Sucrose: Metabolite and signaling molecule

Sucrose metabolism: regulatory mechanisms and pivotal roles in sugar sensing and plant development

Koch, K. E. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.03.014 · Cited by 1,487

Function and regulation of plant invertases: sweet sensations

Roitsch, T. G., & González, M. (2004) · Trends in Plant Science · doi:10.1016/j.tplants.2004.10.009 · Cited by 932

Sucrose-Specific Induction of the Anthocyanin Biosynthetic Pathway in Arabidopsis

Solfanelli, C., Poggi, A., Loreti, E., Alpi, A., & Pierdomenico Perata, A. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.072579 · Cited by 879

Sucrose-Specific Induction of Anthocyanin Biosynthesis in Arabidopsis Requires the MYB75/PAP1 Gene

Teng, S., Keurentjes, J. J. B., Bentsink, L., Koornneef, M., & SMEEKENS, S. C. M. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.066688 · Cited by 715

Control of plant development and gene expression by sugar signaling

Gibson, S. I. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.003 · Cited by 697

Suppression of Sucrose Synthase Gene Expression Represses Cotton Fiber Cell Initiation, Elongation, and Seed Development

Ruan, Y., Llewellyn, D. J., & Furbank, R. T. (2003) · The Plant Cell · doi:10.1105/tpc.010108 · Cited by 502

Phloem Transport: Cellular Pathways and Molecular Trafficking

Turgeon, R., & Wolf, S. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092045 · Cited by 451

Normal growth of Arabidopsis requires cytosolic invertase but not sucrose synthase

Barratt, D. H. P., Derbyshire, P., Findlay, K., Pike, M. J., Wellner, N., Lunn, J. E., Feil, R., Simpson, C. E., Maule, A. J., & Smith, A. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900689106 · Cited by 432

Molecular physiology of higher plant sucrose transporters

Sauer, N. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.03.048 · Cited by 423

Evidence for an essential role of the sucrose transporter in phloem loading and assimilate partitioning.

Riesmeier, J. W., Willmitzer, L., & Frommer, W. B. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06229.x · Cited by 419

Sugar signals and the control of plant growth and development

Lastdrager, J., Hanson, J., & SMEEKENS, S. C. M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert474 · Cited by 638

Carbohydrates in plant immunity and plant protection: roles and potential application as foliar sprays

Trouvelot, S., Héloir, M., Poinssot, B., Gauthier, A., Paris, F., Guillier, C., Combier, M., Trdá, L., Daire, X., & Adrian, M. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00592 · Cited by 415

Drought stress condition increases root to shoot ratio via alteration of carbohydrate partitioning and enzymatic activity in rice seedlings

Xu, W., Cui, K., Xu, A., Nie, L., Huang, J., & Peng, S. (2015) · Acta Physiologiae Plantarum · doi:10.1007/s11738-014-1760-0 · Cited by 410

Sugars and plant innate immunity

Moghaddam, M. R. B., & den Ende, W. V. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers129 · Cited by 386

The role of sugar signaling in plant defense responses against fungal pathogens

Morkunas, I., & Ratajczak, L. (2014) · Acta Physiologiae Plantarum · doi:10.1007/s11738-014-1559-z · Cited by 364

Sucrose functions as a signal involved in the regulation of strawberry fruit development and ripening

Jia, H., Wang, Y., Sun, M., Li, B., Han, Y., Zhao, Y., Li, X., Ding, N., Li, C., Ji, W., et al. (2013) · New Phytologist · doi:10.1111/nph.12176 · Cited by 339

Sucrose and invertases, a part of the plant defense response to the biotic stresses

Tauzin, A. S., & Giardina, T. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00293 · Cited by 335

Plant Hormone-Mediated Regulation of Heat Tolerance in Response to Global Climate Change

Li, N., Euring, D., Cha, J. Y., Lin, Z., Lu, M.-Z., Huang, L., & Kim, W. Y. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2020.627969 · Cited by 347

Sucrose signaling in higher plants

Yoon, J., Cho, L., Tun, W., Jeon, J., & An, G. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110703 · Cited by 325

Salt stress resilience in plants mediated through osmolyte accumulation and its crosstalk mechanism with phytohormones

Singh, P., Choudhary, K. K., Chaudhary, N., Gupta, S. K., Sahu, M., Tejaswini, B., & Sarkar, S. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1006617 · Cited by 276

