2017
DOI: 10.1007/978-3-319-49653-5_7
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Lipid Biosynthesis and Regulation in Jatropha, an Emerging Model for Woody Energy Plants

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Cited by 5 publications
(7 citation statements)
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“…Different enzymes involved in FA and lipid biosynthesis have already been identified through genomic and transcriptomic studies (Gu et al ., 2012; Sood and Chauhan, 2015; Ma et al ., 2017); therefore, it is feasible that there are several routes for storage lipid formation in Jatropha seeds. The first route considered in Jatropha cell cultures for glycerolipid assembly in the endoplasmic reticulum (ER) was the Kennedy pathway.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Different enzymes involved in FA and lipid biosynthesis have already been identified through genomic and transcriptomic studies (Gu et al ., 2012; Sood and Chauhan, 2015; Ma et al ., 2017); therefore, it is feasible that there are several routes for storage lipid formation in Jatropha seeds. The first route considered in Jatropha cell cultures for glycerolipid assembly in the endoplasmic reticulum (ER) was the Kennedy pathway.…”
Section: Resultsmentioning
confidence: 99%
“…The initial step of lipid breakdown is catalyzed by lipases, releasing the acyl chains from the TAGs stored in the lipid droplets (here resembling the LBF reaction) located in the cytosol, yielding free FA and glycerol (Huang, 1983; Quettier and Eastmond, 2009; Li‐Beisson et al ., 2013). Glycerol is metabolized to the glycolytic intermediate dihydroxyacetone‐phosphate by the sequential action of the enzymes glycerol kinase and the FAD‐dependent glycerol‐3‐phosphate dehydrogenase, in the cytosol and the mitochondrial inner membrane, respectively (Eastmond, 2004; Quettier and Eastmond, 2009; Ma et al ., 2017). Dihydroxyacetone‐phosphate is then converted into sugars by the process of gluconeogenesis.…”
Section: Resultsmentioning
confidence: 99%
“…PEP can be used to fuel lipid biosynthesis controlled by the plastid FAS molecular complex. Thus, plant lipid biosynthesis occurs within plastid organelles, where the Suc catabolism and hexose oxidation are essential steps to provide a carbon source for de novo lipid biosynthesis [125,126]. The disruption of the glycolytic pathway by the antisense silencing of cytosolic Triose-Phosphate Isomerase (TPI, EC 5.3.1.1) caused an increase in Suc, Glc, Glc-6-P, Fru, fumarate, and isocitrate in the roots of silenced TPI genotypes, which was accompanied by an increased in the total lipid concentration [127].…”
Section: Lipids In Carbon Partitioning To the Arbuscular Mycorrhizamentioning
confidence: 99%
“…The disruption of the glycolytic pathway by the antisense silencing of cytosolic Triose-Phosphate Isomerase (TPI, EC 5.3.1.1) caused an increase in Suc, Glc, Glc-6-P, Fru, fumarate, and isocitrate in the roots of silenced TPI genotypes, which was accompanied by an increased in the total lipid concentration [127]. In parallel to PEP from glycolysis, alternate Suc catabolism sub-products, such as Glc-6-P, can be translocated into the plastids and can subsequently be used to synthesize PEP (Figure 2) in the stroma by plastidic glycolysis to support lipid biosynthesis [126,128].…”
Section: Lipids In Carbon Partitioning To the Arbuscular Mycorrhizamentioning
confidence: 99%
“…The synthesis of fatty acids in plants occurs mainly in plastids by the condensation of malonyl-CoA by KAS enzymes, of which isoform II is responsible for final elongation step in the form of plastids C16:0 ACP to C18:0 ACP (MA et al, 2017). It has been reported that at mature stages of development of Jatropha curcas seeds, the expression of KASII gene tends to be highly induced (GU et al, 2012); once the fatty acid is elongated from C16 to C18, it can subsequently undergo desaturation for obtaining unsaturated fatty acids (WEI et al 2012).…”
Section: Rt-pcrmentioning
confidence: 99%