Aspartate Transcarbamylase Activity Research Articles

Interannual fluctuations in spring pelagic ecosystem productivity in the Bay of Biscay (northeast Atlantic) measured by mesozooplankton aspartate transcarbamylase activity and relationships with anchovy population dynamics

The French part of the continental shelf of the Bay of Biscay (northeast Atlantic) is the habitat of an anchovy (Engraulis encrasicolus L.) population of scientific interest because of its economic importance and the trend towards greater interannual fluctuations in its abundance, particularly as a consequence of variations in recruitment. Each year a 1-month survey of this population and its pelagic environment is undertaken. Among the descriptors of ecosystem function characterized, mesozooplankton aspartate transcarbamylase (ATC) activity is measured with the goal of defining overall productivity of the mesozooplankton communities. Diverse physical forcing factors are responsible for the enhancement of productivity in the Bay of Biscay, and their respective influences vary at interannual scales. We present the results of ATC activity measurements carried out within the anchovy habitat during six consecutive breeding seasons (from 2000 to 2005). A strong correlation was found between mean ATC activity and variations in interannual biomass for the anchovy population (R=0.928; p<0.01). During the study period the anchovy population collapsed, and a particularly low level of ATC activity in the mesozooplankton preceded this event 1 year earlier. Conversely, an increase in anchovy abundance in the year following the collapse was preceded by a return to substantially higher levels of ATC activity. We hypothesize that this relationship may be robust and generally applicable. We speculate on the environmental descriptors necessary to confirm this result, in view of its potential application to the monitoring of this valuable fish population in the Bay of Biscay.

Biological productivity enhancement over a continental shelf break (Bay of Biscay, NE Atlantic) evidenced by mesozooplankton aspartate transcarbamylase activity

During spring 2005, satellite imagery revealed high sea surface chlorophyll a concentrations over the edge of a wide continental shelf in the Bay of Biscay (NE Atlantic). As a descriptor of biological productivity, mesozooplankton aspartate transcarbamylase specific activity was measured in situ during the bloom. Notably high values were detected in the bloom area relative to other parts of the study area.

Do river discharge rates drive the overall functioning of the pelagic ecosystem over the continental shelf of the Bay of Biscay (NE Atlantic)? A comparison of two contrasting years with special reference to anchovy (Engraulis encrasicolus L.) nutritional state

In the 2000 and 2001 springtime periods, mesozooplankton samples were systematically taken during research cruises devoted to the study of the distribution and abundance of small pelagic fishes in the French part of the Bay of Biscay, NE Atlantic, continental shelf. Simultaneous activities of three enzymes were measured in these mesozooplankton samples, to characterize the main features of ecosystem function at a regional scale. The aim was to assess assimilation rates of carbohydrates, through pyruvate kinase activity, and protein, through trypsin activity, by the mesozooplankton community and the resulting overall productivity, through aspartate transcarbamylase activity. The highest influence on the pelagic environment was the strong difference in the freshwater outflow rates from the two main large rivers, the Loire and the Gironde, which was principally responsible for the inter-annual fluctuations of the nutrients in the Bay. This overall influence of river flow results in a characteristic pattern of sea-surface salinity, which was reflected by the phytoplankton biomass distribution. Mesozooplankton enzyme activities showed high variations between the two years. The contrast in the dynamics of the pelagic food web processes between the two consecutive years, with higher activity in 2001, affected the nutritional condition of the zooplanktivorous breeding anchovy Engraulis encrasicolus.

Discoveries in Bacterial Nucleotide Metabolism

Discoveries in Bacterial Nucleotide Metabolism

Neuroendocrine disruption and health effects in Elliptio complanata mussels exposed to aeration lagoons for wastewater treatment

