ライフサイエンスコーパス: photoautotrophic

1 mutant, the resulting strains were no longer photoautotrophic.

2 he total nitrogen provided in the medium for photoautotrophic and 13% for heterotrophic growth.

3 A suppressor strain, LF-1-RVT-1, which is photoautotrophic and capable of processing pre-D1 has a

4 psulatus, strain Mal7, that was incapable of photoautotrophic and chemoautotrophic growth and could n

5 All ten of these mutants were photoautotrophic and evolved oxygen at normal rates.

6 V247M was photoautotrophic and had an essentially normal phenotype

7 iral and cellular replication cycles in both photoautotrophic and heterotrophic bacterial hosts.

8 to wild type (WT) in continuous-light-grown photoautotrophic and mixotrophic cultures, whereas it gr

9 wild-type and the menG mutant strains under photoautotrophic and photomixotrophic conditions were vi

10 han a decrease in thermotolerance under both photoautotrophic and photomixotrophic conditions.

11 ilis and in a small number of organisms with photoautotrophic and thermophilic lifestyles.

12 and/or cyanobacterium (photobiont), the non-photoautotrophic bacteria found in lichen microbiomes ar

13 Cyanobacteria are a group of photoautotrophic bacteria that have traditionally been u

14 Cyanobacteria are important photoautotrophic bacteria with extensive but variable me

15 n previously applied to map carbon fluxes in photoautotrophic bacteria, which involves model-based re

16 molecular players promoting phototropism in photoautotrophic, but not etiolated, seedlings.

17 st rapidly establish its root system and the photoautotrophic capability appropriate to its surroundi

18 Deletion of slr0286 did not affect photoautotrophic capacity in wild type but led to a mark

19 a slug can be sustained in culture solely by photoautotrophic CO(2) fixation for at least 9 months if

20 3 causes significant growth impairment under photoautotrophic conditions and results in hyper-sensiti

21 ate, although the mutant grew normally under photoautotrophic conditions in air.

22 he resulting mutants were able to grow under photoautotrophic conditions, dividing at rates that were

23 Although both mutants grow under photoautotrophic conditions, the rate of PSI-mediated el

24 moderate light, the mutant grew slowly under photoautotrophic conditions, with a doubling time of app

25 e DeltapsbY mutant cells grew normally under photoautotrophic conditions.

26 In a synchronized photoautotrophic culture of Chlamydomonas reinhardtii, c

27 a mechanistic basis for managing the DIC for photoautotrophic cultures through the N source.

28 cteria, chemoautotrophic Thaumarchaeota, and photoautotrophic Cyanobacteria.

29 h (approximately -200 to -400 per thousand), photoautotrophic growth (-150 to -250 per thousand), het

30 C550-H92M lost photoautotrophic growth ability in the absence of Ca(2+)

31 notype with defects in photopigment content, photoautotrophic growth and carbon fixation rates, and s

32 Those mutants exhibiting photoautotrophic growth and oxygen evolution capability

33 enotypes ranging from moderate alteration of photoautotrophic growth and oxygen evolution rates to a

34 tant G342D exhibited moderate alterations of photoautotrophic growth and oxygen evolution.

35 Photoautotrophic growth and photophosphorylation rates w

36 he Ile, Val, and Leu mutants are impaired in photoautotrophic growth and photosynthesis in both low a

37 re and function, and is critical for overall photoautotrophic growth and plant development.

38 e splicing was completely blocked, showed no photoautotrophic growth and synthesis of a truncated D1

39 s were selected for their ability to restore photoautotrophic growth and these describe six nuclear l

40 psbQ inactivation mutants exhibited reduced photoautotrophic growth as well as decreased water oxida

41 tations produced strains that are capable of photoautotrophic growth at moderate light intensity (20

42 ite mutants (pseudorevertants) with restored photoautotrophic growth but still maintaining the E69Q m

43 which encodes a protein system essential for photoautotrophic growth by ferrous iron oxidation, influ

44 Analysis of the photoautotrophic growth capabilities of these mutants, t

45 Distinct from the results obtained with photoautotrophic growth conditions, the results of studi

46 the groESL1 genes was unexpectedly low under photoautotrophic growth conditions.

47 f amino acid and enzyme de novo synthesis in photoautotrophic growth conditions.

