ライフサイエンスコーパス: rich media

1 2 stimulates filamentation, even on nitrogen-rich media.

2 oxidized state in wild-type strains grown in rich media.

3 had no detectable growth defect in nutrient-rich media.

4 itness compared with the euploid ancestor in rich media.

5 Mtb growth in cholesterol media, but not in rich media.

6 incorporation not typically seen in standard rich media.

7 itions, and for biofilm growth, in glutamate-rich media.

8 erve' maintained by E. coli while growing in rich media.

9 d of 99% in predicting nonessential genes in rich media.

10 d to prevent the accumulation of pyruvate in rich media.

11 d receptors, even in the presence of protein-rich media.

12 are also apparent when cystine is used or in rich media.

13 no acids at diverse sense codons in cells in rich media.

14 cytokines, even when stimulated in nutrient-rich media.

15 pattern as cells enter log phase in nutrient-rich media.

16 , although they prefer glucose when grown in rich media.

17 tions, Shewanella oneidensis, in minimal and rich media.

18 ression at levels similar to those seen with rich media.

19 ffect on growth of the bacterium in nutrient-rich media.

20 s, but had no detectable effect on growth in rich media.

21 -independent (HI) cells, cultured on peptone-rich media.

22 ent to disrupt spore germination in nutrient-rich media.

23 m 50 mL of Escherichia coli culture grown in rich media.

24 ir growth was significantly reduced in lipid-rich media.

25 ing growth in glucose-containing or nutrient-rich media.

26 Salmonella grown in the presence of salt in rich media.

27 S. pyogenes was not essential for growth in rich media.

28 A total of 85% of the genome is expressed in rich media.

29 that of the wild-type strain WU2 in vitro in rich media.

30 genes that regulate gab operon expression in rich media.

31 nes are likely to be essential for growth on rich media.

32 robust aerobic growth of Escherichia coli in rich media.

33 urvival after treatment with alpha-factor in rich media.

34 rains displayed wild-type growth kinetics in rich media.

35 pendence on sigma(S) when cells are grown in rich media.

36 ces associated with culturing in minimal and rich media.

37 pores germinated very poorly in a variety of rich media.

38 ll mutants have no apparent growth defect on rich media.

39 f CFU was measured by plate count methods on rich media.

40 ressed at detectable levels during growth in rich media.

41 er stationary-phase cultures after growth in rich media.

42 ive to UV irradiation (UVS) and sensitive to rich media.

43 mutant shows a 40% decreased growth rate in rich media, a drastic reduction in loosely coupled ribos

44 nearly threefold over the number detected in rich media alone.

45 expressed when cells are growing in nutrient-rich media, although different gene groups are affected

46 ty to growth inhibition by some component of rich media and by oxidized thiol compounds.

47 ly, mRNA half-lives were similar in nutrient-rich media and defined media in which the generation tim

48 Saccharomyces lineages grown in rich media and exposed to a nitrogen downshift gradually

49 es the Frz system for vegetative swarming on rich media and for cellular aggregation during fruiting

50 Fungal growth in rich media and minimal media containing select amino aci

51 In rich media and minimal media, the drug combination kills

52 l growth on nonfermentable carbon sources in rich media and normal frequencies of generation of petit

53 s autophagy in mammalian cells maintained in rich media and nutrient permease downregulation in yeast

54 AbHMwfabG is impaired for growth in nutrient rich media and pellicle formation.

55 e onset of nutrient limitation in amino acid rich media and responds to extracellular pyruvate.

56 Cells are large in rich media and small in poor media.

57 ol promoted the growth of the ccmG mutant on rich media and substantially restored spectroscopically

58 e transcriptional response of yeast grown in rich media and treated with rapamycin to investigate the

59 s growth defect at different temperatures in rich media, and analysis of yeast extracts suggests that

60 or normal growth on a variety of minimal and rich media, and any of the proteins is sufficient for no

61 ng is known to generate hydrogen peroxide in rich media, and because catalase and sodium pyruvate are

62 es spores only after prolonged incubation on rich media, and identifies a gene whose predicted protei

63 he wild type and overproduces antibiotics on rich media, and it identifies a gene whose predicted pro

64 (2) per cell than exponential-phase cells in rich media, and such excessive O(2) consumption causes r

65 bility to progress in development in glucose-rich media are manifestations of phenomena that occur in

66 at the enhanced uptake of Co(II) in chloride-rich media arises from the high thermodynamic stability

67 t of these "dark oxygenations" require water-rich media associated with short (1)O(2) lifetimes, and

68 gene requirements for competitive growth in rich media between these two closely related serovars.

69 The two mutants grow normally in rich media but do not grow in defined media lacking arom

70 ants grow well and are slightly elongated in rich media but grow less well than wild-type cells in mi

71 echanism of catabolite repression control in rich media by Crc involves posttranscriptional regulatio

72 LAC include working equally well in nutrient-rich media, conceivably expanding applicability to any o

73 Here, we show that commonly used rich medias contain substantial concentrations of short-

74 rently simple auxotroph did not grow well in rich media containing excess methionine, forming small c

75 to validate gene essentiality predictions in rich media, contextualize intra-screen discrepancies and

76 the addition of modest amounts of acetate to rich media (e.g., tryptone broth).

