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1 (14) C and delta(13) C into four sources-two autotrophic (above - and belowground plant structures) a
2 t these Archaea are organo-heterotrophic and autotrophic acetogens.
3 c evidence for the Ljungdahl-Wood pathway of autotrophic acetyl-CoA biosynthesis in the methanogenic
4 enzyme activities could be detected in other autotrophic alpha-proteobacteria or in gram-positive met
5                                              Autotrophic ammonia oxidizing bacteria (AOB) have been r
6  first time highly effective and sustainable autotrophic ammonia removal in a gas biofilter and there
7                                              Autotrophic ammonium oxidation in membrane-aerated biofi
8 ive tricarboxylic acid cycle, which in these autotrophic anaerobes is the stage for biosynthesis of a
9                                      In many autotrophic anaerobes, PFOR links the Wood-Ljungdahl pat
10  the last common ancestor of life, a complex autotrophic, anaerobic green bacterium.
11       Citrate synthase activity decreased in autotrophic and acetate-containing cultures compared to
12 pyruvate carboxylase activities increased in autotrophic and acetate-containing cultures.
13 eps of phylloquinone synthesis do not become autotrophic and are seedling lethals, even when grown on
14 hytes of the fern Ceratopteris richardii are autotrophic and develop independently of the diploid spo
15 ange on Reco depends on the responses of its autotrophic and heterotrophic components.
16 he microbial fossils, which include putative autotrophic and heterotrophic eukaryotes, are similar to
17 photosynthetic cyanobacteria capable of both autotrophic and heterotrophic growth, with support from
18 nelles that encapsulate critical segments of autotrophic and heterotrophic metabolic pathways; they a
19 re proteinaceous organelles involved in both autotrophic and heterotrophic metabolism.
20 of warming during different seasons affected autotrophic and heterotrophic respiration in a bryophyte
21                                          How autotrophic and heterotrophic respiration sources respon
22                We quantified the response of autotrophic and heterotrophic respiration to permafrost
23  energy sources, which sustain the growth of autotrophic and heterotrophic species whose activities m
24 thylakoids, and it is present in plastids of autotrophic and heterotrophic tissues.
25 s and the vital role of microorganisms, both autotrophic and heterotrophic, in the coupled organic-ma
26 aracterization of the DeltapntA mutant under autotrophic and mixotrophic conditions.
27 In this report, we probed carbon flux during autotrophic and mixotrophic growth of the GSB Chlorobacu
28 thetic machinery in Ochromonas danica during autotrophic and mixotrophic growth.
29 llowing: (a) the RTCA cycle is active during autotrophic and mixotrophic growth; (b) the flux from py
30            Overall, growing season fluxes of autotrophic and old soil heterotrophic respiration incre
31 to increased proportional contributions from autotrophic and young soil respiration and decreased pro
32 thanococcus jannaschii, a hyperthermophilic, autotrophic, and strictly hydrogenotrophic inhabitant of
33 e- and quinone-based S(0)-reducing system in autotrophic archaea and bacteria.
34                                              Autotrophic archaeal and bacterial ammonia-oxidisers (AO
35 ete 1.66-megabase pair genome sequence of an autotrophic archaeon, Methanococcus jannaschii, and its
36              Arsenotrophy, growth coupled to autotrophic arsenite oxidation or arsenate respiratory r
37 tate of the North (heterotrophic) and South (autotrophic) Atlantic oligotrophic gyres, resulting from
38 mes in the carbon-concentrating mechanism of autotrophic bacteria predict the carboxysomal carbonic a
39                                              Autotrophic bacteria rely on various mechanisms to incre
40 ototypes of the BMCs are the carboxysomes of autotrophic bacteria.
