Engineering triacylglycerol accumulation in duckweed (Lemna japonica)

Duckweeds are amongst the fastest growing of higher plants, making them attractive high-biomass targets for biofuel feedstock production. Their fronds have high rates of fatty acid synthesis to meet the demand for new membranes, but triacylglycerols (TAG) only accumulate to very low levels. Here we report on the engineering of Lemna japonica for the synthesis and accumulation of TAG in its fronds. This was achieved by expression of an estradiol-inducible cyan fluorescent protein-Arabidopsis WRINKLED1 fusion protein (CFP-AtWRI1), strong constitutive expression of a mouse diacylglycerol:acyl-CoA acyltransferase2 (MmDGAT), and a sesame oleosin variant (SiOLE(*)). Individual expression of each gene increased TAG accumulation by 1- to 7-fold relative to controls, while expression of pairs of these genes increased TAG by 7- to 45-fold. In uninduced transgenics containing all three genes, TAG accumulation increased by 45-fold to 3.6% of dry weight (DW) without severely impacting growth, and by 108-fold to 8.7% of DW after incubation on medium containing 100 μm estradiol for 4 days. TAG accumulation was accompanied by an increase in total fatty acids of up to three-fold to approximately 15% of DW. Lipid droplets from fronds of all transgenic lines were visible by confocal microscopy of BODIPY-stained fronds. At a conservative 12 tonnes (dry matter) per acre and 10% (DW) TAG, duckweed could produce 350 gallons of oil/acre/year, approximately seven-fold the yield of soybean, and similar to that of oil palm. These findings provide the foundation for optimizing TAG accumulation in duckweed and present a new opportunity for producing biofuels and lipidic bioproducts.     

The accumulation of poly(3-hydroxyalkanoates) in Rhodobacter sphaeroides

In recent years industrial interest has been focussed on the evaluation of poly(3-hydroxyalkanoates) (PHA) as potentially biodegradable plastics for a wide range of technical applications. Studies have been carried out in order to optimize growth and culture conditions for the intracellular formation of PHA in the phototrophic, purple, non-sulfur bacterium Rhodobacter sphaeroides. Its potential to produce polyesters other than poly(3-hydroxybutyrate) (PHB) was investigated. On an industrial scale, the use of photosynthetic bacteria could harness sunlight as an energy source for the production of these materials. R. sphaeroides was grown anaerobically in the light on different carbon sources. Under nitrogenlimiting conditions a PHA content of up to 60 to 70% of the cellular dry weight was detected. In all of the cases studied, the storage polymer contained approximately 98 mol% of 3-hydroxybutyrate (HB) and 2 mol% 3-hydroxyvalerate (HV) monomer units. Decreasing light intensities did not stimulate PHA formation. Compared to Rhodospirillum rubrum (another member of the family of Rhodospirillaceae), R. sphaeroides showed a limited flexibility in its ability to form PHA with varying monomer unit compositions.     

Aluminium accumulation and distribution in the freshwater clams (unionidae)

1. Freshwater unionids (Anodonta anatina L. and Unio pictorum L.) were exposed to aluminium (300 and 900 μg/l, nominal) in continuous (3 weeks) and fluctuating (24 days) acid exposures.2. In addition, accumulation was monitored for 2 weeks under semi-static acid (pH4-5) and circumneutral (pH 6.6-8.3) conditions in hard (35 mg Ca/l) and soft water (3.5 mg Ca/l).3. In addition, a fluctuating exposure of 24 days, consisting of three intermittent pulses which combined low pH (4–5) and high Al (900 μg/l) concentration, was performed.4. The various organs of A. cygnea, collected from a watershed with relatively high heavy metal concentrations, were analyzed for their Al and Cd concentrations.5. The ultimate order of the Al and Cd concentration in these clams was identical: kidney ≥ midgut gland ≥ rest ≥ gill ≥ mantle.6. During the 3 weeks of exposure, the Al concentration in the gills and kidney increased linearly, and saturation level was not reached.7. The Al concentration in the calcium concretion material isolated from the gills was lower than that of the whole organ.8. An elimination period of 12 weeks was needed to reach the background level of Al in the gills, whereas in the kidney the initial Al concentration was reached after 4 weeks of elimination.9. In both species, the ambient pH had a significant effect on the Al accumulation in the gills, whereas the effect of the water hardness was only of minor importance.10. Rapid elimination of the Al accumulated in the gills of U. pictorum during the episodic 3-day exposure was recorded.     

