Influence of Different Types of Carbon Sources on Glucosinolate and Phenolic Compounds in Radish Sprouts
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J. K. Kim | C. Park | H. Yeo | Yeon-Bok Kim | R. Sathasivam | Sang-Un Park | Min-Soon Choi | Y. Park | Subramanian Sankaranarayanan
[1] J. K. Kim,et al. Comparative Analysis of Glucosinolate and Phenolic Compounds in Green and Red Kimchi Cabbage (Brassica rapa L. ssp. pekinensis) Hairy Roots after Exposure to Light and Dark Conditions , 2023, Horticulturae.
[2] J. K. Kim,et al. Impact of Light and Dark Treatment on Phenylpropanoid Pathway Genes, Primary and Secondary Metabolites in Agastache rugosa Transgenic Hairy Root Cultures by Overexpressing Arabidopsis Transcription Factor AtMYB12 , 2023, Life.
[3] J. K. Kim,et al. Metabolic Profiling of Primary and Secondary Metabolites in Kohlrabi (Brassica oleracea var. gongylodes) Sprouts Exposed to Different Light-Emitting Diodes , 2023, Plants.
[4] C. Manach,et al. Systematic Review on the Metabolic Interest of Glucosinolates and Their Bioactive Derivatives for Human Health , 2023, Nutrients.
[5] T. Shalaby,et al. Metabolites, Nutritional Quality and Antioxidant Activity of Red Radish Roots Affected by Gamma Rays , 2022, Agronomy.
[6] R. Capasso,et al. Cruciferous Vegetables and Their Bioactive Metabolites: from Prevention to Novel Therapies of Colorectal Cancer , 2022, Evidence-based complementary and alternative medicine : eCAM.
[7] H. Zhang,et al. The recent advances of glucosinolates and their metabolites: Metabolism, physiological functions and potential application strategies , 2022, Critical reviews in food science and nutrition.
[8] Shylendra Kumar,et al. Functional significance of underutilized high value cruciferous vegetables- an exotic gleam in the gloomy guise of their functional importance , 2022, South African Journal of Botany.
[9] E. Mazzon,et al. Beneficial Health Effects of Glucosinolates-Derived Isothiocyanates on Cardiovascular and Neurodegenerative Diseases , 2022, Molecules.
[10] I. Pires,et al. The Role of Glucosinolates from Cruciferous Vegetables (Brassicaceae) in Gastrointestinal Cancers: From Prevention to Therapeutics , 2022, Pharmaceutics.
[11] S. Park,et al. Expression Analysis of Phenylpropanoid Pathway Genes and Metabolomic Analysis of Phenylpropanoid Compounds in Adventitious, Hairy, and Seedling Roots of Tartary Buckwheat , 2021, Plants.
[12] J. Hodgson,et al. Glucosinolates From Cruciferous Vegetables and Their Potential Role in Chronic Disease: Investigating the Preclinical and Clinical Evidence , 2021, Frontiers in Pharmacology.
[13] O. Franco,et al. Nutritional and phytochemical characterization of radish (Raphanus sativus): A systematic review , 2021, Trends in Food Science & Technology.
[14] Jifang Zhang,et al. A Comparative Metabolomics Study of Flavonoids in Radish with Different Skin and Flesh Colors (Raphanus sativus L.). , 2020, Journal of agricultural and food chemistry.
[15] J. K. Kim,et al. Metabolite Profiling and Comparative Analysis of Secondary Metabolites in Chinese Cabbage, Radish, and Hybrid xBrassicoraphanus. , 2020, Journal of agricultural and food chemistry.
[16] A. Hernández-Almanza,et al. The value of bioactive compounds of cruciferous vegetables (Brassica) as antimicrobials and antioxidants: A review. , 2020, Journal of food biochemistry.
[17] L. Tang,et al. Cruciferous Vegetable Consumption and Stomach Cancer: A Case-Control Study , 2020, Nutrition and cancer.
[18] D. Moreno,et al. Sorting out the Value of Cruciferous Sprouts as Sources of Bioactive Compounds for Nutrition and Health , 2019, Nutrients.
[19] Jung Sun Kim,et al. Anti-Carcinogenic Glucosinolates in Cruciferous Vegetables and Their Antagonistic Effects on Prevention of Cancers , 2018, Molecules.
[20] Choon Nam Ong,et al. Profiling of Phenolic Compounds and Antioxidant Activity of 12 Cruciferous Vegetables , 2018, Molecules.
