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lipid metabolism

32808 relationships annotated with this phrase. Showing first 500 of 32808.
Source entity Relationship Target entity Species
both plastidial LPAATs are required for the biosynthesis under nutrient-replete and nitrogen-starved conditions Phaeodactylum tricornutum
disruption of a plastidial ptATS2 gene could, at least in part, be biochemically and physiologically compensated by the other plastid-located ptATS2 Phaeodactylum tricornutum
C16:3-, C18:2- and C18:3-FAs are remarkably lower in acbp3-2 flower buds Arabidopsis thaliana
recombinant rACBP3 exhibits binding specificity towards very-long-chain (VLC) acyl-CoA thioesters (≥ C22) Arabidopsis thaliana
(ACBP3, AT4G24230) has potential to maintain acyl-CoA pool in anther development Arabidopsis thaliana
DEGs overlapping with CHH-DMRs demonstrated additional connections to protein turnover, carbohydrate, lipid and amino acid metabolism, self-incompatibility system and regulation of gene expression Fragaria vesca
control Dunaliella bardawil cells do not accumulate triglyceride (TAG) Dunaliella bardawil
stearic acid content declined in (ACBP4, AtACBP4, AT3G05420) flower buds Arabidopsis thaliana
shift in acyl-CoA composition specifically in 10:0-, 18:2- and 18:3-CoAs occurs in acbp3-2 and acbp3-3 Arabidopsis thaliana
(ATSCP2, SCP2, AT5G42890) effector is lipid metabolism-related protein Ustilago maydis
formation of dioxygenated MGDGs is (DALL2, AT1G51440) /DALL3-independent Arabidopsis thaliana
cluster D genes play key molecular functions including glucosidase activity, fatty-acyl-CoA reductase and peroxidase activity Hordeum vulgare
ptATS2a and ptATS2b mutants grown with air bubbling showed strikingly reduced TAG accumulation when algal cultures were bubbled with air Phaeodactylum tricornutum
lipid metabolism enzymes are downregulated in (CYP75B1, D501, TT7, AT5G07990) mutants Arabidopsis thaliana
sn-2-OPDA-MGMG may be used as substrate for OPDA synthesis Arabidopsis thaliana
acbp3-2 mutant in Ler-0 anthers exhibits lower 10:0-, 18:2- and 18:3-CoA content Arabidopsis thaliana
overexpression of carotenoid biosynthesis genes affects fatty acid content
DAG moieties are then fully incorporated into all plastidic lipids except phosphatidylglycerol (PtdGro)
C16:0-, C16:1-, C18:0-, and C18:1-FAs are significantly higher in acbp3-2 flower buds Arabidopsis thaliana
diacylglycerol (DAG) has individual roles in each membrane leaflet Arabidopsis thaliana
fatty-acid degradation is part of d-ESR (diatom common environmental stress response) Thalassiosira pseudonana
depletion of (ACBP3, AT4G24230) in -1 of Col-0 resulted in lower 18:2-FA, 18:3-FA and methyl jasmonate content Arabidopsis thaliana
Chlamydomonas reinhardtii lacks phosphatidyl choline (PC) Chlamydomonas reinhardtii
DAG-modifying enzymes exist in multiple membranes
DAGK generates phosphatidic acid (PtdOH) from diacylglycerol (DAG)
PE 34:1 increases in abundance with increasing Pi supply Hypoxis prostrata
AsE246 can affect lipid homeostasis Astragalus sinicus
nitrogen (N) starvation enhances TAG fluorescence increase upon (ATVPS34, PI3K, VPS34, AT1G60490) inhibition Chlamydomonas reinhardtii
FFA levels in the mutant were significantly reduced under –N conditions Chlamydomonas reinhardtii
(PGD1, AT1G64190) lipase positively affects TAG metabolism Chlamydomonas reinhardtii
cerulenin treatment decreases MGDG/DGDG ratio in Chlamydomonas cells Chlamydomonas
TAG accumulation in nitrogen-starved cells requires de novo synthesis of fatty acids Chlamydomonas
peroxisomal β-hydroxyisobutyryl-CoA hydrolase is needed for fatty acid β-oxidation Arabidopsis thaliana
co-presence of microbodies in zoospores is consistent with usage of stored lipids as primary energy source Phytomyxea
primary veins contain linolenic acid (18:3)-bound lipids Arabidopsis thaliana
white petals of xanthophyll esterase double mutant line pcs show upregulation of lipoxygenase (LOX) genes
diacylglycerol (DAG) becomes substrate for DAGK Arabidopsis thaliana
lipid metabolism is enriched in downregulated genes in (CYP75B1, D501, TT7, AT5G07990) Arabidopsis thaliana
CR-bjpcs #1 petals show more abundant DAG and TAG Brassica juncea
DAG and TAG in white flowers are down-accumulated when possessing medium- and long-chain fatty acids at sn-1 position Brassica juncea
depletion of (ACBP3, AT4G24230) in -1 of Col-0 resulted in higher levels of 12:0- and 14:0-fatty acid (FA) content Arabidopsis thaliana
seeds carrying maternal (FIE, FIE1, FIS3, AT3G20740) allele accumulate low oil with altered composition of triacylglycerol (TAG) molecular species Arabidopsis thaliana
intrinsic difference in lipid metabolism between tobacco and Arabidopsis is possible explanation for differential photosynthesis effects Nicotiana tabacum; Arabidopsis thaliana
additional metabolic activities involved in phosphatidic acid (PtdOH) turnover may have been activated in Arabidopsis expressing tpATS1-DAGK Arabidopsis thaliana
recombinant rACBP3 exhibits binding specificity towards phosphatidylethanolamine (PE) Arabidopsis thaliana
ERECTA likely affects acyl-CoA content differently in Col-0 and La-0 Arabidopsis thaliana
lipidomic assay showed that total lipid content was significantly higher in CR-bjpcs #1 than in L12-5 Brassica juncea
diacylglycerol (DAG) is used for triacylglycerol (TAG) production under nitrogen limitation Phaeodactylum tricornutum
unique species of phosphatidylglycerol (PtdGro) were not found in Arabidopsis tpATS1-DAGK lines Arabidopsis thaliana
changes in triacylglycerol (TAG) content in the (ACBP, ACBP6, AtACBP6, AT1G31812) seeds are accompanied by reduction in seed weight in the double and triple mutants Arabidopsis thaliana
altering carotenoid content impacts fatty acid content
MGDG 34:3, DGDG 34:3, and SQDG 34:3 are very strongly represented in all three leaf stages Hypoxis prostrata
34:x PG species (34:2–34:4) are very low in abundance in young leaves compared with mature leaves Hypoxis prostrata
Proteaceae spp. in their natural habitat have relatively high levels of phospholipids in young expanding leaves compared with mature leaves Proteaceae spp.