Cadmium accumulation and oxidative burst in garlic (Allium sativum)

To investigate the temporal sequence of physiological reactions of garlic (Allium sativum) to cadmium (Cd) treatment, seedlings developed from cloves were grown in increasing concentrations of CdCl2, ranging from 1-10 mM, for up to 8 days in sand. Analysis of Cd uptake indicated that most Cd accumulated in roots, but some was also translocated and accumulated in leaves at longer exposure time (after 12h) and higher concentrations (5 and 10mM) of CdCl2. Changes in activities of antioxidative enzymes, including superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT), were characterized in leaves of garlic seedlings. Cd (5 and 10 mM) initially inhibited the activities of SOD and CAT but thereafter recovered or even increased compared with control plants. POD activities at 5 and 10 mM of Cd increased more than 3-4 times over control plants within 12 h and then dropped, but were still higher than controls at the end of the experiment. Otherwise lipid peroxidation enhanced with the increasing of incubation time and concentrations of external Cd. Leaves exposed to 1 mM CdCl2 showed a less pronounced response and only a small reduction in shoot growth. These results suggested that in leaves of garlic seedlings challenged by CdCl2 at higher concentrations, induction of these various enzymes is part of a general defense strategy to cope with overproduction of reactive oxygen. The possible mechanism of antioxidative enzymes changing before Cd accumulation in leaves of garlic seedlings is discussed.     

Cytotoxicity and cellular accumulation of palladium(II) complexes of tetracyclines

We studied the cytotoxic effect and the uptake of Pd(II) complexes of doxycycline (Dox), [Pd(Dox)Cl2], and tetracycline (Tc), [Pd(Tc)Cl2], in chronic myelogenous leukemia cells. The effect of the compounds on macrophage viability was also investigated. Compound 1 is more effective than compound 2 in inhibiting the growth of K562 cells with the IC(50) values of 14.44 and 34.54 microM, respectively. There is a good correlation between cell-growth inhibition and intracellular metal concentrations, determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES). Incubation of the cells with equitoxic concentrations of both compounds yields approximately the same intracellular Pd concentration. At the IC(50) doses, intracellular concentration is ca. 33 x 10(-16) mol/cell for both compounds 1 and 2. This suggests that more [Pd(Tc)Cl2] is needed to produce a cytotoxic effect, because it enters cells more slowly. Both compounds up to 16 microM did not affect the viability of mouse peritoneal macrophages after a 48-h incubation. After 72 h of incubation, the IC(50) values are 22 for [Pd(Dox)Cl2] and 40 microM for [Pd(Tc)Cl(2)]. Therefore, the cytotoxic effect in cancer cells exhibited by both compounds is higher than their effect in macrophages.     

The role of membrane processes in Au(III) and Au(0) accumulation by bacteria

The role of structural and functional factors in the processes of the bacterial cell interaction with colloid Au (0) and ionic Au (III) states has been investigated. It is shown that the bacterial walls of Bacillus sp. 4368 aggregating with colloid gold contain glycoprotein with isoelectric point 11. Glycoprotein from cell walls indifferent to colloid gold strain (Bacillus subtilis 168) has pHiso = 5. At the same time the cells of both strains accumulate Au (III) introduced into a medium in the form of tetrachloroaurate. The process is energy-dependent because it is suppressed by azide, uncouplers of oxidative phosphorylation and dicyclohexyl carbodiimide (DCCD). The role of ATPase of Au (III) accumulation has been studied on Bacillus sp. 4368 plasma membrane vesicles. The ATPase activity is inhibited by 70, 50 and 35-50% by vanadate, DCCD and Au (III), respectively, but it does not change in the presence of dinitrophenol and NaN3. ATP but not ADP and AMP stimulated the Au (III) accumulation by membrane vesicles and prevents the inhibitory action of azide but neither of DNP or DCCD. In the energized state membrane vesicles link gold sol particles. It has been assumed that the Au (III) accumulation is associated with the functioning of transmembrane potential generators, the metal being localized on the membrane surface.     