The purpose of this study was to examine neuroendocrine-disrupting effects of two domestic wastewater aeration lagoons on freshwater mussels. Mussels were caged and placed in two final aeration lagoons for treating domestic wastewaters for 60 days, at a site 1km downstream of the dispersion plume on the eastern shores of the Richelieu River; the western shore served as the reference site. The mussels were analysed for gonad activity, oxidative metabolism of xenobiotics, stress biomarkers and neuroendocrine status (monoamine and arachidonic acid metabolism). The domestic wastewaters produced many different effects at all levels examined. The gonado-somatic index and vitellogenin-like proteins were significantly induced in both aeration lagoons and gonad pyrimidine synthesis (aspartate transcarbamylase activity) was significantly reduced, indicating that vitellogenin-like proteins were produced while DNA synthesis in gametes remained constant. Biomarkers of oxidative metabolism revealed that global heme oxidase (HO), glutathione S-transferase and xanthine (caffeine) oxydoreductase (XOR) activities were significantly induced in at least one of the aeration lagoons, but not downstream of the dispersion plume. The activities of 7-ethoxyresorufin (cytochrome P4501A1), dibenzoylfluorescein (cytochrome P450 3A4 and 3A5) and benzoyloxyresorurufin (cytochrome P450 3A4 and 2B6) dealkylases were readily induced by substances sharing structural similarities with coplanar polyaromatic hydrocarbons and hydroxylated or aminated aromatic or cyclic hydrocarbon compounds such as pharmaceuticals or steroids in the domestic wastewaters. Biomarkers of toxic stress revealed that exposure to aeration lagoons led to increased production of metallothioneins, lipid peroxidation and DNA strand breaks, with decreased heme oxygenase activity. LPO was significantly correlated with XOR, HO and cytochrome P4501A1 activities. Neuroendocrine effects included significant increases in dopamine and serotonin levels and in monoamine oxidase (MAO). Dopamine transport in synaptosome was significantly increased while serotonin transport activity was significantly decreased, suggesting the mussels were in a state of serotonergicity. Moreover, arachidonic acid cyclooxygenase (COX) activity was also readily increased in one aeration lagoon. Aeration lagoons for the treatment of domestic wastewaters are toxic, estrogenic and disrupt the metabolism of monoamines and COX in freshwater mussels.

Health status of Mya arenaria bivalves collected from contaminated sites in Canada (Saguenay Fjord) and Denmark (Odense Fjord) during their reproductive period

The purpose of this study was to examine the health status and gametogenetic activity in Mya arenaria clams collected at various sites in the St. Lawrence Estuary (Quebec, Canada) and in the Odense Fjord (Denmark). Clam soft tissues were analyzed for metals/metalloids and organotin compounds to confirm their exposure to these contaminants. Their health status was assessed by a test battery of biomarkers designed to measure the early biological effects of contaminants, which include expression of defence mechanisms such as xenobiotic conjugation (glutathione S-transferase), expression of stress proteins (i.e., heme oxygenase and metallothioneins), changes in gametogenetic activity, and individual morphometric characteristics. Clam tissues were also examined for the presence of oxidative damage to lipids, formation of DNA strand breaks, and alterations in heme metabolism. The results showed that clams sampled from sites with either ferry activity or intensive boat traffic in marinas were contaminated by metals/metalloids such as Ag, Al, As, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sn, V, and Zn. The clams also contained relatively high amounts of tributyltin (TBT) in their tissues (in the ng TBT/g range for both areas), with digestive glands containing more organotins than did gonadal tissues. Moreover, clams collected from TBT-contaminated sites had higher amounts of tin–heme adducts and lower total heme in their digestive glands. Condition factor, age distribution, and sex ratio were significantly altered in clams from impacted sites in the Saguenay Fjord and accompanied by an increased male/female sex ratio. Gametogenetic activity was also negatively affected, as revealed by reductions in gonadosomatic index, maturation index, aspartate transcarbamylase activity, and vitellogenin-like proteins. The Saguenay Fjord clams displayed a complex pattern of stress responses and damage such as increased heme oxygenase activity, phase 2 conjugation enzyme activity, lipid peroxidation, and altered DNA strand breaks. The integration of biomarker response data into a biomarker index at the whole-individual level (morphometric characteristics) and for various organs (gill, digestive gland, and gonad) revealed that, relative to the control site, morphological characteristics and gonadal activity were most affected at the most contaminated site, while the effects were more pronounced in the digestive gland and gill at moderately impacted sites. We conclude that the health status of M. arenaria clams at these contaminated sites is compromised, with obvious disruption of reproductive activity.

