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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 2) fixation pathways are known to operate in photoautotrophic and chemoautotrophic microorganisms.
6                All ten of these mutants were photoautotrophic and evolved oxygen at normal rates.
7                                    V247M was photoautotrophic and had an essentially normal phenotype
8 iral and cellular replication cycles in both photoautotrophic and heterotrophic bacterial hosts.
9  to wild type (WT) in continuous-light-grown photoautotrophic and mixotrophic cultures, whereas it gr
10  wild-type and the menG mutant strains under photoautotrophic and photomixotrophic conditions were vi
11 han a decrease in thermotolerance under both photoautotrophic and photomixotrophic conditions.
12 ling approaches are amenable to the study of photoautotrophic and secondary metabolism.
13 ilis and in a small number of organisms with photoautotrophic and thermophilic lifestyles.
14  shoot and root tissues of heterotrophic and photoautotrophic Arabidopsis (Arabidopsis thaliana) seed
15  and/or cyanobacterium (photobiont), the non-photoautotrophic bacteria found in lichen microbiomes ar
16                 Cyanobacteria are a group of photoautotrophic bacteria that have traditionally been u
17                  Cyanobacteria are important photoautotrophic bacteria with extensive but variable me
18 n previously applied to map carbon fluxes in photoautotrophic bacteria, which involves model-based re
19  molecular players promoting phototropism in photoautotrophic, but not etiolated, seedlings.
20 gy-dependent NPQ component characteristic of photoautotrophic C. reinhardtii cultures grown at high l
21 st rapidly establish its root system and the photoautotrophic capability appropriate to its surroundi
22           Deletion of slr0286 did not affect photoautotrophic capacity in wild type but led to a mark
23 a slug can be sustained in culture solely by photoautotrophic CO(2) fixation for at least 9 months if
24 3 causes significant growth impairment under photoautotrophic conditions and results in hyper-sensiti
25 ate, although the mutant grew normally under photoautotrophic conditions in air.
26 he resulting mutants were able to grow under photoautotrophic conditions, dividing at rates that were
27             Although both mutants grow under photoautotrophic conditions, the rate of PSI-mediated el
28 moderate light, the mutant grew slowly under photoautotrophic conditions, with a doubling time of app
29 WT cells to high light under mixotrophic and photoautotrophic conditions, with the aox1 strain being
30 e DeltapsbY mutant cells grew normally under photoautotrophic conditions.
31 hic conditions compared to heterotrophic and photoautotrophic conditions.
32 bolic changes between photoheterotrophic and photoautotrophic conditions.
33  deficiency, both under photomixotrophic and photoautotrophic conditions.
34                                      Further photoautotrophic cultivations demonstrated the maximal E
35                            In a synchronized photoautotrophic culture of Chlamydomonas reinhardtii, c
36 a mechanistic basis for managing the DIC for photoautotrophic cultures through the N source.
37 cteria, chemoautotrophic Thaumarchaeota, and photoautotrophic Cyanobacteria.
38 ring for commercial metabolite production in photoautotrophic, cyanobacterial cells is a desirable ve
39 ring for commercial metabolite production in photoautotrophic, cyanobacterial cells is a desirable ve
40 itial pioneers consisted of the cold-adapted photoautotrophic cyanobacterium Nodularia sp. and potent
41                              Chloroplasts in photoautotrophic eukaryotes provide additional sources o
42 h (approximately -200 to -400 per thousand), photoautotrophic growth (-150 to -250 per thousand), het
43                               C550-H92M lost photoautotrophic growth ability in the absence of Ca(2+)
44 notype with defects in photopigment content, photoautotrophic growth and carbon fixation rates, and s
45 in Arabidopsis thaliana (Arabidopsis) blocks photoautotrophic growth and is seedling-lethal.
46                     Those mutants exhibiting photoautotrophic growth and oxygen evolution capability
47 enotypes ranging from moderate alteration of photoautotrophic growth and oxygen evolution rates to a
48 tant G342D exhibited moderate alterations of photoautotrophic growth and oxygen evolution.
