Extracellular Phosphatase Activity Research Articles

Two-Phase Conceptual Framework of Phosphatase Activity and Phosphorus Bioavailability.

The activity of extracellular phosphatases is a dynamic process controlled by both plant roots and microorganisms, which is responsible for the mineralization of soil phosphorus (P). Plants regulate the availability of soil P through the release of root mucilage and the exudation of low-molecular weight organic acids (LMWOAs). Mucilage increases soil hydraulic conductivity as well as pore connectivity, both of which are associated with increased phosphatase activity. The LMWOAs, in turn, stimulate the mineralization of soil P through their synergistic effects of acidification, chelation, and exchange reactions. This article reviews the catalytic properties of extracellular phosphatases and their interactions with the rhizosphere interfaces. We observed a biphasic effect of root metabolic products on extracellular phosphatases, which notably altered their catalytic mechanism. In accordance with the proposed conceptual framework, soil P is acquired by both plants and microorganisms in a coupled manner that is characterized by the exudation of their metabolic products. Due to inactive or reduced root exudation, plants recycle P through adsorption on the soil matrix, thereby reducing the rhizosphere phosphatase activity. The two-phase conceptual framework might assist in understanding P-acquisition (substrate turnover) and P-restoration (phosphatase adsorption by soil) in various terrestrial ecosystems.

Litter inputs and phosphatase activity affect the temporal variability of organic phosphorus in a tropical forest soil in the Central Amazon

PurposeThe tropical phosphorus cycle and its relation to soil phosphorus (P) availability are a major uncertainty in projections of forest productivity. In highly weathered soils with low P concentrations, plant and microbial communities depend on abiotic and biotic processes to acquire P. We explored the seasonality and relative importance of drivers controlling the fluctuation of common P pools via processes such as litter production and decomposition, and soil phosphatase activity.MethodsWe analyzed intra-annual variation of tropical soil phosphorus pools using a modified Hedley sequential fractionation scheme. In addition, we measured litterfall, the mobilization of P from litter and soil extracellular phosphatase enzyme activity and tested their relation to fluctuations in P- fractions.ResultsOur results showed clear patterns of seasonal variability of soil P fractions during the year. We found that modeled P released during litter decomposition was positively related to change in organic P fractions, while net change in organic P fractions was negatively related to phosphatase activities in the top 5 cm.ConclusionWe conclude that input of P by litter decomposition and potential soil extracellular phosphatase activity are the two main factors related to seasonal soil P fluctuations, and therefore the P economy in P impoverished soils. Organic soil P followed a clear seasonal pattern, indicating tight cycling of the nutrient, while reinforcing the importance of studying soil P as an integrated dynamic system in a tropical forest context.

Characterization of extracellular phosphatase activities in periphytic biofilm from paddy field

Periphytic biofilms exist widely in paddy fields, but their influences on the hydrolysis of organic phosphorus (P) have rarely been investigated. In this study, a periphytic biofilm was incubated in a paddy soil solution, and hydrolysis kinetic parameters (half-saturation constant (Km) and maximum catalytic reaction rate (Vmax)), optimal environmental conditions, substrate specificity, and response to different P regimes of the phosphatase activities in the periphytic biofilm were determined, in order to characterize extracellular phosphatase activities in periphytic biofilms from paddy fields. The results indicated that the periphytic biofilm could produce an acid phosphomonoesterase (PMEase), an alkaline PMEases, and a phosphodiesterase (PDEase). These three phosphatases displayed high substrate affinity, with Km values ranging from 141.03 to 212.96 μmol L–1. The Vmax/Km ratios for the phosphatases followed the order of alkaline PMEase > acid PMEase > PDEase, which suggested that the PMEases, especially the alkaline PMEase, had higher catalytic efficiency. The optimal pH was 6.0 for the acid PMEase activity and 8.0 for the PDEase activity, and the alkaline PMEase activity increased with a pH increase from 7.0 to 12.0. The optimal temperature was 50 °C for the PMEases and 60 °C for the PDEase. The phosphatases showed high catalytic efficiency for condensed P over a wide pH range and for orthophosphate monoesters at pH 11.0, except for inositol hexakisphosphate at pH 6.0. The inorganic P supply was the main factor in the regulation of phosphatase activities. These findings demonstrated that the periphytic biofilm tested had high hydrolysis capacity for organic and condensed P, especially under P-limited conditions.