Sexual maturation and related changes in aspartate transcarbamylase activity of gonad tissues in the soft shell clam ( Mya arenaria)

The information on the relation between the gonadal aspartate transcarbamylase (ACTase) activity and the sexual maturation in molluscs is very fragmentary and is still absent in Mya arenaria. The determination of ATCase activity, energy reserves levels and maturation stages were done in gonads of clams. Results showed that the seasonal cycle of storage and utilization of energy reserves in gonads of clams are linked to the bimodal reproduction well known in this bivalve. ATCase activity was high in clams at development and ripe stages, while this activity was low for individuals found in indifferent, spawning or spent stages. This difference can be explained by the fact that during gonad development, gonadal synthetic activity increased following the mitotic events associated to the reproductive cycle. The results presented in this paper have confirmed the link between ATCase activity and gametogenesis in M. arenaria. Further work should be realized in order to assess if ATCase activity could be considered as a potential biomarker to evaluate the disruption of sexual maturation in clams collected in sites such as the St. Lawrence estuary.

Characterization of aspartate transcarbamylase activity from gonads of the soft shell clam, Mya arenaria

Aspartate transcarbamylase (ATCase, EC 2.1.3.2) has been shown to be a good index of the reproductive cycle in marine molluscs. However, this enzyme has never been studied in the soft shell clam Mya arenaria. The characteristics of gonadal ATCase of the soft shell clam, Mya arenaria were therefore determined since we need powerful tools to assess the degree of effects of endocrine disruptors in this species at risk. Enzyme kinetic values observed at pH 8.3 were significantly lower than those measured at pH 9.4. The optimal conditions for the enzyme assays were reached in the presence of a 10 mM of substrate concentration and at pH 9.2 for 60 min at 37 °C. We have found that the enzyme was heat sensitive, markedly activated by DMSO and DMF, but no effect was observed with ethanol, ATP or CTP. However, clam ATCase activity was partly inhibited by the addition of CuSO 4 and PHMB to the medium, an inhibition that could be attributed to the presence of SH sites in cysteine residues localized in the catalytic site of this enzyme. All these results will be very useful in the near future to study the gametogenetic process of Mya arenaria, since little is known about the factors that control the physiological process of reproduction in this bivalve of ecological and economic importance. Studies of variations of the activity of aspartate transcarbamylase will also be useful as a potential biomarker to evaluate the disruption of gametogenesis in clams exposed to endocrine disruptors in situ.

Overexpression of the 18 kDa and 22/24 kDa FGF-2 isoforms results in differential drug resistance and amplification potential.

We investigated the role of low molecular weight (LMW) and high molecular weight (HMW) isoforms of basic fibroblast growth factor 2 (FGF-2) in the expression of transformation-related phenotypic alterations, drug sensitivity modulation, and gene amplification potential. For this purpose, we used NIH 3T3 and A31 cells transfected with different cDNA FGF-2 constructs allowing expression of the different proteins. Both cell lines showed marked phenotypic alterations when expressing the LMW FGF-2 or the four HMW FGF-2 isoforms: they acquired a transformed morphology, grew at higher saturation densities in 10% serum, and exhibited anchorage-independent growth and increased invasive potential. However, HMW FGF-2-expressing cells also grew in 1% serum and their invasive potential was lower than in cells expressing all FGF-2 forms or LMW FGF-2 alone. We have grown the different cell lines under a selective pressure of N-(phosphonacetyl)-l-aspartate (PALA), a drug which specifically inhibits the aspartate transcarbamylase activity of the multifunctional carbamyl-P-synthetase/aspartate transcarbamylase/dihydro-orotase genes (CAD) enzyme (and thus inhibits de novo pyrimidine biosynthesis) and selects for cells with amplified copies of the CAD gene. Our results demonstrate that aberrant expression of the LMW FGF-2 and/or HMW FGF-2 isoforms differently modulates drug resistance and gene amplification properties in the NIH 3T3 and A31 cell lines by differential amplification of the CAD gene. Coexpression of all isoforms appears to be necessary to obtain cumulative effects and nuclear-targeted HMW FGF-2 has a pivotal role in such a cooperation.