[21] Y. Hwang,et al. Dietary intake of soy and cruciferous vegetables and treatment-related symptoms in Chinese-American and non-Hispanic White breast cancer survivors , 2018, Breast Cancer Research and Treatment.
[22] S. Banihani. Radish (Raphanus sativus) and Diabetes , 2017, Nutrients.
[23] J. K. Kim,et al. Effect of Carbon Sources and Sucrose Concentrations on Shoot Organogenesis of Aloe saponaria , 2016 .
[24] C. Park,et al. Influence of Different Carbohydrates on Flavonoid Accumulation in Hairy Root Cultures of Scutellaria baicalensis , 2016, Natural product communications.
[25] Sun-Ju Kim,et al. Chungpihongsim radish (Raphanus sativus L. cv. Chungpihongsim) ameliorates ethanol-induced gastric injury in rats , 2016, Oriental Pharmacy and Experimental Medicine.
[26] J. K. Kim,et al. Metabolic Profiling and Antioxidant Assay of Metabolites from Three Radish Cultivars (Raphanus sativus) , 2016, Molecules.
[27] S. Park,et al. Methyl Jasmonate- and Light-Induced Glucosinolate and Anthocyanin Biosynthesis in Radish Seedlings , 2015, Natural product communications.
[28] P. Avato,et al. Brassicaceae: a rich source of health improving phytochemicals , 2015, Phytochemistry Reviews.
[29] R. Socha,et al. Phenolic profile and antioxidant activity in selected seeds and sprouts. , 2014, Food chemistry.
[30] S. Park,et al. Glucosinolate accumulation in three important radish ('Raphanus sativus') cultivars , 2013 .
[31] L. A. Biasi,et al. Fox grape cv. Bordô (Vitis labrusca L.) and grapevine cv. Chardonnay (Vitis vinifera L.) cultivated in vitro under different carbohydrates, amino acids and 6-Benzylaminopurine levels , 2013 .
[32] G. Sablok,et al. Review: role of carbon sources for in vitro plant growth and development , 2013, Molecular Biology Reports.
[33] D. Durzan,et al. Cell and Tissue Culture in Forestry , 2012, Forestry Sciences.
[34] M. Jeyaraj,et al. Optimization of Carbon Source for Hairy Root Growth and Withaferin A and Withanone Production in Withania somnifera , 2012, Natural product communications.
[35] M. Rajesh,et al. Chitosan enhances withanolides production in adventitious root cultures of Withania somnifera (L.) Dunal , 2012 .
[36] Qiaomei Wang,et al. Sucrose enhances the accumulation of anthocyanins and glucosinolates in broccoli sprouts. , 2011, Food chemistry.
[37] S. Amiri,et al. Enhancement of callus induction and regeneration efficiency from embryo cultures of Datura stramonium by adjusting carbon sources and concentrations , 2011 .
[38] S. Park,et al. Anthocyanin accumulation and expression of anthocyanin biosynthetic genes in radish (Raphanus sativus). , 2011, Journal of agricultural and food chemistry.
[39] M. Maziah,et al. Flavonoids production in Hydrocotyle bonariensis callus tissues , 2011 .
[40] Qiaomei Wang,et al. Effect of sucrose and mannitol on the accumulation of health-promoting compounds and the activity of metabolic enzymes in broccoli sprouts , 2011 .
[41] Qiaomei Wang,et al. Effect of salt stress on phenolic compounds, glucosinolates, myrosinase and antioxidant activity in radish sprouts , 2010 .
[42] L. Tian,et al. Sugars induce anthocyanin accumulation and flavanone 3-hydroxylase expression in grape berries , 2009, Plant Growth Regulation.
[43] P. Weathers,et al. Sugars proportionately affect artemisinin production , 2007, Plant Cell Reports.
[44] Pung-Ling Huang,et al. Enhancement of growth and regeneration efficiency from embryogenic callus cultures of Oncidium ‘Gower Ramsey’ by adjusting carbohydrate sources , 2006 .
[45] E. Baena-González,et al. Sugar sensing and signaling in plants: conserved and novel mechanisms. , 2006, Annual review of plant biology.
[46] M. S. Narayan,et al. Various Hexoses and di-hexoses Differently Influence Growth, Morphology and Pigment Synthesis in Transformed Root Cultures of Red Beet (Beta vulgaris) , 2004, Plant Cell, Tissue and Organ Culture.
[47] P. Weathers,et al. Alteration of biomass and artemisinin production in Artemisia annua hairy roots by media sterilization method and sugars , 2004, Plant Cell Reports.