young leaves with increasing inorganic phosphate (Pi) availability had lower group II (a) and III sulfolipid levels Hakea prostrata
all phospholipids in Arabidopsis show positive correlation with inorganic phosphate (Pi) supply Arabidopsis thaliana
βC-plastoglobuli proteome contains three proteins with close homology to (PES, AT5G14520) from Arabidopsis Dunaliella bardawil
Phosphatidylinositol 3-kinase (ATVPS34, PI3K, VPS34, AT1G60490) signaling is connected to lipid metabolism
Most (ATVPS34, PI3K, VPS34, AT1G60490) KD lines showed increased total lipid content Chlamydomonas reinhardtii
GPD2 gene connects carbon assimilation and gluconeogenesis to TAG synthesis Chlamydomonas reinhardtii
Lipidome of Haberlea rhodopensis leaves shows 143 annotated lipids from 10 neutral and polar lipid classes Haberlea rhodopensis
bacteria accumulates wax
(LIP1, AT5G64813) lipase negatively affects TAG metabolism Chlamydomonas reinhardtii
20:5 occupancy in the galactolipids of (ATTCP-1, CCT1, TCP-1, AT3G20050) and (PECT1, AT2G38670) was lower under normal conditions compared with wild-type Nannochloropsis oceanica
tight apposition of cytosolic triacylglycerol (TAG) storage body with the surface of the plastid is consistent with route from chloroplast glycerolipids to triacylglycerol (TAG) Phaeodactylum tricornutum
phosphatidic acid (PA) is a central metabolite of primary lipid metabolism Phaeodactylum tricornutum
additional endoplasmic reticulum (ER)-located lysophosphatidic acid acyltransferases (LPAATs) will extend our appreciation of the individual contribution of lysophosphatidic acid acyltransferases (LPAATs) to lipid metabolism Phaeodactylum tricornutum
wounding causes levels of sn-1-, sn-2-OPDA-MGMG and sn-2-18:3-MGMG in veins to fall sn-1-, sn-2-OPDA-MGMG and sn-2-18:3-MGMG levels in veins Arabidopsis thaliana
CR-bjpcs #1 petals show significantly higher levels of glycerophospholipids Brassica juncea
gene encoding a Lipid Transfer Protein family member showed altered expression in (NZZ, SPL, AT4G27330) mutant Arabidopsis thaliana
PtdOH phosphatase activity is known to be associated with inner envelope
(DALL2, AT1G51440) (PLA-Iγ3, ) is PLA-Iγ3 Arabidopsis thaliana
Enhanced malic enzyme activity in AtME2 events resulted in higher levels of linoleic acid Glycine max
(ACBP3, AT4G24230) has potential role in binding fatty-acyl-CoA-thioesters in the phloem Arabidopsis thaliana
diacylglycerol (DAG) does not accumulate stably to high levels
N-DGD1 and tpATS1 lines indicated that both have increased radioactivity in phosphatidic acid (PtdOH) and lyso-phosphatidic acid (l-PtdOH) compared with wild type Arabidopsis thaliana
10:0- and 18:3-CoA levels in anthers of (NZZ, SPL, AT4G27330) mutant were lower than Ler-0 Arabidopsis thaliana
RNAi-mediated suppression of CrLPAAT2 caused a reduction of triacylglycerol (TAG) content Chlamydomonas
acbp3-1 × er-1 exhibits lower 10:0- and 18:3-CoA Arabidopsis thaliana
fatty acid composition was altered in acbp3-2 and acbp3-3 Arabidopsis thaliana
genes involved in lipid binding pathway were significantly enriched in GO enrichment analysis Oryza sativa
CrLPAAT2 has a negligible role under nutrient-replete conditions Chlamydomonas
OsOSC10 modulates expression of genes associated with lipid transporting Oryza sativa
abundant presence of chloroplast glycerolipid C16 fatty acids (FAs) in triacylglycerol (TAG) could be supported by route from chloroplast glycerolipids to triacylglycerol (TAG) Phaeodactylum tricornutum
phosphatidic acid (PtdOH) accumulation is apparently prevented in outer leaflet of the outer envelope membrane Arabidopsis thaliana
Acyl-CoA-binding proteins (ACBPs) bind acyl-CoA esters
diacyl galactolipids (DGs) have statistically similar resting levels in c1x11 mutant and wild-type Arabidopsis thaliana
10:0-, 18:2- and 18:3-CoA content in anthers of acbp3-2 and acbp3-3 were lower than Ler-0 control Arabidopsis thaliana
ptATS2a mutants showed a greater extent of decrease in the amount of triacylglycerols (TAGs) Phaeodactylum tricornutum
Arabidopsis tpATS1-DAGK lines had fatty acid profiles of total phosphatidylglycerol (PtdGro) closely examined for unique species Arabidopsis thaliana
phosphatidylglycerol (PtdGro) profiles showed consistently reduced 16:3 and increased 18:2 acyl groups Arabidopsis thaliana
(DALL1, PLA-I[beta]2, AT4G16820) (PLA-Iβ2, ) is PLA-Iβ2 Arabidopsis thaliana
formation of dioxygenated MGDGs is LOX6-dependent Arabidopsis thaliana
Acyl-CoA-binding proteins (ACBPs) maintain intracellular acyl-CoA pools and transport acyl-CoA thioesters in lipid metabolism
(ACBP3, AT4G24230) mutations -2 and -3 reduced 10:0-, 18:2- and 18:3-CoA content in Ler-0 Arabidopsis thaliana
highly-expressed transcripts and proteins of (ACBP3, AT4G24230) in Ler-0 anthers maintain anther acyl-CoA pool Arabidopsis thaliana
plastidial acyl-CoA:glycerol-3-phosphate acyltransferase 1 (AtCLO1, ATPXG1, ATS1, CLO1, AT4G26740) will extend our appreciation of the individual contribution of lysophosphatidic acid acyltransferases (LPAATs) to lipid metabolism Phaeodactylum tricornutum
SAD6-overexpressing line (SAD6-OE) shows increased levels of endoplasmic reticulum-specific phospholipids Arabidopsis thaliana
Gene encoding galactolipid galactosyltransferase in Haberlea rhodopensis is down-regulated during dark treatment Haberlea rhodopensis
PC levels in (cL37, PSRP5, AT3G56910) increased dramatically during this period 4-day time course
cht7 mutant shows compromised hydrolysis of TAG Chlamydomonas reinhardtii
DGTS in (ATTCP-1, CCT1, TCP-1, AT3G20050) had a decreased proportion of 20:5 Nannochloropsis oceanica
cerulenin treatment produces fluctuations in C18 fatty acids Chlamydomonas
cerulenin treatment decreases relative content of C18:1 Δ9 fatty acid Chlamydomonas
LIPOXYGENASE O may be responsible for traits such as ripening rate and sensitivity to environmental changes Vitis vinifera (Cabernet Sauvignon and Pinot Noir)
plastid-lipid associated protein PAP is chloroplast phosphoprotein Arabidopsis thaliana
transcript profile consistent with observed reduction in fatty acid contents Thalassiosira pseudonana
disruption of ptATS2 caused a dramatic decrease in the content of storage triacylglycerols (TAGs) Phaeodactylum tricornutum
diacylglycerol (DAG) is converted into phosphatidic acid (PtdOH) Escherichia coli
arbutin allows bulk conversion of phosphatidylglycerol (PtdGro) to diacylglycerol (DAG) Escherichia coli
lipid species found primarily in chloroplast account for 75 percent of polar leaf lipids in Arabidopsis Arabidopsis thaliana
(PES, AT5G14520) enzymes have dual function in degradation of polar lipids and conversion to TAG
GO categories relate to lipid metabolism Solanum lycopersicum
(ATVPS34, PI3K, VPS34, AT1G60490) inhibition with 3-methyladenine (3MA) increases triacylglycerol (TAG) fluorescence Chlamydomonas reinhardtii
Triacylglyceride (TAG) lipids in Haberlea rhodopensis accumulate upon darkness but decrease upon recovery Haberlea rhodopensis
