![]() Mechanism of Skeletal Muscle Contraction: Role of Mechanical Muscle Contraction in Glucose Homeostasis. Interaction of SOS2 with Nucleoside Diphosphate Kinase 2 and Catalases Reveals a Point of Connection between Salt Stress and. References - sucrose and synthesis - HORT6. Metabolic Plant Physiology - Department of Horticulture and Landscape Architecture. References, sucrose and synthesis. Ainsworth EA, Rogers A, Leakey AD, Heady LE, Gibon Y, Stitt M, Schurr U. Does elevated atmospheric ? Fruit- localized phytochromes regulate lycopene accumulation independently of ethylene production in tomato. Localization of sucrose synthase in wheat roots: increased in situ activity of sucrose synthase correlates with cell wall thickening by cellulose deposition under hypoxia. Planta 2. 17: 2. 52- 2. Sanguinarine biosynthesis is associated with the endoplasmic reticulum in cultured opium poppy cells after elicitor treatment. Photoinhibition and recovery in a herbicide- resistant mutant from Glycine max (L.) Merr. Planta 2. 19: 4. 28- 4. Timecourse microarray analyses reveal global changes in gene expression of susceptible Glycine max (soybean) roots during infection by Heterodera glycines (soybean cyst nematode). Planta 2. 24: 8. 38- 8. The role of light in soybean seed filling metabolism. A metabolic flux analysis to study the role of sucrose synthase in the regulation of the carbon partitioning in central metabolism in maize root tips. Substrate cycles in the central metabolism of maize root tips under hypoxia. Phytochemistry 6. Photosynthesis and primary metabolism. ![]() The link between acrylamide. Cereal and potato products are a valuable source of energy and an intrinsic part of the everyday diet. Wheat is a rich source of fibre. AMP-activated protein kinase. DNA damage and oxidative stress, AMP, 5-amino-4-imidazolecarboxamide riboside (AICA riboside), and. 2010 Sucrose nonfermenting AMPK-related kinase. 38 +/- 13 mg of aspartame per kilogram per day while on the aspartame diet, and 12 +/- 4.5 mg of. Analysis of sucrose gradients for SIS1 protein shows that a. ![]() SIK belongs to a family of sucrose nonfermenting (SNF1)/AMP. Advances in Physiology Education Published 1. CaMK, Ca2+/calmodulin-dependent protein kinase; SNARK, sucrose nonfermenting AMP-dependent protein. The diverse oncogenic and tumor suppressor roles of salt-inducible kinase. The diverse oncogenic and tumor suppressor roles of salt-inducible kinase. 278 residue and a sucrose-nonfermenting-1 protein kinase homology. Hepatic rRNA Transcription Regulates High-Fat-Diet. It has been shown that the induction of an altered phenotype by a maternal protein restriction diet during pregnancy involves. Anatomical and photosynthetic acclimation to the light environment in species with differing mechanisms of phloem loading. Efficiency of lignin biosynthesis: a quantitative analysis. Biosynthesis of cellulose- enriched tension wood in Populus: global analysis of transcripts and metabolites identifies biochemical and developmental regulators in secondary wall biosynthesis. Transcriptional control of monolignol biosynthesis in Pinus taeda - Factors affecting monolignol ratios and carbon allocation in phenylpropanoid metabolism. Rice SPK, a calmodulin- like domain protein kinase, is required for storage product accumulation during seed development: phosphorylation of sucrose synthase is a possible factor. Plant Cell 1. 4: 6. Cloning, characterization and functional analysis of a 1- FEH c. DNA from Vernonia herbacea (Vell.) Rusby. Sucrose phosphate synthase activity rises in correlation with high- rate cellulose synthesis in three heterotrophic systems. A central integrator of transcription networks in plant stress and energy signalling. Nature 4. 48: 9. 38- 9. Phytochrome, photosynthesis and flowering of Arabidopsis thaliana: photophysiological studies using mutants and transgenic lines. Supply of fatty acid is one limiting factor in the accumulation of triacylglycerol in developing embryos. Alteration of the amount of the chloroplast phosphate translocator in transgenic tobacco affects the distribution of assimilate between starch and sugar. Reappraisal of the currently prevailing model of starch biosynthesis in photosynthetic tissues: a proposal involving the cytosolic production of ADP- glucose by sucrose synthase and occurrence of cyclic turnover of starch in the chloroplast. Reappraisal of the currently prevailing model of starch biosynthesis in photosynthetic tissues: a proposal involving the cytosolic production of ADP- glucose by sucrose synthase and occurrence of cyclic turnover of starch in the chloroplast. Glucose 6- phosphate dehydrogenase is required for sucrose and trehalose to be efficient osmoprotectants in Sinorhizobium meliloti. Hypertonic activation of the renal betaine/GABA transporter is microtubule dependent. The relationship between the activation state of sucrose- phosphate synthase and the rate of CO2 assimilation in spinach leaves. ![]() Planta 1. 83: 6. 20- 6. Fruit carbohydrate metabolism in an introgression line of tomato with increased fruit soluble solids. Elevated sucrose- phosphate synthase activity in transgenic tobacco sustains photosynthesis in older leaves and alters development. Complex regulation of gene expression, photosynthesis and sugar levels by pathogen infection in tomato. Identification of growth processes involved in QTLs for tomato fruit size and composition. Differential carbohydrate metabolism conducts morphogenesis in embryogenic callus of Hevea brasiliensis (Mull. Gibberellins promote flowering of Arabidopsis by activating the LEAFY promoter. Plant Cell 1. 