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energy metabolism

10990 relationships annotated with this phrase. Showing first 500 of 10990.
Source entity Relationship Target entity Species
adenylates not exchanged with cytosol during the day occurs in plastids Arabidopsis thaliana
Rubisco activase (RCA, AT2G39730) activity is dependent on ATP/ADP ratio
acetyl-CoA is part of d-ESR (diatom common environmental stress response) Thalassiosira pseudonana
resting-cell formation involves catabolism of storage compounds Thalassiosira pseudonana
genes associated with inorganic pyrophosphate (PPi)-dependent alternative pathways of phosphorylation reactions are contained in clusters 22, 1, and 17 Rorippa amphibia; Rorippa sylvestris; Arabidopsis thaliana
fermentation has lower ATP yield compared to oxidative respiration
Phosphorus (P) is component of ATP
ATP levels dropped significantly by 30% in Rorippa amphibia Rorippa amphibia
Halophila uninervis restored several TCA cycle intermediates to pre-treatment levels during marine heatwave recovery period Halophila uninervis
metabolic suppression facilitates reduction of energy consumption
inadequate levels of intracellular energy levels can result in intracellular acidification yeast; human; plant
diatom Chaetoceros socialis upregulates catabolic pathways such as the tricarboxylic acid cycle Chaetoceros socialis
cellular energy state in plants is affected by CO2 concentration
branched-chain amino acids (BCAAs), such as isoleucine and valine can provide alternative energy source to plants by producing energy-rich compounds (e.g. acetyl-CoA)
new proline effector genes further link proline accumulation to cellular energy status Arabidopsis thaliana
plastids exchange adenylates with cytosol mainly at night for ATP import Arabidopsis thaliana
submergence stress causes energy crisis due to reduced photosynthesis rate
AMPK (AMP-activated protein kinase) can act to restore energy balance by switching on alternative catabolic pathways that generate ATP
repression of photosynthesis and aerobic respiration results in energy and carbohydrate crisis
acetyl-CoA, α-ketoglutarate, succinyl-CoA, fumarate, or oxaloacetate utilized in TCA cycle for energy production Thalassiosira pseudonana
ATP availability is compromised by increased energy costs for Na+ detoxification Zea mays
plants growing under NPC showed decrease in ATP accumulation Arabidopsis thaliana
Thalassiosira pseudonana metabolizes various compounds as sources of energy during process of forming resting cells Thalassiosira pseudonana
elevated AMP : ATP ratios have been observed to be characteristic for reduced metabolism Austrofundulus limnaeus; Artemia franciscana
high CO2 causes sharp decrease in ATP level
proteasome activity has high ATP demand ATP consumption
ATP levels did not decrease in Rorippa sylvestris Rorippa sylvestris
H+ efflux reversal to influx is possibly related to progressive ATP depletion Zea mays
submergence leads to repression of photosynthesis
diatom Chaetoceros socialis upregulates glyoxylate cycle Chaetoceros socialis
genes PFPA2, PFPB2, (ACD1, LLS1, PAO, AT3G44880) and (ATCPO-I, HEMF1, LIN2, AT1G03475) are strongly induced under submergence in Rorippa species Rorippa amphibia; Rorippa sylvestris
transcriptomic evidence suggests similar metabolic changes occur in C. socialis spores and T. pseudonana resting cells Chaetoceros socialis; Thalassiosira pseudonana
reduced ATP content and elevated AMP levels indicative of energy deficiency Thalassiosira pseudonana
potential decrease in quantity of Rubisco and light-harvesting complex proteins would have impact on energy and carbon balance Haberlea rhodopensis
exhaustion of starch and lipid reserves may cause starvation
regulation of organellar energy-gaining processes is required to substitute for chloroplastic ATP synthesis Hordeum vulgare
futile cycle uses up energy in the form of ATP
maintenance of mitochondrial respiration activity may be prioritized over photosynthesis Arabidopsis thaliana
long-term darkness induces energy starvation
submergence resulted in the repression of many energy-consuming pathways Rorippa sylvestris; Rorippa amphibia; Arabidopsis thaliana; Oryza sativa
marker genes for energy or sugar starvation are not more strongly induced in R. amphibia than in R. sylvestris Rorippa amphibia; Rorippa sylvestris
mitochondrial ATP synthases, ankyrin domain-containing proteins, and sterol-acyl desaturase were identified with increased expression in AI cells versus EAE sacs and decreased expression in both mutants Hieracium praealtum
Pi deficiency of the growth medium might prevent generation of ATP Arabidopsis thaliana
disturbance of the mitochondrial electron transport chain (mETC) leads to drop in ATP levels
activity-based probes have been used to study activities of ATP-binding proteins
down-regulation of malate dehydrogenase in the two cellular compartments notable in DILS and DLS Hordeum vulgare
UspA overexpression lines effect on proline accumulation suggests connection to cellular energy status Arabidopsis thaliana
ATP levels in T411–N were slightly lower than in T411+N Chlamydomonas reinhardtii
increased expression of key genes of gluconeogenesis and glycolysis along with up-regulation of glyoxysomal enzymes Hordeum vulgare
acetyl-CoA bypassed TCA cycle in the mutant Chlamydomonas reinhardtii
mitochondrial tricarboxylic acid (TCA) cycle provides reducing equivalents for other cell compartments
(TOR, AT1G50030) controls at transcriptional level mitochondrial oxidative function
lipid degradation involves succinate synthesis within glyoxysomes Hordeum vulgare
antimycin A has no major effect on ATP/ADP ratio Arabidopsis thaliana
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) protoplasts exhibit high ATP/ADP ratio Arabidopsis thaliana
repression of Rubisco saves carbon and energy Haberlea rhodopensis
ontology analysis detected cellular bioenergetics Chlamydomonas reinhardtii
triacylglycerols serve as energy and carbon sources Haberlea rhodopensis
ontology analysis detected ATP synthesis Chlamydomonas reinhardtii
UspA proteins whether all of them bind or hydrolyze ATP Arabidopsis thaliana
small percentage of total amount of four lipid classes can provide enough energy and carbon to compensate for shortages in darkness Haberlea rhodopensis
sulfur is present in lipoic acid
inorganic pyrophosphate (PPi) powers proton pumps
DP and IDL treatments after 6 d of darkening showed divergent photosynthetic and respiratory capacities
futile cycle associated with the inner envelope membrane effectively depletes the plant of energy resources Arabidopsis thaliana