TAG 52:7 in Haberlea rhodopensis leaves is highly abundant following exposure to extended darkness and recovery Haberlea rhodopensis
lipid transfer route is rather termed omega pathway Nannochloropsis oceanica
moderate reduction in 20:5 in (ATTCP-1, CCT1, TCP-1, AT3G20050) and (PECT1, AT2G38670) under normal conditions suggests the possibility that DGTS partly supports the metabolic roles of PC and PE Nannochloropsis oceanica
cerulenin fully prevents detection of lipid droplets (LDs) in nitrogen-limited cells Chlamydomonas
MGDG is structural lipid of thylakoid membrane protein complexes Chlamydomonas
triglyceride content rose until day 70 of darkness and then dropped and remained at low levels from day 84 on resting cell formation Thalassiosira pseudonana
ptATS2a mutants showed a greater extent of decrease in the amount of TAGs compared to ptATS2b mutants Phaeodactylum tricornutum
ptATS2a and ptATS2b mutants showed strikingly reduced triacylglycerol (TAG) accumulation Phaeodactylum tricornutum
acyl-CoA-dependent acylation of the sn-3 position by diacylglycerol acyltransferase (DGAT) produces triacylglycerol (TAG) Phaeodactylum tricornutum
lipidic profiles showed significant shift in across elevation gradient Atriplex imbricata
diacylglycerol kinase (DAGK) presence in the outer leaflet of the outer envelope membrane results in phosphatidic acid (PtdOH) accumulation is not observed Arabidopsis thaliana
36:x sulfoquinovosyldiacylglycerol (SQDG) species showed typically documented decrease with increasing inorganic phosphate (Pi) supply in Hakea prostrata Hakea prostrata
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
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) down-regulates proteins involved in TAG degradation Arabidopsis thaliana
parental line (PL) accumulated triacylglycerol (TAG) Chlamydomonas reinhardtii
drought stress tolerance is dependent on ability to maintain fatty acid (FA) desaturation activity
crown gall tumors contains elevated levels of α-linolenic acid (18:3) Arabidopsis thaliana
CLD and βC-plastoglobuli are involved in broad range of lipid biosynthesis and degradation reactions versus more specific degradation of chloroplast membrane lipids Dunaliella bardawil
fatty acid synthesis in B. rapa is a highly compartmentalized process compartmentalized process Brassica rapa
lipid-related proteins (mosaic death1 and esterase) interacted with IDH and (LKR, LKR/SDH, SDH, AT4G33150)
integrated omics and network analyses of (ATVPS34, PI3K, VPS34, AT1G60490) KD established nexus between signaling, growth, and metabolism and the regulation of membrane lipid turnover Chlamydomonas reinhardtii
T411 mutant uses initial acetate available for FFA synthesis followed by TAG accumulation Chlamydomonas reinhardtii
cht7 mutant exhibits compromised hydrolysis of triacylglycerols Chlamydomonas reinhardtii
ECH1 is needed for β-oxidation of unsaturated fatty acids Chlamydomonas reinhardtii
DGTS and MGDG may rather compete for the two major 20:5 destinations in extraplastidic and plastidic membranes Nannochloropsis oceanica
20:5 transfer to plastid galactolipids is not mediated by DGTS Nannochloropsis oceanica
inhibition of FAS by cerulenin results in drop of MGDG levels Chlamydomonas
lipid species that accumulated in leaves with P-toxicity symptoms differ from ones found in young leaves or in mature leaves of P-limited plants Hypoxis prostrata
free palmitoleic acid and TAG species (TAG 50:4, 50:5, and 52:7) show same profile as select group of glycerolipids in group III (a) Hypoxis prostrata
MGDG 34:1 and DGDG 34:1 decrease in abundance and PE 34:1 increases in abundance with increasing Pi supply Hypoxis prostrata
AsE246 RNAi nodules have significantly lower phosphatidylinositol (PI) content Astragalus sinicus
SAD6-OE plants contained lower levels of stearic acid Arabidopsis thaliana
(AAD6, FTM1, HUP7, SAD6, AT1G43800) catalyzes desaturation of stearic acid to oleic acid Arabidopsis thaliana
11 groups of interactions are related to amino acid metabolism (27%), mETC/ATP synthesis (13%), signaling (11%), lipid metabolism (5%), nitrogen metabolism (3%), and stress (19%) Arabidopsis thaliana
Genes encoding phospholipase D isoforms in Haberlea rhodopensis are down-regulated during dark treatment Haberlea rhodopensis
Lipid analyses in bta1l and OEBTA1L suggested negative correlation between the amount of DGTS and MGDG Nannochloropsis oceanica
omega pathway detail is unresolved Nannochloropsis oceanica
PC and PE are important for producing the 20:5 used for the formation of the chloroplast membrane Nannochloropsis oceanica
highest Pi supply results in significant drop in PC and PE levels in young leaves Hypoxis prostrata
complete reversal of normal Pi-dependent lipid-remodeling profile shows PG levels decrease with increasing Pi supply in mature and senescing leaves Hypoxis prostrata
sulfolipid SQDG 34:4 and its more saturated precursors SQDG 34:1, 34:2, and 34:3 increase 4- to 6-fold in both mature and senescing leaves at two highest Pi supplies regardless of whether leaves are healthy or have P-toxicity symptoms Hypoxis prostrata
phospholipid levels in senescing leaves did not decrease to same extent during early stage of leaf senescence as they do in other plants Hakea prostrata
crown galls with high (AAD6, FTM1, HUP7, SAD6, AT1G43800) levels have increased levels of unsaturated FA s in glycerolipids Arabidopsis thaliana
balance of molecular species is unchanged even when chlorophyll content/photosynthesis is perturbed Brassica rapa
fatty acid (FA) composition showed no significant change in T411 mutant Chlamydomonas reinhardtii
Genes encoding phospholipase in Haberlea rhodopensis are induced in darkness Haberlea rhodopensis
(LIP1, AT5G64813) and (PGD1, AT1G64190) define respective class of TAG-hydrolyzing and TAG-producing lipases Chlamydomonas reinhardtii
lipid metabolism was greatly repressed in mutant anthers Zea mays
more saturated precursors of PE and galactolipids with 34:1 to 34:3 acyl chains are much more abundant in young than in mature leaves Hypoxis prostrata
(AtSSI2, FAB2, LDW1, SSI2, AT2G43710) or FATTY ACID BIOSYNTHESIS2 catalyze desaturation of stearic acid to oleic acid Arabidopsis thaliana
fad3-2 mutant is known to contain reduced amounts of trienoic FA s of extraplastidic phospholipids Arabidopsis thaliana
nutrient starvation induces membrane lipid hydrolysis Chlamydomonas reinhardtii
PC as a major membrane component and both DG2 and PD1a lines have more HFA-PC at 0 DAS than (cL37, PSRP5, AT3G56910)
(FAE1, KCS18, AT4G34520) has more than 8 μg seed⁻¹ total oil seed oil content
polar lipids tested included DGTS, digalactosyldiacylglycerol, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylinositol, and sulfoquinovosyldiacylglycerol Chlamydomonas reinhardtii
DGTS may be important as a store for 20:5 in extraplastidic membranes Nannochloropsis oceanica
DGTS is not crucial for delivering 20:5 from the ER to chloroplast membranes Nannochloropsis oceanica
