁻¹ on day 25, respectively. Low (20.8%, 30%) and high (50%) oxygen concentration supplies were unfavorable to cell growth and saponin accumulation. The results indicate that oxygen supplementation to bioreactor-based ginseng cultures was beneficial for biomass accumulation and saponin production.     

Enhancement of growth and gymnodimine production by the marine dinoflagellate, Karenia selliformis

Because of its novel bioactive properties the production of gymnodimine for use as a pharmaceutical precursor has aroused interest. The dinoflagellate, Karenia selliformis produces gymnodimine when grown in bulk culture using GP + selenium medium but the growth rates (μ) and levels of gymnodimine are low (μ, 0.05 days⁻¹; gymnodimine 250 μg L⁻¹ max). We describe the effects of organic acid additions (acetate, glycolate, alanine and glutamate additions and combinations of these) in enhancing growth and gymnodimine production in axenic cultures. The most effective organic acid combinations in decreasing order were: glycolate/alanine > acetate > glycolate. Glycolate/alanine optimised gymnodimine production by prolonging growth (maximum cell yield, 1.76 × 10⁵ cells mL⁻¹; gymnodimine, 1260 μg L⁻¹; growth rate (μ), 0.2 days⁻¹) compared to the control (growth maximum cell yield, 7.8 × 10⁴ cells mL⁻¹; gymnodimine, 780 μg L⁻¹; μ, 0.17 days⁻¹). Acetate enhanced gymnodimine by stimulating growth rate (μ, 0.23 days⁻¹) and the large concentration of gymnodimine per cell (16 pg cell⁻¹ cf. 9.8 pg cell⁻¹ for the control) suggests a role for this compound in gymnodimine biosynthesis. Amending culture media with Mn²⁺ additions resulted in slightly decreased growth in control cultures and increased the gymnodimine while in glycolate/alanine cultures growth was stimulated but gymnodimine production decreased. The results suggest that the organic acid can enhance gymnodimine production by either enhancing growth maximum or the biosynthetic pathway.     

Biomass production and carbon dioxide fixation by Aphanothece microscopica Nägeli in a bubble column photobioreactor

The objective of the present study was to evaluate the growth kinetics of Aphanothece microscopica Nägeli under different conditions of temperature, light intensity and CO₂ concentration. The growth kinetics of the microorganism and carbon biofixation were evaluated using a central composite design, considering five different temperature levels (21.5, 25, 30, 35 and 38.5 °C), light intensities (0.96, 3, 6, 9 and 11 klux) and carbon dioxide concentrations (3, 15, 25, 50 and 62%). The results obtained showed the effects of temperature, light intensity and CO₂ concentration (p < 0.05) on the photosynthetic metabolism of the microorganism. Response surface methodology was adequate for process optimisation, providing a carbon fixation rate to the order of 109.2 mg L⁻¹ h⁻¹ under conditions of 11 klux, 35 °C and 15% carbon dioxide, representing an increase of 58.1% as compared to the conditions tested initially.     

Bipyridylium quaternary salts and related compounds. V. Pulse radiolysis studies of the reaction of paraquat radical with oxygen. Implications for the mode of action of bipyridyl herbicides

1. Rate constants for reduction of paraquat ion (1,1′-dimethyl-4,4′-bipyridy-lium, PQ²⁺) to paraquat radical (PQ⁺·) by e⁻_aq and CO₂⁻· have been measured by pulse radiolysis. Reduction by e⁻_aq is diffusion controlled (k = 8.4·10¹⁰ M⁻¹·s⁻¹) and reduction by CO₂⁻· is also very fast k = 1.5·10¹⁰ M⁻¹·s⁻¹).

2. The reaction of paraquat radical with oxygen has been analysed to give rate constants of 7.7·10⁸ M⁻¹·s⁻¹ and 6.5·10⁸ M⁻¹·s⁻¹ for the reactions of paraquat radical with O₂ and O₂⁻·, respectively. The similarity in these rate constants is in marked contrast to the difference in redox potentials of O₂ and O₂⁻· (− 0.59 V and + 1.12 V, respectively).

3. These rate constants, together with that for the self-reaction of O₂⁻·, have been used to calculate the steady-state concentration of O₂⁻· under conditions thought to apply at the site of reduction of paraquat in the plant cell. On the basis of these calculations the decay of O₂⁻· appears to be governed almost entirely by its self-reaction, and the concentration 5 μm away from the thylakoid is still 90% of that at the thylakoid itself. Thus, O₂⁻· persists long enough to diffuse as far as the chloroplast envelope and tonoplast, which are the first structures to be damaged by paraquat treatment. O₂⁻· is therefore sufficiently long-lived to be a candidate for the phytotoxic product formed by paraquat in plants.     

