ライフサイエンスコーパス: minimal media

1 th carbohydrate amendment in Cedars-specific minimal media.

2 B. pseudomallei DeltagspD grown in rich and minimal media.

3 a but grow less well than wild-type cells in minimal media.

4 measuring bacterial growth rates on lactose minimal media.

5 to erect aerial hyphae and differentiate on minimal media.

6 xual reproduction when grown on glucose (1%) minimal media.

7 itive to oxidative stress and grew poorly on minimal media.

8 of Escherichia coli K-12 MG1655 to growth in minimal media.

9 vels of ptsG mRNA and grow poorly in glucose-minimal media.

10 Delta trpF E. coli strain from starvation on minimal media.

11 ary phase, carbon starvation, or rich versus minimal media.

12 ly robust biofilm cultures) in both rich and minimal media.

13 cell growth at most temperatures in rich and minimal media.

14 e dispensable for E. coli growth in rich and minimal media.

15 wild type for chemotaxis, grown in rich and minimal media.

16 48 cells were highly motile in both rich and minimal media.

17 tly functional to permit growth on succinate minimal media.

18 of gene expression during growth in rich and minimal media.

19 revisiae grown in either 14N or 15N-enriched minimal media.

20 lection in Luria-Bertani (LB) and in glucose minimal media.

21 cold-shock in either defined rich or defined minimal media.

22 -chain poly P and are defective in growth in minimal media.

23 as performed on cells grown in both rich and minimal media.

24 res thiamin and nicotinic acid for growth in minimal media.

25 re produced in both rich complex and defined minimal media.

26 alter the growth rate of E. coli in rich or minimal media.

27 s were defective for growth on nitrogen-rich minimal media.

28 ve been measured for cells grown in rich and minimal media.

29 to be nonessential in both rich and glucose-minimal media.

30 eas E. coli is a saprophyte that can grow on minimal media.

31 ing from 0 to 1 mM in both nutrient-rich and minimal media.

32 essential and synthetic lethal reactions and minimal media.

33 Tumor-isolated cells placed in minimal media also contained rare ER(-)PR(-)CK5(+) cells

34 ly coupled during growth in both complex and minimal media, although they exhibit different patterns

35 S. meliloti bluB mutant is unable to grow in minimal media and fails to establish a symbiosis with al

36 ssion of avrRpt2, hrpZ, and hrpL in vitro in minimal media and in vivo when infiltrated into Arabidop

37 l growths of S. cerevisiae grown in rich and minimal media and independent MudPIT analyses of each we

38 otein kinase was expressed to high levels on minimal media and uniformly isotopically enriched with 1

39 at 37 degrees C in defined rich and defined minimal media, and after a shift to 15 degrees C for eit

40 antibiotics on rich media, fails to grow on minimal media, and identifies a gene whose predicted pro

41 controls some genes differently in rich and minimal media, and that Snf/Swi control is exerted at th

42 This is true of cells grown in rich or minimal media, and the principal regulation of mug is at

43 ants were analyzed in both nutrient-rich and minimal media, and the results confirmed the presence of

44 chvD-lacZ fusion, occurred in both rich and minimal media as well as under conditions that induce vi

45 ligosaccharides, and peptides in complex and minimal media at 98 and 72 degrees C to the same extent

46 quired for the growth of vegetative cells in minimal media at very low inoculum densities, as well as

47 X expression is enhanced 3-fold by growth on minimal media but not induced by N-methyl-L-tryptophan,

48 ent RapiGest from cells grown under rich and minimal media conditions using 14N and 15N ammonium sulf

49 Cells of Bacillus species grown in rich and minimal media contained low levels of GB, but GB levels

50 , five bacterial species were cultured in M9 minimal media containing a range of glucose concentratio

51 Fungal growth in rich media and minimal media containing select amino acids/peptides was

52 imately 2400 cytosolic proteins expressed in minimal media depend absolutely on the GroEL/GroES chape

53 n contrast, many of the genes upregulated in minimal media encoded enzymes for synthesis of amino aci

54 g growth on nonfermentable carbon sources in minimal media for the mis1 deletion strain but not for t

55 sing the enzyme in Escherichia coli grown on minimal media in the presence of a number of divalent me

56 he presence of toluidine blue or on glycerol minimal media in the presence of zinc, suggesting that a

57 In minimal media incubated under high CO2, the canB mutant

58 th aerobically and anaerobically in rich and minimal media, indicating that it is not specifically as

59 ma factor, sigma(S), when cells are grown in minimal media, it shows only a modest dependence on sigm

60 oth PCR and failure of the mutant to grow on minimal media lacking aromatic amino acids.

61 g a disruption in argE was unable to grow on minimal media lacking supplemental arginine and formed f

62 DGC genes stimulated growth in both rich and minimal media of a Shigella flexneri mutant that produce

63 cerevisiae strain S288C grown in either 14N minimal media or 15N-enriched minimal media were mixed a

64 Much of the ability to grow on GABA-amended minimal media or in Arabidopsis pop2-1 leaves could be r

65 , including Luria-Bertani (LB) medium, or in minimal media or under heat shock or ethanol stress cond

66 measurements of >2,500 proteins in rich and minimal media provide a detailed view of the cellular re

67 l eradication with subsequent adventitia but minimal media repopulation.

68 PII and GlnK have a severe growth defect on minimal media, resulting from elevated expression of the

69 2 MG1655 grown on either lactate or glycerol minimal media showed that (1) growth phenotypes at the e

70 how that the glucose concentration in the M9 minimal media strongly affects the concentration of sulf

71 by slowing the growth rate of each strain in minimal media, suggesting that certain gene products are

72 In complete minimal media supplemented with GABA, the mutant grew le

73 rate but also become sensitive to alanine in minimal media supplemented with glucose and ammonium.

74 titer exceeding 350 mg.L(-1) was obtained in minimal media supplemented with glucose.

75 -requiring strain grew strongly on synthetic minimal media supplemented with methionine, aspartate or

76 ts was achieved by growing cells in modified minimal media that contained geneticin (G418).

77 In minimal media, the Fis deficiency only reduced the DNA a

78 ency via fitness profiling in rich (YPD) and minimal media to identify all genes that confer a haploi

79 Using defined minimal media to simulate the intracellular pH and Mg2+

80 d-type and Deltafnr strains grown in glucose minimal media under aerobic or anaerobic conditions.

81 tations were grown in both nutrient-rich and minimal media under steady-state conditions known to alt

82 ae proteome resulting from cultures grown in minimal media using galactose, glucose, or raffinose as

83 Saccharomyces cerevisiae cultured in rich or minimal media was analyzed by oligonucleotide arrays and

84 f the acid-resistance phenotype in acidified minimal media was dependent upon the supplementation of

85 in either 14N minimal media or 15N-enriched minimal media were mixed and digested into a complex pep

86 nds and sulfonates as sole sulfur sources in minimal media when Met30 was present.

87 ts under anaerobic, mesophilic conditions in minimal media with acetate as the sole source of energy

88 Growth of P. gingivalis strain A7436 in a minimal media with normal human serum as a source of hem

89 genes is induced via CreBC during growth in minimal media, with the exception of malE, which is more

90 induce autophagy upon switch from a rich to minimal media without nitrogen starvation.