49                                              Photoautotrophic growth and photophosphorylation rates w
50 he Ile, Val, and Leu mutants are impaired in photoautotrophic growth and photosynthesis in both low a
51 re and function, and is critical for overall photoautotrophic growth and plant development.
52 ifferentiation, a critical process for plant photoautotrophic growth and survival.
53 e splicing was completely blocked, showed no photoautotrophic growth and synthesis of a truncated D1
54 s were selected for their ability to restore photoautotrophic growth and these describe six nuclear l
55 -like protein (CPSFL1) that is necessary for photoautotrophic growth and vesicle formation at the inn
56  psbQ inactivation mutants exhibited reduced photoautotrophic growth as well as decreased water oxida
57 tations produced strains that are capable of photoautotrophic growth at moderate light intensity (20
58 ite mutants (pseudorevertants) with restored photoautotrophic growth but still maintaining the E69Q m
59 which encodes a protein system essential for photoautotrophic growth by ferrous iron oxidation, influ
60                              Analysis of the photoautotrophic growth capabilities of these mutants, t
61      Distinct from the results obtained with photoautotrophic growth conditions, the results of studi
62 ains grown under both photoheterotrophic and photoautotrophic growth conditions.
63 the groESL1 genes was unexpectedly low under photoautotrophic growth conditions.
64 f amino acid and enzyme de novo synthesis in photoautotrophic growth conditions.
65 phaeroides under both photoheterotrophic and photoautotrophic growth conditions.
66 does not accumulate cyanophycin and shows no photoautotrophic growth defect.
67 he LTO1 promoter is associated with a severe photoautotrophic growth defect.
68 he porA-1 and PORA RNAi lines display severe photoautotrophic growth defects, which can be partially
69 yledon expansion during the establishment of photoautotrophic growth depends on ABCB19-mediated auxin
70 esting that inactivation of Slr0399 leads to photoautotrophic growth in D2R8.
71 um Synechocystis sp PCC 6803 is required for photoautotrophic growth in fluctuating light and acts ea
72                                              Photoautotrophic growth in nature requires the accumulat
73 photosystem II is known to lead to a loss of photoautotrophic growth in Synechocystis sp. PCC 6803.
74 tion of frameshift mutations and can restore photoautotrophic growth in the presence of a mutation th
75                               Restoration of photoautotrophic growth in this mutant was caused by ear
76                                     However, photoautotrophic growth of Chlamydomonas strains contain
77                                              Photoautotrophic growth of flvB mutants was indistinguis
78                                              Photoautotrophic growth of mutants obtained varied from
79 ergy conversion, could support the sustained photoautotrophic growth of non-photosynthetic microorgan
80 ier in the thylakoid lumen and essential for photoautotrophic growth of plants.
81                                              Photoautotrophic growth of the double mutant is severely
82 ons (12 h of light and 12 h of dark), normal photoautotrophic growth of the mutant is completely rest
83 coccus PCC6301 rbcLS genes enabled anaerobic photoautotrophic growth of the R.capsulatus deletion str
84 nverted to the corresponding perthiol during photoautotrophic growth on sulfide, suggesting that GASH
85 ron donor for carbon dioxide fixation during photoautotrophic growth or for ammonia synthesis during
86  these mutations did not result in a loss of photoautotrophic growth or in significantly altered PS I
87 val of these protein products does not alter photoautotrophic growth or PSII fluorescence properties.
88 nd Gly mutants in high light is reduced, but photoautotrophic growth rate is not affected.
89                                 Although the photoautotrophic growth rate of the Deltasll1951 strain
90 M chloride), it exhibited a severely reduced photoautotrophic growth rate.
91 ylakoids was comparable to the change in the photoautotrophic growth rate.
92 eletion of ndb genes led to small changes in photoautotrophic growth rates and respiratory activities
93                                          The photoautotrophic growth rates of wild type and mutants i
94 The mechanism by which the S79F mutant loses photoautotrophic growth remains to be established.
95  introduction of an antibiotic cassette, and photoautotrophic growth resulted in the generation of a
96 s, and that the PsbQ protein is required for photoautotrophic growth under low light conditions.