Pb and Zn accumulation in a Cd-hyperaccumulator (Viola baoshanensis)

Viola baoshanensis has been identified as a Cd-hyperaccumulator, however, its ability to accumulate Pb or Zn is less certain. Therefore, this study focused on determining whether or not V. baoshanensis can accumulate Pb or Zn, by means of field survey, hydroponic and pot experiments. In addition, we also tried to obtain further information on the Cd hyperaccumulating characteristics of this species. Under field conditions, V. baoshanensis accumulated on average 1090 mg Cd kg(-1), 1902 mg Pb kg(-1) and 3428 mg Zn kg(-1) in its shoots, respectively. In hydroponic and pot experiments, V. baoshanensis showed high tolerance to Cd, Pb, and Zn, as well as the ability to accumulate exceptionally high concentrations of the three elements in its shoots (> 2% Cd, > 1% Pb, and > 0.5% Zn on a dry matter basis). These results, taken together, suggested that V. baoshanensis is not only a Cd-hyperaccumulator, but also a strong accumulator of Pb and Zn.     

Phosphorus requirements and nitrogen accumulation by three mungbean (Vigna radiata (L) Welzek) cultivars

A promising approach for overcoming poor crop yields in phosphorus (P)-deficient soils is to exploit the genetic variation among plants to grow under low P conditions. We examined the P requirements of three mungbean cultivars, T-77, MI-5 and E-72, using four P rates, 0, 30, 60 and 90 mg P kg^-1 soil (designated P₀, P₁, P₂ and P₃, respectively). Nodulation was highest in T-77, and unlike the other cultivars, nodule numbers were not increased by P application. Similarly, growth of T-77 was the highest, and was not influenced by P rates. In contrast shoot yields of MI-5 and E-72 at P₀ were only 76 and 65%, respectively, of the maximum obtained under P application. Nodule dry weight and the amount of N fixed (Ndfa) in each cultivar was enhanced by P application, with T-77 generally giving the lowest response, and accumulating the highest Ndfa. The data suggest a higher P requirement for N₂ fixation (especially for T-77) than for growth. All plants increased their P uptake as P rates increased, with T-77 accumulating the highest amount of P at each P level. Differences in the physiological P use efficiency, PPUE (g shoot mg^-1 P) among genotypes were generally not significant, neither were there any consistent trends as P rates changed. The ability to absorb P therefore appeared to be more important than PPUE in enhancing growth. We conclude from our data that it is possible by selection to obtain plants capable of good growth and high N₂ fixation in soils of low P; cultivar T-77 is a good example.     

Cadmium effects and accumulation in cultures ofProrocentrum micans (dinophyta)

Effects and accumulation of cadmium were studied in unialgal 10-1 batch-culture experiments with the dinoflagellateProrocentrum micans Ehrenberg. Tests were made using sterile filtered North Sea water enriched with nitrate and phosphate only in order to avoid disturbances by complex formation. Cadmium was added to the cultures in amounts of 100 to 0.13μg l⁻¹. In one series it was added at the start of the experiments and in a second one after a growth period of 1 week. Addition of only 1.2μg Cd l⁻¹ reduces multiplication rates and maximum cell densities of the algae. Not until 0.4μg Cd⁻¹ does growth correspond to that of the controls. Cadmium concentrations were measured, after filtration, in the culture medium and in the biomass by means of flameless AAS. The cadmium content in algae increased from 2.7μg g⁻¹ (dry weight) in controls to 500μg g⁻¹ (dry weight) in media containing 100μg Cd l⁻¹. Uptake occurred rapidly during the first few days of the experiments, slowed down somewhat during exponential growth stage, and increased during decay of the cultures. Cadmium content of culture media remained nearly constant (Series 1) or decreased only slowly during experimental time (Series 2). The highest concentration factor was measured in the controls. It decreased with increasing metal concentration in the medium and increased with experimental time. Structural modifications of the cells were visible after Lugol fixation only, indicating brittleness of the cell walls.P. micans has shown to be extremely sensitive to cadmium and to accumulate this metal.     