Plants mitigate restrictions to phosphatase activity in metal contaminated soils

Soil anthropogenic contaminants can limit enzymatic nutrient mineralization, either by direct regulation or via impacts on the microbial community, thus affecting plant growth in agricultural and non-agricultural soils. The impact on phosphatase activity of mixing two contaminated, post-industrial rail yard soils was investigated; one was vegetated and had high phosphatase function, the other was barren and had low enzymatic function. The two soils had different abiotic properties, including contaminant load, vegetation cover, soil aggregate size distribution, and phosphatase potential. An experimental gradient was established between the two soils to systematically vary the abiotic properties and microbial community composition of the two soils, creating a gradient of novel ecosystems. The time dependence of extracellular phosphatase activity, soil moisture, and organic matter content was assessed along this gradient in the presence and absence of plants. Initially, mixtures with higher percentages of functional, vegetated soil had higher phosphatase activities. Phosphatase activity remained unchanged through time (65 days) in all soil mixtures in unplanted pots, but it increased in planted pots. For example, in the presence of plants, phosphatase activity increased from 0.6 ± 0.1 to 2.4 ± 0.3 μmol•h−1•gdry soil−1 from day one to day 65 in the 1:1 functional:barren soil mixture. The presence of plants also promoted moisture retention. Inoculation of poorly functioning soil with 10% of the functional soil with its microbial community did not, over 65 days, revitalize the poorly functioning soil. The findings showed that abiotic limitations to enzymatic activity in barren brownfield soils could be mitigated by establishing primary production but not by the addition of enzymatically active microbial communities alone.

Extracellular phosphoesterases of invertebrate origin: underrated actors in phosphorus recycling?

Extracellular enzymes contribute substantially to the remineralisation of organic matter in aquatic systems. Marine invertebrates release endogenous enzymes through activities such as sloppy feeding or egestion, but the significance of such processes is widely unexplored. We compared functional key properties such as activity, stability, and apparent molecular masses of extracellular phosphatases from faeces of the marine crustaceans Idotea balthica, Palaemon varians, and Homarus gammarus with those of their digestive organs. A fluorescent substrate was used to examine enzyme activity qualitatively on agarose plates and quantitatively in microplate assays. Apparent molecular masses and enzyme stability were examined by native substrate gel electrophoresis (NSGE). Active extracellular phosphatase were present in the faeces of all tested species. NSGE activity band patterns were similar in digestive tissue extracts and faeces extracts. The initial enzyme activity retained for about 2 days, but thereafter rapidly decreased. Activity band patterns of digestive organs and faeces of I. balthica remained consistent for up to 72 h. Antibiotic treatment did not reduce phosphatase activity in the faeces of I. balthica and H. gammarus but in the faeces P. varians. Because of the comparatively high activities in the faeces, the electrophoretic similarity between faeces and digestive organs, and the limited durability of the enzymes in faeces extracts, we conclude that the studied crustaceans release predominantly endogenous, rather than bacterial phosphatases through faeces. These can substantially contribute to the pool of active extracellular phosphatases and the recycling of phosphorus in aquatic systems. The wider physiological and ecological context is discussed.

The effect of Frankia and multiple ectomycorrhizal fungil species on Alnus growing in low fertility soil

Plant interactions with single symbionts of nitrogen fixing bacteria or mycorrhizal fungi are well studied. However, less is known about how plants interact with multiple symbiont species. The aim of this study was to assess whether multiple symbionts had a synergistic effect on host plant performance compared with a single symbiont and whether increasing the number of non-specific fungal species would increase plant performance due to niche complementarity. Green alder (Alnus viridis ssp. crispa) were inoculated with non-specific ectomycorrhizal fungi (Lactarius torminosus, Lactarius theiogalus, Hebeloma crustuliniforme) alone or in combination, with and without Frankia, and grown in nutrient-poor soil. Frankia significantly increased plant growth by 48.5%, doubled the proportion of plants forming ectomycorrhizae, as well as increased root extracellular phosphatase activity by 8.8% compared to non-Frankia treatments. However, increasing number of fungal species decreased nodulated plant biomass. Plants that formed a Hartig net had reduced nodule number and nodule biomass allocation, as well as total nodule activity compared with plants with no Hartig net. Our results indicated that Frankia inoculation provided benefit for both host plants and ectomycorrhizal fungi in the nutrient-poor soil, while ectomycorrhizal fungi did not. These negative effects of mycorrhizal fungi are likely dependent on soil nutrient P availability.

