Plant Biotechnology
Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 13 No. 4, Issue of July 15, 2010
© 2010 by Pontificia Universidad Católica de Valparaíso -- Chile Received September 9, 2009 / Accepted March 17, 2010
DOI: 10.2225/vol13-issue4-fulltext-12
REPORT

Rapid multiplication and in vitro production of leaf biomass in Kaempferia galanga through tissue culture

Reena Parida
Centre of Biotechnology
Siksha ‘O’ Anusandhan University
PO- Khandagiri, Bhubaneswar-751030
Orissa, India 

Sujata Mohanty
Centre of Biotechnology
Siksha ‘O’ Anusandhan University
PO- Khandagiri, Bhubaneswar-751030
Orissa, India 

Ananya Kuanar
Centre of Biotechnology
Siksha ‘O’ Anusandhan University
PO- Khandagiri, Bhubaneswar-751030
Orissa, India 

Sanghamitra Nayak*
Centre of Biotechnology
Siksha ‘O’ Anusandhan University
PO- Khandagiri, Bhubaneswar-751030
Orissa, India
E-mail: sanghamitran@yahoo.com

*Corresponding author

Keywords: growth regulators, Kaempferia, in vitro propagation, leaf biomass.

Abbreviations:

BA: Benzyladenine
Ads: Adenine sulphate
IAA: Indoleacetic acid
IBA: Indolebutyric acid
NAA: Napthaleneacetic acid
RAPD: Random Amplified Polymorphic DNA

Abstract   Full Text

An efficient protocol has been established for rapid multiplication and in vitro production of leaf biomass in Kaempferia galanga L, a rare medicinal plant. Different plant growth regulators like Benzyladenine (BA), Indoleacetic acid (IAA), Indolebutyric acid (IBA), Napthaleneacetic acid (NAA) and adenine sulphates (Ads) have been tried for induction of multiple shoots using lateral bud of rhizome as explants. The highest rate of shoot multiplication (11.5 ± 0.6) shoot/explant as well as leaf biomass production (7.4 ± 0.3) gram/explant was observed on Murashige and Skoog medium supplemented with Benzyladenine (1 mg/l) and Indoleacetic acid (0.5 mg/l). Data of shoot multiplication and leaf biomass production were statistically analysed. Upon excission of leaves after 2 months of culture under sterile condition, the base of each plantlet was transferred to fresh media which could produce the same leaf biomass within another 2 months in a 50 ml culture tube containing 20 ml and 250 ml conical flasks containing 30 ml Murashige and Skoog medium. The rate of multiplication and leaf biomass production remained unchanged in subsequent subcultures. The regenerated plantlets were acclimatized in greenhouse and subsequently transferred to the field. Survival rate of the plantlets under ex vitro condition was 95 percent. Genetic fidelity of the regenerants was confirmed using random amplified polymorphic DNA (RAPD) marker. The protocol could be commercially utilized for large scale production of true-to-type plantlets and as an alternative method of leaf biomass production in Kaempferia galanga.

Supported by UNESCO / MIRCEN network