Fluorometric measurement of alkaline phosphatase activity in algae

SUMMARY. Using both cultures of algae and natural populations, alkaline phosphatase activity located on the cell surface has been measured by a fluorometric procedure. This was done in order to establish optimum standard conditions for the measurement of this activity as an indicator of phosphorus deficiency and to provide a means of interpreting alkaline phosphatase measurements on natural phytoplankton populations. A concentration of 10 μM o-methylfluorescein phosphate saturates or nearly saturates the reaction in a variety of situations. In most trials, rates increased with temperature to or beyond 35°C. Optimum pH values in the range 7–10 were observed. In six of the algae examined, maximum alkaline phosphatase activities were dependent on external calcium at 100 μM or more. One alga, Synura uvella , showed acid phosphatase activity, peaking at pH 5–6, induced by phosphorus deficiency. Based on comparisons between P-sufficient and P-deficient cultures, alkaline phosphatase activities in excess of 0.1 μmol o-methylfluorescein phosphate hydrolysed per mg dry weight per h or 0.1 μmol per μg ATP per h are suggested as indicative of phosphorus deficiency.     

Interplay between vitamin E and phosphorus availability in the control of longevity in Arabidopsis thaliana

Background and Aims Vitamin E helps to control the cellular redox state by reacting with singlet oxygen and preventing the propagation of lipid peroxidation in thylakoid membranes. Both plant ageing and phosphorus deficiency can trigger accumulation of reactive oxygen species, leading to damage to the photosynthetic apparatus. This study investigates how phosphorus availability and vitamin E interact in the control of plant longevity in the short-lived annual Arabidopsis thaliana.Methods The responses of tocopherol cyclase (VTE1)- and γ-tocopherol methyltransferase (VTE4)-null mutants to various levels of phosphorus availability was compared with that of wild-type plants. Longevity (time from germination to rosette death) and the time taken to pass through different developmental stages were determined, and measurements were taken of photosynthetic efficiency, pigment concentration, lipid peroxidation, vitamin E content and jasmonate content.Key Results The vte1 mutant showed accelerated senescence under control conditions, excess phosphorus and mild phosphorus deficiency, suggesting a delaying, protective effect of α-tocopherol during plant senescence. However, under severe phosphorus deficiency the lack of α-tocopherol paradoxically increased longevity in the vte1 mutant, while senescence was accelerated in wild-type plants. Reduced photoprotection in vitamin E-deficient mutants led to increased levels of defence chemicals (as indicated by jasmonate levels) under severe phosphorus starvation in the vte4 mutant and under excess phosphorus and mild phosphorus starvation in the vte1 mutant, indicating a trade-off between the capacity for photoprotection and the activation of chemical defences (jasmonate accumulation).Conclusions Vitamin E increases plant longevity under control conditions and mild phosphorus starvation, but accelerates senescence under severe phosphorus limitation. Complex interactions are revealed between phosphorus availability, vitamin E and the potential to synthesize jasmonates, suggesting a trade-off between photoprotection and the activation of chemical defences in the plants.     

Localization of acid phosphatase activity in maize root under phosphorus deficiency

The effect of phosphorus deficiency on acid phosphatase activity in the apical, middle and basal parts of the root of maize plants was followed. The supernatant obtained by centrifuging the homogenate of plant tissue at 1500 ×g was further centrifuged at 18 000 ×g, the sediment being marked as fraction II and the supernatant as fraction III. The results obtained document the fact that acid phosphatase activity of the two fractions of all analyzed root segments was higher in plants cultured in nutrient medium without phosphate than in those containing phosphorus in nutrient medium. In most cases this difference was significant to highly significant. The results of experiments proved unambiguously a higher enzymatic activity in all root segments in fraction III than in fraction II. In fraction III the highest acid phosphatase activity was found in the apical part, in fraction II in the basal part of the root.     