Seasonal stability of sulfuric acid accumulation in the Dictyotales (Phaeophyceae)

Concerning the accumulation of S0₄^2‐ in cells, three types of species are known in the Dictyotales: (i) acidic type (high H₂S0₄ accumulation); (ii) high MgS0₄ accumulation type; and (iii) nonacidic type (low S0₄^2‐ accumulation). Seasonal changes of intracellular pH and concentrations of inorganic ions were examined in six dictyotalean species. In acidic species (Dictyopteris prolifera (Okamura) Okamura and Spatoglossum eras‐sum J. Tanaka), intracellular concentrations of S0₄^2‐ and H⁺ estimated by pH were high through all seasons. In high MgS0₄ accumulating species (Dictyotasp. and Padina arborescens Holmes), intracellular concentrations of S0₄^2‐ and Mg²⁺ were high through all seasons. In nonacidic species (Dictyota dichotoma (Hudson) Lamouroux and Dictyopteris undulata Holmes), intracellular concentration of sulfuric acid ion was low all year round.     

Cell-specific accumulation of Drosophila proteasomes (MCP) during early development

The proteasome (MCP) is a high relative molecular mass multicatalytic proteinase complex composed of nonidentical protein subunits. We have investigated the cellular distribution of the enzyme complex during Drosophila embryogenesis using the proteasome specific antibodies N19- 35 and N19-28 for immunocytology. Antibody staining of whole-mount embryos shows that during embryogenesis proteasomes are present in proliferating cells and that their accumulation and turnover is differentially regulated. Our data suggest that the proteasome may serve different proteolytic processes and that the enzyme may be involved in cell-specific proteolytic events required for cell proliferation and morphogenesis during early Drosophila development.     

Bis(thiosemicarbazone) copper complexes: mechanism of intracellular accumulation

The molecular basis of Alzheimer’s disease has not been clearly established, but disruption of brain metal ion homeostasis, particularly copper and zinc, might be closely involved in the pathogenesis of this disease and its characteristic β-amyloid neuropathological features. The use of complexes of copper with bis(thiosemicarbazones) ([Cu(btsc)]) has been proposed for the treatment of Alzheimer’s disease. Their mode of action could involve modulation of the concentration of copper or zinc, and it has been suggested that the compounds can modulate the production of β-amyloid peptide at the neuron level. Furthermore, it has been reported that [Cu(btsc)] complexes can be reduced inside the cells. However, to our knowledge the intracellular reduction of these compounds has never been demonstrated. Thus, the goal of our study was to increase understanding of the mechanism of intracellular accumulation of [Cu(btsc)] complexes. Our results reveal that the intracellular concentration of copper inside the cells is very high and that these compounds are not P-glycoprotein substrates. This protein is a key element of the low permeability properties of the blood–brain barrier. Furthermore, no intracellular reduction of cupric ions was detected. Finally, once inside the cells, the complexes undergo aggregation, strongly suggesting that aggregation of complexes is the driving force responsible for their intracellular accumulation.     