chloroplastic isocitrate dehydrogenase isoform activation may supplement mitochondrial catabolism with 2-oxoglutarate Hordeum vulgare
down-regulation of AMPK is associated with decreased ATP Chlamydomonas reinhardtii
phosphorus is essential structural component of ATP
starch acting as ATP sink in (ADT3, PD1, AT2G27820) /4/5/6 plants was supported by measurements of ATP/ADP ratios Arabidopsis thaliana
mechanisms to prevent over-reduction of chloroplastic thylakoid membrane components involve mitochondria
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) plants show increased ATP/ADP ratio
alternative oxidase (AOX) activity is potentially wasteful
drastic changes in cellular energetics in the (ATVPS34, PI3K, VPS34, AT1G60490) KD result from altered metabolic pathways Chlamydomonas reinhardtii
sulfur (S) is an important component of lipoic acid
ATP measured using enzymatic assays coupled to NADPH formation
import assay contains MgATP
higher ATP/ADP ratios in (ADT3, PD1, AT2G27820) /4/5/6 suggested restricted ATP consumption in (ADT3, PD1, AT2G27820) /4/5/6 Arabidopsis thaliana
restoration of TCA cycle intermediates in Halophila uninervis was likely linked to low light adaptation Halophila uninervis
resting-cell formation in Thalassiosira pseudonana is energy demanding process Thalassiosira pseudonana
adenosine triphosphate (ATP) powers proton pumps
sucrose functions as substrate for glycolysis and TCA cycle in light
plant cells in metabolically suppressed state must be resourceful in utilization of various energy sources to yield ATP Arabidopsis thaliana
wild-type protoplasts maintain stable ATP/ADP ratio Arabidopsis thaliana
ADP-Glc/ADP antiport ensures balanced adenylate stoichiometry in stroma and cytosol Zea mays
Rca-α isoforms are better able to stabilize ATPase activity at high temperature
respiration is third fundamental pathway of energy metabolism
proline (Pro) may function as alternative energy source
arrest of protein translation and triggering of protein catabolism effectively switches plants from autotrophy to heterotrophy Arabidopsis thaliana
ATP concentration predicted based on phosphoglycerate kinase and glucose-1-phosphate adenylyltransferase is fivefold lower than concentrations reported in the literature Arabidopsis thaliana
electron transport and photosynthesis/light harvesting complexes continue to be over-represented amongst up- and down-regulated probesets at 14 hpi
increased efflux of glucose and fructose to the cytosol could provide immediate energy source
plants regulate and coordinate energy demands during particular growth and developmental stages
u-ATP9 male-sterile lines have unchanged ATP/ADP ratio
(ATTPS1, TPS1, AT1G78580) is especially required in metabolic sinks with high energy demand Arabidopsis thaliana
mitochondrial dysfunction causes decrease in adenine nucleotides levels Arabidopsis thaliana
Sesaminol diglucoside [SDG(β1→6)] mediates enhancement of energy consumption Mus musculus
copper (Cu) is essential for energy production in chloroplasts and mitochondria
mitragynine intake is related to reduction in weight gain rat
decreased respiratory capacity of complex I affected adenylate concentration Cucumis sativus
triacylglycerols (TAGs) serves as energy and carbon reserve
energy category proteins mainly included glycolysis and photosynthesis proteins
diminished photosynthesis and/or respiration reduces overall energy status of the cell
fertilization places unique demands on energy production
Futile cycle between glucose-6P shunt and Calvin–Benson–Bassham (CBB) cycle consumes ATP
feeding cycles control daily energy levels
primary role of sucrose suggested to be energetic
ratio of ADP/ATP is high (>1.0) causes reductions of ATPase activity and Rubisco activation activity
hypoxic stress causes 50% reduction in cellular ATP levels
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) protein kinase controls plant's energy balance Arabidopsis thaliana
u-ATP9 male-sterile lines have low adenylate levels
Futile cycle between glucose-6P shunt and Calvin–Benson–Bassham (CBB) cycle leaves the NADPH level unchanged
triacylglycerols (TAGs) is involved in ATP production
Tre6-P content and ATP/AMP ratio in mutant anthers were significantly reduced ms33-6038 anthers Zea mays
other energy management pathways remain to be identified Chlamydomonas reinhardtii
transcripts with delayed translation, ATP-independent bypasses, alternative respiratory pathway and 4-aminobutyric acid shunt together confer bioenergetic advantages to meet energy demands upon rehydration Craterostigma plantagineum
plant GS pathway uses approximately 15% of total cellular ATP account
abundances of most amino acids are changed when ATP supply of plastid is diminished
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) enhances ATP-generating capacity
Probable malate dehydrogenase (PMDH1, AT2G22780) has expected function energy Arabidopsis thaliana
growth of pollen tube places unique demands on energy production
reduced fumaric acid content together with lower photosynthesis efficiency and carbohydrate production and increased pool of free amino acids suggests that plants rely on protein degradation rather than photosynthesis to obtain energy Arabidopsis thaliana
young proliferating leaves require large energy investments Pisum sativum
chloroplast and mitochondrion require coordination of activity between optimal energy metabolism
short- and long-term respiratory acclimation is linked with lower energy requirements for cellular maintenance in response to increasing temperatures Agrostis scabra
energy and lipid metabolism proteins levels increase at 12 days after anthesis (DAA) Triticum aestivum
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) kinase promotes catabolism
low plastidial Pi concentration impedes ATP synthesis
lipids serve as storage sources for energy
integrative analysis of transcriptome, proteome and metabolite data was performed with emphasis on energy metabolism Craterostigma plantagineum
respiration has less impact on yield potential than energy efficiency
shift in redox components can limit functioning of plastidial and mitochondrial electron transport chains Arabidopsis thaliana
NLR proteins catalyze breakdown of ATP into ADP and free phosphate ion
nutrients serve as energetic resources
TGS are likely to act as energy reserves consumed during seedling establishment and growth Arabidopsis thaliana
plants cope with lower energy production through increased catabolism
oxoglutarate can be used to provide ATP
haems are essential cofactors for many biological processes
reducing PARP activity could reduce impact of environmental stresses on cellular energy homeostasis
hypoxia in phloem leads to decreased energy charge
