Dependence of the early steps of chlorophyll(ide) synthesis on respiration in dark-grown Euglena gracilis

Protochlorophyll(ide) disappearance and chlorophyll(ide) accumulation, in dark-grown Euglena, promoted by series of actinic light flashes, have been followed by in vivo fluorescence measurements. The data show that chlorophyll(ide) accumulation is biphasic, i.e., there is an initial rapid phase followed by a slower linear phase. The linear phase is highly dependent on flash frequency and on cell respiration whereas the initial phase is much less affected by these factors. It is concluded that dark-grown cells contain a limited pool of phototransformable protochlorophyll(ide); once this pool is exhausted, its reformation and/or the synthesis of some unknown metabolite necessary for the photoreduction appears to be dependent on respiration.     

Studies on polyamine biosynthesis in Euglena gracilis.

Euglene gracilis (strain Z) was found to contain five polyamines which could be separated by high-pressure cation-exchange chromatography. 1,3-Diaminopropane, putrescine, norspermidine (N-(3-aminopropyl)-1,3-diaminopropane), spermidine and norspermine (N,N'-bis(aminopropyl)-1,3-diaminopropane) were identified. Biosynthesis of putrescine in E. gracilis proceeds through decarboxylation of L-ornithine, no arginine decarboxylase (EC 4.1.1.19) activity could be detected. The properties of the enzymes ornithine decarboxylase (EC 4.1.1.17) and S-adenosylmethionine decarboxylase (EC 4.1.1.50) in this alga were found to be similar to those of the enzymes isolated from animal tissues or yeast cells. A bioxynthetic scheme is proposed which relates the different polyamines occurring in E. gracilis.     

Fatty acid synthesis in mitochondria of Euglena gracilis

A malonyl-CoA-independent fatty acid synthetic system, different from the systems in other subcellular fractions, occurred in mitochondria of Euglena gracilis. The system had ability to synthesize fatty acids directly from acetyl-CoA as both primer and C2 donor using NADH as an electron donor. Fatty acids were synthesized by reversal of beta-oxidation with the exception that enoyl-CoA reductase functioned instead of acyl-CoA dehydrogenase in degradation system. A fairly high activity of enoyl-CoA reductase was found on various enoyl-CoA substrates (C4-C12) with NADH or NADPH. Three species of enoyl-CoA reductase, distinct from each other by their chain-length specificity, were found in Euglena mitochondria, and one of them was highly specific for crotonyl-CoA. It is also discussed that the mitochondrial fatty-acid synthetic system contributes to wax ester fermentation, the anaerobic energy-generating system found in the organism.     

Studies on uroporphyrinogen decarboxylase of etiolated Euglena gracilis Z

1. A 423-fold purified fraction of uroporphyrinogen decarboxylase (EC 4.1.1.37) showing a specific activity of 770 units/mg protein has been employed in order to study some properties in etiolated Euglena gracilis Z. 2. Uroporphyrinogen decarboxylase has a relative molecular mass of 54,000, an optimum pH of 7.2 and exhibits Michaelis-Menten kinetics, employing both uroporphyrinogen I and uroporphyrinogen III as substrates. 3. Anaerobic conditions seem not to be necessary for uroporphyrinogen decarboxylase activity. Neither EDTA nor cysteine affected enzyme activity, whereas dithiothreitol produced a remarkable activation of coproporphyrinogen formation. 4. Kinetic data employing both substrates showed an accumulation of porphyrinogen (i.e. hexa- and hepta-porphyrin) containing six or seven COOH groups, depending on the uroporphyrinogen concentration used. 5. An unusual elution profile of the intermediates on Sephacryl S-200 was found.     

Studies on the isolation and purification of chloroplasts from Euglena gracilis

Summary A method has been developed for the isolation of chloroplasts from Euglena gracilis grown under mixotrophic conditions. This method utilizes sucrose density-gradient centrifugation in the AXII zonal rotor and allows the rapid preparation of large amounts of chloroplasts free from contaminating whole cells and other cytoplasmic materials. The majority of the isolated chloroplasts appear intact in phase contrast and electron micrographs. The purified chloroplast fraction contains DNA, the major species of which has a density of 1.682 g/cm³. The species of DNA having a density of 1.707 g/cm³ seemed to result from the presence of contaminating nuclear fragments which could be removed by isopycnic flotation.This research was supported in part by a grant from USPHS No. AM-07189 (to J. M. E.), American Cancer Society Fellowship No. PF-443 (to J.F.P.) and grant No. 2972E06 from the Office of Sponsored Research, University of Florida (to J.F.P.). Univ. of Fla. Agr. Exp. Stat. No. 4538.     

Changes in chlorophyll a fluorescence in Euglena gracilis and Chlamydomonas reinhardtii after exposure to wood-ash

Recycling of wood-ash to boreal forests has been suggested to prevent depletion of essential soil nutrient or reduce the negative effects of acidification of surface waters. The aim of this investigation was to study the effects of different concentrations of wood-ash (5, 10 and 12.5 g l⁻¹ diluted in cultivating medium) on chlorophyll a fluorescence in Euglena gracilis and Chlamydomonas reinhardtii under laboratory conditions. The green alga C. reinhardtii was more susceptible to wood-ash solutions than the flagellate E. gracilis. Two different forms of wood-ash solutions were tested. In the first solution no adjustment of pH was made and after 7 days of incubation with wood-ash the pH for the different wood-ash concentrations (5, 10 and 12.5 g l⁻¹) were 8, 9 and 11, respectively. In the second solution, the pH was adjusted to 7. The results show that no negative effect on fluorescence yield (F_v/F_m), relative electron transport rate (ETR), photochemical quenching (qP) or non-photochemical quenching (NPQ) was observed in E. gracilis. In contrast, C. reinhardtii displayed strong inhibition at concentrations of 10 and 12.5 g l⁻¹ with non-adjusted pH. The negative effects of high pH on photochemical activity in C. reinhardtii could either be related to (1) the destruction of the ΔpH across the thylakoid membranes or (2) other parts in the photosynthetic systems that are negatively affected by changing pH. The results indicate that elevated pH levels due to wood-ash application could be an environmental stress factor to phytoplankton communities and may lead to loss of diversity among primary producers in aquatic ecosystems. If wood-ash application was to become general practice in or near aquatic ecosystems a rapid change in pH induced by wood-ash must be avoided.     