DGDG levels in mature leaves showing P-toxicity symptoms are higher than in mature leaves without toxicity symptoms Hypoxis prostrata
some of the most abundant sulfolipids are found in lipid remodeling group II (b) Hypoxis prostrata
34:x sulfolipids (SQDG 34:1–34:4) are very low in abundance in young leaves compared with mature leaves Hypoxis prostrata
lower phosphatidylglycerol (PG) levels in mature Hakea prostrata leaves appear to be accompanied by compensatory increase in sulfolipid species of 34:x acyl chain configuration Hakea prostrata
(AtSSI2, FAB2, LDW1, SSI2, AT2G43710) has well-documented enzymatic function as S-ACP desaturase Arabidopsis thaliana
algae hydrolyze membrane lipids similar to plants
reduced FA synthesis and decreased PC expansion leading to the retention of HFA in both polar and storage lipids
(APG7, ATAPG7, ATATG7, ATG7, PEUP4, AT5G45900) knockout plants display decreased levels of fatty acids in seeds Arabidopsis thaliana
galactolipid concentrations in senescing leaves do not respond to Pi availability Hypoxis prostrata
proportions of galactolipids and triacylglycerol (TAG) in senescing leaves were much smaller than those in mature leaves Hakea prostrata
crown gall tumors shows decreased levels of monogalactosyl diglyceride (MGDG) Arabidopsis thaliana
enzymes in βC-plastoglobuli proteome are localized in lipid-metabolizing pathways Dunaliella bardawil
fatty acid synthesis is highly regulated process Brassica rapa
misregulated lipase genes in cht7 are promising candidates for reverse genetic studies Chlamydomonas reinhardtii
(PGD1, AT1G64190) encodes MGDG-specific lipase Chlamydomonas
metabolic pathways converting photosynthate into seed oil includes biosynthesis of lipids in plastids Brassica napus
lyso-PC lipid species accumulate in mature and senescing leaves of plants showing P-toxicity symptoms Hypoxis prostrata
higher abundance of phospholipase transcripts in young leaves suggests these enzymes are not involved in release of inorganic phosphate (Pi) from membrane lipids Hakea prostrata
Agrobacterium tumefaciens-derived crown galls strongly express STEAROYL-ACYL CARRIER PROTEIN Δ9-DESATURASE6 (AAD6, FTM1, HUP7, SAD6, AT1G43800) Arabidopsis thaliana
seed oil composition of B. rapa FPsc plants is stable across changing ratios of R : FR light Brassica rapa
majority of lipases, including putative TAG lipases and lysophospholipases were downregulated in T411–N compared to WT–N Chlamydomonas reinhardtii
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) lines show partially decreased total amounts of phosphatidylcholine (PC) and phosphatidylethanolamine (PE) Arabidopsis thaliana
(ABX45, AS11, ATDGAT, AtDGAT1, DGAT1, RDS1, TAG1, AT2G19450) Arabidopsis mutant has 25% less seed oil than wild-type parent Arabidopsis thaliana
phenotypic analyses of (ATTCP-1, CCT1, TCP-1, AT3G20050) and (PECT1, AT2G38670) suggested that 20:5 are mainly produced through PC and PE and then transferred to plastid galactolipids Nannochloropsis oceanica
lipid catabolism intensified from day 7 onwards of dark-induced leaf senescence (DILS) Hordeum vulgare
Calmodulin (CaM)-binding proteins have physiological functions implicated in phospholipid metabolism
starch (carbohydrate) metabolism-related genes are enriched in B. napus lipid metabolism enzyme set Brassica napus
acyl-CoA synthetase-like protein (AT2G17650) up-regulation by K re-supply is lost in coi1-16 mutant Arabidopsis thaliana
linoleic acid was released from Pi
A9:u-ATP9 and AP3:u-ATP9 transgenic lines show increased expression of Esterase/lipase (MAGL12, AT3G62860) Arabidopsis thaliana
amounts of potential ZmMs33 substrates (free fatty acids such as C16:X and C18:X) were relatively higher in mutant anthers Zea mays
Δ3 FAs from (FAD4, FADA, AT4G27030) + (ATPRX Q, PRXQ, AT3G26060) in yeast accumulated in ER-synthesized phosphatidylcholine (PC) and phosphatidylethanolamine (PE) Saccharomyces cerevisiae
(PLD, PLDALPHA1, AT3G15730) proteins produce phosphatidic acid (PA)
seed oil composition was determined by gas chromatography-mass spectrometry (GC-MS) analysis Brassica rapa
fatty acid synthesis remains regulated even in nonoptimal light environments Brassica rapa
T411 line showed higher TAG fluorescence under high-light stress conditions Chlamydomonas reinhardtii
T411 mutant cells exhibited mildly higher TAG fluorescence Chlamydomonas reinhardtii
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) lines show significantly decreased total levels of phosphatidylglycerol (PG) Arabidopsis thaliana
stress-responsive proteins showed diverse functions in lipid metabolic process Solanum lycopersicum
lipases can affect TAG metabolism both positively and negatively TAG metabolism Chlamydomonas reinhardtii
newly synthesized fatty acids in the form of acyl-ACP must be exported out of plant chloroplasts
triacylglycerol in EV control and bta1 mutant had very low levels of 20:5 with no large difference between EV control and bta1 mutant Nannochloropsis oceanica
increased turnover of phosphatidic acid (PtdOH) in tpATS1 is consistent with increased phospholipase A activity in tpATS1 Arabidopsis thaliana
lipids were analyzed from leaves of 6-week-old, soil-grown wild-type Arabidopsis or DAGK-producing lines Arabidopsis thaliana
tpSSU-DAGK production resulted in relative increase of phosphatidylcholine (PtdCho) levels and relative decreases of monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG) levels at the whole-leaf level Nicotiana tabacum
increased phospholipase A activity was observed for Arabidopsis transgenic lines Arabidopsis thaliana
PC species in mature and senescing leaves show positive correlation with Pi supply group IV Hypoxis prostrata
mature Hakea prostrata leaves showed reduced triacylglycerol (TAG) accumulation Hakea prostrata
gut extracts of Lymantria dispar possess high esterase activity Lymantria dispar
Agrobacterium tumefaciens-derived crown galls strongly express ω3 FATTY ACID DESATURASE3 (AtFAD3, FAD3, AT2G29980) Arabidopsis thaliana
D. bardawil βC-plastoglobuli proteome includes enzymes involved in synthesis and degradation of lipids, carotenoids, terpenoids, quinones, carbohydrate and energy metabolism, stress-related proteins, protein kinases and phosphatases, and signaling proteins Dunaliella bardawil
Genes encoding lipase in Haberlea rhodopensis are induced in darkness Haberlea rhodopensis
16:4 and 18:3 ω3 (major FAs of monogalactosyldiacylglycerol [MGDG]) are major components of monogalactosyldiacylglycerol (MGDG) Chlamydomonas reinhardtii
amount of PC in (ATTCP-1, CCT1, TCP-1, AT3G20050) at low temperatures was less than half compared with wild-type Nannochloropsis oceanica
TURGOR REGULATION DEFECT1 (TOD1, AT5G46220) was demonstrated to have alkaline ceramidase activity Arabidopsis thaliana
(FIB, FIB1a, PGL35, AT4G04020) (FIBRILLIN) is chloroplast phosphoprotein Arabidopsis thaliana