41  protein isolated from the ammonia-oxidizing autotrophic bacterium Nitrosomonas europaea, is shown to
42     Dominating the active community are four autotrophic beta-proteobacterial genera that are capable
43                                     However, autotrophic biological treatment is most environmentally
44 h whole-community chlorophyll a, a proxy for autotrophic biomass, suggest that ecological selection v
45 approach to this question by quantifying the autotrophic carbon budget in 16 forest plots along a 330
46 er, no information exists on what pathway of autotrophic carbon fixation these bacteria might use.
47     All sediments contain abundant genes for autotrophic carbon fixation used in the Calvin-Benson-Ba
48 that the most common form for deep-branching autotrophic carbon-fixation combines two disconnected su
49                                              Autotrophic cells, including phototrophs and chemolithot
50 r parallels with the biochemistry of ancient autotrophic cells, notably the acetyl CoA pathway in arc
51 nerates low potential electrons required for autotrophic CO(2) assimilation.
52 f the reductive tricarboxylic acid cycle for autotrophic CO(2) fixation in epsilon-proteobacteria.
53 r activities of the key enzymes of the known autotrophic CO(2) fixation pathways.
54 pyruvate links the Wood-Ljungdahl pathway of autotrophic CO(2) fixation to the reductive tricarboxyli
55 es, or oilfields, these results suggest that autotrophic CO(2) fixation via the reductive tricarboxyl
56 oxysomes (a polyhedral organelle involved in autotrophic CO(2) fixation), suggesting that the S. ente
57 entral role in the Wood-Ljungdahl pathway of autotrophic CO(2) fixation.
58 entral role in the Wood-Ljungdahl pathway of autotrophic CO(2) fixation.
59 ential importance of mixotrophic rather than autotrophic CO2 fixation pathways in these organisms and
60 d functional analysis attributed most of the autotrophic CO2 fixation to one unique cyanobacterium.
61        This mutant was seedling lethal under autotrophic conditions but could be partially rescued un
62 hic conditions (light and glucose) and under autotrophic conditions in a day/night cycle, which is pr
63 es in the presence of glucose, whereas under autotrophic conditions the mutant did not differ from th
64 1, was able to grow via photosynthesis under autotrophic conditions using H2 as an electron donor and
65 l predictions for cyclic electron flow under autotrophic conditions, and fluxes through the phosphoke
66 l of this transcript increased in high light autotrophic conditions, suggesting that it is involved i
67  genome results in synthetic lethality under autotrophic conditions.
68 arming with increased respiration, increased autotrophic contributions to ecosystem respiration, and
69  persistent shift from heterotrophic to more autotrophic control of the growing season carbon cycle i
70 appropriate biological process for achieving autotrophic conversion of methane (CH(4)) to methanol (C
71 higher than ATP citrate synthase activity in autotrophic cultures.
72           Although it was long considered an autotrophic cyanobacterium, the uptake of organic compou
73  efficiency of anabolism exemplified by this autotrophic cycle perfectly suits the lifestyle of ammon
74                                   The use of autotrophic denitrification in microbial fuel cells (MFC
75 ciently reactive reductants that can promote autotrophic denitrification.
76                     The solid components are autotrophic denitrifying bacteria, autotrophic perchlora
77  that the FCA-mediated thermal adaptation of autotrophic development allows developing seedlings to c
78             Chlorophyll biosynthesis enables autotrophic development of developing seedlings.
79  shifting the chlorophyll-ROS balance toward autotrophic development.
80 nge, resulting in 289% and 281% increases in autotrophic dissolved inorganic N and P use efficiency (
81 cted using DNA extracted from soil and river autotrophic enrichments, a photosynthetic biofilm and a
82 , ndh genes are truncated or deleted in some autotrophic Epidendroideae orchid cp genomes.
83 eron was involved in the negative control of autotrophic events, whereas the plasmid operon was invol
84 nt fashion, the trophic activity may be a DA autotrophic factor.
85         The reaction is involved both in the autotrophic fixation of carbon and in the process of met
86 70 m and 915 m), carbon derived from in situ autotrophic fixation supported a significant fraction of
87  nitrogen, temperature and photosynthesis on autotrophic flux from soils at the ecosystem level.
