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1 ors), chlorophyll (O2 production), and heme (aerobic respiration).
2 f organelles, only some of which function in aerobic respiration.
3  transition from anaerobic photosynthesis to aerobic respiration.
4  transition from anaerobic photosynthesis to aerobic respiration.
5 unique to cytochrome c oxidases and vital to aerobic respiration.
6 fate oxidation to denitrification as well as aerobic respiration.
7 tical molecules produced as a consequence of aerobic respiration.
8 tes an electrochemical Na(+) gradient during aerobic respiration.
9 ore carbon when oxygen becomes available for aerobic respiration.
10 ve lipid essential for electron transport in aerobic respiration.
11 ogenase complex (PDHE1), a central enzyme in aerobic respiration.
12 an electrochemical Na(+) potential driven by aerobic respiration.
13 is utilized in oxygen-limited conditions for aerobic respiration.
14 capable of supporting growth of the cells by aerobic respiration.
15 ansformations ranging from photosynthesis to aerobic respiration.
16 ction in oxic environments and often support aerobic respiration.
17 monoxide as supplemental electron donors for aerobic respiration.
18 inorganic carbon (C) and subsequent, in situ aerobic respiration.
19 normalities of glycolysis, the TCA cycle and aerobic respiration.
20  may reveal new insights on the evolution of aerobic respiration.
21  experiencing oxidative stress downregulates aerobic respiration.
22 s related to innate immunity but suppressing aerobic respiration.
23  that complete denitrification evolved after aerobic respiration.
24 longed to bacterial taxa, gaining energy via aerobic respiration.
25 l radical species generated as byproducts of aerobic respiration.
26 is of primary and secondary metabolites, and aerobic respiration.
27 misfolding of proteins that are critical for aerobic respiration.
28 oinfections and included genes necessary for aerobic respiration.
29 genation, which drives pathogen expansion by aerobic respiration.
30 ion when cultured under conditions promoting aerobic respiration.
31 within a shell of bacterial cells undergoing aerobic respiration.
32 cal gas normally produced in the body during aerobic respiration.
33 h, saNOS also plays a modulatory role during aerobic respiration.
34 duced owing to decreased NADH oxidization by aerobic respiration.
35 in which growth of the pathogen is fueled by aerobic respiration.
36  and eukaryotes for energy production during aerobic respiration.
37 een fermentation, anaerobic respiration, and aerobic respiration.
38 cherichia coli is able to conserve energy by aerobic respiration.
39 chment provides C. rodentium with oxygen for aerobic respiration.
40 o detrimental effects on cell energetics and aerobic respiration.
41 tch for the transition between anaerobic and aerobic respiration.
42 imeric enzyme that executes the last step in aerobic respiration.
43 nucleotide metabolism, LPS biosynthesis, and aerobic respiration.
44 imethyl sulfoxide (DMSO) and plays a role in aerobic respiration.
45 unities for improved energy conservation via aerobic respiration.
46 otection and switching between anaerobic and aerobic respiration.
47  while largely suppressing those involved in aerobic respiration-a strategy counterproductive under a
48 00 +/- 9,000 muatm could not be explained by aerobic respiration alone.
49 fferentially regulate many genes involved in aerobic respiration, an essential pathway for sporulatio
50 ion profiles for three diverse growth modes--aerobic respiration, anaerobic respiration in the dark,
51 e is different when cells generate energy by aerobic respiration, anaerobic respiration, or photosynt
52       Several essential metabolisms, such as aerobic respiration and acid tolerance, were likely acqu
53 tes of pyruvate conversion to acetyl-CoA for aerobic respiration and anaerobic fermentation, respecti
54 nuclear genome indicates a capacity for both aerobic respiration and anaerobic metabolism with concom
55 en species (ROS) are metabolic byproducts of aerobic respiration and are responsible for maintaining
56 imetic AICAR or by antimycin A, which blocks aerobic respiration and causes acidification, increased
57 evolution by facilitating the development of aerobic respiration and complex multicellular life.
58       All DOM sources significantly enhanced aerobic respiration and denitrification of the biofilm w
59 dative stress both endogenously generated by aerobic respiration and exogenously produced by host pha
60  coexisting mitochondrial metabolic pathways-aerobic respiration and fermentative malate dismutation.