galactolipids showed negative correlation with inorganic phosphate (Pi) supply in all except senescing leaves Hakea prostrata
crown gall tumors shows increased levels of phosphatidylinositol (PI) Arabidopsis thaliana
oil composition might remain constant field settings where mutual shading between plants may occur Brassica rapa
relative oil content per seed weight showed no significant change Brassica rapa
(ATVPS34, PI3K, VPS34, AT1G60490) inhibition with 3MA increases lipid content Chlamydomonas reinhardtii
Previous transcriptomic studies in C. reinhardtii identified up-regulation of various lipases following N depletion Chlamydomonas reinhardtii
continuous production of FFA in T411 compensates for decreased acyl-chain accumulation following arrested lipid hydrolysis Chlamydomonas reinhardtii
down-regulated lipid-related gene encoding esterase/lipase similar to (CUS2, AT5G33370) is involved in cuticle formation Arabidopsis thaliana
MGDG is monogalactosyl diacylglycerol Chlamydomonas
apolipoprotein D-related is chloroplast phosphoprotein Arabidopsis thaliana
young Hakea prostrata leaves showed altered lipid profile Hakea prostrata
drought stress- and oxidative stress-challenged Arabidopsis crown gall tumors have shaped pool of unsaturated FAs in (AAD6, FTM1, HUP7, SAD6, AT1G43800) and (AtFAD3, FAD3, AT2G29980) desaturases Arabidopsis thaliana
different lipid-metabolizing enzymes in CLD and βC-plastoglobuli were identified in CLD and βC-plastoglobuli proteomes Dunaliella bardawil
PG 32:1 in Haberlea rhodopensis leaves diminishes in dark condition but accumulates following 1-week recovery Haberlea rhodopensis
131 genes predicted to encode lipase, phospholipase, or patatin were sorted through and assigned as 9 TAG-hydrolyzing lipases and 23 TAG-producing lipases Chlamydomonas reinhardtii
(ATTCP-1, CCT1, TCP-1, AT3G20050) at low temperatures did not have a decreased level of plastidic 20:5 Nannochloropsis oceanica
(APG7, ATAPG7, ATATG7, ATG7, PEUP4, AT5G45900) knockout rice plants display decreased TAG content in pollen grains Oryza sativa
loss-of-function Chlamydomonas mutant deficient in the MGDG-specific lipase (PGD1, AT1G64190) showed relative increase in MGDG abundance and hyperstacking of the thylakoid grana Chlamydomonas
(ATSEC14, SEC14, AT4G39180) cytosolic factor family protein is chloroplast phosphoprotein Arabidopsis thaliana
36:x sulfoquinovosyldiacylglycerol (SQDG) species clustered in group II (b) Hakea prostrata
crown gall tumors shows increased levels of phosphatidylethanolamine (PE) Arabidopsis thaliana
crown galls with high (AAD6, FTM1, HUP7, SAD6, AT1G43800) levels do not have increased levels of unsaturated FA s in sphingolipids Arabidopsis thaliana
peroxisomes are responsible for fatty acid β-oxidation
algal class III phosphatidylinositol 3-kinase (ATVPS34, PI3K, VPS34, AT1G60490) knockdown leads to higher lipid content Chlamydomonas reinhardtii
Most (ATVPS34, PI3K, VPS34, AT1G60490) KD lines showed increased TAG content Chlamydomonas reinhardtii
FFA levels in the mutant were higher in +N conditions Chlamydomonas reinhardtii
Chloroplast lipids (MGDG and DGDG) in Haberlea rhodopensis are reduced in darkness, especially during 30-d dark period, but increase following recovery Haberlea rhodopensis
higher accumulation and mobilization of HFA-TAG in DG2 and PD1a is opposite to the effect expected by hypothesis that HFA is toxic to the cell
lipolytic products from TAGs between 6 and 12 h of N resupply were not subjected to β-oxidation cycle Chlamydomonas reinhardtii
16:4 and 18:3 ω3 stored in TAGs during N deprivation comprised approximately 25% of 16:4 and 18:3 ω3 Chlamydomonas reinhardtii
DGTS provides 20:5 for the sn-1 positions of galactolipids Monodus subterraneus
SQDG 34:1 and SQDG 36:3 are associated with group II (a) alongside all three PG species Hypoxis prostrata
occurrence of phytyl esters is common in plants
crown gall tumors shows reduced levels of roughanic acid (16:3) Arabidopsis thaliana
ssi2-2 mutant shows increased levels of stearic acid (18:0) Arabidopsis thaliana
(BADC1, BLP3, AT3G56130) in combination with (BADC2, BLP1, AT1G52670) mutation resulted in significant increases of triacylglycerol (TAG) content Arabidopsis thaliana
roles of PC and PE cannot be fully compensated by excess DGTS Nannochloropsis oceanica
cerulenin prevents TAG synthesis in nitrogen-limited cells Chlamydomonas
stromally targeted tpATS1-DAGK-producing Arabidopsis differ from previously reported stromally targeted tpSSU-DAGK-producing tobacco Arabidopsis thaliana; Nicotiana tabacum
enzymes in Chlamydomonas reinhardtii lipid droplet are involved in lipid metabolism Chlamydomonas reinhardtii
mature and senescing leaves with P-toxicity symptoms have higher levels of free fatty acids Hypoxis prostrata
young Hakea prostrata leaves had 1.5-fold greater phospholipid fraction Hakea prostrata
digalactosyldiacylglycerol (DGDG) and sulfoquinovosyldiacylglycerol (SQDG) species increased 3-fold in sections farther up maize leaf blade compared with leaf base Zea mays
most remarkable and unusual response to increasing inorganic phosphate (Pi) supply was decrease in phosphatidylglycerol (PG) levels in mature Hakea prostrata leaves Hakea prostrata
fad7-1/fad8-1 double mutant produces less plastidic galactolipid trienoic FA s compared with wild type Arabidopsis thaliana
fatty acids released from storage lipids such as TAG are used as alternative substrates for respiration
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) lines showed changes in lipid levels Arabidopsis thaliana
MGDG synthesis genes were not candidates for CHT7-specific regulation Chlamydomonas reinhardtii
(APG7, ATAPG7, ATATG7, ATG7, PEUP4, AT5G45900) knockout rice plants display absence of lipid droplets in tapetal cells Oryza sativa
sulfolipid concentrations in mature leaves showing P-toxicity symptoms are higher than in mature leaves without toxicity symptoms Hypoxis prostrata
absence of DGDG 34:6 and SQDG 34:6 is consistent with current model for desaturation of acyl chains of thylakoid lipids in chloroplast Hypoxis prostrata
PG is main phospholipid in chloroplast inner envelope and thylakoid membranes Hypoxis prostrata
seeds from wild-type and ein194 mutant plants when compared across two light environments Brassica rapa
oleic acid and linoleic acid increased during starvation Chlamydomonas reinhardtii
inhibition of fatty acid synthesis decreased monogalactosyldiacylglycerol abundance Chlamydomonas reinhardtii
autophagy is needed for lipid droplet accumulation in hepatocytes
each transgenic line has individual pattern of diacylglycerol (DAG), phosphatidic acid (PtdOH), phosphatidylcholine (PtdCho), and triacylglycerol (TAG) steady-state levels Arabidopsis thaliana
lipid droplets have diverse metabolic functions
reduction of (AAD6, FTM1, HUP7, SAD6, AT1G43800) overexpression by RNA interference ( -OE-RNAi) caused regaining of wild-type-like stearic acid and oleic acid levels Arabidopsis thaliana
