ライフサイエンスコーパス: diauxic shift

1 carbohydrate in the media becomes limiting (diauxic shift).

2 er exhausting glucose, generating a reversed diauxic shift.

3 2, two targets of Pdr1, also overgrow at the diauxic shift.

4 agments after rapamycin treatment and during diauxic shift.

5 expression of numerous yeast genes after the diauxic shift.

6 very similar to those in cells undergoing a diauxic shift.

7 the metabolic remodeling associated with the diauxic shift.

8 ells undergo the metabolic transition at the diauxic shift.

9 (Ser(2)) phosphorylation observed during the diauxic shift.

10 n of glycogen accumulation that precedes the diauxic shift.

11 e found that yeast propagated until the post-diauxic shift (72 h) provided better longevity in the bo

12 d, CR increased acetyl-CoA levels during the diauxic shift, along with expression of both acetyl-CoA

13 catabolite repression, the aerobic/anaerobic diauxic shift and amino acid biosynthesis pathway repres

14 /3 and SNO2/3 mRNAs are induced prior to the diauxic shift and decrease in abundance during the postd

15 is down-regulated as cells pass through the diauxic shift and enter stationary phase.

16 and between Saccharomyces species during the diauxic shift and found appreciable cis-acting variation

17 omatin structure closes when cells enter the diauxic shift and growth dramatically slows.

18 Puf3p levels are reduced during the diauxic shift and growth on a nonfermentable carbon sour

19 Expression of GTT1 is induced after diauxic shift and remains high throughout the stationary

20 le: cell cycle, DNA damage, stress response, diauxic shift and sporulation.

21 ss of SVF1 is associated with defects in the diauxic shift and the oxidative stress response.

22 es: cell cycle, DNA damage, stress response, diauxic shift, and sporulation.

23 etabolic reprogramming that occur during the diauxic shift, and the expression patterns of many previ

24 show that genes normally induced during the diauxic shift are not properly induced in a ctk1Delta st

25 period of maximal SNF1 activation beyond the diauxic shift, as indicated by Sak1-dependent T210 phosp

26 premature growth arrest of cells during the diauxic shift, as they adapt to the changing environment

27 e possibility that mitochondria may initiate diauxic shift-associated regulation of nucleus-encoded g

28 We describe a previously unknown type of diauxic shift-dependent modulation of the intracellular

29 cerevisiae following glucose depletion (the diauxic shift) depends on a profound metabolic adaptatio

30 that the yeast DJ-1 homologs have a role in diauxic-shift (DS), characterized by metabolic reprogram

31 Even though diauxic shifts emerge naturally from the model when two

32 atch cultures just before they undergo this "diauxic shift." Essentially the same pattern was found b

33 lysis of expression data from a recent yeast diauxic shift experiment.

34 hese genes were found to be clustered in the diauxic-shift experiment as well.

35 This method has been validated on diauxic shift experiments and reproduces well known effe

36 transition of log phase to stationary phase (diauxic shift) for effective CLS extension.

37 nteracts with Snf1 and is induced during the diauxic shift, had an inhibitory role on invasive growth

38 metabolic adaptations that occur during the diauxic shift have not been fully characterized at the o

39 e genes failed to be up-regulated across the diauxic shift in a manner similar to the Deltaisc1 strai

40 so is observed, at least in part, during the diauxic shift in batch cultures.

41 ested for the ability to efficiently undergo diauxic shift in the presence and absence of Bcl-x(L).

42 direct target genes are also induced by the diauxic shift, in which glucose levels begin to be deple

43 athways and the pathways that respond to the diauxic shift (including glycolysis and the citric acid

44 histone deacetylase complex was required for diauxic shift-induced H4 and H2B deposition onto rDNA ge

45 tive to respiratory metabolism, known as the diauxic shift, is reflected by dramatic rearrangements o

46 during log phase and reassembled during the diauxic shift, largely accounting for the differences in

47 During nutrient limitation (diauxic shift) or after treatment with rapamycin (a spec

48 ells, mRNA content was less abundant in post-diauxic shift phase and even less in stationary phase C.

49 transcripts of many genes increased in post-diauxic shift phase as well as stationary phase.

50 xpressed at higher levels at and beyond post-diauxic shift phase.

51 ermentative to a respiratory metabolism, the diauxic shift represents the stage where major structura

52 ible homodimeric protein that is involved in diauxic shift reprogramming and has glyoxalase activity.

53 the Mot1-repressed genes are involved in the diauxic shift, stress response, mating, or sporulation.

54 can result in biphasic growth curves called "diauxic shifts" that typically arise when microbes are g

55 izes Snf1 activity throughout and beyond the diauxic shift, thus optimizing the coordination of nucle

56 mentable carbon source metabolism during the diauxic shift, thus suggesting a mechanism for the defec

57 ociation of the Arc1p:GluRS complex upon the diauxic shift to respiratory conditions.

58 ing through the cell cycle, sporulation, and diauxic shift were analyzed.

59 onQ) cells are initiated within hours of the diauxic shift, when cells have scavenged all the glucose

60 3 mutants, SNZ1 mRNA is induced prior to the diauxic shift, when SNZ2/3 mRNAs are normally induced.

61 carbon upshifts and downshifts (for example, diauxic shifts) without adjustable parameters.