Understanding how long-term organic amendments increase soil phosphatase activities: Insight into phoD- and phoC-harboring functional microbial populations

In context of the use of organic materials as alternatives for mineral fertilizer, it is important to understand how organic amendments influence soil extracellular phosphatase activities which accelerate the mineralization of organic phosphorus (P). To address this, the current study investigates the influence of organic amendments on acid (ACP) and alkaline (ALP) phosphatase activities in soils and how organic amendments influence these activities from the perspective of microbially-mediated pathways. Herein, a comprehensive meta-analysis of 599 measurements from 106 published studies around the world was performed as well as a field component sourced from a 30-year-old field experiment on fertilization. Based on meta-analysis, organic amendments increased average extracellular ACP and ALP activities by 22% and 53%, respectively, in comparison to the mineral-only fertilization. Observed increases in activities were consistent with significant increases in soil organic carbon (C), total nitrogen (N) and available P contents, and microbial biomass C and N pools. According to the data from the long-term field experiment, we found phoD-harboring species encoding ALP were more closely correlated with phoC-harboring species encoding ACP in organically amended soils, and more network hubs were also observed by organic amendment. Soil C:P and N:P ratios, and microbial biomass C were the main predictors of the abundance, diversity, and composition of the phoC- and phoD-harboring populations. Further analysis revealed that the soil C:P ratio was identified as the dominant predictor of potential ACP and ALP activities. Our work highlights the importance in understanding how soil C:N:P stoichiometry mediates phosphatase-harboring populations in order to determine the downstream consequences of using organic amendments for increasing phosphatase activities.

Soil microbial response to metal contamination in a vegetated and urban brownfield

The ubiquity of urban brownfields presents not only a challenge for environmental managers but also an opportunity to study the functional aspects of degraded ecosystems that are in close contact with human habitation. In this study, we investigate the soil microbial community response to heavy metal contamination at Liberty State Park (LSP), an urban brownfield in Jersey City, NJ, USA. Heavy metal contamination of the soils at LSP is heterogeneous, varying widely across site and among metals. We collected soils along a previously mapped gradient of metal contamination at LSP and sampled soil from a local and uncontaminated reference site (Hutcheson Memorial Forest (HMF)) for comparison. For all soils, we measured soil heavy metal concentrations, soil organic carbon content, bacterial density, and extracellular phosphatase activity as a proxy of ecosystem functioning. Additionally, we analyzed the microbial community composition using high-throughput sequencing. Data show that some sites within LSP have significantly higher phosphatase activity compared to HMF, indicating that some heavily contaminated LSP soils are highly functional. We also found that soil organic carbon and bacterial density have a significant and positive relationship with phosphatase activity. The microbial community analyses showed that the bacterial communities were sensitive to heavy metals and that the composition was significantly affected in particular by copper, zinc, and lead. The fungal communities, however, did not vary significantly with heavy metals. Our results shed important light on the composition and functioning of urban brownfield soils. A deeper understanding of these unique ecosystems is required for successful remediation, restoration and urban sustainability.

Abiotic factors determine functional outcomes of microbial inoculation of soils from a metal contaminated brownfield