Isolation and characterisation of a cDNA clone for a chlorophyll synthesis enzyme from Euglena gracilis. The chloroplast enzyme hydroxymethylbilane synthase (porphobilinogen deaminase) is synthesised with a very long transit peptide in Euglena

A cDNA expression library was constructed from light-grown Euglena gracilis poly(A)-rich RNA in lambda gt11. Antibodies to Euglena hydroxymethylbilane synthase, the third enzyme in the porphyrin biosynthetic pathway, were used to screen the library and a clone encoding part of the sequence of hydroxymethylbilane synthase was identified. This was used to rescreen the library and a full-length clone was isolated, which encoded not only the entire mature protein (Mr 36,927), but also an N-terminal extension of 139 amino acids. The deduced Mr of the whole polypeptide is 51,744, which corresponds to the size of the protein immunoprecipitated from the translation products of Euglena poly(A)-rich RNA. The mature protein is 60-70% similar to hydroxymethylbilane synthase from human erythrocytes and Escherichia coli. The sequence of the N-terminal extension has similarities to both the transit peptides of chloroplast proteins and those for the endoplasmic reticulum. This is the first report both of a cDNA clone for an enzyme of the chlorophyll biosynthetic pathway and of a putative transit peptide for a nuclear-encoded Euglena protein.     

Culture cycle dependence of folate interconversion and related enzymes in Euglena gracilis

Folates are involved in one-carbon metabolism in which one-carbon groups of increasing reduction state (formyl, methylene and methyl) are cyclically accepted and donated by the coenzyme form of folic acid, tetrahydrofolic acid. The latter originates by reduction of dihydrofolic acid, the coenzymatically inactive form. Euglena culture cycle dependence of folate distribution in oxidized, formyl and methyl forms and of enzyme activities for folate interconversion were studied. Distribution levels of all the components examined varied widely during the culture, and many of these changes occurred in the logarithmic phase of growth. In the phase of folate synthesis, there was an appreciable delay in the conversion of oxidized to reduced forms and of formyl to methyl forms. This delay appeared to be correlated with the level of corresponding enzymes. The methyl folate peak coincided with the highest level of total cell folates, at which point a severe repression of folate synthesis began. During the last phase of exponential growth, when cell folate content was reduced to one-fifth and folates had shorter glutamate chains, the level of coenzymatically inactive and inhibitory oxidized forms increased again. The reduced efficiency of the system and the change in growth rate are discussed. The activity patterns of dihydrofolate reductase and methylene tetrahydrofolate reductase were markedly different. The peak in methylene tetrahydrofolate reductase activity coincided with the absence of oxidized folates. A regulation of folate synthesis by the level of methyl folates and of methylene tetrahydrofolate reductase synthesis by the level of oxidized forms is proposed.     

Biosynthetic events required for lag elimination in chlorophyll synthesis in Euglena

Summary Levulinic acid, a competitive inhibitor of aminolevulinic acid dehydratase, cycloheximide, an inhibitor of translation on 89s cytoplasmic ribosomes, and chloramphenicol, an inhibitor of translation on 68s chloroplast ribosomes, are reversible inhibitors of light induced chlorophyll synthesis in resting Euglena gracilis Klebs. When dark grown resting cells are preilluminated for 2 h followed by darkness for 12 h prior to exposure to continuous light, the usual lag period in chlorophyll formation is eliminated. If cycloheximide, chloramphenicol, or levulinic acid are present during either the preillumination period or the subsequent dark period, the lag is reestablished. Only the very beginning of the dark period is sensitive to cycloheximide but the dark period is less sensitive to levulinic acid than is the light period. Exposure of preilluminated cells to cycloheximide or levulinic acid at the time of exposure to continuous illumination completely inhibits chlorophyll synthesis indicating that the potential for rapid chlorophyll synthesis generated by preillumination and a dark period does not result simply from the accumulation of porphyrin precursors. Preillumination has little effect on the development of the capacity to fix CO₂ photosynthetically. These results indicate that the control of chlorophyll formation is more complex than in higher plants and a model based on the formation of certain crucial enzymes in the porphyrin pathway, rather than simply upon the accumulation of aminolevulinic acid is presented to explain the experimental findings.Abbreviations ALA delta amino levulinic acid - CAM chloramphenicol - CEX cycloheximide - chl (ide) chlorophyll (ide) - LEV levulinic acid - pchl (ide) protochlorophyll (ide) Supported by GM14595 from the National Institutes of Health. This paper is No. 9 in the series, Events Surrounding the Early Development of Euglena ChloroplastsMicrobiology Trainee of the National Institutes of Health, Grant No. GM1586. The material in this paper is part of a dissertation submitted by S.D.S. to the Graduate Faculty of Brandeis University in partial fulfillment of the requirements for the Ph.D. Degree.