ライフサイエンスコーパス: Kluyveromyces

1 conserved sequences in telomerase RNAs from Kluyveromyces budding yeasts.

2 at KAT1 was domesticated specifically in the Kluyveromyces clade of the budding yeasts.

3 ermini except for those of the Saccharomyces/Kluyveromyces clade that all contained a region homologo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 Mannan chains of Kluyveromyces lactis mannoproteins are similar to those

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

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

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

34 In Kluyveromyces lactis mutants lacking telomerase, recombi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 In Kluyveromyces lactis, the repeats synthesized by the wil

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

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

55 In Kluyveromyces lactis, we have identified a novel allele

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

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

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

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

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

61 p formation in the unicellular budding yeast Kluyveromyces lactis.

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

63 nant proteins derived from the budding yeast Kluyveromyces lactis.

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

65 om Saccharomyces kluyveri and of PET111 from Kluyveromyces lactis.

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

67 he cytoplasmic linear DNA killer plasmids of Kluyveromyces lactis.

68 on of a recombinant endopolygalacturonase of Kluyveromyces marxianus (KMPG) for the aroma enhancement

69 dustrial interest (Saccharomyces cerevisiae, Kluyveromyces marxianus and kefir) by solid state fermen

70 d and pre-treated immobilized inulinase from Kluyveromyces marxianus NRRL Y 7571 and Aspergillus nige

71 emerged after WGD between the divergence of Kluyveromyces polysporus and Saccharomyces castellii fro

72 ere we report the 3.2 A crystal structure of Kluyveromyces polysporus Argonaute (KpAGO) fortuitously

73 tivity of a catalytically active fragment of Kluyveromyces polysporus Dcr1, which represents the nonc

74 ase RNAs of Saccharomyces cerevisiae and six Kluyveromyces species followed by mutagenesis of the S.

75 ly examine 87 potential interactions between Kluyveromyces waltii proteins, whose one to one ortholog

76 ow evolution compared with the orthologue in Kluyveromyces waltii, a non-WGD species.

77 ome duplication, by sequencing and analysing Kluyveromyces waltii, a related yeast species that diver

78 e speciation event between S. cerevisiae and Kluyveromyces waltii, suggesting that the WGD occurred i

79 a core structure common to Saccharomyces and Kluyveromyces yeast species.