97  in two of these mutants, FVEYPI and FLVYNI, photoautotrophic growth was impaired and the relative va
98         Transformants were selected in which photoautotrophic growth was restored, resulting in 11 vi
99          Pseudorevertants with much improved photoautotrophic growth were also generated for one of t
100      Transformants that were complemented to photoautotrophic growth were selected, and 20 such mutan
101 f C. reinhardtii that require high CO(2) for photoautotrophic growth were tested by complementation g
102   Under continuous light, 3WEZ exhibits poor photoautotrophic growth while growing photoheterotrophic
103 tify mutants that were able to complement to photoautotrophic growth with 1.5% CO(2).
104 s incapable of complementing R.capsulatus to photoautotrophic growth with 5% CO(2) were identified.
105 7 of CP47 were found to be indispensable for photoautotrophic growth, and many amino acid combination
106 ed an increased requirement for chloride for photoautotrophic growth, and two mutants, C8-10 and C8-2
107 The single mutant S79F was also incapable of photoautotrophic growth, but displayed reasonably stable
108 tosynthetic performance, they are capable of photoautotrophic growth, demonstrating that, different f
109 es of heliobacteria that have failed to show photoautotrophic growth, genes encoding enzymes for know
110 e small high-potential redox proteins during photoautotrophic growth, including two high-potential ir
111 t plants lacking xanthophylls are capable of photoautotrophic growth, no plants without carotenes in
112 role in the transition from heterotrophic to photoautotrophic growth, suggesting an important physiol
113 ns redox poise during photoheterotrophic and photoautotrophic growth.
114  at position 268 appeared to be required for photoautotrophic growth.
115 tion, as their mutation led to impairment of photoautotrophic growth.
116  CP47 protein are known to lead to a loss of photoautotrophic growth.
117   The eight mutant strains differed in their photoautotrophic growth.
118 erations in D1 turnover, photosynthesis, and photoautotrophic growth.
119 ut this is not necessarily rate-limiting for photoautotrophic growth.
120 00-fold increase in chloride requirement for photoautotrophic growth.
121 in a discernible phenotype, namely, impaired photoautotrophic growth.
122 seedlings are also defective in establishing photoautotrophic growth.
123 ion is central to the rewiring of plants for photoautotrophic growth.
124 nct proteome demands during heterotrophic or photoautotrophic growth.
125 hich harbored PSII dimers that sustained its photoautotrophic growth.
126 n Synechocystis 6803 resulted in compromised photoautotrophic growth.
127      The vte6 mutant plants are incapable of photoautotrophic growth.
128 eals that the gene function is essential for photoautotrophic growth.
129 t an intact sll0606 gene could fully restore photoautotrophic growth.
130 tic organisms and required for their optimal photoautotrophic growth.
131 omorphogenesis, allowing plants to establish photoautotrophic growth.
132 l properties render it a limiting factor for photoautotrophic growth.
133 4S(PsaC) that mapped to sll0088 and restored photoautotrophic growth.
134 poson mutagenesis to be required for optimal photoautotrophic growth.
135 s of full-length D1, and an 18% reduction in photoautotrophic growth.
136 d an engineered suppressor strain capable of photoautotrophic growth.
137                                              Photoautotrophic H2 production has important implication
138 d model accurately predicts phenotypes under photoautotrophic, heterotrophic, and mixotrophic conditi
139                                         In a photoautotrophic higher plant, Spirodela oligorrhiza, gr
140 suggest that cyanobacteria and other diverse photoautotrophic hosts can be a source for new plant gro
141 s (mixotrophic in the presence of acetate or photoautotrophic in the presence or absence of nitrogen)
142 , four (H117C, H117M, H117N, and H117T) were photoautotrophic in the PS I-containing background.
143                            Until they become photoautotrophic juvenile plants, seedlings depend upon
144 hloroplast function and is essential for the photoautotrophic life-style of plants.