The Sugar-Signaling Hub: Overview of Regulators and Interaction with the Hormonal and Metabolic Network

Sakr, S., Wang, M., Dédaldéchamp, F., Pérez-Garcia, M.-D., Ogé, L., Hamama, L., & Atanassova, R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19092506 · Cited by 273

Metabolic engineering of sugars and simple sugar derivatives in plants

Patrick, J. W., Botha, F. C., & Birch, R. G. (2012) · Plant Biotechnology Journal · doi:10.1111/pbi.12002 · Cited by 260

Sugar Signaling During Fruit Ripening

Durán-Soria, S., Pott, D. M., Osorio, S., & Vallarino, J. G. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.564917 · Cited by 257

Soluble Carbohydrates Regulate Auxin Biosynthesis via PIF Proteins in Arabidopsis

Sairanen, I., Novák, O., Pěnčík, A., Ikeda, Y., Jones, B. J., Sandberg, G., & Ljung, K. (2012) · The Plant Cell · doi:10.1105/tpc.112.104794 · Cited by 255

Photosynthetic sucrose acts as cotyledon-derived long-distance signal to control root growth during early seedling development in Arabidopsis

Kircher, S., & Schöpfer, P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203746109 · Cited by 251

Sucrose signaling in plants: A world yet to be explored

Pontis, H. G., & Martínez-Noël, G. M. A. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.23316 · Cited by 255

Soybean (Glycine max) SWEET gene family: insights through comparative genomics, transcriptome profiling and whole genome re-sequence analysis

Patil, G., Valliyodan, B., Deshmukh, R. K., Prince, S., Nicander, B., Zhao, M., Sonah, H., Song, L., Lin, L., Chaudhary, J., et al. (2015) · BMC Genomics · doi:10.1186/s12864-015-1730-y · Cited by 244

Master regulators in plant glucose signaling networks

Sheen, J. (2014) · Journal of Plant Biology · doi:10.1007/s12374-014-0902-7 · Cited by 242

Plant adaptations to severely phosphorus-impoverished soils

Lambers, H., Martinoia, E., & Renton, M. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.04.002 · Cited by 228

Identification and characterization of fructose 1,6-bisphosphate aldolase genes in Arabidopsis reveal a gene family with diverse responses to abiotic stresses

Lü, W., Tang, X., Huo, Y., Xu, R., Qi, S., Huang, J., Zheng, C., & Wu, C. (2012) · Gene · doi:10.1016/j.gene.2012.04.042 · Cited by 215

Metabolic pathways regulated by γ-aminobutyric acid (GABA) contributing to heat tolerance in creeping bentgrass (Agrostis stolonifera)

Li, Z., Yu, J., Peng, Y., & Huang, B. (2016) · Scientific Reports · doi:10.1038/srep30338 · Cited by 202

Sugar Signaling in Root Responses to Low Phosphorus Availability

Hammond, J. P., & White, P. J. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.175380 · Cited by 211

Metabolite transport and associated sugar signalling systems underpinning source/sink interactions

Griffiths, C. A., Paul, M. J., & Foyer, C. H. (2016) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2016.07.007 · Cited by 170

Allantoin, a stress-related purine metabolite, can activate jasmonate signaling in a MYC2-regulated and abscisic acid-dependent manner

Takagi, H., Ishiga, Y., Watanabe, S., Konishi, T., Egusa, M., Akiyoshi, N., Matsuura, T., Mori, I. C., Hirayama, T., Kaminaka, H., et al. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw071 · Cited by 154

Ready, steady, go! A sugar hit starts the race to shoot branching

Barbier, F. F., Lunn, J. E., & Beveridge, C. A. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.04.004 · Cited by 159

Insight into the Role of Sugars in Bud Burst Under Light in the Rose

Rabot, A., Henry, C., Baaziz, K. B., Mortreau, E., Azri, W., Lothier, J., Hamama, L., Boummaza, R., Leduc, N., Pelleschi, S., et al. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs051 · Cited by 143

Cell‐wall invertases, key enzymes in the modulation of plant metabolism during defence responses

Proels, R. K., & Hückelhoven, R. (2014) · Molecular Plant Pathology · doi:10.1111/mpp.12139 · Cited by 142

Comparative metabolomic profiling in the roots and leaves in contrasting genotypes reveals complex mechanisms involved in post-anthesis drought tolerance in wheat

Kang, Z., Babar, M. A., Khan, N., Guo, J. X., Khan, J., Islam, S., Shrestha, S., & Shahi, D. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213502 · Cited by 139