Comparative Study of the Interactive Effects of Salinity and Phosphorus Availability in Wild (Hordeum maritimum) and Cultivated Barley (H. vulgare)

The present study aimed to compare the effects of phosphorus (P) deficiency applied only or combined with salinity on root response, P partitioning, acid phosphatase activity, and phenolic compounds in wild (Hordeum maritimum) and cultivated (H. vulgare) barley species. Seedlings were grown hydroponically under low or sufficient P supply, with or without 100 mM NaCl for 55 days. Results showed that, when individually applied, P deficiency and salinity restricted the whole plant relative growth rate in both species of barley, with a more pronounced impact of the former stress. These depressive effects were more pronounced in H. vulgare than in H. maritimum. The combined effects of P deficiency and salinity were not additive neither on whole plant RGR nor on root response parameters in both species. The root area, root/shoot P content, root and leaf acid phosphatase activities, and shoot flavonoids contents increased under P deficiency conditions with and without salt in both species. Overall, the relatively better tolerance of H. maritimum plants to P deficiency applied only or combined with salinity could be explained by the capacity of this species to maintain higher P acquisition efficiency in concomitance with a larger root system, a higher root/shoot DW ratio, a higher root/shoot P content, a greater root and leaf acid phosphatase activities, and a higher flavonoid content and antioxidant capacity under combined effects of both stresses. Thus, H. maritimum constitutes a promising model to ameliorate the tolerance of the cultivated barley species under low-P soils and/or saline regions.     

不同形态的磷源对球形棕囊藻生长及碱性磷酸酶的影响

研究了不同浓度和形态的无机磷(DIP)和有机磷(DOP)对球形棕囊藻细胞生长、培养基中磷浓度的变化以及碱性磷酸酶活性的变化的影响。在缺磷和大分子DOP(卵磷脂)作为磷源的情况下,碱性磷酸酶活性迅速提高,在第9天达到了最大值,其活性分别为19.11U和18.28U,显然在缺磷胁迫下和大分子DOP的利用过程中碱性磷酸酶起着重要作用。DIP(磷酸二氢钾)和小分子DOP(β-甘油磷酸钠)都容易直接被球形棕囊藻吸收利用,碱性磷酸酶活性变化不明显。     

Effect of Phosphorus Deficiency and Water Deficit on Phosphatase Activities from Wheat Leaves

Wheat was sown in a phosphorus (P) deficient soil. Plants atlow levels of applied P had lower growth rates and lower concentrationsof phosphate in the shoots than plants grown with ‘highP’. Activities of both insoluble and soluble phosphataseincreased with P deficiency in the mature leaves. Soluble phosphataseactivities increased 2.5–3.0 fold as the concentrationof phosphate in the leaves fell from 0.4% to 0.1% dry weightThis increase was not a consequence of reduced growth, as severenitrogen deficiency had no effect on phosphatase activity. Soluble phosphatase activities were higher in young than inmature leaves, and also increased 3–4 fold with severewater deficit. However these increases in activity were notaccompanied by low concentrations of phosphate. Moreover, solublephosphatase activities in mature leaves of plants grown underconditions of water deficit rapidly decreased after rewatering.In contrast, the high soluble phosphatase activities in matureleaves of P deficient wheat persisted for up to 12 d after theresupply of P to adequate levels.     

Primary production in ten reservoirs in southern Brazil

The growth and phosphatase activity during phosphorus starvation of cultures of Nodularia spumigera Mertens were examined. Stationary phase was reached much sooner in phosphorus-deficient cultures than in phosphorus-sufficient cultures; the growth rate did not change. Phosphatase activities were greatly increased in stationary phase. Diurnal patterns were established for phosphorus-sufficient cultures, but they were not light related. In phosphorus-deficient cultures, an increase in phosphatase activities over a 24 h period was superimposed on a diurnal pattern. Both phosphorus and nitrogen additions lowered the relative phosphatase activities in long term studies, but the effect of phosphorus was much more pronounced. In short term studies, phosphorus appeared to cause an immediate decrease in phosphatase activity, but did not affect phosphatase activity after that for up to 24 h. Nitrogen did not have any short term effect on phosphatase. Phosphatase activity was correlated with changes in the proportion of TCA-insoluble phosphorus (polyphosphates).     