88       Recent advances in the partitioning of autotrophic from heterotrophic respiration processes in
89 e CP43-357K mutation lost their capacity for autotrophic growth and exhibited a drastic reduction in
90              The mutants were not capable of autotrophic growth and produced extremely chlorotic coty
91 ions led us to propose a metabolic model for autotrophic growth by Ca. P. anaerolimi whereby DPO driv
92 veral metabolic pathways in Synechocystis in autotrophic growth conditions without prominent effects
93  germination rate and is unable to establish autotrophic growth due to severe inhibition of cotyledon
94 ere expressed in each case and all permitted autotrophic growth in strains expressing cyt. c-550.
95 gy and carbon for the growing seedling until autotrophic growth is possible.
96                          To learn more about autotrophic growth of methanococci, we isolated nine con
97                   Finally, the potential for autotrophic growth of other Pseudonocardia spp. was expl
98                                          The autotrophic growth rates and maximum concentrations of c
99         Rescue of the DeltarbcL mutation and autotrophic growth stabilizes transgenic plastids in het
100 timum for growth at pH 11 and are capable of autotrophic growth with hydrogen, calcium carbonate and
101 nt undergo photomorphogenesis, which enables autotrophic growth with optimized morphology and physiol
102 ere photosynthetically competent, supporting autotrophic growth, and their respective forms of Rubisc
103                                       During autotrophic growth, carbon dioxide is incorporated into
104  Whereas plastocyanin is essential for photo-autotrophic growth, copper/zinc superoxide dismutase is
105  delays the transition from heterotrophic to autotrophic growth, possibly due to MG toxicity.
106 d reductive directions for heterotrophic and autotrophic growth, respectively, but the control of car
107                                Compared with autotrophic growth, the total pigmentation of O. danica
108 hus making these compounds indispensable for autotrophic growth.
109 naerobic CO(2) fixation for heterotrophic or autotrophic growth.
110 ole in this transition from heterotrophic to autotrophic growth.
111 gative mutant enzyme incapable of supporting autotrophic growth.
112 ion of cellular components but do not permit autotrophic growth.
113 mental conditions during their transition to autotrophic growth.
114 tively, could support photoheterotrophic and autotrophic growth.
115 egative mutant of Rhodobacter sphaeroides to autotrophic growth.
116 obably sugar-fermenting organisms capable of autotrophic growth.
117 e report on pyritized replicas of the iconic autotrophic Gunflintia-Huroniospora microfossil assembla
118                                           An autotrophic H(2)-oxidizing bacterium fixes CO(2) in dark
119 rocesses themselves form and maintain stable autotrophic habitats on the surface of the Greenland ice
120 ich upon germination develop as free-living, autotrophic haploid gametophyte consisting of a small (<
121 tified, indicating significant plasticity in autotrophic, heterotrophic, and diazotrophic strategies
122 e across four different trophic modes, i.e., autotrophic, heterotrophic, photoheterotrophic, and mixo
123            For example, parasitic plants and autotrophic hosts are similar in delta15N (with no parti
124 e community reveals a carbon cycle driven by autotrophic hydrogen oxidizers belonging to novel genera
125 organic carbon via a modified version of the autotrophic hydroxypropionate/hydroxybutyrate cycle of C
126 on of the total marine archaeal community is autotrophic in situ.
127 idans becoming increasingly displaced by the autotrophic iron-oxidizing acidophiles Ferrovum myxofaci
128                                              Autotrophic members of the Sulfolobales (crenarchaeota)
129 photosynthetic robustness drives the optimal autotrophic metabolism at the expense of metabolic versa
130 ral inclusion bodies that play a key role in autotrophic metabolism in many bacteria.
131                                          The autotrophic metabolism of this isolate, and its close ph
132 'Candidatus Altiarchaeum hamiconexum' has an autotrophic metabolism that uses a not-yet-reported Fact
133 athways was found to be critical for optimal autotrophic metabolism.