Growth-limiting quantities and accumulation of molybdenum in Anabaena oscillarioides (Cyanobacteria)

Molybdenum deficiency and accumulation was examined in Anabaena oscillarioides (Cyanobacteria). Molybdenum deficiency was induced by: 1) culturing the cyanobacterium on modified Chu-10 (-N) medium containing 4–5 ng Mo · l⁻¹, or 2) adding tungsten to reversibly inactivate dinitrogenase. Stimulation of dinitrogenase activity, while heterocyst frequencies were decreasing, occurred in the range of 5–40 ng · l⁻¹ of added Mo. Molybdenum deficient A. oscillarioides was able to deplete Mo in the medium. This ability was rapidly lost at higher concentrations of added Mo when this cyanobacterium started to accumulate Mo. These results are of potential use in predicting potential Mo limitation in natural environments.     

Heterochromatin accumulation,disposition and diversity in Gibasis karwinskyana (Commelinaceae)

C-banding differences within Gibasis karwinskyana (Roem & Schult.) Rohw. were reassessed using dual fluorochrome staining. Pronounced differences in C-band pattern between two subspecies with identical basic karyotypes were due to different chromosomal locations of AT-rich and GC-rich heterochromatin. The AT-rich component had an equilocal distribution in the karyotype and has evidently been accumulated at telomeres, as shown by its prevalence in supernumerary segments and B chromosomes. The GC-rich component also varied in amount, but was limited to nucleolus organizing regions (NORs) and centromeres. Centromeres and telomeres are suggested to constitute separate, although perhaps interdependent, centres of heterochromatin amplification. The possible role of nuclear architecture in determining the accumulation, distribution and spread of these sequences is discussed.Abbreviations H Hoechst 33258 - CMA chromomycin A3 - NOR nucleolus organizing region - SS supernumerary segment - Q quinacrine dihydrochloride - H⁺ H etc. indicate enhanced (+) and quenched (-) fluorescence with the stated fluorochrome by H.C. Macgregor     

Senile cataract-related accumulation of Lewis(x) glycolipid in human lens.

A glycosphingolipid that reacted positively to anti-stage-specific embryonic antigen-1 (SSEA-1) antiserum accumulated in human lens in association with aging and senile cataract formation. Since this antiserum recognizes Lewis(x) (Le(x)) structure, Gal beta 1-4(Fuc alpha 1-3)GlcNAc-, which is a typical tumor-associated and differentiation-related saccharide chain, the lens glycolipid was predicted to be a Lex antigen. The glycolipid purified from cataractous lens tissues was indeed a Lex glycolipid, Gal beta 1-4(Fuc alpha 1-3)GlcNAc beta 1-3Gal beta 1- 4Glc beta 1-1 ceramide. Enhanced expression of the Lex glycolipid may affect the organization of lens plasma membranes through Le(x)-Le(x) interactions, as suggested for compaction in mouse preimplantation embryos and embryonic teratocarcinomas, resulting in lens opacification, namely cataract.     

Tc(VII) reduction and accumulation by immobilized cells of Escherichia coli

Resting cells of Escherichia coli, immobilized in a flow-through bioreactor, coupled the oxidation of formate or hydrogen to Tc(VII) reduction and removal from solution. Cells, pregrown anaerobically in a hollow-fiber membrane bioreactor, were challenged with 50 muM Tc(VII) in a carrier solution of phosphate-buffered saline. The radionuclide accumulated within the membrane component of the reactor, corresponding to the localization of the cells. Negligible Tc removal was noted in a reactor containing a mutant deficient in active Tc(VII) reductase, when supplied with formate as an electron donor. Formate or hydrogen was supplied as the electron donor for Tc(VII) reduction to cells immobilized in reactors operated in transverse (crossflow) and direct (dead-end filtration) modes, respectively. Flow-rate activity relationships were used to compare the performance of the reactors. A flow rate of 2.4 mL h(-1) supported the removal of 50% of the Tc from solution in a reactor operated in transverse mode with formate as an electron donor. In contrast, a flow rate of 0.7 mL h(-1), supported comparable Tc removal when hydrogen was introduced to a reactor operated in direct mode. The reduced reactor efficiency, when hydrogen was used as an electron donor, could be attributed, in part, to poor delivery of the gas to the cells. The biocatalyst was highly stable in the reactor; no loss in activity was noted over 200 h of continuous use. (c) 1997 John Wiley & Sons Inc. Biotechnol Bioeng 55: 505-510, 1997.     