Differential strain response in alkaline phosphatase activity to available phosphorus in Microcoleus autumnalis

Toxic, benthic cyanobacterial proliferations have increased in frequency and severity globally and can have negative impacts on aquatic ecosystems, recreation and human health. Microcoleus autumnalis has been associated with numerous animal fatalities and is causing increasing concern. It tends to grow in systems with moderate dissolved inorganic nitrogen and very low dissolved reactive phosphorus. Acquisition of nutrients, particularly phosphorus, from organic sources may explain how M. autumnalis can reach the high biomass in these relatively nutrient deplete environments. In the present study the effect of phosphorus concentration and source on alkaline phosphatase activity was investigated in toxic and non-toxic M. autumnalis strains. Toxic strains exhibited significantly higher alkaline phosphatase activity than non-toxic strains (p < 0.05), and alkaline phosphatase activity increased in all strains under phosphorus-depleted conditions (p < 0.05). Alkaline phosphatase activity was also present in environmental M. autumnalis mats, though at lower levels than in laboratory experiments. The presence of alkaline phosphatase activity indicates that the acquisition of phosphorus from organic phosphorus sources may contribute to the ability of M. autumnalis to grow in systems with low dissolved reactive phosphorus.     

CHARACTERISTICS OF PHOSPHORUS DEFICIENCY IN ANABAENA1

Several aspects of the metabolism and composition of a strain of Anabaena have been studied during phosphorus deficiency. The effects of medium composition, substrate concentration, temperature, pH, and illumination on alkaline phosphatase activity and phosphate uptake have been examined. Of particular interest among these results was the dependence of maximum alkaline phosphatase activity on Ca and of phosphate uptake on Mg. Depletion of dissolved phosphate from the culture medium runs accompanied by a marked increase in alkaline phosphatase activity, initial rate of phosphate uptake, and total amount of phosphate taken up to satisfaction of the phosphorus debt. Readdition of phosphate to a phosphorus-deficient culture resulted in a rapid decline in the ability to take up phosphate but no loss of alkaline phosphatase beyond dilution of activity already present. Entry into phophorus deficiency was accompanied by a loss of heterocysts, a decline in chlorophyll a, protein, RNA, and cellular phosphorus, and an increase in carbohydrate per unit dry weight. The possible use of these changes as physiological indicators of phosphorus limitation in natural situations is discussed.     

Acid phosphatase activity in maize leaves as related to their evolution and phosphorus deficiency

The effect of phosphorus deficiency on the activity of acid phosphatase of the first, second and third leaves of maize plants was followed. The supernatant obtained by centrifuging the homogenate of plant tissue at 1500 ×g was further centrifuged at 18 000 ×g, the sediment marked as fraction II and the supernatant as fraction III. Acid phosphatase activity of fraction II of the first to third leaves was for the whole period of culture higher in plants grown in the nutrient solution without phosphate. In fraction III this relation was established in the first leaf, after 3 days of culture in the second leaf and after 5 days in the third leaf. In all leaves higher enzyme activity was unambiguously determined in fraction III when compared with fraction II. Higher acid phosphatase activity was established in those leaves which were younger in their development, particularly in the first days of culture. With the ageing of leaves the enzyme activity decreased.     

The activities of soil and root acid phosphatase in the nine tropical rain forests that differ in phosphorus availability on Mount Kinabalu, Borneo

Background and aims

Tropical rain forests on deeply weathered soils are increasingly thought to be limited by phosphorus (P), where plants and associated organisms would demonstrate adaptations to efficiently recycle P using acid phosphatase from organic matter. The activities of soil and root acid phosphatase were investigated in nine tropical rain forests that demonstrated a 20-fold difference in the soil organic P pool on Mt. Kinabalu, Borneo.

Methods

Acid phosphatase activity was measured at pH6.0 using p-nitrophenyl phosphate as substrate.

Results

The specific phosphatase activity of tree roots on a soil-surface-area basis was significantly positively related with P-use efficiency of above-ground productivity, suggesting a physiological linkage between above and below-ground systems in the adaptation to P deficiency. The phosphatase activities of soils and roots were significantly negatively correlated with the pool size of soil organic P fractions, suggesting that demand for P determines phosphatase activities.