61           NO was found to reversibly inhibit aerobic respiration and growth.
62 e further explored how Rcf1 and Rcf2 support aerobic respiration and growth.
63 r canonical mitochondrial functions, such as aerobic respiration and haem biosynthesis.
64 disorganized mitochondrial networks, reduced aerobic respiration and increased reactive oxygen specie
65 , the CydAB bd-type oxidase is essential for aerobic respiration and intracellular replication, and c
66 and the presence of either is sufficient for aerobic respiration and intracellular replication.
67 tive oxygen species are byproducts of normal aerobic respiration and ionizing radiation, and they rea
68 en abundance was powered by a combination of aerobic respiration and mixed acid fermentation of simpl
69 lved organic matter (DOM), which can promote aerobic respiration and N removal via denitrification.
70  transformed eukaryotic life, from providing aerobic respiration and photosynthesis to enabling colon
71 x potential (HPQs) for electron transport in aerobic respiration and photosynthesis.
72 one of redox reactions in both anaerobic and aerobic respiration and photosynthesis.
73 c program induced by conditions that inhibit aerobic respiration and prevent bacillus replication.
74 ion, FlhD/FlhC repressed enzymes involved in aerobic respiration and regulated many other metabolic e
75 tosynthetic activity led to the evolution of aerobic respiration and responses to the resulting react
76  mechanisms, particularly, the regulation of aerobic respiration and rRNA processing.
77 ned a large number of genes and expanded its aerobic respiration and salt/UV resistance gene repertoi
78 bes that use atmospheric hydrogen to support aerobic respiration and sometimes carbon fixation.
79 es and porewater geochemistry indicated that aerobic respiration and sulfide oxidation inhibit lithif
80  conditions, while that of genes involved in aerobic respiration and the tricarboxylic acid cycle wer
81 notations suggest Gagatemarchaeaceae perform aerobic respiration and use various organic carbon sourc
82 7 mg L(-1)), while inducing genes related to aerobic respiration and wound repair (at >=167 mg L(-1))
83                Oxygen consumption rate (OCR, aerobic respiration) and extracellular acidification rat
84 asured stable C isotopes of CO(2) and CH(4), aerobic respiration, and CH(4) production and oxidation
85 ain their biological functionalities through aerobic respiration, and even in anoxic conditions throu
86 on of genes involved in ribosome biogenesis, aerobic respiration, and mammalian target of rapamycin c
87 es associated with enhanced cell metabolism, aerobic respiration, and mitochondrial function, all ass
88 p protects V. fischeri from NO inhibition of aerobic respiration, and removes NO under both oxic and
89  hydroperoxyl (superoxide) as a byproduct of aerobic respiration, and the demonstrated cytoprotective
90 ions by first consuming dissolved oxygen via aerobic respiration, and then directing extracellular el
91  species (ROS) arise through normal cellular aerobic respiration, and, in combination with external s
92 osa O(2) is actively depleted by S. flexneri aerobic respiration-and not host neutrophils-during infe
93  the extent of the HZ, a single process like aerobic respiration (AR) can be limited by both DOM ther
94 ay constrain the metabolic platform in which aerobic respiration arose.
95  isolation (hot-spring biofilm) revealed (an)aerobic respiration as population segregation factor acr
96   These compounds, produced during bacterial aerobic respiration as well as by the host immune system
97 F-1's functions by showing that it modulates aerobic respiration as well.
98 hen taken advantage of to develop a cellular aerobic respiration assay.
99 ee organisms use DNA repair, translation and aerobic respiration associated processes to modulate the
100 aled enrichment in oxidative stress-inducing aerobic respiration at the expense of microbial vitamin
101 uvate metabolism, resulting in a decrease in aerobic respiration at the location of injury following
102                                       During aerobic respiration, Bacillus subtilis utilizes three te
103 ient in either Rcf1 or Rcf2 proteins can use aerobic respiration-based metabolism for growth, but the
104 strate for alternative energy production via aerobic respiration, biosynthesis of primary and seconda
105 ated intimate attachment is not required for aerobic respiration but for hydrogen peroxide (H(2)O(2))
106 wth inhibition under conditions that require aerobic respiration, but does not affect growth under an
107  produce energy is to metabolize the food by aerobic respiration, but the fastest way is to metaboliz
108             Altogether, our results identify aerobic respiration by bacteria as a previously unknown
109       Therefore, we reasoned that inhibiting aerobic respiration by inducing systemic hypoxaemia woul
110 ch indicated that gut hypoxia was not due to aerobic respiration by the gut microbiota but did depend
111 ete submergence represses photosynthesis and aerobic respiration, causing rapid mortality in most ter
112 neurons that are activated by the product of aerobic respiration, CO2.