Whole community microbial inoculation can improve soil function in contaminated environments. Here we conducted a case study to investigate whether biotic factors (inoculum) or abiotic factors (soil base) have more impact on the extracellular enzymatic activities in a whole community microbial inoculation. To this end, we cross-inoculated microbial communities between two heavy metal-contaminated soils, with high and low extracellular enzyme activities, respectively. We measured extracellular phosphatase activity, a proxy for soil function, after self- and cross-inoculation of microbial communities into sterilized soils, and all activities were normalized to non-inoculated controls. We found that inoculation increased phosphatase activity in the soils. For soils treated with different inocula, we found significant differences in the microbial community compositions but no significant differences in the extracellular phosphatase activities normalized to their respective sterilized, non-inoculated controls (4.7 ± 1.8 and 3.3 ± 0.5 for soils inoculated with microbial communities from 146 to 43, respectively). On the other hand, normalized phosphatase activities between the two soil bases were significantly different (4.1 ± 0.12 and 1.9 ± 0.12 for soil bases 146 and 43, respectively) regardless of the source of the inoculum that did not vary between soil bases. The results indicate that the abiotic properties of the soils were a significant predictor for phosphatase activity but not for the end-point composition of the microbial community. The findings suggest that targeted microbial inocula from metal contaminated soils can increase phosphatase activity, and likely soil functioning in general, but the degree to which this happens depends on the abiotic environment, in this case, metal contamination.

An Experimental Insight into Extracellular Phosphatases - Differential Induction of Cell-Specific Activity in Green Algae Cultured under Various Phosphorus Conditions.

Extracellular phosphatase activity (PA) has been used as an overall indicator of P depletion in lake phytoplankton. However, detailed insights into the mechanisms of PA regulation are still limited, especially in the case of acid phosphatases. The novel substrate ELF97 phosphate allows for tagging PA on single cells in an epifluorescence microscope. This fluorescence-labeled enzyme activity (FLEA) assay enables for autecological studies in natural phytoplankton and algal cultures. We combined the FLEA assay with image analysis to measure cell-specific acid PA in two closely related species of the genus Coccomyxa (Trebouxiophyceae, Chlorophyta) isolated from two acidic lakes with distinct P availability. The strains were cultured in a mineral medium supplied with organic (beta-glycerol phosphate) or inorganic (orthophosphate) P at three concentrations. Both strains responded to experimental conditions in a similar way, suggesting that acid extracellular phosphatases were regulated irrespectively of the origin and history of the strains. We found an increase in cell-specific PA at low P concentration and the cultures grown with organic P produced significantly higher (ca. 10-fold) PA than those cultured with the same concentrations of inorganic P. The cell-specific PA measured in the cultures grown with the lowest organic P concentration roughly corresponded to those of the original Coccomyxa population from an acidic lake with impaired P availability. The ability of Coccomyxa strains to produce extracellular phosphatases, together with tolerance for both low pH and metals can be one of the factors enabling the dominance of the genus in extreme conditions of acidic lakes. The analysis of frequency distribution of the single-cell PA documented that simple visual counting of ‘active’ (labeled) and ‘non-active’ (non-labeled) cells can lead to biased conclusions regarding algal P status because the actual PA of the ‘active’ cells can vary from negligible to very high values. The FLEA assay using image cytometry offers a strong tool in plankton ecology for exploring P metabolism.

Growth, extracellular alkaline phosphatase activity, and kinetic characteristic responses of the bloom-forming toxic cyanobacterium, Microcystis aeruginosa, to atmospheric particulate matter (PM2.5, PM2.5-10, and PM>10).

Atmospheric particulate matter (APM), commonly seen and widely excited in environment, appears great enough to influence the biochemical processes in aquatic microorganisms and phytoplankton. Understanding the response of cyanobacteria to various factors is fundamental for eutrophication control. To clarify the response of cyanobacteria to APM, the effects of PM2.5, PM2.5-10, and PM>10 on Microcystis aeruginosa were researched. Variabilities in cell density, chlorophyll a, soluble protein, malondialdehyde, extracellular activity, and kinetic parameters of alkaline phosphatase were evaluated by lab-cultured experiments. Results showed that the PM2.5 had a slight stimulation impact on the growth and enhanced both of the 48- and 72-h extracellular alkaline phosphatase activity (APA), the affinity of alkaline phosphatase for substrate, and the 72-h maximum enzymatic reaction velocity (Vmax). Moreover, the stimulations in extracellular APA and Vmax enhanced with the increasing exposure concentrations. We also found there were no obvious distinctions on the effects of growth and alkaline phosphatase in M. aeruginosa between PM2.5-10 and PM>10 exposure groups. Obviously, inhibitory effects on growth existed in 4.0 and 8.0mg/L PM2.5-10 and 8.0mg/L PM>10 at 120h. Furthermore, PM2.5-10 and PM>10 exerted inhibitory effects on the extracellular APA during the 72-h exposure. Simultaneously, the Vmax was notably inhibited and the affinity of alkaline phosphatase for substrate was more inseparable compared with control in PM2.5-10 and PM>10 treatments. Nevertheless, the inhibitors in extracellular APA and kinetic parameters were unrelated to PM2.5-10 and PM>10 exposure concentrations. Two-way ANOVA results revealed that there were significant interactions between exposure concentration and diameter of APM on the 120-h cell density, soluble protein content, APA, and 72h APA of M. aeruginosa. These results in our study would be meaningful to further researches on relationships between APM deposition and cyanobacterial bloom.