Conclusions

It is suggested that tree roots and soil microbes develop more active phosphatases in response to the chronic shortage of soil P, which forms the basis for an important functional role for the efficient acquisition of P from soil organic matter.     

Dynamics of water-extractable phosphorus during the degradation of Microcystis aeruginosa by four bacteria species

We carried out a laboratory experiment for studying the dynamics of water-extractable phosphorus release during the decomposition of dead Microcystis aeruginosa driven by the four bacteria strains. Our results showed that water-extractable phosphorus had significant correlation to alkaline phosphatase but without obvious correlation to acid phosphatase, suggesting that alkaline phosphatase was the primary enzyme decomposing organic phosphorus. Also, water-extractable phosphorus exhibited an obvious correlation to pH, indicating that the alkaline environment contributed to the release of water-extractable phosphorus. The quantity of bacteria hardly correlated to the release of water-extractable phosphorus for all species. This could result from decrease of bacterial quantity after consumption of substrate in closed system. Obvious variation in water-extractable phosphorus was observed across the strains in two water treatments. Sporolactobacillus sp. and Bacillus macerans had the strongest ability for decomposing organic phosphorus among five strain treatments in the lake water. In the distilled water, Bacillus sp. had the strongest ability to degrade organic phosphorus. In both water treatments, mixed species exhibited intermediate ability for decomposing organic phosphorus. It was true that water quality strongly affected the release of phosphorus by regulating phosphatase activity.     

Differential Senescence of Maize Hybrids following Ear Removal : I. Whole Plant

Visual senescence symptoms and associated changes in constituent contents of three field-grown maize (Zea mays L.) hybrids (Pioneer brand 3382, B73 × Mo17, and Farm Service brand 854) were compared in response to ear removal. Whole plants were harvested at eight intervals during the grain-filling period, and analyzed for dry matter, total N and nitrate N, phosphorus, sugars, and starch.

Upper leaves of earless P3382 and B73 × Mo17 showed reddish discoloration by 25 days after anthesis (DAA) and all leaves had lost most of their chlorophyll by 40 DAA. In striking contrast, leaves of earless FS854 plants remained green and similar in appearance to eared controls throughout the grain-filling period.

For all hybrids, ear removal led to a decrease in dry weight, reduced N, total N, and phosphorus contents of the total plant, and an increase in carbohydrate content of the leaves and stalks, relative to respective controls. Although changes in carbohydrate and N contents, which previously had been associated with senescence, were observed for all earless hybrids, these changes were followed by accelerated senescence and early death only for P3382 and B73 × Mo17. By 30 DAA, earless P3382 and B73 × Mo17 plants ceased to accumulate dry weight, total N, and phosphorus, indicating a termination of major metabolic activities. In contrast, earless FS854 plants retained a portion of these metabolic activities until 58 DAA, indicating a role for roots in determining rate of senescence development. Thus, the course of senescence was more accurately reflected by measurements of metabolic activities than by measurements of metabolite contents at any given time. These results show that the ear per se does not dictate the rate or completion of the senescence process, and implicated an association between the continued accumulation of N and associated root activities with the delayed senescence pattern of the earless FS854 plants. It is evident that studies involving control of senescence among species must also consider genotypic influences within species.

     

Seasonal activity of non-specific acid and alkaline phosphatases in beech (<Emphasis Type="Italic">Fagus sylvatica</Emphasis>) leaves

The activities of acid and alkaline phosphatases along with phosphorus content in leaves of European beech (Fagus sylvatica L.) were studied for a period from April to October. The phosphorus content of beech leaves was highest in April, at the beginning of the vegetation period; from May to October it was twofold lower than in April. Acid phosphatase activity (per unit fresh weight) in leaves collected from the middle part of the crown decreased significantly in May and July compared to the enzyme activity in April. In both the low and middle parts of the crown, the acid phosphatase activity had a peak in August, and thereafter decreased in September and October. No correlations between acid phosphatase activity and phosphorus concentrations were found. Alkaline phosphatase activity was very low and in some cases near the detection limit during the whole observation period.     

