ライフサイエンスコーパス: batch culture

1 the second phase respiratory growth rate in batch cultures).

2 stress response of each cell line during fed-batch culture.

3 tative interactors of a protein using Y2H in batch culture.

4 ast and follow their expression over time in batch culture.

5 PA titer to 34.93 +/- 2.99 g.L(-1) in a fed-batch culture.

6 e how the cell copes with As(V) generated in batch culture.

7 ynthetic enzymes) proteins in the CCR versus batch culture.

8 s that characterize typical diatom growth in batch culture.

9 waste products (pyruvate and acetate) during batch culture.

10 caused a haploinsufficient phenotype in semi-batch culture.

11 nges for S. marcescens during cultivation in batch culture.

12 ecific environment, Luria-Bertani broth (LB) batch culture.

13 is maximal during mid- to late-log growth in batch culture.

14 activities during growth in a pH-controlled batch culture.

15 d can be maximized by nutrient starvation in batch culture.

16 idyl-peptidase), produced in a pH-controlled batch culture.

17 e concentrations and other conditions during batch cultures.

18 hematical model of mixed-substrate growth in batch cultures.

19 m deltaH cells growing on H2 plus CO2 in fed-batch cultures.

20 xtended to non-balanced growth conditions in batch cultures.

21 cell to maximise production performance from batch cultures.

22 imise volumetric productivity and yield from batch cultures.

23 en subjected to in vitro digestion and fecal batch cultures.

24 he presence of different nitrogen sources in batch cultures.

25 s that can be associated with experiments in batch cultures.

26 occus MED4 grown in P-limited chemostats and batch cultures.

27 t least in part, during the diauxic shift in batch cultures.

28 siological condition normally encountered in batch cultures.

29 ir-liquid interface in stationary or shaking batch cultures.

30 bacteria to 1100 generations of evolution in batch cultures.

31 the CDC, were expressed periodically in our batch culture, albeit a mere 10% of the cells divided as

32 lor optical control of transcription both in batch culture and in patterns across a lawn of engineere

33 osynthesis was important for fitness in semi-batch culture and modelling of this regime showed that r

34 7 ethanol, 2 CO2, and 2.6 H2 when growing in batch culture and to 2 acetate, 2 CO2, and 4 H2 when gro

35 en with various limiting nitrogen sources in batch culture and with ammonia, the optimal nitrogen sou

36 ydrogenase complex, impairs survival of both batch cultures and biofilms.

37 )- or nitrogen (N)-limited growth in adapted batch cultures and cultures subjected to nutrient shifts

38 of individual cells both in stationary phase batch cultures and during continuous growth.

39 embedded in a polysaccharide matrix both in batch cultures and under flow conditions in microfluidic

40 Results of monitoring a batch culture are presented as well as analysis of a cul

41 nvariant conditions whereas serially diluted batch cultures are complex and dynamic.

42 cell material when the strains were grown in batch culture at either high or low external concentrati

43 igested corn stover with equal efficiency in batch culture at low pH.

44 The implementation of batch cultures at the nanoliter scale has been difficult

45 mL air , simulating a small leak into 30 mL batch culture bottle, had no measurable impact on benzen

46 o grows slowly at low NH4+ concentrations in batch culture, but only at pH values below 7.

47 Examination of batch cultures by flow cytofluorometry with monoclonal a

48 s for headspace gas analysis above bacterial batch cultures by spectroscopy, Raman spectroscopy enhan

49 a strong stress response in the auxotrophic batch cultures, cell cycle arrest, if it occurs at all,

50 y by a standardized assay, where aliquots of batch-cultured cells are rapidly pipetted into a hypoton

51 In nutrient-replete exponentially growing batch cultures, concentrations ranged from 2% to 6%, whi

52 r environment (exometabolomics) over time in batch culture conditions can provide rich phenotypic dat

53 When bacteria are grown in a batch culture containing a mixture of two growth-limitin

54 ment substantial residual synchronization in batch cultures, contrary to assumptions of asynchrony.

55 putational comparison between continuous and batch cultures could explain seemingly conflicting exper

56 conditions tested, the daily growth rates in batch cultures decreased steadily over time, and station

57 Escherichia coli cells that are aged in batch culture display an increased fitness referred to a

58 f phi(napF-lacZ) expression during growth in batch culture displayed a complex pattern in response to

59 for the gradual decrease of growth rates in batch cultures during log phase, culminating with the on

60 t is important to note that during long-term batch culture, environmental conditions are in flux.

61 nabling continuous single-cell tracking in a batch culture experiencing unperturbed nutrient exhausti

62 Batch culture experiments on minimal medium revealed tha

63 of mixing on plasmid transfer, we performed batch culture experiments using three different plasmids

64 f the predominant clone, parallel and serial batch culture experiments were performed.

65 Using long-term batch culture experiments, we examined coccolithophore g

66 far unknown N isotope effects of anammox in batch culture experiments.

