Glycine cleavage and generation of one-carbon units in Euglena gracilis

Euglena gracilis Klebs (strain Z) was maintained in division synchronized autotrophic culture, receiving either air (low CO₂) or 5% CO₂ in     

Generation of one-carbon units in methionine-supplemented Euglena cells

The possible effect of L-methionine supplements on the folate metabolism of division-synchronized Euglena gracilis (strain Z) cells has been examined. Cells receiving 1 mM L-methionine for four cell cycles were examined for folate derivatives, prior to and during cell division. Before cell division, methionine-supplemented cells contained less formylfolate but more methylfolate than unsupplemented cells. During division, both types of folates were present in lower concentrations in the supplemented cells. Growth in methionine for 10 and 34 hr also increased the levels of free aspartate, threonine, serine, cysteine and methionine relative to the controls. Methionine-supplemented cells contained ca 50% of the 10-formyltetrahydrofolate synthetase (EC 6.3.4.3) activity per cell of unsupplemented control cultures and specific enzyme activity was reduced ca 90%. Supplemented cells contained almost twice as much serine hydroxymethyltransferase (EC 2.1.2.1) activity per cell but comparable levels of glycollate dehydrogenase. Growth in methionine also reduced the incorporation of formate-¹⁴C] into serine, RNA, DNA, adenine and protein methionine. In contrast, incorporation of glycine-[2-¹⁴C] and serine-[3-¹⁴C] into folate-related products was not greatly altered by this treatment. Levels of radioactivity in these products suggested that formate was a more important C₁ unit source than glycine or serine when growth occurred in unsupplemented medium. It is concluded that methionine reduces formylfolate production by an effect on the cellular levels of formyltetrahydrofolate synthetase.     

ULTRASTRUCTURE OF PHACUS TRYPANON (EUGLENOPHYCEAE) WITH AN EMPHASIS ON STRIATED FIBER AND MICROTUBULE ARRANGEMENT

Phacus trypanon Pochmann is a photosynthetic euglenoid that is known to have typical characteristics of the Euglenales. The ultrastructure of P. trypanon was examined with particular attention being given to the striated fibers of both the basal body complex and feeding apparatus and microtubule arrangement. As in other euglenoids, the basal body complex was associated with the striated and fibrous fibers. The singlet microtubules at the reservoir level were arranged into doublets by a successive linkage of the existing adjacent microtubules at the transition level, and doublets were rearranged into a three-over-two pattern of cytoskeletal microtubules that were continuous with the subpellicular microtubules. The most striking feature of the feeding apparatus of P. trypanon was the prominent striated fiber that originated from the reservoir membrane and became arc shaped with electron-opaque bands at the lower canal level. The reinforcing microtubular band (MTR)/pocket of P. trypanon was associated with a prominent striated fiber that may act as a nucleating site for the semicircular microtubules, which surround the canal. The striated fiber and MTR/pocket are usually only found in those taxa that have a well-developed feeding apparatus and lack plastids; therefore, we speculate that the ingestion apparatus is functional in P. trypanon , which likely diverged in the early history of the photosynthetic green euglenoids.     

PHYLOGENY OF THE EUGLENALES INFERRED FROM PLASTID LSU rDNA SEQUENCES1

To gain insights into the phylogeny of the Euglenales, we analyzed the plastid LSU rDNA sequences from 101 strains of the photosynthetic euglenoids belonging to nine ingroup genera (Euglena, Trachelomonas, Strombomonas, Monomorphina, Cryptoglena, Colacium, Discoplastis, Phacus, and Lepocinclis) and two outgroup genera (Eutreptia and Eutreptiella). Bayesian and maximum‐likelihood (ML) analyses resulted in trees of similar topologies and four major clades: a Phacus and Lepocinclis clade; a Colacium clade; a Trachelomonas, Strombomonas, Monomorphina, and Cryptoglena clade; and a Euglena clade. The Phacus and Lepocinclis clade was the sister group of all other euglenalian genera, followed by Discoplastis spathirhyncha (Skuja) Triemer and the Colacium clade, respectively, which was inconsistent with their placement based on nuclear rDNA genes. The Trachelomonas, Strombomonas, Monomorphina, and Cryptoglena clade was sister to the Euglena clade. The loricate genera, Trachelomonas and Strombomonas, were closely related to each other, while Monomorphina and Cryptoglena also grouped together. The Euglena clade formed a monophyletic lineage comprising most species from taxa formerly allocated to the subgenera Calliglena and Euglena. However, within this genus, none of the subgenera was monophyletic.     