Response to Phosphate Deprivation in Brassica nigra Suspension Cells : Enhancement of Intracellular, Cell Surface, and Secreted Phosphatase Activities Compared to Increases in Pi-Absorption Rate

Suspension cells of Brassica nigra responded to Pi deprivation by increasing their potential for Pi influx and by raising the active levels of intracellular, cell surface, and secreted acid phosphatases. These responses, however, were temporally distinct. Phosphate influx capacity increased 15-fold in parallel to a 10-fold decrease in endogenous Pi during 7 days of culture in basal growth medium. In contrast, intracellular and cell surface phosphatase activities changed only after alterations in cellular phosphorus status had been in place for a number of days. Even in nutrient sufficient cells the secretion of phosphatase remained relatively high as did the activities of the other phosphatases. The cell surface acid phosphatase had a K_m of approximately 10 times that of the influx process and molybdate was a much stronger inhibitor of this phosphatase activity. From these results it appears that Pi absorption and the production or activation of phosphatases are regulated in a distinct manner. In addition, Pi uptake into Brassica nigra cells does not appear to directly involve the cell surface phosphatase under Pi-deficient conditions.     

Mixed plantations of Metasequoia glyptostroboides and Bischofia polycarpa change soil fungal and archaeal communities and enhance soil phosphorus availability in Shanghai,China

Soil degradation has been found in urban forests in Shanghai, especially in the pure plantations. Mixed plantations are considered to improve soil quality because they can stimulate organic matter cycling and increase soil carbon and nutrient content. Although soil microbes play crucial roles in regulating soil biogeochemical processes, little is known about how mixed plantations affect soil microbial communities, including bacteria, archaea, and fungi. Here, we evaluated soil chemical properties, abundances and compositions of soil bacterial, archaeal, and fungal communities, and enzyme activities in pure and mixed Metasequoia glyptostroboides and Bischofia polycarpa plantations, located in Shanghai, China. The results showed that soil available phosphorus content in the mixed plantation of M. glyptostroboides and B. polycarpa was significantly higher than that in pure plantations, while no significant difference was observed in the content of soil organic carbon, total and available nitrogen, total and available potassium among the three studied plantations. We found higher fungal abundance in the mixed plantation, when compared to both pure plantations. Moreover, fungal abundance was positively correlated with the content of soil available phosphorus. No significant difference was found in the abundance and diversity of bacterial and archaeal community among the three studied plantations. A similarity analysis (ANOSIM) showed that mixed plantation significantly altered the community composition of archaea and fungi, accompanied with an increase of alkaline phosphatase activity. However, ANOSIM analysis of bacterial communities showed that there was no significant group separation among different plantations. Overall, results from this study indicated that fungal and archaeal communities were more sensitive to aboveground tree species than bacterial community. Moreover, mixed plantations significantly increased the activity of alkaline phosphatase and the content of soil available phosphorus, suggesting that afforestation with M. glyptostroboides and B. polycarpa is an effective way to alleviate phosphorus deficiency in urban forests in Shanghai, China.     

Changes in phosphatase activity in phosphorus-deficient Spirodela

Summary Onset of phosphorus deficiency in Spirodela oligorrhiza was accompanied by a 50-fold increase in phosphatase activity of cell extracts. The enzyme behaved like other plant acid phosphatase, and was both inhibited and repressed by inorganic phosphate. The phosphatase activity comprised at least three isozymes. Two, of low molecular weight, were present only in P-deficient Spirodela; one of high molecular weight was also present, though in smaller amounts, in normal Spirodela. Presence of 2-thiouracil during onset of P-deficiency partly inhibited the development of phosphatase activity. The nature and role of the increased phosphatase activity in P-deficient plants are discussed.     