67 flavanol-induced bacterial changes in mixed-batch culture experiments.

68 detected, after 1 day of sugar starvation in batch culture, expression was mostly in individual bacte

69 , and a subsequent pH-controlled, anaerobic, batch-culture fermentation model reflective of the dista

70 sulfate is essentially identical to that of batch cultures growing in the same medium just before th

71 Coincident with phenazine production during batch culture growth, Fe(II) becomes the majority of the

72 lobacter crescentus revealed that in finite (batch) cultures (in which all offspring accumulate), the

73 ence of carbon dioxide, TSST-1 production in batch cultures increased from negligible levels in the p

74 ovine serum albumin or casein/L was added to batch cultures inoculated with feces from 4 healthy volu

75 ally, we show that ribosome hibernation in a batch culture is induced at an approximately two-fold lo

76 occurs when nutrients are fully exhausted in batch cultures is not observed in the chemostat, indicat

77 nd gene expression levels in exponential fed-batch cultures is reported.

78 coli from exhibiting detectable escape from batch cultures, its long-term effectiveness is unknown.

79 te closely resembling those of corresponding batch cultures just before they exhaust the nutrient.

80 onds most closely with the state of cells in batch cultures just before they undergo this "diauxic sh

81 eady and unsteady continuous (chemostat) and batch culture laboratory experiments.

82 stem can effectively replace the traditional batch culture methods with nanoliter volumes of bacteria

83 ssurized (i.e., system pressure below 1 atm) batch cultures, nitrogen (or other inert gases) is used

84 Batch culture of biofilms on peg lids is a versatile met

85 We discovered that a prototrophic batch culture of budding yeast, growing in a phosphate-l

86 In this study, we show that a batch culture of CH4ts shifted from 30 to 42 degrees C u

87 relative proportions were time dependent in batch cultures of A. niger.

88 The ELISA method was applied to batch cultures of C. thermocellum grown on Avicel.

89 hydrolysates was optimised (80.2g/g) in fed-batch cultures of R. toruloides leading to a total dry w

90 t similar uncoupling occurs in budding yeast batch cultures of Saccharomyces cerevisiae and Issatchen

91 Glucose-limited batch cultures of yeast go through two sequential expone

92 Chlorophyll allomers were measured in batch-cultures of O. tauri in parallel with maximum quan

93 amine and glutamate pools for cells grown in batch culture on different nitrogen sources that yielded

94 Here, we report that R. albus 7 grown in batch culture on glucose contained, besides a ferredoxin

95 ccharomyces cerevisiae cells was explored in batch cultures on a minimal medium containing glucose as

96 f jucara pulp, using pH-controlled anaerobic batch cultures reflective of the distal region of the hu

97 Cellulase protein production by Avicel-grown batch cultures represented approximately 20% of cell mas

98 Donors grown in batch culture retained conjugative competence following

99 Analysis of alo transcription in batch culture revealed a potential transcription start l

100 Previous batch culture studies determined that the de novo establ

101 An in vitro batch culture study model with different carbon sources,

102 Sulfide formation in fecal batch cultures supplemented with both bovine serum album

103 Included are a batch culturing system for sustained growth of subject-s

104 n the intestinal tract than conditions using batch culture techniques to investigate adherence and bi

105 deterministic cell cycle IBM model fails the batch culture test, because it has an abrupt drop in cel

106 Based on growth studies in batch culture, the Amt protein of Salmonella typhimurium

107 In anaerobic batch culture, the halophile Halomonas halodenitrificans

108 ive to the experimental simplicity of serial batch culture, the opposite is true of the environments

109 f marine phytoplankton grown in bench-scale, batch cultures: the diatom, Pseudonitzshia delicatissima

110 ochlorococcus strain MED4 to P starvation in batch culture to P-limited growth in chemostat culture.

111 possible manipulations that can operate on a batch culture to synchronize cells within the cell cycle

112 riments that were performed in chemostats or batch cultures under a spectrum of environmental perturb

113 n/consumption were obtained for denitrifying batch cultures under four conditions: initial COD:N rati

114 govern the growth at different phases in the batch culture were also identified.

115 r growth of Methylocella spp. in small-scale batch culture were overcome by growth in fermentor cultu

116 Moreover, cell division rates in fed-batch cultures were positively correlated with the dilut

117 S. oneidensis batch cultures were provided with lactate, Fe(III), and

118 When batch cultures were shifted from aerobic N-replete to an

119 the first could support growth on formate in batch culture where formate was in excess.

120 effect was observed on the biomass yield in batch culture, whereas no growth rate enhancement was ev

121 sistance development is generally studied in batch cultures which conceals the heterogeneity in cellu

122 However, laboratory studies use batch cultures, which simplify reality and focus on popu

123 nt for the persistence of S. mutans grown in batch culture with excess glucose and then starved of gl

124 yeast Saccharomyces cerevisiae in bioreactor batch cultures yielded variants that grow as multicellul