Sugars, the clock and transition to flowering

Moghaddam, M. R. B., & den Ende, W. V. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00022 · Cited by 137

Photoreceptor effects on plant biomass, resource allocation, and metabolic state

Yang, D., Seaton, D. D., Krahmer, J., & Halliday, K. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601309113 · Cited by 145

Soybean GmbZIP123 gene enhances lipid content in the seeds of transgenic Arabidopsis plants

Song, Q., Li, Q., Liu, Y.-F., Zhang, F.-X., Ma, B., Zhang, W.-K., Man, W., Du, W.-G., Wang, G., Chen, S.-Y., et al. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert238 · Cited by 134

Fructose sensitivity is suppressed in Arabidopsis by the transcription factor ANAC089 lacking the membrane-bound domain

Li, P., Wind, J. J., Shi, X., Zhang, H., Hanson, J., SMEEKENS, S. C. M., & Teng, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018665108 · Cited by 131

Emerging Roles of SWEET Sugar Transporters in Plant Development and Abiotic Stress Responses

Gautam, T., Dutta, M., Jaiswal, V., Zinta, G., Gahlaut, V., & Kumar, S. (2022) · Cells · doi:10.3390/cells11081303 · Cited by 128

Ethylene involvement in the regulation of heat stress tolerance in plants

Poór, P., Nawaz, K., Gupta, R., Ashfaque, F., & Khan, M. I. R. (2021) · Plant Cell Reports · doi:10.1007/s00299-021-02675-8 · Cited by 133

Effect of exogenous sucrose on anthocyanin synthesis in postharvest strawberry fruit

Li, D., Zhang, X., Xu, Y., Li, L., Aghdam, M. S., & Luo, Z. (2019) · Food Chemistry · doi:10.1016/j.foodchem.2019.03.042 · Cited by 126

Sweet immunity in the plant circadian regulatory network

Moghaddam, M. R. B., & den Ende, W. V. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert046 · Cited by 118

Regulation of fruit and seed response to heat and drought by sugars as nutrients and signals

Liu, Y., Offler, C. E., & Ruan, Y. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00282 · Cited by 117

Aluminum toxicity in plant cells: Mechanisms of cell death and inhibition of cell elongation

Yamamoto, Y. (2018) · Soil Science & Plant Nutrition · doi:10.1080/00380768.2018.1553484 · Cited by 115

Sugar enhances waterlogging‐induced adventitious root formation in cucumber by promoting auxin transport and signalling

Qi, X., Li, Q., Shen, J., Qian, C., Xu, X., Xu, Q., & Chen, X. (2020) · Plant Cell & Environment · doi:10.1111/pce.13738 · Cited by 112

Comparison of Sugar Profile between Leaves and Fruits of Blueberry and Strawberry Cultivars Grown in Organic and Integrated Production System

Akšić, M. F., Tosti, T. B., Sredojević, M., MILIVOJEVIC, J. M., Meland, M., & Natić, M. (2019) · Plants · doi:10.3390/plants8070205 · Cited by 120

Overexpression of Sucrose Phosphate Synthase Enhanced Sucrose Content and Biomass Production in Transgenic Sugarcane

Anur, R. M., Mufithah, N., Sawitri, W. D., Sakakibara, H., & Sugiharto, B. (2020) · Plants · doi:10.3390/plants9020200 · Cited by 109

New insights into the evolution and functional divergence of the SWEET family in Saccharum based on comparative genomics

Hu, W., Hua, X., Zhang, Q., Wang, J., Shen, Q., Zhang, X., Wang, K., Yu, Q., Lin, Y., Ming, R., et al. (2018) · BMC Plant Biology · doi:10.1186/s12870-018-1495-y · Cited by 107

The genetic architecture of amylose biosynthesis in maize kernel

Li, C., Huang, Y., Huang, R., Wu, Y., & Wang, W. (2017) · Plant Biotechnology Journal · doi:10.1111/pbi.12821 · Cited by 103

Sucrose-induced Receptor Kinase SIRK1 Regulates a Plasma Membrane Aquaporin in Arabidopsis

Wu, X., Sánchez‐Rodríguez, C., Pertl-Obermeyer, H., Obermeyer, G., & Schulze, W. X. (2013) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.029579 · Cited by 103

The Plastidic Sugar Transporter pSuT Influences Flowering and Affects Cold Responses