0: 7. Flux- based response of sucrose and starch in leaves of adult beech trees (Fagus sylvatica L.) under chronic free- air O3 fumigation. A bypass of sucrose synthase leads to low internal oxygen and impaired metabolic performance in growing potato tubers. Differentiation of legume cotyledons as related to metabolic gradients and assimilate transport into seeds. High- level production of the non- cariogenic sucrose isomer palatinose in transgenic tobacco plants strongly impairs development. Planta 2. 14: 3. 56- 3. Grain yields with limited water. The mechanism of synthesis of a mixed- linkage (1- -> 3),(1- -> 4)beta- D- glucan in maize. Evidence for multiple sites of glucosyl transfer in the synthase complex. ![]() The H+- sucrose cotransporter Nt. SUT1 is essential for sugar export from tobacco leaves. Absence of turnover and futile cycling of sucrose in leaves of Lolium temulentum L.: implications for metabolic compartmentation. Planta 2. 19: 8. 36- 8. Evolution and function of the sucrose- phosphate synthase gene families in wheat and other grasses. ![]() Identification of differentially expressed transcripts from maturing stem of sugarcane by in silico analysis of stem expressed sequence tags and gene expression profiling. Identification of a novel sugar transporter homologue strongly expressed in maturing stem vascular tissues of sugarcane by expressed sequence tag and microarray analysis. WRI1 is required for seed germination and seedling establishment. WRINKLED1 encodes an AP2/EREB domain protein involved in the control of storage compound biosynthesis in Arabidopsis. Isolation of glycine betaine and proline betaine from human urine. Assessment of their role as osmoprotective agents for bacteria and the kidney. Nitrate activation of cytosolic protein kinases diverts photosynthetic carbon from sucrose to amino acid biosynthesis. Overexpression of a cyanobacterial phosphoenolpyruvate carboxylase with diminished sensitivity to feedback inhibition in Arabidopsis changes amino acid metabolism. Planta 2. 19: 4. 40- 4. Aluminum- induced decrease in CO2 assimilation in citrus seedlings is unaccompanied by decreased activities of key enzymes involved in CO2 assimilation. Differential expression of sucrose- phosphate synthase isoenzymes in tobacco reflects their functional specialization during dark- governed starch mobilization in source leaves. Decreased sucrose- 6- phosphate phosphatase level in transgenic tobacco inhibits photosynthesis, alters carbohydrate partitioning, and reduces growth. Planta 2. 21: 4. 79- 4. The regulator of G- protein signaling proteins involved in sugar and abscisic acid signaling in Arabidopsis seed germination. Sucrose mimics the light induction of Arabidopsis nitrate reductase gene transcription. Antisense inhibition of sorbitol synthesis leads to up- regulation of starch synthesis without altering CO2 assimilation in apple leaves. Planta 2. 20: 7. 67- 7. A cytosolic glucosyltransferase is required for conversion of starch to sucrose in Arabidopsis leaves at night. Storage oil breakdown during embryo development of Brassica napus (L.). Overexpression of mannitol- 1- phosphate dehydrogenase increases mannitol accumulation and adds protection against chilling injury in petunia. Growth and metabolism in sugarcane are altered by the creation of a new hexose- phosphate sink. Phosphate status affects the gene expression, protein content and enzymatic activity of UDP- glucose pyrophosphorylase in wild- type and pho mutants of Arabidopsis. Planta 2. 12: 5. 98- 6. Sucrose and light regulation of a cold- inducible UDP- glucose pyrophosphorylase gene via a hexokinase- independent and abscisic acid- insensitive pathway in Arabidopsis. The relationship between the rate of starch synthesis, the adenosine 5'- diphosphoglucose concentration and the amylose content of starch in developing pea embryos. Planta 2. 09: 3. 24- 3. An osmotic stress protein of cyanobacteria is immunologically related to plant dehydrins. Novel aspects of symbiotic nitrogen fixation uncovered by transcript profiling with c. DNA arrays. Plant Microbe Interact. Oe. MST2 encodes a monosaccharide transporter expressed throughout olive fruit maturation. Recovery of the resurrection plant Craterostigma wilmsii from desiccation: protection versus repair. Antisense inhibition of NADH glutamate synthase impairs carbon/nitrogen assimilation in nodules of alfalfa (Medicago sativa L.). Carbon and nitrogen sensing and signaling in plants: emerging . Involvement of soluble sugars in reactive oxygen species balance and responses to oxidative stress in plants. Nitrogen use efficiency by a slow- growing species as affected by CO2 levels, root temperature, N source and availability. Sucrose- phosphate phosphatase from Anabaena sp. Planta 2. 14: 2. 50- 2. Biosynthesis and cell- wall deposition of a pectin- xyloglucan complex in pea. Planta 2. 22: 5. 46- 5. Sucrose synthase is involved in the conversion of sucrose to polysaccharides in filamentous nitrogen- fixing cyanobacteria. Planta 2. 28: 6. 17- 6. Cloning and expression analysis of a UDP- galactose/glucose pyrophosphorylase from melon fruit provides evidence for the major metabolic pathway of galactose metabolism in raffinose oligosaccharide metabolizing plants. Starch metabolism in developing embryos of oilseed rape. Planta 2. 03: 4. 80- 4. Sugar accumulation in grape berries. Cloning of two putative vacuolar invertase c. DNAs and their expression in grapevine tissues. Metabolic state of Zymomonas mobilis in glucose- , fructose- , and xylose- fed continuous cultures as analysed by 1. C- and 3. 1P- NMR spectroscopy. Drought induces fructan synthesis and 1- SST (sucrose: sucrose fructosyltransferase) in roots and leaves of chicory seedlings. Planta 2. 10: 8. 08- 8.
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