77 the nrf promoter is known to be repressed in rich media, especially in the presence of glucose, but t

78 ch, although capable of growing well in iron-rich media, failed to prosper under iron chelation.

79 n morphogenesis, overproduces antibiotics on rich media, fails to grow on minimal media, and identifi

80 he transcription factor Pho4, slow growth on rich media, failure to grow using galactose, lactate or

81 In rich media, FLO11 is regulated by mating type; it is exp

82 When cultured in rich media in shake flasks, pEVOL was capable of produci

83 n secreted by this strain of B. anthracis in rich media in vitro.

84 s undetectable during growth in a variety of rich media, including Luria-Bertani (LB) medium, or in m

85 biomes were grown for 7 d on either nutrient-rich media-including a modification of SHI medium, brain

86 in blood (output pool) compared to growth in rich media (input pool) were identified using DNA microa

87 yces cerevisiae cells transferred from spent rich media into water live for weeks, whereas the same c

88 from Bacillus thuringiensis spores grown in rich media is [N(1)C(4)H(12)](+).

89 P. putida cultivation in lignin-rich media is characterized by an abundant exoproteome t

90 receptor Atg36 by the casein kinase Hrr25 in rich media is repressed by the ATPase activity of Pex1/6

91 st, Thr4, although dispensable for growth in rich media, is essential in phosphate-depleted or galact

92 In rich media, loss of PBPs 2c and 4 resulted in no obvious

93 n exponentially growing cultures in nutrient-rich media, meaning knowledge of such interactions under

94 Despite an impaired fitness in rich media, melanogenic mutants can inhibit their wild-t

95 Stress in nutrient-rich media necessitated SgrS regulation of only sugar tr

96 nal molecule luteolin in defined minimal and rich media or of strains altered in the expression of ke

97 Ion exchange in nanoporous clay-rich media plays an integral role in water, nutrient, an

98 In nutrient-limited, but not rich, media, RBT was 200-fold more potent than rifampin.

99 Furthermore, when grown in rich media (repressing conditions), wild-type cells yiel

100 dium from stationary-phase cultures grown in rich media resulted in the premature activation of each

101 inization, and ammonia release on amino acid-rich media, similar to stp2Delta and ahr1Delta stp2Delta

102 When grown in rich media, single-celled organisms such as yeast and ba

103 ugh unable to germinate in standard nutrient-rich media, spores lacking SleB, CwlJ1, and CwlJ2 are ab

104 ype repression of FLO11 in diploids grown in rich media suffices to explain the inability of these ce

105 rain is able to form fruiting bodies on semi-rich media, suggest that Pkn5 and Pkn6 have reciprocal r

106 ompU2 displayed wild-type growth kinetics in rich media, suggesting that this is the true phenotype o

107 nder anaerobic conditions, cultures grown on rich media supplemented with d-glucose or glycerol produ

108 that it grows larger and faster in nutrient-rich media than in nutrient-poor media.

109 ates enable robust transport within disorder-rich media through integer invariants inextricably tied

110 toylation as cells transition from growth in rich media to a growth-arrested state during nutrient de

111 mical libraries have traditionally relied on rich media to ensure rapid bacterial growth in high-thro

112 nd expression data from yeast cells grown in rich media to learn the transcriptional network specific

113 h efficiency, low background and facility in rich media, tolC selection is a broadly applicable metho

114 Comparisons made between rich media under aerobic conditions vs low-oxygen condit

115 Repression of srrAB in rich media under aerobic growth conditions shows that Sr

116 y, even against bacteria growing in nutrient-rich media under favorable conditions.

117 y-state diversity of 63 species growing on a rich media, using consumption and production fluxes infe

118 ng early stages of fungal growth in nutrient-rich media, variants found herein could be linked to nut

119 mes more toxic than HDI monomer when protein-rich media was used.

120 tionally, using phenotypic data collected in rich media, we explored the fitness landscape, finding e

121 In cells growing rapidly in nutrient-rich media, we find that RNAP is organized in 2-8 bands.

122 utants that can sustain hyphal elongation in rich media, we found hog1, ssk2, and pbs2 mutants of the

123 under multiple time-points during growth in rich media, we show that the binding regions of the two

124 for the Fis-deficiency, but during growth in rich media when the demand for ribosomes is high, this c

125 iratory mucosa and can be cultivated only on rich media, whereas E. coli is a saprophyte that can gro

126 , single cells (blastospores) predominate in rich media, whereas filaments composed of elongated cell

127 significant bacterial reduction in nutrient rich media, wherein experimental conditions more closely

128 ut1(-) segregant ( fut1(s) ) was obtained in rich media, which showed severe growth defects accompani

129 e 13 ACPPs exert antimicrobial activities in rich media with broad spectrum of antibacterial activiti

130 t wild-type strain when cultured in nutrient-rich media with or without CO(2) in the atmosphere, alth

131 Gal- YAH1 cells were grown in standard rich media (YPD and YPGal) under O 2 or argon atmosphere