ライフサイエンスコーパス: Euglena

1 aracterized in five other euglenoid species, Euglena anabaena, Euglena granulata, Euglena myxocylindr

2 The complex chloroplasts of Euglena and dinoflagellates are surrounded by three memb

3 er eukaryotic world; organisms as diverse as EUGLENA: and nematode worms, including Caenorhabditis el

4 The giant viruses in the genome of Euglena are relatives of important animal pathogens, suc

5 -time interaction with swarms of phototactic Euglena cells hosted on a cloud laboratory.

6 Euglena chloroplast protein precursors are transported a

7 All Euglena chloroplast protein precursors have functionally

8 e in known rpoA sequences, the question of a Euglena chloroplast rpoA gene was re-examined.

9 Euglena gracilis (E. gracilis) has been proposed as one

10 oalgae, Chlamydomonas reinhardtii (ChRe) and Euglena gracilis (EuGr), and HeLa cells in their native

11 sochrysis galbana, a Delta8 -desaturase from Euglena gracilis and a Delta5 -desaturase from Mortierel

12 l-free video-rate metabolite imaging of live Euglena gracilis and statistical analysis of intracellul

13 otide profiling in two representative algae, Euglena gracilis and the toxin-producing microalga Prymn

14 e two strands of the chloroplast genome from Euglena gracilis are asymmetric with regards to nucleoti

15 When the sequence of the Euglena gracilis chloroplast genome was reported in 1993

16 cDNA predicted to encode the mature form of Euglena gracilis chloroplast translational initiation fa

17 nslational initiation factor 3 (IF3chl) from Euglena gracilis consists of an internal region homologo

18 tamic acid, we isolated cyclic peptides from Euglena gracilis containing asparagine and non-proteinog

19 nslational initiation factor 3 (IF3chl) from Euglena gracilis contains a central region (homology dom

20 erobic Hg uptake, whereas DOM harvested from Euglena gracilis did not exhibit this same pronounced ef

21 amino acids and polyamines, most abundant in Euglena gracilis DOM, were positively correlated to incr

22 Euglena gracilis harbours secondary green plastids, but

23 Euglena gracilis is a photosynthetic flagellate possessi

24 ethod in the case of the swimming microalgae Euglena gracilis trapped in light-defined billiard geome

25 ctories and flagellar shapes of specimens of Euglena gracilis We achieved this task by using high-spe

26 biosynthesis in chloroplasts of the protist Euglena gracilis We show that, rather than comparable un

27 oded hsp60 gene from the euglenoid protozoan Euglena gracilis were cloned and sequenced.

28 ate measurements of the behavior of the alga Euglena gracilis when exposed to controlled light fields

29 gent ATP synthase dimer from mitochondria of Euglena gracilis, a member of the phylum Euglenozoa that

30 Euglena gracilis, a microalgal species of unicellular fl

31 Euglena gracilis, a photosynthetic and highly adaptable

32 anosoma brucei, a lethal human parasite, and Euglena gracilis, a photosynthetic protist.

33 of giant viruses integrated in the genome of Euglena gracilis, an ecologically and industrially relev

34 bed in bacteria, the photosynthetic excavate Euglena gracilis, and the heterokont Ochromonas spp.

35 h research has focused on the model organism Euglena gracilis, other members of the euglenids have no

36 e (Chlorella pyrenoidsa, Chlorella vulgaris, Euglena gracilis, Scenedesmus obliquus, and Chlamydomona

37 We also identify a locus in Euglena gracilis, which is similarly required for Z-ISO

38 zymes and also contains the cytosolic FBA of Euglena gracilis.

39 ty with the cyclic AMP-dependent kinase from Euglena gracilis.

40 inensis, and weaker in Porphyra purpurea and Euglena gracilis.

41 ents (GEVEs) in the genome of the microalgae Euglena gracilis.

42 d discuss a model for flagellar mechanics in Euglena gracilis.

43 e other euglenoid species, Euglena anabaena, Euglena granulata, Euglena myxocylindracea, Euglena stel

44 than the higher plants, but within the algae Euglena is found to have several unusual features which

45 deletion constructs of the precursor to the Euglena light-harvesting chlorophyll a/b-binding protein

46 ostelium, Dunaliella, Ectocarpus, Emiliania, Euglena, Micromonas, Naegleria, Nephroselmis, Paramecium

47 t freshly harvested DOM from Chlorophyte and Euglena mutabilis strongly inhibited aerobic and anaerob

48 pecies, Euglena anabaena, Euglena granulata, Euglena myxocylindracea, Euglena stellata and Euglena vi

49 a cyanobacteria to the chloroplast genome of Euglena myxocylindracea.

50 le being only distantly related to all other Euglena plastid introns and maturases.

51 The Euglena plastid, as the product of many genomes, combine

52 The Euglena precursor to the small subunit of ribulose-15-bi

53 gether with the structural similarity of all Euglena presequences, these results demonstrate that chl

54 immunoelectronmicroscopy have shown that in Euglena, proteins are transported from the ER to the Gol

55 e in vivo and in vitro experiments show that Euglena pSSU is inserted into the ER membrane and transp

56 All seven Euglena rpoA genes have either one or three group III in

57 Additionally, Euglena rpoA proteins lack a C-terminal domain required

58 s and blooms of the potentially ichthyotoxic Euglena sanguinea phytoplankton.

59 Quite surprisingly, we found that Euglena scatters with a nearly Lambertian cosine law, re

60 The rpoA gene products in Euglena spp. appear to be the most variable in this gene

61 Euglena spp. are phototrophic flagellates with considera

62 Euglena granulata, Euglena myxocylindracea, Euglena stellata and Euglena viridis, and in the Astasia

63 tes (fungi, plants, animals, slime mold, and euglena) synthesize Asn-linked glycans (Alg) by means of

64 uglena myxocylindracea, Euglena stellata and Euglena viridis, and in the Astasia longa plastid genome

65 ansport route from cytoplasm to chloroplast, Euglena was pulse labeled with 35S-sulfate and the organ

66 otein trees placed apicoplast as a sister to Euglena within the green lineage.