113 chrome C oxidase genes, suggesting increased aerobic respiration compared to diet-fed larvae.
114                             The emergence of aerobic respiration created unprecedented bioenergetic a
115 apsulatus utilizes two terminal oxidases for aerobic respiration, cytochrome cbb(3) and ubiquinol oxi
116 s, but continuous growth eventually leads to aerobic respiration defects, reduced mtDNA content, and
117  hypoxia, leads to reduced ATP production by aerobic respiration, driving cells to rely more on fatty
118 lay a role during the sudden interruption of aerobic respiration due to causes such as hypoxia, thior
119 curtailed the fitness advantage conferred by aerobic respiration during C. rodentium infection.
120 sults indicate a role for V. fischeri AOX in aerobic respiration during NO stress.
121 e repair enzyme that is required to maximize aerobic respiration efficiency by preventing succinate d
122 ry complexes, supporting the hypothesis that aerobic respiration evolved after oxygenic photosynthesi
123                                              Aerobic respiration evolved by bricolage, with modules c
124 pathways, already present in bacteria before aerobic respiration evolved, offer a solution to the str
125  annexins, lipid transporters and enzymes of aerobic respiration), from which a link with lipid oxida
126                              In this system, aerobic respiration generally maintains anoxic groundwat
127                                              Aerobic respiration generates reactive oxygen species th
128                 Tricarboxylic acid cycle and aerobic respiration genes are strongly PHX in all five g
129 transcriptional pauses in EMP glycolysis and aerobic respiration genes by Gre factors safeguards Salm
130  Embden-Meyerhof-Parnas (EMP) glycolysis and aerobic respiration genes.
131 ganelle, even when its canonical function of aerobic respiration has been apparently lost.
132                             Mitochondria and aerobic respiration have been suggested to be required f
133 RNA expression level of genes related to the aerobic respiration (HIF-1alpha, c-Myc, LDHA, PDK1 and V
134     Metabolomics analysis revealed increased aerobic respiration, improved electron transport chain f
135 AB aa 3-type oxidase is required neither for aerobic respiration in air nor for intracellular growth.
136                                              Aerobic respiration in bacteria, Archaea, and mitochondr
137 ion inhibited cytochrome bd oxidase-mediated aerobic respiration in E. coli only in the presence of D
138 d not inhibit cytochrome bd oxidase-mediated aerobic respiration in E. coli, even when D. piger was p
139 gulator for the switch between anaerobic and aerobic respiration in Escherichia coli and many other b
140  Q (Q) is a redox active lipid essential for aerobic respiration in eukaryotes.
141 s more efficient than O(2) metabolism during aerobic respiration in foraminifera from the Peruvian OM
142 ted mandelalides are effective inhibitors of aerobic respiration in living cells.
143 dult stem cells and somatic cells can rescue aerobic respiration in mammalian cells with nonfunctiona
144                                   Modern day aerobic respiration in mitochondria involving complex I
145 n enrichment for metabolites associated with aerobic respiration in samples from patients with open i
146 egulon mechanisms shift metabolism away from aerobic respiration in the face of dwindling oxygen avai
147  in the post-diauxic phase, showed defective aerobic respiration in the post-diauxic phase but retain
148 s, enabling a more detailed understanding of aerobic respiration in this organism.
149 tochondrial homeostasis, including decreased aerobic respiration, increased oxidant stress, and mitoc
150                                              Aerobic respiration is a fundamental energy-generating p
151                                     Although aerobic respiration is a hallmark of eukaryotes, a few u
152 rom reactive oxygen species generated during aerobic respiration is a major cause of genetic damage t
153                                              Aerobic respiration is essential to almost all eukaryote
154                Here we provide evidence that aerobic respiration is required for commensal and pathog
155                                              Aerobic respiration is required for optimal efficiency o
156                                              Aerobic respiration is several times more energetically
157 tress engendered in situations as diverse as aerobic respiration, ischemia reperfusion, and inflammat
158       Since mitochondria are responsible for aerobic respiration, it is expected that mtDNA mutationa
159           Capsule biosynthesis also requires aerobic respiration, leading us to hypothesize that caps
160 ndicates that the capacity of halophiles for aerobic respiration may have been acquired through later
161 existing cardiomyocytes, and is regulated by aerobic-respiration-mediated oxidative DNA damage.