TETREUTREPTIA POMQUETENSIS GEN. ET SP. NOV. (EUGLENOPHYCEAE): A QUADRIFLAGELLATE,PHOTOTROPHIC MARINE EUGLENOID1

A new euglenoid genus and species, Tetreutreptia pomquetensis, is described from winter waters of Maritime Canada. This phototrophic species is characterized by four emergent heterodynamic flagella, two about the length of the cell and two less than one-half this length. Tetreutreptia pomquetensis has features in common with species of Eutreptiella while it differs in several respects from any of the described species of that genus. It could be assigned to the order Eutreptiales or Euglenamorphales sensu Leedale or the order Euglenales sensu Farmer. This new alga has a narrow range of temperature tolerance; it grows best from 0° to 7° C and dies at temperatures above 10° C. The optimum salinity for growth was near full-strength seawater. Growth conditions for the alga define the conditions whence this species was isolated.     

MULTIGENE ANALYSES OF PHOTOSYNTHETIC EUGLENOIDS AND NEW FAMILY,PHACACEAE (EUGLENALES)1

Bayesian and maximum‐likelihood (ML) analyses of the combined multigene data (nuclear SSU rDNA, and plastid SSU and LSU rDNA) were conducted to evaluate the phylogeny of photosynthetic euglenoids. The combined data set consisted of 108 strains of photosynthetic euglenoids including a colorless sister taxon. Bayesian and ML analyses recovered trees of almost identical topology. The results indicated that photosynthetic euglenoids were divided into two major clades, the Euglenaceae clade (Euglena, Euglenaria, Trachelomonas, Strombomonas, Monomorphina, Cryptoglena, Colacium) and the Phacaceae clade (Phacus, Lepocinclis, Discoplastis). The Euglenaceae clade was monophyletic with high support and subdivided into four main clades: the Colacium, the Strombomonas and Trachelomonas, the Cryptoglena and Monomorphina, and the Euglena and Euglenaria clades. The genus Colacium was positioned at the base of the Euglenaceae and was well supported as a monophyletic lineage. The loricate genera (Strombomonas and Trachelomonas) were located at the middle of the Euglenaceae clade and formed a robust monophyletic lineage. The genera Cryptoglena and Monomorphina also formed a well‐supported monophyletic clade. Euglena and the recently erected genus Euglenaria emerged as sister groups. However, Euglena proxima branched off at the base of the Euglenaceae. The Phacaceae clade was also a monophyletic group with high support values and subdivided into three clades, the Discoplastis, Phacus, and Lepocinclis clades. The genus Discoplastis branched first, and then Phacus and Lepocinclis emerged as sister groups. These genera shared a common characteristic, numerous small discoid chloroplasts without pyrenoids. These results clearly separated the Phacaceae clade from the Euglenaceae clade. Therefore, we propose to limit the family Euglenaceae to the members of the Euglena clade and erect a new family, the Phacaceae, to house the genera Phacus, Lepocinclis, and Discoplastis.     

