Fiziol. rast. genet. 2023, vol. 55, no. 5, 417-425, doi: https://doi.org/10.15407/frg2023.05.417

The effect of the tem­perature stress on the growth and content of bioactive compounds in the «hairy» roots Bidens pilosa L.

Matvieieva N.A.1, Duplij V.P.1,2, Ra­tushnyak Ya.I.1

  1. Institute of Cell Biology and Genetic Engineering, National Academy of Sciences of Ukraine 148 Akademika Zabolotnogo St., Kyiv, 03143, Ukraine
  2. Institute of Plant Physiology and Genetics, National Academy of Sciences of Ukraine 31/17 Vasylkivska, St., Kyiv, 03022, Ukraine

Genetic transformation using Agrobacterium rhizogenes can lead to variability in the content of compounds synthesized in different lines of «hairy» roots. Such differences may cause disparities in the survival of the samples under the effects of low and high temperatures as a stress factor. The analysis of such variability makes it possible to assess the impact of transformation on plants’ adaptive potential and to identify opportunities for increasing the content of compounds with antioxidant properties. This work aimed to compare the characteristics of the response of different lines of Bidens pilosa L. «hairy» roots to the effect of short-term temperature stress. For this purpose, the roots were cultivated in vitro and short-term exposed to low (7 °C) and high (36 °C) temperatures. The increase in the fresh weight, the content of flavonoids, and antioxidant activity were determined. The peculiarities of the response of «hairy» roots of different lines to the effect of short-term temperature stress were revealed. Differences in growth rate, synthesis of metabolites (flavonoids), and antioxidant activity of extracts from different root lines under the influence of temperature stress were observed. In particular, only the roots of one line were able to grow after a short-term temperature increase to 36 °C; the specific content of flavonoids significantly increased after the influence of both low and high temperatures; low-temperature stress did not affect antioxidant activity while increasing temperature led to an increase in antioxidant activity. Such features can probably be related to the differences between the lines, which are the separate transformation events and can differ from each other both in the place of insertion of transferred genes, in particular rol genes, and in the copy number and activity of genes which, accordingly, affects the metabolism of plant cells.

Keywords: Bidens pilosa L., Agrobacterium rhizogenes-mediated transformation, «hairy» roots, temperature stress, flavonoids, antioxidant activity

Fiziol. rast. genet.
2023, vol. 55, no. 5, 417-425

Full text and supplemented materials

Free full text: PDF  

References

1. Chen, K. & Otten, L. (2017). Natural Agrobacterium transformants: recent results and some theoretical considerations. Front. Plant Sci., 8, 283312. https://doi.org/10.3389/fpls.2017.01600

2. Chandra, S. (2012). Natural plant genetic engineer Agrobacterium rhizogenes: Role of T-DNA in plant secondary metabolism. Biotech. Let., 34, No. 3, pp. 407-415. https://doi.org/10.1007/s10529-011-0785-3

3. Bulgakov, V.P., Shkryl, Y.N., Veremeichik, G.N., Gorpenchenko, T.Y. & Vereshchagina, Y.V. (2013). Recent advances in the understanding of agrobacterium rhizogenes-derived genes and their effects on stress resistance and plant metabolism. Springer, Berlin, Heidelberg, pp. 1-22. https://doi.org/10.1007/10_2013_179

4. Dilshad, E., Noor, H., Nosheen, N., Gilani, S.R., Ali, U. & Khan, M.A. (2021). Influence of rol genes for enhanced biosynthesis of potent natural products (pp. 379-404), USA: John Wiley & Sons. https://doi.org/10.1002/9781119640929.ch13

5. Khan, A.N. & Dilshad, E. (2023). Enhanced antioxidant and anticancer potential of artemisia carvifolia buch transformed with rol a gene. Metabolites, 13, No. 3, 351. https://doi.org/10.3390/metabo13030351

6. Hussain, S., Awan, T.H., Waraich, E.A., Awan, M.I., Hussain, S., Awan, T.H., Waraich, E.A. & Awan, M.I. (Eds.). (2023). Plant abiotic stress responses and tolerance mechanisms. IntechOpen. https://doi.org/10.5772/intechopen.102138

7. Jaakola, L. & Hohtola, A. (2010). Effect of latitude on flavonoid biosynthesis in plants. Plant, Cell & Environ., 33, No. 8, pp. 1239-1247. https://doi.org/10.1111/j.1365-3040.2010.02154.x

