ライフサイエンスコーパス: heat resistance

1 if germinants are removed, and loss of spore heat resistance.

2 ore core dehydration and a decrease in spore heat resistance.

3 ndent manner, with reduced dosage decreasing heat resistance.

4 action, as well as to de novo acquisition of heat-resistance.

5 important to accurately determine bacteria's heat resistances.

6 osa primarily in stationary phase and boosts heat resistance 100-fold when expressed in Escherichia c

7 We find a wide range of heterogeneous heat resistance and a trade-off between average yield an

8 bmh1Delta-induced heat resistance and CLS extension require the general st

9 similar to endospores in ultrastructure, in heat resistance and in the presence of dipicolinic acid.

10 race, which is associated with slow growth, heat resistance and longevity.

11 The superdormant spores had higher wet-heat resistance and lower core water content than the or

12 role for IMPDH in remodelling metabolism and heat resistance, and provides evidence that Ap4A can fun

13 dged by the kinetics of flaA-gfp expression, heat resistance, and sodium sensitivity.

14 ores of Clostridium perfringens possess high heat resistance, and when these spores germinate and ret

15 cribed to intracellular trehalose, including heat resistance, are not due to the presence of trehalos

16 Korea, and research is required to increase heat resistance as a solution against climate change.

17 and wild-type cells, suggesting induction of heat resistance at low growth rates is independent of re

18 ified as type F because of their exceptional heat resistance but later identified as type C strains.

19 1 capsid coding that is sufficient to confer heat resistance but not bleach resistance.

20 a 1 degrees C warming scenario as increased heat resistance cannot be achieved without a reduction i

21 rocess-like and operating conditions such as heat resistance, contact with organic solvents, steriliz

22 , and dacC and wild-type spores had the same heat resistance, cortex structure, and germination and o

23 and sporulation, and ywhE spores had normal heat-resistance, cortex structure, and germination and o

24 ithin mammalian orthoreovirus that regulates heat resistance, disassembly kinetics, and replicative f

25 s of two Bacillus species, the early loss in heat resistance during germination is most likely due to

26 creases of Actinobacteria encoding genes for heat resistance, fast growth, and pyrogenic carbon utili

27 scopic morphology, production of extrolites, heat-resistance fungi, and sequencing of DNA regions.

28 and IB by a more acidic pH optimum, greater heat resistance, greater sensitivity to alkylating agent

29 Recently elevated heat resistance in gamma-proteobacterial species was sho

30 Higher heat resistance in later bleaching events was detected i

31 ng competent state and also confers cellular heat resistance in vivo.

32 d index, yield stability, relative heat, and heat resistance indices, while duplicate gene interactio

33 Heat resistance is a proxy for long-term aggregation pro

34 tation and maximum temperature, showing that heat resistance is an important determinant of Drosophil

35 The latter event is puzzling, since spore heat resistance is due largely to core water content, wh

36 Knowledge of bacteria's heat resistance is essential for developing effective th

37 Bacterial spore heat resistance is primarily dependent upon dehydration

38 e found, but the existence of tradeoffs with heat resistance may suggest caution in unilateral use of

39 cause human food-borne illness share a spore heat resistance mechanism that likely favors their survi

40 ntal matrices, and the use of elasticity and heat resistance observations to differentiate TRWPs from

41 proteins play no significant role in the wet heat resistance of B. subtilis spores.

42 In addition, the inherent heat resistance of cotton facilitates its high-temperatu

43 thermal stabilities, and for the first time heat resistance of fractions (mono-, dichlorogenic acids

44 to-DNA ratio and a structure that shares the heat resistance of mature AAV particles.

45 duces the characteristic shape, pigment, and heat resistance of stationary-phase L. pneumophila.

46 germination, heat activation optima, and wet-heat resistance of superdormant spores and the heterogen

47 cell morphology, growth, sporulation, spore heat resistance, or spore germination and outgrowth.

48 iable cells and showed that they have normal heat resistance properties.

49 alyses we showed that phylogenetic signal in heat resistance reflects phylogenetic inertia rather tha

50 iated TAG accumulation was found to increase heat resistance, since nonacclimated pdat1 mutant seedli

51 6), which is a secondary explosive with high heat resistance (Tdec =310 degrees C).

52 10-fold-lower viability and far less UV and heat resistance than spores overexpressing SspC(wt).

53 e lower core wet densities and levels of wet heat resistance than wild-type or ger3 spores.

54 The immobilized enzyme possessed a better heat-resistance than free enzyme.

55 growth and restored a small amount of UV and heat resistance to alpha- beta- spores.

56 sion in vivo of hsp110 conferred substantial heat resistance to both Rat-1 and HeLa cells.

57 he sigma(G) regulon, are shown to confer dry-heat resistance to dormant spores.

58 his protein did not restore UV radiation and heat resistance to spores lacking the majority of their

59 isteria monocytogenes that provides enhanced heat resistance to the food-borne pathogen enabling pers

60 Notably, EEC exhibited heat resistance up to 200 degrees C and stabilized above

61 way of interpreting both heat tolerance and heat resistance was developed, differentiating genotypes