scholarly journals Purified Quercetin From in vitro Cell Suspension Cultures of Caesalpinia pulcherrima Sw. and Its Antimicrobial Potentials

Author(s):  
GM Greeshma ◽  
JM Aswathy ◽  
Murukan Greeshma ◽  
Lawarence Bosco ◽  
Murugan K

Tribal people use the flower extract of <em>Caesalpinia pulcherrima<strong> </strong></em>to cure liver, stomach and skin disorders in Indian traditional medicine. This study aimed to evaluate the protective roles of purified quercetin extracted from suspension culture of <em>C. pulcherrima</em> against selected bacterial and fungal pathogens. A simple protocol was developed for callus production using leaf explants<em>.</em> 2, 4-D (2.5 mg/l), BAP (2.5 mg/l) + kin (1 mg/ml) was effective for optimal callus induction. Subsequently, cell suspension culture was established.  Role of effect of elicitors in cell suspension culture was carried. Sucrose, ABA and salicylic acid (SA) at different concentrations influenced cell biomass and quercetin accumulation. Cells cultured in the medium fortified with 45 g/L sucrose without ABA/SA showed the highest quercetin content (16.5 mg/g). Flavonoids was purified, fractionated by HPLC-DAD followed by NMR revealed the presence of quercetin, isoquercetin, quercetrin, rutin, quercetin 3-O-β-D-xyloside, quercetin 3-Oarabinopyranoside, quercetin 3-O- α-arabinopyranosyl (1→2) β-galactopyranoside,  isorhamnetin 3-O-rutinoside and an unknown compound. Subsequently, anthocyanin was evaluated for antimicrobial activity against selected Gram-positive bacteria (<em>S. aureus, Bacillus subtilis</em>, and <em>Enterococcus faecalis</em><em>)</em>, Gram-negative bacteria (<em>E. coli, </em>and <em>Pseudomonas aeruginosa</em>) and fungi such as <em>Aspergillus flavus, Candida albicans </em>and <em>Trichophyton rubrum</em>. Quercetin was found to be active against four bacteria and the fungi- <em>Candida albicans</em>. The highest inhibitory effects were found on <em>S. aureus</em> and <em>Enterococcus faecalis</em>. Gram negative bacteria showed more resistance i.e., with insignificant MIC and MBC values. Among the fungi, <em>Aspergillus flavus</em> and <em>Trichophyton rubrum</em> displayed remarkable MIC and MKC values. These results suggest that quercetin may be used as a natural antimicrobial agent. Future works are designed to trace the molecular mechanism of antimicrobial potentiality of quercetin against these tested pathogens

Plants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 664
Author(s):  
M. Moniruzzaman ◽  
Yun Zhong ◽  
Zhifeng Huang ◽  
Huaxue Yan ◽  
Lv Yuanda ◽  
...  

Agrobacterium-mediated transformation of epicotyl segment has been used in Citrus transgenic studies. The approach suffers, however, from limitations such as occasionally seed unavailability, the low transformation efficiency of juvenile tissues and the high frequency of chimeric plants. Therefore, a suspension cell culture system was established and used to generate transgenic plants in this study to overcome the shortcomings. The embryonic calli were successfully developed from undeveloped ovules of the three cultivars used in this study, “Sweet orange”-Egyptian cultivar (Citrus sinensis), “Shatangju” (Citrus reticulata) and “W. Murcott” (Citrus reticulata), on three different solid media. Effects of media, genotypes and ages of ovules on the induction of embryonic calli were also investigated. The result showed that the ovules’ age interferes with the callus production more significantly than media and genotypes. The 8 to 10 week-old ovules were found to be the best materials. A cell suspension culture system was established in an H+H liquid medium. Transgenic plants were obtained from Agrobacterium-mediated transformation of cell suspension as long as eight weeks subculture intervals. A high transformation rate (~35%) was achieved by using our systems, confirming BASTA selection and later on by PCR confirmation. The results demonstrated that transformation of cell suspension should be more useful for the generation of non-chimeric transgenic Citrus plants. It was also shown that our cell suspension culture procedure was efficient in maintaining the vigor and regeneration potential of the cells.


2014 ◽  
Vol 38 ◽  
pp. 76-82 ◽  
Author(s):  
Zohreh JALALPOUR ◽  
Leila SHABANI ◽  
Ladan AFGHANI ◽  
Majid SHARIFI-TEHRANI ◽  
Sayed-Asadollah AMINI

2008 ◽  
Vol 3 (11) ◽  
pp. 1398-1406 ◽  
Author(s):  
Stephanus J. Ferreira ◽  
Jens Kossmann ◽  
James R. Lloyd ◽  
Jan-Hendrik Groenewald

2012 ◽  
Vol 10 (1) ◽  
pp. 34 ◽  
Author(s):  
Dipto Bhattacharyya ◽  
Ragini Sinha ◽  
Srijani Ghanta ◽  
Amrita Chakraborty ◽  
Saptarshi Hazra ◽  
...  

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