145 sphate (PAP), which evolved to establish the photoautotrophic lifestyle and are instrumental in the i
146 es in vivo is a major challenge in analyzing photoautotrophic metabolism and engineering improved pho
147                                 Knowledge of photoautotrophic metabolism in the natural environment o
148 g constitutes a geochemical paradox, in that photoautotrophic metabolism will tend to precipitate car
149 tial gene and physiological data specific to photoautotrophic metabolism.
150 ight on the impact of the dosage form of the photoautotrophic microalga Nannochloropsis in enriched t
151  chain polyunsaturated fatty acids producing photoautotrophic microalgae in one study.
152  while being stable in the lipid extracts of photoautotrophic microalgae.
153 iptional networks revealed that the dominant photoautotrophic microbes in each environment (Ostreococ
154 he attributes of photosystems from different photoautotrophic model organisms, namely the purple bact
155  Coupling of strong experimental support and photoautotrophic modeling methods thus resulted in a hig
156             Using combinatorial mutagenesis, photoautotrophic mutants of Synechocystis sp. PCC 6803 h
157 em II properties were studied in a number of photoautotrophic mutants of Synechocystis sp. PCC 6803,
158 hrough the NDA2 catalytic hub in response to photoautotrophic N deprivation sustains cell viability w
159 l progression begins with establishment of a photoautotrophic N-fixing bacterial mat on bare soil.
160 of the respiratory oxidases had no effect on photoautotrophic or photomixotrophic growth.
161       We show how this can occur in a single photoautotrophic organism, representing a previously und
162 n of a dark-grown seedling into a pigmented, photoautotrophic organism.
163                                              Photoautotrophic organisms fix inorganic carbon (Ci) by
164 ealed mechanism' expands the distribution of photoautotrophic organisms into hostile regions where th
165  phosphoglycolate was extensively studied in photoautotrophic organisms, including plants, algae, and
166                                           As photoautotrophic organisms, plants produce an incredible
167 uggests that these mutations led to a normal photoautotrophic phenotype.
168 pansions that may explain the distinguishing photoautotrophic phenotypes observed.
169                                              Photoautotrophic plankton in the surface ocean release o
170                  When cells are shifted from photoautotrophic planktonic growth to light-activated he
171 indicate that the NDH complex can be lost in photoautotrophic plant species.
172 transcriptome data showed that 47 out of 660 photoautotrophic plants and all the heterotrophic plants
173 logical evidence to support nitrification by photoautotrophic plants.
174 ole as evolutive templates for the origin of photoautotrophic processes by combining primary protecti
175 included the decline of the oligotrophic and photoautotrophic Prochlorococcus and the enrichment of h
176                                      Several photoautotrophic pseudorevertants of this mutant have be
177 trophic mutant lacking the T271-K277 region, photoautotrophic pseudorevertants were generated with sh
178 d to the genome of the unicellular, obligate photoautotrophic red alga Cyanidioschyzon merolae.
179 of CH(4) (delta(13)C-CH(4)) indicates direct photoautotrophic release as the most likely source of ox
180 8) tail is an obligate heterotroph to obtain photoautotrophic revertants.
181 interest is the switch from heterotrophic to photoautotrophic seedling growth, for which cytoplasmic
182  a quiescent dry seed to an actively growing photoautotrophic seedling is a complex and crucial trait
183 ings reaching the light differ from those in photoautotrophic seedlings.
184                                   Plants are photoautotrophic sessile organisms that use environmenta
185 esia (Wakatobi) corals have declined and the photoautotrophic sponge Lamellodysidea herbacea is now a
186  and mcd5 mutants were initially isolated as photoautotrophic suppressors of the petD 5' mutants LS2
187 between a heterotrophic host and an internal photoautotrophic symbiont.
188 13)Cs provide molar Ci assimilation rates of photoautotrophic Synechocystis cultures.
189 ncrease the probability of transition from a photoautotrophic to a heterotrophic life history.
190 l manipulations and chemical genetics at the photoautotrophic transition checkpoint, we reveal that s
191 ences involved in positive regulation during photoautotrophic versus chemoautotrophic growth, suggest
192 pression was dependent on growth conditions (photoautotrophic versus mixotrophic).
193                   The A249T mutant, although photoautotrophic, was affected by artificial quinones, b

 
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