ライフサイエンスコーパス: photoinhibition

1 n the efficiency and rate of photosynthesis (photoinhibition).

2 volution, and protects photosytem II against photoinhibition.

3 was associated with increased sensitivity to photoinhibition.

4 tem II function and increases sensitivity to photoinhibition.

5 r further oxidation of ChlZ and irreversible photoinhibition.

6 when dark-grown, the effect is unrelated to photoinhibition.

7 h air, although they have less resistance to photoinhibition.

8 Q) and its role in protecting plants against photoinhibition.

9 er UV-B stress, which mitigated UV-B-induced photoinhibition.

10 tive stress during a process that can induce photoinhibition.

11 opy architecture and the diurnal dynamics of photoinhibition.

12 onged high-light exposure caused accelerated photoinhibition.

13 tosystem II reaction center is vulnerable to photoinhibition.

14 y light sensitive and failed to recover from photoinhibition.

15 verreduced and photosystem I is subjected to photoinhibition.

16 nally conclude that mat decline is linked to photoinhibition.

17 volution rate and greater protection against photoinhibition.

18 ent formation of reactive excited states and photoinhibition.

19 and the diatom cells suffered from stronger photoinhibition.

20 es or preventing their accumulation to avoid photoinhibition.

21 n shown directly in plants in the absence of photoinhibition.

22 and to stabilize the Mn(4)Ca cluster against photoinhibition.

23 with a role for the CP43 NFK modification in photoinhibition.

24 ency within the phycobilisome and to prevent photoinhibition.

25 The mutant cells were highly susceptible to photoinhibition.

26 ll content and a reduced recovery rate after photoinhibition.

27 n increased degree of lipid peroxidation and photoinhibition.

28 thylakoid membranes, was most susceptible to photoinhibition.

29 branes, the rate of D1 protein synthesis, or photoinhibition.

30 lar body, and the repair process of D1 after photoinhibition.

31 To avoid chronic photoinhibition, a PSII repair cycle operates to replace

32 This was reflected by a stronger photoinhibition after 24 h of high light (approximately

33 Moreover, S1 photoinhibition after partial adaptation blocked further

34 Model simulations show that photoinhibition alone can result in substantial reductio

35 on; however, increased light can also induce photoinhibition and cause physiological stress in algae

36 Photoinhibition and chlorophyll levels decreased upon ph

37 unit of PSII but is required for repair from photoinhibition and efficient assembly of the PSII RC.

38 isms may increase biomass yields by limiting photoinhibition and increasing light penetration in dens

39 ditions, but exhibits greater sensitivity to photoinhibition and long-term mild heat stress than wild

40 ty of cells to both high temperature-induced photoinhibition and photobleaching was ameliorated by in

41 lated with the extent of photosystem (PS) II photoinhibition and the expression of various (1)O(2) ma

42 naerobiosis preserves PSII from irreversible photoinhibition, and (iii) mutants with enhanced respira

43 temperature on cell growth, photosynthesis, photoinhibition, and nitrate assimilation was examined i

44 var2 mutants are hypersusceptible to photoinhibition, and VAR2 degrades unassembled polypepti

45 underlying molecular mechanisms that lead to photoinhibition are poorly understood.

46 All three isolates showed only minor photoinhibition at 15 microE m(-2) s(-1) and rapid recov

47 bation of PSII protein turnover rates during photoinhibition at elevated temperatures underlies the p

48 plastoquinone-9, resulting in near complete photoinhibition at high light intensity.

49 rvals, features critical for minimization of photoinhibition; (b) a microvolume (5 microL) O2 polarog

50 otodamage to the cofactor-free apo-WOC-PSII (photoinhibition).Bicarbonate does not affect the second

51 e of photosynthetic electron transport or by photoinhibition, but that inactivation of the nitrate/ni

52 me centers, suggesting that qE protects from photoinhibition by preventing overreduction of photosyst

53 ld also have provided effective reduction of photoinhibition by UV radiation.

54 d mutant cells were similar under high-light photoinhibition conditions, as well as in media without

55 ile population increases significantly after photoinhibition, consistent with a role for protein diff

56 This S1 photoinhibition did not impair basic motor patterns, pos

57 Photoinhibition, exacerbated by elevated temperatures, u

58 of the redox component increased the rate of photoinhibition >15-fold.