48 phaeroides under both photoheterotrophic and photoautotrophic growth conditions.

49 ains grown under both photoheterotrophic and photoautotrophic growth conditions.

50 he LTO1 promoter is associated with a severe photoautotrophic growth defect.

51 he porA-1 and PORA RNAi lines display severe photoautotrophic growth defects, which can be partially

52 yledon expansion during the establishment of photoautotrophic growth depends on ABCB19-mediated auxin

53 esting that inactivation of Slr0399 leads to photoautotrophic growth in D2R8.

54 photosystem II is known to lead to a loss of photoautotrophic growth in Synechocystis sp. PCC 6803.

55 Restoration of photoautotrophic growth in this mutant was caused by ear

56 However, photoautotrophic growth of Chlamydomonas strains contain

57 Photoautotrophic growth of flvB mutants was indistinguis

58 Photoautotrophic growth of mutants obtained varied from

59 ier in the thylakoid lumen and essential for photoautotrophic growth of plants.

60 Photoautotrophic growth of the double mutant is severely

61 ons (12 h of light and 12 h of dark), normal photoautotrophic growth of the mutant is completely rest

62 coccus PCC6301 rbcLS genes enabled anaerobic photoautotrophic growth of the R.capsulatus deletion str

63 nverted to the corresponding perthiol during photoautotrophic growth on sulfide, suggesting that GASH

64 ron donor for carbon dioxide fixation during photoautotrophic growth or for ammonia synthesis during

65 these mutations did not result in a loss of photoautotrophic growth or in significantly altered PS I

66 val of these protein products does not alter photoautotrophic growth or PSII fluorescence properties.

67 nd Gly mutants in high light is reduced, but photoautotrophic growth rate is not affected.

68 Although the photoautotrophic growth rate of the Deltasll1951 strain

69 ylakoids was comparable to the change in the photoautotrophic growth rate.

70 M chloride), it exhibited a severely reduced photoautotrophic growth rate.

71 eletion of ndb genes led to small changes in photoautotrophic growth rates and respiratory activities

72 The photoautotrophic growth rates of wild type and mutants i

73 The mechanism by which the S79F mutant loses photoautotrophic growth remains to be established.

74 introduction of an antibiotic cassette, and photoautotrophic growth resulted in the generation of a

75 s, and that the PsbQ protein is required for photoautotrophic growth under low light conditions.

76 in two of these mutants, FVEYPI and FLVYNI, photoautotrophic growth was impaired and the relative va

77 Transformants were selected in which photoautotrophic growth was restored, resulting in 11 vi

78 Pseudorevertants with much improved photoautotrophic growth were also generated for one of t

79 Transformants that were complemented to photoautotrophic growth were selected, and 20 such mutan

80 f C. reinhardtii that require high CO(2) for photoautotrophic growth were tested by complementation g

81 Under continuous light, 3WEZ exhibits poor photoautotrophic growth while growing photoheterotrophic

82 tify mutants that were able to complement to photoautotrophic growth with 1.5% CO(2).

83 s incapable of complementing R.capsulatus to photoautotrophic growth with 5% CO(2) were identified.

84 7 of CP47 were found to be indispensable for photoautotrophic growth, and many amino acid combination

85 ed an increased requirement for chloride for photoautotrophic growth, and two mutants, C8-10 and C8-2

86 The single mutant S79F was also incapable of photoautotrophic growth, but displayed reasonably stable

87 tosynthetic performance, they are capable of photoautotrophic growth, demonstrating that, different f

88 es of heliobacteria that have failed to show photoautotrophic growth, genes encoding enzymes for know

89 e small high-potential redox proteins during photoautotrophic growth, including two high-potential ir

90 role in the transition from heterotrophic to photoautotrophic growth, suggesting an important physiol

91 ion is central to the rewiring of plants for photoautotrophic growth.

92 at position 268 appeared to be required for photoautotrophic growth.

93 tion, as their mutation led to impairment of photoautotrophic growth.

94 CP47 protein are known to lead to a loss of photoautotrophic growth.

95 n Synechocystis 6803 resulted in compromised photoautotrophic growth.

96 The eight mutant strains differed in their photoautotrophic growth.

97 erations in D1 turnover, photosynthesis, and photoautotrophic growth.

98 ut this is not necessarily rate-limiting for photoautotrophic growth.