Patzke, K., Prananingrum, P., Klemens, P. A. W., Trentmann, O., Rodrigues, C. M., Keller, I., Fernie, A. R., Geigenberger, P., Bölter, B., Lehmann, M., et al. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.01036 · Cited by 99

Alterations in plant sugar metabolism: signatory of pathogen attack

Kanwar, P., & Jha, G. (2018) · Planta · doi:10.1007/s00425-018-3018-3 · Cited by 96

UDP-Glucose: A Potential Signaling Molecule in Plants?

van Rensburg, H. C. J., & den Ende, W. V. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2017.02230 · Cited by 94

Effects of soil water stress on fruit yield, quality and their relationship with sugar metabolism in ‘Gala’ apple

Wang, Y., Liu, L., Wang, Y., Tao, H., Fan, J., Zhao, Z., & Guo, Y. (2019) · Scientia Horticulturae · doi:10.1016/j.scienta.2019.108753 · Cited by 92

Sugar and Light Effects on the Condition of the Photosynthetic Apparatus of Arabidopsis thaliana Cultured in vitro

Eckstein, A., Zięba, P., & Gabryś, H. (2011) · Journal of Plant Growth Regulation · doi:10.1007/s00344-011-9222-z · Cited by 93

Sugar transporters and their molecular tradeoffs during abiotic stress responses in plants

Salvi, P., Agarrwal, R., Kajal, Gandass, N., Manna, M., Kaur, H., & Deshmukh, R. K. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13652 · Cited by 92

Comparative Transcriptome Analysis Reveals Critical Function of Sucrose Metabolism Related-Enzymes in Starch Accumulation in the Storage Root of Sweet Potato

Zhang, K., Wu, Z., Tang, D., Luo, K., Lu, H., Liu, Y., Dong, J., Wang, X., Lv, C., Wang, J., et al. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00914 · Cited by 88

Cell division and turgor-driven stem elongation in juvenile plants: A synthesis

Kutschera, U., & Niklas, K. J. (2013) · Plant Science · doi:10.1016/j.plantsci.2013.02.004 · Cited by 91

Spatio-Temporal Dynamics of Fructan Metabolism in Developing Barley Grains

Peukert, M., Thiel, J., Peshev, D., Weschke, W., den Ende, W. V., Mock, H., & Matros, A. (2014) · The Plant Cell · doi:10.1105/tpc.114.130211 · Cited by 90

WRKY18 and WRKY53 Coordinate with HISTONE ACETYLTRANSFERASE1 to Regulate Rapid Responses to Sugar

Chen, Q., Xu, X., Xu, D., Zhang, H., Zhang, C., & Li, G. (2019) · PLANT PHYSIOLOGY · doi:10.1104/pp.19.00511 · Cited by 90

Leaf area and photosynthesis of newly emerged trifoliolate leaves are regulated by mature leaves in soybean

Wu, Y., Gong, W., Wang, Y., Yong, T., Yang, F., Liu, W., Wu, X., Du, J., Shu, K., Liu, J., et al. (2018) · Journal of Plant Research · doi:10.1007/s10265-018-1027-8 · Cited by 88

Starches—from current models to genetic engineering

Sonnewald, U., & Koßmann, J. (2012) · Plant Biotechnology Journal · doi:10.1111/pbi.12029 · Cited by 87

How Sugars Might Coordinate Chloroplast and Nuclear Gene Expression during Acclimation to High Light Intensities

Hausler, R., Heinrichs, L., Schmitz, J., & Flügge, U. (2014) · Molecular Plant · doi:10.1093/mp/ssu064 · Cited by 81

Plant Sucrose Transporters from a Biophysical Point of View

Geiger, D. (2011) · Molecular Plant · doi:10.1093/mp/ssr029 · Cited by 81

Raffinose Family Oligosaccharides Act As Galactose Stores in Seeds and Are Required for Rapid Germination of Arabidopsis in the Dark

Gangl, R., & Tenhaken, R. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01115 · Cited by 80

Molecular basis for optimizing sugar metabolism and transport during fruit development

Chen, T., Zhang, Z., Li, B., Qin, G., & Tian, S. (2021) · aBIOTECH · doi:10.1007/s42994-021-00061-2 · Cited by 78

Transcriptome Analysis and Functional Genomics of Sugarcane

Manners, J. M., & Casu, R. E. (2011) · Tropical Plant Biology · doi:10.1007/s12042-011-9066-5 · Cited by 70