futile ATP hydrolysis increases cellular demand for ATP
phosphorylation modulates enzyme activity and specificity of ATP synthase
coordinated changes in composition of mitochondrion and chloroplast may be sufficient to maintain energy metabolism and photosynthesis Nicotiana tabacum
cured fungus shows lower ATP production Gigaspora margarita
energy-use efficiency is one of the principal factors explaining successful invasion of Wedelia trilobata Wedelia trilobata
flexible chloroplast–mitochondrion interactions can overcome major lesions in energy metabolism
respiratory inhibitor presence poise of energy metabolism will be favouring over-reduction of stroma and ATP deficiency Nicotiana tabacum
algal cells likely exploit other energy management pathways Chlamydomonas reinhardtii
maintenance respiration increased rates of during sugarcane development and maturation contribute to reduced growth phenomenon (RGP) sugarcane
chloroplasts during energy starvation such as prolonged darkness strongly depend on the supply of ATP
mitochondria are found in aerobic eukaryotic cells
electron transfer flavoprotein (ETF) complex enables catabolism of a range of alternative substrates under times of extreme C limitation
ATP content was significantly reduced in mutant anthers at stages 8 and 9 Zea mays
energy-producing pathways have evolved to interact to regulate carbon metabolism in microalgae
ascorbate plays role in co-ordinating rates of respiration and photosynthesis
down-regulation of maintenance processes can conserve carbon and energy
ATP-independent bypasses may play role in energy management Craterostigma plantagineum
OsDRP1e is localized to mitochondrion
elevated AMP levels suggests low-energy status Symplocarpus renifolius
Fructose bisphosphate aldolase (AtFBA5, DEG22, FBA5, AT4G26530) has expected function energy Arabidopsis thaliana
physiological co-operation of the aerobic cortex and hypoxic–anoxic stele seems likely to involve possible transfer of high energy compounds produced in the aerobic cortex to the hypoxic–anoxic stele
UDP-glucose pyrophosphorylase (OsDP5) was down-regulated to a lesser extent in heat-tolerant rice lines compared with heat-sensitive lines on day 5 heat-tolerant and heat-sensitive rice lines Oryza sativa
SnRK1-mediated induction or repression of ~1000 genes switches from anabolism to catabolism
(PXY, TDR, AT5G61480) controls energy production and conversion Oryza sativa
energy category proteins most played roles in glycolysis, respiration, and tricarboxylic acid (TCA) pathway
nucleotide transporter (NTT, WIP2, AT3G57670) mediates import of ATP into photosynthetically inactive plastids
Glc-6-P can interact with signalling systems as potential inhibitor of the energy sensor sucrose non-fermenting 1 (SNF1)-related kinase 1 (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090)
sugars serves as major metabolic fuel
SNF1 and AMP-activated kinases have been primarily studied as metabolic regulator activated in response to energy deprivation Saccharomyces cerevisiae; mammals
metabolic inhibitors may exert their effect by perturbing the pre-existing cellular energy status Oryza sativa
excessive nodule development over-consumes energy from plant energy resources
Probable malate dehydrogenase (PMDH1, AT2G22780) is located in peroxisome Arabidopsis thaliana
starch is normally considered to be major energy source for germinating cereal grain
cytochrome pathway (v cyt) matches ATP demand Nicotiana sylvestris
decreased ATP level under heavy metal stress is an important factor in enzyme deactivation
proline activates ATP synthesis and activation of enzymes
Glyceraldehyde-3-phosphate dehydrogenase B (GAPB, AT1G42970) is located in chloroplast Arabidopsis thaliana
low N2 fixation in S-deficient legumes is proposed to be due to low ATP supply legumes
up-regulation of transcripts related to the energy producing pathways suggests high energy demand was imposed on transgenic cotton to support the cellular energy consumption resulting from the induction of multiple metabolic and host defence responses
nucleotide transporter (NTT, WIP2, AT3G57670) mediates import of ATP into non-green plastids
enhanced starch accumulation in VHb-expressing hybrid aspen lines points to changes in cellular energy metabolism Populus tremula × tremuloides
mitochondrial function plays vital role in optimizing photosynthesis
Agrostis scabra maintains significantly lower maintenance cost at 27 °C or 37 °C Agrostis scabra
ABC transporters function in an ATP-dependent process
citrate, fumarate, malate, and succinate showed decreases of -4 to -50-fold in Clipper roots after 5 weeks of salt stress Hordeum vulgare
stamen tissues appear to increase mitochondrial mass or metabolic activity
15 proteins 60% belonged to energy category
mitochondrial ATPase β-subunit changed expression only in radicles of Patio Solanum lycopersicum
biosensors monitor metabolic state via energy equivalents
elevated AMP levels suggests high ATP consumption Symplocarpus renifolius
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) kinase has roles in regulating energy metabolism
increases in (ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) and AOX combined with large increase in cATP synthase protein amount Nicotiana tabacum
(TOR, AT1G50030) signalling is activated through glycolysis and mitochondrial respiration
putative GDP dissociation inhibitor (OsUP19) was up-regulated in both heat-tolerant and heat-sensitive rice lines under high temperature stress high temperature stress Oryza sativa
energy metabolism (photosystem I supercomplex) seemed to be downregulated later in infection Vitis vinifera
metabolic nodes integrate energy status
photosynthetic machinery adjustment maintains ATP level Nicotiana sylvestris
use of OAA from carboxylation of (PAS2, PEP, PEPINO, AT5G10480) for N assimilation and N transport necessitates no further reductive step and thus energy loss for the nodules
regulatory networks govern energy conversion
metabolite cycling is a form of futile ATP hydrolysis
drought stress mainly affects respiration
glucose deprivation leads to fall in energy charge potentials
sucrose-supplemented flowers maintain higher level of ATP compared with control flowers control flowers without sucrose
depletion of ATP could neither be responsible for decrease of H+-ATPase activity Arabidopsis thaliana
ATP:ADP in a root segment as a whole with a hypoxic–anoxic stele becomes 2.4 in maize Zea mays
DGs were involved in energy metabolism Oryza sativa
light and/or carbon responsive genes are involved in energy production Arabidopsis thaliana
sucrose supplementation to cut tulip flowers could generate adenosine triphosphate (ATP) Tulipa sp.