Multiple‐stressor effects on river biofilms under different hydrological conditions

Summary We studied the relative importance of environmental factors (river flow, nutrients, dissolved organic matter) and organic micro‐pollutants [herbicides, insecticides, industrial organic compounds, personal care products, antibiotics and pharmaceuticals, (PhCs)] to the structure and function of epilithic biofilms under various hydrological conditions and land uses. Biofilms from four river basins in the Iberian Peninsula (Llobregat, Ebro, Júcar and Guadalquivir) were analysed in summer–autumn during a wet period and base‐flow conditions. The sites experienced different levels of pollution. We used variance partitioning (Redundancy Detrended Analysis, RDA) to link environmental stressors to the structure and function of biofilms, which were assessed as diatom community composition, algal biomass, photosynthetic activity, bacterial density and extracellular phosphatase activity. RDAs showed that industrial organic compounds, herbicides and PhC products were the pollutants most strongly associated with measures of biofilm structure and function, whereas dissolved inorganic nitrogen, dissolved organic carbon and hydrological variability were the environmental factors most strongly associated with biofilm responses. Thicker biofilms developing during base flow were most affected by pollutants and nutrients. In contrast, thinner biofilms developing during periods of high river flow were less affected by chemicals.

Effect of Cobalt on Synthesis of Extracellular Alkaline Phosphatase Production from Bacillus sp.

Various species of Bacillus isolated from soil were characterized and tested for their ability to produce extracellular alkaline phosphatase. Six strains of Bacillus demonstrated significant activity as compared to Bacillus subtilis6633 in optimized Bacillus medium ATCC 552. Highest levels of extracellular alkaline phosphatase activity were observed with 1% whey, in the presence 0·1mM CoCl2(10.4 U/ml/min). This trend was observed in five of the six strains tested.

Carbon and Nitrogen Sources Influence Tricalcium Phosphate Solubilization and Extracellular Phosphatase Activity by Talaromyces flavus.

The aim of this work was to study phosphate (P) solubilization (and the processes involved in this event) by Talaromyces flavus (BAFC 3125) as a function of carbon and/or nitrogen sources. P solubilization was evaluated in NBRIP media supplemented with different carbon (glucose, sorbitol, sucrose, and fructose) and nitrogen (L-asparagine, urea, ammonium sulfate (AS), and ammonium nitrate (AN) combinations. The highest P solubilization was related to the highest organic acid production (especially gluconic acid) and pH drop for those treatments where glucose was present. Also P solubilization was higher when an inorganic nitrogen source was supplemented to the media when compared to an organic one. Although not being present an organic P source, phosphatase activity was observed. This shows that P mineralization and P solubilization can occur simultaneously, and that P mineralization is not induced by the enzyme substrate. The combination that showed highest P solubilization was for AN-glucose. The highest acid phosphatase activity was for AS-fructose, while for alkaline phosphatase were for AS-fructose and AN-fructose. Acid phosphatase activity was higher than alkaline. P solubilization and phosphatase activity (acid and alkaline) were influenced by the different carbon-nitrogen combinations. A better understanding of phosphate-solubilizing fungi could bring a better use of soil P.