Decreased pCO(2) accumulation by eliminating bicarbonate addition to high cell-density cultures

High-density perfusion cultivation of mammalian cells can result in elevated bioreactor CO(2) partial pressure (pCO(2)), a condition that can negatively influence growth, metabolism, productivity, and protein glycosylation. For BHK cells in a perfusion culture at 20 x 10(6) cells/mL, the bioreactor pCO(2) exceeded 225 mm Hg with approximate contributions of 25% from cellular respiration, 35% from medium NaHCO(3), and 40% from NaHCO(3) added for pH control. Recognizing the limitations to the practicality of gas sparging for CO(2) removal in perfusion systems, a strategy based on CO(2) reduction at the source was investigated. The NaHCO(3) in the medium was replaced with a MOPS-Histidine buffer, while Na(2)CO(3) replaced NaHCO(3) for pH control. These changes resulted in 63-70% pCO(2) reductions in multiple 15 L perfusion bioreactors, and were reproducible at the manufacturing-scale. Bioreactor pCO(2) values after these modifications were in the 68-85 mm Hg range, pCO(2) reductions consistent with those theoretically expected. Low bioreactor pCO(2) was accompanied by both 68-123% increased growth rates and 58-92% increased specific productivity. Bioreactor pCO(2) reduction and the resulting positive implications for cell growth and productivity were brought about by process changes that were readily implemented and robust. This philosophy of pCO(2) reduction at the source through medium and base modification should be readily applicable to large-scale fed-batch cultivation of mammalian cells.     

Excessive aluminium accumulation in the pea mutant E107 (brz)

E107 is a pleiotropic mutant of peaPisum sativum cv. ‘Sparkle’, characterized by forming few nodules and developing bronze necrotic spots on older leaves. The mutant accumulates Al and has symptoms typical of Al toxicity. The lateral roots of E107 are fewer (40%) and shorter (50%) than those of its parent. High concentrations of Al accumulate in E107 shoots (1000 mg kg^-1) and roots (3000 mg kg^-1), and three-week old E107 plants extrude 2.5 times more protons than ‘Sparkle’ plants of similar age. Al concentrations of the roots of the mutant and of its parent ‘Sparkle’ are similar for the first two weeks of growth. Thereafter they differ. In 2 week old plants Al continues to accumulate in excessive amounts in E107 primary and lateral roots whereas in ‘Sparkle’ roots, it reaches a plateau. In E107, Al is erratically distributed in the walls of root hairs and epidermal cells in both primary and lateral roots. Some of these cells have also Al in their nucleus.     

The accumulation and synthesis of betaine in winter skate (Leucoraja ocellata)

The present study investigated aspects of betaine metabolism in an elasmobranch fish, the winter skate (Leucoraja ocellata). Based on the level of choline dehydrogenase (ChoDH) activity, the liver and kidney appear to be the major sites of betaine synthesis and the mitochondrial localization of ChoDH and betaine aldehyde dehydrogenase (BADH) indicates that the metabolic organization of betaine synthesis in winter skate is similar to other vertebrates. Food deprivation did not affect white muscle betaine content, and prolonged starvation (70 days) appeared to decrease the total hepatic betaine synthetic capacity. There was no decrease in ChoDH or BADH activity at the mitochondrial level with starvation, suggesting any decrease is due to catabolism of hepatic reserves rather than downregulation of betaine synthesis. Skates fed a high betaine diet (frozen squid approximately 55 micromol g(-1)) had elevated white muscle betaine content compared to those fed a low betaine diet (frozen herring <2 micromol g(-1)); however, high dietary betaine intake did not affect the activity of betaine synthesizing enzymes in liver. Acclimation to elevated salinity (120 and 130% seawater) did not result in an increase in white muscle betaine content. Taken as a whole, the present data suggest that diet is a major determinant of muscle betaine in the winter skate and that betaine is of marginal importance as an intracellular osmolyte in this species.