Compartmentalization of Metabolites and Enzymatic Mediation in Nutritive Cells of Cecidomyiidae Galls on Piper Arboreum Aubl. (Piperaceae)

Bragança, G. P. P., de Oliveira, D. C., & Isaías, R. M. D. S. (2016) · Journal of Plant Studies · doi:10.5539/jps.v6n1p11 · Cited by 73

Arabidopsis Sucrose Transporter SUT4 Interacts with Cytochrome b5-2 to Regulate Seed Germination in Response to Sucrose and Glucose

Li, Y., Li, L., Fan, R., Peng, C., Sun, H., Zhu, S., Wang, X., Zhang, L., & Zhang, D. (2012) · Molecular Plant · doi:10.1093/mp/sss001 · Cited by 66

Loss of the two major leaf isoforms of sucrose-phosphate synthase in Arabidopsis thaliana limits sucrose synthesis and nocturnal starch degradation but does not alter carbon partitioning during photosynthesis

Volkert, K., Debast, S., Voll, L. M., Voll, H., Schießl, I., Hofmann, J., Schneider, S., & Börnke, F. A. J. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru282 · Cited by 64

Transcriptome analysis reveals the accumulation mechanism of anthocyanins in ‘Zijuan’ tea (Camellia sinensis var. asssamica (Masters) kitamura) leaves

Li, J., Lv, X., Wang, L., Qiu, Z., Song, X., Lin, J., & Chen, W. (2016) · Plant Growth Regulation · doi:10.1007/s10725-016-0183-x · Cited by 65

Omics Approaches for Understanding Grapevine Berry Development: Regulatory Networks Associated with Endogenous Processes and Environmental Responses

Serrano, A., Espinoza, C., Armijo, G., Inostroza‐Blancheteau, C., Poblete, E., Meyer‐Regueiro, C., Arce, A., Parada, F., Santibáñez, C., & Arce‐Johnson, P. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01486 · Cited by 64

Glucose Uptake via STP Transporters Inhibits in Vitro Pollen Tube Growth in a HEXOKINASE1-Dependent Manner in Arabidopsis thaliana

Rottmann, T., Fritz, C., Sauer, N., & Stadler, R. (2018) · The Plant Cell · doi:10.1105/tpc.18.00356 · Cited by 64

Effects of preharvest regulation of ethylene on carbohydrate metabolism of apple (Malus domestica Borkh cv. Starkrimson) fruit at harvest and during storage

Sun, Y., Shi, Z., Jiang, Y., Zhang, X., Li, X., & Li, F. (2020) · Scientia Horticulturae · doi:10.1016/j.scienta.2020.109748 · Cited by 64

Genome-wide identification and expression analysis of SWEET gene family in Litchi chinensis reveal the involvement of LcSWEET2a/3b in early seed development

Xie, H., Wang, D., Qin, Y., Ma, A., Fu, J., Qin, Y., Hu, G., & Zhao, J. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-2120-4 · Cited by 59

Plant glucose transporter structure and function

Geiger, D. (2020) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-020-02449-3 · Cited by 59

Sugar regulation of SUGAR TRANSPORTER PROTEIN 1 (STP1) expression in Arabidopsis thaliana

Córdoba, E., Aceves-Zamudio, D., Hernández-Bernal, A. F., Ramos-Vega, M., & León, P. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru394 · Cited by 59

Phloem loading in rice leaves depends strongly on the apoplastic pathway

Wang, G., Wu, Y., Ma, L. M., Lin, Y., Hu, Y., Li, M., Li, W., Ding, Y., & Chen, L. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab085 · Cited by 57

Light modulated activity of root alkaline/neutral invertase involves the interaction with 14‐3‐3 proteins

Gao, J. Q., van Kleeff, P. J. M., Oecking, C., Li, K. W., Erban, A., Kopka, J., Hincha, D. K., & BOER, A. H. D. (2014) · The Plant Journal · doi:10.1111/tpj.12677 · Cited by 57

Engineering α-amylase levels in wheat grain suggests a highly sophisticated level of carbohydrate regulation during development

Whan, A., Dielen, A., Mieog, J. C., Bowerman, A. F., Robinson, H. M., Byrne, K. A., Colgrave, M. L., Larkin, P. J., Howitt, C. A., Morell, M. K., et al. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru299 · Cited by 57

Genome-wide identification and expression profiling analysis of sucrose synthase (SUS) and sucrose phosphate synthase (SPS) genes family in Actinidia chinensis and A. eriantha

Liao, G., Li, Y., Wang, H., Liu, Q., Zhong, M., Jia, D., Huang, C., & Xu, X. (2022) · BMC Plant Biology · doi:10.1186/s12870-022-03603-y · Cited by 55

Sucrose induced osmotic stress and photoperiod regimes enhanced the biomass and production of antioxidant secondary metabolites in shake-flask suspension cultures of Prunella vulgaris L.