Biomass and potential feeding, respiration and growth of zooplankton in the Bransfield Strait (Antarctic Peninsula) during austral summer

Biomass (as dry weight and protein content), gut fluorescence, electron transfer system (ETS) and aspartate transcarbamylase (ATC) activities were studied in different size fractions (200–500, 500–1000 μm and 1–14 mm) in the Bransfield Strait (Antarctic Peninsula) during January 1993. Very low values of zooplankton biomass were observed in all the size classes studied. About 56% of total biomass was due to the large size fraction (1–14 mm) while the smallest one (200–500 μm) accounted for about 26%. Gut fluorescence values increased in relation to the size class considered, as expected, being the differences from the smaller to the highest size fractions of orders of magnitude. Calculated ingestion rates showed that about 60–80% of total zooplankton ingestion (<14 mm) was due to the smaller organisms. Higher average values and higher variability of specific ETS activity was observed in the smaller size fraction while no differences between size classes were observed for the specific ATC activity. Biomass, gut fluorescence, ETS and ATC activities were not significantly different between the Bellingshausen and Weddell waters, although higher standard deviation was normally found at the former area. With the restrictions of using the above indices to estimate physiological rates, potential grazing of mesozooplankton (<14 mm) accounted for a rather low portion (<10%) of the primary production. The index of growth showed high values, suggesting no food limitation of mesozooplankton. Therefore, other processes such as predation should account for the very low biomass found and for the fate of a large portion of primary production.

Biochemical indices for instantaneous growth estimation in young cephalopod Sepia officinalisL.

Aspartate transcarbamylase (ATCase) activity was used to estimate instantaneous growth in young cuttlefish (Sepia officinalis) reared under different diet conditions, and compared with estimation obtained by RNA concentration. During the first month of life, the changes in ATCase activity and RNA content of muscle are related to growth. ATCase appears to be a good index of growth during the first stage of intense cell multiplication. ATCase activity is correlated to food intake up to a maximum ration, but decreases when animals are more than 40 days old. The approach of using ATCase activity as a biochemical index for estimating short-term change in growth rates of young cuttlefish in experimental rearing could be extended to young cephalopods collected in the field, and used to predict the effect of biotic factors in recruitment.

Sources of seasonal variability in mesozooplankton aspartate transcarbamylase activity in coastal waters off Plymouth, UK

Some investigators have proposed aspartate transcarbamylase (ATCase) activity as an overall index of mesozooplankton productivity. However, seasonal changes in mesozooplankton species composition have never been investigated as a possible source of variation in ATCase activity. In this study, we investigate mesozooplankton composition in terms of (i) developmental stages, (ii) species and developmental stages body mass and (iii) species composition, and their relationship to ATCase activity. In controlled laboratory conditions, ATCase activity variability was closely related to changes in somatic growth rate of the copepod Calanus helgolandicus, but was not related to changes in nucleic acid concentrations. It can be argued, however, that the activity of this enzyme is partially involved in copepod somatic productivity, and should be a good index of embryogenesis. In addition, changes in ATCase activity were not significantly influenced by variability in mesozooplankton biomass, when investigated both on inter- and intraspecific levels. Finally, when a complete seasonal cycle was investigated at a fixed station off Plymouth (English Channel), ATCase activity was not correlated with the abundance of any mesozooplankton species apart from copepodites and adult C.helgolandicus. Furthermore, ATCase activity measured both on mesozooplankton and female C.helgolandicus was significantly correlated (R2 = 0.72, n = 33, P < 0.001) throughout the year, apart from April. At that particular time of the year, ATCase activity was in phase with the peak of abundance of copepod eggs and nauplii. It is suggested that mesozooplankton peaks of ATCase activity reflect two periods in the life history of the copepod: embryogenesis and terminal moult. We propose further experiments to test this hypothesis and to promote the development of molecular biomarkers in order to characterize specific zooplankton metabolic processes.

ATCase activity, RNA:DNA ratio, gonad development stage, and egg production in the female copepod Calanus helgolandicus

Some investigators have proposed the measurement of aspartate transcarbamylase (ATCase) activity as a suitable technique for estimating zooplankton productivity. However, this technique has never been comprehensively evaluated under controlled laboratory conditions nor compared extensively with other productivity techniques in the field. This paper describes such an evaluation, using the reproduction of the calanoid copepod Calanus helgolandicus as an index of germinal growth, an important aspect of zooplankton productivity. ATCase activity and RNA:DNA ratio both increased significantly with increasing gonad maturation. In addition, ATCase activity in females responded immediately to changing food conditions, whilst changes in egg production lagged behind by ≃24 h. Shifting the ATCase data by 24 h revealed a significant and positive correlation of ATCase activity with egg production. However, in well-fed females, ATCase activity assayed at constant temperature was apparently independent of environmental temperature conditions, whilst egg production was temperature-dependent. In the field, ATCase activity was significantly correlated with egg production only in autumn and winter; when a complete seasonal cycle was considered, no correlation was found between the two measurements. These findings suggest that ATCase is involved partially in either germinal growth and/or in other biosynthetic processes of female C. helgolandicus; thus, ATCase activity does not reflect copepod egg-production with any certainty.

