2017
DOI: 10.1007/s11738-017-2349-1
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Comparative proteomics analysis of the effect of combined red and blue lights on sugarcane somatic embryogenesis

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Cited by 37 publications
(26 citation statements)
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“…Glycolysis, a key and ubiquitous metabolic pathway by which the plant cell converts carbohydrates to the energetic coin ATP, is a central pathway to generate energy and metabolic intermediaries that sustain the biosynthesis of intra- and extra-cellular molecules required by the cell. Proteins of the glycolysis pathway such as phosphofructokinase, fructose-1,6-biphosphate aldolase, glyceraldehyde-3-phosphate dehydrogenase, triosephosphate isomerase, phosphoglycerate mutase, 2,3-bisphosphoglycerate-independent phosphoglycerate mutase, phosphoglycerate kinase, enolase, and pyruvate decarboxylase were reported to be more abundant in the EC stage of African oil palm ( Silva et al, 2014 ), G. hirsutum ( Ge et al, 2017 ), maize ( Sun et al, 2013 ; Varhaníková et al, 2014 ; Ge et al, 2017 ), saffron ( Sharifi et al, 2012 ), Cyphomandra betacea ( Correia et al, 2012b ), Musa ( Kumaravel et al, 2017 ), Vitis vinifera ( Zhang et al, 2009 ), Larix principis-rupprechtii ( Beversdorf, 1987 ; Zhao et al, 2015a ), A. angustifolia ( dos Santos et al, 2016 ), P. nigra ( Klubicová et al, 2017 ), Theobroma cacao ( Niemenak et al, 2015 ), and sugarcane ( Heringer et al, 2017 ).…”
Section: Glycolysis-supplied Energy Leads Embryo Formationmentioning
confidence: 99%
See 1 more Smart Citation
“…Glycolysis, a key and ubiquitous metabolic pathway by which the plant cell converts carbohydrates to the energetic coin ATP, is a central pathway to generate energy and metabolic intermediaries that sustain the biosynthesis of intra- and extra-cellular molecules required by the cell. Proteins of the glycolysis pathway such as phosphofructokinase, fructose-1,6-biphosphate aldolase, glyceraldehyde-3-phosphate dehydrogenase, triosephosphate isomerase, phosphoglycerate mutase, 2,3-bisphosphoglycerate-independent phosphoglycerate mutase, phosphoglycerate kinase, enolase, and pyruvate decarboxylase were reported to be more abundant in the EC stage of African oil palm ( Silva et al, 2014 ), G. hirsutum ( Ge et al, 2017 ), maize ( Sun et al, 2013 ; Varhaníková et al, 2014 ; Ge et al, 2017 ), saffron ( Sharifi et al, 2012 ), Cyphomandra betacea ( Correia et al, 2012b ), Musa ( Kumaravel et al, 2017 ), Vitis vinifera ( Zhang et al, 2009 ), Larix principis-rupprechtii ( Beversdorf, 1987 ; Zhao et al, 2015a ), A. angustifolia ( dos Santos et al, 2016 ), P. nigra ( Klubicová et al, 2017 ), Theobroma cacao ( Niemenak et al, 2015 ), and sugarcane ( Heringer et al, 2017 ).…”
Section: Glycolysis-supplied Energy Leads Embryo Formationmentioning
confidence: 99%
“…Lipid transfer proteins, a collection of extracellular proteins with a secretory peptide, are thought to participate in the movement of surface lipids required for the formation of wax and cutin ( Wirtz, 1991 ; Li-Beisson et al, 2013 ). A lipid transfer protein was upregulated in CSE from G. hirsutum ( Ge et al, 2014 ) and phospholipid transfer protein 1 was upregulated during somatic embryo maturation of sugarcane embryos in a light quality-dependent fashion (meaning embryo maturation under white light plus medium blue, red, and far-red) ( Heringer et al, 2017 ), suggesting that surface lipids are an essential factor in embryo maturation.…”
Section: Fatty Acidsmentioning
confidence: 99%
“…The ideal protein extraction method should capture as many contents and proteins as possible while minimizing degradation and contamination (including phenolic compounds, starches, oils, and cell wall polysaccharides) . Therefore, the urea/thiourea protocol, which involves grinding a sample in liquid nitrogen, resuspending the sample in urea/thiourea extraction buffer (consisting of 7 m urea, 2 m thiourea, 1% dithiothreitol (DTT), 2% Triton X‐100, and protease inhibitors), and collecting the supernatant following centrifugation (Figure ), is preferred for surveying embryogenic callus or somatic embryo proteomes . In samples with a high contaminant load, the previously used trichloroacetic acid (TCA)/acetone precipitation (10% TCA in acetone) method, followed by resuspension in urea/thiourea buffer (Figure ), can be used.…”
Section: Evolution Of the Plant Proteomic Platformmentioning
confidence: 99%
“…Additional and complementary approaches in proteomics, such as phosphoproteomics, subcellular proteomics, and mass spectrometry immunohistochemistry (MSIHC), have great potential as complementary methods to help elucidate particular aspects of cellular metabolism. Recent publications have suggested that the gel‐free workflow will be the initial step to achieve a thorough overview of cellular proteins related to somatic embryogenesis competence and development . In addition to generating a catalog of proteins, proteomics can provide real biological knowledge; however, this achievement first requires the use of plant model systems.…”
Section: Further Perspectivesmentioning
confidence: 99%
“…Over the last few years, the expression profiles of SE related genes and other differentially expressed genes during SE had been extensively excavated by RNA-seq sequencing in various species, including Gossypium hirsutum [9][10][11][12] [ [22], Rice [23], Lilium pumilum [24], Mangosteen [25], Papaya [26], and Triticum aestivum [27]. Meanwhile, the comparative proteome analysis during SE also characterized numerous proteins that associated with SE in many plant species, such as Maize [28], Papaya [29], Cacao [30], Sugarcane [31], Musa. spp [32], and Gossypium hirsutum [33].…”
Section: Introductionmentioning
confidence: 99%