8. Dong, N. & Lin, H. (2021). Contribution of phenylpropanoid metabolism to plant development and plant-environment interactions. J. Integr. Plant Biol., 63, No. 1, pp. 180-209. https://doi.org/10.1111/jipb.13054

9. Satyakam, Zinta, G., Singh, R.K. & Kumar, R. (2022). Cold adaptation strategies in plants - an emerging role of epigenetics and antifreeze proteins to engineer cold resilient plants. Front. Genet., 13, 909007. https://doi.org/10.3389/fgene.2022.909007

10. Choi, S., Kwon, Y.R., Hossain, M.A., Hong, S.W., Lee, B. ha & Lee, H. (2009). A mutation in ELA1, an age-dependent negative regulator of PAP1/MYB75, causes UV- and cold stress-tolerance in Arabidopsis thaliana seedlings. Plant Sci., 176, No. 5, pp. 678-686. https://doi.org/10.1016/j.plantsci.2009.02.010

11. Dela, G., Or, E., Ovadia, R., Nissim-Levi, A., Weiss, D. & Oren-Shamir, M. (2003). Changes in anthocyanin concentration and composition in 'Jaguar' rose flowers due to transient high-temperature conditions. Plant Sci., 164, No. 3, pp. 333-340. https://doi.org/10.1016/S0168-9452(02)00417-X

12. Ferreira, J.F.S., Luthria, D.L., Sasaki, T. & Heyerick, A. (2010). Flavonoids from Artemisia annua L. as antioxidants and their potential synergism with Artemisinin against malaria and cancer. Molecules, 15, No. 5, pp. 3135-3170. https://doi.org/10.3390/molecules15053135

13. PДkal, A. & Pyrzynska, K. (2014). Evaluation of aluminium complexation reaction for flavonoid content assay. Food Anal. Methods, 7, No. 9, pp. 1776-1782. https://doi.org/10.1007/s12161-014-9814-x

14. Zhao, H., Fan, W., Dong, J., Lu, J., Chen, J., Shan, L., Lin, Y. & Kong, W. (2008). Evaluation of antioxidant activities and total phenolic contents of typical malting barley varieties. Food Chem., 107, No. 1, pp. 296-304. https://doi.org/10.1016/j.foodchem.2007.08.018

15. Shomali, A., Das, S., Arif, N., Sarraf, M., Zahra, N., Yadav, V., Aliniaeifard, S., Chauhan, D.K. & Hasanuzzaman, M. (2022). Diverse physiological roles of flavonoids in plant environmental stress responses and tolerance. Plants, 11, No. 22, 3158. https://doi.org/10.3390/plants11223158

16. Boo, H.O., Chon, S.U. & Lee, S.Y. (2006). Effects of temperature and plant growth regulators on anthocyanin synthesis and phenylalanine ammonia-lyase activity in chicory (Cichorium intybus L.). J. Horticult. Sci. and Biotech., 81, No. 3, pp. 478-482. https://doi.org/10.1080/14620316.2006.11512091

17. Schulz, E., Tohge, T., Zuther, E., Fernie, A.R. & Hincha, D.K. (2016). Flavonoids are determinants of freezing tolerance and cold acclimation in Arabidopsis thaliana. Sci. Rep., 6, No. 1, 34027. https://doi.org/10.1038/srep34027

18. Albert, A., Sareedenchai, V., Heller, W., Seidlitz, H.K. & Zidorn, C. (2009). Temperature is the key to altitudinal variation of phenolics in Arnica montana L. cv. ARBO. Oecologia, 160, No. 1, pp. 1-8. https://doi.org/10.1007/s00442-009-1277-1

19. Matvieieva, N.A., Ratushnyak, Y.I., Duplij, V.P., Shakhovsky, A.M. & Kuchuk, M.V. (2021). Effect of temperature stress on the Althaea officinalis's «Hairy» roots carrying the human interferon a2b gene. Cytology and Genetics, 55, No. 3, pp. 207-212. https://doi.org/10.3103/S0095452721030051

20. Matvieieva, N., Havryliuk, O., Duplij, V. & Drobot, K. (2018). The effect of high temperature on the flavonoid accumulation in Artemisia «hairy» roots. Agrobiodiversity for Improving Nutrition, Health and Life Quality, No. 2, pp. 262-267. https://doi.org/10.15414/agrobiodiversity.2018.2585-8246.262-267