Molecular Characterization of Monocrotophos Hydrolyzing Soil Fungal Strain Penicillium aculeatum ITCC 7980.10

A B S T R A C T Pesticides poses great threat to the environmental sustainability by affecting its microbial flora and fauna. Fungi are well known for the secretion of extracellular hydrolases for the degradation of these hazardous chemicals from its ambient environment. Hydrolase secreting soil fungi Penicillium aculeatum ITCC 7980.10 was selected for the study of its monocrotophos degrading efficiency under in vitro conditions in phosphorus free liquid culture medium. Fungal strain was molecularly characterized by 18S rDNA analysis as Penicillium aculeatum JQ660374. Monocrotophos degrading efficiency of the isolate was studied under optimum conditions each, at an interval of 5 days for 15 days incubation period. The isolated strain possessed meagre extracellular phosphatase activity 28.33 ± 0.40 U which resulted in the formation of 614.62 ± 0.38 µg ml -1 inorganic phosphates. Degradation process was studied by spectrophotometric analysis at 254nm, HPTLC and FTIR. Spectrophotometric analysis revealed 98.88% degradation of monocrotophos with a prominent decrease in the standard peak of monocrotophos (standard rf 0.19- 0.21) within 15 days of incubation as evident by HPTLC chromatograms. Molecular mechanism as studied by FTIR analysis revealed hydrolytic cleavage of vinyl bond with the formation of PO –4 . Degradation of monocrotophos followed first order kinetics with the rate constant (k deg ) of 0.0115 day -1 and half life of 2.53 days. The results of the study conclude that Penicillium aculeatum JQ660374 could be used as an efficient candidate for the detoxification of monocrotophos contaminated sites.

English

Ectomycorrhizal fungi have been shown to improve on the phosphorus nutrition of their plant partners and acid phosphatase activities are thought to be important in the uptake process. The effect of nitrogen source and presence/absence of phosphorus in the experimental medium on acid phosphatase activity of Scleroderma sinnamariense, an ectomycorrhizal fungus associated with Gnetum spp.in Cameroon, was determined in comparison to Pisolithus tinctorius. The effect of internal mycelial phosphorus status of the inoculum on acid phosphatase activity was also studied. Results show that the absence of phosphorus in the assay medium stimulated cell bound acid phosphatase activity. Extracellular phosphatase activity was less than cell bound activity by a factor of 100.   Key words: Acid phosphatase, cell-bound activity, Scleroderma sinnamariense, ectomycorrhizal fungus.

Differentiating Intracellular from Extracellular Alkaline Phosphatase Activity in Soil by Sonication

Differentiating intracellular from extracellular enzyme activity is important in soil enzymology, but not easy. Here, we report on an adjusted sonication method for the separation of intracellular from extracellular phosphatase activity in soil. Under optimal sonication conditions [soil:water ratio = 1/8 (w/v) and power density = 15 watt ml-1], the activity of alkaline phosphomonoesterase (phosphatase) in a Haplic Cambisol soil increased with sonication time in two distinct steps. A first plateau of enzyme activity was reached between 60 and 100 s, and a second higher plateau after 300 s. We also found that sonication for 100 s under optimal conditions activated most (about 80%) of the alkaline phosphatase that was added to an autoclaved soil, while total bacteria number was not affected. Sonication for 300 s reduced the total bacteria number by three orders of magnitude but had no further effects on enzyme activity. Our results indicate that the first plateau of alkaline phosphatase activity was derived from extracellular enzymes attached to soil particles, and the second plateau to the combination of extracellular and intracellular enzymes after cell lysis. We conclude that our adjusted sonication method may be an alternative to the currently used physiological and chloroform-fumigation methods for differentiating intracellular from extracellular phosphatase activity in soil. Further testing is needed to find out whether this holds for other soil types.

Distribution of actinomycetes in different soil ecosystems and effect of media composition on extracellular phosphatase activity