Diurnal starch accumulation and utilization in phosphorus-deficient soybean plants

The effects of phosphorus deficiency on carbohydrate accumulation and utilization in 34-day-old soybean (Glycine max L. Merr.) plants were characterized over a diurnal cycle to evaluate the mechanisms by which phosphorus deficiency restricts plant growth. Phosphorus deficiency decreased the net CO₂ exchange rate throughout the light period. The decrease in the CO₂ exhange rate was associated with a decrease in stomatal conductance and an increase in the internal CO₂ concentration. These observations indicate that phosphorus deficiency increased mesophyll resistance. Assimilate export rate from the youngest fully expanded leaves was decreased by phosphorus deficiency, whereas starch concentrations in these leaves were increased. Higher starch concentrations in phosphorus-deficient youngest fully expanded leaves resulted from a longer period of net starch accumulation and a shorter period of net starch degradation relative to those for phosphorus-sufficient controls. Phosphorus deficiency decreased sucrose-P synthase activity by 27% (averaged over the diurnal cycle), and essentially eliminated diurnal variation in sucrose-P-synthase activity. Diurnal variations in nonstructural carbohydrate concentrations in leaves and stems were also less pronounced in phosphorus-deficient plants than in controls. In phosphorus-deficient plants, only 30% of the whole plant starch present at the end of a light phase was utilized during the subsequent 12-hour dark phase as compared with 68% for phosphorus-sufficient controls. Although phosphorus deficiency decreased the CO₂ exchange rate and whole plant leaf area, accumulation of high starch concentrations in leaves and stems and restricted starch utilization in the dark indicate that growth processes (i.e. sink activities) were restricted to a greater extent than photosynthetic capacity. Further experimentation is required to determine whether decreased starch utilization in phosphorus-deficient plants is the cause or the result of restricted growth.     

Effects of Photosynthesis on Bacterial Phosphatase Production in Biofilms

The fraction of bacteria displaying phosphatase activity within natural photosynthetic biofilms was examined in relation to phosphorus limitation and algal photosynthesis. An artificial substrate that forms a fluorescent precipitate was used in conjunction with the nucleic acid stain DAPI to enumerate extracellular phosphatase expression by biofilm bacteria exposed to different photosynthetic activities and phosphorus supplies. The proportion of bacteria displaying phosphatase activity changed in response to the presence or absence of algal photosynthesis. In general, phosphate-deprived biofilms had positive linear trends in bacterial phosphatase activity (p <0.001), with greater proportions of bacteria displaying phosphatase under photosynthetic inhibition compared to active photosynthesis. Under sufficient phosphate supplies, biofilms had negative linear trends (p <0.05) or were lower in the proportion of bacteria displaying phosphatase activity in the presence of algal photosynthesis, whereas bacterial phosphatase activity was generally maintained when photosynthesis was inhibited. it is suggested that the amount of extracellular organic carbon released within the biofilm matrix during photosynthesis indirectly affected bacterial phosphatase synthesis.     

磷胁迫对不同杉木无性系酸性磷酸酶活性的影响

 缺磷是限制目前农林业产量的一个重要因子,传统的农林业生产主要通过施肥和土壤改良来满足植物对磷的需求,近年来人们开始发掘磷高效利用植物来替代传统方法提高磷的利用效率。杉木(Cunninghamia lanceolata)是我国亚热带地区最重要的造林树种之一,生长快、材质好、产量高,在中国人工林经营中占有重要地位。为揭示磷素胁迫条件下杉木无性系酸性磷酸酶的变化规律和筛选磷高效利用杉木无性系,通过土培试验,设计4种磷素处理水平(正常供磷16 mg•kg－1、轻度磷胁迫8 mg•kg－1、中度磷胁迫4 mg•kg－1、重度磷胁迫0 mg•kg－1),进行磷素胁迫条件下不同杉木无性系酸性磷酸酶(APA)活性的比较研究。结果表明：缺磷条件下1年生杉木叶片和根际的APA活性明显高于正常供磷处理。随缺磷时间的延长、不同杉木无性系酸性磷酸酶的变化规律不同,其中8号、24号、37号无性系叶片和根际的APA活性明显高于正常供磷处理;5号、9号无性系根际APA活性虽然增幅较大,但其叶片酶活性变化较小;3号、23号、34号无性系整体而言对磷胁迫不敏感,缺磷条件不对其叶片APA及根系APA活性造成显著影响。在磷胁迫条件下,杉木无性系可通过叶片及根际酸性磷酸酶活性的增强来适应环境磷缺乏,但不同杉木无性系对磷缺乏的适应性存在明显差异,因此能否将APA活性作为杉木无性系磷效率的评价指标之一仍需作进一步研究。