ライフサイエンスコーパス: phototrophic

1 that depend entirely on bacterial prey; (3) phototrophic algae that depend only on light and inorgan

2 dation-reduction balancing mechanisms during phototrophic anaerobic respiration.

3 mes have already been reduced in free-living phototrophic ancestors of apicomplexan parasites, and su

4 arameter representing proportional mixing of phototrophic and heterotrophic nutritional strategies.

5 Purple non-sulphur phototrophic bacteria (PNSB) are excellent models for an

6 oductive microbial ecosystem, including both phototrophic bacteria and eukaryotes, living in a strati

7 evious data-limited phylogenetic analyses of phototrophic bacteria and indicate that the core compone

8 that photosynthetically competent anoxygenic phototrophic bacteria are abundant in the upper open oce

9 The green phototrophic bacteria contain a unique complement of chl

10 Aerobic, anoxygenic, phototrophic bacteria containing bacteriochlorophyll a (

11 The purple phototrophic bacteria elaborate a specialized intracytop

12 ein, whereas plants, cyanobacteria, and some phototrophic bacteria possess an O2-dependent enzyme, th

13 It is known that anoxygenic phototrophic bacteria require the Calvin cycle to accept

14 ng cyclases between cyanobacteria and purple phototrophic bacteria reveals three classes of the O2-de

15 MTA metabolism to ethylene formation in the phototrophic bacteria Rhodospirillum rubrum and Rhodopse

16 The purple phototrophic bacteria synthesize an extensive system of

17 rotective mechanism of likely importance for phototrophic bacteria that encounter light and oxygen.

18 nobacteria are a recently described group of phototrophic bacteria that is a major focus of photosynt

19 The green sulfur bacteria, the Chlorobi, are phototrophic bacteria that oxidize sulfide and deposit e

20 The majority of anoxygenic phototrophic bacteria use BchE, an O2-sensitive [4Fe-4S]

21 on of light and oxygen encountered by purple phototrophic bacteria, but the efficiency of such protec

22 pex taxa are consistent with those of extant phototrophic bacteria; those for a somewhat lower delta(

23 Several phototrophic bacterial clades are thought to have evolve

24 of the thermophilic, filamentous anoxygenic phototrophic bacterium Chloroflexus aurantiacus has been

25 action center (RC) in the thermophilic green phototrophic bacterium Chloroflexus aurantiacus.

26 proteins of the green filamentous anoxygenic phototrophic bacterium Chloroflexus aurantiacus.

27 ons of oxygen limitation, this facultatively phototrophic bacterium forms an intracytoplasmic membran

28 rothrix halophila," a filamentous anoxygenic phototrophic bacterium found in Baja California Sur, Mex

29 The facultative phototrophic bacterium Rhodobacter capsulatus contains o

30 arboxylase/oxygenase (Rubisco) employing the phototrophic bacterium Rhodobacter capsulatus was used t

31 e photosynthetic apparatus in the anoxygenic phototrophic bacterium Rhodobacter sphaeroides 2.4.1.

32 PpsR from the anoxygenic phototrophic bacterium Rhodobacter sphaeroides has been

33 osynthesis control RNA Z) of the facultative phototrophic bacterium Rhodobacter sphaeroides is induce

34 wth in the presence of 1O2, we show that the phototrophic bacterium Rhodobacter sphaeroides mounts a

35 ve recently established that the facultative phototrophic bacterium Rhodobacter sphaeroides, like the

36 In the purple phototrophic bacterium Rhodobacter sphaeroides, many pro

37 rmine the role of GSH-FDH in the facultative phototrophic bacterium Rhodobacter sphaeroides.

38 tase was purified from the purple non-sulfur phototrophic bacterium Rhodobacter sulfidophilus.

39 anaerobic degradation of p-coumarate by the phototrophic bacterium Rhodopseudomonas palustris and fo

40 This enzyme was purified from the phototrophic bacterium Rhodopseudomonas palustris by seq

41 ation of benzoate has been described for the phototrophic bacterium Rhodopseudomonas palustris.

42 hbaA, were identified and sequenced from the phototrophic bacterium Rhodopseudomonas palustris.