Effects of sulfur dioxide on the development of powdery mildew of cucumber

Environment is a major factor that does influence host parasite relationships. Air pollution caused by SO₂ may directly alter the environment around the plant and pathogen. It is hypothesised that plants may respond differently to foliar pathogens in air polluted environments. To test this hypothesis, effects of intermittent exposures of SO₂ at 143, 286 and 571 μg m⁻³ were investigated on the development of powdery mildew of cucumber (Cucumis sativa) caused by Sphaerotheca fuliginea, using pre-, post- and concomitant-inoculation exposures in closed-top chambers. Sulfur dioxide (except 143 μg m⁻³) and the fungus acting alone caused chlorosis and/or necrosis, and mildew colonies on leaves, respectively and both reduced the plant growth and yield of cucumber. Fungus colonization was relatively greater on the plants exposed to 143 μg SO₂ m⁻³, but at the higher concentrations, the colonies were greatly suppressed. Gas injury on fungus-infected plants was also less in the other treatments. Conidia of S. fuliginea collected from exposed plants varied in size. Conidial germination was considerably greater at 143 μg SO₂ m⁻³. This concentration also promoted germination of the conidia exposed on glass slides. Higher concentrations (286 and 571 μg m⁻³), however, suppressed the germination of conidia from exposed plants or exposed on glass slides. The number of fibrosin bodies declined at all the concentrations. Synergistic effects of 143 μg SO₂ m⁻³ and S. fuliginea were recorded on plant growth and yield of cucumber. Sulfur dioxide at 571 μg m⁻³ and powdery mildew infection had an antagonistic effect on plant growth.     

Mechanisms of H2O2-induced oxidative stress in endothelial cells

Hydrogen peroxide, produced by inflammatory and vascular cells, induces oxidative stress that may contribute to endothelial dysfunction. In smooth muscle cells, H₂O₂ induces production of O₂⁻ by activating NADPH oxidase. However, the mechanisms whereby H₂O₂ induces oxidative stress in endothelial cells are poorly understood. We examined the effects of H₂O₂ on O₂⁻ levels on porcine aortic endothelial cells (PAEC). Treatment with 60 μmol/L H₂O₂ markedly increased intracellular O₂⁻ levels (determined by conversion of dihydroethidium to hydroxyethidium) and produced cytotoxicity (determined by propidium iodide staining) in PAEC. Overexpression of human manganese superoxide dismutase in PAEC reduced O₂⁻ levels and attenuated cytotoxicity resulting from treatment with H₂O₂. L-NAME, an inhibitor of nitric oxide synthase (NOS), and apocynin, an inhibitor of NADPH oxidase, reduced O₂⁻ levels in PAEC treated with H₂O₂, suggesting that both NOS and NADPH oxidase contribute to H₂O₂-induced O₂⁻ in PAEC. Inhibition of NADPH oxidase using apocynin and NOS rescue with L-sepiapterin together reduced O₂⁻ levels in PAEC treated with H₂O₂ to control levels. This suggests interaction-distinct NOS and NADPH oxidase pathways to superoxide. We conclude that H₂O₂ produces oxidative stress in endothelial cells by increasing intracellular O₂⁻ levels through NOS and NADPH oxidase. These findings suggest a complex interaction between H₂O₂ and oxidant-generating enzymes that may contribute to endothelial dysfunction.     

四种常见树木叶片光合模型关键参数对臭氧浓度升高的响应

随着城市化进程的加快, 臭氧(O₃)已经成为中国夏季首要大气污染物。已有研究表明O₃通过气孔进入叶片显著抑制光合作用, 影响陆地生态系统碳水循环过程。但是O₃浓度升高对植物光合和气孔导度模型关键参数影响的研究仍然缺乏。该研究利用开顶式气室, 设置两个O₃处理(CF, 过滤空气; E-O₃, 未过滤空气+ 60 nmol·mol^-1 O₃), 选用4种常见的树木(茶(Camellia sinensis)、复叶槭(Acer negundo)、栾树(Koelreuteria paniculata)和蒙古栎(Quercus mongolica)), 通过测定叶片气体交换参数, 探究O₃浓度升高对植物光合和气孔导度模型关键参数的影响。结果表明: O₃浓度升高显著降低了4种植物的饱和光合速率和光合生化模型参数叶肉导度, 但是O₃对光合生化模型参数最大羧化速率和最大电子传递速率的负效应在不同树种间存在差异。此外, 不同植物气孔导度对O₃的响应也存在差异。通过对最优化气孔导度模型进行参数化, 结果表明O₃显著提高了蒙古栎和复叶槭的斜率参数(g₁), 并显著增加了茶的气孔导度模型截距参数(g₀), 但降低了复叶槭的g₀。在不同O₃处理下4种树木的内源水分利用效率与g₁呈显著线性负相关关系。综上所述, O₃浓度升高显著影响光合生化和气孔导度模型关键参数。     

Effect of chloride ions on the S-state distribution and deactivation kinetics in preparations of the cyanobacterium Anacystis nidulans

The roles of Ca²⁺ and Cl⁻ on the photosynthetic O₂ yield under flash illumination have been examined in EDTA-washed preparations of the cyanobacterium Anacystis nidulans. Especially the effect of Cl⁻ deficiency on the O₂ yield and on the S-state distribution was analyzed. As the results show, omission of both Ca²⁺ and Cl⁻ (Mn²⁺ present) almost totally inhibited O₂ evolution. When Ca²⁺ was replaced by Na⁺, a substantial reduction of the O₂ yield was observed, but only a minor change in the S-state distribution occurred. However, when Cl⁻ was displaced by NO⁻₃, which is equivalent to Cl⁻ deficiency of the water-splitting complex, a substantial reduction of the O₂ yield and in addition a significant change in the S-state distribution was observed. The comparison of deactivation kinetics in NO⁻₃ containing samples with those in control samples indicated that Cl⁻ deficiency allowed accumulation of oxidizing equivalents up to the S₃ state but modified the final step of O₂ evolution. Moreover, those centers which advanced to the S₃ state in the absence of Cl⁻ deactivated in a special way which involved a faster deactivation of S₂ and an increased formation of S₋₁.     

