Heterotrophic cultures of microalgae: Metabolism and potential products

Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture

Seed dormancy provides a mechanism for plants to delay germina- tion until conditions are optimal for survival of the next generation. Dormancy release is regulated by a combination of environmental and endogenous signals with both synergistic and competing effects. Molecular studies of dormancy have correlated changes in transcrip- tomes, proteomes, and hormone levels with dormancy states ranging from deep primary or secondary dormancy to varying degrees of re- lease. The balance of abscisic acid (ABA):gibberellin (GA) levels and sensitivity is a major, but not the sole, regulator of dormancy status. ABA promotes dormancy induction and maintenance, whereas GA promotes progression from release through germination; environ- mental signals regulate this balance by modifying the expression of biosynthetic and catabolic enzymes. Mediators of environmental and hormonal response include both positive and negative regulators, many of which are feedback-regulated to enhance or attenuate the response. The net result is a slightly heterogeneous response, thereby providing more temporal options for successful germination.

Molecular Aspects of Seed Dormancy

†Background Productive agriculture needs a large amount of expensive nitrogenous fertilizers. Improving nitrogen use efficiency (NUE) of crop plants is thus of key importance. NUE definitions differ depending on whether plants are cultivated to produce biomass or grain yields. However, for most plant species, NUE mainly depends on how plants extract inorganic nitrogen from the soil, assimilate nitrate and ammonium, and recycle organic nitrogen. Efforts have been made to study the genetic basis as well as the biochemical and enzymatic mechanisms involved in nitrogen uptake, assimilation, and remobilization in crops and model plants. The detection of the limiting factors that could be manipulated to increase NUE is the major goal of such research. †Scope An overall examination of the physiological, metabolic, and genetic aspects of nitrogen uptake, assimilation and remobilization is presented in this review. The enzymes and regulatory processes manipulated to improve NUE components are presented. Results obtained from natural variation and quantitative trait loci studies are also discussed. †Conclusions This review presents the complexity of NUE and supports the idea that the integration of the numerous data coming from transcriptome studies, functional genomics, quantitative genetics, ecophysiology and soil science into explanatory models of whole-plant behaviour will be promising.

REVIEW: PART OF A SPECIAL ISSUE ON PLANT NUTRITION Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture

The objective of this study was to evaluate the growth of green algae Chlorella sp. on wastewaters sampled from four different points of the treatment process flow of a local municipal wastewater treatment plant (MWTP) and how well the algal growth removed nitrogen, phosphorus, chemical oxygen demand (COD), and metal ions from the wastewaters. The four wastewaters were wastewater before primary settling (#1 wastewater), wastewater after primary settling (#2 wastewater), wastewater after activated sludge tank (#3 wastewater), and centrate (#4 wastewater), which is the wastewater generated in sludge centrifuge. The average specific growth rates in the exponential period were 0.412, 0.429, 0.343, and 0.948 day(-1) for wastewaters #1, #2, #3, and #4, respectively. The removal rates of NH4-N were 82.4%, 74.7%, and 78.3% for wastewaters #1, #2, and #4, respectively. For #3 wastewater, 62.5% of NO3-N, the major inorganic nitrogen form, was removed with 6.3-fold of NO2-N generated. From wastewaters #1, #2, and #4, 83.2%, 90.6%, and 85.6% phosphorus and 50.9%, 56.5%, and 83.0% COD were removed, respectively. Only 4.7% was removed in #3 wastewater and the COD in #3 wastewater increased slightly after algal growth, probably due to the excretion of small photosynthetic organic molecules by algae. Metal ions, especially Al, Ca, Fe, Mg, and Mn in centrate, were found to be removed very efficiently. The results of this study suggest that growing algae in nutrient-rich centrate offers a new option of applying algal process in MWTP to manage the nutrient load for the aeration tank to which the centrate is returned, serving the dual roles of nutrient reduction and valuable biofuel feedstock production.

/pdf/cultivation-of-green-algae-chlorella-sp-in-different-1unomqxaws.pdf

Cultivation of green algae Chlorella sp. in different wastewaters from municipal wastewater treatment plant.

A nitrate reductase (NR)-null mutant of Arabidopsis was constructed that had a deletion of the major NR gene NIA2 and an insertion in the NIA1 NR gene. This mutant had no detectable NR activity and could not use nitrate as the sole nitrogen source. Starch mobilization was not induced by nitrate in this mutant but was induced by ammonium, indicating that nitrate was not the signal for this process. Microarray analysis of gene expression revealed that 595 genes responded to nitrate (5 mm nitrate for 2 h) in both wild-type and mutant plants. This group of genes was overrepresented most significantly in the functional categories of energy, metabolism, and glycolysis and gluconeogenesis. Because the nitrate response of these genes was NR independent, nitrate and not a downstream metabolite served as the signal. The microarray analysis also revealed that shoots can be as responsive to nitrate as roots, yet there was substantial organ specificity to the nitrate response.