Structural and transcriptional analysis of the pyrABCN, pyrD and pyrF genes in Aspergillus nidulans and the evolutionary origin of fungal dihydroorotases.

The six biochemical steps of the de novo pyrimidine biosynthesis pathway are conserved in all known organisms. However, in animals and fungi, unlike prokaryotes, at least the first two activities are grouped on a multifunctional enzyme. Here, we report cloning, mapping and transcriptional characterization of some pyrimidine biosynthesis genes in the filamentous fungus Aspergillus nidulans. The first two steps of the pathway are performed by a multifunctional enzyme comprising the activities of carbamoyl phosphate synthetase (CPSase) and aspartate transcarbamylase (ATCase). This polypeptide is encoded by a 7 kbp cluster gene, pyrABCN, which has a high degree of nucleotide identity with the Ura2 gene in Saccharomyces cerevisiae. The enzyme of the third step, dihydroorotase (DHOase), is encoded by a separate locus, pyrD. However, the pyrABCN gene apparently contains an evolutionary remnant of a DHOase-encoding sequence, similarly to the Ura2 gene of Saccharomyces cerevisiae. The pyrABCN gene is transcribed as a single 7 kb mRNA species. The level of transcripts of pyrABCN, pyrD and, to a lesser degree, pyrF genes responds to the presence of exogenous pyrimidines and to the conditions of pyrimidine starvation. Derepression of pyrABCN and pyrD under pyrimidine starvation is noticeably enhanced in pyrE mutants that accumulate dihydroorotic acid. The pyrABCN gene maps to the distal portion of the right arm of the chromosome VIII, whereas the pyrD gene, in contrast to early genetic data, is closely linked to the brlA gene and located to the right of it. Our data on mitotic recombination should help to verify the genetic map of the chromosome VIII. Comparison of amino acid sequences of active dihydroorotases with related enzymes and with their non-functional homologues in yeast and Aspergillus indicates that the active dihydroorotases from fungi are more similar to ureases and enzymes of the pyrimidine degradation pathway. The 'silent' dihydroorotase domains of the multifunctional enzymes from fungi and active DHOase domains of the multifunctional enzymes in higher eukaryotes are more closely related to bacterial dehydroorotases.

Food intake and growth in reared early juvenile cuttlefish Sepia officinalis L. (Mollusca Cephalopoda)

Abstract Experimental rearing of juvenile cuttlefish was carried out in a semi-closed system for 40 days at 19°C. Different quantities of live food were offered to isolated animals. The actual ingestion rate was enhanced by the amount of food offered, this tendency decreasing with age. Frozen food was ingested at the same rate, but was less effective than live food for growth. The quantity of food ingested during the first 20–30 days of life seems to affect further growth, especially weight increase. Aspartate transcarbamylase activity appeared to be a good indicator for the early phase of growth (first 20–30 days) which is likely due to hyperplasy, and moreover for predicting future growth.

Large-Scale and Mesoscale Distribution of Plankton Biomass and Metabolic Activity in the Northeastern Central Atlantic

Plankton biomass and indices of metabolism and growth [electron transport system (ETS), glutamate dehydrogenase (GDH) and aspartate transcarbamylase (ATC) activities] were studied over a 2,800 km east-west section of the tropical North Atlantic Ocean (21°N) in ;500 µm size classes. On the large-scale, zooplankton (>;200 µm) enzymatic activities increased westward in the study section, where large cyanobacteria chains (Trichodesmium spp.) were observed. Parallel to it, an increase in medium calanoids (1–2 mm length) was observed towards the western part of the transect, whereas small calanoids (<1 mm) were dominant throughout the boundary area of the subtropical gyre. Microplankton ETS and mesoplankton ETS and ATC activities seemed to match the wave length of low frequency waves. Our results suggest that such waves are related to the observed enhancement of metabolic activity of micro- and mesoplankton. The large-scale and mesoscale variability observed give evidence of the inadequacy of assuming a steady-state picture of the euphotic zone of tropical and subtropical waters.