energy metabolism has positive correlation with morphological features of the mitochondria
respiratory activity of plant mitochondria has been studied using thermogenic and non-thermogenic plants
system-wide reprogramming in cellular metabolic processes balances energy demand and energy production Arabidopsis thaliana
mitochondrial respiration is main source of ATP in root tissues
V1 catalytic domain is involved in ATP hydrolysis
differentially expressed proteins participate in energy metabolism Synechocystis sp. PCC 6803
heat is generated by many reactions in energy metabolism are exothermic in the forward direction reactions in energy metabolism
growth decline at extreme [K+]ext (40 mM) may be a consequence of energetic drain from futile cycling of K+ and NH4+ Oryza sativa; Hordeum vulgare
transporters are involved in the provision of energy-rich metabolites
cessation of oxidative phosphorylation causes severe energy deficits
adenylate energy charge (AEC) level in sucrose-supplemented flowers is maintained at >0.8 at all stages until day 9 day 9 of petal development
α-ketoglutarate, aconitate, citrate, isocitrate, malate, and succinate were at 2-15-fold higher levels in salt-treated Sahara leaves Hordeum vulgare
ADP consumption through oxidative phosphorylation is part of steady-state recycling of ADP
trap closure in Dionaea muscipula results in loss of ATP (29%) Dionaea muscipula
myo inositol and its phosphorylated derivatives play important roles in cellular energy currency
putative GDP dissociation inhibitor (OsUP19) expression was lower after 5 d of high temperature stress in heat-tolerant and heat-sensitive rice lines Oryza sativa
water-deficit stress causes deleterious effects on photosynthesis
reverse genetic approaches underscore interconnection between photosynthesis and respiration
positive correlation between energy metabolism and total mitochondrial number is a well known feature in brown adipose tissues
lack of oxygen directly causes shortage of cellular energy supply (ATP)
decreased energy charge may lead to dramatic metabolic starvation subsequent to decreased assimilate uptake in cell Vitis vinifera
mitochondrial energy production is limited causes starch-derived glucose contribution as osmoticum and energy source
electron flow through non-phosphorylating pathways is not limited by adenylate control
gap between increasing energy demand and impaired ability for energy provision widens at pod formation
(GLC, AT1G65450) outflow and mtHXK activity stimulates ADP recycling
O2 deficiency results in severe energy deficits
intracellular high energy phosphate content is reflected by adenylate energy charge (AEC) adenylate energy charge (AEC)
(ATCAD4, CAD, CAD-C, CAD4, AT3G19450) ATPase (AAA1) is involved in energy metabolism, ATP binding, and oxidative phosphorylation Helianthus annuus
ADP production by mtHXK, bound to the mitochondrial outer membrane is part of steady-state recycling of ADP
lack of ATP probably caused decrease in glutamate utilization by GS and asparagine synthetase Medicago truncatula
adenylate energy charge (AEC) level in control flowers drops below 0.75 after 3 d day 3 of petal development
AMP : ATP ratios increased over time course of resting cell formation Thalassiosira pseudonana
Phosphorus (P) plays key roles in plant energy balance
orthogroups associated with oxidation–reduction and metabolic processes were over-represented in ferns Ceratopteris richardii; Polypodium vulgare
sulfide treatment had significant effect on ATP concentration Arabidopsis thaliana
resting cells possess elevated levels of AMP Thalassiosira pseudonana
net H+ efflux reversal to influx in SKT1506 indicates less favorable energy status Zea mays
higher ATP content in R. sylvestris might indicate higher energy demand of elongation growth in R. amphibia Rorippa amphibia; Rorippa sylvestris
tolerance to low oxygen levels requires tight balance between energy use for growth and ATP generation through glycolysis and fermentation Arabidopsis thaliana; Oryza sativa; Rorippa amphibia; Rorippa sylvestris
gene expression of energy production in the mutant was altered energy metabolism Arabidopsis thaliana
glycolysis rather than respiration in meristematic cells occurs in hypoxic conditions Zea mays
38 (ASHH2, CCR1, CLI186, EFS, LAZ2, SDG8, AT1G77300) target genes cover metabolic pathways in energy use Arabidopsis thaliana
decreases in root respiration can conserve carbon and energy
protein phosphorylation depends on energetic status of the cell
hexoses formed from sucrose cleavage are used for respiration
CCM metabolites play a central role in energy production
AtSnRK1α1/2 activation results in increase of catabolism Arabidopsis thaliana
balance between ATP and NADPH maintenance highlighted importance of setting correct division of maintenance energy consumption
Cytoplasmic ATP generation frees up carbon for anabolism Zea mays
later leaf development shows mitochondria switch from respiration to photorespiration Zea mays
constraint on relative activities of generic ATPase and NADPH oxidase was necessary to introduce account for maintenance costs
ATP demand for maintenance may be lower in dark conditions Chlamydomonas reinhardtii
plants treated with sulfide under NPC showed significantly higher accumulation of ATP Arabidopsis thaliana
increase in labile organic C compound decomposition aids in energy conservation
meristematic cells at the base of the stalk probably utilize glycolysis rather than respiration Zea mays
mitochondrial alternative electron transport (mAET) partitions energy between foliar nitrogen assimilation and carbon assimilation Arabidopsis thaliana
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) activity correlates with repression of ZmbZIP11 and ZmDPS (negative (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) targets) Zea mays
effects of chemical stress on energy metabolism suggested by modifications of carbon balance and carbon utilization Lolium perenne
UDP-glucose pyrophosphorylase (OsDP5) was down-regulated to a greater extent in heat-tolerant rice lines compared with heat-sensitive lines under high temperature stress for day 1 heat-tolerant and heat-sensitive rice lines Oryza sativa