59 essure at photosystem II, and no evidence of photoinhibition, implying a better dynamic regulation to

60 e required for low-temperature recovery from photoinhibition in Arabidopsis.

61 Inspiratory-phase photoinhibition in Arch-transfected mice during inspirat

62 in thermal dissipation ability and enhanced photoinhibition in excess light conditions.

63 omponent of NPQ that is necessary to prevent photoinhibition in excess light.

64 rong control over the rate of photosystem II photoinhibition in isolated thylakoid membranes.

65 Detailed investigation of photoinhibition in the triple mutant revealed that the r

66 Therefore, photoinhibition is always observed when the rate of phot

67 Photoinhibition of CeM projectors impairs fear condition

68 Dorsal striatal photoinhibition of ChIs in lesioned ChAT(cre/cre) mice e

69 Our results show that photoinhibition of ChIs in the dorsal striatum and pharm

70 Unilateral photoinhibition of delay activity in the ALM or thalamus

71 Photoinhibition of FPTase activity by Compound 1 is prev

72 ed mouse hippocampal neurons enabled precise photoinhibition of individual spikes in trains of up to

73 triggered changes in protein expression and photoinhibition of photosystem I (PSI) and resulted in t

74 pe exposed to mild light stress that invokes photoinhibition of photosystem II without causing photoo

75 ht stress than PSII as shown by the stronger photoinhibition of PSI and increased rate of singlet oxy

76 The flv4-2/OE mutant is more resistant to photoinhibition of PSII and exhibits a more oxidized sta

77 Increased susceptibility to photoinhibition of PSII in stm6 demonstrates that the MO

78 We found that temporally precise photoinhibition of somatosensory cortex (S1) applied con

79 Similarly, photoinhibition of the ALM diminished thalamic activity.

80 Photoinhibition of the thalamus caused a short-latency a

81 rmal firing rates in the left mPFC; however, photoinhibition of these neurons induced social avoidanc

82 Here, we evaluate the effects of photoinhibition on long-term carbon gain (over 1 d) in t

83 Significant photoinhibition only occurred at Chl concentrations belo

84 f light level and occurred in the absence of photoinhibition or lipid peroxidation suggests that the

85 of ATP and NADPH must be balanced to prevent photoinhibition or photodamage.

86 tein deficiency did not significantly affect photoinhibition or turnover of photosystem II-associated

87 inactivation results from an FtsH-sensitive photoinhibition process.

88 RTN photoinhibition reduced breathing equally during non-REM

89 Photoinhibition reduces photosynthetic productivity; how

90 52L, and W352A, exhibit an increased rate of photoinhibition relative to wild type.

91 During persistent apneas, prolonged photoinhibition restored rhythmic breathing.

92 bic potentiometric titrations of the rate of photoinhibition revealed a redox component with a midpoi

93 osses to the atmosphere, and a lower risk of photoinhibition, roles that justify its vast presence in

94 mpensate for the impaired photosynthesis and photoinhibition sensitivity.

95 spiratory duration, whereas expiratory-phase photoinhibition shortened the latency until the next ins

96 ates that potato may be a useful species for photoinhibition studies.

97 h increased DHAR expression experienced less photoinhibition than did wild-type plants following expo

98 d show that younger leaves are less prone to photoinhibition than older leaves.

99 had higher degrees of lipid peroxidation and photoinhibition than the vtc2 mutant.

100 ow light growth, but it is more sensitive to photoinhibition than the wild type.

101 th higher qE capacity were more resistant to photoinhibition than the wild type.

102 fad8 triple mutant, were more susceptible to photoinhibition than wild-type Arabidopsis, whereas one

103 e pre-steady-state lag phase and to suppress photoinhibition, thereby improving the accuracy of t(lag

104 The mutant was susceptible to photoinhibition under pulsing but not constant light.

105 ae decreased simultaneously, indicating that photoinhibition underlies the observed decreased photosy

106 Significant photoinhibition was also observed following exposure to

107 Such a photoinhibition was paralleled by significant damage to

108 The extent of photoinhibition was the same in all of the mutants, sugg

109 nts showed impaired growth and photosystem I photoinhibition when exposed to fluctuating light, demon

110 amage of photosystem II (PSII) thus avoiding photoinhibition which can decrease plant fitness and pro