Actinomycetes are widely distributed in different habitats and involved in important processes. Therefore, evaluation of their distribution is important in understanding their ecological role. Ninety seven samples were taken from different soil ecosystems (forest, pasture, rain-fed and irrigated cultivated land) located in various climatic zones in the province of Golestan, Northeast Iran. The number of actinomycetes as well as pH value, organic carbon (OC) and soil salinity expressed as electrical conductivity (EC) showed significant differences in the soil ecosystems under investigation. The number of actinomycetes decreased from 2.86 * 10 6cfu g-1 in irrigated cultivated land to 7* 105 cfu g-1 in pasture (p<0.01). In pastures, the number of actinomycetes was negatively correlated with EC (r=-0.60, n=15, p<0.001) and pH (r=-0.59, n=15, p<0.001). In other soil ecosystems under investigation no significant correlations between soil pH, OC and EC and the number of actinomycetes could be found. In forest soils, the number of actinomycetes was significantly dependent (p<0.05) on climate. A significantly higher population was observed under semi-arid conditions compared to all other climatic zones (humid, sub-humid, Mediterranean). Because many soil microorganisms are able to transform different forms of insoluble organic and inorganic phosphorus into a soluble form suitable for plant uptake, the capacity of the isolated actinomycetes to secrete phosphatase activity was determined under laboratory conditions. A huge variation in the capacities to produce acid and alkaline phosphatases among the different isolates was observed. These enzyme activities and the capacities to hydrolyze phytate in the fermentation broth were significantly dependent on medium composition. In general, substitution of arginine and glycerol in the modified glycerol arginine medium (MGA) with other nitrogen and carbon sources resulted in a significant reduction of phytate dephosphorylation.

Drought episode modulates the response of river biofilms to triclosan

The consequences of global change on rivers include altered flow regime, and entrance of compounds that may be toxic to biota. When water is scarce, a reduced dilution capacity may amplify the effects of chemical pollution. Therefore, studying the response of natural communities to compromised water flow and to toxicants is critical for assessing how global change may affect river ecosystems. This work aims to investigate how an episode of drought might influence the response of river biofilms to pulses of triclosan (TCS). The objectives were to assess the separate and combined effects of simulated drought (achieved through drastic flow alteration) and of TCS exposure on biofilms growing in artificial channels. Thus, three-week-old biofilms were studied under four conditions: Control (normal water flow); Simulated Drought (1 week reduced flow+2 days interrupted flow); TCS only (normal water flow plus a 48-h pulse of TCS); and Simulated Drought+TCS. All channels were then left for 2 weeks under steady flow conditions, and their responses and recovery were studied. Several descriptors of biofilms were analyzed before and after each step. Flow reduction and subsequent interruption were found to provoke an increase in extracellular phosphatase activity, bacterial mortality and green algae biomass. The TCS pulses severely affected biofilms: they drastically reduced photosynthetic efficiency, the viability of bacteria and diatoms, and phosphate uptake. Latent consequences evidenced significant combined effects caused by the two stressors. The biofilms exposed only to TCS recovered far better than those subjected to both altered flow and subsequent TCS exposure: the latter suffered more persistent consequences, indicating that simulated drought amplified the toxicity of this compound. This finding has implications for river ecosystems, as it suggests that the toxicity of pollutants to biofilms may be exacerbated following a drought.

PHOSPHATE DEFICIENCY AFFECTS ACID PHOSPHATASE ACTIVITY AND GROWTH OF TWO WHEAT VARIETIES

The effects of phosphate deficiency on the plant growth and acid phosphatase activity in two wheat cultivars (Triticum aestivum L. cv. ‘Bryza’ and ‘Opatka’) were studied. Pi content decreased significantly in the shoots and roots of all plants grown for one to three weeks in the nutrient medium without phosphate (−P). Phosphate starvation affected growth of both wheat cultivars in a similar way: significantly decreased shoot and root mass, especially after three weeks growth on −P medium, even up to 8–11% of control. However the ratio of root/shoot fresh weight of −P plants increased (2–3 times more than control). The shoot height of −P wheat plants decreased to about 50–60% of the control after two to three weeks of culture; less affected by Pi deficiency was root elongation—no significant changes were observed for both wheat cultivars during one to three weeks of culture. Phosphate deficiency increased the activity of extracellular and intracellular acid phosphatases in comparison to phosphate-sufficient plants. The increase of intracellular acid phosphatase activity in leaves and roots was generally more significant in ‘Bryza’ cultivar as compared to ‘Opatka’, especially after two to three weeks of growth on −P medium. The increase of root surface acid phosphatase activity was the highest for Pi-deficient wheat cv. ‘Bryza’, after three weeks of culture in the −P medium. Generally, the increase of activity of acid phosphatases secreted by the roots of −P wheat plants was higher than those of intracellular acid phosphatases. These results indicate an important role of acid phosphatases in the acclimation of both wheat cultivars to early Pi deficiency.