[48] G. He,et al. Optimization of elicitors and precursors for paclitaxel production in cell suspension culture of Taxus chinensis in the presence of nutrient feeding , 2004 .
[49] T. Sotiropoulos,et al. In vitro Propagation of the Peach Rootstock: The Effect of Different Carbon Sources and Types of Sealing Material on Rooting , 2004, Biologia Plantarum.
[50] M. Hara,et al. Enhancement of anthocyanin biosynthesis by sugar in radish (Raphanus sativus) hypocotyl , 2003 .
[51] L. Lardet,et al. Differential carbohydrate metabolism conducts morphogenesis in embryogenic callus of Hevea brasiliensis (Müll. Arg.). , 2002, Journal of experimental botany.
[52] Saurabh Chattopadhyay,et al. Production of podophyllotoxin by plant cell cultures of Podophyllum hexandrum in bioreactor. , 2002, Journal of bioscience and bioengineering.
[53] S. Gibson,et al. Plant sugar-response pathways. Part of a complex regulatory web. , 2000, Plant physiology.
[54] B. Cuenca,et al. Influence of carbon source on shoot multiplication and adventitious bud regeneration in in vitro beech cultures , 2000, Plant Growth Regulation.
[55] J. Mérillon,et al. Sugar sensing and Ca2+-calmodulin requirement in Vitis vinifera cells producing anthocyanins. , 2000, Phytochemistry.
[56] H. Harada,et al. Micropropagation ofPrunus mume , 1996, Plant Cell, Tissue and Organ Culture.
[57] K. Ohba,et al. In vitro regeneration of Alnus cremastogyne Burk from epicotyl explants , 1996, Plant Cell Reports.
[58] A. Romano,et al. Role of carbohydrates in micropropagation of cork oak , 1995, Plant Cell, Tissue and Organ Culture.
[59] J. Sheen,et al. Sugar sensing in higher plants. , 1994, The Plant cell.
[60] B. Swedlund,et al. Sorbitol as the Primary Carbon Source for the Growth of Embryogenic Callus of Maize , 1993, Plant physiology.
[61] Xiaoling Yu,et al. Improved shoot multiplication of mature hazelnut (Corylus avellana L.) in vitro using glucose as a carbon source , 1993, Plant Cell Reports.
[62] S. Kwak,et al. Improvement of the catharanthine productivity in hairy root cultures ofCatharanthus roseus by using monosaccharides as a carbon source , 1992, Biotechnology Letters.
[63] F. Skoog,et al. A revised medium for rapid growth and bio assays with tobacco tissue cultures , 1962 .
[64] K. Paek,et al. Sucrose regulated enhanced induction of anthraquinone, phenolics, flavonoids biosynthesis and activities of antioxidant enzymes in adventitious root suspension cultures of Morinda citrifolia (L.) , 2011, Acta Physiologiae Plantarum.
[65] D. Barnes,et al. Phytochemical composition and biological activity of 8 varieties of radish (Raphanus sativus L.) sprouts and mature taproots. , 2011, Journal of food science.
[66] Hanan A. A. Taie. Antioxidant activities, total anthocyanins, phenolics and flavonoids contents of some sweetpotato genotypes under stress of different concentrations of sucrose and sorbitol. , 2009 .
[67] S. Korban,et al. Factors affectingin vitro establishment and shoot proliferation ofRosa hybrida L. andRosa Chinensis minima , 2008, In Vitro Cellular & Developmental Biology - Plant.
[68] Ansar Ali,et al. COMPARISON OF SUCROSE AND SORBITOL AS MAIN CARBON ENERGY SOURCES IN MICROPROPAGATION OF PEACH ROOTSTOCK GF-677 , 2007 .
[69] Trejgell Alina,et al. The effect of carbon source on callus induction and regeneration ability in Pharbitis nil , 2006, Acta Physiologiae Plantarum.
[70] L. Vieira,et al. The effects of silver nitrate and different carbohydrate sources on somatic embryogenesis in Coffea canephora , 2004, Plant Cell, Tissue and Organ Culture.
[71] L. Przywara,et al. Rola cukrowcow w roslinnych kulturach in vitro , 1999 .
[72] N. Welander,et al. Regulation of in vitro shoot multiplication in Syringa, Alnus and Malus by different carbon sources , 1989 .
[73] H. Beevers,et al. Absorption of Sugars by Plant Tissues. , 1964, Plant physiology.