162  environmental heme is a means of activating aerobic respiration metabolism.
163 al for many cellular processes, ranging from aerobic respiration, metabolite biosynthesis, ribosome a
164  onset of villus elongation, suggesting that aerobic respiration might function as a regulator of vil
165                     I therefore suggest that aerobic respiration must have developed early in the Arc
166 ession in P. aerophilum were associated with aerobic respiration, nitrate respiration, arsenate respi
167 ence of nitrate there is stratification with aerobic respiration occurring in the outer oxic layer an
168                                    Moreover, aerobic respiration occurs at internalized mitochondrial
169 s rise to molecular oxygen that supports the aerobic respiration of E. coli.
170 inhibition of cytochrome bd oxidase-mediated aerobic respiration of Escherichia coli in the murine la
171 olisms at specific environmental conditions: aerobic respiration of glucose in freshwater, anaerobic
172 egulated the expression of genes involved in aerobic respiration of ovarian cancer cells.
173 by inhibiting cytochrome bd oxidase-mediated aerobic respiration of the commensal.
174 ting first-order catalytic rate constant for aerobic respiration on iron was 7,400 s(-1).
175 thways and determined that genes involved in aerobic respiration or mitochondrial DNA replication wer
176     Mitochondria maintain a constant rate of aerobic respiration over a wide range of oxygen levels.
177                 Mitochondria are the site of aerobic respiration, producing ATP via oxidative phospho
178 egulation of metabolic parameters, including aerobic respiration, proton motive force (Deltap), and s
179 icantly enhanced, including sugar transport, aerobic respiration, pyruvate breakdown, and the glyoxyl
180 o be the main reason SQR is expressed during aerobic respiration rather than the related enzyme fumar
181                                  In terms of aerobic respiration, resD functions upstream of ctaA, a
182 crucial role in folding important players in aerobic respiration such as the beta-subunit of the ATP
183 c removal of ROS strongly increases rates of aerobic respiration, sulfate reduction and hydrogen accu
184 ate a connection between the Krebs cycle and aerobic respiration that directs electrons along a singl
185 ion is an important factor in the inertia to aerobic respiration that is evident in the transition fr
186 ctaA is one of the several genes involved in aerobic respiration that requires ResD for in vivo expre
187   The mitochondria provided the capacity for aerobic respiration, the creation of the eukaryotic cell
188 ycling in upland soils is entirely driven by aerobic respiration; the impact of anaerobic microsites
189     Red blood cells (RBCs) are essential for aerobic respiration through delivery of oxygen to distan
190 is during metabolic depression but engage in aerobic respiration through the tricarboxylic acid cycle
191 ing revealed bacterial formate oxidation and aerobic respiration to be overrepresented metabolic path
192 cherichia coli, which we have shown requires aerobic respiration to compete successfully in the mouse
193                    While the transition from aerobic respiration to denitrification is well-studied,
194  cause of urinary tract infections, requires aerobic respiration to establish infection in the bladde
195                     ABPP showed a shift from aerobic respiration to ethanol fermentation and utilizat
196 uction can shift cellular bioenergetics from aerobic respiration to glycolysis, yet RCAN1-1L has very
197 antly, it is proposed that the adaptation of aerobic respiration to low oxygen environments resulted
198 el after 2 days, suggesting that maintaining aerobic respiration under conditions of nitrosative stre
199                             The evolution of aerobic respiration was likely linked to the origins of
200                  The biological toolkits for aerobic respiration were critical for the rise and diver
201 tion, is able to functionally replace SQR in aerobic respiration when conditions are used to allow th
202 dent respiration under hypoxic conditions to aerobic respiration, when accumulated nitric oxide react
203 ed the short-term influence of tobramycin on aerobic respiration within a PAO1 colony.
204 ectron transport and eventually cessation of aerobic respiration within the cell.
205 rgistic impacts of oxygen and temperature on aerobic respiration would have made marine animals more

 
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