Fazal, H., Abbasi, B. H., Ahmad, N., Ali, M., & Ali, S. (2015) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-015-0915-z · Cited by 55

Light regulates alternative splicing outcomes via the TOR kinase pathway

Riegler, S., Servi, L., Scarpin, M. R., Herz, M. A. G., Kubaczka, M. G., Venhuizen, P., Meyer, C., Brunkard, J. O., Kalyna, M., Barta, A., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109676 · Cited by 55

Effects of fruit bagging on anthocyanins, sugars, organic acids, and color properties of ‘Granny Smith’ and ‘Golden Delicious’ during fruit maturation

Liu, Y., Zhang, X., & Zhao, Z. (2012) · European Food Research and Technology · doi:10.1007/s00217-012-1896-3 · Cited by 54

Impact of concurrent overexpression of cytosolic glutamine synthetase (GS1) and sucrose phosphate synthase (SPS) on growth and development in transgenic tobacco

Seger, M., Gebril, S., Tabilona, J., Peel, A., & Sengupta‐Gopalan, C. (2014) · Planta · doi:10.1007/s00425-014-2165-4 · Cited by 53

Sucrose synthase: An enzyme with multiple roles in plant physiology

Li, J., Hu, Y., Hu, J., Xie, Q., Chen, X., & Qi, X. (2024) · Journal of Plant Physiology · doi:10.1016/j.jplph.2024.154352 · Cited by 51

Characters related to higher starch accumulation in cassava storage roots

Li, Y., Zhao, J., Wu, S.-M., Fan, X., Luo, X., & Chen, B. (2016) · Scientific Reports · doi:10.1038/srep19823 · Cited by 51

Proteomics of phosphate use and deprivation in plants

Alexova, R., & Millar, A. H. (2012) · PROTEOMICS · doi:10.1002/pmic.201200266 · Cited by 50

Identification of the Carbohydrate and Organic Acid Metabolism Genes Responsible for Brix in Tomato Fruit by Transcriptome and Metabolome Analysis

Li, N., Wang, J., Wang, B., Huang, S., Hu, J., Yang, T., Asmutola, P., Lan, H., & Yu, Q. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.714942 · Cited by 49

There and back again: An evolutionary perspective on long-distance coordination of plant growth and development

Wheeldon, C. D., & Bennett, T. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.06.011 · Cited by 51

In and out of the plant storage vacuole

Etxeberria, E., Pozueta‐Romero, J., & Gonzalez, P. (2012) · Plant Science · doi:10.1016/j.plantsci.2012.03.010 · Cited by 47

Pronounced Phenotypic Changes in Transgenic Tobacco Plants Overexpressing Sucrose Synthase May Reveal a Novel Sugar Signaling Pathway

Nguyen, Q. A., Luan, S., Wi, S. G., Bae, H., Lee, D.-S., & Bae, H. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01216 · Cited by 47

Photosynthesis in the seeds of chloroembryophytes

Николаевна, С. Г., & Medvedev, S. S. (2016) · Russian Journal of Plant Physiology · doi:10.1134/s1021443715060163 · Cited by 47

Constitutive overexpression of the sucrose transporter SoSUT1 in potato plants increases arbuscular mycorrhiza fungal root colonization under high, but not under low, soil phosphorus availability

Gabriel‐Neumann, E., Neumann, G., Leggewie, G., & George, E. (2011) · Journal of Plant Physiology · doi:10.1016/j.jplph.2010.11.026 · Cited by 47

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Wang, J., Lu, Y., Zhang, X., Hu, W., Lin, L., Deng, Q., Xia, H., Liang, D., & Lv, X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052828 · Cited by 40

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Dahiya, A., Saini, R., Saini, H. S., & Devi, A. (2017) · Journal of Pharmacognosy and Phytochemistry · Cited by 8

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Sucrose Metabolism

Lunn, J. E. (2008) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0021259 · Cited by 18