134 the synthesis of other proteins required for autotrophic metabolism.
135 al trends in carbon-heterotrophic and carbon-autotrophic metabolism.
136 eterotrophic and obligately or facultatively autotrophic methylotrophs.
137                  Four different omega-3 rich autotrophic microalgae, Phaeodactylum tricornutum, Nanno
138                                              Autotrophic microbes can acquire electrons from solid do
139 al indicative of their origin from primarily autotrophic microbes.
140 ical barrier to SCN(-) biodegradation for an autotrophic microbial consortium enriched from mine tail
141          Microbial fuel cells operating with autotrophic microorganisms are known as biophotovoltaic
142 ell as seasonal shifts from heterotrophic to autotrophic microorganisms associated with increases in
143 fluxes in P. tricornutum were calculated for autotrophic, mixotrophic and heterotrophic growth condit
144 as reinhardtii cultured under nine different autotrophic, mixotrophic, and heterotrophic conditions d
145 study carbohydrate metabolism of algae under autotrophic, mixotrophic, and heterotrophic conditions u
146 erential assimilation of fungal protein, and autotrophic, mycorrhizal plants are lower in 15N than th
147 asure the contributions of heterotrophic and autotrophic N2-producing metabolisms (denitrification an
148                               Oxygen-limited autotrophic nitrification/denitrification (OLAND), appli
149  Hydroxylamine oxidoreductase (HAO) from the autotrophic nitrifying bacterium Nitrosomonas europaea c
150  Hydroxylamine oxidoreductase (HAO) from the autotrophic nitrifying bacterium Nitrosomonas europaea c
151                            To understand how autotrophic nitrifying organisms respond to inorganic ca
152 ic basis for energy and biomass synthesis in autotrophic nitrifying organisms, which in turn are cruc
153                                              Autotrophic nitrogen removal from municipal wastewater e
154                                              Autotrophic nitrogen removal is regarded as a resource e
155 OM use by Trichodesmium as an alternative to autotrophic nutrition in oligotrophic open ocean waters.
156 rkers of an MCG community that may either be autotrophic or feeding on (13) C-depleted organic substr
157  metalloenzyme that is vitally important for autotrophic organism as it catalyzes the first and rate-
158                                              Autotrophic organisms obtain phosphorus from the environ
159                            Higher plants, as autotrophic organisms, are effective sources of molecule
160 s often the limiting factor in the growth of autotrophic organisms, intrinsically linking the nitroge
161 irst step of carbon dioxide fixation in most autotrophic organisms.
162 ced by photosynthesis within an ecosystem by autotrophic organisms.
163  gene expression in plants, which are biotin autotrophic organisms.
164 gests a role for this enzyme in the proposed autotrophic origin of life.
165 more energy efficient than any other aerobic autotrophic pathway.
166 hic growth, genes encoding enzymes for known autotrophic pathways in other phototrophic organisms, in
167 nents are autotrophic denitrifying bacteria, autotrophic perchlorate-reducing bacteria, heterotrophic
168 ut only those with a strategy that is mostly autotrophic persisted with high nutrient supply, and the
169 that the MSP-D159N mutant suppresses the non-autotrophic phenotype of MSP-R163L (or vice versa) in th
170                                              Autotrophic photosynthesis by PSI-deficient mutants was
171 lysogeny occurs in natural populations of an autotrophic picoplankton (Synechococcus) and that there
172                                              Autotrophic picoplankton dominate primary production ove
173 e to viral infection seen in common forms of autotrophic picoplankton.
174 fferent from that in either heterotrophic or autotrophic plant tissues or in most other organisms: (i
175 es of the 15N/14N (expressed as delta15N) of autotrophic plants, mycoheterotrophic plants, parasitic
176 e specialized towards mycorrhizal fungi than autotrophic plants.