enhanced/uninhibited FFA synthesis is proven trait of malignancy
extensive lipid transport from the ER to the plastid must take place in Nannochloropsis Nannochloropsis oceanica
cerulenin treatment enriches C18:1 Δ11 fatty acid Chlamydomonas
A9:u-ATP9 and AP3:u-ATP9 transgenic lines show decreased expression of Palmitoyl protein thioesterase family protein (AT5G47340) Arabidopsis thaliana
(ABCD1, ACN2, AtABCD1, CTS, PED3, PXA1, AT4G39850) likely transports fatty acids
CzDGTT3 is an exception to DGAT activity in most DGATs from Chlorella zofingiensis Chlorella zofingiensis
plastoglobuli are involved in synthesis and degradation of lipids
sulfolipid concentrations do not decrease with increasing Pi supply Hypoxis prostrata
MGDG 34:6 species are detected in all leaf stages Hypoxis prostrata
additional diluted oil samples from wild-type plants were tested and found no difference between ratio of 18:2 to 18:1 fatty acids from seeds in white light or low R : FR light Brassica rapa
Sulfoquinovosyldiacylglycerol (SQDG) lipids in Haberlea rhodopensis are reduced in darkness, especially during 30-d dark period, but increase following recovery Haberlea rhodopensis
lipid bodies accumulate upon extended darkness
galactolipids MGDG and DGDG constitute bulk of membrane lipids in chloroplasts
TAG in parental line (PL) reached basal steady state in the next 6 h 12 h of N resupply Chlamydomonas reinhardtii
18:1 Δ9 and other FAs decreased after N resupply Chlamydomonas reinhardtii
(BADC1, BLP3, AT3G56130) (BADC3, BLP2, AT3G15690) double mutant had TFA and TAG per seed significantly higher than wild-type plants Arabidopsis thaliana
cerulenin treatment produces no significant effect on digalactosyl diacylglycerol (DGDG) content Chlamydomonas
down-regulation of C- and D-type of phospholipase genes in dark-induced leaf senescence (DILS) Hordeum vulgare
phospholipases are well known to be involved in lipid catabolism
glycosyltransferases (GTs) play roles in lipid metabolism
10:0- and 18:3-CoA content in anthers of acbp3-1 and er-1 mutants declined in comparison to Col-0 control Arabidopsis thaliana
disruption of either ptATS2 resulted in a significant decrease in the amounts of triacylglycerols (TAGs) Phaeodactylum tricornutum
genes showing similar transcriptional response in both A9:u-ATP9 and AP3:u-ATP9 transgenic lines include 19 genes related to lipid metabolism Arabidopsis thaliana
six HXXXD-type acyltransferase genes include FACT, (ABS1, BIA1, AT4G15400) and (BAT1, PIZ, AT4G31910) Arabidopsis thaliana
flux estimation studies have studied regulation of lipid metabolism Glycine max; Zea mays; Brassica napus; Helianthus annuus; Arabidopsis thaliana
phosphatidic acid (PA) is product of PLD-mediated hydrolysis Arabidopsis thaliana
algal PDATs have possible roles in membrane remodeling
AtPDAT1 does not exhibit lipase and phospholipase activities with broad substrate preferences Arabidopsis thaliana
digalactosyldiacylglycerol (DGDG) in PBMs is reported to be derived from host root cells Glycine max
GmPLDα1OE overproduced PA
phosphatidic acid (PtdOH) and many other extraplastidic phospholipids can be converted to diacylglycerol (DAG)
major product of DAGK assay was lyso-phosphatidic acid (l-PtdOH) Arabidopsis thaliana
homeostasis between TAG and membrane lipid hydrolysis exists in algae
genes in cluster C11 were enriched in lipid transport and lipid localization Triticum aestivum
relative abundance of 16:4 and 18:3 ω3 in parental line (PL) following N resupply increased gradually N resupply Chlamydomonas reinhardtii
phosphatidic acid (PtdOH) is either rapidly converted to other lipids Arabidopsis thaliana
phospholipase D alpha (PLDα) activity is very prominent in metabolically active organs in Arabidopsis Arabidopsis thaliana
T411 mutant continuously produces FFAs, akin to tumor cells Chlamydomonas reinhardtii; Homo sapiens
TAG lipases in many species have shown preference for specific fatty acids
betaine lipid synthase (BTA1) is typical example of NR-specific gene Chlamydomonas reinhardtii
inability of cht7 to readjust MGDG may be consequence of delay in TAG turnover Chlamydomonas reinhardtii
(LIP1, AT5G64813) gene has important role in TAG and diacylglycerol metabolism Solanum lycopersicum
major chloroplast membrane lipids are relatively higher in WT anthers Zea mays
Sl-LIP8 is predicted to act upon MGDG and phospholipids Solanum lycopersicum
lipidomics analysis identified ultra-accumulated α-linolenic acid (ALA) released from phosphatidylcholine Arabidopsis thaliana
GmPLDα1KD mutant roots show significantly higher levels of DGDG
lipid storage plastoglobules accumulate in rep-1 chloroplasts Arabidopsis thaliana
LCAT-PLA 1 enzymes show homology to plant phospholipid: sterol O-acyltransferase (PSAT)
oxPAP transformant decreased PG level Synechocystis sp. PCC 6803
non-specific PLC (NPC) hydrolyzes phosphatidylcholine (PC)
(AtPLAIVB, PLA IVB, PLP5, AT4G37060) is patatin-related phospholipase A (pPLA) gene Arabidopsis thaliana
(AtPLAIVC, PLA V, PLAIII{beta}, PLP4, AT4G37050) is patatin-related phospholipase A (pPLA) gene Arabidopsis thaliana
mitochondria house lipid biosynthesis
free ALA content in FAD3-OE lines is up to 4- and 2.5-fold higher than in WT and FL2-OE respectively Arabidopsis thaliana
Brassica napus contains fatty acids Brassica napus
contents of seven lipid components (44 molecule species) were significantly reduced in mutant anthers Zea mays
Δ3 FAs from (FAD4, FADA, AT4G27030) + (ATPRX Q, PRXQ, AT3G26060) in yeast are less abundant on mitochondria-synthesized phosphatidylglycerol (PG, ~2.7 mol%) Saccharomyces cerevisiae
One KEGG pathway (KO00071) involves lipid metabolism
Alpha-linolenic acid and linoleic acid are PUFAs and common substrates for LOX
acyl-ACP thioesterase is involved in biosynthesis of very-long-chain fatty acids (VLCFA)
bottom-up reconstruction of metabolic network of Jatropha curcas is supported by labeling experiments Jatropha curcas
linolenic acid is the major fatty acid in Arabidopsis leaves Arabidopsis thaliana
Sl-LIP8 protein cleaves multiple lipid substrates into FFAs including linoleic and linolenic acids Solanum lycopersicum
MGDG in PBMs is reported to be derived from host root cells Glycine max
16:1t is synthesized on and is exclusive to phosphatidylglycerol (PG) Arabidopsis thaliana
pah1pah2 double mutant showed increased PA level compared with WT Arabidopsis thaliana
lipid anabolism and catabolism in the primary root (PR) were gradually strengthened throughout the growing season Aconitum kusnezoffii
DAG pool in KO lines showed increase in 20:5/16:0 form Phaeodactylum tricornutum
prenylcysteine lyase is localized to lysosomal membranes
palmitic acid was released from PC
(PLIP1, AT3G61680) is phosphatidylglycerol lipase Arabidopsis thaliana
monogalactosyldiacylglycerol 36:6 (MGDG) distribution was found to be not affected by treatment Zea mays
(PLD, PLDALPHA1, AT3G15730) proteins function in membrane degradation
