Assessment of genetic, biochemical fidelity, and therapeutic activity of in vitro regenerated Hedychium coronarium

被引:4
作者
Behera, Shashikanta [1 ,2 ]
Kar, Subrat K. [4 ]
Monalisa, Kumari [1 ]
Mohapatra, Soumyajit [1 ,5 ]
Meher, Rajesh K. [2 ]
Barik, Durga P. [1 ]
Panda, Pratap C. [6 ]
Naik, Pradeep K. [2 ]
Naik, Soumendra K. [1 ,3 ]
机构
[1] Ravenshaw Univ, Dept Bot, Cuttack 753003, Odisha, India
[2] Sambalpur Univ, Ctr Excellence Nat Prod & Therapeut, Dept Biotechnol & Bioinformat, Sambalpur 768019, Odisha, India
[3] Ravenshaw Univ, Ctr Excellence Environm & Publ Hlth, Cuttack 753003, Odisha, India
[4] Rivaara Labs, BS-3,B-Wing,Kamal Palace, Nagpur 440010, Maharashtra, India
[5] CSIR, Cent Inst Med & Aromat Plants, Lucknow 226015, Uttar Pradesh, India
[6] Siksha O Anusandhan, Ctr Biotechnol, Sch Pharmaceut Sci, Bhubaneswar 751003, Odisha, India
关键词
Anticancer activity; Antioxidant activity; Callus; Organogenesis; Essential oil; PLANT-REGENERATION; CHEMICAL-COMPOSITION; ESSENTIAL OIL; J; KOENIG; AGAR CONCENTRATION; LEAF EXPLANTS; META-TOPOLIN; ANTIOXIDANT; CALLUS; IDENTIFICATION;
D O I
10.1007/s11627-023-10383-z
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Hedychium coronarium J. Koenig is a rhizomatous herb (Zingiberaceae family) and is well known for its uses in traditional systems of medicine for the treatment of various diseases. The plant has been over-exploited and enlisted as a threatened species in India. Thus, there is an urgent attention required for its conservation. Here, a callus-mediated in vitro plant regeneration protocol was developed using leaf sheath of H. coronarium. The optimal medium for callus induction (85.0%) and subsequent proliferation was found to be MS basal medium augmented with 3.0 mg L-1 N-6-benzyladenine (BA), 0.5 mg L-1 alpha-naphthaleneacetic acid (NAA), and 3.0% sucrose, and gelled with 0.5% agar. Optimum callus-mediated shoot organogenesis (78.3%; ca. 11.4 shoots/0.5 g of callus) was obtained on MS medium supplemented with 3.0 mg L-1 BA after 6 wk of culture. All the in vitro regenerated shoots were rooted (8.5 roots/shoot) successfully on plant growth regulator-free MS medium. About 90% plantlets were acclimatized on the planting tray filled with garden soil and sand (1:1). Transfer of these plants to larger pots containing garden soil and subsequent field transfer under full sun resulted in cent-percent survival. Monomorphic banding profile obtained using Random Amplified Polymorphic DNA (RAPD) and Inter Simple Sequence Repeat (ISSR) markers ascertained the clonal fidelity of the in vitro regenerated plants. Similarly, the biochemical fidelity of the in vitro regenerated plants vis-a-vis mother plant was ascertained by comparing the composition of essential oil through gas chromatography/mass spectrometry (GC/MS) analysis. Furthermore, the antioxidant activities estimated by DPPH and ABTS free radical scavenging assay and anticancer activities evaluated against two cell lines, i.e., MCF 7 and MDA-MB 231, also confirmed comparable effectiveness of in vitro regenerated plants to that of the mother plant. Thus, the study has the potential to provide a platform to achieve sustainability by using the in vitro regenerated H. coronarium in place of naturally available population.
引用
收藏
页码:602 / 620
页数:19
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