Endogenous brassinosteroids in microalgae exposed to salt and low temperature stress

References

• Bajguz, A. (2000). Effect of brassinosteroids on nucleic acids and protein content in cultured cells of Chlorella vulgaris. Plant Physiology and Biochemistry, 38: 209–215.
   Web of Science ®Google Scholar
• Bajguz, A. (2002). Brassinosteroids and lead as stimulators of phytochelatins synthesis in Chlorella vulgaris. Journal of Plant Physiology, 159: 321–324.
   Web of Science ®Google Scholar
• Bajguz, A. (2009a). Isolation and characterization of brassinosteroids from algal cultures of Chlorella vulgaris Beijernck (Trebouxiophyceae). Journal of Plant Physiology, 166: 1946–1949.
   PubMed Web of Science ®Google Scholar
• Bajguz, A. (2009b). Brassinosteroid enhanced the level of abscisic acid in Chlorella vulgaris subjected to short-term heat stress. Journal of Plant Physiology, 166: 882–886.
   PubMed Web of Science ®Google Scholar
• Bajguz, A. (2010). An enhancing effect of exogenous brassinolide on the growth and antioxidant activity in Chlorella vulgaris cultures under heavy metal stress. Environmental and Experimental Botany, 68: 175–179.
   Web of Science ®Google Scholar
• Bajguz, A. (2011). Suppression of Chlorella vulgaris growth by cadmium, lead and copper stress and its restoration by endogenous brassinolide. Archives of Environmental Contamination and Toxicology, 60: 406–416.
   PubMed Web of Science ®Google Scholar
• Bajguz, A. & Asami, T. (2004). Effects of brassinazole, an inhibitor of brassinosteroid biosynthesis, on light- and dark-grown Chlorella vulgaris. Planta, 218: 869–877.
   PubMed Web of Science ®Google Scholar
• Bajguz, A. & Czerpak, R. (1998). Physiological and biochemical role of brassinosteroids and their structure-activity relationship in the green alga Chlorella vulgaris Beijerinck (Chlorophyceae). Journal of Plant Growth Regulation, 71: 131–139.
   Web of Science ®Google Scholar
• Bajguz, A. & Piotrowska-Niczyporuk, A. (2013). Synergistic effect of auxin and brassinosteroids on the growth and regulation of metabolite content in the green alga Chlorella vulgaris (Trebouxiophyceae). Plant Physiology and Biochemistry, 71: 290–297.
   PubMed Web of Science ®Google Scholar
• Bajguz, A. & Piotrowska-Niczyporuk, A. (2014). Interactive effect of brassinosteroids and cytokinins on growth, chlorophyll, monosaccharide and protein content in the green alga Chlorella vulgaris (Trebouxiophyceae). Plant Physiology and Biochemistry, 80: 176–183.
   PubMed Web of Science ®Google Scholar
• Bajguz, A. & Tretyn, A. (2003). The chemical characteristic and distribution of brassinosteroids in plants. Phytochemistry, 62: 1027–1046.
   PubMed Web of Science ®Google Scholar
• Bajguz, A., Bajguz, A.J. & Tryniszewska, E.A. (2013). Recent advances in medicinal applications of brassinosteroids, a group of plant hormones. In Studies in Natural Products Chemistry, vol. 40 (Atta-ur-Rahman, F.R.S., editor), 33–49. Elsevier, Amsterdam.
   Google Scholar
• Bartwell, A., Mall, R., Lohani, P., Guru, S.K. & Arora, S. (2013). Role of secondary metabolites and brassinosteroids in plant defense against environmental stresses. Journal of Plant Growth Regulation, 32: 216–232.
   Web of Science ®Google Scholar
• Bold, H.C. (1949). The morphology of Chlamydomonas chlamydogma sp. nov. Bulletin of the Torrey Botanical Club, 76: 101–108.
   Google Scholar
• Fariduddin, Q., Yusuf, M., Ahmad, I. & Ahmad, A. (2014). Brassinosteroids and their role in response of plants to abiotic stress. Biologia Plantarum, 58: 9–17.
   Web of Science ®Google Scholar
• Fujioka, S. & Yokota, T. (2003). Biosynthesis and metabolism of brassinosteroids. Annual Review of Plant Biology, 54: 137–164.
   PubMed Web of Science ®Google Scholar
• Oklestková, J., Rárová, L., Kvasnica, M. & Strnad, M. (2015). Brassinosteroids: synthesis and biological activities. Phytochemical Reviews, 14: 1053–1072.
   Web of Science ®Google Scholar
• Park, S.H., Han, K.S., Kim, T.W., Shim, J.K., Takatsuto, S., Yokoto, T. & Kim, S.K. (1999). In vivo and in vitro conversion of teasterone to typhasterol in cultured cells of Marchantia polymorpha. Plant and Cell Physiology, 40: 955–960.
   Web of Science ®Google Scholar
• Rajewska, I., Talarek, M. & Bajguz, A. (2016). Brassinosteroids and response of plants to heavy metal action. Frontiers in Plant Science, 7: 629.
   PubMed Web of Science ®Google Scholar
• Stirk, W.A., Bálint, P., Tarkowská, D., Novák, O., Strnad, M., Ördög, V. & van Staden, J. (2013a). Hormone profiles in microalgae: Gibberellins and brassinosteroids. Plant Physiology and Biochemistry, 70: 348–353.
   PubMed Web of Science ®Google Scholar
• Stirk, W.A., Ördög, V., Novák, O., Rolčík, J., Strnad, M., Bálint, P. & van Staden, J. (2013b). Auxin and cytokinin relationships in 24 microalgal strains. Journal of Phycology, 49: 459–467.
   PubMed Web of Science ®Google Scholar
• Stirk, W.A., Tarkowská, D., Turečová, V., Strnad, M. & van Staden, J. (2014). Abscisic acid, gibberellins and brassinosteroids in Kelpak®, a commercial seaweed extract made from Ecklonia maxima. Journal of Applied Phycology, 26: 561–567.
   Web of Science ®Google Scholar
• Takatsuto, S., Abe, H. & Gamoh, K. (1990). Evidence for brassinosteroids in strobilus of Equisetum arvense L. Agricultural and Biological Chemistry, 54: 1057–1059.
   Web of Science ®Google Scholar
• Tarkowská, D., Novák, O., Oklestková, J. & Strnad, M. (2016). The determination of 22 natural brassinosteroids in a minute sample of plant tissue by UHPLC-MS/MS. Analytical and Bioanalytical Chemistry, 408: 6799–6812.
   PubMed Web of Science ®Google Scholar
• Yokota, T., Kim, S.K., Fukui, Y., Takahashi, N., Takeuchi, Y. & Takematsu, T. (1987). Brassinosteroids and sterols from a green alga, Hydrodictyon reticulatum: configuration at C-24. Phytochemistry, 26: 503–506.
   Web of Science ®Google Scholar