overexpression of CsLPAT2 decreased free ALA Arabidopsis thaliana
LCAT-family enzymes includes PSAT
digalactosyl diacylglycerol (DGDG) (34:1) and malvidin were found to be differentially accumulated in response to (AFB1, ATGRH1, GRH1, AT4G03190) treatment Zea mays
treatment with ABA promotes increase in PA from PLDα1-catalyzed hydrolysis of PC in leaves
Arabidopsis and cress are known to store lipids
scutellum did not contain any high levels of PLs during germination Avena sativa
conversion of glycerol 3-phosphate to glycerol is catalysed by glycerol 3-phosphatase
5-phosphatases (5-PTases; i.e. (CVP2, AT1G05470) (CVL1, AT2G32010) ) normally degrade phosphatidylinositol 4,5-bisphosphate (PIP2) Arabidopsis thaliana
PLDα2 activity modulates membrane lipid metabolism
rhizobial infection increases transcript levels of PLDs, PLCs and DGKs
brassinolide (BL) treatment does not increase phosphatidic acid (PA) content Nicotiana tabacum
DEFECTIVE ANTHER DEHISCENCE 1 (DAD1, AT2G44810) has phospholipase A 1 (PLA 1) activity Arabidopsis thaliana
Patatin-related PLA enzymes have substrate preference for galactolipids
palmitic acid was released from Pi
PG in yeast is very minor lipid Saccharomyces cerevisiae
Sl-LIP8 mainly catalyzes hydrolysis of ester bonds of TAGs Solanum lycopersicum
different PA molecules, such as di18:1 PA and di18:2 PA, or 18:1-18:2PA fluctuate after rhizobial infections and during nodulation
chloroplast hosts lipid biosynthesis
10 lipid components required for chloroplast membrane development are widely used to investigate gene function in lipid metabolism of chloroplast membranes
decreased contents of MGDG, DGDG, and SQDG in anther tissue reflected reduced amounts in anther En chloroplast membranes Zea mays
16:1t may have function(s) beyond being a moiety in a specific structural lipid of the photosynthetic membrane under normal conditions
triacylglycerols have important physiological roles in photosynthetic organisms
triacylglycerols (TAGs) participates in essential physiological processes
phosphatidic acid (PA) is involved in lipid metabolism
lipid mQTL analysis of IL population from S. lycopersicum cv. M82 and S. pennellii cross identified locus in chromosome 9 region linked to altered C18 glycerolipid content Solanum lycopersicum; Solanum pennellii
yams had greater proportion of odd-chain fatty acids
SlLIP1 is triacylglycerol (TAG) lipase Solanum lycopersicum
energy expenditures affect lipid metabolism Jatropha curcas
metabolic network of Jatropha curcas was used to characterize distribution of fluxes under three carbon growth scenarios Jatropha curcas
inhibition of fatty acid (FA) synthesis contributes more to reduction in fatty acid (FA) accumulation in CsFAD3-OE Arabidopsis thaliana
main lipids detected in tomato fruits invariant between WT and sibling PH13 lines Solanum lycopersicum
Ser/Asp catalytic (DYAD, SWI1, AT5G51330) serves as essential catalytic dyad for lipid hydrolytic activity
Phaeodactylum tricornutum ecotypes (ATPT1, PHT1;1, PT1, AT5G43350) and Pt4 have non-polar lipids representing diacylglycerols (DAG) and triacylglycerols (TAG) Phaeodactylum tricornutum
plant seed oil composition can be manipulated to deliver enhanced fatty acid compositions suitable for feed or fuel
PR-10 proteins bind fatty acids
phosphatidylethanolamine (PE) is increased in nodules compared with roots
active lipophagy might be critical for triacylglycerol metabolism and energy homeostasis in guard cells of suba1 plants Arabidopsis thaliana
lipid biosynthesis and FA accumulation are regulated by plant hormones Arabidopsis thaliana
plant peroxisomes play a pivotal role in storage oil mobilization
higher amounts of free fatty acids in mutant anthers possibly due to ineffective usage in lipid metabolic processes caused by loss of ZmMs33 function Zea mays
flux estimation studies have studied lipid metabolism in seed tissues Glycine max; Zea mays; Brassica napus; Helianthus annuus; Arabidopsis thaliana
triacylglycerols (TAGs) is involved in membrane lipid remodeling
nitrogen (N) starvation activates distinct metabolic pathway for triacylglycerol (TAG) accumulation
PLDα1 knockout Arabidopsis plants display defect because of low PA level Arabidopsis thaliana
increased Caleosin and lipid A export ATP-binding/permease protein MsbA indicates high lipid metabolism Triticum aestivum
supplementation of CO2 into culture decreased PG content Synechocystis sp. PCC 6803
EPA accumulates particularly in galactolipids such as MGDG and DGDG Phaeodactylum tricornutum
non-specific PLC (NPC) hydrolyzes phosphatidylethanolamine (PE)
(ATSEC14, SEC14, AT4G39180) mutants fully active for PtdIns transfer in vitro but defective in PtdCho binding and transfer fail to stimulate PtdIns(4)P production in vivo
(ATSEC14, SEC14, AT4G39180) stimulates Pik1 PtdIns 4-OH kinase activity
Sec14-dependent PtdIns presentation stimulates PtdIns(4)P production
phosphatidylcholine (PC) and phosphatidylethanolamine (PE) species decreased by more than 3-fold in sections farther up maize leaf blade compared with leaf base Zea mays
AsE246 RNAi nodules have significantly lower phosphatidylcholine (PC) content Astragalus sinicus
(AAD6, FTM1, HUP7, SAD6, AT1G43800) restores (AtSSI2, FAB2, LDW1, SSI2, AT2G43710) loss of function Arabidopsis thaliana
nutrient starvation leads to triacylglycerol (TAG) synthesis Chlamydomonas reinhardtii
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) lines show almost unaffected levels of phosphatidylserine and ceramides Arabidopsis thaliana
lipid anabolism and catabolism in the lateral root (LR) and leaf between 71 and 80 days after sprouting (DAS) showed only downregulated differentially expressed genes (DEGs) between 71 and 80 days after sprouting (DAS) Aconitum kusnezoffii
Physaria possesses lesquerolic acid (C20-HFA) in seed oil Physaria
DGDG (34:1) was stored in collenchyma of treated leaf Zea mays
transcription factors identified in this study may participate in inhibition of de novo fatty acid biosynthesis and TAG assembly
PAP level might determine ratio between PG and glycolipids Synechocystis sp. PCC 6803
MGDG content under HC reached more than half of total membrane lipid content Synechocystis sp. PCC 6803
defects in (ATSEC14, SEC14, AT4G39180) proteins cause vitamin E deficiency Homo sapiens
(ATSEC14, SEC14, AT4G39180) integrates two antagonistic lipid pathways
(PXY, TDR, AT5G61480) mutant shows greatly changed aliphatic compositions of anther Oryza sativa
genes encoding proteins involved in FA biosynthesis, elongation, transport, and degradation were expressed during early stage of seeds (3–19 DAF) Brassica napus
tapetosomes contain alkanes
plant lipids are essential as precursors to a wide range of important metabolites
Sl-LIP8 protein can hydrolyze 18:2 and 18:3 acyl groups from TAGs and PCs Solanum lycopersicum
BILs and gene expression profiles strategy was recently adopted to confirm candidature of lipase for mQTL responsible for TAG and DAG breakdown Solanum lycopersicum