43 he anaerobic oxidation of CO to CO(2) in the phototrophic bacterium Rhodospirillum rubrum.

44 domonas palustris is a purple, facultatively phototrophic bacterium that uses hydrogen gas as an elec

45 des 2.4.1T is a purple nonsulfur facultative phototrophic bacterium which exhibits remarkable metabol

46 n of benzoate and related compounds from the phototrophic bacterium, Rhodopseudomonas palustris.

47 Ppr from the purple phototrophic bacterium, Rhodospirillum centenum (also kn

48 The purple phototrophic bacterium, Thermochromatium tepidum, contai

49 ive bacteriochlorophyll (BChl)-synthesizing, phototrophic bacterium.

50 the porous ikaite is colonized by endolithic phototrophic biofilms serving as a substrate for grazing

51 In the presence of riboflavin, the phototrophic biomass in the anodic compartment produced

52 netic event can result in the acquisition of phototrophic capabilities in an otherwise chemoorganotro

53 rocess model or PPM) was developed for mixed phototrophic communities subjected to day/night cycling.

54 e changed with time and structurally similar phototrophic communities were found at the soil surface

55 ith novel combinations of photosynthetic and phototrophic components that have not yet been described

56 viour of tomato leaf under heterotrophic and phototrophic conditions.

57 vented when respiration is impaired or under phototrophic conditions.

58 e of riboflavin upon illumination of a mixed phototrophic culture enriched from a freshwater pond at

59 Nanowires produced by the oxygenic phototrophic cyanobacterium Synechocystis PCC6803 and th

60 ime-dependent resource allocation problem of phototrophic diurnal growth and may serve as a general f

61 The distribution of GSH in phototrophic eubacteria indicates that GSH synthesis evo

62 ociation between a heterotrophic or possibly phototrophic eukaryotic host and a photosynthetic eukary

63 lysis revealed that FixK regulates anaerobic phototrophic expression of other target genes with FixK

64 he pio operon are essential and specific for phototrophic Fe(II) oxidation in R. palustris TIE-1.

65 ophic iron oxidation), that is necessary for phototrophic Fe(II) oxidation.

66 Phototrophic Fe(II)-oxidizing bacteria couple the oxidat

67 f this process because, until recently, most phototrophic Fe(II)-oxidizing bacteria have been genetic

68 Here we examine this issue for the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas

69 etic and spectroscopic measurements that the phototrophic Fe(II)-oxidizing bacterium Rhodopseudomonas

70 rine Synechococcus, the second-most abundant phototrophic group in the marine environment, is partly

71 was constructed and found to be incapable of phototrophic growth and impaired in intracytoplasmic mem

72 e CO(2)-anaplerotic pathway is active during phototrophic growth and that isoleucine is mainly synthe

73 We formulate phototrophic growth as an autocatalytic process and solv

74 seq was used to identify genes essential for phototrophic growth by the purple bacterium Rhodopseudom

75 ds to specific metabolic circumstances under phototrophic growth conditions.

76 The cloned ycf5 gene also complements the phototrophic growth deficiency in strain B6 of C. reinha

77 tosynthesis, thereby permitting survival and phototrophic growth during the light period.

78 wild-type level is insufficient for rescuing phototrophic growth impairment of the prrA mutant, where

79 xidation during sulfide-dependent chemo- and phototrophic growth in bacteria.

80 While they are crucial for phototrophic growth of cyanobacterial cells, biogenesis

81 a genetic suppressor approach that restored phototrophic growth of mutants originally defective for

82 uctoisomerase, did not significantly inhibit phototrophic growth of the cyanobacterium, nor did it af

83 and pyruvate, can be assimilated during the phototrophic growth of the GSBs, in the presence of CO(2

84 he puhA gene alone was sufficient to restore phototrophic growth provided that recombination occurred

85 oxidoreductase complex IE was essential for phototrophic growth under strictly anaerobic conditions

86 ocation of cellular resources during diurnal phototrophic growth using a genome-scale metabolic recon

87 g an R. sphaeroides regA-deficient mutant to phototrophic growth with restored regulated synthesis of

88 The selected (phototrophic growth) as well as the unselected (holocyto

89 e are either absent or down-regulated during phototrophic growth, implying that the OTCA cycle is not

90 these were proteins encoded by subset of the phototrophic growth-essential genes.