shading compromises energy status
sugars resulting from cell wall dissolution contribute energy for the young seedling Hordeum vulgare
Low T6P levels induce maximal activation of (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) (major energy sensor) Zea mays
helicase utilizes energy from hydrolysis of nucleoside triphosphates (NTPs)
ATPases next largest group in Transport category triticale stigma proteome Triticale
fully functional organellar DNA (orgDNA) at early stages of organellar development is needed for subsequent respiration and photosynthesis Zea mays
higher respiratory activity in mitochondrion in (AGY1, AtcpSecA, SECA1, AT4G01800) is in response to defective photosynthetic activity Arabidopsis thaliana
free energy is used for ATP production
increase in the efficiency of photosynthesis under non-saturating light conditions would result in new ATP requirements Arabidopsis thaliana
maize class II TPS enzymes play regulatory role in responding to and/or managing energy resources Zea mays
mitochondrial subset based exclusively on prediction was not enriched in energy functions Oryza sativa
remainder of ATP budget is used for maintenance Arabidopsis thaliana
tightly bound outer membrane mtHXK produces ADP that can be transported through both mitochondrial membranes
ascorbate biosynthesis is linked to photosynthesis
carbohydrates serve as sole source of energy
switch from anabolism to catabolism promotes survival in lieu of growth
eutypine uncouples mitochondrial oxidative phosphorylation Vitis vinifera
ADP-glucose pyrophosphorylase large subunit (OsDP3) was down-regulated to a lesser extent in heat-tolerant rice lines compared with heat-sensitive lines on day 5 heat-tolerant and heat-sensitive rice lines Oryza sativa
resynthesis of starch during degradation may result in futile ATP consumption Arabidopsis thaliana
48 h incubation in darkness leads to intracellular energy depletion
ATP increase may compensate for starvation and sustain essential cellular processes Chlamydomonas reinhardtii
T411 line had highly reduced ATP levels despite the induction of autophagy Chlamydomonas reinhardtii
shutdown of photosynthesis- and photorespiration-related genes saves valuable resources Haberlea rhodopensis
genes in energy metabolism category were significantly overrepresented in class 1
disintegration of chloroplasts correlated with activation of chloroplast isocitrate dehydrogenase Hordeum vulgare
lipid droplets (LDs) ensure energy storage
ATP levels under –N were higher in wild-type cells Chlamydomonas reinhardtii
class III (ATVPS34, PI3K, VPS34, AT1G60490) mediates homeostasis of lipid, starch, FFA, and ATP Chlamydomonas reinhardtii
malate dehydrogenase genes specific for the two cellular compartments were found down-regulated dark-induced leaf senescence (DILS) progression beyond day 7 Hordeum vulgare
ATP-related genes are repressed and up-regulated during 17–21 DAF
subset of mitochondrial proteins defined exclusively by orthology was enriched in energy functions Oryza sativa
increasing temperature caused marked reduction in carbon conversion efficiency Arabidopsis thaliana
photorespiration controls photosynthesis Arabidopsis thaliana
TCA depletion in roots could originate from increasing energy demand for ATP synthase and ATPase-dependent copper exclusion Lolium perenne
mitochondrial durability within the same timeframe as activation of glyoxylate cycle Hordeum vulgare
relatively more durable mitochondria appear to reutilize and recycle carbon substrates that likely originate from the degradation of proteins, lipids, and other organic cellular compounds Hordeum vulgare
derepression of flowering and ABA-responsive pathways in (AtLHP1, LHP1, TFL2, AT5G17690) mutant comes with high energetic cost Arabidopsis thaliana
(ASHH2, CCR1, CLI186, EFS, LAZ2, SDG8, AT1G77300) targets is enriched in energy metabolism biological process Arabidopsis thaliana
ADP was determined in protoplasts exposed to light Arabidopsis thaliana
down-regulation of malate dehydrogenase in the two cellular compartments apparently related to suppression of chloroplastic glyceraldehyde-3-phosphate dehydrogenase Hordeum vulgare
expression cluster 6 was enriched for energy metabolism (GO 0006091; P = 2 × 10−14) Panicum hallii
transcription of mitochondrion-encoded respiratory complexes in the mutant was induced respiratory complex expression Arabidopsis thaliana
inhibition of DNA binding of PIFs by phytochrome may occur in the absence of ATP
Some of these studies suggested roles for energy metabolism Zea mays
wild-type embryo cells at 7 days after pollination (DAP) contained abundant mitochondria Zea mays
accurate prediction of fluxes through energy-transforming pathways requires taking into account several other energy costs
increased membrane leakage at elevated temperature make major contributions to increased ATP maintenance costs Arabidopsis thaliana
hyper-osmotic conditions caused small decrease in proportion of NADPH used for maintenance Arabidopsis thaliana
mitochondrial oxidative phosphorylation (OXPHOS) is responsible for ATP production
no major effects on intermediate metabolites in glycolysis and TCA cycle suggests that energy metabolism was not affected
fluxes through energy-transforming pathways (glycolysis, oxidative pentose phosphate pathway (OPPP) and tricarboxylic acid (TCA) cycle) are greatly under-estimated by FBA when solely constrained by biomass synthesis
maintenance ATP demand in E. coli was 7.6 mmol ATP g DW −1 h −1 Escherichia coli
addition of single extra constraint, flux ratio of glycolysis to OPPP allows ATP and NADPH maintenance costs to be accounted for
33% of total ATP produced in heterotrophic Arabidopsis cells was used for maintenance under control conditions Arabidopsis thaliana
decreased PSII efficiency probably involves complex mechanisms relying on interdependence between mitochondria and chloroplasts
plant UCPs are involved in regulation of energy metabolism
heavy metal stress (Cd, Cu, Ni) decreases ATP content Cucumis sativus
multicellular and complex tissue organization results in specific energy demands Zea mays
trehalose and T6P include storage of chemical energy
greater TAG breakdown acts to compensate for lack of starch Arabidopsis thaliana
