Preprint Article Version 1 Preserved in Portico This version is not peer-reviewed

Micropropagation of Rare Scutellaria Havanensis Jacq. And Preliminary Studies on Antioxidant Capacity and Anti-cancer Potential

Version 1 : Received: 14 August 2021 / Approved: 16 August 2021 / Online: 16 August 2021 (14:50:44 CEST)

How to cite: Irvin, L.; Zavala Ortiz, Y.; Rivera, K.R.; Nanda Vaidya, B.; Sherman, S.H.; Negron Berrios, J.A.; Joshee, N.; Arun, A. Micropropagation of Rare Scutellaria Havanensis Jacq. And Preliminary Studies on Antioxidant Capacity and Anti-cancer Potential. Preprints 2021, 2021080346 (doi: 10.20944/preprints202108.0346.v1). Irvin, L.; Zavala Ortiz, Y.; Rivera, K.R.; Nanda Vaidya, B.; Sherman, S.H.; Negron Berrios, J.A.; Joshee, N.; Arun, A. Micropropagation of Rare Scutellaria Havanensis Jacq. And Preliminary Studies on Antioxidant Capacity and Anti-cancer Potential. Preprints 2021, 2021080346 (doi: 10.20944/preprints202108.0346.v1).

Abstract

We report the development of in vitro propagation protocols through adventitious shoot induction pathway for a rare and medicinal Scutellaria havanensis. In vitro propagation studies using nodal explants showed MS medium supplemented with 10µM 6-Benzylaminopurine induced highest number of adventitious shoots in a time dependent manner. A ten - day incubation was optimum for shoot bud induction as longer exposures resulted in hyperhydricity of the explants and shoots induced. We also report preliminary evidence of Agrobacterium tumefaciens EHA105 - mediated gene transfer transiently expressing of green fluorescent protein in this species. Transformation studies exhibited amenability of various explant tissues, internode being the most receptive. As the plant has medicinal value, research was carried out to evaluate its potential antioxidant capacity and the efficacy of methanolic leaf extracts in curbing the viability of human colorectal cancer cell line HCT116. Comparative total polyphenol, and flavonoid content measurement of fresh and air dried leaf extract revealed that the fresh leaf extracts contain higher total polyphenol and flavonoid content. The HCT 116 cell viability assessed by colorimetric assay using a 3-(4, 5-dimethyl-thiazol-2-yl)-2, 5-diphenyltetrazolium bromide, showed a steady growth inhibition after 24 hours of incubation. Scanning Electron Microscopy of leaf surface revealed high density of glandular and non-glandular trichomes. This research provides basis for the conservation of this rare plant and future phytochemical screening and clinical research.

Keywords

Conservation; HCT 116 cells; polyphenol; trichomes

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