ultra-accumulated α-linolenic acid (ALA) is released from phosphatidylcholine Arabidopsis thaliana
GmPLDα1 mutant roots show higher levels of DGD2 and MGD2 coinciding with higher levels of DGDG and MGDG
(ATRBL11, AtRBL9, RBL11, RBL9, AT5G25752) has no known function in lipid metabolism Arabidopsis thaliana
pgsA mutant increased MGDG content Synechocystis sp. PCC 6803
contigs annotated as involved in secondary metabolism, lipid metabolism and ascorbate–glutathione (GSH) cycle equally represented regardless of hydration state Craterostigma plantagineum
Phaeodactylum tricornutum ecotypes (ATPT1, PHT1;1, PT1, AT5G43350) and Pt4 have glycerolipid profiles dominated by MGDG, SQDG, DGDG and phosphatidylcholine (PC) Phaeodactylum tricornutum
DAG pool in KO lines showed disappearance of 16:1/16:1 form Phaeodactylum tricornutum
noncatalytic protein characteristics such as interactions and stoichiometry importance of plant lipid metabolism
(ATRBL10, ATRBL14, RBL10, RBL14, AT3G17611) affects lipid metabolism in the chloroplast Arabidopsis thaliana
protein interactors of (ATRBL10, ATRBL14, RBL10, RBL14, AT3G17611) are involved in lipid metabolism Arabidopsis thaliana
boron (B) deficiency influences lipid metabolic processes Arabidopsis thaliana
59 putative lipid-related genes modification in expression of identified Zea mays
fatty acid unsaturation in olive is affected by ambient light
increasing lipid unsaturation may be achieved by post-transcriptional/translational modifications of (AtFAD2, FAD2, AT3G12120) or other desaturase isoforms Gossypium hirsutum
major portion of total fatty acids at stage C were likely to be from membrane lipids
enoyl CoA hydratase (bin code 11.9.4.3) was upregulated at 80 days after sprouting (80 DAS) in the primary root (PR) Aconitum kusnezoffii
phospholipase A enzymes cleave phospho- and galactolipids
pPLA proteins possess phospholipase A 2 activity
(AtPLAIVA, PLA IVA, PLP1, AT4G37070) possess phospholipase A activity Arabidopsis thaliana
(AT1G47780) encodes acyl-protein thioesterase involved in fatty acid synthesis
PG is only phospholipid present Arabidopsis thaliana
enzymatic assays in vitro were performed to confirm the function of Sl-LIP8 in cleaving glycerolipids Solanum lycopersicum
downregulation of key enzymes participating in JA biosynthesis helping to accumulate polyunsaturated fatty acid (PUFA) and maintain membrane fluidity in winter
phosphatidylcholine (PC) is increased in nodules compared with roots
phosphatidic acid synthesis occurs in seed coat Arabidopsis thaliana
brefeldin A causes accumulation of triacylglycerols in plastoglobules Chlamydomonas
overexpression of PAP reduced PG content Synechocystis sp. PCC 6803
lipid droplets accumulate in leaf cells of the (ABCI14, TGD1, AT1G19800) and (PDE320, TGD4, AT3G06960) mutants Arabidopsis thaliana
altered lipid binding affinity of FBN proteins affects the accumulation of certain compounds in PGs depending on the environmental condition Arabidopsis thaliana
(ACBP4, AtACBP4, AT3G05420) functions in floral lipidic metabolism Arabidopsis thaliana
PAD overexpression cells have higher MGDG levels Phaeodactylum tricornutum
[1-14C]linolenate percentages increased in phospholipids with rising temperature
effects of R/FR on saturated fatty acids occurred in both upper and lower sections of internode internode sections Helianthus annuus
erucic acid in yellow lupine cotyledons were vestigial quantities Lupinus luteus
Andean lupine oil contains a high amount of oleic and linoleic acids Lupinus mutabilis
TAG metabolism plays an important role in membrane lipid remodeling
KO lines had significant increase in PC Phaeodactylum tricornutum
S-acylation of (AtNPC4, NPC4, AT3G03530) in C terminus is conserved and required for phosphosphingolipid hydrolysis Arabidopsis thaliana; Brassica napus
enhanced de novo fatty acid biosynthetic flux could contribute to accumulation of PA Arabidopsis thaliana
LCAT-PLA 1 enzymes show homology to plant phospholipid: diacylglycerol acyltransferase (ATPDAT, PDAT, PDAT1, AT5G13640)
pgsA mutant increased SQDG content Synechocystis sp. PCC 6803
turnover of membrane lipids might be important rather than de novo synthesis of lipids Synechocystis sp. PCC 6803
non-acylating (AtNPC4, NPC4, AT3G03530) C533A mutant fails to functionally restore glycosyl inositol phosphoryl ceramide (GIPC) level to wild-type level Arabidopsis thaliana
leaf oil bodies contain phospholipases Arabidopsis thaliana
leaf oil bodies contain triacylglycerol lipases Arabidopsis thaliana
wheat grown at higher temperatures had higher levels of saturated fatty acids
KO lines had significant increase in PG Phaeodactylum tricornutum
chloroplast lipid profiles characterized by presence of phosphatidylglycerol (PG)
u-ATP9 plants display modification in expression of genes involved in lipid metabolism Arabidopsis thaliana
A9:u-ATP9 and AP3:u-ATP9 transgenic lines show increased expression of Very long chain fatty acid (VLCFA) condensing enzyme (AtCER6, AtCUT1, CER6, CUT1, G2, KCS6, POP1, AT1G68530) Arabidopsis thaliana
Non-specific phospholipase Cs (NPCs) are responsible for membrane lipid remodeling
(NPC6, AT3G48610) has role in seed triacylglycerol (TAG) content under normal growth conditions Arabidopsis thaliana
GDSL-like lipases (Os10g30290, Os07g47210, Os06g47910, Os06g14630) were up-regulated in (PXY, TDR, AT5G61480) mutant Oryza sativa
glycerol 3-phosphate is produced from glycerol by enzyme glycerol kinase
Tung lipid metabolic genes were identified based on orthology with established set of Arabidopsis genes
(GLES1, TGD5, AT1G27695) stomatal guard cells have WT levels of plastidial-pathway-specific lipids (34:6-MGDG, 34:3-DGDG, and 34:4-phosphatidylglycerol) Arabidopsis thaliana
leaf oil bodies contain lipoxygenases Arabidopsis thaliana
TAG metabolism affects acyl-CoA and DAG pools
ER pathway of lipid metabolism contributes differentially to plastid morphology maintenance in non-mesophyll plastids Arabidopsis thaliana
neoxanthin is found solely in high light plastoglobules Arabidopsis thaliana
polar lipids particularly include galactolipids Phaeodactylum tricornutum
protein–protein interactions is important for regulation of plant lipid metabolism Arabidopsis thaliana
sphingolipids are phytochemical class
acyl-CoA thioesterase is upregulated in PtMYB14 overexpression lines Picea glauca; Pinus taeda
biosynthesis of fatty acid and lipid is precursor of 2-butyl-l-octanol
Wax-deficient anther1 mutants exhibit abnormal lipid content in tissues including the tapetum Oryza sativa
(PXY, TDR, AT5G61480) has ability to regulate genes related to lipid metabolism Oryza sativa
(ACBP5, AtACBP5, AT5G27630) binds and transfers cytosolic oleoyl-CoA esters Arabidopsis thaliana
caleosins have been demonstrated to play critical roles in lipid trafficking/turnover plants
ER pathway of lipid metabolism contributes differentially to plastid morphology maintenance in mesophyll plastids Arabidopsis thaliana