177 itrification or the more recently discovered autotrophic process, anaerobic ammonia oxidation (anammo
178                            Heterotrophic and autotrophic production data together with small subunit
179          However, warming can also stimulate autotrophic production leading to increased ecosystem ca
180 e ecosystem known to be supported by in situ autotrophic production, and it contains the only terrest
181                                    Thus, the autotrophic productive capacity of large aquatic ecosyst
182 The RTCA pathway occurs in several groups of autotrophic prokaryotes, including the green sulfur bact
183 espiration (Rs) and its components, that is, autotrophic (Ra) and heterotrophic (Rh) respiration.
184 esponses of Rs and its two components [i.e., autotrophic (Ra) and heterotrophic (Rh) respiration] to
185 cing equivalents, such as H2, which then fed autotrophic reduction of CO2 to methane.
186  mycoheterotrophic Ericaceae and their close autotrophic relatives.
187 arge portion of each bioreactor community is autotrophic, relying not on molasses in reactor feed but
188 ood vs foliage production (NPPfoliage ), and autotrophic respiration (Ra ) vs all biomass production
189                                              Autotrophic respiration (Ra) was calculated by subtracti
190 roductivity (GPP) and continuously increased autotrophic respiration (Ra).
191 fer the impacts of environmental stresses on autotrophic respiration and carbon-use-efficiency, with
192 h component of net primary production (NPP), autotrophic respiration and heterotrophic respiration is
193          Tight coupling between below-ground autotrophic respiration and the availability of recently
194 phic respiration will be more sensitive than autotrophic respiration if precipitation increases in th
195 sence of drought, with extended decreases in autotrophic respiration in the three driest plots.
196 ut dominant contribution to ER switched from autotrophic respiration in wet years to heterotrophic in
197                                 If increased autotrophic respiration is balanced by increased primary
198 the proportion of photosynthate allocated to autotrophic respiration is not sensitive to temperature.
199                                              Autotrophic respiration ranged from 40 to 70% of Reco an
200 he Rs decrease was mainly due to a decreased autotrophic respiration rate (Ra).
201 t increase in RH was offset by a decrease in autotrophic respiration such that the total ecosystem re
202 al NPP, trees prioritized growth by reducing autotrophic respiration that was unrelated to growth.
203     Despite the physiological acclimation of autotrophic respiration to warming, increases in tempera
204      First, the models predicted declines in autotrophic respiration under prolonged drought in contr
205 rbon to partition ecosystem respiration into autotrophic respiration, associated with production, and
206     However, towards the end of the drought, autotrophic respiration, especially in roots and stems,
207 dences of gross primary production (GPP) and autotrophic respiration, the fraction of GPP respired by
208 tosynthesis and release by decomposition and autotrophic respiration.
209 erotrophic respiration and very low daylight autotrophic respiration.
210 ons to growth; feedbacks to nutrient uptake; autotrophic respiration; and the impact of low soil mois
211  development of a germinating embryo into an autotrophic seedling is arrested under conditions of wat
212  zone, and large lakes may exhibit shifts in autotrophic structure analogous to the regime shifts see
213 n of algal production), or simply a shift in autotrophic structure with no net decline in PP?
214 y of in situ SCN(-) bioremediation involving autotrophic sulfur-oxidizing bacteria.
215   Thermodynamic calculations showed that the autotrophic synthesis of all 20 protein-forming amino ac
216 is inconsistent with known heterotrophic and autotrophic thaumarchaeal lifestyles.
217  that is a net producer of fixed carbon (net autotrophic) throughout the year, with episodic events n
218 e predominantly in heterotrophic rather than autotrophic tissues, at least under standard growth cond
219                           This shift from an autotrophic to a heterotrophic profile occurred concurre
220 osystem respiration, and increased ratios of autotrophic to heterotrophic respiration.
221 L. cf. luymesi can be sufficient to fuel net autotrophic total dissolved inorganic carbon uptake.
222  the debate are that it is either hetero- or autotrophic, which suggests either substantial unaccount
223 )MPT-dependent activities were also found in autotrophic Xanthobacter strains.

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