TCA cycle inhibition caused a comparable physiological response to ETC/complex V inhibition Arabidopsis thaliana
38 (ASHH2, CCR1, CLI186, EFS, LAZ2, SDG8, AT1G77300) target genes cover metabolic pathways in energy production Arabidopsis thaliana
chloroplast-to-nucleus retrograde signalling and chloroplast-to-mitochondrion signalling in (AGY1, AtcpSecA, SECA1, AT4G01800) adjust metabolic networks to cope with insufficient energy supply Arabidopsis thaliana
ADP-glucose pyrophosphorylase large subunit (OsDP3) was down-regulated under high temperature stress in heat-tolerant and heat-sensitive rice lines Oryza sativa
respiratory metabolism has functional role in illuminated leaf
expression changes in glycolysis, TCA cycle, and ETC enzymes suggests heterotic plants require optimized enzyme levels for sufficient energy production Zea mays
ATP occurs in each of these compartments Arabidopsis thaliana
ATP content is less reduced in R. sylvestris than in R. amphibia under submergence Rorippa amphibia; Rorippa sylvestris
ATP increases specifically in shoots Arabidopsis thaliana
ATP and ADP concentrations remained constant when expressed with respect to cytosol volume
rice genotypes differing in submergence tolerance [M202 versus M202 (SUB1, AT4G08810) ] express PFP genes at different levels under submerged conditions Oryza sativa
selective translation of specific mRNAs avoids excessive energy consumption Arabidopsis thaliana
hyper-osmotic conditions caused substantial reduction in proportion of ATP used for maintenance Arabidopsis thaliana
Cytoplasmic ATP generation has benefit of eliminating major source of reactive oxygen species (ROS) Zea mays
transcriptional modules defined from genes showing opposite gene expression patterns during S3 and S5 stages included regulatory gene circuits (TFs–regulatory motifs–target genes) involved in energy production Cicer arietinum
PFPA2 and PFPB2 are associated with inorganic pyrophosphate (PPi)-dependent alternative pathways of phosphorylation reactions Rorippa amphibia; Rorippa sylvestris; Arabidopsis thaliana
exogenous sulfide increases ATP concentration Arabidopsis thaliana
alcohol fermentation and lactate production supply ATP Thalassiosira pseudonana
ketogenesis supplies fuel and ATP Thalassiosira pseudonana
Phosphocreatine releases substantial energy upon hydrolysis
ATP : AMP ratio changed gradually resting cell formation Thalassiosira pseudonana
catabolism of stored compounds is crucial for development of resting cells Thalassiosira pseudonana
higher abundance of chloroplasts in fern guard cells may reflect over-representation of orthogroups associated with oxidation–reduction and metabolic processes Ceratopteris richardii; Polypodium vulgare
KCN treatment resulted in a significant drop in MgATP 2− Arabidopsis thaliana
epigenetic marks by (ASHH2, CCR1, CLI186, EFS, LAZ2, SDG8, AT1G77300) possibly function to coordinate broad genome-wide regulation of genes involved in energy supply and demand Arabidopsis thaliana
functioning TCA cycle is critical for mitigation of light-dependent energy deprivation in seagrasses Halophila uninervis
transcriptomic changes largely reflect biochemical changes related to energy status Thalassiosira pseudonana
PTR via ToxA activity may divert cell energy
ATP is adenosine triphosphate
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) protein kinase inhibits energy-consuming anabolic processes Arabidopsis thaliana
transgenic plants with reduced PARP activity reduce energy consumption
AMPK (AMP-activated protein kinase) can act to restore energy balance by switching off anabolic pathways and other processes consuming ATP
ATP and ADP metabolism is affected in hvtdf1 mutant Hordeum vulgare
fatty acid beta oxidation uses lipids as an energy source Chaetoceros socialis
submergence leads to repression of aerobic respiration
H+-ATPase operation comes with high carbon cost
conserved biophysical traits observable at the single-cell level can be associated with major metabolic changes
(RCA, AT2G39730) possesses ATP-hydrolyzing enzyme activity
sulfide restores ATP levels Arabidopsis thaliana
higher dark respiratory rate in the leaves under elevated CO2 concentrations is driven by greater abundance of transcripts involved in glycolysis, the TCA cycle, and mitochondrial electron transport energy metabolism Solanum lycopersicum
light-deprived Halophila uninervis leaves likely relied on warmer temperatures to restore TCA cycle intermediates Halophila uninervis
Rozella allomycis relies on host mitochondria to source ATP Rozella allomycis
ATP and ADP are rapidly exchanged over mitochondrial membrane Arabidopsis thaliana
sharp decrease in ATP level at high CO2 causes significant decrease in the ATP : ADP ratio
ATP to ADP ratio remained unchanged in Rorippa amphibia and Rorippa sylvestris Rorippa amphibia; Rorippa sylvestris
GO term carbohydrate catabolic process was enriched with 7.2% in PM vs PF comparison Physcomitrella patens
parasite consuming the major polysaccharide storage provides rapid energy Maullinia ectocarpii
ATP hydrolysis by plasma membrane H+-ATPase consumes high amounts of energy
oxygen transport significant for energy demands of symbionts Medicago truncatula
IFQA affects expression of genes related to energy metabolism maize
(TOR, AT1G50030) is necessary for maintenance of mitochondrial oxidative function
N-terminal TF fragments in nucleus activates genes involved in mitochondrial metabolism higher plants
inorganic phosphate (Pi) is required for ATP synthesis
rapid and specific exchange of molecules between cytosol and mitochondrial matrix is required for metabolic activities
inhibition of glycolysis is accompanied by low ATP and ADP levels Arabidopsis thaliana
guard cells detected to contain several metabolites participating in glycolysis and the TCA cycle Arabidopsis thaliana
resting cells possess reduced ATP content Thalassiosira pseudonana
energy costs in plants are potentially higher than in microbial systems
2cysprxA/B mutant has slightly increased ATP levels, ATP/ADP ratios and energy charges
iCre1355 metabolic model uses experimentally determined values for energy requirements for growth and maintenance Chlamydomonas reinhardtii
