ライフサイエンスコーパス: Kluyveromyces lactis

1 p formation in the unicellular budding yeast Kluyveromyces lactis.

2 etylase, we studied Sir2 from another yeast, Kluyveromyces lactis.

3 nant proteins derived from the budding yeast Kluyveromyces lactis.

4 tional ancestral gene as is still present in Kluyveromyces lactis.

5 om Saccharomyces kluyveri and of PET111 from Kluyveromyces lactis.

6 idues in the telomerase RNA of budding yeast Kluyveromyces lactis.

7 he cytoplasmic linear DNA killer plasmids of Kluyveromyces lactis.

8 agues demonstrate that, in the budding yeast Kluyveromyces lactis, a DNA rearrangement associated wit

9 se Gal4 binding sites are not present in the Kluyveromyces lactis ACC1 gene.

10 isiae and the homologous KLLA0A09713 gene of Kluyveromyces lactis allow for cross-complementation of

11 bility of ICE to divergent yeasts, including Kluyveromyces lactis and alternative S. cerevisiae strai

12 ial beta-galactosidases (Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae) was analyse

13 beta-galactosidases from Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae.

14 sidase preparations from Aspergillus oryzae, Kluyveromyces lactis and Bacillus circulans.

15 at shock transcription factor from the yeast Kluyveromyces lactis and had shown it to be highly alpha

16 ase activity, as previously observed for the Kluyveromyces lactis and human telomerase RNA pseudoknot

17 led to monitor carboxylic acid production by Kluyveromyces lactis and Saccharomyces cerevisiae during

18 provided evidence that in the budding yeasts Kluyveromyces lactis and Saccharomyces cerevisiae, the t

19 egy to isolate LCB2 homologs from the yeasts Kluyveromyces lactis and Schizosaccharomyces pombe and a

20 e three-dimensional structure of Gal80p from Kluyveromyces lactis and show that it is structurally ho

21 st Saccharomyces cerevisiae, the dairy yeast Kluyveromyces lactis and the human pathogen Candida albi

22 and gamma-subunits of ATP synthase in yeast Kluyveromyces lactis and trypanosome Trypanosoma brucei.

23 ree yeast species (Saccharomyces cerevisiae, Kluyveromyces lactis, and Debaryomyces hansenii) are rem

24 We show here, by using Kluyveromyces lactis cells containing two types of telom

25 Telomeres in the budding yeast Kluyveromyces lactis consist of perfectly repeated 25-bp

26 dy, we uncovered a domesticated transposase, Kluyveromyces lactis hobo/Activator/Tam3 (hAT) transposa

27 the yeast heat-shock transcription factor of Kluyveromyces lactis (HSF_KL) suggests that these prolin

28 We present the 3.0-A crystal structure of Kluyveromyces lactis Hsv2, which shares significant sequ

29 Solubilisation of beta-galactosidase from Kluyveromyces lactis in Aerosol-OT water-in-isooctane mi

30 CrPV-IRES bound to the ribosome of the yeast Kluyveromyces lactis in both the canonical and rotated s

31 pression of the lactose-galactose regulon in Kluyveromyces lactis is induced by lactose or galactose

32 airy industry, and the enzyme from the yeast Kluyveromyces lactis is most widely used.

33 ing yeasts Saccharomyces cerevisiae (Sc) and Kluyveromyces lactis (Kl).

34 owever, deletion of the PNT1 orthologue from Kluyveromyces lactis, KlPNT1, caused a clear nonrespirat

35 Origin positions in four other yeasts-Kluyveromyces lactis, Lachancea kluyveri, Lachancea walt

36 The mannan chains of Kluyveromyces lactis mannoproteins are similar to those

37 The mannan chains of Kluyveromyces lactis mannoproteins are similar to those

38 Mannan chains of Kluyveromyces lactis mannoproteins are similar to those

39 The corresponding domain of the yeast Kluyveromyces lactis Mig1 conferred glucose-regulated Ms

40 We report the crystal structure of Kluyveromyces lactis MIND and examine its partner intera

41 from MDCK cells of a recently characterized Kluyveromyces lactis mutant deficient in Golgi transport

42 In Kluyveromyces lactis mutants lacking telomerase, recombi

43 Saccharomyces cerevisiae, S. carlsbergensis, Kluyveromyces lactis, Neurospora crassa, Aspergillus nid

44 Yarrowia lipolytica and Kluyveromyces lactis occur as part of Stilton cheese mic

45 in a telomerase-deletion mutant of the yeast Kluyveromyces lactis occurs through a roll-and-spread me

46 The solution NMR structure of the Kluyveromyces lactis pseudoknot, presented here, reveals

47 the telomerase RNA gene (TER1) in the yeast Kluyveromyces lactis results in gradual loss of telomeri

48 Here we report the crystal structure of Kluyveromyces lactis Rtr1, which reveals a new type of z

49 Golgi apparatus and of a mutant of the yeast Kluyveromyces lactis specifically defective in the trans

50 We characterized two mutations in the Kluyveromyces lactis telomerase RNA gene (TER1) template

51 knot elements in human and the budding yeast Kluyveromyces lactis telomerase RNAs contain unusual tri

52 The Kluyveromyces lactis ter1-16T strain contains mutant tel

53 omerase RNA gene (TER1) of the budding yeast Kluyveromyces lactis that were predicted to lead to synt

54 In the budding yeast Kluyveromyces lactis, the incorporation of certain mutan

55 In Kluyveromyces lactis, the repeats synthesized by the wil

56 In the yeast Kluyveromyces lactis, the telomerase RNA (Ter1) template

57 ing ALT cells, such as the stn1-M1 mutant of Kluyveromyces lactis, the telomeres appear to be continu

58 zyme that converts the petite-negative yeast Kluyveromyces lactis to petite-positive.

59 In Kluyveromyces lactis, we have identified a novel allele

60 ed mating type and Sir proteins in the yeast Kluyveromyces lactis, which contains cryptic copies of t

61 plication and found that Orc1 from the yeast Kluyveromyces lactis, which diverged from S. cerevisiae

62 died telomere length regulation in the yeast Kluyveromyces lactis, which has long (25 base pairs) hom

63 Using the KlCYC1 gene of the yeast Kluyveromyces lactis, which includes a single promoter a

64 chore proteins Nkp1 and Nkp2, from the yeast Kluyveromyces lactis, with nanoflow electrospray ionizat