99 00-fold increase in chloride requirement for photoautotrophic growth.

100 in a discernible phenotype, namely, impaired photoautotrophic growth.

101 seedlings are also defective in establishing photoautotrophic growth.

102 The vte6 mutant plants are incapable of photoautotrophic growth.

103 nct proteome demands during heterotrophic or photoautotrophic growth.

104 eals that the gene function is essential for photoautotrophic growth.

105 t an intact sll0606 gene could fully restore photoautotrophic growth.

106 tic organisms and required for their optimal photoautotrophic growth.

107 l properties render it a limiting factor for photoautotrophic growth.

108 4S(PsaC) that mapped to sll0088 and restored photoautotrophic growth.

109 poson mutagenesis to be required for optimal photoautotrophic growth.

110 s of full-length D1, and an 18% reduction in photoautotrophic growth.

111 d an engineered suppressor strain capable of photoautotrophic growth.

112 ns redox poise during photoheterotrophic and photoautotrophic growth.

113 Photoautotrophic H2 production has important implication

114 d model accurately predicts phenotypes under photoautotrophic, heterotrophic, and mixotrophic conditi

115 In a photoautotrophic higher plant, Spirodela oligorrhiza, gr

116 s (mixotrophic in the presence of acetate or photoautotrophic in the presence or absence of nitrogen)

117 , four (H117C, H117M, H117N, and H117T) were photoautotrophic in the PS I-containing background.

118 hloroplast function and is essential for the photoautotrophic life-style of plants.

119 g constitutes a geochemical paradox, in that photoautotrophic metabolism will tend to precipitate car

120 tial gene and physiological data specific to photoautotrophic metabolism.

121 chain polyunsaturated fatty acids producing photoautotrophic microalgae in one study.

122 iptional networks revealed that the dominant photoautotrophic microbes in each environment (Ostreococ

123 Coupling of strong experimental support and photoautotrophic modeling methods thus resulted in a hig

124 Using combinatorial mutagenesis, photoautotrophic mutants of Synechocystis sp. PCC 6803 h

125 em II properties were studied in a number of photoautotrophic mutants of Synechocystis sp. PCC 6803,

126 hrough the NDA2 catalytic hub in response to photoautotrophic N deprivation sustains cell viability w

127 of the respiratory oxidases had no effect on photoautotrophic or photomixotrophic growth.

128 We show how this can occur in a single photoautotrophic organism, representing a previously und

129 n of a dark-grown seedling into a pigmented, photoautotrophic organism.

130 uggests that these mutations led to a normal photoautotrophic phenotype.

131 pansions that may explain the distinguishing photoautotrophic phenotypes observed.

132 Photoautotrophic plankton in the surface ocean release o

133 When cells are shifted from photoautotrophic planktonic growth to light-activated he

134 indicate that the NDH complex can be lost in photoautotrophic plant species.

135 transcriptome data showed that 47 out of 660 photoautotrophic plants and all the heterotrophic plants

136 logical evidence to support nitrification by photoautotrophic plants.

137 Several photoautotrophic pseudorevertants of this mutant have be

138 trophic mutant lacking the T271-K277 region, photoautotrophic pseudorevertants were generated with sh

139 d to the genome of the unicellular, obligate photoautotrophic red alga Cyanidioschyzon merolae.

140 8) tail is an obligate heterotroph to obtain photoautotrophic revertants.

141 a quiescent dry seed to an actively growing photoautotrophic seedling is a complex and crucial trait

142 Plants are photoautotrophic sessile organisms that use environmenta

143 esia (Wakatobi) corals have declined and the photoautotrophic sponge Lamellodysidea herbacea is now a

144 and mcd5 mutants were initially isolated as photoautotrophic suppressors of the petD 5' mutants LS2

145 between a heterotrophic host and an internal photoautotrophic symbiont.

146 ncrease the probability of transition from a photoautotrophic to a heterotrophic life history.

147 l manipulations and chemical genetics at the photoautotrophic transition checkpoint, we reveal that s

148 ences involved in positive regulation during photoautotrophic versus chemoautotrophic growth, suggest

149 pression was dependent on growth conditions (photoautotrophic versus mixotrophic).

150 The A249T mutant, although photoautotrophic, was affected by artificial quinones, b