minimum rate of ATP synthesis in mitochondria during dark growth was higher than value calculated for growth and starch synthesis in light Chlamydomonas reinhardtii
MFA did not directly affect indicates that oxidative phosphorylation Arabidopsis thaliana
components of energy metabolism pathways showed consistently different expression in higher-heterosis hybrids compared to low-heterosis hybrid Zea mays
male germinal cells divert carbon into alternative pathways that avoid producing reactive oxygen species (ROS) Zea mays
pgl3-1 mutation is not the result of general energy deficiency Arabidopsis thaliana
Pareto optimality analysis explores trade-off between ATP and NADPH production for maintenance
ATPase reaction is reaction r52 in cytosol
proteins involved in the generation of precursor metabolites and energy, or in photosynthesis (light reactions) were clearly down-regulated in the double mutant Arabidopsis thaliana
both mutations ( (CEF, AT3G44340) and complex I deficiency) cause a decrease in ATP/NAD(P)H ratio
Mutation in (P1w, RPP1.1, RPP1A, AT1G01100) highlighted effects on energy metabolism Arabidopsis thaliana
ATP turnover is increased due to higher energy need during mitosis I
energization of the leaves was unchanged among mutants and wild-type under both light conditions
LC/MS analysis examines phosphorylated adenine nucleotides Arabidopsis thaliana
rate of ATP synthesis for maintenance in dark decreased as specific rate of TAG consumption increased Chlamydomonas reinhardtii
(ASD, ATA1, TA1, AT3G42960) aleurone exhibits reduced level of ATP content Oryza sativa
fatty acid de novo synthesis requires large amounts of reducing equivalents (NADPH)
apyrases may be related to regulation of the energy charge of cell
AtSnRK1α1/2 activation results in reduction of anabolism Arabidopsis thaliana
germinal initials are enriched in gene sets involved in cytoplasmic ATP generation Zea mays
2cysprx mutant depicted higher ATP levels in normal light and high light Arabidopsis thaliana
lipids can be catabolized by catabolism of stored carbon
DEGs are enriched in pathways related to energy metabolism Paeonia suffruticosa
PPi-dependent alternative pathways have potential benefit for energy metabolism in plants under low-oxygen stress Rorippa amphibia; Rorippa sylvestris; Arabidopsis thaliana; Oryza sativa
energy efficiency has major impact on yield potential
energy substrate in primary root (PR) was preferentially consumed by plant Aconitum kusnezoffii
lipids is energy storage molecules
T411 cells have reduced survival because decreased ATP levels compromise essential cellular functioning Chlamydomonas reinhardtii
minimizing synthesis of photosynthesis-related proteins may enable economizing on valuable energy and nutrient resources Haberlea rhodopensis
down-regulation of malate dehydrogenase in the two cellular compartments indicates that glyoxylic and citric acid cycles might be compromised Hordeum vulgare
respiratory activity provides nitrogenase with 16 molecules of ATP and 8 electrons
plants growing in normal air showed higher accumulation of ATP Arabidopsis thaliana
ATP content changed gradually resting cell formation Thalassiosira pseudonana
ADP measured using coupling to NADH utilization
decreased ATP/AMP ratio suggests low energy status in mutant anthers Zea mays
grade I class iii "TCA & respiratory chain" encompasses 10.3% (232) of the regulated genes Zea mays
organisms lacking complex I compensate through degeneration or rearrangement of the respiratory chain
regulation of organellar energy-gaining processes required in both DILS and DLS Hordeum vulgare
persulfidated proteins found under NPC are mainly involved in glycolysis, the TCA cycle, and mitochondrial electron transport energy metabolism routes Arabidopsis thaliana
drop in ATP affects cytoplasmic pH control Thalassiosira pseudonana
fatty acids and triacylglycerols serve as primary energy sources for mature resting cells Thalassiosira pseudonana
AMP level remains steady phosphate (Pi) starvation Arabidopsis thaliana
starch consumption rate in dark constrained to rate of production under light (3.08 × 10−4 mmol (g DW h)−1) resulted in maximum rate of ATP synthesis for cell maintenance of 1.11 mmol (g DW h)−1 which is 39% of assumed value Chlamydomonas reinhardtii
up-regulation of glyoxysomal citrate synthase and mitochondrial succinate dehydrogenase supported by conclusion that mitochondria reutilize and recycle carbon substrates Hordeum vulgare
UspA domain proteins in bacteria may act as switches that detect cellular energy or metabolic status
(ATVPS34, PI3K, VPS34, AT1G60490) signaling cascade independently influences energy homeostasis Chlamydomonas reinhardtii
ATP levels in T411–N were considerably lower than in WT–N Chlamydomonas reinhardtii
energy normally dissipated through AP (alternative pathway) diverted to other metabolic pathways
pyruvate released in mimosine degradation reaction may enter tricarboxylic acid cycle Leucaena leucocephala
photosynthesis produces ATP
(AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) integrates energy and stress signaling Arabidopsis thaliana
bypassing the TCA cycle results in highly reduced ATP levels under prolonged starvation Chlamydomonas reinhardtii
cool temperature most likely led to decline in energy production Oryza sativa
increased proline accumulation in nucleoside triphosphate hydrolase (AT1G33290) mutants suggests link of proline accumulation to energy status Arabidopsis thaliana
reduced carbon possibly liberated from cell wall modification/degradation can be catabolized to yield ATP Arabidopsis thaliana
higher branched-chain amino acids in shaded Halophila uninervis leaves suggests that this seagrass can access alternative energy production pathways during longer periods of light deprivation Halophila uninervis
decline in ATP content triggers increase in intracellular viscosity within yeast cells yeast
transgenic mice overexpressing a truncated version of HMGA2 are obese Mus musculus
mitochondria and nuclei integrity seems related to availability of recycled carbon substrates from degradation of proteins, lipids, and other organic cellular compounds Hordeum vulgare
(AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) plants show increased ATP level
severe energy limitation likely causes slow growth and compromised development and seed set in (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) rpoTmp plants Arabidopsis thaliana
pyruvate eventually feeds into TCA cycle Chlamydomonas reinhardtii
genes related to oxidative phosphorylation, carbon fixation, and photosynthesis were included in class 1
increases of succinic acid, pyruvic acid, oxaloacetic acid, G6P and F6P in guard cells suggest accelerated energy production process Arabidopsis thaliana
metabolic model findings pinpoint energy expenditures Jatropha curcas
sucrose could speed up generation of energy after rehydration
TAG consumption rate in dark constrained to not exceed TAG production rate under light (9.87 × 10−3 mmol (g DW h)−1) resulted in no growth and energy reserves used for ATP synthesis for cell maintenance at rate of 0.59 mmol (g DW h)−1 Chlamydomonas reinhardtii
high cATP synthase activity fulfilling cellular ATP demands Nicotiana tabacum
genes associated with electron transport, energy pathways, and structural molecule activities were significantly underrepresented in the aox1a-specific gene set Arabidopsis thaliana
(ATBHLH029, ATBHLH29, ATFIT1, BHLH029, FIT, FIT1, FRU, AT2G28160) stored in root vacuoles may serve as important source of energy for actively growing cells
regulation of AOX may be tied into energy and stress signaling pathways in wide variety of eukaryotes
chloroplast isocitrate dehydrogenase activation apparently necessary for 2-oxoglutarate anabolic export Hordeum vulgare
Koshihikari showed modified abundance of several subunits of cytochrome C oxidase Oryza sativa
higher PMF in (ADT3, PD1, AT2G27820) /4/5/6 agrees with data indicating restricted ATP consumption Arabidopsis thaliana
vacuolar sugars can serve as important carbohydrate source during energy starvation
ATP/ADP ratios for (ADT3, PD1, AT2G27820) /4/5/6 were higher compared with ATP/ADP ratios in wild type Arabidopsis thaliana
generated glucose (Glc) from remobilized β-glucans could serve as energy source under conditions of sugar depletion Hordeum vulgare
combination of (ATVPS34, PI3K, VPS34, AT1G60490) and AMPK might have major role in maintaining cellular ATP levels in C. reinhardtii Chlamydomonas reinhardtii
UspA mutants effect on proline accumulation suggests connection to cellular energy status Arabidopsis thaliana
C. reinhardtii continues to actively generate ATP in mitochondria through the TCA cycle Chlamydomonas reinhardtii
energy-limiting conditions under which plant is not able to use all the carbohydrate reserves
prolonged darkness will ultimately lead to exhaustion of starch and lipid reserves
reduced photosynthesis and electron transport eventually also inhibits respiration
4mC-methylated genes show enrichment GO for oxidative phosphorylation Casuarina equisetifolia
ATP appears important for cell survival Nicotiana tabacum
tricarboxylic acid cycle (TCAC) has canonical role in cellular energy production
changes in composition of mitochondrion and chloroplast ensured sufficient mitochondrial electron sink capacity and chloroplast ATP-generating capacity Nicotiana tabacum
AMP-activated kinases act to inhibit (TOR, AT1G50030) (target of rapamycin)
changes in TAG synthesis and increased starch levels might radically alter cellular energy metabolism Chlamydomonas reinhardtii
severe oxygen deficiency leads to insufficiency in ATP for energy-demanding processes
similar patterns of TCA cycle restoration were absent under Shade treatment at control temperatures Halophila uninervis
diatom Chaetoceros socialis upregulates fatty acid beta oxidation Chaetoceros socialis
genes PFPA2, PFPB2, (ACD1, LLS1, PAO, AT3G44880) and (ATCPO-I, HEMF1, LIN2, AT1G03475) are not induced in Arabidopsis Arabidopsis thaliana
positional information modulates energy activities within the cell
(ATVPS34, PI3K, VPS34, AT1G60490) mutant displayed fundamental shift in intracellular energy flux Chlamydomonas reinhardtii
increased mitochondrial activity is needed to compensate for lack of energy production in chloroplasts Haberlea rhodopensis
inhibition of glyoxylic and citric acid cycles does not seem to preclude function of glyoxylic acid cycle to supplement cytosolic gluconeogenesis Hordeum vulgare
BZR1-dependent GA-regulated transcriptome controls photosynthesis
maintenance requirement was experimentally determined for cells in continuous light Chlamydomonas reinhardtii
light uptake rate was assumed to be determined solely by energy requirements for CO2 fixation, functional biomass production and starch synthesis Chlamydomonas reinhardtii
AtMBP-1 coordinates energy metabolism Arabidopsis thaliana
ATP quantification assay showed that ORF182 expression resulted in significant ATP decrease by 52.1% Escherichia coli
eukaryotic metatranscriptome in marine sediments was dominated by metabolic genes of diatoms, particularly other Thalassiosirales Thalassiosira pseudonana; other Thalassiosirales
cytoplasmic acidification greatly decreases metabolism Thalassiosira pseudonana
T. pseudonana resting cell formation is characterized by catabolism of stored compounds Thalassiosira pseudonana
cellular ATP concentrations dropped on Day 56 Thalassiosira pseudonana
sulfide regulates cellular energy status by sharply increasing the concentration of ATP Arabidopsis thaliana
AMP : ATP ratios peaked on day 84 with approximately 20-fold increase Thalassiosira pseudonana
major transcriptional switch observed during late maturation included several nuclear-encoded mitochondrial proteins that are markers of large reorganization of energy metabolism Coffea canephora
contribution of TAGs to energy for maintenance and cell division cannot be ruled out dark conditions Chlamydomonas reinhardtii
period of darkness results in plant consumption of all of its reserves
cell growth and proliferation are energy-consuming processes energy regulation Arabidopsis thaliana
cell energization was determined by quantifying adenylate levels Arabidopsis thaliana
phosphate (PO₄³⁻; Pᵢ) is key component of energy metabolism and signal transduction
starch is preferred carbon source for cell maintenance in dark Chlamydomonas reinhardtii