91 sis, that were not known to be essential for phototrophic growth.

92 was also enhanced over normal levels during phototrophic growth.

93 s essential for light-dependent greening and phototrophic growth.

94 regulated, as was the bop gene, required for phototrophic growth.

95 chlorosomes as light-harvesting antennae for phototrophic growth.

96 riven by reduced ferredoxin generated during phototrophic growth.

97 was previously considered indispensable for phototrophic growth.

98 gens, whereas the major thiol in the aerobic phototrophic halobacteria is gamma-glutamylcysteine.

99 -gene operon, designated the pio operon (for phototrophic iron oxidation), that is necessary for phot

100 The pioABC operon is required for phototrophic iron oxidative (photoferrotrophic) growth b

101 The spatial organization of the phototrophic layer resembles microbial mats growing on s

102 traditionally been thought to be an ancient phototrophic lineage, genomics has revealed a much great

103 faster growing CO2 fixers, better adapted to phototrophic living in the oligotrophic open ocean-the m

104 ife strategies arose from a once free-living phototrophic marine alga.

105 however, debate continues over how different phototrophic mechanisms and the bacteria that contain th

106 constructed evolutionary relationships among phototrophic mechanisms based on a phylogeny of core ant

107 There are two types of phototrophic mechanisms in the Bacteria: reaction center

108 s and molecular clock analyses, we show that phototrophic members of the Chloroflexi phylum are not p

109 gineer cellular metabolism; however, GEMs of phototrophic metabolism have been limited by the lack of

110 t and bioenergy production, using engineered phototrophic microbial communities.

111 Metagenomic data from the phototrophic microbial mats of alkaline siliceous hot sp

112 m, assess the level of sub-optimal growth in phototrophic microbial mats, and elucidate the extent an

113 Phototrophic microorganisms have significant potential a

114 We propose that periphytic phototrophic microorganisms such as algae likely affect

115 lar-weight thiol composition of a variety of phototrophic microorganisms to ascertain how evolution o

116 While this is an expected response among phototrophic microorganisms, the ability of chemotrophic

117 generate reactive intermediates that damage phototrophic microorganisms.

118 We analyzed different CMAs produced by phototrophic or nitrate-reducing microbial Fe(II) oxidat

119 Glycolipids are mainly found in phototrophic organisms (like plants and cyanobacteria),

120 Phototrophic organisms exhibit a highly dynamic proteome

121 Phototrophic organisms such as plants, photosynthetic ba

122 lity of metabolic strategies that evolved in phototrophic organisms under diurnal conditions.

123 ymes for known autotrophic pathways in other phototrophic organisms, including ribulose bisphosphate

124 ed a strong influence on the paleoecology of phototrophic plankton in Kusai Lake.

125 lumped pathway metabolic model (denoted the phototrophic process model or PPM) was developed for mix

126 rectly compare the intrinsic growth rates of phototrophic prokaryotes and eukaryotes from the equator

127 In the facultatively phototrophic proteobacterium Rhodobacter sphaeroides, fo

128 senting the 4.6-Mb genome of the facultative phototrophic proteobacterium, Rhodobacter sphaeroides 2.

129 In the facultative phototrophic (Ps) bacterium Rhodobacter capsulatus, it i

130 l genes encoding photosynthetic functions in phototrophic purple bacteria are not present in the heli

131 tathione amide and its perthiol, produced by phototrophic purple sulfur bacteria and apparently invol

132 ite the fact that heliobacteria are the only phototrophic representatives of the bacterial phylum Fir

133 re pairing fermentative Escherichia coli and phototrophic Rhodopseudomonas palustris.

134 xic state with sulfate-reducing bacteria and phototrophic sulfur bacteria.

135 r bacterium (GSB) that is a model system for phototrophic sulfur oxidation.

136 s) originally inoculated with biomass from a phototrophic system at a wastewater treatment plant.