/pdf/genomic-analysis-of-the-nitrate-response-using-a-nitrate-3q5cy9lzmb.pdf

Genomic Analysis of the Nitrate Response Using a Nitrate Reductase-Null Mutant of Arabidopsis

Response to Zemojtel et al: Plant nitric oxide synthase: back to square one

This investigation shows diurnal variations in the xylem sap composition of poplar (Populus tremula × P. alba). All major macronutrients reached a maximum concentration in the first half of the light period and decreased to the middle of the night. The relative abundance of the nutrients did not change during the day. The sap flow, which responded very fast to the environmental changes (2.2-fold increase within 10–20 min of illumination), reached a maximum value in the second half of the light period. Transpiration (and photosynthesis) was constant throughout the light phase. The calculated translocation rates displayed a maximum in the first half of the light period and therefore did not fit the time course of sap flow. During the night, translocation rates were 63–69% lower than the maximum. The regulation of nutrient translocation is discussed taking the active xylem loading into account. The axial distribution located the nitrate assimilation in younger leaves and storage of nitrate (and other macronutrients) in older leaves. Nitrate and potassium concentrations in the xylem sap did not change along the plant axis. However, the sap flow was greater in younger shoot sections than in older sections. We assume that the greater demand for nitrate in the younger shoot section was satisfied via an increased volume flow rather an increased nitrate concentration.

Nutrient translocation in the xylem of poplar--diurnal variations and spatial distribution along the shoot axis.

Bark, wood, and root tissues of several Populus species contain a 32- and a 36-kilodalton polypeptide which undergo seasonal fluctuations and are considered to be storage proteins. These two proteins are abundant in winter and not detectable in summer as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunodetection. An antibody raised against the 32-kilodalton storage protein of Populus trichocarpa (T. & G.) cross-reacts with the 36-kilodalton protein of this species. The synthesis of the 32- and 36-kilodalton proteins can be induced in micropropagated plants by short-day conditions in the growth chamber. These proteins are highly abundant in structural roots, bark, and wood and combined represent >25% of the total soluble proteins in these tissues. Nitrate concentration in the leaves and nitrate uptake rate decreased dramatically when LD plants were transferred to short-day conditions; the protein content in leaves was unaffected. A decrease of the 32- and 36-kilodalton polypeptides occurs after transferring induced plants back to LD conditions. Both polypeptides are glycosylated and can be efficiently purified by affinity chromatography using concanavalin A-Sepharose 4B. The 32- and the 36-kilodalton polypeptides have identical basic isoelectric points and both consist of at least three isoforms. The storage proteins show a loss in apparent molecular mass after deglycosylation with trifluoromethanesulfonic acid. It is concluded that the 32- and 36-kilodalton polypeptides are glycoforms differing only in the extent of glycosylation. The relative molecular mass of the native storage protein was estimated to be 58 kilodalton, using gel filtration. From the molecular mass and the elution pattern it is supposed that the storage protein occurs as a heterodimer composed of one 32- and one 36-kilodalton subunit. Preliminary data suggest the involvement of the phytochrome system in the induction process of the 32- and 36-kilodalton polypeptides.

Vegetative Storage Proteins in Poplar Induction and Characterization of a 32- and a 36-Kilodalton Polypeptide

Nitrate uptake was followed continuously in cultures of Chlorella sorokiniana using ionsensitive electrodes. During the lifecycle of the synchronous cell cultures, a drastic increase occurred in the first hour after the onset of the light. Nitrate uptake rate was shown to be dependent on illumination intensity, nitrate concentration, and temperature. These results point to an energy-linked uptake process. From the different timecourses of nitrate uptake rate and nitrate reductase activation, one can conclude that the increased nitrate reductase activity after light onset is regulated via nitrate uptake. Further evidence for a regulation in this direction is shown by the action of ammonium on nitrate uptake and nitrate reductase activity. The results are discussed in terms of the regulation of the nitrate consuming system.

Rudolf Tischner

Papers

Genomic Analysis of the Nitrate Response Using a Nitrate Reductase-Null Mutant of Arabidopsis

Response to Zemojtel et al: Plant nitric oxide synthase: back to square one

Nutrient translocation in the xylem of poplar--diurnal variations and spatial distribution along the shoot axis.

Vegetative Storage Proteins in Poplar Induction and Characterization of a 32- and a 36-Kilodalton Polypeptide

Nitrate uptake and nitrate reduction in synchronous Chlorella