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1 K. lactis sir2 and sir4 mutant strains showed partial de
2 K. lactis sir2 mutants are more sensitive than the wild
3 K. lactis telomerase RNA, encoded by the TER1 gene, is a
6 cerevisiae, we determined the structure of a K. lactis CBF3 complex by electron cryomicroscopy at ~4
7 iring: unlike S. cerevisiae and C. albicans, K. lactis integrates nutritional signals, by means of Rm
8 than the wild type to ethidium bromide, and K. lactis sir4 mutants are more resistant phenotypes tha
9 ted in two budding yeasts, S. cerevisiae and K. lactis, have shown recombination can replenish termin
11 f the COX2 and COX3 mRNAs of S. kluyveri and K. lactis have little similarity to each other or to tho
12 controlling the amount of Y. lipolytica and K. lactis during production offers potential to manipula
14 s in centromeric nucleosome assembly between K. lactis and S. cerevisiae, we determined the structure
15 the template and the precision of copying by K. lactis telomerase to examine primer elongation within
22 tity with the corresponding transporter from K. lactis but showed 53% amino acid sequence identity to
24 age of lactose hydrolysis by the immobilized K. lactis beta-galactosidase using genipin as a crosslin
25 e Mig1 revealed short patches of homology in K. lactis and K. marxianus Mig1 that might be Msn5-inter
26 The various phenotypes of sir mutants in K. lactis and S. cerevisiae, however, revealed unanticip
27 this model, we demonstrate here that RTE in K. lactis occurs by amplification of a sequence originat
34 Increasing the inoculum concentration of K. lactis resulted in decreased variation between replic
35 models inoculated with low concentrations of K. lactis exhibited blue cheese-related attributes, asso
36 cent-activated cell sorter after labeling of K. lactis cells with fluorescein isothiocyanate (FITC) c
41 und by DNA-blot hybridization to S. pombe or K. lactis genomic DNA, and no antigenically related prot
48 We have now cloned the gene encoding the K. lactis Golgi membrane N-acetylglucosaminyltransferase
49 We have now cloned the gene encoding the K. lactis Golgi membrane UDP-GlcNAc transporter by compl
51 tants defective in telomere maintenance, the K. lactis telomere fusions retained their telomeric DNA
52 of Ndc10 and discuss potential models of the K. lactis centromeric nucleosome that account for the ex
53 of the 5-nt repeats defining the ends of the K. lactis telomerase RNA template in telomerase transloc
54 formed with a genomic library from wild-type K. lactis in a pKD1-derived vector; transformants were i
55 1% (v/v), the maximum GOS concentration with K. lactis beta-galactosidase was achieved in 1 and 5h at