Cerium-based ultracytochemical localization of aspartate transcarbamylase activity in the cell membrane complex of Saccharomyces cerevisiae

Aspartate transcarbamylase (ATCase) activity was localized ultracytochemically in the yeast Saccharomyces cerevisiae by precipitation of its reaction product orthophosphate as cerium phosphate. We prefixed yeast cells with ice-cold 1% glutaraldehyde for 30 min which preserved 80% of ATCase activity. Cells were washed and incubated with ATCase substrates (aspartate, carbamyl phosphate) plus cerium chloride, and postfixed by osmium tetroxide. In cells from exponential batch cultures, deposits of cerium phosphate delineated simultaneously or alternatively membranes of the secretory pathway: nuclear envelope, endoplasmic reticulum, Golgi complex and the plasmalemma; mitochondrial membranes and intramitochondrial fibrous component were labelled as well. Deposits of cerium phosphate were never observed in the nucleoplasm. Cells incubated in the absence of cerium or ATCase substrates and mutant S. cerevisiae cells lacking ATCase activity served as controls. Small round electron-dense condensates were found to be randomly distributed within some cells, both in control and experimental runs, in the nucleoplasm, cytoplasm and mitochondrial matrix and represented undefined osmicated endogenous compounds. Our results suggest that the synthesis of pyrimidine precursors occurs in membranes, where compounds such as UDP-glucose and CDP-diglycerides are needed for membrane and/or yeast cell wall synthesis. The possible contribution of ATCase activity found in the nuclear envelope to nucleic acid synthesis remains to be clarified.

Multiple mechanisms of N-phosphonacetyl-L-aspartate resistance in human cell lines: carbamyl-P synthetase/aspartate transcarbamylase/dihydro-orotase gene amplification is frequent only when chromosome 2 is rearranged.

Rodent cells resistant to N-phosphonacetyl-L-aspartate (PALA) invariably contain amplified carbamyl-P synthetase/aspartate transcarbamylase/dihydro-orotase (CAD) genes, usually in widely spaced tandem arrays present as extensions of the same chromosome arm that carries a single copy of CAD in normal cells. In contrast, amplification of CAD is very infrequent in several human tumor cell lines. Cell lines with minimal chromosomal rearrangement and with unrearranged copies of chromosome 2 rarely develop intrachromosomal amplifications of CAD. These cells frequently become resistant to PALA through a mechanism that increases the aspartate transcarbamylase activity with no increase in CAD copy number, or they obtain one extra copy of CAD by forming an isochromosome 2p or by retaining an extra copy of chromosome 2. In cells with multiple chromosomal aberrations and rearranged copies of chromosome 2, amplification of CAD as tandem arrays from rearranged chromosomes is the most frequent mechanism of PALA resistance. All of these different mechanisms of PALA resistance are blocked in normal human fibroblasts.

A Continuous Spectrophotometric Assay for Aspartate Transcarbamylase and ATPases

A new continuous coupled uv-spectrophotometric assay is described for two phosphate-releasing enzymes, aspartate transcarbamylase and ATPase of herpes simplex virus (HSV). Phosphate release is coupled to the phosphorolysis of the nucleoside analog 7-methylinosine (m7Ino) catalyzed by purine nucleoside phosphorylase. When this reaction is monitored at 291 nm, the coupled assay can readily detect 10 nmol Pireleased/min. Our method offers advantages over a recently reported continuous assay devised for measuring aspartate transcarbamylase activity using the nucleoside analog methylthioguanosine (MESG) as the linking substrate. In contrast to MESG, m7Ino is easily and inexpensively synthesized and is also commercially available. The spectrophotometric signal at 291 nm, produced by the difference in the extinction coefficients between nucleoside substrate and the base product, is significant over a much wider pH range than the signal difference between MESG and its phosphorolysis product at 360 nm. Saturation curves for aspartate and carbamyl phosphate and pH rate profiles have been reproduced using the purine nucleoside phosphorylase/m7Ino coupled assay. Initial velocity patterns constructed over micromolar to millimolar concentrations of aspartate and carbamyl phosphate yielded four kinetic parameters simultaneously. To further illustrate the application of this coupled assay, kinetic parameters were determined for the DNA-dependent ATPase reaction of HSV helicase–primase.

Aspartate transcarbamylase activity for the assessment of mesozooplankton production: New aspects from oceanic areas

Aspartate transcarbamylase activity for the assessment of mesozooplankton production: New aspects from oceanic areas