Phylogeny and taxonomic revision of plastid-containing euglenophytes based on SSU rDNA sequence comparisons and synapomorphic signatures in the SSU rRNA secondary structure

Sequence comparisons and a revised classification of the Euglenophyceae were based on 92 new SSU rDNA sequences obtained from strains of Euglena, Astasia, Phacus, Trachelomonas, Colacium, Cryptoglena, Lepocinclis, Eutreptia, Eutreptiella and Tetreutreptia. Sequence data also provided molecular signatures for taxa from genus to class level in the SSU rRNA secondary structure, revealed by a novel approach (search for non-homoplasious synapomorphies) and used for taxonomic diagnoses. Photosynthetic euglenoids and secondary heterotrophs formed a clade, designated as Euglenophyceae (emend.) with two orders: Euglenales and Eutreptiales. The mostly marine Eutreptiales (Eutreptia, Eutreptiella; not Distigma) comprised taxa with two or four emergent flagella (the quadriflagellate Tetreutreptia was integrated within Eutreptiella). The Euglenales (freshwater genera with < or = one emergent flagellum) formed nine clades and two individual branches (single strains); however, only two clades were congruent with traditional genera: Trachelomonas (incl. Strombomonas) and Colacium. Euglena was polyphyletic and diverged into four independent clades (intermixed with Astasia, Khawkinea and Lepocinclis) and two individual branches (e.g. E. polymorpha). Phacus was also subdivided into Phacus s. str. and two combined lineages (mixed with Lepocinclis spp. or Cryptoglena). In consequence, Euglena (s. str.), Phacus and other genera were emended and one lineage (mixed Phacus/Lepocinclis-clade) was recognized as the previously neglected genus Monomorphina Mereschkowsky (1877). The sister clade of Phacus s. str. (mixed Euglena/Lepocinclis-clade) was identified as Lepocinclis Perty (emended).     

Biotransformation of enones with biocatalysts — two enone reductases from Astasia longa

The stereochemistry and mechanism in the reduction of the C–C double bond of carvone by the cultured cells of Astasia longa, a nonchlorophyllous cell line classified in Euglenales, was studied. The reduction of the C–C double bond of carvone with the cultured cells involved the anti-addition of hydrogen atom from the si face at the -position and the re face at the β-position of carbonyl group. Two different enone reductases were isolated from the cultured cells of A. longa. Both reductases catalyzed stereospecifically the anti-addition of hydrogen atoms from the si face at C-1 and the re face at C-6. However, one of the reductases participated in a hydrogen transfer of the pro-4R hydrogen of NADH to C-6 position of carvone and the other used the pro-4S hydrogen of NADH.     

Properties of purified chloroplastic and cytoplasmicvalyl- and leucyl-tRNA synthetases from Euglena gracilis

The catalytic properties of purified chloroplastic and cytoplasmic valyl- and leucyl-tRNA synthetasesfrom Euglena gracilis were studied and compare     

MORPHOLOGICAL SEPARATION OF THE EUGLENOID GENERA TRACHELOMONAS AND STROMBOMONAS (EUGLENOPHYTA) BASED ON LORICA DEVELOPMENT AND POSTERIOR STRIP REDUCTION1

Since the separation of the Trachelomonas Ehrenberg subgroup “Saccatae” into a new genus, Strombomonas Deflandre (1930) , there has been some question as to its validity. Deflandre's separation was based entirely on characteristics of the lorica, including the shape of the lorica, the lack of a distinctive collar, possession of a tailpiece, lack of ornamentation, and the ability of Strombomonas species to aggregate particles on the surface of the lorica. Recent molecular analyses indicated that the loricate taxa (Trachelomonas and Strombomonas) formed a single monophyletic clade; however, the phylogenetic relationship of Strombomonas to Trachelomonas remains unclear because only two Strombomonas taxa have been sequenced to date. In this study, we evaluated the monophyly of the loricate genera using two sets of morphological characters, lorica development and pellicle strip reduction. Lorica development in Strombomonas occurred from the anterior of the cell to the posterior, forming a shroud over the protoplast. In Trachelomonas, a layer of mucilage was excreted over the entire protoplast, followed by creation of the collar at the anterior end. Taxa from both genera underwent exponential strip reduction at the anterior and posterior poles. In Strombomonas only one reduction was visible in the anterior pole, whereas in most Trachelomonas species two reductions were visible. Likewise, Strombomonas species possessed two whorls of strip reduction in the posterior end compared with a single whorl of strip reduction in Trachelomonas species. These morphological characters support the separation of Trachelomonas and Strombomonas as distinct genera.