Continuous production of green cells of Haematococcus pluvialis: Modeling of the irradiance effect

This paper presents a model for the continuous production of green cells of the microalga Haematococcus pluvialis, in both indoor and outdoor conditions. To develop this model, the influence of irradiance and dilution rate on the performance of continuous cultures of H. pluvialis was studied in the laboratory but simulating outdoor conditions. Characterization of the cultures included biomass productivity, fluorescence of chlorophylls, pigment content, elemental composition of the biomass, cell density, cell size, homogeneity and nitrate consumption rate. Results showed that the optimal dilution rate was 0.04 h⁻¹, and that higher external irradiance resulted in higher biomass productivity in all cases, with a maximum value of 0.58 g L⁻¹day⁻¹. Continuous cultures were stable for more than 3 months, in spite of photoinhibition at noon, producing homogeneous biomass with a stable biochemical composition and cell morphology at each steady state. Astaxanthin accumulation was not observed in spite of the high levels of irradiance essayed, and cells remained in the flagellated-palmeloids green form whatever the culture conditions. High dilution rates produced small cells of 22 μm diameter, with a high nitrogen content of up to 10.0% d.wt. The average irradiance within the reactor was the main factor determining the behaviour of the cultures, although the external irradiance impinging on the reactor surface also influenced the results, indicating the existence of photoinhibition. The influence of both external and average irradiance on the growth of H. pluvialis was modelized. The accuracy of the model obtained was verified on a 0.22 m³ outdoor tubular photobioreactor operated in both discontinuous and continuous mode, obtaining a maximum biomass productivity of 0.68 g L⁻¹day⁻¹. The model reproduced the experimental data of biomass concentration and productivity, cell size and nitrate consumption, providing to be a powerful tool for optimizing the design and operation of outdoor photobioreactors for the production of green cells of H. pluvialis.     

Photoinhibition of photosynthesis in Lemna gibba as induced by the interaction between light and temperature. I. Photosynthesis in vivo

The floating angiosperm Lemna gibba L. was exposed for 2 h to various combinations of photosynthetic photon flux densities and temperature. The extent of photoinhibition of photosynthesis was assayed by measuring the net CO₂ uptake before and after a photoinhibitory treatment, and the time course for photoinhibition was studied. It was found that the maximum quantum yield and the light-saturated rate of CO₂ uptake were affected by the interaction between light and temperature during the photoinhibitory treatment. At a constant photon flux density of 650 μmol m⁻² s⁻¹ the extent of photoinhibition increased with decreasing temperature showing that even a chilling-resistant plant like L. gibba is much more susceptible to photoinhibition at chilling temperatures. About 60% photoinhibition of the quantum yield for CO₂ uptake could be obtained either by a high photon flux density of 1 750 μmol m⁻² s⁻¹ and 25°C or by a moderate photon flux density of 650 μmol m⁻² s⁻¹ and 3°C. The time courses of recovery from 60% photoinhibition produced by either of these two treatments were similar, indicating that the nature of the photoinhibition was intrinsically similar. The extent of photoinhibition was related to the amount of light absorbed in excess to what could be handled by photosynthesis at that temperature. The vital importance of photosynthesis in alleviating photoinhibition is discussed.     

Biological phosphorus removal in sequencing batch reactor with single-stage oxic process

The performance of biological phosphorus removal (BPR) in a sequencing batch reactor (SBR) with single-stage oxic process was investigated using simulated municipal wastewater. The experimental results showed that BPR could be achieved in a SBR without anaerobic phase, which was conventionally considered as a key phase for BPR. Phosphorus (P) concentration 0.22–1.79 mg L⁻¹ in effluent can be obtained after 4 h aeration when P concentration in influent was about 15–20 mg L⁻¹, the dissolved oxygen (DO) was controlled at 3 ± 0.2 mg L⁻¹ during aerobic phase and pH was maintained 7 ± 0.1, which indicated the efficiencies of P removal were achieved 90% above. Experimental results also showed that P was mainly stored in the form of intracellular storage of polyphosphate (poly-P), and about 207.235 mg phosphates have been removed by the discharge of rich-phosphorus sludge for each SBR cycle. However, the energy storage poly-β-hydroxyalkanoates (PHA) was almost kept constant at a low level (5–6 mg L⁻¹) during the process. Those results showed that phosphate could be transformed to poly-P with single-stage oxic process without PHA accumulation, and BPR could be realized in net phosphate removal.